locus-tag	class	description
J171_00023	ENOG4108C33	Resolvase
J171_00028	ENOG4105D13	transposase
J171_00032	ENOG4108C33	Resolvase
J171_00041	ENOG4105CVE	Lytic murein transglycosylase
J171_00072	ENOG4105CMA	conjugation trbi family protein
J171_00094	ENOG4105XMH	SpoVT AbrB domain protein
J171_00095	ENOG4108C33	Resolvase
J171_00099	ENOG4105D13	transposase
J171_00103	ENOG4108C33	Resolvase
J171_00104	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)
J171_00105	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)
J171_00106	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)
J171_00108	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)
J171_00110	ENOG4108K0D	peptidase, M48
J171_00116	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)
J171_00118	ENOG4105CQX	Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol (By similarity)
J171_00123	ENOG4105CKF	membrane protein involved in aromatic hydrocarbon degradation
J171_00127	ENOG4105CN1	protease
J171_00128	ENOG41063SB	peptidase
J171_00130	ENOG4107VAM	peptidase, m28
J171_00135	ENOG4105DQ4	alcohol dehydrogenase
J171_00136	ENOG4105BZ8	glutamate synthase
J171_00137	ENOG4105CBC	glutamate synthase
J171_00141	ENOG4105CUJ	penicillin amidase
J171_00143	ENOG4105EXG	Transcriptional regulator
J171_00145	ENOG4107Y2G	Glycosyl transferase (Group 1
J171_00146	ENOG4105D3Q	Sugar transferase
J171_00147	ENOG4105EAG	UDP-N-acetylglucosamine 2-epimerase
J171_00149	ENOG4108UHC	Glycosyl transferase, wecb taga cpsf family
J171_00150	ENOG4107RA4	Glycosyl transferase (Group 1
J171_00154	ENOG4105CAQ	asparagine synthetase
J171_00157	ENOG4105CMR	udp-glucose 4-epimerase
J171_00160	ENOG4105BZ1	(ABC) transporter
J171_00166	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)
J171_00184	ENOG4108I5C	dEAD DEAH box helicase
J171_00185	ENOG4108UT2	hemolysin iii
J171_00188	ENOG4107FW0	short-chain dehydrogenase reductase
J171_00189	ENOG4105CHR	reductase
J171_00194	ENOG4105DYS	nad(p)h dehydrogenase (quinone)
J171_00205	ENOG41067RQ	csbd family
J171_00209	ENOG4105D4Y	metalloprotease
J171_00214	ENOG4105K63	Thioredoxin
J171_00215	ENOG4105CSH	Transporter
J171_00223	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
J171_00229	ENOG4105CZI	D-fructose-1,6-bisphosphate 1-phosphohydrolase class 1
J171_00230	ENOG4105CGF	Aromatic amino acid aminotransferase
J171_00231	ENOG4105CHB	tonB-dependent Receptor
J171_00233	ENOG41082W1	Cupin 2, conserved barrel domain protein
J171_00234	ENOG4105C26	Dehydrogenase
J171_00239	ENOG4105DMF	Dehydrogenase
J171_00241	ENOG4105BZU	Histidine kinase
J171_00242	ENOG4105WH1	Two component transcriptional regulator luxr family
J171_00246	ENOG4108M3R	transcriptional activator CadC
J171_00247	ENOG4105RKW	reductase (By
J171_00262	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)
J171_00263	ENOG4105CG3	alpha amylase, catalytic region
J171_00264	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)
J171_00267	ENOG4105EBR	Carboxylesterase
J171_00270	ENOG4105DR6	Trap dicarboxylate transporter, dctp subunit
J171_00272	ENOG4105CG6	trap dicarboxylate transporter dctm subunit
J171_00273	ENOG4105DSG	hydrolase family 43
J171_00274	ENOG4105ETE	Transcriptional regulator (LacI family
J171_00275	ENOG4105D50	Catalyzes the isomerization of 5-dehydro-4-deoxy-D- glucuronate to 3-deoxy-D-glycero-2,5-hexodiulosonate (By similarity)
J171_00276	ENOG4105CHR	reductase
J171_00278	ENOG4107TDE	lipolytic protein G-D-S-L family
J171_00281	ENOG4105MIR	Phenylalanine 4-monooxygenase
J171_00282	ENOG4108YXU	transcriptional regulator AsnC family
J171_00283	ENOG4105CNM	Receptor
J171_00284	ENOG4105D78	K07001 NTE family protein
J171_00286	ENOG4105DKW	ABC transporter
J171_00289	ENOG4108IJ8	ABC transporter
J171_00290	ENOG4105E90	ABC transporter
J171_00299	ENOG4105D1F	ATP-binding protein
J171_00300	ENOG4105M4E	phosphohistidine phosphatase, SixA
J171_00302	ENOG4107RZC	phospholipase d
J171_00303	ENOG4105KA0	thioesterase Superfamily protein
J171_00311	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
J171_00312	ENOG4105C5F	glutamine synthetase
J171_00314	ENOG4105BZU	Histidine kinase
J171_00315	ENOG4105CUX	Signal transduction histidine kinase
J171_00316	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
J171_00317	ENOG4108Z7T	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
J171_00318	ENOG4108Z7T	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
J171_00319	ENOG4105I9P	Metallothiol transferase which confers resistance to fosfomycin by catalyzing the addition of a thiol cofactor to fosfomycin. L-cysteine is probably the physiological thiol donor (By similarity)
J171_00321	ENOG4105CHU	acetyl-coa acetyltransferase
J171_00328	ENOG4107YZP	Rhodanese domain protein
J171_00329	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)
J171_00330	ENOG4105CSF	NADPH-dependent glycerol-3-phosphate dehydrogenase
J171_00332	ENOG4105C7K	acetolactate synthase
J171_00333	ENOG4108TQ9	Histidine kinase
J171_00334	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
J171_00338	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)
J171_00341	ENOG4105E2T	synthase III
J171_00342	ENOG4107R3N	Filamentation induced by cAMP protein fic
J171_00343	ENOG4108J2P	Alpha beta hydrolase fold
J171_00344	ENOG4105PI0	Ferredoxin
J171_00345	ENOG410680H	amp-dependent synthetase and ligase
J171_00347	ENOG4107VBM	3-beta hydroxysteroid dehydrogenase isomerase
J171_00349	ENOG4105CPF	Cell wall formation (By similarity)
J171_00351	ENOG4105CNK	Required, probably indirectly, for the hydroxylation of 2-octaprenylphenol to 2-octaprenyl-6-hydroxy-phenol, the fourth step in ubiquinone biosynthesis (By similarity)
J171_00353	ENOG4105DR9	pseudouridine synthase
J171_00355	ENOG4108YZN	class I peptide chain release factor
J171_00357	ENOG4105D44	asparaginase
J171_00358	ENOG4105DGW	oligopeptidase A
J171_00364	ENOG4107R11	Transcriptional regulator
J171_00365	ENOG4107QP3	malate synthase g
J171_00367	ENOG4105BZU	Histidine kinase
J171_00374	ENOG4107QX3	carboxylase
J171_00375	ENOG4105C1G	acyl-Coa dehydrogenase
J171_00386	ENOG4105CKI	cobalamin synthesis protein
J171_00388	ENOG4108TZV	Membrane
J171_00390	ENOG4105D6Z	AFG1 family ATPase
J171_00391	ENOG4105K56	Transcriptional regulator
J171_00392	ENOG4108ZHJ	Organic hydroperoxide resistance protein
J171_00397	ENOG4105CJH	Alcohol dehydrogenase zinc-binding domain protein
J171_00400	ENOG4108R99	pseudouridine synthase
J171_00401	ENOG4108KPZ	tonB-dependent Receptor
J171_00403	ENOG4105CQ7	ATP-dependent helicase
J171_00404	ENOG4108W15	Protein of unknown function (DUF1456)
J171_00405	ENOG4105VT2	5-hydroxyisourate hydrolase
J171_00406	ENOG4105E1J	oxidoreductase
J171_00410	ENOG4105C5R	Aminotransferase
J171_00412	ENOG4105EQ2	LysR family Transcriptional regulator
J171_00413	ENOG4107RTG	Major Facilitator superfamily
J171_00415	ENOG4105CFB	Gamma-glutamyltranspeptidase (EC 2.3.2.2)
J171_00417	ENOG4105DU0	nucleoside hydrolase
J171_00419	ENOG4105C7N	Xanthine uracil vitamin C permease
J171_00422	ENOG4105ETT	transcriptional Regulator, LysR family
J171_00423	ENOG4105F8V	Hydrolase, tatD family
J171_00426	ENOG4106NZI	LysR family Transcriptional regulator
J171_00427	ENOG4105D94	Major Facilitator Superfamily
J171_00430	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)
J171_00431	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
J171_00435	ENOG4105E3W	Two component transcriptional regulator (Winged helix family
J171_00436	ENOG4105EB3	Histidine kinase
J171_00437	ENOG4105C1P	efflux transporter, rnd family, mfp subunit
J171_00438	ENOG4105BZS	acriflavin resistance protein
J171_00439	ENOG4105ENJ	RND efflux system, outer membrane lipoprotein
J171_00441	ENOG4105DAE	Methylenetetrahydrofolate reductase
J171_00442	ENOG4105WPN	DNA integration recombination invertion protein
J171_00443	ENOG4105DZ2	Transcriptional regulator
J171_00444	ENOG4108UZX	fmn reductase
J171_00447	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)
J171_00449	ENOG4105ECR	NmrA family
J171_00457	ENOG4105C01	Dihydroxy-acid dehydratase
J171_00460	ENOG4108Z0R	Transferase
J171_00461	ENOG4105D2S	major facilitator superfamily
J171_00462	ENOG4105CPI	Metal Dependent Phosphohydrolase
J171_00468	ENOG41072AC	4-hydroxybenzoate 3-monooxygenase
J171_00471	ENOG4108JQ0	Key enzyme in the regulation of glycerol uptake and metabolism (By similarity)
J171_00472	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)
J171_00473	ENOG4105C6V	Glycerol-3-phosphate dehydrogenase
J171_00474	ENOG4105E98	transcriptional regulator DeoR family
J171_00479	ENOG4105CHU	acetyl-coa acetyltransferase
J171_00482	ENOG4107RAW	3-carboxy-cis-cis-muconate cycloisomerase
J171_00483	ENOG4105F2Z	3-oxoadipate enol-lactonase
J171_00484	ENOG4108UWZ	4-Carboxymuconolactone decarboxylase
J171_00486	ENOG4107HP6	Transcriptional regulator
J171_00489	ENOG4105MH3	Protein of unknown function (DUF2490)
J171_00490	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)
J171_00497	ENOG4107EXU	Short-chain dehydrogenase reductase Sdr
J171_00498	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)
J171_00500	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)
J171_00501	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)
J171_00502	ENOG41081UC	Inherit from COG: Competence protein
J171_00503	ENOG4105C4G	Synthesis of 3-octaprenyl-4-hydroxybenzoate (By similarity)
J171_00515	ENOG4105VS8	Flagellar biosynthetic protein fliq
J171_00519	ENOG4108HR8	type iii secretion
J171_00523	ENOG4107Y59	type iii secretion
J171_00526	ENOG4108JIR	Flagellum-specific ATP synthase
J171_00528	ENOG4108TN6	type iii secretion
J171_00529	ENOG4105K44	type iii secretion
J171_00531	ENOG4105FTC	Lytic transglycosylase catalytic
J171_00534	ENOG4105EGS	Mechanosensitive ion channel
J171_00535	ENOG4107RES	phosphoglycerol transferase I
J171_00537	ENOG4105CKW	Inner membrane protein yedI
J171_00538	ENOG4105BZU	Histidine kinase
J171_00539	ENOG4105CXW	Synthesizes alpha-1,4-glucan chains using ADP-glucose (By similarity)
J171_00540	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)
J171_00541	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)
J171_00546	ENOG4105K4T	epimerase
J171_00547	ENOG4107ZQV	short-chain dehydrogenase reductase
J171_00553	ENOG4105BZS	acriflavin resistance protein
J171_00554	ENOG4105CHR	reductase
J171_00557	ENOG4105C1J	atp-dependent rna helicase
J171_00561	ENOG4105CPP	Dehydrogenase, E1 component
J171_00562	ENOG4107RUY	(E1 component), alpha subunit
J171_00564	ENOG4105HJ8	Catalyzes the oxidative cleavage of the L-tryptophan (L- Trp) pyrrole ring (By similarity)
J171_00565	ENOG4105DUX	Transporter
J171_00568	ENOG4105E6K	4-Hydroxyphenylpyruvate dioxygenase
J171_00569	ENOG4105F1J	Homogentisate 1,2-dioxygenase
J171_00572	ENOG4105KJM	monovalent cation h antiporter subunit g
J171_00573	ENOG4105W4C	monovalent cation H antiporter subunit F
J171_00575	ENOG4107R4Z	monovalent cation h antiporter subunit d
J171_00576	ENOG4108ZE9	Monovalent cation H antiporter subunit C
J171_00577	ENOG4105D65	subunit l
J171_00581	ENOG4105NVB	glycoside hydrolase, family 19
J171_00585	ENOG4105C8V	SAICAR synthetase
J171_00586	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)
J171_00589	ENOG4105KD7	acetyltransferase
J171_00590	ENOG4107TE5	Lipid kinase
J171_00591	ENOG4105CRQ	synthase (Component I)
J171_00593	ENOG4105DDQ	anthranilate synthase
J171_00595	ENOG4108I0Q	anthranilate phosphoribosyltransferase
J171_00596	ENOG4105DK0	Indole-3-glycerol phosphate synthase
J171_00598	ENOG4107RYR	Transcriptional regulator, Crp Fnr family
J171_00599	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)
J171_00601	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)
J171_00602	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)
J171_00603	ENOG4108UJD	30S ribosomal protein S9
J171_00606	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)
J171_00607	ENOG4108UQY	Iron-storage protein
J171_00608	ENOG4105BZU	Histidine kinase
J171_00613	ENOG4108YX9	iron--sulfur cluster insertion protein erpA
J171_00617	ENOG4105DH2	Converts cobyric acid to cobinamide by the addition of aminopropanol on the F carboxylic group (By similarity)
J171_00620	ENOG4108J8Q	Catalyzes the facilitated diffusion of 2-acyl-glycero-3- phosphoethanolamine (2-acyl-GPE) into the cell (By similarity)
J171_00623	ENOG4105EM2	membrane
J171_00624	ENOG4105C12	Phosphoribosylglycinamide synthetase
J171_00626	ENOG4105DC1	bifunctional purine biosynthesis protein purh
J171_00627	ENOG4108UMZ	Cdp-alcohol phosphatidyltransferase
J171_00628	ENOG4105E8V	Alpha Beta Hydrolase Fold protein
J171_00629	ENOG41077RS	Phosphatase
J171_00634	ENOG4108HPI	phosphatidate Cytidylyltransferase
J171_00635	ENOG4105VY0	Activates ribosomal RNA transcription. Plays a direct role in upstream activation of rRNA promoters (By similarity)
J171_00640	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
J171_00643	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
J171_00645	ENOG4105KM4	Acetyl-CoA carboxylase, biotin carboxyl carrier protein
J171_00646	ENOG4108Z38	Catalyzes a trans-dehydration via an enolate intermediate (By similarity)
J171_00647	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)
J171_00648	ENOG4105VF7	tolerance protein
J171_00651	ENOG4105VV6	START domain-containing protein
J171_00653	ENOG4105E1F	short-chain dehydrogenase reductase
J171_00654	ENOG4108K8S	endonuclease I
J171_00655	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
J171_00656	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
J171_00659	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)
J171_00664	ENOG4105CE6	Adenylation and deadenylation of glutamate--ammonia ligase (By similarity)
J171_00665	ENOG4105EX9	Membrane
J171_00668	ENOG4108RDT	NADH dehydrogenase NAD(P)H nitroreductase)
J171_00669	ENOG4108YYC	ycei family
J171_00674	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)
J171_00677	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)
J171_00678	ENOG4108K6F	triphosphoribosyl-dephospho-CoA synthase
J171_00680	ENOG4105CJF	Malonyl coA-acyl carrier protein transacylase
J171_00682	ENOG4105DRR	Transcriptional regulator, GntR family
J171_00690	ENOG4105DAQ	Component of the pyruvate dehydrogenase (PDH) complex, that catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2) (By similarity)
J171_00693	ENOG4107GJV	short-chain dehydrogenase reductase
J171_00696	ENOG4105PDP	Short chain dehydrogenase
J171_00698	ENOG4105CHF	Glutathione S-transferase
J171_00703	ENOG4105EYF	MMPL domain protein
J171_00704	ENOG4105C5Z	peptidase
J171_00705	ENOG4107QS8	(LipO)protein
J171_00706	ENOG4105BZU	Histidine kinase
J171_00710	ENOG4105DFI	Membrane
J171_00711	ENOG4105F87	Dehydratase
J171_00716	ENOG4105D7N	magnesium and cobalt transport protein CorA
J171_00718	ENOG4105E53	ec 3.2.1.28
J171_00726	ENOG4105C8Q	Methyl-accepting chemotaxis
J171_00727	ENOG4106R7G	Glycoside hydrolase family 5
J171_00728	ENOG4105CHH	sulfate transporter
J171_00729	ENOG4105BZU	Histidine kinase
J171_00732	ENOG4105C3A	Involved in the biosynthesis of osmoregulated periplasmic glucans (OPGs) (By similarity)
J171_00734	ENOG4108HRK	Histidine kinase
J171_00735	ENOG4108NEV	two component transcriptional regulator, LytTR family
J171_00736	ENOG4105D6W	Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps (By similarity)
J171_00742	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)
J171_00745	ENOG4105WD1	Membrane
J171_00747	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)
J171_00749	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)
J171_00750	ENOG4108R5P	Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery (By similarity)
J171_00751	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)
J171_00756	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)
J171_00757	ENOG4105BZU	Histidine kinase
J171_00758	ENOG4105CD8	aminopeptidase N
J171_00761	ENOG4105DZG	Dehydrogenase
J171_00762	ENOG4108Q1J	Extracellular solute-binding protein, family 3
J171_00767	ENOG4108JU9	GAF modulated sigma54 specific transcriptional regulator Fis family
J171_00769	ENOG4105DFF	Rod shape-determining protein mreb
J171_00770	ENOG4105N3I	Involved in formation and maintenance of cell shape (By similarity)
J171_00773	ENOG4105CNI	cell division protein FtsW
J171_00774	ENOG4107WN4	Polygalacturonase
J171_00775	ENOG4105CVE	Lytic murein transglycosylase
J171_00776	ENOG4105K6T	rare lipoprotein A
J171_00777	ENOG4105DZ1	carboxypeptidase
J171_00780	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)
J171_00781	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)
J171_00782	ENOG4105CN1	protease
J171_00784	ENOG4105EGI	Transcriptional regulator
J171_00793	ENOG4108J5G	6-phosphogluconate dehydrogenase
J171_00794	ENOG4105D9R	oxidoreductase
J171_00795	ENOG4105W4M	Transport-associated protein
J171_00796	ENOG4105BZU	Histidine kinase
J171_00798	ENOG4105BZU	Histidine kinase
J171_00800	ENOG4105CHR	reductase
J171_00808	ENOG4105GVR	general secretion pathway protein D
J171_00809	ENOG4107QHF	type ii secretion system protein e
J171_00810	ENOG4105D7Q	type ii secretion system
J171_00811	ENOG4108VAU	general secretion pathway protein G
J171_00812	ENOG4105VWV	general secretion pathway protein h
J171_00815	ENOG4108RTD	type II secretion system protein K
J171_00821	ENOG4105CNT	hydrolase family 2
J171_00825	ENOG4105FDP	GntR family transcriptional regulator
J171_00827	ENOG4105ETE	Transcriptional regulator (LacI family
J171_00828	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
J171_00829	ENOG4105CE4	GlcNAc 6-P deacetylase
J171_00831	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
J171_00832	ENOG4105CZ6	Can catalyze the oxidation of choline to betaine aldehyde and betaine aldehyde to glycine betaine (By similarity)
J171_00833	ENOG4105C26	Dehydrogenase
J171_00834	ENOG4105C94	Transporter
J171_00836	ENOG4108Z33	Thiol disulfide Interchange Protein
J171_00839	ENOG4106RE7	Cytochrome
J171_00840	ENOG4105WHM	Necessary for normal cell division and for the maintenance of normal septation (By similarity)
J171_00841	ENOG4105CY0	Metallo-Beta-Lactamase
J171_00844	ENOG4105JJR	Histidine kinase
J171_00845	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
J171_00850	ENOG4108QBQ	Catalyzes the condensation of formaldehyde and glutathione to S-hydroxymethylglutathione (By similarity)
J171_00852	ENOG4105C1I	TRANSCRIPTIONAl REGULATOR GntR family
J171_00853	ENOG4105JAB	phenazine biosynthesis protein, phzf family
J171_00856	ENOG4105C5H	ABC transporter
J171_00858	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)
J171_00859	ENOG4108Z11	Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes (By similarity)
J171_00861	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)
J171_00865	ENOG4105C66	Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate (By similarity)
J171_00866	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)
J171_00867	ENOG4107YIM	Involved in the transcription termination process (By similarity)
J171_00868	ENOG4105CG2	Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 (By similarity)
J171_00872	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)
J171_00873	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)
J171_00874	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)
J171_00875	ENOG4105C08	Histidine kinase
J171_00876	ENOG4105EEX	Two component transcriptional regulator (Winged helix family
J171_00879	ENOG4105CQB	FAD linked oxidase domain protein
J171_00880	ENOG4105S2T	inner membrane protein YbcI
J171_00881	ENOG41082RQ	UPF0102 protein
J171_00888	ENOG4108V6E	Cell division protein mraZ
J171_00889	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
J171_00890	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)
J171_00891	ENOG4105CJN	penicillin-binding protein
J171_00892	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)
J171_00893	ENOG4108EQQ	Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein (By similarity)
J171_00894	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
J171_00896	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)
J171_00897	ENOG4105DFU	Cell wall formation (By similarity)
J171_00898	ENOG4105CPF	Cell wall formation (By similarity)
J171_00899	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)
J171_00900	ENOG4105CIT	This protein may be involved in anomalous filament growth. May be a component of the septum (By similarity)
J171_00901	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)
J171_00902	ENOG4105C7C	involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
J171_00904	ENOG4105DR5	peptidase
J171_00905	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
J171_00906	ENOG4105M6F	mutator MutT protein
J171_00908	ENOG4105SYT	Methylenetetrahydrofolate reductase
J171_00921	ENOG4105DXX	methyltransferase
J171_00922	ENOG4105C3E	May play a key role in the regulation of the intracellular concentration of adenosylhomocysteine (By similarity)
J171_00925	ENOG4105CCA	Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle (By similarity)
J171_00930	ENOG4105D6F	Phosphatase
J171_00931	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
J171_00933	ENOG4107R6G	Catalyzes the S-adenosylmethionine monomethyl esterification of trans-aconitate (By similarity)
J171_00934	ENOG4105CEH	Catalyzes the synthesis of dihydrouridine a modified base found in the D-loop of most tRNAs (By similarity)
J171_00937	ENOG4108RVA	ribokinase
J171_00938	ENOG4105D9N	nucleoside
J171_00939	ENOG4105CPC	Aldo Keto reductase
J171_00941	ENOG4105D05	Receptor
J171_00946	ENOG4105EFS	Binding-protein-dependent transport systems, inner membrane component
J171_00949	ENOG4105E2B	Taurine dioxygenase
J171_00951	ENOG4108I0Y	(ABC) transporter
J171_00952	ENOG4108UJV	acyl-CoA thioesterase i
J171_00953	ENOG4105ETX	regulatoR
J171_00954	ENOG4105DHQ	Histidine kinase
J171_00956	ENOG41080IJ	Diacylglycerol kinase
J171_00960	ENOG4105C3B	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
J171_00961	ENOG4105C0V	Provides the sole de novo source of dTMP for DNA biosynthesis (By similarity)
J171_00964	ENOG4107SM7	Transcriptional regulator
J171_00965	ENOG4107T8P	acyl-Coa dehydrogenase
J171_00966	ENOG4105D7T	ABC transporter
J171_00967	ENOG4105EFS	Binding-protein-dependent transport systems, inner membrane component
J171_00969	ENOG4105D4R	Catalyzes the desulfonation of aliphatic sulfonates (By similarity)
J171_00970	ENOG4108UZX	fmn reductase
J171_00975	ENOG4105DEF	Extracellular solute-binding protein, family 5
J171_00977	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
J171_00980	ENOG4105DDT	Hydrolyzes diadenosine 5',5'''-P1,P4-tetraphosphate to yield ADP (By similarity)
J171_00981	ENOG4105NWN	ApaG protein
J171_00982	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)
J171_00983	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)
J171_00984	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)
J171_00985	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)
J171_00989	ENOG4108WBT	adenosyltransferase
J171_00991	ENOG4105D0A	hydroxylase
J171_00992	ENOG4105EAK	ubiquinone biosynthesis hydroxylase, ubiH ubiF VisC COQ6 family
J171_00999	ENOG4105DDW	LysR family Transcriptional regulator
J171_01002	ENOG4108D7R	p-hydroxycinnamoyl CoA hydratase lyase
J171_01008	ENOG4105EZ6	Catalyzes the 2'-O-methylation at nucleotide C2498 in 23S rRNA (By similarity)
J171_01011	ENOG4105DXC	membrane
J171_01012	ENOG4105CX6	glutaminyL-tRNA synthetase
J171_01015	ENOG4105BZU	Histidine kinase
J171_01016	ENOG4105BZU	Histidine kinase
J171_01017	ENOG4105WH1	Two component transcriptional regulator luxr family
J171_01019	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)
J171_01021	ENOG4105CW3	Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway (By similarity)
J171_01022	ENOG4105NXH	GreA GreB family elongation factor
J171_01023	ENOG4105C5Q	Transcriptional regulator
J171_01026	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)
J171_01030	ENOG4105C2M	dna polymerase I
J171_01036	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)
J171_01041	ENOG4105W8H	transhydrogenase (subunit alpha
J171_01042	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)
J171_01045	ENOG4105CM2	brancheD-chain amino acid aminotransferase
J171_01046	ENOG4105RX7	peptidase S8 and S53, subtilisin, kexin, sedolisin
J171_01047	ENOG4105RX7	peptidase S8 and S53, subtilisin, kexin, sedolisin
J171_01048	ENOG4105RX7	peptidase S8 and S53, subtilisin, kexin, sedolisin
J171_01049	ENOG4108Z66	YbaK ebsC protein
J171_01054	ENOG4105CS1	NAD(P)H quinone oxidoreductase
J171_01055	ENOG4107S2Z	UPF0761 membrane protein
J171_01056	ENOG4107QX9	Thiol disulfide interChange protein
J171_01059	ENOG4105CSR	polyphosphate kinase 2
J171_01060	ENOG4108RIR	Molybdenum cofactor biosynthesis protein
J171_01062	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
J171_01063	ENOG4105C7E	Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) (By similarity)
J171_01064	ENOG4105DJQ	tetratricopeptide tpr_2 repeat protein
J171_01065	ENOG4105QVB	outer membrane lipoprotein LolB
J171_01066	ENOG4105CTR	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
J171_01068	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
J171_01069	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)
J171_01070	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
J171_01071	ENOG4105C3G	gtp-binding protein
J171_01075	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
J171_01077	ENOG4105PM1	preprotein translocase subunit SecE
J171_01078	ENOG4105E5V	Participates in transcription elongation, termination and antitermination (By similarity)
J171_01079	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
J171_01080	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)
J171_01081	ENOG4108VZM	50s ribosomal protein L10
J171_01082	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)
J171_01084	ENOG4108IIJ	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
J171_01085	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
J171_01086	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)
J171_01087	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)
J171_01088	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)
J171_01089	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
J171_01090	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
J171_01091	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)
J171_01092	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)
J171_01093	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)
J171_01094	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
J171_01095	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
J171_01096	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)
J171_01097	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
J171_01098	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
J171_01099	ENOG41083MP	50s ribosomal protein l29
J171_01100	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
J171_01101	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
J171_01102	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
J171_01103	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
J171_01104	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)
J171_01105	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)
J171_01106	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)
J171_01107	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)
J171_01108	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)
J171_01110	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
J171_01111	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)
J171_01112	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
J171_01113	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)
J171_01114	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)
J171_01115	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
J171_01116	ENOG4108ZT0	50S ribosomal protein l17
J171_01117	ENOG41080I0	Required for disulfide bond formation in some periplasmic proteins. Acts by oxidizing the DsbA protein (By similarity)
J171_01119	ENOG4105C7V	phospho-2-dehydro-3-deoxyheptonate aldolase
J171_01121	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)
J171_01124	ENOG4107XH4	PPIases accelerate the folding of proteins (By similarity)
J171_01125	ENOG4105D9Z	Catalyzes the reversible oxidation of malate to oxaloacetate (By similarity)
J171_01126	ENOG4108K3A	Glutathione S-transferase
J171_01128	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
J171_01129	ENOG4105CIS	alcohol dehydrogenase
J171_01130	ENOG4105CDV	Ompa motb domain protein
J171_01132	ENOG4108R99	pseudouridine synthase
J171_01134	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)
J171_01135	ENOG4105DE7	Sulfate ABC transporter periplasmic sulfate-binding protein
J171_01136	ENOG4108I5D	sulfate abc transporter
J171_01138	ENOG4108IJ6	ABC transporter
J171_01140	ENOG4105CPQ	Dehydrogenase
J171_01142	ENOG4105HSS	phospholipase C
J171_01145	ENOG4105CVJ	phosphoglycerate mutase
J171_01146	ENOG4105DPM	folylpolyglutamate synthase Dihydrofolate synthase
J171_01149	ENOG4105CBA	glutamine phosphoribosylpyrophosphate amidotransferase
J171_01150	ENOG4105ED9	Protein of unknown function (DUF455)
J171_01152	ENOG4108YP4	Metalloprotease, specifically cleaves on the N-terminal side of aspartyl, glutamyl and cysteic acid residues (By similarity)
J171_01154	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)
J171_01156	ENOG4105EYK	Phosphatidylglycerophosphatase B
J171_01157	ENOG4105BZF	Glycosyl transferase (Group 1
J171_01158	ENOG4105C9X	ppx gppa phosphatase
J171_01159	ENOG4105CUU	Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) (By similarity)
J171_01160	ENOG4105BZU	Histidine kinase
J171_01161	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
J171_01162	ENOG4105ERG	peptidase m48, ste24p
J171_01163	ENOG4105VW4	glutaredoxin 3
J171_01165	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)
J171_01199	ENOG4105BZU	Histidine kinase
J171_01202	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
J171_01203	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)
J171_01204	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)
J171_01210	ENOG4105EIN	peptidylprolyl cis-trans isomerase
J171_01213	ENOG4108RW0	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
J171_01215	ENOG4108UMW	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
J171_01216	ENOG4107RZZ	dna polymerase iii epsilon subunit
J171_01217	ENOG4108ZF3	Phosphatase
J171_01220	ENOG4105DKP	glycosyl transferase, family 9
J171_01221	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)
J171_01222	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)
J171_01223	ENOG4105CM1	Catalyzes, together with MoaC, the conversion of 5'-GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
J171_01224	ENOG4108YXW	Together with MoaA, is involved in the conversion of 5'- GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
J171_01225	ENOG4105M00	molybdopterin converting factor, subunit 1
J171_01226	ENOG4108ZAF	Molybdopterin
J171_01236	ENOG4107QMP	dna polymerase iii subunits gamma and tau
J171_01237	ENOG4105KDX	Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection (By similarity)
J171_01238	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)
J171_01239	ENOG4105K59	histidine triad (HIT) protein
J171_01241	ENOG4105F8C	transglutaminase domain-containing protein
J171_01243	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
J171_01245	ENOG41089I4	Inherit from COG: Glycosyl transferase, family 2
J171_01247	ENOG4108UHJ	MAF-like protein
J171_01248	ENOG4105FCQ	metal-binding, possibly nucleic acid-binding protein
J171_01249	ENOG4105VGS	50s ribosomal protein l32
J171_01250	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)
J171_01252	ENOG4105CJF	Malonyl coA-acyl carrier protein transacylase
J171_01253	ENOG4105CHR	reductase
J171_01254	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
J171_01255	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
J171_01257	ENOG4105HHA	aminodeoxychorismate lyase
J171_01258	ENOG4107QRG	dna polymerase iii
J171_01262	ENOG4108JU7	Transcriptional regulator
J171_01263	ENOG4105CR4	methylisocitrate lyase
J171_01264	ENOG4105BZN	citrate synthase
J171_01265	ENOG4108I0Z	Aconitate hydratase
J171_01266	ENOG4105YAJ	CopG Arc MetJ
J171_01268	ENOG4105C7F	AcnD-accessory protein PrpF
J171_01271	ENOG4105DN3	alpha-2-macroglobulin domain protein
J171_01274	ENOG4108JQB	penicillin-binding protein 1C
J171_01280	ENOG4105M3Z	response regulator
J171_01282	ENOG4107QJR	hflk protein
J171_01283	ENOG4105EPW	hflc protein
J171_01285	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
J171_01286	ENOG4105CD8	aminopeptidase N
J171_01288	ENOG4105F6U	Short-chain dehydrogenase reductase Sdr
J171_01289	ENOG4108XFH	Transcriptional regulator
J171_01302	ENOG4105CVJ	phosphoglycerate mutase
J171_01303	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)
J171_01305	ENOG4105BZP	glycoside hydrolase 15-related
J171_01306	ENOG4105CYX	Short-chain dehydrogenase reductase Sdr
J171_01307	ENOG4105CWX	Alpha-1,2-mannosidase
J171_01311	ENOG4105C3M	thioredoxin reductase
J171_01316	ENOG4105C7W	Xanthine dehydrogenase
J171_01317	ENOG4105DIP	Molybdopterin dehydrogenase FAD-binding
J171_01318	ENOG4107XKX	isoquinoline 1-oxidoreductase, alpha subunit
J171_01325	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)
J171_01328	ENOG4105C0B	DNA polymerase III (alpha subunit)
J171_01331	ENOG4105EPD	Oligopeptide transporter, Opt family
J171_01334	ENOG4105DRY	peptidase s9 prolyl oligopeptidase active site domain protein
J171_01337	ENOG4106AXJ	AraC family transcriptional regulator
J171_01343	ENOG4105CV8	reductase
J171_01344	ENOG4105EBR	Carboxylesterase
J171_01345	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
J171_01348	ENOG4105C2C	drug resistance transporter, Bcr CflA
J171_01351	ENOG4105DIJ	Phosphoethanolamine transferase
J171_01354	ENOG4105ETX	regulatoR
J171_01355	ENOG4105DHQ	Histidine kinase
J171_01357	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)
J171_01358	ENOG4107QMS	site-determining protein
J171_01359	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)
J171_01361	ENOG4105BZU	Histidine kinase
J171_01362	ENOG4105WH1	Two component transcriptional regulator luxr family
J171_01370	ENOG4107SPG	Catalyzes two reactions the first one is the production of beta-formyl glycinamide ribonucleotide (GAR) from formate, ATP and beta GAR
J171_01372	ENOG4105DWA	May conjugate Arg from its aminoacyl-tRNA to the N- termini of proteins containing an N-terminal aspartate or glutamate
J171_01377	ENOG4105C29	acyl-CoA thioesterase
J171_01380	ENOG4108TGP	Thioesterase superfamily protein
J171_01381	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)
J171_01382	ENOG4105KK9	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
J171_01383	ENOG4105K46	50S ribosomal protein l27
J171_01384	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
J171_01385	ENOG4105KQV	Binds directly to 16S ribosomal RNA (By similarity)
J171_01386	ENOG4105CJR	Integral membrane protein (MviN
J171_01387	ENOG4105DTN	riboflavin biosynthesis protein ribF
J171_01388	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)
J171_01389	ENOG4105M02	This protein specifically catalyzes the removal of signal peptides from prolipoproteins (By similarity)
J171_01390	ENOG4105C48	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
J171_01392	ENOG4105E2S	oxidase) subunit II
J171_01393	ENOG4105BZ9	Cytochrome C oxidase, subunit I
J171_01394	ENOG4105CCU	oxidase (Subunit III)
J171_01395	ENOG41090KH	cytochrome o ubiquinol oxidase (subunit iv)
J171_01397	ENOG4105DNJ	May play a role in the repair of endogenous alkylation damage (By similarity)
J171_01398	ENOG4105KAF	membrAne
J171_01401	ENOG4105CJX	Molecular chaperone. Has ATPase activity (By similarity)
J171_01403	ENOG4107MMM	Anti-sigma-factor antagonist
J171_01404	ENOG4105FUA	antagonist
J171_01405	ENOG4105QD0	anti-sigma regulatory factor serine threonine protein kinase
J171_01407	ENOG4105BZU	Histidine kinase
J171_01412	ENOG4105KCV	RNA signal recognition particle 4.5S RNA
J171_01413	ENOG4105C08	Histidine kinase
J171_01414	ENOG4107Z5C	methylesterase
J171_01415	ENOG4105BZU	Histidine kinase
J171_01416	ENOG4105BZU	Histidine kinase
J171_01417	ENOG4105CQZ	Histidine kinase
J171_01420	ENOG4105CZZ	Alpha-N-arabinofuranosidase (EC 3.2.1.55)
J171_01421	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)
J171_01422	ENOG4105CRE	cytochrome C
J171_01423	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
J171_01424	ENOG4107QWG	2-Nitropropane dioxygenase
J171_01426	ENOG4105K5M	30s ribosomal protein S16
J171_01427	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)
J171_01428	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
J171_01429	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)
J171_01430	ENOG4107QJQ	Mate efflux family protein
J171_01431	ENOG4107QJQ	Mate efflux family protein
J171_01434	ENOG4105VEJ	Heat shock protein
J171_01435	ENOG4105C1X	Bifunctional enzyme with both catalase and broad- spectrum peroxidase activity (By similarity)
J171_01437	ENOG4105D86	that it carries out the mismatch recognition step. This protein has a weak ATPase activity (By similarity)
J171_01440	ENOG4105CNA	YD repeat protein
J171_01444	ENOG4105CNT	hydrolase family 2
J171_01445	ENOG4106FKC	arabinogalactan endo-1,4-beta-galactosidase
J171_01448	ENOG4105C26	Dehydrogenase
J171_01449	ENOG4105C1G	acyl-Coa dehydrogenase
J171_01450	ENOG4105E39	Enoyl-CoA hydratase
J171_01451	ENOG4105DYT	3-hydroxyacyl-CoA dehydrogenase
J171_01452	ENOG4105CF3	3-Hydroxyisobutyrate dehydrogenase
J171_01454	ENOG4105DYT	3-hydroxyacyl-CoA dehydrogenase
J171_01455	ENOG4105EMN	RNA polymerase sigma factor
J171_01457	ENOG4105C0H	protease
J171_01458	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)
J171_01459	ENOG4105C3F	Signal peptidase i
J171_01461	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)
J171_01462	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)
J171_01463	ENOG41071DT	Involved in DNA repair and RecF pathway recombination (By similarity)
J171_01465	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
J171_01466	ENOG41080ZE	Adenylate cyclase
J171_01467	ENOG4107ZXU	DSBA oxidoreductase
J171_01468	ENOG4108QDE	fad dependent oxidoreductase
J171_01469	ENOG4105EXX	Deoxyribodipyrimidine photolyase-related protein
J171_01470	ENOG4107QPA	Cleaves GlcNAc linked beta-1,4 to MurNAc tripeptides (By similarity)
J171_01471	ENOG4108UGV	hypoxanthine phosphoribosyltransferase
J171_01472	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)
J171_01473	ENOG4105VEQ	Cold shock protein
J171_01474	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)
J171_01476	ENOG4107QRT	dEAD DEAH box helicase
J171_01477	ENOG4107T0X	DNA ligase
J171_01479	ENOG4107T0X	DNA ligase
J171_01482	ENOG4105BZU	Histidine kinase
J171_01485	ENOG4105CHU	acetyl-coa acetyltransferase
J171_01489	ENOG4108VKG	metal-dependent hydrolase
J171_01492	ENOG4105KSC	Transcriptional regulator, TraR DksA family
J171_01495	ENOG4105DFF	Rod shape-determining protein mreb
J171_01496	ENOG4108YZY	peptidylprolyl cis-trans isomerase
J171_01498	ENOG4108Z8G	Alkylphosphonate utilization operon protein PhnA
J171_01499	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
J171_01500	ENOG4105F27	Major Facilitator
J171_01510	ENOG4105M4H	endoribonuclease L-psp
J171_01511	ENOG4105CV9	cyclopropane-fatty-acyl-phospholipid synthase
J171_01514	ENOG4105CV9	cyclopropane-fatty-acyl-phospholipid synthase
J171_01519	ENOG4105K6V	RNA polymerase
J171_01522	ENOG4108R3D	Electron transport complex
J171_01524	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)
J171_01527	ENOG4105DA5	(ABC) transporter
J171_01528	ENOG4108YZK	glyoxalase bleomycin resistance protein dioxygenase
J171_01529	ENOG4108IQI	permease
J171_01530	ENOG4107QK5	Homocysteine s-methyltransferase
J171_01540	ENOG4108YXA	Membrane
J171_01543	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)
J171_01545	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
J171_01546	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)
J171_01547	ENOG4105DAF	Involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
J171_01548	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)
J171_01549	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)
J171_01552	ENOG4105DZP	Membrane-associated zinc metalloprotease
J171_01553	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)
J171_01554	ENOG4105KNE	Phosphatidate cytidylyltransferase
J171_01555	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
J171_01556	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)
J171_01557	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
J171_01558	ENOG4105BZU	Histidine kinase
J171_01559	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)
J171_01560	ENOG4105CE9	30S ribosomal protein S2
J171_01567	ENOG4105CA1	Removes the N-terminal methionine from nascent proteins (By similarity)
J171_01568	ENOG4105E1P	Modifies, by uridylylation or deuridylylation the PII (GlnB) regulatory protein (By similarity)
J171_01570	ENOG4105KUZ	arsenate reductase
J171_01571	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)
J171_01572	ENOG4105CAQ	asparagine synthetase
J171_01574	ENOG4108ESX	Receptor
J171_01577	ENOG4108UWD	Iron-storage protein
J171_01578	ENOG4105FQ6	thiopurine methyltransferase
J171_01580	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)
J171_01584	ENOG4105CW7	secretion protein, HlyD family
J171_01585	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
J171_01589	ENOG4105DUX	Transporter
J171_01595	ENOG4105DGW	oligopeptidase A
J171_01596	ENOG4108V06	Glutathione peroxidase
J171_01597	ENOG4105DP0	ferredoxin-NADP reductase
J171_01599	ENOG4107GFK	fumarate
J171_01602	ENOG4105HDD	phospholipase
J171_01604	ENOG4105VEQ	Cold shock protein
J171_01607	ENOG4105CUZ	uba thif-type nad fad binding protein
J171_01608	ENOG4105F8V	Hydrolase, tatD family
J171_01611	ENOG4105C1G	acyl-Coa dehydrogenase
J171_01613	ENOG4108K3A	Glutathione S-transferase
J171_01614	ENOG4105CAQ	asparagine synthetase
J171_01616	ENOG4105CDU	Replicative dna helicase
J171_01617	ENOG4105CVP	deoxyribo-dipyrimidine photolyase
J171_01618	ENOG4105CDV	Ompa motb domain protein
J171_01620	ENOG4105CR8	Transcriptional regulator
J171_01627	ENOG4105BZU	Histidine kinase
J171_01629	ENOG4106TD9	Diguanylate cyclase
J171_01656	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
J171_01657	ENOG4108Z1B	Cyclase dehydrase
J171_01659	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)
J171_01660	ENOG41090R7	Ferric uptake
J171_01661	ENOG4105C4F	May be involved in recombinational repair of damaged DNA (By similarity)
J171_01662	ENOG4105CI8	Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons (By similarity)
J171_01663	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
J171_01664	ENOG4105CFG	Acts as a chaperone (By similarity)
J171_01665	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)
J171_01667	ENOG4107XGF	functions in a salvage pathway. Uses pyridoxamine (By similarity)
J171_01674	ENOG4105C5Q	Transcriptional regulator
J171_01675	ENOG4105BZ1	(ABC) transporter
J171_01677	ENOG4108URH	decarboxylase
J171_01679	ENOG4105C7S	Dehydrogenase
J171_01680	ENOG4105C7P	2-oxoglutarate dehydrogenase, E1
J171_01682	ENOG4105EZE	Cupin 4 family protein
J171_01684	ENOG4107QTF	adenylosuccinate lyase
J171_01686	ENOG4105C37	(CBS) domain
J171_01692	ENOG4105CZV	ABC transporter
J171_01693	ENOG410811P	TRANSCRIPTIONAl REGULATOR GntR family
J171_01696	ENOG4108V1T	peptidylprolyl cis-trans isomerase
J171_01697	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
J171_01698	ENOG41069P5	Protein slyX homolog
J171_01701	ENOG4105ETE	Transcriptional regulator (LacI family
J171_01703	ENOG4105D7K	pfkb domain protein
J171_01705	ENOG4105C3R	Methionine synthase
J171_01706	ENOG4105C3R	Methionine synthase
J171_01708	ENOG4105C1G	acyl-Coa dehydrogenase
J171_01711	ENOG4105C40	3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs (By similarity)
J171_01713	ENOG4105C2N	RNA methyltransferase TrmH family group 3
J171_01714	ENOG4105BZU	Histidine kinase
J171_01715	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)
J171_01717	ENOG4108UTW	Plays a role in the regulation of phosphate uptake
J171_01718	ENOG4105BZY	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
J171_01719	ENOG4105E2Z	phosphate ABC transporter (Permease
J171_01720	ENOG4105C8U	phosphate abc transporter
J171_01721	ENOG4107QMV	Part of the ABC transporter complex PstSACB involved in phosphate import (By similarity)
J171_01725	ENOG4107B2H	carbonic anhydrase
J171_01726	ENOG4105CHH	sulfate transporter
J171_01727	ENOG4105CSM	endonuclease III
J171_01729	ENOG4105E39	Enoyl-CoA hydratase
J171_01730	ENOG4108V1T	peptidylprolyl cis-trans isomerase
J171_01731	ENOG4105P8F	nudix hydrolase
J171_01732	ENOG4105KHC	sulfurtransferase
J171_01738	ENOG4105C5H	ABC transporter
J171_01739	ENOG4105C4H	Specifically methylates the guanine in position 2445 (m2G2445) and the guanine in position 2069 (m7G2069) of 23S rRNA (By similarity)
J171_01740	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)
J171_01744	ENOG4105CJB	Exodeoxyribonuclease I
J171_01745	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)
J171_01746	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)
J171_01748	ENOG4105C3W	Catalyzes the oxidative ring opening of 3- hydroxyanthranilate to 2-amino-3-carboxymuconate semialdehyde, which spontaneously cyclizes to quinolinate (By similarity)
J171_01749	ENOG41077A9	carbonic anhydrase
J171_01758	ENOG4105WH1	Two component transcriptional regulator luxr family
J171_01765	ENOG4105C5S	asparaginyl-tRNA synthetase
J171_01766	ENOG4108YX9	iron--sulfur cluster insertion protein erpA
J171_01767	ENOG4108ZDX	Binds together with S18 to 16S ribosomal RNA (By similarity)
J171_01768	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)
J171_01769	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
J171_01771	ENOG4107NPY	receptor for the septal ring structure, may anchor it to the inner-membrane (By similarity)
J171_01773	ENOG4105CIH	Imidazole acetol-phosphate transaminase
J171_01774	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)
J171_01775	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)
J171_01777	ENOG4105C35	Catalyzes the interconversion of methylthioribose-1- phosphate (MTR-1-P) into methylthioribulose-1-phosphate (MTRu-1-P) (By similarity)
J171_01778	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)
J171_01779	ENOG4105DZG	Dehydrogenase
J171_01781	ENOG4105CGP	Urocanate hydratase
J171_01783	ENOG4105C84	Histidine ammonia-lyase
J171_01784	ENOG4105CI2	imidazolone-5-propionate hydrolase
J171_01792	ENOG4105DQ2	Is probably involved in the electron transfer between its heme and the molybdenum cofactor of the reductase catalytic subunit YedY (By similarity)
J171_01793	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)
J171_01794	ENOG4107QM1	Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine (By similarity)
J171_01796	ENOG4105CMY	5-enolpyruvylshikimate-3-phosphate synthase
J171_01799	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)
J171_01800	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)
J171_01801	ENOG4105CC0	LysR family Transcriptional regulator
J171_01812	ENOG4105C8Q	Methyl-accepting chemotaxis
J171_01816	ENOG4105ETX	regulatoR
J171_01820	ENOG4105KWW	Biogenesis protein
J171_01821	ENOG4107QX9	Thiol disulfide interChange protein
J171_01822	ENOG4105DA4	cytochrome c-type biogenesis protein
J171_01823	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)
J171_01825	ENOG41060IM	Heme exporter protein
J171_01828	ENOG4105EMN	RNA polymerase sigma factor
J171_01839	ENOG4105EGZ	biosynthesis protein
J171_01845	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
J171_01847	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)
J171_01850	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)
J171_01852	ENOG41079KZ	Major Facilitator Superfamily
J171_01853	ENOG4105DEN	Luciferase family
J171_01858	ENOG4105CJ3	phosphate transporter
J171_01861	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)
J171_01863	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
J171_01864	ENOG4105CXR	Phospho-2-dehydro-3-deoxyoctonate aldolase
J171_01866	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
J171_01867	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)
J171_01868	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)
J171_01869	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)
J171_01870	ENOG4106NZV	Responsible for synthesis of pseudouridine from uracil- 13 in transfer RNAs (By similarity)
J171_01871	ENOG4108DG9	Smr protein MutS2
J171_01872	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
J171_01873	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)
J171_01874	ENOG4108UM1	dedA family
J171_01875	ENOG4108K5P	(LipO)protein
J171_01878	ENOG4105HBR	Rna-binding protein
J171_01879	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)
J171_01880	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)
J171_01881	ENOG4105EEI	dihydropteroate synthase
J171_01882	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)
J171_01883	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)
J171_01884	ENOG4105C1N	GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis (By similarity)
J171_01885	ENOG4107TH8	cina domain protein
J171_01886	ENOG4105CNK	Required, probably indirectly, for the hydroxylation of 2-octaprenylphenol to 2-octaprenyl-6-hydroxy-phenol, the fourth step in ubiquinone biosynthesis (By similarity)
J171_01887	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)
J171_01888	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)
J171_01889	ENOG4105Y3E	Modulates RecA activity (By similarity)
J171_01890	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)
J171_01891	ENOG4105VM8	Could accelerate the degradation of some genes transcripts potentially through selective RNA binding (By similarity)
J171_01893	ENOG4107SDU	Methyl-accepting chemotaxis
J171_01895	ENOG4105CWB	LysR family transcriptional Regulator
J171_01900	ENOG4105DWF	phosphomethylpyrimidine kinase
J171_01903	ENOG4108IAB	Phoh family
J171_01904	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
J171_01907	ENOG4107TUS	Dihydrodipicolinate synthase
J171_01909	ENOG4108Z4U	Ferredoxin
J171_01910	ENOG4105EI3	2-dehydro-3-deoxygalactonokinase EC 2.7.1.58
J171_01912	ENOG4105CXK	mandelate racemase muconate lactonizing
J171_01913	ENOG4108RTU	Aldolase
J171_01923	ENOG4105CMG	Carbohydrate kinase
J171_01924	ENOG4105C93	Xylose Isomerase
J171_01928	ENOG4108KNB	n-acetylmuramoyl-l-alanine amidase
J171_01929	ENOG4105DZA	Converts GTP to 7,8-dihydroneopterin triphosphate (By similarity)
J171_01933	ENOG4105DJ0	Poly(A) Polymerase
J171_01934	ENOG4105K8U	2-Amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase
J171_01935	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
J171_01936	ENOG4108IAA	Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate (By similarity)
J171_01937	ENOG4108Z2X	Catalyzes the pyruvoyl-dependent decarboxylation of aspartate to produce beta-alanine (By similarity)
J171_01938	ENOG4107QP8	phosphohexose isomerase
J171_01945	ENOG4105KU2	hydrolase family 5
J171_01946	ENOG4108UYB	regulatoR
J171_01948	ENOG4105C4E	Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate (By similarity)
J171_01949	ENOG410841Q	phosphoesterase PA-phosphatase related protein
J171_01952	ENOG4108SXK	Transporter Drug Metabolite Exporter family
J171_01953	ENOG4105D4A	Cell wall formation (By similarity)
J171_01954	ENOG4107QYT	Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor (By similarity)
J171_01957	ENOG4105C26	Dehydrogenase
J171_01960	ENOG4105CND	Glycosyl transferase, family 2
J171_01961	ENOG4107BJW	polysaccharide deacetylase
J171_01964	ENOG41067NU	
J171_01965	ENOG41067NU	
J171_01974	ENOG4105DS0	Transcriptional regulator, Crp Fnr family
J171_01975	ENOG4105CUT	histidyl-tRNA synthetase
J171_01977	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)
J171_01978	ENOG4105CEK	Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine (By similarity)
J171_01979	ENOG4105CIH	Imidazole acetol-phosphate transaminase
J171_01980	ENOG4105ECC	imidazole-glycerol-phosphate dehydratase
J171_01981	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)
J171_01982	ENOG4105CJV	Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase
J171_01983	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)
J171_01984	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
J171_01987	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)
J171_01988	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)
J171_01989	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)
J171_01990	ENOG4105CUB	amino acid
J171_01991	ENOG4105CUB	amino acid
J171_01993	ENOG4108JQ1	Dehydrogenase
J171_01994	ENOG4105CQB	FAD linked oxidase domain protein
J171_01998	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)
J171_02000	ENOG4105CBH	Hydroxymethylglutaryl-CoA lyase
J171_02004	ENOG4105CE1	Ferrous iron transport protein b
J171_02007	ENOG4105C1I	TRANSCRIPTIONAl REGULATOR GntR family
J171_02008	ENOG4108RPX	mosc domain containing protein
J171_02009	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
J171_02010	ENOG4105C1M	carbamoyl-phosphate synthetase glutamine chain
J171_02012	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
J171_02013	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)
J171_02015	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
J171_02023	ENOG4105DY9	regulatoR
J171_02024	ENOG4105CG1	Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA (By similarity)
J171_02025	ENOG4105CRK	lysyL-tRNA synthetase
J171_02026	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
J171_02027	ENOG4105BZU	Histidine kinase
J171_02028	ENOG41060WC	Enoyl-CoA hydratase
J171_02029	ENOG4105CEY	Amp-dependent synthetase and ligase
J171_02031	ENOG4107QM5	aconitate hydratase
J171_02034	ENOG4107QIJ	Aconitate hydratase 2
J171_02035	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)
J171_02036	ENOG4105BZU	Histidine kinase
J171_02037	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
J171_02038	ENOG4108Z4W	Probably deamidates glutamine residues to glutamate on methyl-accepting chemotaxis receptors (MCPs), playing an important role in chemotaxis (By similarity)
J171_02039	ENOG4105BZU	Histidine kinase
J171_02040	ENOG4105C8Q	Methyl-accepting chemotaxis
J171_02041	ENOG4105C8Q	Methyl-accepting chemotaxis
J171_02042	ENOG4105C8Q	Methyl-accepting chemotaxis
J171_02043	ENOG4105C8Q	Methyl-accepting chemotaxis
J171_02044	ENOG4105C8Q	Methyl-accepting chemotaxis
J171_02046	ENOG4105C8Q	Methyl-accepting chemotaxis
J171_02048	ENOG4105C8Q	Methyl-accepting chemotaxis
J171_02049	ENOG4105C8Q	Methyl-accepting chemotaxis
J171_02049	ENOG4105C8Q	Methyl-accepting chemotaxis
J171_02051	ENOG4105C8Q	Methyl-accepting chemotaxis
J171_02052	ENOG4105CBS	Chea signal transduction histidine kinase
J171_02053	ENOG4108VYJ	response regulator receiver protein
J171_02055	ENOG4108V3W	Chemotaxis protein, CheW
J171_02056	ENOG4107QJE	Chromosome Partitioning Protein
J171_02057	ENOG4105ER2	Ompa motb domain protein
J171_02058	ENOG4105E14	MotA TolQ exbB proton channel
J171_02077	ENOG4105C4X	radical SAM domain protein
J171_02080	ENOG4105CBS	Chea signal transduction histidine kinase
J171_02082	ENOG4108VYJ	response regulator receiver protein
J171_02083	ENOG4105DN4	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
J171_02084	ENOG4107R21	site-determining protein
J171_02085	ENOG4105FZW	flagellar biosynthesis regulator FlhF
J171_02086	ENOG4105D7B	Flagellar biosynthesis protein flha
J171_02087	ENOG4105D00	flagellar biosynthetic protein flhB
J171_02088	ENOG4105BZU	Histidine kinase
J171_02089	ENOG4105BZU	Histidine kinase
J171_02090	ENOG4105BZU	Histidine kinase
J171_02091	ENOG4105D19	Role in flagellar biosynthesis (By similarity)
J171_02092	ENOG4105VS8	Flagellar biosynthetic protein fliq
J171_02094	ENOG4105CN7	Flagellar biosynthetic protein FliP
J171_02095	ENOG4105K0P	flagellar biosynthesis protein
J171_02096	ENOG4105DD5	Flagellar motor switch protein
J171_02097	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)
J171_02101	ENOG4108JIR	Flagellum-specific ATP synthase
J171_02103	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)
J171_02104	ENOG4105C1F	The M ring may be actively involved in energy transduction (By similarity)
J171_02105	ENOG4105VQ0	flagellar hook-basal body complex protein fliE
J171_02106	ENOG4107RGC	Glycosyl transferase, family 2
J171_02112	ENOG4105CHR	reductase
J171_02113	ENOG4105H9W	Short-chain dehydrogenase reductase Sdr
J171_02114	ENOG4108P1X	synthase
J171_02117	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
J171_02118	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
J171_02119	ENOG4105DTW	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
J171_02123	ENOG4105MQ3	flagellar protein FliS
J171_02124	ENOG4107W9T	flagellar hook-associated
J171_02126	ENOG4105DTJ	flagellar hook-associated protein
J171_02128	ENOG4108ZW7	flagellar rod assembly protein muramidase flgj
J171_02129	ENOG4105D92	Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation (By similarity)
J171_02130	ENOG4107W7W	Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation (By similarity)
J171_02131	ENOG4105CGA	flagellar basal-body rod protein FlgG
J171_02132	ENOG4108KPB	Flagellar basal-body rod protein FlgF
J171_02133	ENOG4105BZE	flagellar hook protein, FlgE
J171_02134	ENOG410822I	Flagellar hook capping protein
J171_02135	ENOG4108ZC9	flagellar basal-body rod protein flgc
J171_02137	ENOG4107R88	Chemotaxis protein (CheV)
J171_02141	ENOG4105BZU	Histidine kinase
J171_02142	ENOG4105BZU	Histidine kinase
J171_02144	ENOG4105BZU	Histidine kinase
J171_02148	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
J171_02150	ENOG4105KAE	Involved in the modulation of the specificity of the ClpAP-mediated ATP-dependent protein degradation (By similarity)
J171_02151	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
J171_02152	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)
J171_02153	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)
J171_02155	ENOG4105C3M	thioredoxin reductase
J171_02156	ENOG4105CNU	cell division protein FtsK
J171_02158	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)
J171_02160	ENOG4105D1H	recombination factor protein RarA
J171_02162	ENOG41082MI	Protein CrcB homolog
J171_02164	ENOG4105CHU	acetyl-coa acetyltransferase
J171_02167	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)
J171_02168	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
J171_02170	ENOG4105HSZ	Cytoskeletal protein that is involved in cell-shape control through regulation of the length of the long axis (By similarity)
J171_02172	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)
J171_02173	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
J171_02174	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
J171_02175	ENOG4105D06	uba thif-type nad fad binding protein
J171_02182	ENOG4105CGK	Exodeoxyribonuclease III
J171_02184	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
J171_02185	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)
J171_02188	ENOG4105C56	H( )-stimulated, divalent metal cation uptake system (By similarity)
J171_02189	ENOG4105KST	dependent repressor
J171_02190	ENOG4108Z6B	deaminase
J171_02191	ENOG4108RBP	3'-to-5' exoribonuclease specific for small oligoribonucleotides (By similarity)
J171_02194	ENOG4105CF9	Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation dephosphorylation (By similarity)
J171_02198	ENOG4106PT6	cdpdiacylglycerol-serine O-phosphatidyltransferase
J171_02200	ENOG4105D1N	poly(r)-hydroxyalkanoic acid synthase, class
J171_02205	ENOG4105BZM	domain protein
J171_02206	ENOG4105BZU	Histidine kinase
J171_02214	ENOG4105N7H	Cytochrome
J171_02219	ENOG4108UHU	Aldolase
J171_02220	ENOG4105C01	Dihydroxy-acid dehydratase
J171_02221	ENOG4108Q79	6-phosphogluconolactonase (EC 3.1.1.31)
J171_02222	ENOG4105CHC	glucokinase (EC 2.7.1.2)
J171_02225	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)
J171_02227	ENOG410612Q	succinate dehydrogenase (cytochrome b-556 subunit)
J171_02232	ENOG410681N	tpr repeat protein
J171_02234	ENOG4105D60	lipoprotein releasing system transmembrane protein
J171_02235	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)
J171_02237	ENOG4108EC8	DNA internalization-related competence protein ComEC
J171_02240	ENOG4105BZ1	(ABC) transporter
J171_02241	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)
J171_02242	ENOG4105CET	Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria (By similarity)
J171_02245	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)
J171_02246	ENOG4105BZQ	cdp-diacylglycerol-glycerol-3-phosphate 3-phosphatidyltransferase
J171_02250	ENOG4105C0W	non-ribosomal peptide synthetase
J171_02251	ENOG4105CEY	Amp-dependent synthetase and ligase
J171_02256	ENOG4108KU3	Integrase
J171_02258	ENOG4107QQG	Dehydrogenase
J171_02260	ENOG4108V1T	peptidylprolyl cis-trans isomerase
J171_02262	ENOG4105C72	UPF0176 protein
J171_02264	ENOG4105C03	ribonuclease
J171_02265	ENOG4105EI2	Pseudouridine synthase
J171_02266	ENOG4108NST	exported protein
J171_02267	ENOG4105DUN	Mediates zinc uptake. May also transport other divalent cations (By similarity)
J171_02269	ENOG41090A4	Pterin carbinolamine dehydratase
J171_02270	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)
J171_02281	ENOG4105EWI	Short-chain dehydrogenase reductase Sdr
J171_02288	ENOG4105W39	Membrane
J171_02294	ENOG4105DY9	regulatoR
J171_02302	ENOG4108ZXC	Two component transcriptional regulator, luxr family
J171_02307	ENOG4108N8X	transition metal ion binding
J171_02309	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)
J171_02311	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)
J171_02314	ENOG4107SFI	Major Facilitator superfamily
J171_02317	ENOG4105CHJ	isochorismatase hydrolase
J171_02320	ENOG4105WH1	Two component transcriptional regulator luxr family
J171_02323	ENOG4105DND	Transcriptional regulator
J171_02325	ENOG4105EVH	UPF0753 protein
J171_02330	ENOG4108YGG	dna repair protein
J171_02335	ENOG4105DFP	Integrase
J171_02338	ENOG4105E0K	tonB-dependent siderophore receptor
J171_02342	ENOG4106A2Z	transcriptional regulator antitoxin, MazE
J171_02347	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)
J171_02350	ENOG4105NRM	Membrane
J171_02356	ENOG4105C42	Type I secretion membrane fusion protein (HlyD
J171_02357	ENOG4108JJA	ABC, transporter
J171_02359	ENOG4107QJE	Chromosome Partitioning Protein
J171_02367	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)
J171_02368	ENOG4105NI8	Cytosine-specific methyltransferase
J171_02380	ENOG4105DFS	Conserved Protein
J171_02383	ENOG4107AQZ	Membrane
J171_02386	ENOG4108X0B	nad(p)h dehydrogenase (quinone)
J171_02387	ENOG4108K3A	Glutathione S-transferase
J171_02388	ENOG4105CTU	Proline racemase
J171_02391	ENOG4105DJ2	Major Facilitator Superfamily
J171_02392	ENOG4105R1U	AraC Family Transcriptional Regulator
J171_02422	ENOG41088T4	Helicase IV
J171_02438	ENOG4105ZXK	Dehydrogenase
J171_02443	ENOG4105W5Q	DNA repair protein (RadC
J171_02450	ENOG4105DFP	Integrase
J171_02451	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
J171_02452	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)
J171_02453	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)
J171_02455	ENOG4105CKD	glutathione-regulated potassium-efflux system protein
J171_02456	ENOG4105C3Y	UTP-glucose-1-phosphate uridylyltransferase
J171_02458	ENOG4105ESV	Glycosyl transferase, family 4
J171_02459	ENOG4105CFV	Tetratricopeptide repeat protein
J171_02461	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)
J171_02462	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)
J171_02463	ENOG4105CAT	Cytidine monophosphate kinase
J171_02464	ENOG4105YK5	50S ribosomal protein L36
J171_02467	ENOG4105DWY	Agmatine deiminase
J171_02473	ENOG4105DRS	transport system, permease
J171_02474	ENOG4105F0P	binding-protein-dependent transport systems inner membrane Component
J171_02480	ENOG4105K9H	YciI-like protein
J171_02481	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)
J171_02482	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)
J171_02483	ENOG4105FE9	pseudouridine synthase
J171_02487	ENOG4105CHM	Aminotransferase
J171_02488	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)
J171_02489	ENOG4105CA5	Required for the export of heme to the periplasm for the biogenesis of c-type cytochromes (By similarity)
J171_02490	ENOG41060IM	Heme exporter protein
J171_02492	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)
J171_02493	ENOG4105DA4	cytochrome c-type biogenesis protein
J171_02495	ENOG4105KWW	Biogenesis protein
J171_02496	ENOG4108M1T	Cytochrome c-type biogenesis protein
J171_02499	ENOG4108JJ8	(ABC) transporter
J171_02500	ENOG4108JJ9	ABC, transporter
J171_02501	ENOG4105C4M	(Ubiquinol oxidase) subunit I
J171_02502	ENOG4105CFY	cytochrome d ubiquinol oxidase, subunit ii
J171_02507	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)
J171_02508	ENOG4105CGT	Catalyzes the transfer of a phosphate group to glutamate to form glutamate 5-phosphate which rapidly cyclizes to 5- oxoproline (By similarity)
J171_02510	ENOG4105CH7	arginosuccinase
J171_02511	ENOG4105C0N	N-acetylglutamate semialdehyde dehydrogenase
J171_02513	ENOG4105CAS	nag kinase
J171_02516	ENOG4105CDH	Citrulline--aspartate ligase
J171_02517	ENOG4105DBV	ornithine carbamoyltransferase
J171_02519	ENOG4105C8N	cysteinyl-tRNA synthetase
J171_02520	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)
J171_02522	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
J171_02523	ENOG4105VAS	Could be involved in insertion of integral membrane proteins into the membrane (By similarity)
J171_02524	ENOG4105CD3	dihydroorotase
J171_02528	ENOG4105CPD	ethanolamine ammonia-lyase
J171_02529	ENOG4107FQ9	ethanolamine ammonia-lyase
J171_02540	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)
J171_02541	ENOG4108HWB	Non-specific O-methyltransferase that catalyzes the 2 O- methylation steps in the ubiquinone biosynthetic pathway (By similarity)
J171_02542	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)
J171_02544	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)
J171_02545	ENOG4105CK3	Lysine 2,3-aminomutase YodO family protein
J171_02546	ENOG4105BZU	Histidine kinase
J171_02549	ENOG4105ECY	inositol monophosphatase
J171_02550	ENOG4105CK4	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
J171_02553	ENOG4105C5H	ABC transporter
J171_02554	ENOG4105C1J	atp-dependent rna helicase
J171_02555	ENOG4109003	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis (By similarity)
J171_02556	ENOG4105CNG	UPF0061 protein
J171_02558	ENOG4108RXX	maleylacetoacetate isomerase
J171_02559	ENOG4105VEQ	Cold shock protein
J171_02560	ENOG4108VWS	Yaeq family
J171_02561	ENOG4105CBX	hi0933 family
J171_02563	ENOG4105D0M	Protease HtpX homolog
J171_02564	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)
J171_02565	ENOG4105CHR	reductase
J171_02569	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)
J171_02570	ENOG4105C5C	n-acetylmuramoyl-l-alanine amidase
J171_02571	ENOG4105K8N	protein family UPF0079, ATPase
J171_02572	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)
J171_02573	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)
J171_02574	ENOG4105DVS	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
J171_02576	ENOG4105E6M	Sulphatase-modifying factor protein
J171_02579	ENOG4105DQE	DNA ligase
J171_02593	ENOG4105C26	Dehydrogenase
J171_02595	ENOG4105MP0	transposase
J171_02615	ENOG4108V3W	Chemotaxis protein, CheW
J171_02616	ENOG4105C8Q	Methyl-accepting chemotaxis
J171_02617	ENOG4108VX5	3-methyladenine DNA glycosylase
J171_02618	ENOG4107QRT	dEAD DEAH box helicase
J171_02621	ENOG4105KB2	stringent starvation protein b
J171_02622	ENOG4107MKT	Stringent starvation protein a
J171_02623	ENOG4105EIX	cytochrome c1
J171_02624	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)
J171_02625	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)
J171_02626	ENOG4105E4C	Lytic transglycosylase catalytic
J171_02629	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)
J171_02630	ENOG4105C9A	Phoh family
J171_02632	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)
J171_02634	ENOG4108JU5	Magnesium and cobalt efflux protein
J171_02638	ENOG4105D38	putrescine abc transporter
J171_02639	ENOG4105F38	ABC transporter, permease
J171_02640	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
J171_02644	ENOG4107RUE	extracellular solute-binding protein family 1
J171_02645	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)
J171_02648	ENOG4105CFQ	glutamine synthetase
J171_02649	ENOG4105CJP	fad dependent oxidoreductase
J171_02650	ENOG4105BZU	Histidine kinase
J171_02651	ENOG4105W3S	hemerythrin-like, metal-binding protein
J171_02652	ENOG4105CSH	Transporter
J171_02654	ENOG4107QKC	Oxidoreductase alpha (molybdopterin) subunit
J171_02655	ENOG4107H9G	Necessary for formate dehydrogenase activity (By similarity)
J171_02656	ENOG4105FCD	Major Facilitator
J171_02659	ENOG4106BRA	Membrane
J171_02660	ENOG4105BZU	Histidine kinase
J171_02661	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
J171_02662	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
J171_02663	ENOG4105C7I	Dehydrogenase
J171_02665	ENOG4105C1P	efflux transporter, rnd family, mfp subunit
J171_02666	ENOG4105BZS	acriflavin resistance protein
J171_02667	ENOG4108M60	Transcriptional regulator
J171_02668	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)
J171_02669	ENOG4105DE4	1-phosphofructokinase
J171_02670	ENOG4105DM4	PTS System
J171_02678	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)
J171_02679	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)
J171_02680	ENOG4105VIE	preprotein translocase, subunit YajC
J171_02681	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)
J171_02682	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)
J171_02690	ENOG4105CZ5	Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate (By similarity)
J171_02691	ENOG4105E08	Glycoside hydrolase, family 9
J171_02692	ENOG4105CFB	Gamma-glutamyltranspeptidase (EC 2.3.2.2)
J171_02693	ENOG4105K5D	4fe-4S ferredoxin iroN-sulfur binding
J171_02696	ENOG4108ZEF	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate (By similarity)
J171_02697	ENOG4106H78	methyltransferase
J171_02698	ENOG4105CJX	Molecular chaperone. Has ATPase activity (By similarity)
J171_02714	ENOG4107QTZ	amino acid
J171_02717	ENOG4105DC7	peptidase M24
J171_02719	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
J171_02722	ENOG41080HI	glycine oxidase
J171_02723	ENOG4105CTU	Proline racemase
J171_02725	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)
J171_02726	ENOG4105CEN	a g-specific adenine glycosylase
J171_02727	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)
J171_02728	ENOG4105CQZ	Histidine kinase
J171_02731	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)
J171_02734	ENOG4105QNF	Outer membrane lipoprotein
J171_02736	ENOG4105CSU	acyl-Coa dehydrogenase
J171_02738	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)
J171_02742	ENOG4107VBM	3-beta hydroxysteroid dehydrogenase isomerase
J171_02743	ENOG4108JMX	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
J171_02744	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)
J171_02749	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
J171_02751	ENOG4107Y2G	Glycosyl transferase (Group 1
J171_02756	ENOG4105D3Q	Sugar transferase
J171_02760	ENOG4105WJX	transcriptional regulator MERR family
J171_02761	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)
J171_02762	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
J171_02763	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
J171_02764	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)
J171_02765	ENOG41082NX	50s ribosomal protein l35
J171_02767	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)
J171_02768	ENOG4105C22	threonyL-tRNA synthetase
J171_02769	ENOG4105ETE	Transcriptional regulator (LacI family
J171_02771	ENOG4107RBJ	symporter
J171_02777	ENOG4105CG3	alpha amylase, catalytic region
J171_02789	ENOG4106E4H	Type IV secretory pathway VirB3 family protein
J171_02793	ENOG4105CMA	conjugation trbi family protein
J171_02800	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)
J171_02819	ENOG4105ED4	portal protein
J171_02828	ENOG4105NVB	glycoside hydrolase, family 19
J171_02844	ENOG4108HRK	Histidine kinase
J171_02845	ENOG4105EWT	decarboxylase family
J171_02846	ENOG4108KPZ	tonB-dependent Receptor
J171_02847	ENOG41076UM	multiple antibiotic resistance (MarC)-related protein
J171_02849	ENOG4105M2J	Glutaredoxin
J171_02850	ENOG4105CK4	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
J171_02851	ENOG4105CY8	phosphoribosylaminoimidazole carboxylase atpase subunit
J171_02852	ENOG4108UM6	Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) (By similarity)
J171_02854	ENOG4105D18	nicotinate-nucleotide pyrophosphorylase
J171_02856	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
J171_02857	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
J171_02858	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
J171_02859	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)
J171_02860	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)
J171_02861	ENOG4105CHV	Transcription elongation factor NusA
J171_02862	ENOG4105K7D	Required for maturation of 30S ribosomal subunits (By similarity)
J171_02864	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)
J171_02865	ENOG4105C8S	subunit m
J171_02866	ENOG4105D65	subunit l
J171_02868	ENOG4105DF2	NADH dehydrogenase subunit j
J171_02869	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)
J171_02870	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)
J171_02871	ENOG4107R0R	NADH dehydrogenase subunit g
J171_02872	ENOG4107QIZ	NADH dehydrogenase
J171_02873	ENOG4105GKE	subunit e
J171_02874	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)
J171_02875	ENOG4105CYU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
J171_02876	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)
J171_02877	ENOG4105KWU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
J171_02880	ENOG4105CP7	Triose-phosphate isomerase
J171_02881	ENOG4107FW0	short-chain dehydrogenase reductase
J171_02884	ENOG4105BZU	Histidine kinase
J171_02887	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
J171_02888	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)
J171_02889	ENOG4105F6H	The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate (By similarity)
J171_02891	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
J171_02893	ENOG4108ZGB	N-(5'-phosphoribosyl)anthranilate isomerase
J171_02894	ENOG4105DI7	Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs (By similarity)
J171_02898	ENOG4105CM3	Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate (By similarity)
J171_02899	ENOG4105C5I	Dehydrogenase
J171_02900	ENOG4105D10	5-enolpyruvylshikimate-3-phosphate phospholyase
J171_02901	ENOG4105C76	Specifically methylates the 50S ribosomal protein L3 on a specific glutamine residue (By similarity)
J171_02903	ENOG4105DJ4	phosphatidylserine decarboxylase
J171_02905	ENOG4105D7A	ATP-binding protein
J171_02906	ENOG4107VIJ	nudix hydrolase
J171_02909	ENOG4108RRZ	Transcription elongation factor GreB
J171_02910	ENOG4105CBM	Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 (By similarity)
J171_02915	ENOG4105DHP	deoxycytidine triphosphate deaminase
J171_02920	ENOG4105C9K	Endothelin-converting enzyme 1
J171_02921	ENOG4105C9K	Endothelin-converting enzyme 1
J171_02925	ENOG4105DC8	reductase
J171_02926	ENOG4105MWK	D-amino acid dehydrogenase, small subunit
J171_02928	ENOG41090X3	Peptidyl-prolyl cis-trans isomerase
J171_02929	ENOG4105K4H	Nlp p60 protein
J171_02930	ENOG4105K4H	Nlp p60 protein
J171_02932	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)
J171_02934	ENOG4105G6Z	alkaline phosphatase
J171_02935	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)
J171_02936	ENOG41067QG	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
J171_02937	ENOG4105CTB	Polyprenyl synthetase
J171_02940	ENOG4105CMS	peptidase U62, modulator of DNA gyrase
J171_02941	ENOG4105N42	UPF0307 protein
J171_02942	ENOG4105D1U	peptidase U62 modulator of DNA gyrase
J171_02944	ENOG4105QD6	exported protein
J171_02945	ENOG4105C03	ribonuclease
J171_02946	ENOG4108Z03	MAF-like protein
J171_02947	ENOG4105MPN	Membrane
J171_02950	ENOG4108UXA	Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA (By similarity)
J171_02953	ENOG4108Z1W	Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) (By similarity)
J171_02956	ENOG4105C8T	Leucyl-tRNA synthetase
J171_02958	ENOG4107QR8	Thioredoxin
J171_02963	ENOG4105WG9	Conserved Protein
J171_02964	ENOG4108R5K	PPIases accelerate the folding of proteins (By similarity)
J171_02971	ENOG4105BZ1	(ABC) transporter
J171_02977	ENOG4105ENJ	RND efflux system, outer membrane lipoprotein
J171_02978	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
J171_02979	ENOG4105BZU	Histidine kinase
J171_02981	ENOG4105FQP	Beta-lactamase
J171_02982	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)
J171_02985	ENOG4105BZU	Histidine kinase
J171_02986	ENOG4105FE9	pseudouridine synthase
J171_02987	ENOG4105BZU	Histidine kinase
J171_02997	ENOG4105D03	DNA-3-methyladenine glycosylase II
J171_03000	ENOG4105CMQ	Chloride channel
J171_03004	ENOG4105UGU	tonB-dependent Receptor
J171_03011	ENOG4108FN7	Aldo keto reductase
J171_03012	ENOG4105F27	Major Facilitator
J171_03013	ENOG4105CC0	LysR family Transcriptional regulator
J171_03015	ENOG4105CF7	AraC family transcriptional regulator
J171_03017	ENOG4108JGH	Tetr family transcriptional regulator
J171_03018	ENOG4105ENJ	RND efflux system, outer membrane lipoprotein
J171_03019	ENOG4105BZS	acriflavin resistance protein
J171_03020	ENOG4105C1P	efflux transporter, rnd family, mfp subunit
J171_03022	ENOG4105MYN	Zinc uptake regulation protein
J171_03023	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)
J171_03028	ENOG4105CT7	inner membrane cred family protein
J171_03030	ENOG4105EB3	Histidine kinase
J171_03031	ENOG4105E3W	Two component transcriptional regulator (Winged helix family
J171_03032	ENOG4105D6S	protein involved in catabolism of external DNA
J171_03034	ENOG4108JA2	transcriptioN-repair coupling factor
J171_03041	ENOG4105CBS	Chea signal transduction histidine kinase
J171_03042	ENOG4105C8Q	Methyl-accepting chemotaxis
J171_03043	ENOG4108V3W	Chemotaxis protein, CheW
J171_03044	ENOG4105BZU	Histidine kinase
J171_03045	ENOG4105BZU	Histidine kinase
J171_03046	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
J171_03047	ENOG4107RZC	phospholipase d
J171_03048	ENOG4105C9K	Endothelin-converting enzyme 1
J171_03050	ENOG4105DKJ	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
J171_03051	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)
J171_03053	ENOG4105EUB	pirin domain protein
J171_03056	ENOG4105EUB	pirin domain protein
J171_03057	ENOG4105D22	carbon starvation protein
J171_03058	ENOG4105VCD	cytoplasmic protein
J171_03069	ENOG4107XAN	XdhC and CoxI family
J171_03070	ENOG4105C7W	Xanthine dehydrogenase
J171_03071	ENOG4105DIP	Molybdopterin dehydrogenase FAD-binding
J171_03072	ENOG4107XKX	isoquinoline 1-oxidoreductase, alpha subunit
J171_03083	ENOG4108UUM	single-stranded DNA-binding protein
J171_03084	ENOG4105EAH	synthase
J171_03086	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
J171_03089	ENOG4105CFH	Aspartokinase
J171_03090	ENOG4105JAB	phenazine biosynthesis protein, phzf family
J171_03091	ENOG4105JAB	phenazine biosynthesis protein, phzf family
J171_03093	ENOG4108Z9K	Osmotically inducible protein
J171_03094	ENOG4105CXT	aspartate transcarbamylase
J171_03095	ENOG4107Y66	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
J171_03096	ENOG4108UJU	UPF0301 protein
J171_03097	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
J171_03100	ENOG4108E16	pectate lyase
J171_03101	ENOG4105CZX	twitching motility protein
J171_03102	ENOG4105CZX	twitching motility protein
J171_03103	ENOG4105DFA	alanine racemase domain protein
J171_03104	ENOG4105II7	pyrroline-5-carboxylate reductase
J171_03106	ENOG4105FAA	peptidase M23
J171_03110	ENOG4108Z0Z	intracellular protease Pfpi family
J171_03114	ENOG4105C3K	feS assembly ATPase SufC
J171_03115	ENOG4105JRK	feS assembly protein SufD
J171_03116	ENOG4105C9B	Cysteine desulfurase
J171_03119	ENOG4108IU3	tonb-dependent siderophore receptor
J171_03120	ENOG4107E2E	PKHD-type hydroxylase
J171_03125	ENOG4105CJ2	(LipO)protein
J171_03126	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)
J171_03129	ENOG41083P1	competence protein ComEA helix-hairpin-helix repeat protein
J171_03130	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)
J171_03132	ENOG4105EHM	Aminoglycoside phosphotransferase
J171_03133	ENOG4108S0S	Nucleotidyl transferase
J171_03135	ENOG4105C02	permease
J171_03137	ENOG4105CXB	phosphoribosylaminoimidazole synthetase
J171_03139	ENOG4108V3E	phosphoribosylglycinamide formyltransferase
J171_03143	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
J171_03145	ENOG4105C2X	Arabinose 5-phosphate isomerase
J171_03146	ENOG4108Z4R	3-deoxy-d-manno-octulosonate 8-phosphate phosphatase
J171_03148	ENOG4105WI0	lipopolysaccharide transport periplasmic protein lptA
J171_03149	ENOG4108IUZ	ABC transporter
J171_03150	ENOG4105DTW	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
J171_03151	ENOG41080QH	sigma 54 modulation protein ribosomal protein S30EA
J171_03152	ENOG4107RM2	PTS IIA-like nitrogen-regulatory protein PtsN
J171_03153	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)
J171_03154	ENOG4105C21	Displays ATPase and GTPase activities (By similarity)
J171_03156	ENOG41080Z8	PHOSPHOCARRIER protein
J171_03157	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)
J171_03158	ENOG4105CJW	magnesium transporter
J171_03159	ENOG4107UWA	esterase
J171_03160	ENOG4105CFY	cytochrome d ubiquinol oxidase, subunit ii
J171_03161	ENOG4105C4M	(Ubiquinol oxidase) subunit I
J171_03163	ENOG4105C85	amino acid
J171_03164	ENOG4108NFF	pectate lyase
J171_03167	ENOG4105CUB	amino acid
J171_03170	ENOG4108MHS	Lysyl endopeptidase
J171_03172	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)
J171_03173	ENOG4105QV4	Tryptophan halogenase
J171_03178	ENOG4108Z4X	TRANSCRIPTIONal
J171_03181	ENOG4106032	Glutathionylspermidine synthase
J171_03186	ENOG4108P9J	Phage shock protein A
J171_03188	ENOG4108S7T	Catalyzes the oxidation of either pyridoxine 5'- phosphate (PNP) or pyridoxamine 5'-phosphate (PMP) into pyridoxal 5'-phosphate (PLP) (By similarity)
J171_03189	ENOG4105KHV	Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate (By similarity)
J171_03190	ENOG4105D49	3-dehydroquinate synthase
J171_03192	ENOG4105CFZ	Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III (By similarity)
J171_03205	ENOG4108JUA	Transcriptional regulator
J171_03206	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
J171_03207	ENOG4105BZU	Histidine kinase
J171_03208	ENOG4105BZU	Histidine kinase
J171_03210	ENOG4105BZU	Histidine kinase
J171_03211	ENOG4108YYC	ycei family
J171_03215	ENOG4105EJQ	L-serine dehydratase
J171_03217	ENOG4105CFH	Aspartokinase
J171_03218	ENOG4105C28	cystathionine
J171_03219	ENOG4106TYC	homoserine o-acetyltransferase (EC 2.3.1.31)
J171_03221	ENOG4105DR5	peptidase
J171_03222	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)
J171_03223	ENOG4108UT2	hemolysin iii
J171_03224	ENOG41066T0	asmA family
J171_03225	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)
J171_03227	ENOG4108VKV	Monofunctional biosynthetic peptidoglycan transglycosylase
J171_03228	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)
J171_03230	ENOG4105D05	Receptor
J171_03232	ENOG4108IG5	Transcriptional regulator
J171_03234	ENOG4107QPN	acyl-Coa dehydrogenase
J171_03239	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)
J171_03240	ENOG4105D43	The glycine cleavage system catalyzes the degradation of glycine (By similarity)
J171_03242	ENOG4107QX8	SPFH domain, Band 7 family protein
J171_03243	ENOG4105KK4	UPF0060 membrane protein
J171_03244	ENOG4105DXN	mazG family
J171_03245	ENOG4108RNI	3'(2')5'-bisphosphate nucleotidase
J171_03246	ENOG4107RK2	ADP-ribose diphosphatase NudE
J171_03248	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)
J171_03249	ENOG4105CHC	glucokinase (EC 2.7.1.2)
J171_03252	ENOG4105VRS	hydrolase family 18
J171_03253	ENOG4105E2D	ec 3.2.1.52
J171_03258	ENOG4107QTZ	amino acid
J171_03260	ENOG4105F8D	glycoside hydrolase family 4
J171_03262	ENOG4105CWX	Alpha-1,2-mannosidase
J171_03269	ENOG4106N3A	copper homeostasis protein cutc
J171_03271	ENOG4105D9U	N-acetyltransferase
J171_03274	ENOG4105CBS	Chea signal transduction histidine kinase
J171_03275	ENOG4105C8Q	Methyl-accepting chemotaxis
J171_03277	ENOG4105M3Z	response regulator
J171_03278	ENOG4108UNF	response regulator
J171_03279	ENOG4105D7Z	glutathione synthase
J171_03281	ENOG41065RQ	ADP-ribosylation crystallin J1
J171_03282	ENOG41072GX	Peptidase M22 Glycoprotease
J171_03283	ENOG4105DVT	helicase
J171_03285	ENOG4105BZ4	penicillin-binding protein
J171_03288	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)
J171_03289	ENOG4105JIE	May be involved in the transport of PQQ or its precursor to the periplasm (By similarity)
J171_03290	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)
J171_03291	ENOG4105Z85	coenzyme PQQ synthesis
J171_03292	ENOG4105EZY	Pyrroloquinoline quinone biosynthesis protein E
J171_03295	ENOG4105CHC	glucokinase (EC 2.7.1.2)
J171_03297	ENOG4105CQ7	ATP-dependent helicase
J171_03299	ENOG4105C9U	ATP-dependent DNA helicase RecQ
J171_03306	ENOG4105C8Q	Methyl-accepting chemotaxis
J171_03310	ENOG410903D	sensor protein
J171_03311	ENOG4105FD2	Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) (By similarity)
J171_03313	ENOG4105EIZ	Catalyzes the conversion of 6-carboxy-5,6,7,8- tetrahydropterin (CPH4) to 7-carboxy-7-deazaguanine (CDG) (By similarity)
J171_03315	ENOG4105KCK	Peptidoglycan-associated lipoprotein
J171_03316	ENOG4107R6Y	Involved in the TonB-independent uptake of proteins (By similarity)
J171_03319	ENOG4105E02	MotA TolQ exbB proton channel
J171_03320	ENOG4107YD3	Thioesterase
J171_03321	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)
J171_03323	ENOG4105DFH	Transport of potassium into the cell (By similarity)
J171_03324	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)
J171_03325	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)
J171_03326	ENOG4105CDY	transcriptional regulatory protein
J171_03329	ENOG4105C9M	aspartyl-trna synthetase
J171_03332	ENOG4108ISG	Major Facilitator
J171_03335	ENOG4105HSS	phospholipase C
J171_03338	ENOG4105ETT	transcriptional Regulator, LysR family
J171_03340	ENOG4105C5H	ABC transporter
J171_03341	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)
J171_03343	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)
J171_03344	ENOG4107RNH	Outer membrane receptor FepA
J171_03346	ENOG4105CKD	glutathione-regulated potassium-efflux system protein
J171_03351	ENOG4105GAV	receptor
J171_03354	ENOG4105C6X	Major Facilitator
J171_03356	ENOG4105CU5	Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine (By similarity)
J171_03361	ENOG4105CUP	Catalyzes the synthesis of alpha-ribazole-5'-phosphate from nicotinate mononucleotide (NAMN) and 5,6- dimethylbenzimidazole (DMB) (By similarity)
J171_03362	ENOG4108YZT	Adenosylcobinamide kinase
J171_03363	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)
J171_03364	ENOG4105EFT	decarboxylase
J171_03366	ENOG4105DH2	Converts cobyric acid to cobinamide by the addition of aminopropanol on the F carboxylic group (By similarity)
J171_03367	ENOG41068B1	Cob-I-yrinic acid a,c-diamide adenosyltransferase
J171_03370	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)
J171_03372	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
J171_03373	ENOG4105E2Y	ABC, transporter
J171_03374	ENOG4105EFS	Binding-protein-dependent transport systems, inner membrane component
J171_03375	ENOG4105GVF	(ABC) transporter
J171_03376	ENOG4105CPC	Aldo Keto reductase
J171_03377	ENOG4105CPU	Monooxygenase
J171_03378	ENOG4107ZSV	Receptor
J171_03379	ENOG41082IR	Excinuclease ABC C subunit domain protein
J171_03386	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)
J171_03387	ENOG4108K4C	ec 3.1.3.12
J171_03388	ENOG4105BZP	glycoside hydrolase 15-related
J171_03389	ENOG4105C1K	alpha-alpha-trehalose-phosphate synthase
J171_03390	ENOG4105DZG	Dehydrogenase
J171_03391	ENOG4105C8Q	Methyl-accepting chemotaxis
J171_03392	ENOG4105KIR	Thiol-disulfide oxidoreductase dcc
J171_03395	ENOG4105C34	Pseudouridine synthase
J171_03396	ENOG4106SNF	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane
J171_03398	ENOG4105C4K	Nad synthetase
J171_03404	ENOG4105CVE	Lytic murein transglycosylase
J171_03409	ENOG4108X1T	PAAR repeat-containing protein
J171_03414	ENOG4105CH8	Succinyl-CoA ligase ADP-forming subunit alpha
J171_03415	ENOG4105CMV	Succinyl-CoA synthetase subunit beta
J171_03416	ENOG4107TUY	Histidine kinase
J171_03417	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
J171_03419	ENOG4107QHF	type ii secretion system protein e
J171_03420	ENOG4107QHF	type ii secretion system protein e
J171_03421	ENOG4107QHF	type ii secretion system protein e
J171_03425	ENOG4105EHH	Cleaves type-4 fimbrial leader sequence and methylates the N-terminal (generally Phe) residue (By similarity)
J171_03426	ENOG4108ZQD	Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A (By similarity)
J171_03431	ENOG4105BZU	Histidine kinase
J171_03432	ENOG4105ETX	regulatoR
J171_03434	ENOG4105D9I	Responsible for the addition of glutamate residues to the C-terminus of ribosomal protein S6 (By similarity)
J171_03448	ENOG4105W5Q	DNA repair protein (RadC
J171_03453	ENOG4105CQZ	Histidine kinase
J171_03454	ENOG4105CQZ	Histidine kinase
J171_03479	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)
J171_03480	ENOG4105CZ1	Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA (By similarity)
J171_03485	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)
J171_03487	ENOG4105ETE	Transcriptional regulator (LacI family
J171_03493	ENOG4105EIB	trna rrna methyltransferase
J171_03495	ENOG4105CD8	aminopeptidase N
J171_03504	ENOG4105BZS	acriflavin resistance protein
J171_03506	ENOG4105C3T	may be the GTPase, regulating ATP sulfurylase activity (By similarity)
J171_03507	ENOG4105C11	sulfate adenylyltransferase), subunit 2
J171_03508	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)
J171_03509	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)
J171_03510	ENOG4105ET3	Reduction of activated sulfate into sulfite (By similarity)
J171_03514	ENOG4105BZU	Histidine kinase
J171_03516	ENOG4107R11	Transcriptional regulator
J171_03517	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)
J171_03520	ENOG4108UVJ	appr-1-p processing domain protein
J171_03521	ENOG4107R1Y	fructose-bisphosphate aldolase
J171_03522	ENOG4105CA9	Pyruvate kinase
J171_03524	ENOG4105BZA	Phosphoglycerate kinase
J171_03529	ENOG4105C17	glyceraldehyde-3-phosphate dehydrogenase
J171_03531	ENOG4105EIF	outer membrane protein W
J171_03532	ENOG4105EIF	outer membrane protein W
J171_03534	ENOG4107S76	domain protein
J171_03535	ENOG4108S6J	ABC transporter, periplasmic molybdate-binding protein
J171_03536	ENOG4105E0C	molybdate abc transporter
J171_03537	ENOG4105CGB	Part of the ABC transporter complex ModABC involved in molybdenum import. Responsible for energy coupling to the transport system (By similarity)
J171_03544	ENOG4107Y2H	ErfK ybiS ycfS ynhG family protein
J171_03545	ENOG4105DR5	peptidase
J171_03547	ENOG4105CNM	Receptor
J171_03548	ENOG4107SKW	Inherit from COG: Alpha beta hydrolase
J171_03549	ENOG4105CV1	Transketolase (EC 2.2.1.1)
J171_03550	ENOG4105CK2	sodium dicarboxylate symporter
J171_03552	ENOG4107QVM	von Willebrand factor, type A
J171_03556	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
J171_03558	ENOG4105E4G	Type IV pilus
J171_03563	ENOG4108JQC	penicillin-binding protein 1A
J171_03567	ENOG4105NRA	50s ribosomal protein l31 type b
J171_03568	ENOG4105DU0	nucleoside hydrolase
J171_03569	ENOG4105CB5	ATP-dependent DNA helicase recG
J171_03570	ENOG4105KME	endoribonuclease L-psp
J171_03571	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)
J171_03572	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)
J171_03573	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
J171_03574	ENOG4105DSJ	YicC domain protein
J171_03575	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)
J171_03577	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)
J171_03578	ENOG4105CSA	Coproporphyrinogen iii oxidase
J171_03581	ENOG4105D9Y	Splits dipeptides with a prolyl residue in the C- terminal position (By similarity)
J171_03583	ENOG4107RAQ	aminopeptidase
J171_03586	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)
J171_03588	ENOG4105MK2	5-formyltetrahydrofolate cyclo-ligase
J171_03590	ENOG4105E66	phosphoriboisomerase A
J171_03592	ENOG41063JG	Transcriptional regulator
J171_03593	ENOG4105VCQ	rubredoxin
J171_03594	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)
J171_03597	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
J171_03598	ENOG41061ZR	Transcriptional regulator
J171_03600	ENOG4105CIH	Imidazole acetol-phosphate transaminase
J171_03606	ENOG4105C8Y	Acetylornithine aminotransferase
J171_03607	ENOG4105EYW	Ion transport protein
J171_03610	ENOG410841Q	phosphoesterase PA-phosphatase related protein
J171_03611	ENOG4105FFC	UPF0187 protein
J171_03613	ENOG4105DFU	Cell wall formation (By similarity)
J171_03614	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)
J171_03617	ENOG4105EAY	pump that utilizes the energy of pyrophosphate hydrolysis as the driving force for
J171_03619	ENOG4105F0N	pyrophosphate phospho-hydrolase
J171_03622	ENOG4105ECQ	AraC Family Transcriptional Regulator
J171_03623	ENOG4108M3R	transcriptional activator CadC
J171_03624	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)
J171_03627	ENOG4105C8Q	Methyl-accepting chemotaxis
J171_03628	ENOG4105CFB	Gamma-glutamyltranspeptidase (EC 2.3.2.2)
J171_03629	ENOG4105C6M	Alpha-keto-beta-hydroxylacyl reductoisomerase
J171_03632	ENOG4105C7B	Threonine dehydratase
J171_03633	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)
J171_03634	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)
J171_03635	ENOG4105MQS	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
J171_03636	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
J171_03637	ENOG4108MP6	LysR family Transcriptional regulator
J171_03640	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)
J171_03641	ENOG4105DFG	type I secretion outer membrane protein
J171_03642	ENOG4105D8A	3-Deoxy-D-manno-octulosonic-acid transferase
J171_03643	ENOG4105D1S	lipid A biosynthesis
J171_03648	ENOG4105C6K	Malic enzyme
J171_03649	ENOG4105CK2	sodium dicarboxylate symporter
J171_03651	ENOG4105CQZ	Histidine kinase
J171_03652	ENOG4105CSH	Transporter
J171_03654	ENOG4105F04	LysR family Transcriptional regulator
J171_03655	ENOG4105CPC	Aldo Keto reductase
J171_03659	ENOG4105WH1	Two component transcriptional regulator luxr family
J171_03660	ENOG4106JDA	Phosphoglycerate transport regulatory protein PGTC
J171_03661	ENOG4105DHQ	Histidine kinase
J171_03664	ENOG4105D4T	Citrate transporter
J171_03666	ENOG4105CHR	reductase
J171_03667	ENOG4105ETE	Transcriptional regulator (LacI family
J171_03670	ENOG4107QW3	Sucrose phosphorylase
J171_03673	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)
J171_03677	ENOG4105CNM	Receptor
J171_03687	ENOG4108RMV	DegV Family
J171_03688	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)
J171_03692	ENOG4105EJG	cellulose synthase
J171_03693	ENOG4105K2Z	endo-1,4-d-glucanase (EC 3.2.1.4)
J171_03694	ENOG4107EEX	Cellulose synthase regulator protein
J171_03695	ENOG4107QZ7	Cellulose synthase catalytic subunit
J171_03699	ENOG4107RH7	Nicotinate phosphoribosyltransferase
J171_03709	ENOG4106S9K	Transcriptional regulator
J171_03711	ENOG4105GVR	general secretion pathway protein D
J171_03713	ENOG410678M	general secretion pathway protein M
J171_03714	ENOG41090VX	general secretion pathway protein L
J171_03715	ENOG4105UV2	general secretion pathway protein K
J171_03716	ENOG41069G9	General secretion pathway protein J
J171_03718	ENOG4105WMT	general secretion pathway protein h
J171_03720	ENOG4105D7Q	type ii secretion system
J171_03721	ENOG4107QHF	type ii secretion system protein e
J171_03722	ENOG4105RX7	peptidase S8 and S53, subtilisin, kexin, sedolisin
J171_03723	ENOG4105EUR	Domain-Containing protein
J171_03724	ENOG4105RX7	peptidase S8 and S53, subtilisin, kexin, sedolisin
J171_03725	ENOG4105EUR	Domain-Containing protein
J171_03726	ENOG4108ETH	Formylglycinamide ribotide synthetase
J171_03727	ENOG4105T95	Thiol disulfide interChange protein
J171_03728	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)
J171_03731	ENOG4108K5H	permease YjgP YjgQ family protein
J171_03733	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)
J171_03736	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)
J171_03742	ENOG4106PT6	cdpdiacylglycerol-serine O-phosphatidyltransferase
J171_03744	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)
J171_03745	ENOG4105VFQ	Histone family protein nucleoid-structuring protein H-NS
J171_03748	ENOG4105DHJ	ABC, transporter
J171_03749	ENOG4108SNX	Mammalian cell entry related domain protein
J171_03752	ENOG4105DWH	electron transfer flavoprotein-ubiquinone oxidoreductase
J171_03756	ENOG4107QKV	phosphomannomutase
J171_03757	ENOG4105CJT	Mannose-1-phosphate guanylyltransferase
J171_03759	ENOG4105DBZ	Dtdp-4-dehydrorhamnose reductase
J171_03760	ENOG4108URP	Dtdp-4-dehydrorhamnose 3,5-epimerase
J171_03763	ENOG4105BZJ	Electron transfer flavoprotein
J171_03764	ENOG4105C10	Electron transfer flavoprotein
J171_03767	ENOG4105IQ5	FAD linked oxidase domain protein
J171_03770	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)
J171_03771	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
J171_03778	ENOG4105EY8	ABC transporter
J171_03780	ENOG4105C28	cystathionine
J171_03785	ENOG4105CZX	twitching motility protein
J171_03786	ENOG4108RXX	maleylacetoacetate isomerase
J171_03788	ENOG4105C1J	atp-dependent rna helicase
J171_03791	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)
J171_03792	ENOG4107ZIF	6-carboxy-5,6,7,8-tetrahydropterin synthase
J171_03794	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)
J171_03797	ENOG4105NIV	Esterase
J171_03798	ENOG4107RNH	Outer membrane receptor FepA
J171_03799	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)
J171_03800	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)
J171_03801	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)
J171_03804	ENOG4105DGW	oligopeptidase A
J171_03807	ENOG4105E3B	Multicopper oxidase
J171_03815	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
J171_03816	ENOG4105DJY	efflux transporter, rnd family, mfp subunit
J171_03817	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)
J171_03818	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)
J171_03819	ENOG4107RBB	ABC transporter, permease
J171_03821	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
J171_03822	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)
J171_03825	ENOG4105KNM	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
J171_03826	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)
J171_03827	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)
J171_03828	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
J171_03829	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)
J171_03830	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)
J171_03831	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)
J171_03832	ENOG4107RAZ	it plays a direct role in the translocation of protons across the membrane (By similarity)
J171_03836	ENOG4107QN2	dihydrolipoyl dehydrogenase
J171_03838	ENOG4107QSN	dihydrolipoamide acetyltransferase
J171_03844	ENOG4105D01	(LipO)protein
J171_03845	ENOG4108UMI	ABC transporter, permease
J171_03846	ENOG4108JEI	Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system (By similarity)
J171_03847	ENOG4108EHX	EamA-like transporter family
J171_03848	ENOG4108VPT	UPF0234 protein
J171_03850	ENOG4105BZU	Histidine kinase
J171_03853	ENOG4107EXU	Short-chain dehydrogenase reductase Sdr
J171_03854	ENOG4107YBY	Hydrolase
J171_03855	ENOG4105I08	Pseudouridine synthase
J171_03856	ENOG4105D8J	Specifically methylates the guanine in position 1207 of 16S rRNA in the 30S particle (By similarity)
J171_03860	ENOG4105BZU	Histidine kinase
J171_03864	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
J171_03865	ENOG4105MWK	D-amino acid dehydrogenase, small subunit
J171_03866	ENOG4105EW9	transcriptional regulator AsnC family
J171_03870	ENOG4107RD7	Flagellar Motor Protein, MotA
J171_03871	ENOG4105ER2	Ompa motb domain protein
J171_03876	ENOG4105E3A	(ABC) transporter
J171_03877	ENOG4105DA5	(ABC) transporter
J171_03878	ENOG4105EEQ	Na H antiporter
J171_03880	ENOG4108UN4	phage SPO1 DNA polymerase-related protein
J171_03882	ENOG4105C8E	extradiol ring-cleavage dioxygenase class IIi protein subunit b
J171_03884	ENOG4105CBN	LysR family transcriptional regulator
J171_03886	ENOG4105CPC	Aldo Keto reductase
J171_03888	ENOG4105C9K	Endothelin-converting enzyme 1
J171_03892	ENOG4107QTZ	amino acid
J171_03894	ENOG4108VAC	response regulator
J171_03895	ENOG4105C2F	Histidine kinase
J171_03898	ENOG4108Z9Z	response to DNA damage stimulus
J171_03899	ENOG4105WEF	catalase
J171_03902	ENOG4105BZU	Histidine kinase
J171_03905	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
J171_03907	ENOG4105C4M	(Ubiquinol oxidase) subunit I
J171_03908	ENOG4105CFY	cytochrome d ubiquinol oxidase, subunit ii
J171_03911	ENOG4105CYX	Short-chain dehydrogenase reductase Sdr
J171_03912	ENOG4105CMR	udp-glucose 4-epimerase
J171_03916	ENOG4105BZ1	(ABC) transporter
J171_03919	ENOG4105E2A	Dehydrogenase
J171_03931	ENOG4105CIG	ABC transporter
J171_03934	ENOG4108UQ8	endoribonuclease L-psp
J171_03940	ENOG4105C8Q	Methyl-accepting chemotaxis
J171_03944	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)
J171_03958	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
J171_03959	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)
J171_03960	ENOG4105D1S	lipid A biosynthesis
J171_03961	ENOG4108Z7F	N-acetyltransferase
J171_03969	ENOG4105CYJ	ribosomal RNA small subunit methyltransferase B
J171_03970	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)
J171_03971	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)
J171_03972	ENOG4108WZM	domain protein
J171_03973	ENOG4105C79	DNA protecting protein DprA
J171_03974	ENOG4108RPN	Protein smg homolog
J171_03977	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)
J171_03978	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)
J171_03981	ENOG4107ZQV	short-chain dehydrogenase reductase
J171_03983	ENOG4105D07	Signal peptide peptidase, SppA
J171_03984	ENOG4107QI1	Mate efflux family protein
J171_03988	ENOG4105C25	Primosomal protein n'
J171_03989	ENOG4108TGY	Glutathione S-transferase
J171_03993	ENOG4105EN6	Membrane
J171_03994	ENOG4105DEK	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
J171_03995	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)
J171_03996	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
J171_03997	ENOG4105CRP	Part of the ABC transporter FtsEX involved in
J171_03998	ENOG4105CAK	Cell division ATP-binding protein ftsE
J171_03999	ENOG4105C1J	atp-dependent rna helicase
J171_04000	ENOG4105K63	Thioredoxin
J171_04001	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)
J171_04002	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)
J171_04003	ENOG4105ETT	transcriptional Regulator, LysR family
J171_04005	ENOG4105E9K	Isocitrate dehydrogenase
J171_04008	ENOG4105FB9	CRISPR-associated protein
J171_04013	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)
J171_04014	ENOG4105KCF	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). Functions as a ssRNA-specific endoribonuclease (By similarity)
J171_04016	ENOG4109066	lysm domain bon superfamily protein
J171_04017	ENOG4107R1K	Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1) (By similarity)
J171_04018	ENOG4105CH2	amidohydrolase
J171_04019	ENOG4105ENT	Efflux transporter rnd family, mfp subunit
J171_04020	ENOG4105BZS	acriflavin resistance protein
J171_04022	ENOG4105E32	cytoplasmic protein
J171_04030	ENOG4108UQS	dipeptidase
J171_04031	ENOG4108VBV	N-Acetylmuramoyl-L-alanine amidase
J171_04033	ENOG4105DTQ	mandelate racemase muconate lactonizing
J171_04035	ENOG4105D5Q	Arginine ornithine antiporter
J171_04038	ENOG4108Z12	YiaAB two helix domain-containing protein
J171_04040	ENOG4107QK4	glycoside hydrolase, family 3 domain protein
J171_04041	ENOG4107ZVW	dihydroneopterin aldolase
J171_04042	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)
J171_04043	ENOG4105VCC	30S ribosomal protein S21
J171_04044	ENOG4105KTH	gatB Yqey
J171_04045	ENOG4107S2Z	UPF0761 membrane protein
J171_04046	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)
J171_04047	ENOG4105DHU	Bile acid
J171_04049	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)
J171_04054	ENOG4107QS1	Cytochrome C Oxidase, Subunit III
J171_04055	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)
J171_04058	ENOG4105CV4	Subunits I and II form the functional core of the enzyme complex. Electrons originating in cytochrome c are transferred via heme a and Cu(A) to the binuclear center formed by heme a3 and Cu(B) (By similarity)
J171_04060	ENOG4105C26	Dehydrogenase
J171_04068	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)
J171_04069	ENOG4105DR5	peptidase
J171_04070	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)
J171_04072	ENOG4105EYM	Major Facilitator superfamily
J171_04073	ENOG4105CGK	Exodeoxyribonuclease III
J171_04074	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)
J171_04076	ENOG4107QJE	Chromosome Partitioning Protein
J171_04077	ENOG4105FA0	parb-like partition protein
J171_04080	ENOG4105CKK	Glycosyl transferase, family 2
J171_04084	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)
J171_04085	ENOG4105CJS	Phosphopantothenoylcysteine decarboxylase
J171_04086	ENOG4105W5Q	DNA repair protein (RadC
J171_04087	ENOG4105C75	arginyL-tRNA synthetase
J171_04090	ENOG4105EMU	Dehydrogenase
J171_04091	ENOG4105EXC	Acyl-transferase
J171_04093	ENOG4105CEY	Amp-dependent synthetase and ligase
J171_04094	ENOG4105DP5	Catalyzes the biosynthesis of agmatine from arginine (By similarity)
J171_04095	ENOG4105CCX	Catalyzes the production of spermidine from putrescine and decarboxylated S-adenosylmethionine (dcSAM), which serves as an aminopropyl donor (By similarity)
J171_04100	ENOG4108YZA	Nitrogen regulatory protein pii
J171_04101	ENOG4105W0Z	cytoplasmic protein
J171_04102	ENOG4105C0P	Mg chelatase subunit ChlI
J171_04108	ENOG4105CMM	transposase
J171_04116	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)
J171_04125	ENOG4105C0P	Mg chelatase subunit ChlI
J171_04128	ENOG41066DG	(EAL) domain protein
J171_04131	ENOG4105EJ2	Transcriptional regulator
J171_04137	ENOG4105E0Y	RtcB Protein
J171_04145	ENOG4105ECP	epimerase
J171_04146	ENOG4105XJC	Two component transcriptional regulator (Winged helix family
J171_04147	ENOG4105DHQ	Histidine kinase
J171_04151	ENOG4105C0H	protease
J171_04155	ENOG4105DSF	transport protein
J171_04156	ENOG4107URF	beta-phospho-glucomutase
J171_04157	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)
J171_04160	ENOG4107VGR	Catalase
J171_04163	ENOG4108S01	response regulator
J171_04164	ENOG4108ZGX	Histidine kinase
J171_04165	ENOG4105ENT	Efflux transporter rnd family, mfp subunit
J171_04166	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)
J171_04170	ENOG4105FR1	rard protein
J171_04172	ENOG4105FDR	Membrane
J171_04175	ENOG4108NNI	Beta-lactamase domain-containing protein
J171_04176	ENOG4105C31	Tryptophanyl-tRNA synthetase
J171_04177	ENOG4105VDW	Csbd family
J171_04189	ENOG4105HJX	Biotin- acetyl-CoA-carboxylase ligase
J171_04194	ENOG4105EB3	Histidine kinase
J171_04195	ENOG4105XJC	Two component transcriptional regulator (Winged helix family
J171_04197	ENOG4105CEH	Catalyzes the synthesis of dihydrouridine a modified base found in the D-loop of most tRNAs (By similarity)
J171_04200	ENOG4105CH6	catalase
J171_04201	ENOG4105DVT	helicase
J171_04204	ENOG4105E2X	shikimate dehydrogenase
J171_04206	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)
J171_04210	ENOG4105D52	delta-aminolevulinic acid dehydratase
J171_04215	ENOG4105CYM	Glutathione S-transferase
J171_04219	ENOG4105QV4	Tryptophan halogenase
J171_04222	ENOG4108IUW	ABC transporter
J171_04224	ENOG4105VZ8	Transcriptional regulator
J171_04228	ENOG4105PGM	cation diffusion facilitator family transporter
J171_04230	ENOG4105E0K	tonB-dependent siderophore receptor
J171_04232	ENOG4105ECQ	AraC Family Transcriptional Regulator
J171_04233	ENOG4108JA0	Oxidoreductase, FAD NAD(P)-binding domain protein
J171_04234	ENOG4105DA5	(ABC) transporter
J171_04235	ENOG4105E3A	(ABC) transporter
J171_04238	ENOG41063V1	Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid (By similarity)
J171_04244	ENOG4105E05	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
J171_04245	ENOG4107QYD	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
J171_04247	ENOG4105CD5	CoA-binding domain protein
J171_04248	ENOG4105CJW	magnesium transporter
J171_04249	ENOG4108UHE	carbonic anhydrase
J171_04251	ENOG4105D8W	glucose-6-phosphate 1-dehydrogenase
J171_04252	ENOG4105BZP	glycoside hydrolase 15-related
J171_04256	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
J171_04258	ENOG4106N3V	dolichyl-phosphate beta-D-mannosyltransferase (EC 2.4.1.83)
J171_04269	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)
J171_04270	ENOG4105E9Q	Acyl-transferase
J171_04272	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
J171_04277	ENOG4105DRY	peptidase s9 prolyl oligopeptidase active site domain protein
J171_04280	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)
J171_04281	ENOG4105C2M	dna polymerase I
J171_04287	ENOG4105D9P	serine threonine protein kinase
J171_04288	ENOG4108ZF3	Phosphatase
J171_04295	ENOG4105CS6	Rhs element vgr protein
J171_04303	ENOG4105D6F	Phosphatase
J171_04310	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
J171_04315	ENOG4108WC9	type VI secretion system effector, hcp1 family
J171_04321	ENOG4105C4R	Atp-dependent dna helicase
J171_04323	ENOG4105CQX	Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol (By similarity)
J171_04324	ENOG4108KB2	LysR family Transcriptional regulator
J171_04325	ENOG4105JSC	dimethylmenaquinone methyltransferase
J171_04327	ENOG4105KHM	amidohydrolase 2
J171_04328	ENOG4105W0E	50S ribosomal protein L33
J171_04329	ENOG4105KDC	50s ribosomal protein l28
J171_04331	ENOG4105ENT	Efflux transporter rnd family, mfp subunit
J171_04335	ENOG4105D28	Specifically methylates the N7 position of a guanine in 16S rRNA (By similarity)
J171_04336	ENOG4105DGI	Alkaline phosphatase
J171_04342	ENOG4105CGK	Exodeoxyribonuclease III
J171_04344	ENOG4105E2R	ROK family
J171_04346	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)
J171_04348	ENOG4107QN1	sodium solute
J171_04349	ENOG41062QD	Membrane
J171_04351	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)
J171_04357	ENOG4105DSG	hydrolase family 43
J171_04360	ENOG4105I7Z	Short-chain dehydrogenase reductase Sdr
J171_04361	ENOG4105ERH	Fumarylacetoacetate hydrolase
J171_04362	ENOG4105DIA	mandelate racemase muconate lactonizing
J171_04364	ENOG4105QJH	Domain of unknown function (DUF718)
J171_04365	ENOG4105EDR	glucose galactose transporter
J171_04366	ENOG4108K2P	TRANSCRIPTIONal
J171_04367	ENOG4108UI1	Probably functions as a manganese efflux pump (By similarity)
J171_04368	ENOG4105BZU	Histidine kinase
J171_04370	ENOG4105E2V	Glycosyltransferase 36
J171_04371	ENOG4105CT4	transporter
J171_04372	ENOG4108Z67	carbohydrate kinase, thermoresistant glucokinase family
J171_04377	ENOG4105MA0	exported protein
J171_04378	ENOG4105CFU	surface antigen
J171_04383	ENOG4108JJA	ABC, transporter
J171_04386	ENOG4108HMW	glycyl-tRNA synthetase, alpha subunit
J171_04387	ENOG4107QHF	type ii secretion system protein e
J171_04389	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
J171_04391	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)
J171_04392	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)
J171_04395	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
J171_04398	ENOG4105DH7	May be involved in recombination (By similarity)
J171_04399	ENOG4105CB3	Required for the thiolation of cytidine in position 32 of tRNA, to form 2-thiocytidine (s(2)C32) (By similarity)
J171_04400	ENOG4105C93	Xylose Isomerase
J171_04401	ENOG4105ETE	Transcriptional regulator (LacI family
J171_04402	ENOG4105D0H	Alpha-glucuronidase (EC 3.2.1.139)
J171_04404	ENOG4105CXK	mandelate racemase muconate lactonizing
J171_04407	ENOG4105DEI	Mannitol dehydrogenase
J171_04415	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
J171_04416	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
J171_04422	ENOG4105D9F	endo-1,4-beta-xylanase (EC 3.2.1.8)
J171_04423	ENOG4105CNT	hydrolase family 2
J171_04424	ENOG4105D2H	Uronic isomerase
J171_04430	ENOG4105CT4	transporter
J171_04431	ENOG4105DT9	hydrolase family 43
J171_04442	ENOG4105E55	glycerol-3-phosphate acyltransferase
J171_04444	ENOG4105ETE	Transcriptional regulator (LacI family
J171_04447	ENOG4105QV4	Tryptophan halogenase
J171_04448	ENOG4106EG9	Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) (By similarity)
J171_04449	ENOG4105CUR	5'-nucleotidase, lipoprotein e(p4) family
J171_04451	ENOG4108YXG	UPF0502 protein
J171_04454	ENOG4105C4R	Atp-dependent dna helicase
J171_04455	ENOG4107104	thymidine kinase
J171_04456	ENOG4105BZU	Histidine kinase
J171_04457	ENOG4105DJ9	glucan biosynthesis protein
J171_04459	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)
J171_04466	ENOG4105DKK	Benzoate
J171_04470	ENOG4105DSB	aldose 1-epimerase
J171_04472	ENOG4105K5B	UPF0225 protein
J171_04473	ENOG4105EJ9	Membrane
J171_04477	ENOG4105EUJ	GTP cyclohydrolase i
J171_04479	ENOG4105ZQC	membrane protein AaeX
J171_04480	ENOG4105Y49	secretion protein, HlyD family
J171_04482	ENOG4105DR8	Membrane
J171_04483	ENOG4105CSH	Transporter
J171_04485	ENOG4105CQX	Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol (By similarity)
J171_04501	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
J171_04512	ENOG4107QKA	exodeoxyribonuclease V beta
J171_04513	ENOG4105DSY	exodeoxyribonuclease V, gamma
J171_04515	ENOG4105DHJ	ABC, transporter
J171_04516	ENOG4105CY3	ABC transporter, permease
J171_04517	ENOG4107PE3	Mammalian cell entry related domain protein
J171_04520	ENOG410903C	(LipO)protein
J171_04522	ENOG4108V06	Glutathione peroxidase
J171_04524	ENOG4107QSV	RmuC domain protein
J171_04525	ENOG4105CIS	alcohol dehydrogenase
J171_04526	ENOG4105EJC	lysr family transcriptional regulator
J171_04528	ENOG4108TGY	Glutathione S-transferase
J171_04530	ENOG4105CUB	amino acid
J171_04531	ENOG4105CWX	Alpha-1,2-mannosidase
J171_04532	ENOG4105NRM	Membrane
J171_04533	ENOG4105BZU	Histidine kinase
J171_04534	ENOG4108IXP	Carbohydrate diacid transcriptional activator CdaR
J171_04535	ENOG4105BZW	Glycerate kinase
J171_04536	ENOG4105CSP	Major Facilitator Superfamily
J171_04539	ENOG4105DR4	Methyltransferase
J171_04541	ENOG4105DU1	integral membrane protein, terc
J171_04543	ENOG4106MZZ	glycerophosphoryl diester phosphodiesterase
J171_04546	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)
J171_04547	ENOG4108ZJ4	polysaccharide deacetylase
J171_04548	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
J171_04549	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)