locus-tag	class	description
J168_00005	ENOG4108C33	Resolvase
J168_00017	ENOG4108C33	Resolvase
J168_00029	ENOG4108C33	Resolvase
J168_00036	ENOG4108C33	Resolvase
J168_00040	ENOG4106RHG	Yeca family
J168_00045	ENOG4108C33	Resolvase
J168_00046	ENOG4105XMH	SpoVT AbrB domain protein
J168_00071	ENOG4105CNU	cell division protein FtsK
J168_00079	ENOG4106RHG	Yeca family
J168_00083	ENOG4105CI4	it binds specifically double-stranded DNA at a 9 bp consensus (dnaA box) 5'-TTATC CA A CA A-3'. DnaA binds to ATP and to acidic phospholipids (By similarity)
J168_00084	ENOG4105CZ8	DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity. The beta chain is required for initiation of replication once it is clamped onto DNA, it slides freely (bidirectional and ATP- independent) along duplex DNA (By similarity)
J168_00085	ENOG4105C3X	it is required for DNA replication and normal SOS inducibility. RecF binds preferentially to single-stranded, linear DNA. It also seems to bind ATP (By similarity)
J168_00087	ENOG4105C7D	DNA gyrase negatively supercoils closed circular double- stranded DNA in an ATP-dependent manner and also catalyzes the interconversion of other topological isomers of double-stranded DNA rings, including catenanes and knotted rings (By similarity)
J168_00089	ENOG4108K0D	peptidase, M48
J168_00095	ENOG4105CSZ	Catalyzes the complicated ring closure reaction between the two acyclic compounds 1-deoxy-D-xylulose-5-phosphate (DXP) and 3-amino-2-oxopropyl phosphate (1-amino-acetone-3-phosphate or AAP) to form pyridoxine 5'-phosphate (PNP) and inorganic phosphate (By similarity)
J168_00097	ENOG4105CQX	Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol (By similarity)
J168_00102	ENOG4105CKF	membrane protein involved in aromatic hydrocarbon degradation
J168_00106	ENOG4105CN1	protease
J168_00107	ENOG41063SB	peptidase
J168_00109	ENOG4107VAM	peptidase, m28
J168_00119	ENOG4105DT9	hydrolase family 43
J168_00120	ENOG4105CT4	transporter
J168_00126	ENOG4105D2H	Uronic isomerase
J168_00127	ENOG4105CNT	hydrolase family 2
J168_00128	ENOG4105D9F	endo-1,4-beta-xylanase (EC 3.2.1.8)
J168_00134	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
J168_00142	ENOG4105DEI	Mannitol dehydrogenase
J168_00145	ENOG4105CXK	mandelate racemase muconate lactonizing
J168_00147	ENOG4105D0H	Alpha-glucuronidase (EC 3.2.1.139)
J168_00148	ENOG4105ETE	Transcriptional regulator (LacI family
J168_00149	ENOG4105C93	Xylose Isomerase
J168_00150	ENOG4105CB3	Required for the thiolation of cytidine in position 32 of tRNA, to form 2-thiocytidine (s(2)C32) (By similarity)
J168_00151	ENOG4105DH7	May be involved in recombination (By similarity)
J168_00154	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
J168_00157	ENOG4105X8U	Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. Together with TatC, TatB is part of a receptor directly interacting with Tat signal peptides. TatB may form an oligomeric binding site that transiently accommodates folded Tat precursor proteins before their translocation (By similarity)
J168_00158	ENOG4105DCX	Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. Together with TatB, TatC is part of a receptor directly interacting with Tat signal peptides (By similarity)
J168_00160	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
J168_00162	ENOG4107QHF	type ii secretion system protein e
J168_00163	ENOG4108HMW	glycyl-tRNA synthetase, alpha subunit
J168_00165	ENOG4107RDJ	Sulfotransferase
J168_00170	ENOG4105D05	Receptor
J168_00171	ENOG4105CFU	surface antigen
J168_00172	ENOG4105MA0	exported protein
J168_00178	ENOG4108Z67	carbohydrate kinase, thermoresistant glucokinase family
J168_00179	ENOG4105CT4	transporter
J168_00180	ENOG4105E2V	Glycosyltransferase 36
J168_00182	ENOG4105BZU	Histidine kinase
J168_00183	ENOG4108UI1	Probably functions as a manganese efflux pump (By similarity)
J168_00184	ENOG4108K2P	TRANSCRIPTIONal
J168_00185	ENOG4105EDR	glucose galactose transporter
J168_00186	ENOG4105QJH	Domain of unknown function (DUF718)
J168_00188	ENOG4105DIA	mandelate racemase muconate lactonizing
J168_00189	ENOG4105ERH	Fumarylacetoacetate hydrolase
J168_00190	ENOG4105I7Z	Short-chain dehydrogenase reductase Sdr
J168_00193	ENOG4105DSG	hydrolase family 43
J168_00199	ENOG4108IQF	Catalyzes the conversion of acetate into acetyl-CoA (AcCoA), an essential intermediate at the junction of anabolic and catabolic pathways. AcsA undergoes a two-step reaction. In the first half reaction, AcsA combines acetate with ATP to form acetyl-adenylate (AcAMP) intermediate. In the second half reaction, it can then transfer the acetyl group from AcAMP to the sulfhydryl group of CoA, forming the product AcCoA (By similarity)
J168_00201	ENOG41062QD	Membrane
J168_00202	ENOG4107QN1	sodium solute
J168_00204	ENOG4105DBD	Chaperone involved in the correct folding and assembly of outer membrane proteins. Recognizes specific patterns of aromatic residues and the orientation of their side chains, which are found more frequently in integral outer membrane proteins. May act in both early periplasmic and late outer membrane-associated steps of protein maturation (By similarity)
J168_00206	ENOG4105E2R	ROK family
J168_00208	ENOG4105CGK	Exodeoxyribonuclease III
J168_00214	ENOG4105DGI	Alkaline phosphatase
J168_00215	ENOG4105D28	Specifically methylates the N7 position of a guanine in 16S rRNA (By similarity)
J168_00219	ENOG4105ENT	Efflux transporter rnd family, mfp subunit
J168_00221	ENOG4105KDC	50s ribosomal protein l28
J168_00222	ENOG4105W0E	50S ribosomal protein L33
J168_00223	ENOG4105KHM	amidohydrolase 2
J168_00225	ENOG4105JSC	dimethylmenaquinone methyltransferase
J168_00226	ENOG4108KB2	LysR family Transcriptional regulator
J168_00227	ENOG4105CQX	Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol (By similarity)
J168_00229	ENOG4105C4R	Atp-dependent dna helicase
J168_00235	ENOG4108WC9	type VI secretion system effector, hcp1 family
J168_00240	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
J168_00247	ENOG4105D6F	Phosphatase
J168_00255	ENOG4105CS6	Rhs element vgr protein
J168_00262	ENOG4108ZF3	Phosphatase
J168_00263	ENOG4105D9P	serine threonine protein kinase
J168_00269	ENOG4105C2M	dna polymerase I
J168_00270	ENOG4105DBS	Key enzyme in heme biosynthesis. Catalyzes the oxidative decarboxylation of propionic acid side chains of rings A and B of coproporphyrinogen III (By similarity)
J168_00273	ENOG4105DRY	peptidase s9 prolyl oligopeptidase active site domain protein
J168_00278	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
J168_00280	ENOG4105E9Q	Acyl-transferase
J168_00281	ENOG4108YXN	Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs (By similarity)
J168_00291	ENOG4106N3V	dolichyl-phosphate beta-D-mannosyltransferase (EC 2.4.1.83)
J168_00293	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
J168_00297	ENOG4105BZP	glycoside hydrolase 15-related
J168_00298	ENOG4105D8W	glucose-6-phosphate 1-dehydrogenase
J168_00300	ENOG4108UHE	carbonic anhydrase
J168_00301	ENOG4105CJW	magnesium transporter
J168_00302	ENOG4105CD5	CoA-binding domain protein
J168_00304	ENOG4107QYD	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
J168_00305	ENOG4105E05	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
J168_00311	ENOG41063V1	Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid (By similarity)
J168_00314	ENOG4105E3A	(ABC) transporter
J168_00315	ENOG4105DA5	(ABC) transporter
J168_00316	ENOG4108JA0	Oxidoreductase, FAD NAD(P)-binding domain protein
J168_00317	ENOG4105ECQ	AraC Family Transcriptional Regulator
J168_00319	ENOG4105E0K	tonB-dependent siderophore receptor
J168_00321	ENOG4105PGM	cation diffusion facilitator family transporter
J168_00325	ENOG4105VZ8	Transcriptional regulator
J168_00327	ENOG4108IUW	ABC transporter
J168_00330	ENOG4105QV4	Tryptophan halogenase
J168_00334	ENOG4105CYM	Glutathione S-transferase
J168_00339	ENOG4105D52	delta-aminolevulinic acid dehydratase
J168_00343	ENOG4107EER	Component of the sulfite reductase complex that catalyzes the 6-electron reduction of sulfite to sulfide. This is one of several activities required for the biosynthesis of L- cysteine from sulfate. The flavoprotein component catalyzes the electron flow from NADPH - FAD - FMN to the hemoprotein component (By similarity)
J168_00345	ENOG4105E2X	shikimate dehydrogenase
J168_00348	ENOG4105DVT	helicase
J168_00349	ENOG4105CH6	catalase
J168_00352	ENOG4105CEH	Catalyzes the synthesis of dihydrouridine a modified base found in the D-loop of most tRNAs (By similarity)
J168_00354	ENOG4105XJC	Two component transcriptional regulator (Winged helix family
J168_00355	ENOG4105EB3	Histidine kinase
J168_00360	ENOG4105HJX	Biotin- acetyl-CoA-carboxylase ligase
J168_00372	ENOG4105VDW	Csbd family
J168_00373	ENOG4105C31	Tryptophanyl-tRNA synthetase
J168_00374	ENOG4108NNI	Beta-lactamase domain-containing protein
J168_00377	ENOG4105FDR	Membrane
J168_00382	ENOG4105D6C	Part of the ABC transporter complex MacAB involved in macrolide export. Transmembrane domains (TMD) form a pore in the inner membrane and the ATP-binding domain (NBD) is responsible for energy generation (By similarity)
J168_00383	ENOG4105ENT	Efflux transporter rnd family, mfp subunit
J168_00384	ENOG4108ZGX	Histidine kinase
J168_00385	ENOG4108S01	response regulator
J168_00388	ENOG4107VGR	Catalase
J168_00391	ENOG4105BZ6	Presumably involved in the processing and regular turnover of intracellular proteins. Catalyzes the removal of unsubstituted N-terminal amino acids from various peptides (By similarity)
J168_00392	ENOG4107URF	beta-phospho-glucomutase
J168_00393	ENOG4105DSF	transport protein
J168_00397	ENOG4105C0H	protease
J168_00401	ENOG4105DHQ	Histidine kinase
J168_00402	ENOG4105XJC	Two component transcriptional regulator (Winged helix family
J168_00403	ENOG4105ECP	epimerase
J168_00411	ENOG4105E0Y	RtcB Protein
J168_00417	ENOG4105EJ2	Transcriptional regulator
J168_00420	ENOG41066DG	(EAL) domain protein
J168_00423	ENOG4105C0P	Mg chelatase subunit ChlI
J168_00424	ENOG4105W0Z	cytoplasmic protein
J168_00425	ENOG4108YZA	Nitrogen regulatory protein pii
J168_00430	ENOG4105CCX	Catalyzes the production of spermidine from putrescine and decarboxylated S-adenosylmethionine (dcSAM), which serves as an aminopropyl donor (By similarity)
J168_00431	ENOG4105DP5	Catalyzes the biosynthesis of agmatine from arginine (By similarity)
J168_00432	ENOG4105CEY	Amp-dependent synthetase and ligase
J168_00434	ENOG4105EXC	Acyl-transferase
J168_00435	ENOG4105EMU	Dehydrogenase
J168_00438	ENOG4105C75	arginyL-tRNA synthetase
J168_00439	ENOG4105W5Q	DNA repair protein (RadC
J168_00440	ENOG4105CJS	Phosphopantothenoylcysteine decarboxylase
J168_00441	ENOG4108Z1K	This enzyme is involved in nucleotide metabolism it produces dUMP, the immediate precursor of thymidine nucleotides and it decreases the intracellular concentration of dUTP so that uracil cannot be incorporated into DNA (By similarity)
J168_00445	ENOG4105CKK	Glycosyl transferase, family 2
J168_00448	ENOG4105FA0	parb-like partition protein
J168_00449	ENOG4107QJE	Chromosome Partitioning Protein
J168_00451	ENOG4107QP2	Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) (By similarity)
J168_00452	ENOG4105CGK	Exodeoxyribonuclease III
J168_00453	ENOG4105EYM	Major Facilitator superfamily
J168_00455	ENOG4105ED7	Catalyzes the specific phosphorylation of 1,6-anhydro-N- acetylmuramic acid (anhMurNAc) with the simultaneous cleavage of the 1,6-anhydro ring, generating MurNAc-6-P. Is required for the utilization of anhMurNAc either imported from the medium or derived from its own cell wall murein, and thus plays a role in cell wall recycling (By similarity)
J168_00456	ENOG4105DR5	peptidase
J168_00457	ENOG4105DA0	Catalyzes the attachment of tyrosine to tRNA(Tyr) in a two-step reaction tyrosine is first activated by ATP to form Tyr- AMP and then transferred to the acceptor end of tRNA(Tyr) (By similarity)
J168_00464	ENOG4105ERD	Involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. Acts as DNA glycosylase that recognizes and removes damaged bases. Has a preference for oxidized purines, such as 7,8-dihydro-8-oxoguanine (8-oxoG). Has AP (apurinic apyrimidinic) lyase activity and introduces nicks in the DNA strand. Cleaves the DNA backbone by beta-delta elimination to generate a single-strand break at the site of the removed base with both 3'- and 5'-phosphates (By similarity)
J168_00466	ENOG4105DJ9	glucan biosynthesis protein
J168_00467	ENOG4105BZU	Histidine kinase
J168_00468	ENOG4107104	thymidine kinase
J168_00469	ENOG4105C4R	Atp-dependent dna helicase
J168_00472	ENOG4108YXG	UPF0502 protein
J168_00474	ENOG4105CUR	5'-nucleotidase, lipoprotein e(p4) family
J168_00475	ENOG4106EG9	Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) (By similarity)
J168_00476	ENOG4105QV4	Tryptophan halogenase
J168_00479	ENOG4105ETE	Transcriptional regulator (LacI family
J168_00481	ENOG4105E55	glycerol-3-phosphate acyltransferase
J168_00489	ENOG4105DQ4	alcohol dehydrogenase
J168_00490	ENOG4105BZ8	glutamate synthase
J168_00491	ENOG4105CBC	glutamate synthase
J168_00495	ENOG4105CUJ	penicillin amidase
J168_00497	ENOG4105EXG	Transcriptional regulator
J168_00500	ENOG4105D3Q	Sugar transferase
J168_00501	ENOG4105EAG	UDP-N-acetylglucosamine 2-epimerase
J168_00503	ENOG4108UHC	Glycosyl transferase, wecb taga cpsf family
J168_00504	ENOG4107RA4	Glycosyl transferase (Group 1
J168_00510	ENOG4105CAQ	asparagine synthetase
J168_00513	ENOG4105CMR	udp-glucose 4-epimerase
J168_00516	ENOG4105BZ1	(ABC) transporter
J168_00522	ENOG4105D1C	Catalyzes the ATP- as well as the pyrophosphate- dependent phosphorylation of a specific serine residue in HPr, a phosphocarrier protein of the phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS). HprK P also catalyzes the pyrophosphate-producing, inorganic phosphate-dependent dephosphorylation (phosphorolysis) of seryl-phosphorylated HPr (P- Ser-HPr). The two antagonistic activities of HprK P are regulated by several intracellular metabolites, which change their concentration in response to the absence or presence of rapidly metabolisable carbon sources (glucose, fructose, etc.) in the growth medium. Therefore, by controlling the phosphorylation state of HPr, HPrK P is a sensor enzyme that plays a major role in the regulation of carbon metabolism and sugar transport it mediates carbon catabolite repression (CCR), and regulates PTS-catalyzed carbohydrate uptake and inducer exclusion (By similarity)
J168_00540	ENOG4108I5C	dEAD DEAH box helicase
J168_00541	ENOG4108UT2	hemolysin iii
J168_00544	ENOG4107FW0	short-chain dehydrogenase reductase
J168_00545	ENOG4105CHR	reductase
J168_00550	ENOG4105DYS	nad(p)h dehydrogenase (quinone)
J168_00561	ENOG41067RQ	csbd family
J168_00565	ENOG4105D4Y	metalloprotease
J168_00570	ENOG4105K63	Thioredoxin
J168_00571	ENOG4105CSH	Transporter
J168_00579	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
J168_00585	ENOG4105CZI	D-fructose-1,6-bisphosphate 1-phosphohydrolase class 1
J168_00586	ENOG4105CGF	Aromatic amino acid aminotransferase
J168_00587	ENOG4105CHB	tonB-dependent Receptor
J168_00589	ENOG41082W1	Cupin 2, conserved barrel domain protein
J168_00590	ENOG4105C26	Dehydrogenase
J168_00595	ENOG4105DMF	Dehydrogenase
J168_00597	ENOG4105BZU	Histidine kinase
J168_00598	ENOG4105WH1	Two component transcriptional regulator luxr family
J168_00602	ENOG4108M3R	transcriptional activator CadC
J168_00603	ENOG4105RKW	reductase (By
J168_00619	ENOG4105EP6	Maltosyltransferase that uses maltose 1-phosphate (M1P) as the sugar donor to elongate linear or branched alpha-(1- 4)- glucans. Is involved in a branched alpha-glucan biosynthetic pathway from trehalose, together with TreS, Mak and GlgB (By similarity)
J168_00620	ENOG4105CG3	alpha amylase, catalytic region
J168_00621	ENOG4105C9C	Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position (By similarity)
J168_00624	ENOG4105EBR	Carboxylesterase
J168_00627	ENOG4105DR6	Trap dicarboxylate transporter, dctp subunit
J168_00629	ENOG4105CG6	trap dicarboxylate transporter dctm subunit
J168_00630	ENOG4105DSG	hydrolase family 43
J168_00631	ENOG4105ETE	Transcriptional regulator (LacI family
J168_00632	ENOG4105D50	Catalyzes the isomerization of 5-dehydro-4-deoxy-D- glucuronate to 3-deoxy-D-glycero-2,5-hexodiulosonate (By similarity)
J168_00633	ENOG4105CHR	reductase
J168_00635	ENOG4107TDE	lipolytic protein G-D-S-L family
J168_00639	ENOG4105MIR	Phenylalanine 4-monooxygenase
J168_00640	ENOG4108YXU	transcriptional regulator AsnC family
J168_00641	ENOG4105CNM	Receptor
J168_00642	ENOG4105D78	K07001 NTE family protein
J168_00644	ENOG4105DKW	ABC transporter
J168_00647	ENOG4108IJ8	ABC transporter
J168_00648	ENOG4105E90	ABC transporter
J168_00657	ENOG4105D1F	ATP-binding protein
J168_00658	ENOG4105M4E	phosphohistidine phosphatase, SixA
J168_00660	ENOG4107RZC	phospholipase d
J168_00661	ENOG4105KA0	thioesterase Superfamily protein
J168_00669	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
J168_00670	ENOG4105C5F	glutamine synthetase
J168_00672	ENOG4105BZU	Histidine kinase
J168_00673	ENOG4105CUX	Signal transduction histidine kinase
J168_00674	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
J168_00675	ENOG4108Z7T	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
J168_00676	ENOG4108Z7T	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
J168_00679	ENOG4105CHU	acetyl-coa acetyltransferase
J168_00686	ENOG4107YZP	Rhodanese domain protein
J168_00687	ENOG4105IX2	One of the proteins required for the normal export of preproteins out of the cell cytoplasm. It is a molecular chaperone that binds to a subset of precursor proteins, maintaining them in a translocation-competent state. It also specifically binds to its receptor SecA (By similarity)
J168_00688	ENOG4105CSF	NADPH-dependent glycerol-3-phosphate dehydrogenase
J168_00690	ENOG4105C7K	acetolactate synthase
J168_00691	ENOG4108TQ9	Histidine kinase
J168_00692	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
J168_00696	ENOG4108UIQ	Methylates the ribose at the nucleotide 34 wobble position in the two leucyl isoacceptors tRNA(Leu)(CmAA) and tRNA(Leu)(cmnm5UmAA). Catalyzes the methyl transfer from S- adenosyl-L-methionine to the 2'-OH of the wobble nucleotide (By similarity)
J168_00699	ENOG4105E2T	synthase III
J168_00700	ENOG4107R3N	Filamentation induced by cAMP protein fic
J168_00701	ENOG4107R3N	Filamentation induced by cAMP protein fic
J168_00702	ENOG4108J2P	Alpha beta hydrolase fold
J168_00703	ENOG4105PI0	Ferredoxin
J168_00704	ENOG410680H	amp-dependent synthetase and ligase
J168_00706	ENOG4107VBM	3-beta hydroxysteroid dehydrogenase isomerase
J168_00708	ENOG4105CPF	Cell wall formation (By similarity)
J168_00710	ENOG4105CNK	Required, probably indirectly, for the hydroxylation of 2-octaprenylphenol to 2-octaprenyl-6-hydroxy-phenol, the fourth step in ubiquinone biosynthesis (By similarity)
J168_00712	ENOG4105DR9	pseudouridine synthase
J168_00714	ENOG4108YZN	class I peptide chain release factor
J168_00716	ENOG4105D44	asparaginase
J168_00717	ENOG4105DGW	oligopeptidase A
J168_00723	ENOG4107R11	Transcriptional regulator
J168_00724	ENOG4107QP3	malate synthase g
J168_00726	ENOG4105BZU	Histidine kinase
J168_00732	ENOG4107QX3	carboxylase
J168_00733	ENOG4105C1G	acyl-Coa dehydrogenase
J168_00744	ENOG4105CKI	cobalamin synthesis protein
J168_00746	ENOG4108TZV	Membrane
J168_00748	ENOG4105D6Z	AFG1 family ATPase
J168_00749	ENOG4105K56	Transcriptional regulator
J168_00750	ENOG4108ZHJ	Organic hydroperoxide resistance protein
J168_00755	ENOG4105CJH	Alcohol dehydrogenase zinc-binding domain protein
J168_00758	ENOG4108R99	pseudouridine synthase
J168_00760	ENOG4108KPZ	tonB-dependent Receptor
J168_00762	ENOG4105CQ7	ATP-dependent helicase
J168_00763	ENOG4108W15	Protein of unknown function (DUF1456)
J168_00764	ENOG4105VT2	5-hydroxyisourate hydrolase
J168_00765	ENOG4105E1J	oxidoreductase
J168_00769	ENOG4105C5R	Aminotransferase
J168_00771	ENOG4105EQ2	LysR family Transcriptional regulator
J168_00772	ENOG4107RTG	Major Facilitator superfamily
J168_00774	ENOG4105CFB	Gamma-glutamyltranspeptidase (EC 2.3.2.2)
J168_00776	ENOG4105DU0	nucleoside hydrolase
J168_00778	ENOG4105C7N	Xanthine uracil vitamin C permease
J168_00781	ENOG4105ETT	transcriptional Regulator, LysR family
J168_00782	ENOG4105F8V	Hydrolase, tatD family
J168_00785	ENOG4106NZI	LysR family Transcriptional regulator
J168_00786	ENOG4105D94	Major Facilitator Superfamily
J168_00788	ENOG4105D3C	The physiological role of BioH is to remove the methyl group introduced by BioC when the pimeloyl moiety is complete. It allows to synthesize pimeloyl-ACP via the fatty acid synthetic pathway through the hydrolysis of the ester bonds of pimeloyl-ACP esters (By similarity)
J168_00789	ENOG4105NDF	NAD-dependent protein deacetylase which modulates the activities of several enzymes which are inactive in their acetylated form. May also have NAD-dependent lysine demalonylase and desuccinylase activity (By similarity)
J168_00790	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
J168_00794	ENOG4105E3W	Two component transcriptional regulator (Winged helix family
J168_00795	ENOG4105EB3	Histidine kinase
J168_00796	ENOG4105C1P	efflux transporter, rnd family, mfp subunit
J168_00797	ENOG4105BZS	acriflavin resistance protein
J168_00798	ENOG4105ENJ	RND efflux system, outer membrane lipoprotein
J168_00800	ENOG4105DAE	Methylenetetrahydrofolate reductase
J168_00801	ENOG4105WPN	DNA integration recombination invertion protein
J168_00802	ENOG4105DZ2	Transcriptional regulator
J168_00803	ENOG4108UZX	fmn reductase
J168_00806	ENOG4105CAX	The 2-keto-3-deoxygluconate permease transports the degraded pectin products into the bacterial cell, where they serve as carbon and energy sources. This is a hydrogen coupled transport system (By similarity)
J168_00808	ENOG4105ECR	NmrA family
J168_00816	ENOG4105C01	Dihydroxy-acid dehydratase
J168_00819	ENOG4108Z0R	Transferase
J168_00820	ENOG4105D2S	major facilitator superfamily
J168_00821	ENOG4105CPI	Metal Dependent Phosphohydrolase
J168_00827	ENOG41072AC	4-hydroxybenzoate 3-monooxygenase
J168_00830	ENOG4108JQ0	Key enzyme in the regulation of glycerol uptake and metabolism (By similarity)
J168_00831	ENOG4105D8C	Channel that permits osmotically driven movement of water in both directions. It is involved in the osmoregulation and in the maintenance of cell turgor during volume expansion in rapidly growing cells. It mediates rapid entry or exit of water in response to abrupt changes in osmolarity (By similarity)
J168_00832	ENOG4105C6V	Glycerol-3-phosphate dehydrogenase
J168_00833	ENOG4105E98	transcriptional regulator DeoR family
J168_00838	ENOG4105CHU	acetyl-coa acetyltransferase
J168_00841	ENOG4107RAW	3-carboxy-cis-cis-muconate cycloisomerase
J168_00842	ENOG4105F2Z	3-oxoadipate enol-lactonase
J168_00843	ENOG4108UWZ	4-Carboxymuconolactone decarboxylase
J168_00845	ENOG4107HP6	Transcriptional regulator
J168_00848	ENOG4105MH3	Protein of unknown function (DUF2490)
J168_00849	ENOG4107RE5	NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 (By similarity)
J168_00856	ENOG4107EXU	Short-chain dehydrogenase reductase Sdr
J168_00857	ENOG4105D3C	The physiological role of BioH is to remove the methyl group introduced by BioC when the pimeloyl moiety is complete. It allows to synthesize pimeloyl-ACP via the fatty acid synthetic pathway through the hydrolysis of the ester bonds of pimeloyl-ACP esters (By similarity)
J168_00859	ENOG4107EEK	Catalyzes the decarboxylative condensation of pimeloyl- acyl-carrier protein and L-alanine to produce 8-amino-7- oxononanoate (AON), acyl-carrier protein , and carbon dioxide (By similarity)
J168_00860	ENOG4105CZF	Catalyzes the conversion of dethiobiotin (DTB) to biotin by the insertion of a sulfur atom into dethiobiotin via a radical- based mechanism (By similarity)
J168_00861	ENOG41081UC	Inherit from COG: Competence protein
J168_00862	ENOG4105C4G	Synthesis of 3-octaprenyl-4-hydroxybenzoate (By similarity)
J168_00874	ENOG4105VS8	Flagellar biosynthetic protein fliq
J168_00878	ENOG4108HR8	type iii secretion
J168_00882	ENOG4107Y59	type iii secretion
J168_00885	ENOG4108JIR	Flagellum-specific ATP synthase
J168_00887	ENOG4108TN6	type iii secretion
J168_00888	ENOG4105K44	type iii secretion
J168_00890	ENOG4105FTC	Lytic transglycosylase catalytic
J168_00893	ENOG4105EGS	Mechanosensitive ion channel
J168_00894	ENOG4107RES	phosphoglycerol transferase I
J168_00897	ENOG4105CKW	Inner membrane protein yedI
J168_00898	ENOG4105BZU	Histidine kinase
J168_00899	ENOG4105CXW	Synthesizes alpha-1,4-glucan chains using ADP-glucose (By similarity)
J168_00900	ENOG4105C9C	Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position (By similarity)
J168_00901	ENOG4105C9C	Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position (By similarity)
J168_00906	ENOG4105K4T	epimerase
J168_00907	ENOG4107ZQV	short-chain dehydrogenase reductase
J168_00913	ENOG4105BZS	acriflavin resistance protein
J168_00914	ENOG4105CHR	reductase
J168_00916	ENOG4105C1J	atp-dependent rna helicase
J168_00920	ENOG4105CPP	Dehydrogenase, E1 component
J168_00921	ENOG4107RUY	(E1 component), alpha subunit
J168_00923	ENOG4105HJ8	Catalyzes the oxidative cleavage of the L-tryptophan (L- Trp) pyrrole ring (By similarity)
J168_00924	ENOG4105DUX	Transporter
J168_00927	ENOG4105E6K	4-Hydroxyphenylpyruvate dioxygenase
J168_00928	ENOG4105F1J	Homogentisate 1,2-dioxygenase
J168_00931	ENOG4105KJM	monovalent cation h antiporter subunit g
J168_00932	ENOG4105W4C	monovalent cation H antiporter subunit F
J168_00934	ENOG4107R4Z	monovalent cation h antiporter subunit d
J168_00935	ENOG4108ZE9	Monovalent cation H antiporter subunit C
J168_00936	ENOG4105D65	subunit l
J168_00941	ENOG4105NVB	glycoside hydrolase, family 19
J168_00945	ENOG4105C8V	SAICAR synthetase
J168_00946	ENOG41066UG	Regulatory DnaK co-chaperone. Direct interaction between DnaK and DjlA is needed for the induction of the wcaABCDE operon, involved in the synthesis of a colanic acid polysaccharide capsule, possibly through activation of the RcsB RcsC phosphotransfer signaling pathway. The colanic acid capsule may help the bacterium survive conditions outside the host (By similarity)
J168_00950	ENOG4107TE5	Lipid kinase
J168_00951	ENOG4105CRQ	synthase (Component I)
J168_00953	ENOG4105DDQ	anthranilate synthase
J168_00955	ENOG4108I0Q	anthranilate phosphoribosyltransferase
J168_00956	ENOG4105DK0	Indole-3-glycerol phosphate synthase
J168_00958	ENOG4107RYR	Transcriptional regulator, Crp Fnr family
J168_00959	ENOG4105FDS	Catalyzes the decarboxylation of S-adenosylmethionine to S-adenosylmethioninamine (dcAdoMet), the propylamine donor required for the synthesis of the polyamines spermine and spermidine from the diamine putrescine (By similarity)
J168_00961	ENOG4108S0N	Oxygenase that introduces the hydroxyl group at carbon five of 2-nonaprenyl-3-methyl-6-methoxy-1,4-benzoquinol resulting in the formation of 2-nonaprenyl-3-methyl-5-hydroxy-6-methoxy-1,4- benzoquinol (By similarity)
J168_00962	ENOG4108UM5	This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly (By similarity)
J168_00963	ENOG4108UJD	30S ribosomal protein S9
J168_00966	ENOG4105EJF	Accelerates the degradation of transcripts by removing pyrophosphate from the 5'-end of triphosphorylated RNA, leading to a more labile monophosphorylated state that can stimulate subsequent ribonuclease cleavage (By similarity)
J168_00967	ENOG4108UQY	Iron-storage protein
J168_00968	ENOG4105BZU	Histidine kinase
J168_00973	ENOG4108YX9	iron--sulfur cluster insertion protein erpA
J168_00976	ENOG4105DH2	Converts cobyric acid to cobinamide by the addition of aminopropanol on the F carboxylic group (By similarity)
J168_00979	ENOG4108J8Q	Catalyzes the facilitated diffusion of 2-acyl-glycero-3- phosphoethanolamine (2-acyl-GPE) into the cell (By similarity)
J168_00982	ENOG4105EM2	membrane
J168_00983	ENOG4105C12	Phosphoribosylglycinamide synthetase
J168_00985	ENOG4105DC1	bifunctional purine biosynthesis protein purh
J168_00986	ENOG4108UMZ	Cdp-alcohol phosphatidyltransferase
J168_00987	ENOG4105E8V	Alpha Beta Hydrolase Fold protein
J168_00988	ENOG41077RS	Phosphatase
J168_00993	ENOG4108HPI	phosphatidate Cytidylyltransferase
J168_00994	ENOG4105VY0	Activates ribosomal RNA transcription. Plays a direct role in upstream activation of rRNA promoters (By similarity)
J168_00999	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
J168_01003	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
J168_01005	ENOG4105KM4	Acetyl-CoA carboxylase, biotin carboxyl carrier protein
J168_01006	ENOG4108Z38	Catalyzes a trans-dehydration via an enolate intermediate (By similarity)
J168_01007	ENOG4105CSG	Required to facilitate the formation of correct disulfide bonds in some periplasmic proteins and for the assembly of the periplasmic c-type cytochromes. Acts by transferring electrons from cytoplasmic thioredoxin to the periplasm. This transfer involves a cascade of disulfide bond formation and reduction steps (By similarity)
J168_01008	ENOG4105VF7	tolerance protein
J168_01011	ENOG4105VV6	START domain-containing protein
J168_01013	ENOG4105E1F	short-chain dehydrogenase reductase
J168_01014	ENOG4108K8S	endonuclease I
J168_01015	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
J168_01016	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
J168_01019	ENOG4105E99	Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) (By similarity)
J168_01024	ENOG4105CE6	Adenylation and deadenylation of glutamate--ammonia ligase (By similarity)
J168_01025	ENOG4105EX9	Membrane
J168_01028	ENOG4108RDT	NADH dehydrogenase NAD(P)H nitroreductase)
J168_01029	ENOG4108YYC	ycei family
J168_01034	ENOG4105WSE	Subunit of malonate decarboxylase, it is an acyl carrier protein to which acetyl and malonyl thioester residues are bound via a 2'-(5''-phosphoribosyl)-3'-dephospho-CoA prosthetic group and turn over during the catalytic mechanism (By similarity)
J168_01037	ENOG41065ZS	Transfers 2'-(5-triphosphoribosyl)-3'-dephosphocoenzyme- A to the apo- acyl-carrier-protein of the malonate decarboxylase to yield holo- acyl-carrier-protein (By similarity)
J168_01038	ENOG4108K6F	triphosphoribosyl-dephospho-CoA synthase
J168_01040	ENOG4105CJF	Malonyl coA-acyl carrier protein transacylase
J168_01042	ENOG4105DRR	Transcriptional regulator, GntR family
J168_01050	ENOG4105DAQ	Component of the pyruvate dehydrogenase (PDH) complex, that catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2) (By similarity)
J168_01053	ENOG4107GJV	short-chain dehydrogenase reductase
J168_01056	ENOG4105PDP	Short chain dehydrogenase
J168_01058	ENOG4105CHF	Glutathione S-transferase
J168_01067	ENOG4105CD8	aminopeptidase N
J168_01069	ENOG4105EIB	trna rrna methyltransferase
J168_01075	ENOG4105ETE	Transcriptional regulator (LacI family
J168_01077	ENOG4105M2E	Channel that opens in response to stretch forces in the membrane lipid bilayer. May participate in the regulation of osmotic pressure changes within the cell (By similarity)
J168_01082	ENOG4105CZ1	Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA (By similarity)
J168_01083	ENOG4105CA8	Catalyzes the rearrangement of 1-deoxy-D-xylulose 5- phosphate (DXP) to produce the thiazole phosphate moiety of thiamine. Sulfur is provided by the thiocarboxylate moiety of the carrier protein ThiS. In vitro, sulfur can be provided by H(2)S (By similarity)
J168_01090	ENOG4105CNA	YD repeat protein
J168_01096	ENOG4105VUH	addiction module killer protein
J168_01104	ENOG4105W5Q	DNA repair protein (RadC
J168_01110	ENOG4107QMH	DNA methylase
J168_01128	ENOG4105D9I	Responsible for the addition of glutamate residues to the C-terminus of ribosomal protein S6 (By similarity)
J168_01130	ENOG4105ETX	regulatoR
J168_01131	ENOG4105BZU	Histidine kinase
J168_01136	ENOG4108ZQD	Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A (By similarity)
J168_01137	ENOG4105EHH	Cleaves type-4 fimbrial leader sequence and methylates the N-terminal (generally Phe) residue (By similarity)
J168_01141	ENOG4107QHF	type ii secretion system protein e
J168_01142	ENOG4107QHF	type ii secretion system protein e
J168_01144	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
J168_01145	ENOG4107TUY	Histidine kinase
J168_01146	ENOG4105CMV	Succinyl-CoA synthetase subunit beta
J168_01147	ENOG4105CH8	Succinyl-CoA ligase ADP-forming subunit alpha
J168_01152	ENOG4108X1T	PAAR repeat-containing protein
J168_01202	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
J168_01203	ENOG4105CQZ	Histidine kinase
J168_01216	ENOG4105ED4	portal protein
J168_01220	ENOG4105CQ3	Poorly processive error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by polIV. Exhibits no 3-5 exonuclease (proofreading) activity. May be involved in translesional synthesis in conjunction with the beta clamp from polIII (By similarity)
J168_01222	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
J168_01223	ENOG4105BZU	Histidine kinase
J168_01226	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
J168_01227	ENOG4105CCQ	Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins (By similarity)
J168_01228	ENOG4105CHN	ATP-dependent specificity component of the Clp protease. It directs the protease to specific substrates. Can perform chaperone functions in the absence of ClpP (By similarity)
J168_01234	ENOG4105EIN	peptidylprolyl cis-trans isomerase
J168_01237	ENOG4108RW0	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
J168_01239	ENOG4108UMW	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
J168_01240	ENOG4107RZZ	dna polymerase iii epsilon subunit
J168_01241	ENOG4108ZF3	Phosphatase
J168_01244	ENOG4105DKP	glycosyl transferase, family 9
J168_01245	ENOG4108W7E	Catalyzes the ATP-dependent phosphorylation of the 3- deoxy-D-manno-octulosonic acid (Kdo) residue in Kdo-lipid IV(A) at the 4-OH position (By similarity)
J168_01246	ENOG4105IES	Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA (By similarity)
J168_01247	ENOG4105CM1	Catalyzes, together with MoaC, the conversion of 5'-GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
J168_01248	ENOG4108YXW	Together with MoaA, is involved in the conversion of 5'- GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
J168_01249	ENOG4105M00	molybdopterin converting factor, subunit 1
J168_01250	ENOG4108ZAF	Molybdopterin
J168_01260	ENOG4107QMP	dna polymerase iii subunits gamma and tau
J168_01261	ENOG4105KDX	Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection (By similarity)
J168_01262	ENOG4105F3K	May play a role in DNA repair. It seems to be involved in an RecBC-independent recombinational process of DNA repair. It may act with RecF and RecO (By similarity)
J168_01263	ENOG4105K59	histidine triad (HIT) protein
J168_01265	ENOG4105F8C	transglutaminase domain-containing protein
J168_01267	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
J168_01269	ENOG41089I4	Inherit from COG: Glycosyl transferase, family 2
J168_01272	ENOG4108UHJ	MAF-like protein
J168_01273	ENOG4105FCQ	metal-binding, possibly nucleic acid-binding protein
J168_01274	ENOG4105VGS	50s ribosomal protein l32
J168_01275	ENOG4105CCZ	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids (By similarity)
J168_01277	ENOG4105CJF	Malonyl coA-acyl carrier protein transacylase
J168_01278	ENOG4105CHR	reductase
J168_01279	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
J168_01280	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
J168_01282	ENOG4105HHA	aminodeoxychorismate lyase
J168_01283	ENOG4107QRG	dna polymerase iii
J168_01287	ENOG4108JU7	Transcriptional regulator
J168_01288	ENOG4105CR4	methylisocitrate lyase
J168_01289	ENOG4105BZN	citrate synthase
J168_01290	ENOG4108I0Z	Aconitate hydratase
J168_01291	ENOG4105YAJ	CopG Arc MetJ
J168_01293	ENOG4105C7F	AcnD-accessory protein PrpF
J168_01296	ENOG4105DN3	alpha-2-macroglobulin domain protein
J168_01299	ENOG4108JQB	penicillin-binding protein 1C
J168_01305	ENOG4105M3Z	response regulator
J168_01307	ENOG4107QJR	hflk protein
J168_01308	ENOG4105EPW	hflc protein
J168_01311	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
J168_01312	ENOG4105CD8	aminopeptidase N
J168_01314	ENOG4105F6U	Short-chain dehydrogenase reductase Sdr
J168_01315	ENOG4108XFH	Transcriptional regulator
J168_01328	ENOG4105CVJ	phosphoglycerate mutase
J168_01329	ENOG4107Z4K	Catalyzes the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. Together with NAD(P)HX epimerase, which catalyzes the epimerization of the S- and R-forms, the enzyme allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration (By similarity)
J168_01331	ENOG4105BZP	glycoside hydrolase 15-related
J168_01332	ENOG4105CYX	Short-chain dehydrogenase reductase Sdr
J168_01333	ENOG4105CWX	Alpha-1,2-mannosidase
J168_01337	ENOG4105C3M	thioredoxin reductase
J168_01342	ENOG4105C7W	Xanthine dehydrogenase
J168_01343	ENOG4105DIP	Molybdopterin dehydrogenase FAD-binding
J168_01344	ENOG4107XKX	isoquinoline 1-oxidoreductase, alpha subunit
J168_01351	ENOG4105DS7	Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair (By similarity)
J168_01354	ENOG4105C0B	DNA polymerase III (alpha subunit)
J168_01357	ENOG4105EPD	Oligopeptide transporter, Opt family
J168_01360	ENOG4105DRY	peptidase s9 prolyl oligopeptidase active site domain protein
J168_01363	ENOG4106AXJ	AraC family transcriptional regulator
J168_01368	ENOG4108JA2	transcriptioN-repair coupling factor
J168_01370	ENOG4105D6S	protein involved in catabolism of external DNA
J168_01371	ENOG4105E3W	Two component transcriptional regulator (Winged helix family
J168_01372	ENOG4105EB3	Histidine kinase
J168_01374	ENOG4105CT7	inner membrane cred family protein
J168_01379	ENOG4105C20	Catalyzes the attachment of glutamate to tRNA(Glu) in a two-step reaction glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu) (By similarity)
J168_01380	ENOG4105MYN	Zinc uptake regulation protein
J168_01382	ENOG4105C1P	efflux transporter, rnd family, mfp subunit
J168_01383	ENOG4105BZS	acriflavin resistance protein
J168_01384	ENOG4105ENJ	RND efflux system, outer membrane lipoprotein
J168_01385	ENOG4108JGH	Tetr family transcriptional regulator
J168_01387	ENOG4105CF7	AraC family transcriptional regulator
J168_01389	ENOG4105CC0	LysR family Transcriptional regulator
J168_01390	ENOG4105F27	Major Facilitator
J168_01391	ENOG4108FN7	Aldo keto reductase
J168_01397	ENOG4105UGU	tonB-dependent Receptor
J168_01401	ENOG4105CMQ	Chloride channel
J168_01414	ENOG4105BZU	Histidine kinase
J168_01415	ENOG4105FE9	pseudouridine synthase
J168_01416	ENOG4105BZU	Histidine kinase
J168_01419	ENOG4108YYX	Globally modulates RNA abundance by binding to RNase E (Rne) and regulating its endonucleolytic activity. Can modulate Rne action in a substrate-dependent manner by altering the composition of the degradosome. Modulates RNA-binding and helicase activities of the degradosome (By similarity)
J168_01420	ENOG4105FQP	Beta-lactamase
J168_01422	ENOG4105BZU	Histidine kinase
J168_01423	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
J168_01424	ENOG4105ENJ	RND efflux system, outer membrane lipoprotein
J168_01430	ENOG4105BZ1	(ABC) transporter
J168_01438	ENOG4108R5K	PPIases accelerate the folding of proteins (By similarity)
J168_01439	ENOG4105WG9	Conserved Protein
J168_01444	ENOG4107QR8	Thioredoxin
J168_01446	ENOG4105C8T	Leucyl-tRNA synthetase
J168_01449	ENOG4108Z1W	Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) (By similarity)
J168_01452	ENOG4108UXA	Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA (By similarity)
J168_01455	ENOG4105MPN	Membrane
J168_01456	ENOG4108Z03	MAF-like protein
J168_01457	ENOG4105C03	ribonuclease
J168_01458	ENOG4105QD6	exported protein
J168_01460	ENOG4105D1U	peptidase U62 modulator of DNA gyrase
J168_01461	ENOG4105N42	UPF0307 protein
J168_01462	ENOG4105CMS	peptidase U62, modulator of DNA gyrase
J168_01465	ENOG4105CTB	Polyprenyl synthetase
J168_01466	ENOG41067QG	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
J168_01467	ENOG4105D3U	Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine (By similarity)
J168_01468	ENOG4105G6Z	alkaline phosphatase
J168_01470	ENOG41082K6	Converts the free carboxyl group of a malonyl-thioester to its methyl ester by transfer of a methyl group from S-adenosyl- L-methionine (SAM). It allows to synthesize pimeloyl-ACP via the fatty acid synthetic pathway (By similarity)
J168_01472	ENOG4105K4H	Nlp p60 protein
J168_01473	ENOG4105K4H	Nlp p60 protein
J168_01474	ENOG41090X3	Peptidyl-prolyl cis-trans isomerase
J168_01476	ENOG4105MWK	D-amino acid dehydrogenase, small subunit
J168_01477	ENOG4105DC8	reductase
J168_01481	ENOG4105C9K	Endothelin-converting enzyme 1
J168_01482	ENOG4105C9K	Endothelin-converting enzyme 1
J168_01487	ENOG4105DHP	deoxycytidine triphosphate deaminase
J168_01492	ENOG4105CBM	Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 (By similarity)
J168_01493	ENOG4108RRZ	Transcription elongation factor GreB
J168_01496	ENOG4107VIJ	nudix hydrolase
J168_01497	ENOG4105D7A	ATP-binding protein
J168_01499	ENOG4105DJ4	phosphatidylserine decarboxylase
J168_01501	ENOG4105C76	Specifically methylates the 50S ribosomal protein L3 on a specific glutamine residue (By similarity)
J168_01502	ENOG4105D10	5-enolpyruvylshikimate-3-phosphate phospholyase
J168_01503	ENOG4105C5I	Dehydrogenase
J168_01504	ENOG4105CM3	Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate (By similarity)
J168_01508	ENOG4105DI7	Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs (By similarity)
J168_01509	ENOG4108ZGB	N-(5'-phosphoribosyl)anthranilate isomerase
J168_01511	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
J168_01513	ENOG4105F6H	The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate (By similarity)
J168_01514	ENOG4107QTG	Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl- CoA (By similarity)
J168_01515	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
J168_01518	ENOG4105BZU	Histidine kinase
J168_01521	ENOG4107FW0	short-chain dehydrogenase reductase
J168_01522	ENOG4105CP7	Triose-phosphate isomerase
J168_01525	ENOG4105KWU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
J168_01526	ENOG4105ES3	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
J168_01527	ENOG4105CYU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
J168_01528	ENOG4105CQV	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
J168_01529	ENOG4105GKE	subunit e
J168_01530	ENOG4107QIZ	NADH dehydrogenase
J168_01531	ENOG4107R0R	NADH dehydrogenase subunit g
J168_01532	ENOG4105CMZ	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient. This subunit may bind ubiquinone (By similarity)
J168_01533	ENOG4105P3U	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
J168_01534	ENOG4105DF2	NADH dehydrogenase subunit j
J168_01536	ENOG4105D65	subunit l
J168_01537	ENOG4105C8S	subunit m
J168_01538	ENOG4105CNR	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
J168_01540	ENOG4105K7D	Required for maturation of 30S ribosomal subunits (By similarity)
J168_01541	ENOG4105CHV	Transcription elongation factor NusA
J168_01542	ENOG4107QHU	One of the essential components for the initiation of protein synthesis. Protects formylmethionyl-tRNA from spontaneous hydrolysis and promotes its binding to the 30S ribosomal subunits. Also involved in the hydrolysis of GTP during the formation of the 70S ribosomal complex (By similarity)
J168_01543	ENOG4105KG7	Associates with free 30S ribosomal subunits (but not with 30S subunits that are part of 70S ribosomes or polysomes). Essential for efficient processing of 16S rRNA. May interact with the 5'-terminal helix region of 16S rRNA (By similarity)
J168_01544	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
J168_01545	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
J168_01546	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
J168_01548	ENOG4105D18	nicotinate-nucleotide pyrophosphorylase
J168_01550	ENOG4108UM6	Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) (By similarity)
J168_01551	ENOG4105CY8	phosphoribosylaminoimidazole carboxylase atpase subunit
J168_01552	ENOG4105CK4	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
J168_01553	ENOG4105M2J	Glutaredoxin
J168_01555	ENOG41076UM	multiple antibiotic resistance (MarC)-related protein
J168_01556	ENOG4108KPZ	tonB-dependent Receptor
J168_01557	ENOG4105EWT	decarboxylase family
J168_01558	ENOG4108HRK	Histidine kinase
J168_01570	ENOG4108YGG	dna repair protein
J168_01575	ENOG4105EVH	UPF0753 protein
J168_01577	ENOG4105DND	Transcriptional regulator
J168_01580	ENOG4105WH1	Two component transcriptional regulator luxr family
J168_01583	ENOG4105CHJ	isochorismatase hydrolase
J168_01586	ENOG4107SFI	Major Facilitator superfamily
J168_01589	ENOG4105CB8	Multifunctional enzyme that catalyzes the SAM-dependent methylation of uroporphyrinogen III at position C-2 and C-7 to form precorrin-2 and then position C-12 or C-18 to form trimethylpyrrocorphin 2. It also catalyzes the conversion of precorrin-2 into siroheme. This reaction consists of the NAD- dependent oxidation of precorrin-2 into sirohydrochlorin and its subsequent ferrochelation into siroheme (By similarity)
J168_01591	ENOG4105CB8	Multifunctional enzyme that catalyzes the SAM-dependent methylation of uroporphyrinogen III at position C-2 and C-7 to form precorrin-2 and then position C-12 or C-18 to form trimethylpyrrocorphin 2. It also catalyzes the conversion of precorrin-2 into siroheme. This reaction consists of the NAD- dependent oxidation of precorrin-2 into sirohydrochlorin and its subsequent ferrochelation into siroheme (By similarity)
J168_01593	ENOG4108N8X	transition metal ion binding
J168_01598	ENOG4108ZXC	Two component transcriptional regulator, luxr family
J168_01606	ENOG4105DY9	regulatoR
J168_01612	ENOG4105W39	Membrane
J168_01631	ENOG4105EWI	Short-chain dehydrogenase reductase Sdr
J168_01633	ENOG410626R	Converts the free carboxyl group of a malonyl-thioester to its methyl ester by transfer of a methyl group from S-adenosyl- L-methionine (SAM). It allows to synthesize pimeloyl-ACP via the fatty acid synthetic pathway (By similarity)
J168_01642	ENOG4107RUK	Involved in iron-sulfur cluster biogenesis. Binds a 4Fe- 4S cluster, can transfer this cluster to apoproteins, and thereby intervenes in the maturation of Fe S proteins. Could also act as a scaffold chaperone for damaged Fe S proteins (By similarity)
J168_01643	ENOG41090A4	Pterin carbinolamine dehydratase
J168_01645	ENOG4105DUN	Mediates zinc uptake. May also transport other divalent cations (By similarity)
J168_01646	ENOG4108NST	exported protein
J168_01647	ENOG4105EI2	Pseudouridine synthase
J168_01648	ENOG4105C03	ribonuclease
J168_01650	ENOG4105C72	UPF0176 protein
J168_01652	ENOG4108V1T	peptidylprolyl cis-trans isomerase
J168_01654	ENOG4107QQG	Dehydrogenase
J168_01656	ENOG4108KU3	Integrase
J168_01661	ENOG4105CEY	Amp-dependent synthetase and ligase
J168_01662	ENOG4105C0W	non-ribosomal peptide synthetase
J168_01665	ENOG4105F2I	Transposase
J168_01670	ENOG4105F2I	Transposase
J168_01673	ENOG4105F2I	Transposase
J168_01679	ENOG4105BZK	Transcription regulator that activates transcription by stimulating RNA polymerase (RNAP) recycling in case of stress conditions such as supercoiled DNA or high salt concentrations. Probably acts by releasing the RNAP, when it is trapped or immobilized on tightly supercoiled DNA. Does not activate transcription on linear DNA. Probably not involved in DNA repair (By similarity)
J168_01682	ENOG4105BZK	Transcription regulator that activates transcription by stimulating RNA polymerase (RNAP) recycling in case of stress conditions such as supercoiled DNA or high salt concentrations. Probably acts by releasing the RNAP, when it is trapped or immobilized on tightly supercoiled DNA. Does not activate transcription on linear DNA. Probably not involved in DNA repair (By similarity)
J168_01683	ENOG4105NI8	Cytosine-specific methyltransferase
J168_01688	ENOG4107QJE	Chromosome Partitioning Protein
J168_01695	ENOG4107YH6	single-stranded DNA-binding protein
J168_01696	ENOG4105C73	Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone (By similarity)
J168_01697	ENOG4105NI8	Cytosine-specific methyltransferase
J168_01701	ENOG41080R2	UPF0102 protein
J168_01709	ENOG4105F9F	transposase
J168_01737	ENOG4105W5Q	DNA repair protein (RadC
J168_01760	ENOG4106NZI	LysR family Transcriptional regulator
J168_01768	ENOG4105BZQ	cdp-diacylglycerol-glycerol-3-phosphate 3-phosphatidyltransferase
J168_01769	ENOG4105CII	The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrC both incises the 5' and 3' sides of the lesion. The N-terminal half is responsible for the 3' incision and the C-terminal half is responsible for the 5' incision (By similarity)
J168_01772	ENOG4105CET	Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria (By similarity)
J168_01773	ENOG4105CHD	Transfers the gamma-phosphate of ATP to the 4'-position of a tetraacyldisaccharide 1-phosphate intermediate (termed DS-1- P) to form tetraacyldisaccharide 1,4'-bis-phosphate (lipid IVA) (By similarity)
J168_01774	ENOG4105BZ1	(ABC) transporter
J168_01777	ENOG4108EC8	DNA internalization-related competence protein ComEC
J168_01779	ENOG4105CQU	Part of the ABC transporter complex LolCDE involved in the translocation of mature outer membrane-directed lipoproteins, from the inner membrane to the periplasmic chaperone, LolA. Responsible for the formation of the LolA-lipoprotein complex in an ATP-dependent manner (By similarity)
J168_01780	ENOG4105D60	lipoprotein releasing system transmembrane protein
J168_01782	ENOG410681N	tpr repeat protein
J168_01787	ENOG410612Q	succinate dehydrogenase (cytochrome b-556 subunit)
J168_01789	ENOG4106XY2	Folate-binding protein involved in regulating the level of ATP-DnaA and in the modification of some tRNAs. It is probably a key factor in regulatory networks that act via tRNA modification, such as initiation of chromosomal replication (By similarity)
J168_01792	ENOG4105CHC	glucokinase (EC 2.7.1.2)
J168_01793	ENOG4108Q79	6-phosphogluconolactonase (EC 3.1.1.31)
J168_01794	ENOG4105C01	Dihydroxy-acid dehydratase
J168_01795	ENOG4108UHU	Aldolase
J168_01800	ENOG4105N7H	Cytochrome
J168_01808	ENOG4105BZU	Histidine kinase
J168_01809	ENOG4105BZM	domain protein
J168_01814	ENOG4105D1N	poly(r)-hydroxyalkanoic acid synthase, class
J168_01816	ENOG4106PT6	cdpdiacylglycerol-serine O-phosphatidyltransferase
J168_01820	ENOG4105CF9	Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation dephosphorylation (By similarity)
J168_01823	ENOG4108RBP	3'-to-5' exoribonuclease specific for small oligoribonucleotides (By similarity)
J168_01824	ENOG4108Z6B	deaminase
J168_01825	ENOG4105KST	dependent repressor
J168_01826	ENOG4105C56	H( )-stimulated, divalent metal cation uptake system (By similarity)
J168_01829	ENOG41085AN	Transfers a GMP moiety from GTP to Mo-molybdopterin (Mo- MPT) cofactor (Moco or molybdenum cofactor) to form Mo- molybdopterin guanine dinucleotide (Mo-MGD) cofactor (By similarity)
J168_01830	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
J168_01832	ENOG4105CGK	Exodeoxyribonuclease III
J168_01839	ENOG4105D06	uba thif-type nad fad binding protein
J168_01840	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
J168_01841	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
J168_01842	ENOG4105CNE	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane (By similarity)
J168_01844	ENOG4105HSZ	Cytoskeletal protein that is involved in cell-shape control through regulation of the length of the long axis (By similarity)
J168_01846	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
J168_01847	ENOG4108UGX	Major role in the synthesis of nucleoside triphosphates other than ATP. The ATP gamma phosphate is transferred to the NDP beta phosphate via a ping-pong mechanism, using a phosphorylated active-site intermediate (By similarity)
J168_01850	ENOG4105CHU	acetyl-coa acetyltransferase
J168_01852	ENOG41082MI	Protein CrcB homolog
J168_01854	ENOG4105D1H	recombination factor protein RarA
J168_01856	ENOG4107Y7W	Participates in the translocation of lipoproteins from the inner membrane to the outer membrane. Only forms a complex with a lipoprotein if the residue after the N-terminal Cys is not an aspartate (The Asp acts as a targeting signal to indicate that the lipoprotein should stay in the inner membrane) (By similarity)
J168_01858	ENOG4105CNU	cell division protein FtsK
J168_01859	ENOG4105C3M	thioredoxin reductase
J168_01861	ENOG4108R4Z	Functions in the N-end rule pathway of protein degradation where it conjugates Leu, Phe and, less efficiently, Met from aminoacyl-tRNAs to the N-termini of proteins containing an N-terminal arginine or lysine (By similarity)
J168_01862	ENOG4105K9U	however, it seems to stimulate more or less all the activities of the other two initiation factors, IF-2 and IF-3 (By similarity)
J168_01863	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
J168_01864	ENOG4105KAE	Involved in the modulation of the specificity of the ClpAP-mediated ATP-dependent protein degradation (By similarity)
J168_01866	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
J168_01870	ENOG4105BZU	Histidine kinase
J168_01872	ENOG4105BZU	Histidine kinase
J168_01873	ENOG4105BZU	Histidine kinase
J168_01877	ENOG4107R88	Chemotaxis protein (CheV)
J168_01879	ENOG4108ZC9	flagellar basal-body rod protein flgc
J168_01880	ENOG410822I	Flagellar hook capping protein
J168_01881	ENOG4105BZE	flagellar hook protein, FlgE
J168_01882	ENOG4108KPB	Flagellar basal-body rod protein FlgF
J168_01883	ENOG4105CGA	flagellar basal-body rod protein FlgG
J168_01884	ENOG4107W7W	Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation (By similarity)
J168_01885	ENOG4105D92	Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation (By similarity)
J168_01886	ENOG4108ZW7	flagellar rod assembly protein muramidase flgj
J168_01888	ENOG4105DTJ	flagellar hook-associated protein
J168_01890	ENOG4107W9T	flagellar hook-associated
J168_01891	ENOG4105MQ3	flagellar protein FliS
J168_01895	ENOG4105DTW	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
J168_01896	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
J168_01897	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
J168_01900	ENOG4108P1X	synthase
J168_01901	ENOG4105H9W	Short-chain dehydrogenase reductase Sdr
J168_01902	ENOG4105CHR	reductase
J168_01908	ENOG4107RGC	Glycosyl transferase, family 2
J168_01909	ENOG4105VQ0	flagellar hook-basal body complex protein fliE
J168_01910	ENOG4105C1F	The M ring may be actively involved in energy transduction (By similarity)
J168_01911	ENOG4105CS3	FliG is one of three proteins (FliG, FliN, FliM) that forms the rotor-mounted switch complex (C ring), located at the base of the basal body. This complex interacts with the CheY and CheZ chemotaxis proteins, in addition to contacting components of the motor that determine the direction of flagellar rotation (By similarity)
J168_01913	ENOG4108JIR	Flagellum-specific ATP synthase
J168_01917	ENOG4105D24	FliM is one of three proteins (FliG, FliN, FliM) that forms the rotor-mounted switch complex (C ring), located at the base of the basal body. This complex interacts with the CheY and CheZ chemotaxis proteins, in addition to contacting components of the motor that determine the direction of flagellar rotation (By similarity)
J168_01918	ENOG4105DD5	Flagellar motor switch protein
J168_01919	ENOG4105K0P	flagellar biosynthesis protein
J168_01920	ENOG4105CN7	Flagellar biosynthetic protein FliP
J168_01923	ENOG4105VS8	Flagellar biosynthetic protein fliq
J168_01924	ENOG4105D19	Role in flagellar biosynthesis (By similarity)
J168_01925	ENOG4105BZU	Histidine kinase
J168_01926	ENOG4105BZU	Histidine kinase
J168_01927	ENOG4105BZU	Histidine kinase
J168_01928	ENOG4105D00	flagellar biosynthetic protein flhB
J168_01929	ENOG4105D7B	Flagellar biosynthesis protein flha
J168_01930	ENOG4105FZW	flagellar biosynthesis regulator FlhF
J168_01931	ENOG4107R21	site-determining protein
J168_01932	ENOG4105DN4	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
J168_01933	ENOG4108VYJ	response regulator receiver protein
J168_01935	ENOG4105CBS	Chea signal transduction histidine kinase
J168_01937	ENOG4105C4X	radical SAM domain protein
J168_01952	ENOG41088T4	Helicase IV
J168_01968	ENOG4105ZXK	Dehydrogenase
J168_01973	ENOG4105W5Q	DNA repair protein (RadC
J168_01980	ENOG4105DFP	Integrase
J168_01981	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
J168_01982	ENOG4105CP4	Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth (By similarity)
J168_01983	ENOG4105CN0	Catalyzes the oxidation of 5,10- methylenetetrahydrofolate to 5,10-methenyltetrahydrofolate and then the hydrolysis of 5,10-methenyltetrahydrofolate to 10- formyltetrahydrofolate (By similarity)
J168_01985	ENOG4105CKD	glutathione-regulated potassium-efflux system protein
J168_01986	ENOG4105C3Y	UTP-glucose-1-phosphate uridylyltransferase
J168_01988	ENOG4105ESV	Glycosyl transferase, family 4
J168_01989	ENOG4105CFV	Tetratricopeptide repeat protein
J168_01991	ENOG41080YA	This protein is one of the two subunits of integration host factor, a specific DNA-binding protein that functions in genetic recombination as well as in transcriptional and translational control (By similarity)
J168_01992	ENOG4105CAV	thus facilitating recognition of the initiation point. It is needed to translate mRNA with a short Shine-Dalgarno (SD) purine-rich sequence (By similarity)
J168_01993	ENOG4105CAT	Cytidine monophosphate kinase
J168_01994	ENOG4105YK5	50S ribosomal protein L36
J168_01997	ENOG4105DWY	Agmatine deiminase
J168_02003	ENOG4105DRS	transport system, permease
J168_02004	ENOG4105F0P	binding-protein-dependent transport systems inner membrane Component
J168_02010	ENOG4105K9H	YciI-like protein
J168_02011	ENOG4108KVX	Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpB that pull DNA away from mid-cell into both cell halves (By similarity)
J168_02012	ENOG4105K8I	Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpA that pull DNA away from mid-cell into both cell halves (By similarity)
J168_02013	ENOG4105FE9	pseudouridine synthase
J168_02017	ENOG4105CHM	Aminotransferase
J168_02018	ENOG4107EV4	once thought to export heme, this seems not to be the case, but its exact role is uncertain. Responsible for energy coupling to the transport system (By similarity)
J168_02019	ENOG4105CA5	Required for the export of heme to the periplasm for the biogenesis of c-type cytochromes (By similarity)
J168_02020	ENOG41060IM	Heme exporter protein
J168_02022	ENOG4108ZKK	Heme chaperone required for the biogenesis of c-type cytochromes. Transiently binds heme delivered by CcmC and transfers the heme to apo-cytochromes in a process facilitated by CcmF and CcmH (By similarity)
J168_02023	ENOG4105DA4	cytochrome c-type biogenesis protein
J168_02025	ENOG4105KWW	Biogenesis protein
J168_02026	ENOG4108M1T	Cytochrome c-type biogenesis protein
J168_02029	ENOG4108JJ8	(ABC) transporter
J168_02030	ENOG4108JJ9	ABC, transporter
J168_02031	ENOG4105C4M	(Ubiquinol oxidase) subunit I
J168_02032	ENOG4105CFY	cytochrome d ubiquinol oxidase, subunit ii
J168_02037	ENOG4105C2S	Catalyzes the NADPH dependent reduction of L-gamma- glutamyl 5-phosphate into L-glutamate 5-semialdehyde and phosphate. The product spontaneously undergoes cyclization to form 1-pyrroline-5-carboxylate (By similarity)
J168_02038	ENOG4105CGT	Catalyzes the transfer of a phosphate group to glutamate to form glutamate 5-phosphate which rapidly cyclizes to 5- oxoproline (By similarity)
J168_02040	ENOG4105CH7	arginosuccinase
J168_02041	ENOG4105C0N	N-acetylglutamate semialdehyde dehydrogenase
J168_02043	ENOG4105CAS	nag kinase
J168_02046	ENOG4105CDH	Citrulline--aspartate ligase
J168_02047	ENOG4105DBV	ornithine carbamoyltransferase
J168_02049	ENOG4105C8N	cysteinyl-tRNA synthetase
J168_02050	ENOG4105P9C	Participates in cysteine desulfuration mediated by SufS. Cysteine desulfuration mobilizes sulfur from L-cysteine to yield L-alanine and constitutes an essential step in sulfur metabolism for biosynthesis of a variety of sulfur-containing biomolecules. Functions as a sulfur acceptor for SufS, by mediating the direct transfer of the sulfur atom from the S-sulfanylcysteine of SufS, an intermediate product of cysteine desulfuration process (By similarity)
J168_02052	ENOG4108V7X	Transcription factor that acts by binding directly to the RNA polymerase (RNAP). Required for negative regulation of rRNA expression and positive regulation of several amino acid biosynthesis promoters
J168_02053	ENOG4105VAS	Could be involved in insertion of integral membrane proteins into the membrane (By similarity)
J168_02054	ENOG4105CD3	dihydroorotase
J168_02058	ENOG4105CPD	ethanolamine ammonia-lyase
J168_02059	ENOG4107FQ9	ethanolamine ammonia-lyase
J168_02070	ENOG4108VXP	Specifically catalyzes the dephosphorylation of 2- phosphoglycolate. Is involved in the dissimilation of the intracellular 2-phosphoglycolate formed during the DNA repair of 3'-phosphoglycolate ends, a major class of DNA lesions induced by oxidative stress (By similarity)
J168_02071	ENOG4108HWB	Non-specific O-methyltransferase that catalyzes the 2 O- methylation steps in the ubiquinone biosynthetic pathway (By similarity)
J168_02072	ENOG4105D6T	Catalyzes the deamination of 5-methylthioadenosine and S-adenosyl-L-homocysteine into 5-methylthioinosine and S-inosyl-L- homocysteine, respectively. Is also able to deaminate adenosine (By similarity)
J168_02074	ENOG4105DRH	Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase (By similarity)
J168_02075	ENOG4105CK3	Lysine 2,3-aminomutase YodO family protein
J168_02076	ENOG4105BZU	Histidine kinase
J168_02079	ENOG4105ECY	inositol monophosphatase
J168_02080	ENOG4105CK4	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
J168_02083	ENOG4105C5H	ABC transporter
J168_02084	ENOG4105C1J	atp-dependent rna helicase
J168_02085	ENOG4109003	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis (By similarity)
J168_02086	ENOG4105CNG	UPF0061 protein
J168_02088	ENOG4108RXX	maleylacetoacetate isomerase
J168_02089	ENOG4105VEQ	Cold shock protein
J168_02090	ENOG4108VWS	Yaeq family
J168_02091	ENOG4105CBX	hi0933 family
J168_02093	ENOG4105D0M	Protease HtpX homolog
J168_02094	ENOG4106F3G	Catalyzes the tRNA-independent activation of glutamate in presence of ATP and the subsequent transfer of glutamate onto a tRNA(Asp). Glutamate is transferred on the 2-amino-5-(4,5- dihydroxy-2-cyclopenten-1-yl) moiety of the queuosine in the wobble position of the QUC anticodon (By similarity)
J168_02095	ENOG4105CHR	reductase
J168_02099	ENOG4105DC6	This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex (By similarity)
J168_02100	ENOG4105C5C	n-acetylmuramoyl-l-alanine amidase
J168_02101	ENOG4105K8N	protein family UPF0079, ATPase
J168_02102	ENOG4105DR1	Catalyzes the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. Together with NAD(P)HX epimerase, which catalyzes the epimerization of the S- and R-forms, the enzyme allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration (By similarity)
J168_02103	ENOG4105EH2	Catalyzes the conversion of epoxyqueuosine (oQ) to queuosine (Q), which is a hypermodified base found in the wobble positions of tRNA(Asp), tRNA(Asn), tRNA(His) and tRNA(Tyr) (By similarity)
J168_02104	ENOG4105DVS	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
J168_02106	ENOG4105E6M	Sulphatase-modifying factor protein
J168_02109	ENOG4105DQE	DNA ligase
J168_02123	ENOG4105C26	Dehydrogenase
J168_02125	ENOG4105MP0	transposase
J168_02145	ENOG4108V3W	Chemotaxis protein, CheW
J168_02146	ENOG4105C8Q	Methyl-accepting chemotaxis
J168_02147	ENOG4108VX5	3-methyladenine DNA glycosylase
J168_02148	ENOG4107QRT	dEAD DEAH box helicase
J168_02151	ENOG4105KB2	stringent starvation protein b
J168_02152	ENOG4107MKT	Stringent starvation protein a
J168_02153	ENOG4105EIX	cytochrome c1
J168_02154	ENOG4105DJ5	Component of the ubiquinol-cytochrome c reductase complex (complex III or cytochrome b-c1 complex), which is a respiratory chain that generates an electrochemical potential coupled to ATP synthesis (By similarity)
J168_02155	ENOG4108R5F	Component of the ubiquinol-cytochrome c reductase complex (complex III or cytochrome b-c1 complex), which is a respiratory chain that generates an electrochemical potential coupled to ATP synthesis (By similarity)
J168_02156	ENOG4105E4C	Lytic transglycosylase catalytic
J168_02159	ENOG4105CIW	Catalyzes the methylthiolation of N6- (dimethylallyl)adenosine (i(6)A), leading to the formation of 2- methylthio-N6-(dimethylallyl)adenosine (ms(2)i(6)A) at position 37 in tRNAs that read codons beginning with uridine (By similarity)
J168_02160	ENOG4105C9A	Phoh family
J168_02162	ENOG4105KGE	Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA (By similarity)
J168_02164	ENOG4108JU5	Magnesium and cobalt efflux protein
J168_02168	ENOG4105D38	putrescine abc transporter
J168_02169	ENOG4105F38	ABC transporter, permease
J168_02170	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
J168_02174	ENOG4107RUE	extracellular solute-binding protein family 1
J168_02175	ENOG4108JPX	Catalyzes the transfer of the alpha-amino group from S- adenosyl-L-methionine (SAM) to 7-keto-8-aminopelargonic acid (KAPA) to form 7,8-diaminopelargonic acid (DAPA). It is the only animotransferase known to utilize SAM as an amino donor (By similarity)
J168_02178	ENOG4105CFQ	glutamine synthetase
J168_02179	ENOG4105CJP	fad dependent oxidoreductase
J168_02180	ENOG4105BZU	Histidine kinase
J168_02181	ENOG4105W3S	hemerythrin-like, metal-binding protein
J168_02182	ENOG4105CSH	Transporter
J168_02184	ENOG4107QKC	Oxidoreductase alpha (molybdopterin) subunit
J168_02185	ENOG4107H9G	Necessary for formate dehydrogenase activity (By similarity)
J168_02186	ENOG4105FCD	Major Facilitator
J168_02189	ENOG4106BRA	Membrane
J168_02190	ENOG4105BZU	Histidine kinase
J168_02191	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
J168_02192	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
J168_02193	ENOG4105C7I	Dehydrogenase
J168_02195	ENOG4105C1P	efflux transporter, rnd family, mfp subunit
J168_02196	ENOG4105BZS	acriflavin resistance protein
J168_02197	ENOG4108M60	Transcriptional regulator
J168_02198	ENOG4105BZ3	General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) (By similarity)
J168_02199	ENOG4105DE4	1-phosphofructokinase
J168_02200	ENOG4105DM4	PTS System
J168_02208	ENOG4107QT7	Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA (By similarity)
J168_02209	ENOG4107QN8	Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA (By similarity)
J168_02210	ENOG4105VIE	preprotein translocase, subunit YajC
J168_02211	ENOG4105C6U	Exchanges the guanine residue with 7-aminomethyl-7- deazaguanine in tRNAs with GU(N) anticodons (tRNA-Asp, -Asn, -His and -Tyr). After this exchange, a cyclopentendiol moiety is attached to the 7-aminomethyl group of 7-deazaguanine, resulting in the hypermodified nucleoside queuosine (Q) (7-(((4,5-cis- dihydroxy-2-cyclopenten-1-yl)amino)methyl)-7-deazaguanosine) (By similarity)
J168_02212	ENOG4105E2N	Transfers and isomerizes the ribose moiety from AdoMet to the 7-aminomethyl group of 7-deazaguanine (preQ1-tRNA) to give epoxyqueuosine (oQ-tRNA) (By similarity)
J168_02220	ENOG4105CZ5	Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate (By similarity)
J168_02221	ENOG4105E08	Glycoside hydrolase, family 9
J168_02222	ENOG4105CFB	Gamma-glutamyltranspeptidase (EC 2.3.2.2)
J168_02223	ENOG4105K5D	4fe-4S ferredoxin iroN-sulfur binding
J168_02226	ENOG4108ZEF	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate (By similarity)
J168_02227	ENOG4106H78	methyltransferase
J168_02228	ENOG4105CJX	Molecular chaperone. Has ATPase activity (By similarity)
J168_02244	ENOG4107QTZ	amino acid
J168_02247	ENOG4105DC7	peptidase M24
J168_02249	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
J168_02252	ENOG41080HI	glycine oxidase
J168_02253	ENOG4105CTU	Proline racemase
J168_02255	ENOG4105CCP	Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Acts as a receptor for the complex formed by the signal recognition particle (SRP) and the ribosome-nascent chain (RNC)
J168_02256	ENOG4105CEN	a g-specific adenine glycosylase
J168_02257	ENOG4105KMG	Could be a mediator in iron transactions between iron acquisition and iron-requiring processes, such as synthesis and or repair of Fe-S clusters in biosynthetic enzymes (By similarity)
J168_02258	ENOG4105CQZ	Histidine kinase
J168_02261	ENOG4105DKD	Incises the DNA at the 3' side of a lesion during nucleotide excision repair. Incises the DNA farther away from the lesion than UvrC. Not able to incise the 5' site of a lesion. When a lesion remains because UvrC is not able to induce the 3' incision, Cho incises the DNA. Then UvrC makes the 5' incision. The combined action of Cho and UvrC broadens the substrate range of nucleotide excision repair (By similarity)
J168_02264	ENOG4105QNF	Outer membrane lipoprotein
J168_02266	ENOG4105CSU	acyl-Coa dehydrogenase
J168_02268	ENOG4105C2V	Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) (By similarity)
J168_02272	ENOG4107VBM	3-beta hydroxysteroid dehydrogenase isomerase
J168_02273	ENOG4108JMX	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
J168_02274	ENOG4105CCZ	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids (By similarity)
J168_02279	ENOG4108NQK	Catalyzes the transfer of a glucuronic acid (GlcA) residue from UDP-glucuronate to mannose-alpha-1,3-glucose-beta- 1,4-glucose-P-P-polyisoprenyl to form the lipid-linked tetrasaccharide GlcA-Man-Glc(2)-PP-Pol, with a glucuronic acid- beta-mannose linkage. Is involved in the biosynthesis of the exopolysaccharide xanthan, since it catalyzes the fourth glycosylation step in the assembly of the pentasaccharide-P-P- polyisoprenyl repeating unit of xanthan. Is unable to use the trisaccharide acceptor freed from the pyrophosphate lipid moiety. Does not show specificity for the lipidic portion of the acceptor. Shows diminished activity when tested with 6-O-acetyl-mannose- alpha-1,3-glucose-beta-1,4-glucose-P-P-polyisoprenyl, a
J168_02281	ENOG4107Y2G	Glycosyl transferase (Group 1
J168_02286	ENOG4105D3Q	Sugar transferase
J168_02290	ENOG4105WJX	transcriptional regulator MERR family
J168_02291	ENOG4108ZUF	This protein is one of the two subunits of integration host factor, a specific DNA-binding protein that functions in genetic recombination as well as in transcriptional and translational control (By similarity)
J168_02292	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
J168_02293	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
J168_02294	ENOG4108YZX	Binds directly to 23S ribosomal RNA and is necessary for the in vitro assembly process of the 50S ribosomal subunit. It is not involved in the protein synthesizing functions of that subunit (By similarity)
J168_02295	ENOG41082NX	50s ribosomal protein l35
J168_02297	ENOG4108UUX	IF-3 binds to the 30S ribosomal subunit and shifts the equilibrum between 70S ribosomes and their 50S and 30S subunits in favor of the free subunits, thus enhancing the availability of 30S subunits on which protein synthesis initiation begins (By similarity)
J168_02298	ENOG4105C22	threonyL-tRNA synthetase
J168_02299	ENOG4105ETE	Transcriptional regulator (LacI family
J168_02301	ENOG4107RBJ	symporter
J168_02307	ENOG4105CG3	alpha amylase, catalytic region
J168_02313	ENOG4105C93	Xylose Isomerase
J168_02314	ENOG4105CMG	Carbohydrate kinase
J168_02324	ENOG4108RTU	Aldolase
J168_02325	ENOG4105CXK	mandelate racemase muconate lactonizing
J168_02327	ENOG4105EI3	2-dehydro-3-deoxygalactonokinase EC 2.7.1.58
J168_02328	ENOG4108Z4U	Ferredoxin
J168_02330	ENOG4107TUS	Dihydrodipicolinate synthase
J168_02333	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
J168_02334	ENOG4108IAB	Phoh family
J168_02337	ENOG4105DWF	phosphomethylpyrimidine kinase
J168_02342	ENOG4105CWB	LysR family transcriptional Regulator
J168_02344	ENOG4107SDU	Methyl-accepting chemotaxis
J168_02346	ENOG4105VM8	Could accelerate the degradation of some genes transcripts potentially through selective RNA binding (By similarity)
J168_02347	ENOG4105CIM	Catalyzes the attachment of alanine to tRNA(Ala) in a two-step reaction alanine is first activated by ATP to form Ala- AMP and then transferred to the acceptor end of tRNA(Ala). Also edits incorrectly charged Ser-tRNA(Ala) and Gly-tRNA(Ala) via its editing domain (By similarity)
J168_02348	ENOG4105Y3E	Modulates RecA activity (By similarity)
J168_02349	ENOG4105C68	Can catalyze the hydrolysis of ATP in the presence of single-stranded DNA, the ATP-dependent uptake of single-stranded DNA by duplex DNA, and the ATP-dependent hybridization of homologous single-stranded DNAs. It interacts with LexA causing its activation and leading to its autocatalytic cleavage (By similarity)
J168_02350	ENOG4105DS7	Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair (By similarity)
J168_02351	ENOG4105CNK	Required, probably indirectly, for the hydroxylation of 2-octaprenylphenol to 2-octaprenyl-6-hydroxy-phenol, the fourth step in ubiquinone biosynthesis (By similarity)
J168_02352	ENOG4107TH8	cina domain protein
J168_02353	ENOG4105C1N	GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis (By similarity)
J168_02354	ENOG4105KW8	RNA chaperone that binds small regulatory RNA (sRNAs) and mRNAs to facilitate mRNA translational regulation in response to envelope stress, environmental stress and changes in metabolite concentrations. Also binds with high specificity to tRNAs (By similarity)
J168_02355	ENOG4105DKX	Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 in tRNAs that read codons beginning with uridine, leading to the formation of N6-(dimethylallyl)adenosine (i(6)A) (By similarity)
J168_02356	ENOG4105EEI	dihydropteroate synthase
J168_02357	ENOG4105C3H	Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins (By similarity)
J168_02358	ENOG4105F7M	Specifically methylates the uridine in position 2552 of 23S rRNA at the 2'-O position of the ribose in the fully assembled 50S ribosomal subunit (By similarity)
J168_02359	ENOG4105HBR	Rna-binding protein
J168_02362	ENOG4108K5P	(LipO)protein
J168_02363	ENOG4108UM1	dedA family
J168_02364	ENOG4105E26	Catalyzes the methyl esterification of L-isoaspartyl residues in peptides and proteins that result from spontaneous decomposition of normal L-aspartyl and L-asparaginyl residues. It plays a role in the repair and or degradation of damaged proteins (By similarity)
J168_02365	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
J168_02366	ENOG4108DG9	Smr protein MutS2
J168_02367	ENOG4106NZV	Responsible for synthesis of pseudouridine from uracil- 13 in transfer RNAs (By similarity)
J168_02368	ENOG4108UH8	Involved in the biosynthesis of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP), two major building blocks of isoprenoid compounds. Catalyzes the conversion of 4- diphosphocytidyl-2-C-methyl-D-erythritol 2-phosphate (CDP-ME2P) to 2-C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-CPP) with a corresponding release of cytidine 5-monophosphate (CMP) (By similarity)
J168_02369	ENOG4105CE5	Catalyzes the formation of 4-diphosphocytidyl-2-C- methyl-D-erythritol from CTP and 2-C-methyl-D-erythritol 4- phosphate (MEP) (By similarity)
J168_02370	ENOG4105XX3	Essential cell division protein. May link together the upstream cell division proteins, which are predominantly cytoplasmic, with the downstream cell division proteins, which are predominantly periplasmic (By similarity)
J168_02371	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
J168_02373	ENOG4105CXR	Phospho-2-dehydro-3-deoxyoctonate aldolase
J168_02374	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
J168_02376	ENOG4105C7D	DNA gyrase negatively supercoils closed circular double- stranded DNA in an ATP-dependent manner and also catalyzes the interconversion of other topological isomers of double-stranded DNA rings, including catenanes and knotted rings (By similarity)
J168_02379	ENOG4105CJ3	phosphate transporter
J168_02384	ENOG4105DEN	Luciferase family
J168_02385	ENOG41079KZ	Major Facilitator Superfamily
J168_02387	ENOG4105CQU	Part of the ABC transporter complex LolCDE involved in the translocation of mature outer membrane-directed lipoproteins, from the inner membrane to the periplasmic chaperone, LolA. Responsible for the formation of the LolA-lipoprotein complex in an ATP-dependent manner (By similarity)
J168_02390	ENOG4107R5M	Catalyzes the transfer of a N-acetyl-glucosamine moiety to 1D-myo-inositol 3-phosphate to produce 1D-myo-inositol 2- acetamido-2-deoxy-glucopyranoside 3-phosphate in the mycothiol biosynthesis pathway (By similarity)
J168_02392	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
J168_02398	ENOG4105EGZ	biosynthesis protein
J168_02409	ENOG4105EMN	RNA polymerase sigma factor
J168_02412	ENOG41060IM	Heme exporter protein
J168_02414	ENOG4108ZKK	Heme chaperone required for the biogenesis of c-type cytochromes. Transiently binds heme delivered by CcmC and transfers the heme to apo-cytochromes in a process facilitated by CcmF and CcmH (By similarity)
J168_02415	ENOG4105DA4	cytochrome c-type biogenesis protein
J168_02416	ENOG4107QX9	Thiol disulfide interChange protein
J168_02417	ENOG4105KWW	Biogenesis protein
J168_02421	ENOG4105ETX	regulatoR
J168_02425	ENOG4105C8Q	Methyl-accepting chemotaxis
J168_02434	ENOG4108YGG	dna repair protein
J168_02439	ENOG4105DFP	Integrase
J168_02442	ENOG4105E0K	tonB-dependent siderophore receptor
J168_02446	ENOG4106A2Z	transcriptional regulator antitoxin, MazE
J168_02451	ENOG4105CHI	Involved in the active translocation of vitamin B12 (cyanocobalamin) across the outer membrane to the periplasmic space. It derives its energy for transport by interacting with the trans-periplasmic membrane protein TonB (By similarity)
J168_02453	ENOG4105NRM	Membrane
J168_02458	ENOG4105C42	Type I secretion membrane fusion protein (HlyD
J168_02459	ENOG4108JJA	ABC, transporter
J168_02461	ENOG4107QJE	Chromosome Partitioning Protein
J168_02470	ENOG4105C73	Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone (By similarity)
J168_02471	ENOG4108IYH	Dna topoisomerase
J168_02472	ENOG4105NI8	Cytosine-specific methyltransferase
J168_02484	ENOG4105DFS	Conserved Protein
J168_02499	ENOG4105E14	MotA TolQ exbB proton channel
J168_02500	ENOG4105ER2	Ompa motb domain protein
J168_02501	ENOG4107QJE	Chromosome Partitioning Protein
J168_02502	ENOG4108V3W	Chemotaxis protein, CheW
J168_02504	ENOG4108VYJ	response regulator receiver protein
J168_02505	ENOG4105CBS	Chea signal transduction histidine kinase
J168_02506	ENOG4105C8Q	Methyl-accepting chemotaxis
J168_02508	ENOG4105C8Q	Methyl-accepting chemotaxis
J168_02508	ENOG4105C8Q	Methyl-accepting chemotaxis
J168_02509	ENOG4105C8Q	Methyl-accepting chemotaxis
J168_02511	ENOG4105C8Q	Methyl-accepting chemotaxis
J168_02513	ENOG4105C8Q	Methyl-accepting chemotaxis
J168_02514	ENOG4105C8Q	Methyl-accepting chemotaxis
J168_02515	ENOG4105C8Q	Methyl-accepting chemotaxis
J168_02516	ENOG4105C8Q	Methyl-accepting chemotaxis
J168_02517	ENOG4105C8Q	Methyl-accepting chemotaxis
J168_02518	ENOG4105C8Q	Methyl-accepting chemotaxis
J168_02519	ENOG4105C8Q	Methyl-accepting chemotaxis
J168_02521	ENOG4108V3W	Chemotaxis protein, CheW
J168_02523	ENOG4105C8Q	Methyl-accepting chemotaxis
J168_02524	ENOG4105BZU	Histidine kinase
J168_02525	ENOG4108Z4W	Probably deamidates glutamine residues to glutamate on methyl-accepting chemotaxis receptors (MCPs), playing an important role in chemotaxis (By similarity)
J168_02526	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
J168_02527	ENOG4105BZU	Histidine kinase
J168_02528	ENOG41074FZ	May increase the rate of spontaneous hydrolysis of aminoacrylate to malonic semialdehyde. Required to remove a toxic intermediate produce in the pyrimidine nitrogen degradation (By similarity)
J168_02529	ENOG4107QIJ	Aconitate hydratase 2
J168_02532	ENOG4107QM5	aconitate hydratase
J168_02534	ENOG4105CEY	Amp-dependent synthetase and ligase
J168_02535	ENOG41060WC	Enoyl-CoA hydratase
J168_02536	ENOG4105BZU	Histidine kinase
J168_02537	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
J168_02538	ENOG4105CRK	lysyL-tRNA synthetase
J168_02539	ENOG4105CG1	Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA (By similarity)
J168_02540	ENOG4105DY9	regulatoR
J168_02548	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
J168_02550	ENOG4108UKH	Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides (By similarity)
J168_02551	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
J168_02553	ENOG4105C1M	carbamoyl-phosphate synthetase glutamine chain
J168_02554	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
J168_02555	ENOG4108RPX	mosc domain containing protein
J168_02556	ENOG4105C1I	TRANSCRIPTIONAl REGULATOR GntR family
J168_02559	ENOG4105CE1	Ferrous iron transport protein b
J168_02563	ENOG4105CBH	Hydroxymethylglutaryl-CoA lyase
J168_02565	ENOG4105FUQ	Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase (By similarity)
J168_02569	ENOG4105CQB	FAD linked oxidase domain protein
J168_02570	ENOG4108JQ1	Dehydrogenase
J168_02572	ENOG4105CUB	amino acid
J168_02573	ENOG4105CUB	amino acid
J168_02574	ENOG4107QY0	Catalyzes the dehydration of methylthioribulose-1- phosphate (MTRu-1-P) into 2,3-diketo-5-methylthiopentyl-1- phosphate (DK-MTP-1-P) (By similarity)
J168_02575	ENOG4108CAF	Catalyzes 2 different reactions between oxygene and the acireductone 1,2-dihydroxy-3-keto-5-methylthiopentene (DHK-MTPene) depending upon the metal bound in the active site. Fe-containing acireductone dioxygenase (Fe-ARD) produces formate and 2-keto-4- methylthiobutyrate (KMTB), the alpha-ketoacid precursor of methionine in the methionine recycle pathway. Ni-containing acireductone dioxygenase (Ni-ARD) produces methylthiopropionate, carbon monoxide and formate, and does not lie on the methionine recycle pathway (By similarity)
J168_02576	ENOG4106YVY	Bifunctional enzyme that catalyzes the enolization of 2,3-diketo-5-methylthiopentyl-1-phosphate (DK-MTP-1-P) into the intermediate 2-hydroxy-3-keto-5-methylthiopentenyl-1-phosphate (HK-MTPenyl-1-P), which is then dephosphorylated to form the acireductone 1,2-dihydroxy-3-keto-5-methylthiopentene (DHK-MTPene) (By similarity)
J168_02579	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
J168_02580	ENOG4105C0S	IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisF subunit catalyzes the cyclization activity that produces IGP and AICAR from PRFAR using the ammonia provided by the HisH subunit (By similarity)
J168_02581	ENOG4105CJV	Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase
J168_02582	ENOG4108UJE	IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisH subunit provides the glutamine amidotransferase activity that produces the ammonia necessary to HisF for the synthesis of IGP and AICAR (By similarity)
J168_02583	ENOG4105ECC	imidazole-glycerol-phosphate dehydratase
J168_02584	ENOG4105CIH	Imidazole acetol-phosphate transaminase
J168_02585	ENOG4105CEK	Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine (By similarity)
J168_02586	ENOG4105E21	Catalyzes the condensation of ATP and 5-phosphoribose 1- diphosphate to form N'-(5'-phosphoribosyl)-ATP (PR-ATP). Has a crucial role in the pathway because the rate of histidine biosynthesis seems to be controlled primarily by regulation of HisG enzymatic activity (By similarity)
J168_02588	ENOG4105CUT	histidyl-tRNA synthetase
J168_02589	ENOG4105DS0	Transcriptional regulator, Crp Fnr family
J168_02598	ENOG41067NU	
J168_02599	ENOG41067NU	
J168_02602	ENOG4107BJW	polysaccharide deacetylase
J168_02603	ENOG4105CND	Glycosyl transferase, family 2
J168_02606	ENOG4105C26	Dehydrogenase
J168_02609	ENOG4107QYT	Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor (By similarity)
J168_02610	ENOG4105D4A	Cell wall formation (By similarity)
J168_02611	ENOG4108SXK	Transporter Drug Metabolite Exporter family
J168_02614	ENOG410841Q	phosphoesterase PA-phosphatase related protein
J168_02615	ENOG4105C4E	Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate (By similarity)
J168_02617	ENOG4108UYB	regulatoR
J168_02618	ENOG4105KU2	hydrolase family 5
J168_02625	ENOG4107QP8	phosphohexose isomerase
J168_02626	ENOG4108Z2X	Catalyzes the pyruvoyl-dependent decarboxylation of aspartate to produce beta-alanine (By similarity)
J168_02627	ENOG4108IAA	Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate (By similarity)
J168_02628	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
J168_02629	ENOG4105K8U	2-Amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase
J168_02630	ENOG4105DJ0	Poly(A) Polymerase
J168_02634	ENOG4105DZA	Converts GTP to 7,8-dihydroneopterin triphosphate (By similarity)
J168_02635	ENOG4108KNB	n-acetylmuramoyl-l-alanine amidase
J168_02637	ENOG4105CG3	alpha amylase, catalytic region
J168_02653	ENOG4105CMA	conjugation trbi family protein
J168_02660	ENOG4105CCW	damaged site, the DNA wraps around one UvrB monomer. DNA wrap is dependent on ATP binding by UvrB and probably causes local melting of the DNA helix, facilitating insertion of UvrB beta-hairpin between the DNA strands. Then UvrB probes one DNA strand for the presence of a lesion. If a lesion is found the UvrA subunits dissociate and the UvrB-DNA preincision complex is formed. This complex is subsequently bound by UvrC and the second UvrB is released. If no lesion is found, the DNA wraps around the other UvrB subunit that will check the other stand for damage (By similarity)
J168_02675	ENOG4105CC0	LysR family Transcriptional regulator
J168_02676	ENOG4108V3G	Catalyzes the reductive cleavage of azo bond in aromatic azo compounds to the corresponding amines. Requires NADH, but not NADPH, as an electron donor for its activity (By similarity)
J168_02677	ENOG4105CGR	Catalyzes the attachment of serine to tRNA(Ser). Is also able to aminoacylate tRNA(Sec) with serine, to form the misacylated tRNA L-seryl-tRNA(Sec), which will be further converted into selenocysteinyl-tRNA(Sec) (By similarity)
J168_02680	ENOG4105CMY	5-enolpyruvylshikimate-3-phosphate synthase
J168_02682	ENOG4107QM1	Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine (By similarity)
J168_02683	ENOG4105CCD	The exact function is not known. Can catalyze the reduction of a variety of substrates like dimethyl sulfoxide, trimethylamine N-oxide, phenylmethyl sulfoxide and L-methionine sulfoxide. Cannot reduce cyclic N-oxides. Shows no activity as sulfite oxidase (By similarity)
J168_02684	ENOG4105DQ2	Is probably involved in the electron transfer between its heme and the molybdenum cofactor of the reductase catalytic subunit YedY (By similarity)
J168_02692	ENOG4105CI2	imidazolone-5-propionate hydrolase
J168_02693	ENOG4105C84	Histidine ammonia-lyase
J168_02695	ENOG4105CGP	Urocanate hydratase
J168_02696	ENOG4105DZG	Dehydrogenase
J168_02697	ENOG4105C24	DNA gyrase negatively supercoils closed circular double- stranded DNA in an ATP-dependent manner and also catalyzes the interconversion of other topological isomers of double-stranded DNA rings, including catenanes and knotted rings (By similarity)
J168_02698	ENOG4105C35	Catalyzes the interconversion of methylthioribose-1- phosphate (MTR-1-P) into methylthioribulose-1-phosphate (MTRu-1-P) (By similarity)
J168_02700	ENOG4105CAP	With EpmB is involved in the beta-lysylation step of the post-translational modification of translation elongation factor P (EF-P). Catalyzes the ATP-dependent activation of (R)-beta-lysine produced by EpmB, forming a lysyl-adenylate, from which the beta- lysyl moiety is then transferred to the epsilon-amino group of a conserved specific lysine residue in EF-P (By similarity)
J168_02701	ENOG4105C77	DNA ligase that catalyzes the formation of phosphodiester linkages between 5'-phosphoryl and 3'-hydroxyl groups in double-stranded DNA using NAD as a coenzyme and as the energy source for the reaction. It is essential for DNA replication and repair of damaged DNA (By similarity)
J168_02702	ENOG4105CIH	Imidazole acetol-phosphate transaminase
J168_02704	ENOG4107NPY	receptor for the septal ring structure, may anchor it to the inner-membrane (By similarity)
J168_02706	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
J168_02707	ENOG4105VH8	Binds as a heterodimer with protein S6 to the central domain of the 16S rRNA, where it helps stabilize the platform of the 30S subunit (By similarity)
J168_02708	ENOG4108ZDX	Binds together with S18 to 16S ribosomal RNA (By similarity)
J168_02709	ENOG4108YX9	iron--sulfur cluster insertion protein erpA
J168_02710	ENOG4105C5S	asparaginyl-tRNA synthetase
J168_02717	ENOG4105WH1	Two component transcriptional regulator luxr family
J168_02726	ENOG41077A9	carbonic anhydrase
J168_02727	ENOG4105C3W	Catalyzes the oxidative ring opening of 3- hydroxyanthranilate to 2-amino-3-carboxymuconate semialdehyde, which spontaneously cyclizes to quinolinate (By similarity)
J168_02729	ENOG4105CKY	Catalyzes the cleavage of L-kynurenine (L-Kyn) and L-3- hydroxykynurenine (L-3OHKyn) into anthranilic acid (AA) and 3- hydroxyanthranilic acid (3-OHAA), respectively (By similarity)
J168_02730	ENOG4107RQD	Catalyzes the hydroxylation of L-kynurenine (L-Kyn) to form 3-hydroxy-L-kynurenine (L-3OHKyn). Required for synthesis of quinolinic acid (By similarity)
J168_02731	ENOG4105CJB	Exodeoxyribonuclease I
J168_02735	ENOG4105F91	Catalyzes the phosphorylation of NAD to NADP. Utilizes ATP and other nucleoside triphosphates as well as inorganic polyphosphate as a source of phosphorus (By similarity)
J168_02736	ENOG4105C4H	Specifically methylates the guanine in position 2445 (m2G2445) and the guanine in position 2069 (m7G2069) of 23S rRNA (By similarity)
J168_02737	ENOG4105C5H	ABC transporter
J168_02743	ENOG4105KHC	sulfurtransferase
J168_02744	ENOG4105P8F	nudix hydrolase
J168_02745	ENOG4108V1T	peptidylprolyl cis-trans isomerase
J168_02746	ENOG4105E39	Enoyl-CoA hydratase
J168_02748	ENOG4105CSM	endonuclease III
J168_02749	ENOG4105CHH	sulfate transporter
J168_02750	ENOG4107B2H	carbonic anhydrase
J168_02754	ENOG4107QMV	Part of the ABC transporter complex PstSACB involved in phosphate import (By similarity)
J168_02755	ENOG4105C8U	phosphate abc transporter
J168_02756	ENOG4105E2Z	phosphate ABC transporter (Permease
J168_02757	ENOG4105BZY	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
J168_02758	ENOG4108UTW	Plays a role in the regulation of phosphate uptake
J168_02760	ENOG4105DH5	Responsible for the end-turnover of tRNA specifically removes the terminal AMP residue from uncharged tRNA (tRNA-C-C-A). Also appears to be involved in tRNA biosynthesis (By similarity)
J168_02761	ENOG4105BZU	Histidine kinase
J168_02762	ENOG4105C2N	RNA methyltransferase TrmH family group 3
J168_02764	ENOG4105C40	3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs (By similarity)
J168_02767	ENOG4105C1G	acyl-Coa dehydrogenase
J168_02769	ENOG4105C3R	Methionine synthase
J168_02770	ENOG4105C3R	Methionine synthase
J168_02772	ENOG4105D7K	pfkb domain protein
J168_02774	ENOG4105ETE	Transcriptional regulator (LacI family
J168_02777	ENOG41069P5	Protein slyX homolog
J168_02778	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
J168_02779	ENOG4108V1T	peptidylprolyl cis-trans isomerase
J168_02782	ENOG410811P	TRANSCRIPTIONAl REGULATOR GntR family
J168_02783	ENOG4105CZV	ABC transporter
J168_02789	ENOG4105C37	(CBS) domain
J168_02791	ENOG4107QTF	adenylosuccinate lyase
J168_02793	ENOG4105EZE	Cupin 4 family protein
J168_02795	ENOG4105C7P	2-oxoglutarate dehydrogenase, E1
J168_02796	ENOG4105C7S	Dehydrogenase
J168_02798	ENOG4108URH	decarboxylase
J168_02800	ENOG4105BZ1	(ABC) transporter
J168_02801	ENOG4105C5Q	Transcriptional regulator
J168_02807	ENOG4107XGF	functions in a salvage pathway. Uses pyridoxamine (By similarity)
J168_02809	ENOG4105BZ5	ATP binding to DnaK triggers the release of the substrate protein, thus completing the reaction cycle. Several rounds of ATP-dependent interactions between DnaJ, DnaK and GrpE are required for fully efficient folding. Also involved, together with DnaK and GrpE, in the DNA replication of plasmids through activation of initiation proteins (By similarity)
J168_02810	ENOG4105CFG	Acts as a chaperone (By similarity)
J168_02811	ENOG4105K90	Participates actively in the response to hyperosmotic and heat shock by preventing the aggregation of stress-denatured proteins, in association with DnaK and GrpE. It is the nucleotide exchange factor for DnaK and may function as a thermosensor. Unfolded proteins bind initially to DnaJ
J168_02812	ENOG4105CI8	Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons (By similarity)
J168_02813	ENOG4105C4F	May be involved in recombinational repair of damaged DNA (By similarity)
J168_02814	ENOG41090R7	Ferric uptake
J168_02815	ENOG4105YRI	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane (By similarity)
J168_02817	ENOG4108Z1B	Cyclase dehydrase
J168_02818	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
J168_02847	ENOG4106TD9	Diguanylate cyclase
J168_02849	ENOG4105BZU	Histidine kinase
J168_02856	ENOG4105CR8	Transcriptional regulator
J168_02858	ENOG4105CDV	Ompa motb domain protein
J168_02859	ENOG4105CVP	deoxyribo-dipyrimidine photolyase
J168_02860	ENOG4105CDU	Replicative dna helicase
J168_02862	ENOG4105CAQ	asparagine synthetase
J168_02863	ENOG4108K3A	Glutathione S-transferase
J168_02865	ENOG4105C1G	acyl-Coa dehydrogenase
J168_02868	ENOG4105F8V	Hydrolase, tatD family
J168_02869	ENOG4105CUZ	uba thif-type nad fad binding protein
J168_02872	ENOG4105VEQ	Cold shock protein
J168_02874	ENOG4105HDD	phospholipase
J168_02877	ENOG4107GFK	fumarate
J168_02879	ENOG4105DP0	ferredoxin-NADP reductase
J168_02880	ENOG4108V06	Glutathione peroxidase
J168_02881	ENOG4105DGW	oligopeptidase A
J168_02887	ENOG4105DUX	Transporter
J168_02891	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
J168_02892	ENOG4105CW7	secretion protein, HlyD family
J168_02896	ENOG4105C24	DNA gyrase negatively supercoils closed circular double- stranded DNA in an ATP-dependent manner and also catalyzes the interconversion of other topological isomers of double-stranded DNA rings, including catenanes and knotted rings (By similarity)
J168_02898	ENOG4105FQ6	thiopurine methyltransferase
J168_02899	ENOG4108UWD	Iron-storage protein
J168_02901	ENOG4108ESX	Receptor
J168_02903	ENOG4105CAQ	asparagine synthetase
J168_02904	ENOG4105C9Y	Catalyzes the hydrolysis of N-succinyl-L,L- diaminopimelic acid (SDAP), forming succinate and LL-2,6- diaminoheptanedioate (DAP), an intermediate involved in the bacterial biosynthesis of lysine and meso-diaminopimelic acid, an essential component of bacterial cell walls (By similarity)
J168_02905	ENOG4105KUZ	arsenate reductase
J168_02907	ENOG4105E1P	Modifies, by uridylylation or deuridylylation the PII (GlnB) regulatory protein (By similarity)
J168_02908	ENOG4105CA1	Removes the N-terminal methionine from nascent proteins (By similarity)
J168_02915	ENOG4105CE9	30S ribosomal protein S2
J168_02916	ENOG4105CU7	Associates with the EF-Tu.GDP complex and induces the exchange of GDP to GTP. It remains bound to the aminoacyl-tRNA.EF- Tu.GTP complex up to the GTP hydrolysis stage on the ribosome (By similarity)
J168_02917	ENOG4105BZU	Histidine kinase
J168_02918	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
J168_02919	ENOG4108VCV	Responsible for the release of ribosomes from messenger RNA at the termination of protein biosynthesis. May increase the efficiency of translation by recycling ribosomes from one round of translation to another (By similarity)
J168_02920	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
J168_02921	ENOG4105KNE	Phosphatidate cytidylyltransferase
J168_02922	ENOG4105CEA	Catalyzes the NADP-dependent rearrangement and reduction of 1-deoxy-D-xylulose-5-phosphate (DXP) to 2-C-methyl-D-erythritol 4-phosphate (MEP) (By similarity)
J168_02923	ENOG4105DZP	Membrane-associated zinc metalloprotease
J168_02926	ENOG4105D7M	Catalyzes the N-acylation of UDP-3-O-acylglucosamine using 3-hydroxyacyl-ACP as the acyl donor. Is involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
J168_02927	ENOG4108YXN	Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs (By similarity)
J168_02928	ENOG4105DAF	Involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
J168_02929	ENOG4105D0V	Condensation of UDP-2,3-diacylglucosamine and 2,3- diacylglucosamine-1-phosphate to form lipid A disaccharide, a precursor of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
J168_02930	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
J168_02932	ENOG4107QM9	Component of the acetyl coenzyme A carboxylase (ACC) complex. First, biotin carboxylase catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the carboxyltransferase to acetyl-CoA to form malonyl-CoA (By similarity)
J168_02935	ENOG4108YXA	Membrane
J168_02945	ENOG4107QK5	Homocysteine s-methyltransferase
J168_02946	ENOG4108IQI	permease
J168_02947	ENOG4108YZK	glyoxalase bleomycin resistance protein dioxygenase
J168_02948	ENOG4105DA5	(ABC) transporter
J168_02951	ENOG4105CKH	Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation (By similarity)
J168_02953	ENOG4108R3D	Electron transport complex
J168_02956	ENOG4105K6V	RNA polymerase
J168_02961	ENOG4105CV9	cyclopropane-fatty-acyl-phospholipid synthase
J168_02964	ENOG4105CV9	cyclopropane-fatty-acyl-phospholipid synthase
J168_02965	ENOG4105M4H	endoribonuclease L-psp
J168_02975	ENOG4105F27	Major Facilitator
J168_02976	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
J168_02977	ENOG4108Z8G	Alkylphosphonate utilization operon protein PhnA
J168_02979	ENOG4108YZY	peptidylprolyl cis-trans isomerase
J168_02980	ENOG4105DFF	Rod shape-determining protein mreb
J168_02983	ENOG4105KSC	Transcriptional regulator, TraR DksA family
J168_02986	ENOG4108VKG	metal-dependent hydrolase
J168_02990	ENOG4105CHU	acetyl-coa acetyltransferase
J168_02993	ENOG4105BZU	Histidine kinase
J168_02996	ENOG4107T0X	DNA ligase
J168_02998	ENOG4107T0X	DNA ligase
J168_02999	ENOG4107QRT	dEAD DEAH box helicase
J168_03001	ENOG4107RQD	Catalyzes the hydroxylation of L-kynurenine (L-Kyn) to form 3-hydroxy-L-kynurenine (L-3OHKyn). Required for synthesis of quinolinic acid (By similarity)
J168_03002	ENOG4105VEQ	Cold shock protein
J168_03003	ENOG4107RHB	Catalyzes the reversible phosphorylation of S-methyl-5'- thioadenosine (MTA) to adenine and 5-methylthioribose-1-phosphate. Involved in the breakdown of MTA, a major by-product of polyamine biosynthesis. Responsible for the first step in the methionine salvage pathway after MTA has been generated from S- adenosylmethionine. Has broad substrate specificity with 6- aminopurine nucleosides as preferred substrates (By similarity)
J168_03004	ENOG4108UGV	hypoxanthine phosphoribosyltransferase
J168_03005	ENOG4107QPA	Cleaves GlcNAc linked beta-1,4 to MurNAc tripeptides (By similarity)
J168_03006	ENOG4105EXX	Deoxyribodipyrimidine photolyase-related protein
J168_03007	ENOG4108QDE	fad dependent oxidoreductase
J168_03008	ENOG4107ZXU	DSBA oxidoreductase
J168_03009	ENOG41080ZE	Adenylate cyclase
J168_03010	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
J168_03012	ENOG41071DT	Involved in DNA repair and RecF pathway recombination (By similarity)
J168_03013	ENOG4105CWT	An essential GTPase that binds both GDP and GTP, with rapid nucleotide exchange. Plays a role in 16S rRNA processing and 30S ribosomal subunit biogenesis and possibly also in cell cycle regulation and energy metabolism (By similarity)
J168_03014	ENOG4108ZBM	Digests double-stranded RNA. Involved in the processing of primary rRNA transcript to yield the immediate precursors to the large and small rRNAs (23S and 16S). Also processes some mRNAs, and tRNAs when they are encoded in the rRNA operon (By similarity)
J168_03016	ENOG4105C3F	Signal peptidase i
J168_03017	ENOG4105C4S	Required for accurate and efficient protein synthesis under certain stress conditions. May act as a fidelity factor of the translation reaction, by catalyzing a one-codon backward translocation of tRNAs on improperly translocated ribosomes. Back- translocation proceeds from a post-translocation (POST) complex to a pre-translocation (PRE) complex, thus giving elongation factor G a second chance to translocate the tRNAs correctly. Binds to ribosomes in a GTP-dependent manner (By similarity)
J168_03018	ENOG4105C0H	protease
J168_03020	ENOG4105EMN	RNA polymerase sigma factor
J168_03021	ENOG4105DYT	3-hydroxyacyl-CoA dehydrogenase
J168_03023	ENOG4105CF3	3-Hydroxyisobutyrate dehydrogenase
J168_03024	ENOG4105DYT	3-hydroxyacyl-CoA dehydrogenase
J168_03025	ENOG4105E39	Enoyl-CoA hydratase
J168_03026	ENOG4105C1G	acyl-Coa dehydrogenase
J168_03027	ENOG4105C26	Dehydrogenase
J168_03030	ENOG4106FKC	arabinogalactan endo-1,4-beta-galactosidase
J168_03031	ENOG4105CNT	hydrolase family 2
J168_03035	ENOG4105CNA	YD repeat protein
J168_03038	ENOG4105D86	that it carries out the mismatch recognition step. This protein has a weak ATPase activity (By similarity)
J168_03040	ENOG4105C1X	Bifunctional enzyme with both catalase and broad- spectrum peroxidase activity (By similarity)
J168_03041	ENOG4105VEJ	Heat shock protein
J168_03044	ENOG4107QJQ	Mate efflux family protein
J168_03045	ENOG4108YY1	This protein is located at the 30S-50S ribosomal subunit interface and may play a role in the structure and function of the aminoacyl-tRNA binding site (By similarity)
J168_03046	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
J168_03047	ENOG4108ZR6	An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Probably interacts with S19. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes (By similarity)
J168_03048	ENOG4105K5M	30s ribosomal protein S16
J168_03050	ENOG4107QWG	2-Nitropropane dioxygenase
J168_03051	ENOG4105CB9	Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Binds to the hydrophobic signal sequence of the ribosome-nascent chain (RNC) as it emerges from the ribosomes. The SRP-RNC complex is then targeted to the cytoplasmic membrane where it interacts with the SRP receptor FtsY
J168_03052	ENOG4105CRE	cytochrome C
J168_03053	ENOG4105ENN	converts alpha-aldose to the beta-anomer. It is active on D-glucose, L-arabinose, D-xylose, D-galactose, maltose and lactose (By similarity)
J168_03054	ENOG4105CZZ	Alpha-N-arabinofuranosidase (EC 3.2.1.55)
J168_03057	ENOG4105CQZ	Histidine kinase
J168_03058	ENOG4105BZU	Histidine kinase
J168_03059	ENOG4105BZU	Histidine kinase
J168_03060	ENOG4107Z5C	methylesterase
J168_03061	ENOG4105C08	Histidine kinase
J168_03062	ENOG4105KCV	RNA signal recognition particle 4.5S RNA
J168_03067	ENOG4105BZU	Histidine kinase
J168_03069	ENOG4105QD0	anti-sigma regulatory factor serine threonine protein kinase
J168_03070	ENOG4105FUA	antagonist
J168_03071	ENOG4107MMM	Anti-sigma-factor antagonist
J168_03073	ENOG4105CJX	Molecular chaperone. Has ATPase activity (By similarity)
J168_03076	ENOG4105KAF	membrAne
J168_03077	ENOG4105DNJ	May play a role in the repair of endogenous alkylation damage (By similarity)
J168_03079	ENOG41090KH	cytochrome o ubiquinol oxidase (subunit iv)
J168_03080	ENOG4105CCU	oxidase (Subunit III)
J168_03081	ENOG4105BZ9	Cytochrome C oxidase, subunit I
J168_03082	ENOG4105E2S	oxidase) subunit II
J168_03084	ENOG4105C48	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
J168_03085	ENOG4105M02	This protein specifically catalyzes the removal of signal peptides from prolipoproteins (By similarity)
J168_03086	ENOG4105C07	amino acids such as valine, to avoid such errors it has two additional distinct tRNA(Ile)-dependent editing activities. One activity is designated as 'pretransfer' editing and involves the hydrolysis of activated Val-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Val-tRNA(Ile) (By similarity)
J168_03087	ENOG4105DTN	riboflavin biosynthesis protein ribF
J168_03088	ENOG4105CJR	Integral membrane protein (MviN
J168_03089	ENOG4105KQV	Binds directly to 16S ribosomal RNA (By similarity)
J168_03090	ENOG4105C9R	An essential GTPase which binds GTP, GDP and possibly (p)ppGpp with moderate affinity, with high nucleotide exchange rates and a fairly low GTP hydrolysis rate (By similarity). It may play a role in control of the cell cycle, stress response, ribosome biogenesis and in those bacteria that undergo differentiation, in morphogenesis control
J168_03091	ENOG4105K46	50S ribosomal protein l27
J168_03092	ENOG4105KK9	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
J168_03093	ENOG4105C5U	The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrA is an ATPase and a DNA-binding protein. A damage recognition complex composed of 2 UvrA and 2 UvrB subunits scans DNA for abnormalities. When the presence of a lesion has been verified by UvrB, the UvrA molecules dissociate (By similarity)
J168_03094	ENOG4108TGP	Thioesterase superfamily protein
J168_03097	ENOG4105C29	acyl-CoA thioesterase
J168_03102	ENOG4105DWA	May conjugate Arg from its aminoacyl-tRNA to the N- termini of proteins containing an N-terminal aspartate or glutamate
J168_03104	ENOG4107SPG	Catalyzes two reactions the first one is the production of beta-formyl glycinamide ribonucleotide (GAR) from formate, ATP and beta GAR
J168_03112	ENOG4105WH1	Two component transcriptional regulator luxr family
J168_03113	ENOG4105BZU	Histidine kinase
J168_03115	ENOG4105K7U	Cell division inhibitor that blocks the formation of polar Z ring septums. Rapidly oscillates between the poles of the cell to destabilize FtsZ filaments that have formed before they mature into polar Z rings. Prevents FtsZ polymerization (By similarity)
J168_03116	ENOG4107QMS	site-determining protein
J168_03117	ENOG4105VJP	Prevents the cell division inhibition by proteins MinC and MinD at internal division sites while permitting inhibition at polar sites. This ensures cell division at the proper site by restricting the formation of a division septum at the midpoint of the long axis of the cell (By similarity)
J168_03119	ENOG4105DHQ	Histidine kinase
J168_03120	ENOG4105ETX	regulatoR
J168_03123	ENOG4105DIJ	Phosphoethanolamine transferase
J168_03126	ENOG4105C2C	drug resistance transporter, Bcr CflA
J168_03129	ENOG4105CBI	The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor
J168_03130	ENOG4105EBR	Carboxylesterase
J168_03131	ENOG4105CV8	reductase
J168_03140	ENOG4105CBS	Chea signal transduction histidine kinase
J168_03141	ENOG4105C8Q	Methyl-accepting chemotaxis
J168_03142	ENOG4108V3W	Chemotaxis protein, CheW
J168_03143	ENOG4105BZU	Histidine kinase
J168_03144	ENOG4105BZU	Histidine kinase
J168_03145	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
J168_03146	ENOG4107RZC	phospholipase d
J168_03147	ENOG4105C9K	Endothelin-converting enzyme 1
J168_03149	ENOG4105DKJ	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
J168_03150	ENOG4105Y7X	Selectively cleaves double-stranded DNA at the second phosphodiester bond 3' to a deoxyinosine leaving behind the intact lesion on the nicked DNA. Acts in DNA repair (By similarity)
J168_03152	ENOG4105EUB	pirin domain protein
J168_03155	ENOG4105EUB	pirin domain protein
J168_03156	ENOG4105D22	carbon starvation protein
J168_03157	ENOG4105VCD	cytoplasmic protein
J168_03165	ENOG4107XAN	XdhC and CoxI family
J168_03166	ENOG4105C7W	Xanthine dehydrogenase
J168_03167	ENOG4105DIP	Molybdopterin dehydrogenase FAD-binding
J168_03168	ENOG4107XKX	isoquinoline 1-oxidoreductase, alpha subunit
J168_03171	ENOG4108UUM	single-stranded DNA-binding protein
J168_03172	ENOG4105EAH	synthase
J168_03174	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
J168_03177	ENOG4105CFH	Aspartokinase
J168_03178	ENOG4105JAB	phenazine biosynthesis protein, phzf family
J168_03179	ENOG4105JAB	phenazine biosynthesis protein, phzf family
J168_03181	ENOG4108Z9K	Osmotically inducible protein
J168_03182	ENOG4105CXT	aspartate transcarbamylase
J168_03183	ENOG4107Y66	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
J168_03184	ENOG4108UJU	UPF0301 protein
J168_03185	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
J168_03188	ENOG4108E16	pectate lyase
J168_03189	ENOG4105CZX	twitching motility protein
J168_03190	ENOG4105CZX	twitching motility protein
J168_03191	ENOG4105DFA	alanine racemase domain protein
J168_03192	ENOG4105II7	pyrroline-5-carboxylate reductase
J168_03194	ENOG4105FAA	peptidase M23
J168_03198	ENOG4108Z0Z	intracellular protease Pfpi family
J168_03202	ENOG4105C3K	feS assembly ATPase SufC
J168_03203	ENOG4105JRK	feS assembly protein SufD
J168_03204	ENOG4105C9B	Cysteine desulfurase
J168_03207	ENOG4108IU3	tonb-dependent siderophore receptor
J168_03208	ENOG4107E2E	PKHD-type hydroxylase
J168_03213	ENOG4105CJ2	(LipO)protein
J168_03214	ENOG4107EER	Component of the sulfite reductase complex that catalyzes the 6-electron reduction of sulfite to sulfide. This is one of several activities required for the biosynthesis of L- cysteine from sulfate. The flavoprotein component catalyzes the electron flow from NADPH - FAD - FMN to the hemoprotein component (By similarity)
J168_03217	ENOG41083P1	competence protein ComEA helix-hairpin-helix repeat protein
J168_03218	ENOG4105C9Y	Catalyzes the hydrolysis of N-succinyl-L,L- diaminopimelic acid (SDAP), forming succinate and LL-2,6- diaminoheptanedioate (DAP), an intermediate involved in the bacterial biosynthesis of lysine and meso-diaminopimelic acid, an essential component of bacterial cell walls (By similarity)
J168_03220	ENOG4105EHM	Aminoglycoside phosphotransferase
J168_03221	ENOG4108S0S	Nucleotidyl transferase
J168_03223	ENOG4105C02	permease
J168_03225	ENOG4105CXB	phosphoribosylaminoimidazole synthetase
J168_03227	ENOG4108V3E	phosphoribosylglycinamide formyltransferase
J168_03231	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
J168_03233	ENOG4105C2X	Arabinose 5-phosphate isomerase
J168_03234	ENOG4108Z4R	3-deoxy-d-manno-octulosonate 8-phosphate phosphatase
J168_03236	ENOG4105WI0	lipopolysaccharide transport periplasmic protein lptA
J168_03237	ENOG4108IUZ	ABC transporter
J168_03238	ENOG4105DTW	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
J168_03239	ENOG41080QH	sigma 54 modulation protein ribosomal protein S30EA
J168_03240	ENOG4107RM2	PTS IIA-like nitrogen-regulatory protein PtsN
J168_03241	ENOG4105D1C	Catalyzes the ATP- as well as the pyrophosphate- dependent phosphorylation of a specific serine residue in HPr, a phosphocarrier protein of the phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS). HprK P also catalyzes the pyrophosphate-producing, inorganic phosphate-dependent dephosphorylation (phosphorolysis) of seryl-phosphorylated HPr (P- Ser-HPr). The two antagonistic activities of HprK P are regulated by several intracellular metabolites, which change their concentration in response to the absence or presence of rapidly metabolisable carbon sources (glucose, fructose, etc.) in the growth medium. Therefore, by controlling the phosphorylation state of HPr, HPrK P is a sensor enzyme that plays a major role in the regulation of carbon metabolism and sugar transport it mediates carbon catabolite repression (CCR), and regulates PTS-catalyzed carbohydrate uptake and inducer exclusion (By similarity)
J168_03242	ENOG4105C21	Displays ATPase and GTPase activities (By similarity)
J168_03244	ENOG41080Z8	PHOSPHOCARRIER protein
J168_03245	ENOG4105BZ3	General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) (By similarity)
J168_03246	ENOG4105CJW	magnesium transporter
J168_03247	ENOG4107UWA	esterase
J168_03248	ENOG4105CFY	cytochrome d ubiquinol oxidase, subunit ii
J168_03249	ENOG4105C4M	(Ubiquinol oxidase) subunit I
J168_03251	ENOG4105C85	amino acid
J168_03252	ENOG4108NFF	pectate lyase
J168_03255	ENOG4105CUB	amino acid
J168_03258	ENOG4108MHS	Lysyl endopeptidase
J168_03260	ENOG4107XDQ	Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA (By similarity)
J168_03261	ENOG4105QV4	Tryptophan halogenase
J168_03266	ENOG4108Z4X	TRANSCRIPTIONal
J168_03269	ENOG4106032	Glutathionylspermidine synthase
J168_03274	ENOG4108P9J	Phage shock protein A
J168_03276	ENOG4108S7T	Catalyzes the oxidation of either pyridoxine 5'- phosphate (PNP) or pyridoxamine 5'-phosphate (PMP) into pyridoxal 5'-phosphate (PLP) (By similarity)
J168_03277	ENOG4105KHV	Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate (By similarity)
J168_03278	ENOG4105D49	3-dehydroquinate synthase
J168_03280	ENOG4105CFZ	Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III (By similarity)
J168_03293	ENOG4108JUA	Transcriptional regulator
J168_03294	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
J168_03295	ENOG4105BZU	Histidine kinase
J168_03296	ENOG4105BZU	Histidine kinase
J168_03298	ENOG4105BZU	Histidine kinase
J168_03299	ENOG4108YYC	ycei family
J168_03303	ENOG4105EJQ	L-serine dehydratase
J168_03305	ENOG4105CFH	Aspartokinase
J168_03306	ENOG4105C28	cystathionine
J168_03307	ENOG4106TYC	homoserine o-acetyltransferase (EC 2.3.1.31)
J168_03309	ENOG4105DR5	peptidase
J168_03310	ENOG4105C8A	Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP (By similarity)
J168_03311	ENOG4108UT2	hemolysin iii
J168_03312	ENOG41066T0	asmA family
J168_03313	ENOG4105CP4	Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth (By similarity)
J168_03315	ENOG4108VKV	Monofunctional biosynthetic peptidoglycan transglycosylase
J168_03316	ENOG4105F4C	Redox regulated molecular chaperone. Protects both thermally unfolding and oxidatively damaged proteins from irreversible aggregation. Plays an important role in the bacterial defense system toward oxidative stress (By similarity)
J168_03318	ENOG4105D05	Receptor
J168_03320	ENOG4108IG5	Transcriptional regulator
J168_03322	ENOG4107QPN	acyl-Coa dehydrogenase
J168_03327	ENOG4105KE9	The glycine cleavage system catalyzes the degradation of glycine. The H protein shuttles the methylamine group of glycine from the P protein to the T protein (By similarity)
J168_03328	ENOG4105D43	The glycine cleavage system catalyzes the degradation of glycine (By similarity)
J168_03330	ENOG4107QX8	SPFH domain, Band 7 family protein
J168_03331	ENOG4105KK4	UPF0060 membrane protein
J168_03332	ENOG4105DXN	mazG family
J168_03333	ENOG4108RNI	3'(2')5'-bisphosphate nucleotidase
J168_03334	ENOG4107RK2	ADP-ribose diphosphatase NudE
J168_03336	ENOG4105QF0	Specifically methylates the N3 position of the uracil ring of uridine 1498 (m3U1498) in 16S rRNA. Acts on the fully assembled 30S ribosomal subunit (By similarity)
J168_03337	ENOG4105CHC	glucokinase (EC 2.7.1.2)
J168_03340	ENOG4105VRS	hydrolase family 18
J168_03341	ENOG4105E2D	ec 3.2.1.52
J168_03346	ENOG4107QTZ	amino acid
J168_03348	ENOG4105F8D	glycoside hydrolase family 4
J168_03350	ENOG4105CWX	Alpha-1,2-mannosidase
J168_03357	ENOG4106N3A	copper homeostasis protein cutc
J168_03359	ENOG4105D9U	N-acetyltransferase
J168_03362	ENOG4105CBS	Chea signal transduction histidine kinase
J168_03363	ENOG4105C8Q	Methyl-accepting chemotaxis
J168_03365	ENOG4105M3Z	response regulator
J168_03366	ENOG4108UNF	response regulator
J168_03367	ENOG4105D7Z	glutathione synthase
J168_03369	ENOG41065RQ	ADP-ribosylation crystallin J1
J168_03370	ENOG41072GX	Peptidase M22 Glycoprotease
J168_03371	ENOG4105DVT	helicase
J168_03373	ENOG4105BZ4	penicillin-binding protein
J168_03376	ENOG4105CWR	In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance (By similarity)
J168_03377	ENOG4105JIE	May be involved in the transport of PQQ or its precursor to the periplasm (By similarity)
J168_03378	ENOG41086XE	Ring cyclization and eight-electron oxidation of 3a-(2- amino-2-carboxyethyl)-4,5-dioxo-4,5,6,7,8,9-hexahydroquinoline- 7,9-dicarboxylic-acid to PQQ (By similarity)
J168_03379	ENOG4105Z85	coenzyme PQQ synthesis
J168_03380	ENOG4105EZY	Pyrroloquinoline quinone biosynthesis protein E
J168_03383	ENOG4105CHC	glucokinase (EC 2.7.1.2)
J168_03385	ENOG4105CQ7	ATP-dependent helicase
J168_03387	ENOG4105C9U	ATP-dependent DNA helicase RecQ
J168_03394	ENOG4105C8Q	Methyl-accepting chemotaxis
J168_03398	ENOG410903D	sensor protein
J168_03399	ENOG4105FD2	Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) (By similarity)
J168_03401	ENOG4105EIZ	Catalyzes the conversion of 6-carboxy-5,6,7,8- tetrahydropterin (CPH4) to 7-carboxy-7-deazaguanine (CDG) (By similarity)
J168_03403	ENOG4105KCK	Peptidoglycan-associated lipoprotein
J168_03404	ENOG4107R6Y	Involved in the TonB-independent uptake of proteins (By similarity)
J168_03407	ENOG4105E02	MotA TolQ exbB proton channel
J168_03408	ENOG4107YD3	Thioesterase
J168_03409	ENOG4105CKJ	The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing (By similarity)
J168_03411	ENOG4105DFH	Transport of potassium into the cell (By similarity)
J168_03412	ENOG4105KA4	The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing. RuvA stimulates, in the presence of DNA, the weak ATPase activity of RuvB (By similarity)
J168_03413	ENOG4105NHU	Nuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves the cruciform structure in supercoiled DNA by nicking to strands with the same polarity at sites symmetrically opposed at the junction in the homologous arms and leaves a 5'-terminal phosphate and a 3'-terminal hydroxyl group (By similarity)
J168_03414	ENOG4105CDY	transcriptional regulatory protein
J168_03417	ENOG4105C9M	aspartyl-trna synthetase
J168_03420	ENOG4108ISG	Major Facilitator
J168_03423	ENOG4105HSS	phospholipase C
J168_03426	ENOG4105ETT	transcriptional Regulator, LysR family
J168_03428	ENOG4105C5H	ABC transporter
J168_03429	ENOG4105CHI	Involved in the active translocation of vitamin B12 (cyanocobalamin) across the outer membrane to the periplasmic space. It derives its energy for transport by interacting with the trans-periplasmic membrane protein TonB (By similarity)
J168_03431	ENOG4105CHI	Involved in the active translocation of vitamin B12 (cyanocobalamin) across the outer membrane to the periplasmic space. It derives its energy for transport by interacting with the trans-periplasmic membrane protein TonB (By similarity)
J168_03432	ENOG4107RNH	Outer membrane receptor FepA
J168_03434	ENOG4105CKD	glutathione-regulated potassium-efflux system protein
J168_03439	ENOG4105GAV	receptor
J168_03442	ENOG4105C6X	Major Facilitator
J168_03444	ENOG4105CU5	Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine (By similarity)
J168_03449	ENOG4105CUP	Catalyzes the synthesis of alpha-ribazole-5'-phosphate from nicotinate mononucleotide (NAMN) and 5,6- dimethylbenzimidazole (DMB) (By similarity)
J168_03450	ENOG4108YZT	Adenosylcobinamide kinase
J168_03451	ENOG4105CAA	catalyzes amidations at positions B, D, E, and G on adenosylcobyrinic A,C-diamide. NH(2) groups are provided by glutamine, and one molecule of ATP is hydrogenolyzed for each amidation (By similarity)
J168_03452	ENOG4105EFT	decarboxylase
J168_03454	ENOG4105DH2	Converts cobyric acid to cobinamide by the addition of aminopropanol on the F carboxylic group (By similarity)
J168_03455	ENOG41068B1	Cob-I-yrinic acid a,c-diamide adenosyltransferase
J168_03458	ENOG4105CHI	Involved in the active translocation of vitamin B12 (cyanocobalamin) across the outer membrane to the periplasmic space. It derives its energy for transport by interacting with the trans-periplasmic membrane protein TonB (By similarity)
J168_03460	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
J168_03461	ENOG4105E2Y	ABC, transporter
J168_03462	ENOG4105EFS	Binding-protein-dependent transport systems, inner membrane component
J168_03463	ENOG4105GVF	(ABC) transporter
J168_03464	ENOG4105CPC	Aldo Keto reductase
J168_03465	ENOG4105CPU	Monooxygenase
J168_03466	ENOG4107ZSV	Receptor
J168_03467	ENOG41082IR	Excinuclease ABC C subunit domain protein
J168_03474	ENOG4105CHI	Involved in the active translocation of vitamin B12 (cyanocobalamin) across the outer membrane to the periplasmic space. It derives its energy for transport by interacting with the trans-periplasmic membrane protein TonB (By similarity)
J168_03475	ENOG4108K4C	ec 3.1.3.12
J168_03476	ENOG4105BZP	glycoside hydrolase 15-related
J168_03477	ENOG4105C1K	alpha-alpha-trehalose-phosphate synthase
J168_03478	ENOG4105DZG	Dehydrogenase
J168_03479	ENOG4105C8Q	Methyl-accepting chemotaxis
J168_03480	ENOG4105KIR	Thiol-disulfide oxidoreductase dcc
J168_03483	ENOG4105C34	Pseudouridine synthase
J168_03484	ENOG4106SNF	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane
J168_03486	ENOG4105C4K	Nad synthetase
J168_03492	ENOG4105CVE	Lytic murein transglycosylase
J168_03514	ENOG4105C0C	Catalyzes the oxidation of 3-carboxy-2-hydroxy-4- methylpentanoate (3-isopropylmalate) to 3-carboxy-4-methyl-2- oxopentanoate. The product decarboxylates to 4-methyl-2 oxopentanoate (By similarity)
J168_03516	ENOG4105VW4	glutaredoxin 3
J168_03517	ENOG4105ERG	peptidase m48, ste24p
J168_03518	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
J168_03519	ENOG4105BZU	Histidine kinase
J168_03520	ENOG4105CUU	Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) (By similarity)
J168_03521	ENOG4105C9X	ppx gppa phosphatase
J168_03522	ENOG4105BZF	Glycosyl transferase (Group 1
J168_03523	ENOG4105EYK	Phosphatidylglycerophosphatase B
J168_03525	ENOG4105F10	Catalyzes the hydrolysis of the pyrophosphate bond of UDP-2,3-diacylglucosamine to yield 2,3-diacylglucosamine 1- phosphate (lipid X) and UMP (By similarity)
J168_03527	ENOG4108YP4	Metalloprotease, specifically cleaves on the N-terminal side of aspartyl, glutamyl and cysteic acid residues (By similarity)
J168_03529	ENOG4105ED9	Protein of unknown function (DUF455)
J168_03530	ENOG4105CBA	glutamine phosphoribosylpyrophosphate amidotransferase
J168_03533	ENOG4105DPM	folylpolyglutamate synthase Dihydrofolate synthase
J168_03534	ENOG4105CVJ	phosphoglycerate mutase
J168_03537	ENOG4105HSS	phospholipase C
J168_03539	ENOG4105CPQ	Dehydrogenase
J168_03541	ENOG4108IJ6	ABC transporter
J168_03543	ENOG4108I5D	sulfate abc transporter
J168_03544	ENOG4105DE7	Sulfate ABC transporter periplasmic sulfate-binding protein
J168_03545	ENOG4107EEK	Catalyzes the decarboxylative condensation of pimeloyl- acyl-carrier protein and L-alanine to produce 8-amino-7- oxononanoate (AON), acyl-carrier protein , and carbon dioxide (By similarity)
J168_03547	ENOG4108R99	pseudouridine synthase
J168_03549	ENOG4105CDV	Ompa motb domain protein
J168_03550	ENOG4105CIS	alcohol dehydrogenase
J168_03551	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
J168_03553	ENOG4108K3A	Glutathione S-transferase
J168_03554	ENOG4105D9Z	Catalyzes the reversible oxidation of malate to oxaloacetate (By similarity)
J168_03555	ENOG4107XH4	PPIases accelerate the folding of proteins (By similarity)
J168_03558	ENOG4105C3P	Allows the formation of correctly charged Gln-tRNA(Gln) through the transamidation of misacylated Glu-tRNA(Gln) in organisms which lack glutaminyl-tRNA synthetase. The reaction takes place in the presence of glutamine and ATP through an activated gamma-phospho-Glu-tRNA(Gln) (By similarity)
J168_03560	ENOG4105C7V	phospho-2-dehydro-3-deoxyheptonate aldolase
J168_03562	ENOG41080I0	Required for disulfide bond formation in some periplasmic proteins. Acts by oxidizing the DsbA protein (By similarity)
J168_03563	ENOG4108ZT0	50S ribosomal protein l17
J168_03564	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
J168_03565	ENOG4105G6W	One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the body of the 30S subunit (By similarity)
J168_03566	ENOG4108UHH	Located on the platform of the 30S subunit, it bridges several disparate RNA helices of the 16S rRNA. Forms part of the Shine-Dalgarno cleft in the 70S ribosome (By similarity)
J168_03567	ENOG4108Z04	Located at the top of the head of the 30S subunit, it contacts several helices of the 16S rRNA. In the 70S ribosome it contacts the 23S rRNA (bridge B1a) and protein L5 of the 50S subunit (bridge B1b), connecting the 2 subunits
J168_03568	ENOG4105CGG	The central subunit of the protein translocation channel SecYEG. Consists of two halves formed by TMs 1-5 and 6-10. These two domains form a lateral gate at the front which open onto the bilayer between TMs 2 and 7, and are clamped together by SecE at the back. The channel is closed by both a pore ring composed of hydrophobic SecY resides and a short helix (helix 2A) on the extracellular side of the membrane which forms a plug. The plug probably moves laterally to allow the channel to open. The ring and the pore may move independently (By similarity)
J168_03569	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
J168_03571	ENOG4108RA9	Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body (By similarity)
J168_03572	ENOG4105K4C	This is one of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance (By similarity)
J168_03573	ENOG4108R5J	This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7 L12 stalk, and near the tRNA binding site of the peptidyltransferase center (By similarity)
J168_03574	ENOG4108UJY	One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit (By similarity)
J168_03575	ENOG4105VBI	Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site (By similarity)
J168_03576	ENOG4105CW6	This is 1 of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance. In the 70S ribosome it contacts protein S13 of the 30S subunit (bridge B1b), connecting the 2 subunits
J168_03577	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
J168_03578	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
J168_03579	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
J168_03580	ENOG41083MP	50s ribosomal protein l29
J168_03581	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
J168_03582	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
J168_03583	ENOG4105KAP	The globular domain of the protein is located near the polypeptide exit tunnel on the outside of the subunit, while an extended beta-hairpin is found that lines the wall of the exit tunnel in the center of the 70S ribosome (By similarity)
J168_03584	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
J168_03585	ENOG4105CFD	One of the primary rRNA binding proteins. Required for association of the 30S and 50S subunits to form the 70S ribosome, for tRNA binding and peptide bond formation. It has been suggested to have peptidyltransferase activity
J168_03586	ENOG41080KG	One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome (By similarity)
J168_03587	ENOG4106U5A	One of the primary rRNA binding proteins, this protein initially binds near the 5'-end of the 23S rRNA. It is important during the early stages of 50S assembly. It makes multiple contacts with different domains of the 23S rRNA in the assembled 50S subunit and ribosome (By similarity)
J168_03588	ENOG4105EEE	One of the primary rRNA binding proteins, it binds directly near the 3'-end of the 23S rRNA, where it nucleates assembly of the 50S subunit (By similarity)
J168_03589	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
J168_03590	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
J168_03591	ENOG4105CEJ	Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post- translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome (By similarity)
J168_03592	ENOG4108UHY	One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the head domain of the 30S subunit. Is located at the subunit interface close to the decoding center, probably blocks exit of the E-site tRNA (By similarity)
J168_03593	ENOG4108UKE	Interacts with and stabilizes bases of the 16S rRNA that are involved in tRNA selection in the A site and with the mRNA backbone. Located at the interface of the 30S and 50S subunits, it traverses the body of the 30S subunit contacting proteins on the other side and probably holding the rRNA structure together. The combined cluster of proteins S8, S12 and S17 appears to hold together the shoulder and platform of the 30S subunit (By similarity)
J168_03594	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
J168_03595	ENOG4108IIJ	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
J168_03597	ENOG4105KBC	Seems to be the binding site for several of the factors involved in protein synthesis and appears to be essential for accurate translation (By similarity)
J168_03598	ENOG4108VZM	50s ribosomal protein L10
J168_03599	ENOG4105C64	Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release (By similarity)
J168_03600	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
J168_03601	ENOG4105E5V	Participates in transcription elongation, termination and antitermination (By similarity)
J168_03602	ENOG4105PM1	preprotein translocase subunit SecE
J168_03604	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
J168_03608	ENOG4105C3G	gtp-binding protein
J168_03609	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
J168_03610	ENOG4105KW6	This is one of the proteins that binds to the 5S RNA in the ribosome where it forms part of the central protuberance (By similarity)
J168_03611	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
J168_03613	ENOG4105CTR	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
J168_03614	ENOG4105QVB	outer membrane lipoprotein LolB
J168_03615	ENOG4105DJQ	tetratricopeptide tpr_2 repeat protein
J168_03616	ENOG4105C7E	Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) (By similarity)
J168_03617	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
J168_03619	ENOG4108RIR	Molybdenum cofactor biosynthesis protein
J168_03620	ENOG4105CSR	polyphosphate kinase 2
J168_03623	ENOG4107QX9	Thiol disulfide interChange protein
J168_03624	ENOG4107S2Z	UPF0761 membrane protein
J168_03625	ENOG4105CS1	NAD(P)H quinone oxidoreductase
J168_03630	ENOG4108Z66	YbaK ebsC protein
J168_03631	ENOG4105RX7	peptidase S8 and S53, subtilisin, kexin, sedolisin
J168_03632	ENOG4105RX7	peptidase S8 and S53, subtilisin, kexin, sedolisin
J168_03633	ENOG4105RX7	peptidase S8 and S53, subtilisin, kexin, sedolisin
J168_03634	ENOG4105CM2	brancheD-chain amino acid aminotransferase
J168_03637	ENOG4105C15	The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane (By similarity)
J168_03638	ENOG4105W8H	transhydrogenase (subunit alpha
J168_03642	ENOG4108IIE	The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane (By similarity)
J168_03648	ENOG4105C2M	dna polymerase I
J168_03652	ENOG4105EQY	Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif (By similarity)
J168_03655	ENOG4105C5Q	Transcriptional regulator
J168_03656	ENOG4105NXH	GreA GreB family elongation factor
J168_03657	ENOG4105CW3	Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway (By similarity)
J168_03659	ENOG4107QXP	Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine (By similarity)
J168_03661	ENOG4105WH1	Two component transcriptional regulator luxr family
J168_03662	ENOG4105BZU	Histidine kinase
J168_03663	ENOG4105BZU	Histidine kinase
J168_03666	ENOG4105CX6	glutaminyL-tRNA synthetase
J168_03667	ENOG4105DXC	membrane
J168_03670	ENOG4105EZ6	Catalyzes the 2'-O-methylation at nucleotide C2498 in 23S rRNA (By similarity)
J168_03676	ENOG4108D7R	p-hydroxycinnamoyl CoA hydratase lyase
J168_03678	ENOG4105CEY	Amp-dependent synthetase and ligase
J168_03679	ENOG4105DDW	LysR family Transcriptional regulator
J168_03686	ENOG4105EAK	ubiquinone biosynthesis hydroxylase, ubiH ubiF VisC COQ6 family
J168_03687	ENOG4105D0A	hydroxylase
J168_03689	ENOG4108WBT	adenosyltransferase
J168_03693	ENOG4105E7H	involved in the assembly of LPS in the outer leaflet of the outer membrane. Determines N-hexane tolerance and is involved in outer membrane permeability. Essential for envelope biogenesis (By similarity)
J168_03694	ENOG4105DBD	Chaperone involved in the correct folding and assembly of outer membrane proteins. Recognizes specific patterns of aromatic residues and the orientation of their side chains, which are found more frequently in integral outer membrane proteins. May act in both early periplasmic and late outer membrane-associated steps of protein maturation (By similarity)
J168_03695	ENOG4105CEZ	Catalyzes the NAD(P)-dependent oxidation of 4- (phosphohydroxy)-L-threonine (HTP) into 2-amino-3-oxo-4- (phosphohydroxy)butyric acid which spontaneously decarboxylates to form 3-amino-2-oxopropyl phosphate (AHAP) (By similarity)
J168_03696	ENOG4105D1X	Specifically dimethylates two adjacent adenosines (A1518 and A1519) in the loop of a conserved hairpin near the 3'-end of 16S rRNA in the 30S particle. May play a critical role in biogenesis of 30S subunits (By similarity)
J168_03697	ENOG4105NWN	ApaG protein
J168_03698	ENOG4105DDT	Hydrolyzes diadenosine 5',5'''-P1,P4-tetraphosphate to yield ADP (By similarity)
J168_03700	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
J168_03702	ENOG4105DEF	Extracellular solute-binding protein, family 5
J168_03707	ENOG4108UZX	fmn reductase
J168_03708	ENOG4105D4R	Catalyzes the desulfonation of aliphatic sulfonates (By similarity)
J168_03710	ENOG4105EFS	Binding-protein-dependent transport systems, inner membrane component
J168_03711	ENOG4105D7T	ABC transporter
J168_03712	ENOG4107T8P	acyl-Coa dehydrogenase
J168_03713	ENOG4107SM7	Transcriptional regulator
J168_03716	ENOG4105C0V	Provides the sole de novo source of dTMP for DNA biosynthesis (By similarity)
J168_03717	ENOG4105C3B	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
J168_03721	ENOG41080IJ	Diacylglycerol kinase
J168_03723	ENOG4105DHQ	Histidine kinase
J168_03724	ENOG4105ETX	regulatoR
J168_03725	ENOG4108UJV	acyl-CoA thioesterase i
J168_03726	ENOG4108I0Y	(ABC) transporter
J168_03728	ENOG4105E2B	Taurine dioxygenase
J168_03731	ENOG4105EFS	Binding-protein-dependent transport systems, inner membrane component
J168_03735	ENOG4105D05	Receptor
J168_03737	ENOG4105CPC	Aldo Keto reductase
J168_03738	ENOG4105D9N	nucleoside
J168_03739	ENOG4108RVA	ribokinase
J168_03742	ENOG4105CEH	Catalyzes the synthesis of dihydrouridine a modified base found in the D-loop of most tRNAs (By similarity)
J168_03743	ENOG4107R6G	Catalyzes the S-adenosylmethionine monomethyl esterification of trans-aconitate (By similarity)
J168_03745	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
J168_03746	ENOG4105D6F	Phosphatase
J168_03751	ENOG4105CCA	Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle (By similarity)
J168_03754	ENOG4105C3E	May play a key role in the regulation of the intracellular concentration of adenosylhomocysteine (By similarity)
J168_03755	ENOG4105DXX	methyltransferase
J168_03768	ENOG4105SYT	Methylenetetrahydrofolate reductase
J168_03770	ENOG4105M6F	mutator MutT protein
J168_03771	ENOG4105CI6	Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. Has a central role in coupling the hydrolysis of ATP to the transfer of proteins into and across the cell membrane, serving
J168_03772	ENOG4105DR5	peptidase
J168_03774	ENOG4105C7C	involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
J168_03775	ENOG4105CDK	Essential cell division protein that forms a contractile ring structure (Z ring) at the future cell division site. The regulation of the ring assembly controls the timing and the location of cell division. One of the functions of the FtsZ ring is to recruit other cell division proteins to the septum to produce a new cell wall between the dividing cells. Binds GTP and shows GTPase activity (By similarity)
J168_03776	ENOG4105CIT	This protein may be involved in anomalous filament growth. May be a component of the septum (By similarity)
J168_03777	ENOG4105K7E	Essential cell division protein. May link together the upstream cell division proteins, which are predominantly cytoplasmic, with the downstream cell division proteins, which are predominantly periplasmic. May control correct divisome assembly (By similarity)
J168_03778	ENOG4105CPF	Cell wall formation (By similarity)
J168_03779	ENOG4105DFU	Cell wall formation (By similarity)
J168_03780	ENOG4105DVQ	Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II) (By similarity)
J168_03781	ENOG4105DVQ	Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II) (By similarity)
J168_03783	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
J168_03784	ENOG4108EQQ	Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein (By similarity)
J168_03785	ENOG4107EEN	Catalyzes the addition of meso-diaminopimelic acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan (By similarity)
J168_03786	ENOG4105CJN	penicillin-binding protein
J168_03787	ENOG4106932	Essential cell division protein. May link together the upstream cell division proteins, which are predominantly cytoplasmic, with the downstream cell division proteins, which are predominantly periplasmic (By similarity)
J168_03788	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
J168_03789	ENOG4108V6E	Cell division protein mraZ
J168_03797	ENOG41082RQ	UPF0102 protein
J168_03798	ENOG4105S2T	inner membrane protein YbcI
J168_03799	ENOG4105CQB	FAD linked oxidase domain protein
J168_03802	ENOG4105EEX	Two component transcriptional regulator (Winged helix family
J168_03803	ENOG4105C08	Histidine kinase
J168_03804	ENOG4108R80	One of the components of the high-affinity ATP-driven potassium transport (or KDP) system, which catalyzes the hydrolysis of ATP coupled with the exchange of hydrogen and potassium ions. The C subunit may be involved in assembly of the KDP complex (By similarity)
J168_03805	ENOG4105C8X	One of the components of the high-affinity ATP-driven potassium transport (or KDP) system, which catalyzes the hydrolysis of ATP coupled with the exchange of hydrogen and potassium ions (By similarity)
J168_03806	ENOG4105D9K	One of the components of the high-affinity ATP-driven potassium transport (or KDP) system, which catalyzes the hydrolysis of ATP coupled with the exchange of hydrogen and potassium ions (By similarity)
J168_03810	ENOG4105CG2	Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 (By similarity)
J168_03811	ENOG4107YIM	Involved in the transcription termination process (By similarity)
J168_03812	ENOG4108UTT	Catalyzes the formation of 6,7-dimethyl-8- ribityllumazine by condensation of 5-amino-6-(D- ribitylamino)uracil with 3,4-dihydroxy-2-butanone 4-phosphate. This is the penultimate step in the biosynthesis of riboflavin (By similarity)
J168_03813	ENOG4105C66	Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate (By similarity)
J168_03817	ENOG4105D1W	Converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)- pyrimidinedione 5'-phosphate (By similarity)
J168_03819	ENOG4108Z11	Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes (By similarity)
J168_03820	ENOG4105C65	Catalyzes the reversible interconversion of serine and glycine with tetrahydrofolate (THF) serving as the one-carbon carrier. This reaction serves as the major source of one-carbon groups required for the biosynthesis of purines, thymidylate, methionine, and other important biomolecules. Also exhibits THF- independent aldolase activity toward beta-hydroxyamino acids, producing glycine and aldehydes, via a retro-aldol mechanism (By similarity)
J168_03822	ENOG4105C5H	ABC transporter
J168_03825	ENOG4105JAB	phenazine biosynthesis protein, phzf family
J168_03826	ENOG4105C1I	TRANSCRIPTIONAl REGULATOR GntR family
J168_03828	ENOG4108QBQ	Catalyzes the condensation of formaldehyde and glutathione to S-hydroxymethylglutathione (By similarity)
J168_03833	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
J168_03834	ENOG4105JJR	Histidine kinase
J168_03837	ENOG4105CY0	Metallo-Beta-Lactamase
J168_03838	ENOG4105WHM	Necessary for normal cell division and for the maintenance of normal septation (By similarity)
J168_03839	ENOG4106RE7	Cytochrome
J168_03842	ENOG4108Z33	Thiol disulfide Interchange Protein
J168_03844	ENOG4105C94	Transporter
J168_03845	ENOG4105C26	Dehydrogenase
J168_03846	ENOG4105CZ6	Can catalyze the oxidation of choline to betaine aldehyde and betaine aldehyde to glycine betaine (By similarity)
J168_03847	ENOG4105D4J	Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate
J168_03849	ENOG4105CE4	GlcNAc 6-P deacetylase
J168_03850	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
J168_03851	ENOG4105ETE	Transcriptional regulator (LacI family
J168_03853	ENOG4105FDP	GntR family transcriptional regulator
J168_03857	ENOG4105CNT	hydrolase family 2
J168_03862	ENOG4108RTD	type II secretion system protein K
J168_03865	ENOG4105VWV	general secretion pathway protein h
J168_03866	ENOG4108VAU	general secretion pathway protein G
J168_03867	ENOG4105D7Q	type ii secretion system
J168_03868	ENOG4107QHF	type ii secretion system protein e
J168_03869	ENOG4105GVR	general secretion pathway protein D
J168_03877	ENOG4105CHR	reductase
J168_03879	ENOG4105BZU	Histidine kinase
J168_03881	ENOG4105BZU	Histidine kinase
J168_03882	ENOG4105W4M	Transport-associated protein
J168_03883	ENOG4105D9R	oxidoreductase
J168_03884	ENOG4108J5G	6-phosphogluconate dehydrogenase
J168_03893	ENOG4105EGI	Transcriptional regulator
J168_03895	ENOG4105CN1	protease
J168_03896	ENOG4105C0G	Catalyzes the radical-mediated insertion of two sulfur atoms into the C-6 and C-8 positions of the octanoyl moiety bound to the lipoyl domains of lipoate-dependent enzymes, thereby converting the octanoylated domains into lipoylated derivatives (By similarity)
J168_03897	ENOG4108BDP	Catalyzes the transfer of endogenously produced octanoic acid from octanoyl-acyl-carrier-protein onto the lipoyl domains of lipoate-dependent enzymes. Lipoyl-ACP can also act as a substrate although octanoyl-ACP is likely to be the physiological substrate (By similarity)
J168_03900	ENOG4105DZ1	carboxypeptidase
J168_03901	ENOG4105K6T	rare lipoprotein A
J168_03902	ENOG4105CVE	Lytic murein transglycosylase
J168_03903	ENOG4107WN4	Polygalacturonase
J168_03904	ENOG4105CNI	cell division protein FtsW
J168_03907	ENOG4105N3I	Involved in formation and maintenance of cell shape (By similarity)
J168_03908	ENOG4105DFF	Rod shape-determining protein mreb
J168_03910	ENOG4108JU9	GAF modulated sigma54 specific transcriptional regulator Fis family
J168_03915	ENOG4108Q1J	Extracellular solute-binding protein, family 3
J168_03916	ENOG4105DZG	Dehydrogenase
J168_03919	ENOG4105CD8	aminopeptidase N
J168_03920	ENOG4105BZU	Histidine kinase
J168_03921	ENOG4105DDZ	Methyltransferase required for the conversion of demethylmenaquinone (DMKH2) to menaquinone (MKH2) and the conversion of 2-polyprenyl-6-methoxy-1,4-benzoquinol (DDMQH2) to 2-polyprenyl-3-methyl-6-methoxy-1,4-benzoquinol (DMQH2) (By similarity)
J168_03926	ENOG4105C4N	this subunit has chaperone activity. The binding of ATP and its subsequent hydrolysis by HslU are essential for unfolding of protein substrates subsequently hydrolyzed by HslV. HslU recognizes the N-terminal part of its protein substrates and unfolds these before they are guided to HslV for hydrolysis (By similarity)
J168_03927	ENOG4108R5P	Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery (By similarity)
J168_03928	ENOG4108IYS	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
J168_03930	ENOG4105E4Z	Catalyzes the stereoinversion of LL-2,6- diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso- DAP), a precursor of L-lysine and an essential component of the bacterial peptidoglycan (By similarity)
J168_03932	ENOG4105WD1	Membrane
J168_03935	ENOG4105DKX	Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 in tRNAs that read codons beginning with uridine, leading to the formation of N6-(dimethylallyl)adenosine (i(6)A) (By similarity)
J168_03941	ENOG4105D6W	Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps (By similarity)
J168_03942	ENOG4108NEV	two component transcriptional regulator, LytTR family
J168_03943	ENOG4108HRK	Histidine kinase
J168_03945	ENOG4105C3A	Involved in the biosynthesis of osmoregulated periplasmic glucans (OPGs) (By similarity)
J168_03948	ENOG4105BZU	Histidine kinase
J168_03949	ENOG4105CHH	sulfate transporter
J168_03950	ENOG4106R7G	Glycoside hydrolase family 5
J168_03951	ENOG4105C8Q	Methyl-accepting chemotaxis
J168_03959	ENOG4105E53	ec 3.2.1.28
J168_03961	ENOG4105D7N	magnesium and cobalt transport protein CorA
J168_03967	ENOG4105F87	Dehydratase
J168_03968	ENOG4105DFI	Membrane
J168_03973	ENOG4105BZU	Histidine kinase
J168_03974	ENOG4107QS8	(LipO)protein
J168_03975	ENOG4105C5Z	peptidase
J168_03976	ENOG4105EYF	MMPL domain protein
J168_03981	ENOG4105CHF	Glutathione S-transferase
J168_03986	ENOG4105W5Q	DNA repair protein (RadC
J168_03991	ENOG4105CQZ	Histidine kinase
J168_03998	ENOG4105BZS	acriflavin resistance protein
J168_04000	ENOG4105C3T	may be the GTPase, regulating ATP sulfurylase activity (By similarity)
J168_04001	ENOG4105C11	sulfate adenylyltransferase), subunit 2
J168_04002	ENOG4107EER	Component of the sulfite reductase complex that catalyzes the 6-electron reduction of sulfite to sulfide. This is one of several activities required for the biosynthesis of L- cysteine from sulfate. The flavoprotein component catalyzes the electron flow from NADPH - FAD - FMN to the hemoprotein component (By similarity)
J168_04003	ENOG4105ET1	Component of the sulfite reductase complex that catalyzes the 6-electron reduction of sulfite to sulfide. This is one of several activities required for the biosynthesis of L- cysteine from sulfate (By similarity)
J168_04004	ENOG4105ET3	Reduction of activated sulfate into sulfite (By similarity)
J168_04008	ENOG4105BZU	Histidine kinase
J168_04010	ENOG4107R11	Transcriptional regulator
J168_04011	ENOG4105CB8	Multifunctional enzyme that catalyzes the SAM-dependent methylation of uroporphyrinogen III at position C-2 and C-7 to form precorrin-2 and then position C-12 or C-18 to form trimethylpyrrocorphin 2. It also catalyzes the conversion of precorrin-2 into siroheme. This reaction consists of the NAD- dependent oxidation of precorrin-2 into sirohydrochlorin and its subsequent ferrochelation into siroheme (By similarity)
J168_04014	ENOG4108UVJ	appr-1-p processing domain protein
J168_04015	ENOG4107R1Y	fructose-bisphosphate aldolase
J168_04016	ENOG4105CA9	Pyruvate kinase
J168_04018	ENOG4105BZA	Phosphoglycerate kinase
J168_04023	ENOG4105C17	glyceraldehyde-3-phosphate dehydrogenase
J168_04025	ENOG4105EIF	outer membrane protein W
J168_04026	ENOG4105EIF	outer membrane protein W
J168_04028	ENOG4107S76	domain protein
J168_04029	ENOG4108S6J	ABC transporter, periplasmic molybdate-binding protein
J168_04030	ENOG4105E0C	molybdate abc transporter
J168_04031	ENOG4105CGB	Part of the ABC transporter complex ModABC involved in molybdenum import. Responsible for energy coupling to the transport system (By similarity)
J168_04038	ENOG4107Y2H	ErfK ybiS ycfS ynhG family protein
J168_04039	ENOG4105DR5	peptidase
J168_04041	ENOG4105CNM	Receptor
J168_04042	ENOG4107SKW	Inherit from COG: Alpha beta hydrolase
J168_04043	ENOG4105CV1	Transketolase (EC 2.2.1.1)
J168_04044	ENOG4105CK2	sodium dicarboxylate symporter
J168_04046	ENOG4107QVM	von Willebrand factor, type A
J168_04050	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
J168_04052	ENOG4105E4G	Type IV pilus
J168_04057	ENOG4108JQC	penicillin-binding protein 1A
J168_04061	ENOG4105NRA	50s ribosomal protein l31 type b
J168_04062	ENOG4105DU0	nucleoside hydrolase
J168_04063	ENOG4105CB5	ATP-dependent DNA helicase recG
J168_04064	ENOG4105KME	endoribonuclease L-psp
J168_04065	ENOG4105CWR	In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance (By similarity)
J168_04066	ENOG4105VFG	Promotes RNA polymerase assembly. Latches the N- and C- terminal regions of the beta' subunit thereby facilitating its interaction with the beta and alpha subunits (By similarity)
J168_04067	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
J168_04068	ENOG4105DSJ	YicC domain protein
J168_04069	ENOG4105ED0	Phosphorolytic exoribonuclease that removes nucleotide residues following the -CCA terminus of tRNA and adds nucleotides to the ends of RNA molecules by using nucleoside diphosphates as substrates (By similarity)
J168_04071	ENOG4108V82	Pyrophosphatase that hydrolyzes non-canonical purine nucleotides such as XTP and ITP dITP to their respective monophosphate derivatives. Might exclude non-canonical purines from DNA precursor pool, thus preventing their incorporation into DNA and avoiding chromosomal lesions (By similarity)
J168_04072	ENOG4105CSA	Coproporphyrinogen iii oxidase
J168_04075	ENOG4105D9Y	Splits dipeptides with a prolyl residue in the C- terminal position (By similarity)
J168_04077	ENOG4107RAQ	aminopeptidase
J168_04080	ENOG4105W8B	Activator of cell division through the inhibition of FtsZ GTPase activity, therefore promoting FtsZ assembly into bundles of protofilaments necessary for the formation of the division Z ring. It is recruited early at mid-cell but it is not essential for cell division (By similarity)
J168_04082	ENOG4105MK2	5-formyltetrahydrofolate cyclo-ligase
J168_04084	ENOG4105E66	phosphoriboisomerase A
J168_04086	ENOG41063JG	Transcriptional regulator
J168_04087	ENOG4105VCQ	rubredoxin
J168_04088	ENOG4108UV6	Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP) (By similarity)
J168_04091	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
J168_04092	ENOG41061ZR	Transcriptional regulator
J168_04094	ENOG4105CIH	Imidazole acetol-phosphate transaminase
J168_04100	ENOG4105C8Y	Acetylornithine aminotransferase
J168_04101	ENOG4105EYW	Ion transport protein
J168_04104	ENOG410841Q	phosphoesterase PA-phosphatase related protein
J168_04105	ENOG4105FFC	UPF0187 protein
J168_04107	ENOG4105DFU	Cell wall formation (By similarity)
J168_04108	ENOG4105CC8	Catalyzes the reversible transfer of the terminal phosphate group between ATP and AMP. Plays an important role in cellular energy homeostasis and in adenine nucleotide metabolism (By similarity)
J168_04111	ENOG4105EAY	pump that utilizes the energy of pyrophosphate hydrolysis as the driving force for
J168_04113	ENOG4105F0N	pyrophosphate phospho-hydrolase
J168_04116	ENOG4105ECQ	AraC Family Transcriptional Regulator
J168_04117	ENOG4108M3R	transcriptional activator CadC
J168_04118	ENOG4105CBF	Catalyzes the synthesis of the hydroxymethylpyrimidine phosphate (HMP-P) moiety of thiamine from aminoimidazole ribotide (AIR) in a radical S-adenosyl-L-methionine (SAM)-dependent reaction (By similarity)
J168_04121	ENOG4105C8Q	Methyl-accepting chemotaxis
J168_04122	ENOG4105CFB	Gamma-glutamyltranspeptidase (EC 2.3.2.2)
J168_04123	ENOG4105C6M	Alpha-keto-beta-hydroxylacyl reductoisomerase
J168_04126	ENOG4105C7B	Threonine dehydratase
J168_04127	ENOG4105CYQ	Catalyzes the condensation of the acetyl group of acetyl-CoA with 3-methyl-2-oxobutanoate (2-oxoisovalerate) to form 3-carboxy-3-hydroxy-4-methylpentanoate (2-isopropylmalate) (By similarity)
J168_04128	ENOG4105C0C	Catalyzes the oxidation of 3-carboxy-2-hydroxy-4- methylpentanoate (3-isopropylmalate) to 3-carboxy-4-methyl-2- oxopentanoate. The product decarboxylates to 4-methyl-2 oxopentanoate (By similarity)
J168_04129	ENOG4105MQS	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
J168_04130	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
J168_04131	ENOG4108MP6	LysR family Transcriptional regulator
J168_04134	ENOG4105E26	Catalyzes the methyl esterification of L-isoaspartyl residues in peptides and proteins that result from spontaneous decomposition of normal L-aspartyl and L-asparaginyl residues. It plays a role in the repair and or degradation of damaged proteins (By similarity)
J168_04135	ENOG4105DFG	type I secretion outer membrane protein
J168_04136	ENOG4105D8A	3-Deoxy-D-manno-octulosonic-acid transferase
J168_04137	ENOG4105D1S	lipid A biosynthesis
J168_04143	ENOG4105C6K	Malic enzyme
J168_04144	ENOG4105CK2	sodium dicarboxylate symporter
J168_04146	ENOG4105CQZ	Histidine kinase
J168_04147	ENOG4105CSH	Transporter
J168_04149	ENOG4105F04	LysR family Transcriptional regulator
J168_04150	ENOG4105CPC	Aldo Keto reductase
J168_04154	ENOG4105WH1	Two component transcriptional regulator luxr family
J168_04155	ENOG4106JDA	Phosphoglycerate transport regulatory protein PGTC
J168_04156	ENOG4105DHQ	Histidine kinase
J168_04159	ENOG4105D4T	Citrate transporter
J168_04161	ENOG4105CHR	reductase
J168_04162	ENOG4105ETE	Transcriptional regulator (LacI family
J168_04165	ENOG4107QW3	Sucrose phosphorylase
J168_04168	ENOG4105E06	May play a role in 30S ribosomal subunit biogenesis. Unusual circulary permuted GTPase that catalyzes rapid hydrolysis of GTP with a slow catalytic turnover (By similarity)
J168_04172	ENOG4105CNM	Receptor
J168_04182	ENOG4108RMV	DegV Family
J168_04183	ENOG4108RBJ	Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions (By similarity)
J168_04187	ENOG4105EJG	cellulose synthase
J168_04188	ENOG4105EJG	cellulose synthase
J168_04189	ENOG4105K2Z	endo-1,4-d-glucanase (EC 3.2.1.4)
J168_04190	ENOG4107EEX	Cellulose synthase regulator protein
J168_04191	ENOG4107QZ7	Cellulose synthase catalytic subunit
J168_04194	ENOG4107RH7	Nicotinate phosphoribosyltransferase
J168_04203	ENOG4106S9K	Transcriptional regulator
J168_04205	ENOG4105GVR	general secretion pathway protein D
J168_04207	ENOG410678M	general secretion pathway protein M
J168_04208	ENOG41090VX	general secretion pathway protein L
J168_04209	ENOG4105UV2	general secretion pathway protein K
J168_04210	ENOG41069G9	General secretion pathway protein J
J168_04212	ENOG4105WMT	general secretion pathway protein h
J168_04214	ENOG4105D7Q	type ii secretion system
J168_04215	ENOG4107QHF	type ii secretion system protein e
J168_04216	ENOG4105RX7	peptidase S8 and S53, subtilisin, kexin, sedolisin
J168_04217	ENOG4105EUR	Domain-Containing protein
J168_04218	ENOG4105RX7	peptidase S8 and S53, subtilisin, kexin, sedolisin
J168_04219	ENOG4105EUR	Domain-Containing protein
J168_04220	ENOG4108ETH	Formylglycinamide ribotide synthetase
J168_04221	ENOG4105T95	Thiol disulfide interChange protein
J168_04222	ENOG4105C13	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
J168_04225	ENOG4108K5H	permease YjgP YjgQ family protein
J168_04227	ENOG4105BZ6	Presumably involved in the processing and regular turnover of intracellular proteins. Catalyzes the removal of unsubstituted N-terminal amino acids from various peptides (By similarity)
J168_04230	ENOG4105CA4	amino acids such as threonine, to avoid such errors, it has a posttransfer editing activity that hydrolyzes mischarged Thr-tRNA(Val) in a tRNA-dependent manner (By similarity)
J168_04236	ENOG4106PT6	cdpdiacylglycerol-serine O-phosphatidyltransferase
J168_04238	ENOG4105C90	Catalyzes the attachment of proline to tRNA(Pro) in a two-step reaction proline is first activated by ATP to form Pro- AMP and then transferred to the acceptor end of tRNA(Pro). As ProRS can inadvertently accommodate and process non-cognate amino acids such as alanine and cysteine, to avoid such errors it has two additional distinct editing activities against alanine. One activity is designated as 'pretransfer' editing and involves the tRNA(Pro)-independent hydrolysis of activated Ala-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Ala-tRNA(Pro). The misacylated Cys- tRNA(Pro) is not edited by ProRS (By similarity)
J168_04239	ENOG4105VFQ	Histone family protein nucleoid-structuring protein H-NS
J168_04242	ENOG4105DHJ	ABC, transporter
J168_04243	ENOG4108SNX	Mammalian cell entry related domain protein
J168_04246	ENOG4105DWH	electron transfer flavoprotein-ubiquinone oxidoreductase
J168_04250	ENOG4107QKV	phosphomannomutase
J168_04251	ENOG4105CJT	Mannose-1-phosphate guanylyltransferase
J168_04253	ENOG4105DBZ	Dtdp-4-dehydrorhamnose reductase
J168_04254	ENOG4108URP	Dtdp-4-dehydrorhamnose 3,5-epimerase
J168_04257	ENOG4105BZJ	Electron transfer flavoprotein
J168_04258	ENOG4105C10	Electron transfer flavoprotein
J168_04261	ENOG4105IQ5	FAD linked oxidase domain protein
J168_04262	ENOG4108RG3	short-chain dehydrogenase reductase
J168_04264	ENOG4105CUI	Catalyzes the interconversion between ADP-D-glycero- beta-D-manno-heptose and ADP-L-glycero-beta-D-manno-heptose via an epimerization at carbon 6 of the heptose (By similarity)
J168_04265	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
J168_04268	ENOG4105DDZ	Methyltransferase required for the conversion of demethylmenaquinone (DMKH2) to menaquinone (MKH2) and the conversion of 2-polyprenyl-6-methoxy-1,4-benzoquinol (DDMQH2) to 2-polyprenyl-3-methyl-6-methoxy-1,4-benzoquinol (DMQH2) (By similarity)
J168_04270	ENOG4105CTC	Lipopolysaccharide biosynthesis protein-like protein
J168_04272	ENOG4105EQK	-acetyltransferase
J168_04273	ENOG4105EY8	ABC transporter
J168_04275	ENOG4105C28	cystathionine
J168_04280	ENOG4105CZX	twitching motility protein
J168_04281	ENOG4108RXX	maleylacetoacetate isomerase
J168_04283	ENOG4105C1J	atp-dependent rna helicase
J168_04285	ENOG4105CHI	Involved in the active translocation of vitamin B12 (cyanocobalamin) across the outer membrane to the periplasmic space. It derives its energy for transport by interacting with the trans-periplasmic membrane protein TonB (By similarity)
J168_04286	ENOG4107ZIF	6-carboxy-5,6,7,8-tetrahydropterin synthase
J168_04288	ENOG4105E78	Catalyzes a mechanistically unusual reaction, the ATP- dependent insertion of CO2 between the N7 and N8 nitrogen atoms of 7,8-diaminopelargonic acid (DAPA) to form an ureido ring (By similarity)
J168_04291	ENOG4105NIV	Esterase
J168_04292	ENOG4107RNH	Outer membrane receptor FepA
J168_04293	ENOG4108VXP	Specifically catalyzes the dephosphorylation of 2- phosphoglycolate. Is involved in the dissimilation of the intracellular 2-phosphoglycolate formed during the DNA repair of 3'-phosphoglycolate ends, a major class of DNA lesions induced by oxidative stress (By similarity)
J168_04294	ENOG4105CQ3	Poorly processive error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by polIV. Exhibits no 3-5 exonuclease (proofreading) activity. May be involved in translesional synthesis in conjunction with the beta clamp from polIII (By similarity)
J168_04295	ENOG4108RKI	Necessary for the introduction of cis unsaturation into fatty acids. Catalyzes the dehydration of (3R)-3-hydroxydecanoyl- ACP to E-(2)-decenoyl-ACP and then its isomerization to Z-(3)- decenoyl-ACP. Can catalyze the dehydratase reaction for beta- hydroxyacyl-ACPs with saturated chain lengths up to 16 0, being most active on intermediate chain length (By similarity)
J168_04298	ENOG4105DGW	oligopeptidase A
J168_04301	ENOG4105E3B	Multicopper oxidase
J168_04308	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
J168_04309	ENOG4105DJY	efflux transporter, rnd family, mfp subunit
J168_04310	ENOG4105CQU	Part of the ABC transporter complex LolCDE involved in the translocation of mature outer membrane-directed lipoproteins, from the inner membrane to the periplasmic chaperone, LolA. Responsible for the formation of the LolA-lipoprotein complex in an ATP-dependent manner (By similarity)
J168_04311	ENOG4107RBB	ABC transporter, permease
J168_04312	ENOG4107RBB	ABC transporter, permease
J168_04314	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
J168_04315	ENOG4105BZU	Histidine kinase
J168_04316	ENOG4105CAJ	Catalyzes the last two sequential reactions in the de novo biosynthetic pathway for UDP-N-acetylglucosamine (UDP- GlcNAc). The C-terminal domain catalyzes the transfer of acetyl group from acetyl coenzyme A to glucosamine-1-phosphate (GlcN-1-P) to produce N-acetylglucosamine-1-phosphate (GlcNAc-1-P), which is converted into UDP-GlcNAc by the transfer of uridine 5- monophosphate (from uridine 5-triphosphate), a reaction catalyzed by the N-terminal domain (By similarity)
J168_04320	ENOG4105KNM	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
J168_04321	ENOG4105C4J	Produces ATP from ADP in the presence of a proton gradient across the membrane. The catalytic sites are hosted primarily by the beta subunits (By similarity)
J168_04322	ENOG4105J80	Produces ATP from ADP in the presence of a proton gradient across the membrane. The gamma chain is believed to be important in regulating ATPase activity and the flow of protons through the CF(0) complex (By similarity)
J168_04323	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
J168_04324	ENOG4107S15	F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation (By similarity)
J168_04325	ENOG4107Z6K	F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation (By similarity)
J168_04326	ENOG4105KY6	F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation (By similarity)
J168_04327	ENOG4107RAZ	it plays a direct role in the translocation of protons across the membrane (By similarity)
J168_04331	ENOG4107QN2	dihydrolipoyl dehydrogenase
J168_04333	ENOG4107QSN	dihydrolipoamide acetyltransferase
J168_04339	ENOG4105D01	(LipO)protein
J168_04340	ENOG4108UMI	ABC transporter, permease
J168_04341	ENOG4108JEI	Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system (By similarity)
J168_04342	ENOG4108EHX	EamA-like transporter family
J168_04343	ENOG4108VPT	UPF0234 protein
J168_04345	ENOG4105BZU	Histidine kinase
J168_04348	ENOG4107EXU	Short-chain dehydrogenase reductase Sdr
J168_04350	ENOG4107YBY	Hydrolase
J168_04351	ENOG4105I08	Pseudouridine synthase
J168_04352	ENOG4105D8J	Specifically methylates the guanine in position 1207 of 16S rRNA in the 30S particle (By similarity)
J168_04356	ENOG4105BZU	Histidine kinase
J168_04360	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
J168_04361	ENOG4105MWK	D-amino acid dehydrogenase, small subunit
J168_04362	ENOG4105EW9	transcriptional regulator AsnC family
J168_04366	ENOG4107RD7	Flagellar Motor Protein, MotA
J168_04367	ENOG4105ER2	Ompa motb domain protein
J168_04372	ENOG4105E3A	(ABC) transporter
J168_04373	ENOG4105DA5	(ABC) transporter
J168_04374	ENOG4105EEQ	Na H antiporter
J168_04376	ENOG4108UN4	phage SPO1 DNA polymerase-related protein
J168_04378	ENOG4105C8E	extradiol ring-cleavage dioxygenase class IIi protein subunit b
J168_04380	ENOG4105CBN	LysR family transcriptional regulator
J168_04382	ENOG4105CPC	Aldo Keto reductase
J168_04384	ENOG4105C9K	Endothelin-converting enzyme 1
J168_04388	ENOG4107QTZ	amino acid
J168_04390	ENOG4108VAC	response regulator
J168_04391	ENOG4105C2F	Histidine kinase
J168_04394	ENOG4108Z9Z	response to DNA damage stimulus
J168_04395	ENOG4105WEF	catalase
J168_04398	ENOG4105BZU	Histidine kinase
J168_04401	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
J168_04403	ENOG4105C4M	(Ubiquinol oxidase) subunit I
J168_04404	ENOG4105CFY	cytochrome d ubiquinol oxidase, subunit ii
J168_04407	ENOG4105CYX	Short-chain dehydrogenase reductase Sdr
J168_04408	ENOG4105CMR	udp-glucose 4-epimerase
J168_04412	ENOG4105BZ1	(ABC) transporter
J168_04415	ENOG4105E2A	Dehydrogenase
J168_04427	ENOG4105CIG	ABC transporter
J168_04430	ENOG4108UQ8	endoribonuclease L-psp
J168_04433	ENOG4105C8Q	Methyl-accepting chemotaxis
J168_04437	ENOG4108V3G	Catalyzes the reductive cleavage of azo bond in aromatic azo compounds to the corresponding amines. Requires NADH, but not NADPH, as an electron donor for its activity (By similarity)
J168_04456	ENOG4105CQ3	Poorly processive error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by polIV. Exhibits no 3-5 exonuclease (proofreading) activity. May be involved in translesional synthesis in conjunction with the beta clamp from polIII (By similarity)
J168_04461	ENOG4105ED4	portal protein
J168_04470	ENOG4105NVB	glycoside hydrolase, family 19
J168_04512	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
J168_04513	ENOG4108YYA	Hydrolyzes D-tyrosyl-tRNA(Tyr) into D-tyrosine and free tRNA(Tyr). Could be a defense mechanism against a harmful effect of D-tyrosine (By similarity)
J168_04514	ENOG4105D1S	lipid A biosynthesis
J168_04515	ENOG4108Z7F	N-acetyltransferase
J168_04523	ENOG4105CYJ	ribosomal RNA small subunit methyltransferase B
J168_04524	ENOG4105CAE	Modifies the free amino group of the aminoacyl moiety of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by (I) promoting its recognition by IF2 and (II) impairing its binding to EFTu-GTP (By similarity)
J168_04525	ENOG4108Z02	Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions (By similarity)
J168_04526	ENOG4108WZM	domain protein
J168_04527	ENOG4105C79	DNA protecting protein DprA
J168_04528	ENOG4108RPN	Protein smg homolog
J168_04531	ENOG4105C73	Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone (By similarity)
J168_04532	ENOG4105EK0	Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine (By similarity)
J168_04535	ENOG4107ZQV	short-chain dehydrogenase reductase
J168_04537	ENOG4105D07	Signal peptide peptidase, SppA
J168_04538	ENOG4107QI1	Mate efflux family protein
J168_04542	ENOG4105C25	Primosomal protein n'
J168_04543	ENOG4108TGY	Glutathione S-transferase
J168_04547	ENOG4105EN6	Membrane
J168_04548	ENOG4105DEK	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
J168_04549	ENOG4105D5S	Excises uracil residues from the DNA which can arise as a result of misincorporation of dUMP residues by DNA polymerase or due to deamination of cytosine (By similarity)
J168_04550	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
J168_04551	ENOG4105CRP	Part of the ABC transporter FtsEX involved in
J168_04552	ENOG4105CAK	Cell division ATP-binding protein ftsE
J168_04553	ENOG4105C1J	atp-dependent rna helicase
J168_04554	ENOG4105K63	Thioredoxin
J168_04555	ENOG4105C4P	Facilitates transcription termination by a mechanism that involves Rho binding to the nascent RNA, activation of Rho's RNA-dependent ATPase activity, and release of the mRNA from the DNA template (By similarity)
J168_04556	ENOG4105VS7	Bifunctional enzyme which can phosphorylate or dephosphorylate isocitrate dehydrogenase (IDH) on a specific serine residue. This is a regulatory mechanism which enables bacteria to bypass the Krebs cycle via the glyoxylate shunt in response to the source of carbon. When bacteria are grown on glucose, IDH is fully active and unphosphorylated, but when grown on acetate or ethanol, the activity of IDH declines drastically concomitant with its phosphorylation (By similarity)
J168_04557	ENOG4105ETT	transcriptional Regulator, LysR family
J168_04559	ENOG4105E9K	Isocitrate dehydrogenase
J168_04562	ENOG4105FB9	CRISPR-associated protein
J168_04563	ENOG4105FB9	CRISPR-associated protein
J168_04567	ENOG4105DYN	CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Acts as a dsDNA endonuclease. May be involved in the integration of spacer DNA into the CRISPR cassette (By similarity)
J168_04571	ENOG4109066	lysm domain bon superfamily protein
J168_04572	ENOG4107R1K	Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1) (By similarity)
J168_04573	ENOG4105CH2	amidohydrolase
J168_04574	ENOG4105ENT	Efflux transporter rnd family, mfp subunit
J168_04575	ENOG4105BZS	acriflavin resistance protein
J168_04577	ENOG4105E32	cytoplasmic protein
J168_04585	ENOG4108UQS	dipeptidase
J168_04586	ENOG4108VBV	N-Acetylmuramoyl-L-alanine amidase
J168_04588	ENOG4105DTQ	mandelate racemase muconate lactonizing
J168_04590	ENOG4105D5Q	Arginine ornithine antiporter
J168_04593	ENOG4108Z12	YiaAB two helix domain-containing protein
J168_04595	ENOG4107QK4	glycoside hydrolase, family 3 domain protein
J168_04596	ENOG4107ZVW	dihydroneopterin aldolase
J168_04597	ENOG4105CPM	Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine (By similarity)
J168_04598	ENOG4105VCC	30S ribosomal protein S21
J168_04599	ENOG4105KTH	gatB Yqey
J168_04600	ENOG4107S2Z	UPF0761 membrane protein
J168_04601	ENOG4105C9G	DNA primase is the polymerase that synthesizes small RNA primers for the Okazaki fragments on both template strands at replication forks during chromosomal DNA synthesis (By similarity)
J168_04602	ENOG4105DHU	Bile acid
J168_04604	ENOG4105F1R	Converts heme B (protoheme IX) to heme O by substitution of the vinyl group on carbon 2 of heme B porphyrin ring with a hydroxyethyl farnesyl side group (By similarity)
J168_04609	ENOG4107QS1	Cytochrome C Oxidase, Subunit III
J168_04610	ENOG4105FT1	Exerts its effect at some terminal stage of cytochrome c oxidase synthesis, probably by being involved in the insertion of the copper B into subunit I (By similarity)
J168_04615	ENOG4105C26	Dehydrogenase
J168_04623	ENOG4105DKK	Benzoate
J168_04627	ENOG4105DSB	aldose 1-epimerase
J168_04629	ENOG4105K5B	UPF0225 protein
J168_04630	ENOG4105EJ9	Membrane
J168_04635	ENOG4105EUJ	GTP cyclohydrolase i
J168_04637	ENOG4105ZQC	membrane protein AaeX
J168_04638	ENOG4105Y49	secretion protein, HlyD family
J168_04640	ENOG4105DR8	Membrane
J168_04641	ENOG4105CSH	Transporter
J168_04643	ENOG4105CQX	Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol (By similarity)
J168_04659	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
J168_04670	ENOG4107QKA	exodeoxyribonuclease V beta
J168_04671	ENOG4105DSY	exodeoxyribonuclease V, gamma
J168_04673	ENOG4105DHJ	ABC, transporter
J168_04674	ENOG4105CY3	ABC transporter, permease
J168_04675	ENOG4107PE3	Mammalian cell entry related domain protein
J168_04678	ENOG410903C	(LipO)protein
J168_04680	ENOG4108V06	Glutathione peroxidase
J168_04682	ENOG4107QSV	RmuC domain protein
J168_04683	ENOG4105CIS	alcohol dehydrogenase
J168_04684	ENOG4105EJC	lysr family transcriptional regulator
J168_04686	ENOG4108TGY	Glutathione S-transferase
J168_04688	ENOG4105CUB	amino acid
J168_04689	ENOG4105CWX	Alpha-1,2-mannosidase
J168_04690	ENOG4105NRM	Membrane
J168_04691	ENOG4105BZU	Histidine kinase
J168_04692	ENOG4108IXP	Carbohydrate diacid transcriptional activator CdaR
J168_04693	ENOG4105BZW	Glycerate kinase
J168_04694	ENOG4105CSP	Major Facilitator Superfamily
J168_04697	ENOG4105DR4	Methyltransferase
J168_04699	ENOG4105DU1	integral membrane protein, terc
J168_04701	ENOG4106MZZ	glycerophosphoryl diester phosphodiesterase
J168_04704	ENOG4105C1H	Exhibits a very high intrinsic GTPase hydrolysis rate. Involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA- cmnm(5)s(2)U34 (By similarity)
J168_04705	ENOG4108ZJ4	polysaccharide deacetylase
J168_04706	ENOG4105DHW	Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins
J168_04707	ENOG41067YR	RNaseP catalyzes the removal of the 5'-leader sequence from pre-tRNA to produce the mature 5'-terminus. It can also cleave other RNA substrates such as 4.5S RNA. The protein component plays an auxiliary but essential role in vivo by binding to the 5'-leader sequence and broadening the substrate specificity of the ribozyme (By similarity)