locus-tag	class	description
FE785_00005	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)
FE785_00010	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)
FE785_00015	ENOG41076HS	cation diffusion facilitator family transporter
FE785_00020	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)
FE785_00030	ENOG4105JAB	phenazine biosynthesis protein, phzf family
FE785_00035	ENOG4105VN1	Heat shock protein
FE785_00040	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)
FE785_00055	ENOG4105VEJ	Heat shock protein
FE785_00060	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)
FE785_00085	ENOG4105BZU	Histidine kinase
FE785_00105	ENOG4105ERG	peptidase m48, ste24p
FE785_00110	ENOG4105FE9	pseudouridine synthase
FE785_00115	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)
FE785_00120	ENOG4105CUV	Homoserine Kinase
FE785_00125	ENOG4105C2M	dna polymerase I
FE785_00130	ENOG4105BZU	Histidine kinase
FE785_00145	ENOG4105CF7	AraC family transcriptional regulator
FE785_00150	ENOG4105WHM	Necessary for normal cell division and for the maintenance of normal septation (By similarity)
FE785_00155	ENOG4105EBH	Required during biogenesis of c-type cytochromes (cytochrome c6 and cytochrome f) at the step of heme attachment (By similarity)
FE785_00160	ENOG4105CRE	cytochrome C
FE785_00165	ENOG4108Z33	Thiol disulfide Interchange Protein
FE785_00170	ENOG4105C7K	acetolactate synthase
FE785_00180	ENOG4105C9U	ATP-dependent DNA helicase RecQ
FE785_00185	ENOG4107Y03	Nitroreductase
FE785_00190	ENOG4105C5Q	Transcriptional regulator
FE785_00195	ENOG410903C	(LipO)protein
FE785_00200	ENOG4105D65	subunit l
FE785_00205	ENOG4108ZE9	Monovalent cation H antiporter subunit C
FE785_00210	ENOG4107R4Z	monovalent cation h antiporter subunit d
FE785_00215	ENOG4105SC1	monovalent cation H antiporter subunit E
FE785_00220	ENOG4105W4C	monovalent cation H antiporter subunit F
FE785_00225	ENOG4105KJM	monovalent cation h antiporter subunit g
FE785_00230	ENOG41066VF	YeeE YedE family protein
FE785_00235	ENOG4108VYJ	response regulator receiver protein
FE785_00245	ENOG4108YXU	transcriptional regulator AsnC family
FE785_00250	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)
FE785_00265	ENOG4108YXI	Secondary thiamine-phosphate synthase enzyme
FE785_00270	ENOG4105DGW	oligopeptidase A
FE785_00305	ENOG4105CEY	Amp-dependent synthetase and ligase
FE785_00335	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
FE785_00340	ENOG4105CHG	glycolate oxidase (iron-sulfur subunit)
FE785_00345	ENOG4105EU8	FAD linked oxidase domain protein
FE785_00350	ENOG4105CQB	FAD linked oxidase domain protein
FE785_00355	ENOG4105C5R	Aminotransferase
FE785_00360	ENOG4107XTP	(EAL) domain protein
FE785_00365	ENOG4105CQ7	ATP-dependent helicase
FE785_00375	ENOG4105PFA	Catalyzes the conversion of 5-hydroxyuridine (ho5U) to 5-methoxyuridine (mo5U) at position 34 in tRNA (By similarity)
FE785_00380	ENOG4105DA6	Catalyzes the conversion of 5-methoxyuridine (mo5U) to uridine-5-oxyacetic acid (cmo5U) at position 34 in tRNA. May also participate in the methylation of uridine-5-oxyacetic acid (cmo5U) to uridine-5-oxyacetic acid methyl ester (mcmo5U) (By similarity)
FE785_00385	ENOG4105BZU	Histidine kinase
FE785_00390	ENOG4106S48	Murein-degrading enzyme. May play a role in recycling of muropeptides during cell elongation and or cell division
FE785_00405	ENOG4105BZS	acriflavin resistance protein
FE785_00415	ENOG4108YYH	Nadph-dependent fmn reductase
FE785_00420	ENOG4105BZU	Histidine kinase
FE785_00430	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
FE785_00465	ENOG4105K63	Thioredoxin
FE785_00485	ENOG4107WDG	serine threonine protein kinase
FE785_00495	ENOG4109003	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis (By similarity)
FE785_00500	ENOG4105BZU	Histidine kinase
FE785_00505	ENOG4105CH7	arginosuccinase
FE785_00515	ENOG4105D6W	Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps (By similarity)
FE785_00545	ENOG4105CGK	Exodeoxyribonuclease III
FE785_00550	ENOG4105CIY	formyltetrahydrofolate deformylase
FE785_00555	ENOG4105E0I	Catalyzes the formation of N(4)-acetylcytidine (ac(4)C) at the wobble position of tRNA(Met), by using acetyl-CoA as an acetyl donor and ATP (or GTP) (By similarity)
FE785_00560	ENOG4105E0X	reductase
FE785_00565	ENOG4105CWG	Catalyzes the last two steps in the biosynthesis of 5- methylaminomethyl-2-thiouridine (mnm(5)s(2)U) at the wobble position (U34) in tRNA. Catalyzes the FAD-dependent demodification of cmnm(5)s(2)U34 to nm(5)s(2)U34, followed by the transfer of a methyl group from S-adenosyl-L-methionine to nm(5)s(2)U34, to form mnm(5)s(2)U34 (By similarity)
FE785_00580	ENOG4105CEV	competence damage-inducible protein
FE785_00585	ENOG4105CBX	hi0933 family
FE785_00590	ENOG4105KQ5	peptidylprolyl cis-trans isomerase
FE785_00595	ENOG4105DZ2	Transcriptional regulator
FE785_00600	ENOG4105DSS	Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation (By similarity)
FE785_00625	ENOG4105EHV	domain protein
FE785_00675	ENOG4108Z0R	Transferase
FE785_00680	ENOG4105C1X	Bifunctional enzyme with both catalase and broad- spectrum peroxidase activity (By similarity)
FE785_00685	ENOG4105E2X	shikimate dehydrogenase
FE785_00690	ENOG4105D52	delta-aminolevulinic acid dehydratase
FE785_00705	ENOG4105CM1	Catalyzes, together with MoaC, the conversion of 5'-GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
FE785_00710	ENOG4105M00	molybdopterin converting factor, subunit 1
FE785_00715	ENOG4108ZAF	Molybdopterin
FE785_00720	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
FE785_00725	ENOG4108YXW	Together with MoaA, is involved in the conversion of 5'- GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
FE785_00730	ENOG4105BZU	Histidine kinase
FE785_00735	ENOG41082IR	Excinuclease ABC C subunit domain protein
FE785_00745	ENOG4105BZU	Histidine kinase
FE785_00750	ENOG4105CG6	trap dicarboxylate transporter dctm subunit
FE785_00765	ENOG4105C25	Primosomal protein n'
FE785_00770	ENOG4106T9E	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)
FE785_00775	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)
FE785_00785	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)
FE785_00790	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)
FE785_00795	ENOG4105MJ2	Competence protein
FE785_00800	ENOG4105BZU	Histidine kinase
FE785_00820	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)
FE785_00825	ENOG4105WKS	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. TatA could form the protein-conducting channel of the Tat system (By similarity)
FE785_00830	ENOG4107YU2	histidine triad (hIT) protein
FE785_00835	ENOG4105KPZ	phosphoribosyl-atp pyrophosphatase
FE785_00840	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)
FE785_00845	ENOG4105CJV	Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase
FE785_00850	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)
FE785_00855	ENOG4105ECC	imidazole-glycerol-phosphate dehydratase
FE785_00860	ENOG4105EUH	cytochrome C oxidase, cbb3-type, subunit i
FE785_00875	ENOG4105D6P	C-type cytochrome. Part of the cbb3-type cytochrome c oxidase complex (By similarity)
FE785_00880	ENOG4105C58	cytochrome c oxidase accessory protein ccog
FE785_00915	ENOG4105BZU	Histidine kinase
FE785_00920	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)
FE785_00940	ENOG4105CUC	YeeE YedE family protein
FE785_00950	ENOG4105FDT	acyl-CoA dehydrogenase
FE785_00980	ENOG4105C8Q	Methyl-accepting chemotaxis
FE785_00985	ENOG4107R9T	Catalyzes the formation of 5-methyl-uridine at position 54 (m5U54) in all tRNAs (By similarity)
FE785_00995	ENOG4105BZU	Histidine kinase
FE785_01005	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
FE785_01010	ENOG4105CB3	Required for the thiolation of cytidine in position 32 of tRNA, to form 2-thiocytidine (s(2)C32) (By similarity)
FE785_01035	ENOG4105D37	Low-affinity potassium transport system. Interacts with Trk system potassium uptake protein TrkA (By similarity)
FE785_01040	ENOG4105C1A	potassium transporter peripheral membrane
FE785_01045	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
FE785_01050	ENOG4105ES5	Histidine kinase
FE785_01060	ENOG4105CYJ	ribosomal RNA small subunit methyltransferase B
FE785_01065	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)
FE785_01070	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)
FE785_01075	ENOG4105C79	DNA protecting protein DprA
FE785_01090	ENOG4105C75	arginyL-tRNA synthetase
FE785_01100	ENOG4105BZU	Histidine kinase
FE785_01105	ENOG4105W0Z	cytoplasmic protein
FE785_01110	ENOG4105C0P	Mg chelatase subunit ChlI
FE785_01125	ENOG4105WH1	Two component transcriptional regulator luxr family
FE785_01130	ENOG4105C42	Type I secretion membrane fusion protein (HlyD
FE785_01140	ENOG4107XKF	NMT1 THI5 Like Domain Protein
FE785_01145	ENOG4105BZU	Histidine kinase
FE785_01155	ENOG4105CDV	Ompa motb domain protein
FE785_01160	ENOG4105C0A	alcohol dehydrogenase
FE785_01165	ENOG4105C4R	Atp-dependent dna helicase
FE785_01170	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
FE785_01175	ENOG4107Y49	methyltransferase
FE785_01180	ENOG4108W2P	Methyl-accepting chemotaxis
FE785_01195	ENOG4106NZV	Responsible for synthesis of pseudouridine from uracil- 13 in transfer RNAs (By similarity)
FE785_01200	ENOG4105BZU	Histidine kinase
FE785_01205	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
FE785_01215	ENOG4105BZW	Glycerate kinase
FE785_01230	ENOG4105CK4	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
FE785_01235	ENOG4105VNG	YcgL domain-containing protein
FE785_01245	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
FE785_01250	ENOG410624X	efflux transporter, rnd family, mfp subunit
FE785_01260	ENOG4105CV1	Transketolase (EC 2.2.1.1)
FE785_01265	ENOG4105C17	glyceraldehyde-3-phosphate dehydrogenase
FE785_01270	ENOG4105BZA	Phosphoglycerate kinase
FE785_01275	ENOG4105CA9	Pyruvate kinase
FE785_01280	ENOG4105D2N	Aldolase
FE785_01285	ENOG4105C8Q	Methyl-accepting chemotaxis
FE785_01320	ENOG4105KNY	Microcompartments protein
FE785_01325	ENOG4105KNY	Microcompartments protein
FE785_01330	ENOG4105KNY	Microcompartments protein
FE785_01345	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)
FE785_01360	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)
FE785_01365	ENOG4105C8V	SAICAR synthetase
FE785_01375	ENOG4105DJV	ribulose-phosphate 3-epimerase
FE785_01380	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)
FE785_01385	ENOG4105CRQ	synthase (Component I)
FE785_01390	ENOG4105DDQ	anthranilate synthase
FE785_01395	ENOG4107QYG	anthranilate phosphoribosyltransferase
FE785_01400	ENOG4105DK0	Indole-3-glycerol phosphate synthase
FE785_01405	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
FE785_01425	ENOG4105X3E	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)
FE785_01430	ENOG4105CCX	Catalyzes the production of spermidine from putrescine and decarboxylated S-adenosylmethionine (dcSAM), which serves as an aminopropyl donor (By similarity)
FE785_01440	ENOG4108UKZ	OsmC family
FE785_01465	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)
FE785_01470	ENOG4105DR9	pseudouridine synthase
FE785_01490	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
FE785_01500	ENOG4105PM1	preprotein translocase subunit SecE
FE785_01505	ENOG4105E5V	Participates in transcription elongation, termination and antitermination (By similarity)
FE785_01510	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
FE785_01515	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)
FE785_01520	ENOG4108VZM	50s ribosomal protein L10
FE785_01525	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)
FE785_01530	ENOG4107QIH	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
FE785_01535	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
FE785_01540	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)
FE785_01545	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)
FE785_01550	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)
FE785_01555	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
FE785_01560	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
FE785_01565	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)
FE785_01570	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)
FE785_01575	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)
FE785_01580	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
FE785_01585	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
FE785_01590	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)
FE785_01595	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
FE785_01600	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
FE785_01605	ENOG41083MP	50s ribosomal protein l29
FE785_01610	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
FE785_01615	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
FE785_01620	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
FE785_01625	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
FE785_01630	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)
FE785_01635	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)
FE785_01640	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)
FE785_01645	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)
FE785_01650	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)
FE785_01655	ENOG4105VPB	50S ribosomal protein L30
FE785_01660	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
FE785_01665	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)
FE785_01670	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
FE785_01675	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)
FE785_01680	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)
FE785_01685	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
FE785_01690	ENOG4108ZT0	50S ribosomal protein l17
FE785_01695	ENOG4105F8V	Hydrolase, tatD family
FE785_01700	ENOG4105CUZ	uba thif-type nad fad binding protein
FE785_01715	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)
FE785_01725	ENOG4107RDB	Major Facilitator
FE785_01730	ENOG4108UUM	single-stranded DNA-binding protein
FE785_01735	ENOG4105BZU	Histidine kinase
FE785_01740	ENOG4108TWJ	NADH dehydrogenase subunit 5
FE785_01745	ENOG4105EVH	UPF0753 protein
FE785_01755	ENOG4105CZK	Aspartate kinase
FE785_01760	ENOG4108Z6K	Catalyzes the circularization of gamma-N-acetyl- alpha,gamma-diaminobutyric acid (ADABA) to ectoine (1,4,5,6- tetrahydro-2-methyl-4-pyrimidine carboxylic acid), which is an excellent osmoprotectant (By similarity)
FE785_01765	ENOG4108JPW	Aminotransferase
FE785_01785	ENOG4105EAH	synthase
FE785_01790	ENOG4105KK9	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
FE785_01795	ENOG4105K46	50S ribosomal protein l27
FE785_01800	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
FE785_01805	ENOG4105CGT	Catalyzes the transfer of a phosphate group to glutamate to form glutamate 5-phosphate which rapidly cyclizes to 5- oxoproline (By similarity)
FE785_01810	ENOG4105C8Q	Methyl-accepting chemotaxis
FE785_01815	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
FE785_01820	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
FE785_01830	ENOG4105BZU	Histidine kinase
FE785_01845	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)
FE785_01865	ENOG4108WT6	Carbon dioxide concentrating mechanism protein
FE785_01870	ENOG4108WT6	Carbon dioxide concentrating mechanism protein
FE785_01885	ENOG4105C0N	N-acetylglutamate semialdehyde dehydrogenase
FE785_01890	ENOG4108YX9	iron--sulfur cluster insertion protein erpA
FE785_01895	ENOG4105BZN	citrate synthase
FE785_01900	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)
FE785_01905	ENOG4105DR5	peptidase
FE785_01910	ENOG4105VFE	sira family
FE785_01915	ENOG4107QIB	glycyl-tRNA synthetase, alpha subunit
FE785_01920	ENOG4105C38	Glycyl-tRNA synthetase beta subunit
FE785_01925	ENOG4108ZI0	d,d-heptose 1,7-bisphosphate phosphatase
FE785_01935	ENOG4105E14	MotA TolQ exbB proton channel
FE785_01945	ENOG4106VK6	Flagellar motor protein
FE785_01950	ENOG4105C8Q	Methyl-accepting chemotaxis
FE785_01955	ENOG4108ZX6	Electron transport protein SCO1 SenC
FE785_01960	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)
FE785_01965	ENOG4108S7T	Catalyzes the oxidation of either pyridoxine 5'- phosphate (PNP) or pyridoxamine 5'-phosphate (PMP) into pyridoxal 5'-phosphate (PLP) (By similarity)
FE785_01970	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)
FE785_01980	ENOG4105C8Q	Methyl-accepting chemotaxis
FE785_01985	ENOG4107RHT	methyl-accepting chemotaxis sensory transducer with Pas Pac sensor
FE785_02000	ENOG4105CNG	UPF0061 protein
FE785_02010	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)
FE785_02015	ENOG4107RD7	Flagellar Motor Protein, MotA
FE785_02020	ENOG4105ER2	Ompa motb domain protein
FE785_02025	ENOG4105D06	uba thif-type nad fad binding protein
FE785_02030	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)
FE785_02035	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
FE785_02040	ENOG4105C7E	Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) (By similarity)
FE785_02055	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
FE785_02060	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)
FE785_02065	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
FE785_02070	ENOG4105C3G	gtp-binding protein
FE785_02080	ENOG4105DFP	Integrase
FE785_02105	ENOG4105BZU	Histidine kinase
FE785_02110	ENOG4105BZU	Histidine kinase
FE785_02115	ENOG4105BZU	Histidine kinase
FE785_02145	ENOG4105CNK	Required, probably indirectly, for the hydroxylation of 2-octaprenylphenol to 2-octaprenyl-6-hydroxy-phenol, the fourth step in ubiquinone biosynthesis (By similarity)
FE785_02155	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)
FE785_02165	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)
FE785_02170	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)
FE785_02190	ENOG4108R5P	Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery (By similarity)
FE785_02200	ENOG4105D8A	3-Deoxy-D-manno-octulosonic-acid transferase
FE785_02205	ENOG4105C2X	Arabinose 5-phosphate isomerase
FE785_02215	ENOG4105DW0	Catalyzes the ADP transfer to D-glycero-D-manno-heptose 1-phosphate, yielding ADP-D,D-heptose (By similarity)
FE785_02220	ENOG4105F55	Catalyzes the isomerization of sedoheptulose 7-phosphate in D-glycero-D-manno-heptose 7-phosphate (By similarity)
FE785_02225	ENOG4105CHC	glucokinase (EC 2.7.1.2)
FE785_02230	ENOG4107QQ4	Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans (By similarity)
FE785_02240	ENOG4107SBB	4-alpha-glucanotransferase (EC 2.4.1.25)
FE785_02245	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)
FE785_02250	ENOG4105CXW	Synthesizes alpha-1,4-glucan chains using ADP-glucose (By similarity)
FE785_02260	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
FE785_02265	ENOG4105EAG	UDP-N-acetylglucosamine 2-epimerase
FE785_02300	ENOG4105CPK	Glycosyl transferase (Group 1
FE785_02310	ENOG4107V1M	polysaccharide export protein
FE785_02335	ENOG4105E3R	(LipO)protein
FE785_02340	ENOG4105CMR	udp-glucose 4-epimerase
FE785_02350	ENOG4108URP	Dtdp-4-dehydrorhamnose 3,5-epimerase
FE785_02360	ENOG4105C1B	dTDP-glucose 4-6-dehydratase
FE785_02365	ENOG4108I19	Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis (By similarity)
FE785_02395	ENOG4105EGZ	biosynthesis protein
FE785_02400	ENOG4105K64	Glycosyl transferase, family 2
FE785_02410	ENOG4105CGN	Glycosyl transferase (Group 1
FE785_02415	ENOG4105D3Q	Sugar transferase
FE785_02425	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
FE785_02450	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)
FE785_02465	ENOG4105KXI	murein peptide amidase A
FE785_02470	ENOG4105CZX	twitching motility protein
FE785_02475	ENOG4105CZX	twitching motility protein
FE785_02485	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)
FE785_02490	ENOG4108M8S	permease YjgP YjgQ family protein
FE785_02495	ENOG4108K5H	permease YjgP YjgQ family protein
FE785_02505	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
FE785_02515	ENOG4105C3Y	UTP-glucose-1-phosphate uridylyltransferase
FE785_02535	ENOG4108KU3	Integrase
FE785_02545	ENOG4105BZU	Histidine kinase
FE785_02555	ENOG4105IH7	synthase
FE785_02575	ENOG4105BZU	Histidine kinase
FE785_02580	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)
FE785_02585	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)
FE785_02590	ENOG4105VIE	preprotein translocase, subunit YajC
FE785_02595	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)
FE785_02600	ENOG4107RAB	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)
FE785_02605	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)
FE785_02625	ENOG4105CDV	Ompa motb domain protein
FE785_02630	ENOG4105CJW	magnesium transporter
FE785_02635	ENOG41080QH	sigma 54 modulation protein ribosomal protein S30EA
FE785_02640	ENOG4108IUZ	ABC transporter
FE785_02655	ENOG4108Z4R	3-deoxy-d-manno-octulosonate 8-phosphate phosphatase
FE785_02670	ENOG4105DHJ	ABC, transporter
FE785_02675	ENOG4105CY3	ABC transporter, permease
FE785_02680	ENOG4107PE3	Mammalian cell entry related domain protein
FE785_02695	ENOG4105DA5	(ABC) transporter
FE785_02700	ENOG4105E3A	(ABC) transporter
FE785_02710	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
FE785_02715	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)
FE785_02720	ENOG4105CEK	Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine (By similarity)
FE785_02725	ENOG4107QNR	UPF0135 protein
FE785_02730	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)
FE785_02735	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)
FE785_02740	ENOG4105EIX	cytochrome c1
FE785_02745	ENOG4105CBC	glutamate synthase
FE785_02750	ENOG4105DNJ	May play a role in the repair of endogenous alkylation damage (By similarity)
FE785_02755	ENOG4105ISI	outer membrane protein, OMPP1 FadL TodX family
FE785_02765	ENOG4105BZU	Histidine kinase
FE785_02770	ENOG4105ECY	inositol monophosphatase
FE785_02775	ENOG4108JU6	CBS domain protein
FE785_02785	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
FE785_02790	ENOG4105K5M	30s ribosomal protein S16
FE785_02795	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)
FE785_02800	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
FE785_02805	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)
FE785_02810	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)
FE785_02815	ENOG4105T95	Thiol disulfide interChange protein
FE785_02820	ENOG4106MWK	domain protein
FE785_02825	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)
FE785_02830	ENOG4105I03	Flagellin
FE785_02850	ENOG4108YZA	Nitrogen regulatory protein pii
FE785_02860	ENOG4105CE6	Adenylation and deadenylation of glutamate--ammonia ligase (By similarity)
FE785_02865	ENOG4105C5F	glutamine synthetase
FE785_02870	ENOG4105C8U	phosphate abc transporter
FE785_02875	ENOG4105E2Z	phosphate ABC transporter (Permease
FE785_02880	ENOG4105BZY	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
FE785_02885	ENOG4108UTW	Plays a role in the regulation of phosphate uptake
FE785_02890	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FE785_02895	ENOG4105BZU	Histidine kinase
FE785_02905	ENOG410811Q	Ferredoxin
FE785_02925	ENOG4105M85	Bola protein
FE785_02935	ENOG4105DDT	Hydrolyzes diadenosine 5',5'''-P1,P4-tetraphosphate to yield ADP (By similarity)
FE785_02940	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)
FE785_02945	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)
FE785_02950	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)
FE785_02955	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)
FE785_02960	ENOG4105EHM	Aminoglycoside phosphotransferase
FE785_02965	ENOG4108S0S	Nucleotidyl transferase
FE785_02970	ENOG4105FE9	pseudouridine synthase
FE785_02975	ENOG4105VEQ	Cold shock protein
FE785_02980	ENOG4105C09	Bile acid
FE785_02985	ENOG4105BZU	Histidine kinase
FE785_02990	ENOG4105CQZ	Histidine kinase
FE785_02995	ENOG4105D1Q	UPF0246 protein
FE785_03025	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)
FE785_03030	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)
FE785_03035	ENOG4108Z43	UPF0250 protein
FE785_03040	ENOG4105F0I	Aminotransferase
FE785_03045	ENOG4105DZ1	carboxypeptidase
FE785_03050	ENOG4105CNI	cell division protein FtsW
FE785_03055	ENOG4105CJN	penicillin-binding protein
FE785_03065	ENOG4105N3I	Involved in formation and maintenance of cell shape (By similarity)
FE785_03070	ENOG4105DFF	Rod shape-determining protein mreb
FE785_03075	ENOG41080G2	Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) (By similarity)
FE785_03080	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)
FE785_03085	ENOG4105CHT	Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) (By similarity)
FE785_03090	ENOG4105D0M	Protease HtpX homolog
FE785_03110	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)
FE785_03120	ENOG4105M15	transport protein ExbD
FE785_03125	ENOG4105M8K	biopolymer transport protein
FE785_03135	ENOG4105EUZ	Beta-lactamase domain protein
FE785_03140	ENOG4105EAC	phosphoserine phosphatase
FE785_03160	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)
FE785_03165	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
FE785_03170	ENOG4108Z6B	deaminase
FE785_03175	ENOG4108Z4W	Probably deamidates glutamine residues to glutamate on methyl-accepting chemotaxis receptors (MCPs), playing an important role in chemotaxis (By similarity)
FE785_03180	ENOG4105CBS	Chea signal transduction histidine kinase
FE785_03190	ENOG4105CJX	Molecular chaperone. Has ATPase activity (By similarity)
FE785_03195	ENOG4105C5H	ABC transporter
FE785_03215	ENOG4105C17	glyceraldehyde-3-phosphate dehydrogenase
FE785_03220	ENOG4108V1T	peptidylprolyl cis-trans isomerase
FE785_03235	ENOG4107QR8	Thioredoxin
FE785_03240	ENOG4105D86	that it carries out the mismatch recognition step. This protein has a weak ATPase activity (By similarity)
FE785_03245	ENOG4105BZU	Histidine kinase
FE785_03250	ENOG4107TH8	cina domain protein
FE785_03255	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)
FE785_03260	ENOG4105Y3E	Modulates RecA activity (By similarity)
FE785_03265	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)
FE785_03270	ENOG4105CFH	Aspartokinase
FE785_03290	ENOG4105BZU	Histidine kinase
FE785_03315	ENOG4105DQF	Hydrolase
FE785_03320	ENOG4105CC5	ABC transporter
FE785_03325	ENOG4105CC5	ABC transporter
FE785_03330	ENOG4105DIK	(ABC) transporter
FE785_03335	ENOG4105DSE	periplasmic solute binding protein
FE785_03340	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
FE785_03345	ENOG4107RJX	Catalyzes the conversion of 6-carboxy-5,6,7,8- tetrahydropterin (CPH4) to 7-carboxy-7-deazaguanine (CDG) (By similarity)
FE785_03350	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
FE785_03355	ENOG4105MQS	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
FE785_03360	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)
FE785_03365	ENOG4105DR5	peptidase
FE785_03375	ENOG4105CM3	Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate (By similarity)
FE785_03380	ENOG4105DI7	Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs (By similarity)
FE785_03385	ENOG4108ZGB	N-(5'-phosphoribosyl)anthranilate isomerase
FE785_03390	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
FE785_03395	ENOG4105F6H	The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate (By similarity)
FE785_03400	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)
FE785_03405	ENOG4105DPM	folylpolyglutamate synthase Dihydrofolate synthase
FE785_03415	ENOG4105CBA	glutamine phosphoribosylpyrophosphate amidotransferase
FE785_03420	ENOG4105C28	cystathionine
FE785_03425	ENOG4105HBR	Rna-binding protein
FE785_03430	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)
FE785_03435	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)
FE785_03440	ENOG4105EEI	dihydropteroate synthase
FE785_03445	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
FE785_03450	ENOG4105CP7	Triose-phosphate isomerase
FE785_03455	ENOG4107EJC	Preprotein translocase subunit SecG
FE785_03465	ENOG4105KWU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
FE785_03470	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)
FE785_03475	ENOG4105CYU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
FE785_03480	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)
FE785_03495	ENOG4108IEH	NADH dehydrogenase subunit g
FE785_03500	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)
FE785_03505	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)
FE785_03510	ENOG4105DF2	NADH dehydrogenase subunit j
FE785_03515	ENOG4105M5H	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)
FE785_03525	ENOG4105C8S	subunit m
FE785_03530	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)
FE785_03545	ENOG4108KU3	Integrase
FE785_03570	ENOG4105VTW	prevent-host-death family
FE785_03590	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)
FE785_03620	ENOG4105BZU	Histidine kinase
FE785_03625	ENOG4105BZU	Histidine kinase
FE785_03645	ENOG4105RX7	peptidase S8 and S53, subtilisin, kexin, sedolisin
FE785_03655	ENOG4107QJE	Chromosome Partitioning Protein
FE785_03665	ENOG4105CUP	Catalyzes the synthesis of alpha-ribazole-5'-phosphate from nicotinate mononucleotide (NAMN) and 5,6- dimethylbenzimidazole (DMB) (By similarity)
FE785_03670	ENOG4105BZU	Histidine kinase
FE785_03680	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
FE785_03685	ENOG4105BZU	Histidine kinase
FE785_03700	ENOG4105DJY	efflux transporter, rnd family, mfp subunit
FE785_03705	ENOG4108IJF	Heavy metal efflux pump, CzcA
FE785_03725	ENOG4105BZU	Histidine kinase
FE785_03730	ENOG4107R15	K00850 6-phosphofructokinase 1 EC 2.7.1.11
FE785_03735	ENOG4105ZIE	Exonuclease involved in the 3' processing of various precursor tRNAs. Initiates hydrolysis at the 3'-terminus of an RNA molecule and releases 5'-mononucleotides (By similarity)
FE785_03740	ENOG4105DFU	Cell wall formation (By similarity)
FE785_03745	ENOG4105BZU	Histidine kinase
FE785_03765	ENOG4108BPE	-transporting atpase
FE785_03770	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
FE785_03775	ENOG4107QX9	Thiol disulfide interChange protein
FE785_03780	ENOG4105E66	phosphoriboisomerase A
FE785_03800	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)
FE785_03805	ENOG4105C7B	Threonine dehydratase
FE785_03815	ENOG4105DHP	deoxycytidine triphosphate deaminase
FE785_03825	ENOG4108V3E	phosphoribosylglycinamide formyltransferase
FE785_03830	ENOG4105CXB	phosphoribosylaminoimidazole synthetase
FE785_03840	ENOG4108KZ1	Mediates the interaction of DNA replication inititator protein DnaA with DNA polymerase subunit beta sliding clamp (dnaN). Stimulates hydrolysis of ATP-DnaA to ADP-DnaA, rendering DnaA inactive for reinititation, a process called regulatory inhibition of DnaA or RIDA (By similarity)
FE785_03845	ENOG4107ZT5	Thiol disulfide interchange protein
FE785_03860	ENOG4105ENT	Efflux transporter rnd family, mfp subunit
FE785_03875	ENOG4105D6S	protein involved in catabolism of external DNA
FE785_03880	ENOG4105C9W	Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity (By similarity)
FE785_03885	ENOG4105C8Q	Methyl-accepting chemotaxis
FE785_03905	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)
FE785_03930	ENOG4105C4Q	deoxyguanosinetriphosphate triphosphohydrolase-like protein
FE785_03935	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)
FE785_03940	ENOG4105K8N	protein family UPF0079, ATPase
FE785_03945	ENOG4105C5C	n-acetylmuramoyl-l-alanine amidase
FE785_03950	ENOG4105MK2	5-formyltetrahydrofolate cyclo-ligase
FE785_03960	ENOG4105E07	UPF0149 protein
FE785_03965	ENOG4107RAQ	aminopeptidase
FE785_03970	ENOG4105D0A	hydroxylase
FE785_03975	ENOG4105EAK	ubiquinone biosynthesis hydroxylase, ubiH ubiF VisC COQ6 family
FE785_03985	ENOG4105DUM	transcriptional regulator, lysR family
FE785_03990	ENOG4108V1T	peptidylprolyl cis-trans isomerase
FE785_03995	ENOG4105C3M	thioredoxin reductase
FE785_04000	ENOG4105CNU	cell division protein FtsK
FE785_04005	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)
FE785_04010	ENOG4105D1H	recombination factor protein RarA
FE785_04015	ENOG4105WMR	Protein CrcB homolog
FE785_04020	ENOG4105D43	The glycine cleavage system catalyzes the degradation of glycine (By similarity)
FE785_04025	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)
FE785_04030	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
FE785_04040	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)
FE785_04055	ENOG4107R0U	MotA TolQ exbB proton channel
FE785_04060	ENOG4106VK6	Flagellar motor protein
FE785_04065	ENOG4105BZU	Histidine kinase
FE785_04075	ENOG4105BZU	Histidine kinase
FE785_04080	ENOG4105BZU	Histidine kinase
FE785_04100	ENOG4105D3G	Pseudouridine synthase
FE785_04110	ENOG4105C03	ribonuclease
FE785_04115	ENOG4105EI2	Pseudouridine synthase
FE785_04120	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)
FE785_04135	ENOG4105VGS	50s ribosomal protein l32
FE785_04140	ENOG4105C6B	Catalyzes the reversible formation of acyl-phosphate (acyl-PO(4)) from acyl- acyl-carrier-protein (acyl-ACP). This enzyme utilizes acyl-ACP as fatty acyl donor, but not acyl-CoA (By similarity)
FE785_04145	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)
FE785_04150	ENOG4105CJF	Malonyl coA-acyl carrier protein transacylase
FE785_04155	ENOG4105CHR	reductase
FE785_04160	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
FE785_04165	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
FE785_04175	ENOG4105YAZ	4-amino-4-deoxychorismate lyase
FE785_04180	ENOG4105HHA	aminodeoxychorismate lyase
FE785_04185	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
FE785_04195	ENOG4105F8V	Hydrolase, tatD family
FE785_04200	ENOG4105BZ1	(ABC) transporter
FE785_04205	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)
FE785_04235	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
FE785_04240	ENOG4107RHT	methyl-accepting chemotaxis sensory transducer with Pas Pac sensor
FE785_04240	ENOG4107RHT	methyl-accepting chemotaxis sensory transducer with Pas Pac sensor
FE785_04245	ENOG4105BZU	Histidine kinase
FE785_04250	ENOG4105BZU	Histidine kinase
FE785_04255	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
FE785_04260	ENOG4105BZU	Histidine kinase
FE785_04265	ENOG4108PYU	two-component system response regulator
FE785_04275	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
FE785_04290	ENOG4107FW0	short-chain dehydrogenase reductase
FE785_04305	ENOG4105CV9	cyclopropane-fatty-acyl-phospholipid synthase
FE785_04325	ENOG4105BZU	Histidine kinase
FE785_04355	ENOG4105DUM	transcriptional regulator, lysR family
FE785_04360	ENOG4105CVP	deoxyribo-dipyrimidine photolyase
FE785_04375	ENOG4108HW3	(ABC) transporter
FE785_04405	ENOG4105CFQ	glutamine synthetase
FE785_04415	ENOG4105CHC	glucokinase (EC 2.7.1.2)
FE785_04425	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
FE785_04430	ENOG4105EIG	urea carboxylase-associated protein 1
FE785_04440	ENOG4105MRR	Transcriptional regulator (By similarity)
FE785_04450	ENOG4105EFS	Binding-protein-dependent transport systems, inner membrane component
FE785_04455	ENOG4105HJX	Biotin- acetyl-CoA-carboxylase ligase
FE785_04460	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
FE785_04470	ENOG4105CJW	magnesium transporter
FE785_04475	ENOG4105D9I	Responsible for the addition of glutamate residues to the C-terminus of ribosomal protein S6 (By similarity)
FE785_04480	ENOG4105D9I	Responsible for the addition of glutamate residues to the C-terminus of ribosomal protein S6 (By similarity)
FE785_04495	ENOG4105CPC	Aldo Keto reductase
FE785_04500	ENOG4105CH2	amidohydrolase
FE785_04505	ENOG4108JPW	Aminotransferase
FE785_04520	ENOG4107STW	synthase
FE785_04525	ENOG4106N16	had-superfamily hydrolase, subfamily iib
FE785_04540	ENOG4105FCD	Major Facilitator
FE785_04550	ENOG4105EVH	UPF0753 protein
FE785_04570	ENOG4105BZU	Histidine kinase
FE785_04580	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
FE785_04590	ENOG4108Z1B	Cyclase dehydrase
FE785_04610	ENOG41090R7	Ferric uptake
FE785_04615	ENOG4105C4F	May be involved in recombinational repair of damaged DNA (By similarity)
FE785_04620	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)
FE785_04625	ENOG4105CI8	Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons (By similarity)
FE785_04630	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
FE785_04635	ENOG4105CFG	Acts as a chaperone (By similarity)
FE785_04640	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)
FE785_04645	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
FE785_04650	ENOG4105BZU	Histidine kinase
FE785_04655	ENOG4107TT5	NLP P60 protein
FE785_04660	ENOG4105C1M	carbamoyl-phosphate synthetase glutamine chain
FE785_04665	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
FE785_04670	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)
FE785_04685	ENOG4105ED9	Protein of unknown function (DUF455)
FE785_04695	ENOG4105DKQ	ROK family
FE785_04715	ENOG4105E1F	short-chain dehydrogenase reductase
FE785_04720	ENOG41080RH	Thioredoxin
FE785_04730	ENOG4105BZU	Histidine kinase
FE785_04750	ENOG4105CRK	lysyL-tRNA synthetase
FE785_04765	ENOG4108V3W	Chemotaxis protein, CheW
FE785_04770	ENOG4107XVI	synthase
FE785_04775	ENOG4105CTB	Polyprenyl synthetase
FE785_04780	ENOG41080XP	Cbs domain
FE785_04785	ENOG4108IYU	L-aspartate oxidase
FE785_04795	ENOG4105C0H	protease
FE785_04800	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)
FE785_04805	ENOG4105C3F	Signal peptidase i
FE785_04810	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)
FE785_04825	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)
FE785_04830	ENOG4105KJV	Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein (By similarity)
FE785_04840	ENOG4105C09	Bile acid
FE785_04865	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)
FE785_04905	ENOG4105BZU	Histidine kinase
FE785_04910	ENOG4108YZY	peptidylprolyl cis-trans isomerase
FE785_04920	ENOG4105CMV	Succinyl-CoA synthetase subunit beta
FE785_04925	ENOG4105CH8	Succinyl-CoA ligase ADP-forming subunit alpha
FE785_04930	ENOG4105C4K	Nad synthetase
FE785_04935	ENOG4106SNF	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane
FE785_04940	ENOG4105C34	Pseudouridine synthase
FE785_04945	ENOG4105DBW	Multi-copper polyphenol oxidoreductase laccase
FE785_04955	ENOG4105D18	nicotinate-nucleotide pyrophosphorylase
FE785_04975	ENOG4105MHQ	Low-potential electron donor to a number of redox enzymes (By similarity)
FE785_04985	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)
FE785_04990	ENOG4105DAQ	Component of the pyruvate dehydrogenase (PDH) complex, that catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2) (By similarity)
FE785_04995	ENOG4107QSN	dihydrolipoamide acetyltransferase
FE785_05000	ENOG4107QN2	dihydrolipoyl dehydrogenase
FE785_05015	ENOG4105VRT	cytoplasmic protein
FE785_05060	ENOG4105C94	Transporter
FE785_05065	ENOG410620I	Diguanylate cyclase
FE785_05080	ENOG4105C8Q	Methyl-accepting chemotaxis
FE785_05085	ENOG4105C1J	atp-dependent rna helicase
FE785_05095	ENOG4105BZU	Histidine kinase
FE785_05100	ENOG410645S	MarR family Transcriptional regulator
FE785_05110	ENOG4108UPT	UPF0178 protein
FE785_05130	ENOG4105C8E	extradiol ring-cleavage dioxygenase class IIi protein subunit b
FE785_05145	ENOG4108NIW	Leucine export protein LeuE
FE785_05155	ENOG4105BZU	Histidine kinase
FE785_05160	ENOG4108R96	Methyltransferase, YaeB family
FE785_05190	ENOG4105EUB	pirin domain protein
FE785_05195	ENOG4108VBZ	doxx family
FE785_05200	ENOG4105CC0	LysR family Transcriptional regulator
FE785_05210	ENOG4108W1A	pseudouridine synthase
FE785_05220	ENOG4108YZY	peptidylprolyl cis-trans isomerase
FE785_05225	ENOG4108YZY	peptidylprolyl cis-trans isomerase
FE785_05230	ENOG4108YXA	Membrane
FE785_05245	ENOG4105E0C	molybdate abc transporter
FE785_05255	ENOG4105CBM	Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 (By similarity)
FE785_05260	ENOG4105CEP	NADH dehydrogenase
FE785_05265	ENOG4105M78	Catalyzes, although with low efficiency, the sulfur transfer reaction from thiosulfate to cyanide (By similarity)
FE785_05280	ENOG4105CFP	Peptidase U32
FE785_05285	ENOG4105K5D	4fe-4S ferredoxin iroN-sulfur binding
FE785_05305	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
FE785_05310	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)
FE785_05315	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)
FE785_05320	ENOG4105C6P	ATP-dependent serine protease that mediates the selective degradation of mutant and abnormal proteins as well as certain short-lived regulatory proteins. Required for cellular homeostasis and for survival from DNA damage and developmental changes induced by stress. Degrades polypeptides processively to yield small peptide fragments that are 5 to 10 amino acids long. Binds to DNA in a double-stranded, site-specific manner (By similarity)
FE785_05350	ENOG4105CSJ	Enoyl- acyl-carrier-protein reductase NADH
FE785_05355	ENOG4105DEF	Extracellular solute-binding protein, family 5
FE785_05370	ENOG4108JQ5	ABC transporter
FE785_05380	ENOG4105CHR	reductase
FE785_05385	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)
FE785_05390	ENOG4107RFD	Non-specific O-methyltransferase that catalyzes the 2 O- methylation steps in the ubiquinone biosynthetic pathway (By similarity)
FE785_05395	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)
FE785_05400	ENOG4107QM1	Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine (By similarity)
FE785_05405	ENOG4105CQC	Prephenate dehydratase
FE785_05410	ENOG4105CIH	Imidazole acetol-phosphate transaminase
FE785_05420	ENOG4105CMY	5-enolpyruvylshikimate-3-phosphate synthase
FE785_05425	ENOG4105CAT	Cytidine monophosphate kinase
FE785_05430	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)
FE785_05435	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)
FE785_05445	ENOG4106EG9	Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) (By similarity)
FE785_05450	ENOG4108ZDX	Binds together with S18 to 16S ribosomal RNA (By similarity)
FE785_05455	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)
FE785_05465	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
FE785_05470	ENOG4105CDU	Replicative dna helicase
FE785_05475	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
FE785_05480	ENOG41087AY	ADP-Ribose pyrophosphatase
FE785_05490	ENOG4107QI1	Mate efflux family protein
FE785_05495	ENOG4105K5B	UPF0225 protein
FE785_05520	ENOG4105DTW	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FE785_05530	ENOG4105K89	arsenate reductase
FE785_05540	ENOG4107SVC	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
FE785_05545	ENOG4105CEH	Catalyzes the synthesis of dihydrouridine a modified base found in the D-loop of most tRNAs (By similarity)
FE785_05550	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)
FE785_05575	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)
FE785_05605	ENOG4105FE9	pseudouridine synthase
FE785_05610	ENOG4108Z4T	Peptidase M50
FE785_05615	ENOG4107RTD	sua5 ycio yrdc ywlc family protein
FE785_05620	ENOG4105DB7	PHP domain protein
FE785_05625	ENOG4107835	probably involved in intracellular septation (By similarity)
FE785_05630	ENOG4105K9H	YciI-like protein
FE785_05635	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)
FE785_05655	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)
FE785_05660	ENOG4107NPY	receptor for the septal ring structure, may anchor it to the inner-membrane (By similarity)
FE785_05665	ENOG4107S5T	Carbohydrate kinase
FE785_05675	ENOG4107S75	HAD-superfamily hydrolase subfamily IA variant 3
FE785_05680	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
FE785_05710	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
FE785_05715	ENOG4107QID	Threonine synthase
FE785_05725	ENOG4105D6E	homoserine dehydrogenase
FE785_05730	ENOG4105CHM	Aminotransferase
FE785_05745	ENOG4108K5P	(LipO)protein
FE785_05750	ENOG4108UM1	dedA family
FE785_05755	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)
FE785_05765	ENOG4108DG9	Smr protein MutS2
FE785_05770	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)
FE785_05775	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
FE785_05780	ENOG4105CXR	Phospho-2-dehydro-3-deoxyoctonate aldolase
FE785_05785	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
FE785_05790	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)
FE785_05795	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)
FE785_05805	ENOG4105DDY	UPF0142 protein ycaO
FE785_05820	ENOG41081QV	Universal stress protein
FE785_05825	ENOG41072GX	Peptidase M22 Glycoprotease
FE785_05830	ENOG4105DVT	helicase
FE785_05835	ENOG4105YK5	50S ribosomal protein L36
FE785_05840	ENOG4107R88	Chemotaxis protein (CheV)
FE785_05845	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
FE785_05850	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)
FE785_05855	ENOG4105DAF	Involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
FE785_05860	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)
FE785_05865	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)
FE785_05875	ENOG4105E1Z	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane
FE785_05880	ENOG4105DZP	Membrane-associated zinc metalloprotease
FE785_05885	ENOG4105KNE	Phosphatidate cytidylyltransferase
FE785_05895	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)
FE785_05900	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
FE785_05905	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)
FE785_05910	ENOG4105CE9	30S ribosomal protein S2
FE785_05915	ENOG4105CA1	Removes the N-terminal methionine from nascent proteins (By similarity)
FE785_05920	ENOG4105E1P	Modifies, by uridylylation or deuridylylation the PII (GlnB) regulatory protein (By similarity)
FE785_05930	ENOG4105EJ3	Catalyzes the conversion of the cyclic tetrahydrodipicolinate (THDP) into the acyclic N-succinyl-L-2- amino-6-oxopimelate using succinyl-CoA (By similarity)
FE785_05935	ENOG4105KUZ	arsenate reductase
FE785_05940	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)
FE785_05950	ENOG4105C8J	)-transporter
FE785_05955	ENOG4105D4A	Cell wall formation (By similarity)
FE785_05960	ENOG4105VV6	START domain-containing protein
FE785_05965	ENOG4105D64	Mechanosensitive ion channel
FE785_05970	ENOG4107QPA	Cleaves GlcNAc linked beta-1,4 to MurNAc tripeptides (By similarity)
FE785_05980	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
FE785_05985	ENOG4105CJM	Binding-protein-dependent transport systems, inner membrane component
FE785_06000	ENOG4105DFG	type I secretion outer membrane protein
FE785_06005	ENOG41080ZE	Adenylate cyclase
FE785_06010	ENOG4105C6T	cysteine synthase
FE785_06020	ENOG4105C8Q	Methyl-accepting chemotaxis
FE785_06025	ENOG4105C5H	ABC transporter
FE785_06030	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)
FE785_06035	ENOG4105D60	lipoprotein releasing system transmembrane protein
FE785_06040	ENOG4105EN6	Membrane
FE785_06045	ENOG4107SA8	fad-dependent pyridine nucleotide-disulfide oxidoreductase
FE785_06050	ENOG4108JA2	transcriptioN-repair coupling factor
FE785_06060	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)
FE785_06070	ENOG4108KMM	Diguanylate cyclase
FE785_06080	ENOG4108M8H	domain protein
FE785_06090	ENOG4105C6R	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)
FE785_06095	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
FE785_06105	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)
FE785_06120	ENOG4107QZF	nitrite reductase NADPH large subunit
FE785_06125	ENOG4108IFG	nitrite reductase, (NAD(P)H)
FE785_06130	ENOG4107RNU	major facilitator superfamily MFS_1
FE785_06135	ENOG4105D9P	serine threonine protein kinase
FE785_06140	ENOG4105C8Q	Methyl-accepting chemotaxis
FE785_06145	ENOG4105D7T	ABC transporter
FE785_06155	ENOG4105I5W	Transporter
FE785_06170	ENOG41082YX	Transcriptional regulator, arsr family
FE785_06180	ENOG4105CUC	YeeE YedE family protein
FE785_06185	ENOG4107TPS	domain protein
FE785_06195	ENOG4105BZU	Histidine kinase
FE785_06200	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
FE785_06205	ENOG4106VK6	Flagellar motor protein
FE785_06210	ENOG4107R0U	MotA TolQ exbB proton channel
FE785_06215	ENOG4105BZU	Histidine kinase
FE785_06245	ENOG41067CV	Integrase
FE785_06265	ENOG4105BZQ	cdp-diacylglycerol-glycerol-3-phosphate 3-phosphatidyltransferase
FE785_06270	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)
FE785_06275	ENOG4105D07	Signal peptide peptidase, SppA
FE785_06285	ENOG4107QIJ	Aconitate hydratase 2
FE785_06290	ENOG4107QTF	adenylosuccinate lyase
FE785_06295	ENOG4105EZE	Cupin 4 family protein
FE785_06305	ENOG4105BZU	Histidine kinase
FE785_06315	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
FE785_06320	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
FE785_06335	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
FE785_06340	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)
FE785_06345	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)
FE785_06350	ENOG4105CHV	Transcription elongation factor NusA
FE785_06355	ENOG4105K7D	Required for maturation of 30S ribosomal subunits (By similarity)
FE785_06360	ENOG4105DE5	Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity (By similarity)
FE785_06380	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)
FE785_06405	ENOG4105C0B	DNA polymerase III (alpha subunit)
FE785_06410	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)
FE785_06430	ENOG4105E33	succinate dehydrogenase
FE785_06435	ENOG41086VE	Flavinator of succinate dehydrogenase
FE785_06440	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)
FE785_06445	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
FE785_06450	ENOG4105KAE	Involved in the modulation of the specificity of the ClpAP-mediated ATP-dependent protein degradation (By similarity)
FE785_06460	ENOG4108Z8G	Alkylphosphonate utilization operon protein PhnA
FE785_06475	ENOG4105CDY	transcriptional regulatory protein
FE785_06480	ENOG4105BZU	Histidine kinase
FE785_06485	ENOG4105CR7	Catalyzes the transfer of selenium from selenophosphate for conversion of 2-thiouridine to 2-selenouridine at the wobble position in tRNA (By similarity)
FE785_06490	ENOG4105D4F	Synthesizes selenophosphate from selenide and ATP (By similarity)
FE785_06495	ENOG4108B1Q	Ribonuclease
FE785_06525	ENOG4108R99	pseudouridine synthase
FE785_06530	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
FE785_06535	ENOG41075W9	High frequency lysogenization protein HflD homolog
FE785_06545	ENOG4105EIN	peptidylprolyl cis-trans isomerase
FE785_06550	ENOG4108VYJ	response regulator receiver protein
FE785_06555	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
FE785_06560	ENOG4105C49	Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine (By similarity)
FE785_06570	ENOG4105EPW	hflc protein
FE785_06575	ENOG4107QJR	hflk protein
FE785_06580	ENOG4105C1N	GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis (By similarity)
FE785_06585	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)
FE785_06590	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)
FE785_06600	ENOG4105D1F	ATP-binding protein
FE785_06610	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)
FE785_06615	ENOG4105DGN	Electron transport complex
FE785_06620	ENOG4108R3D	Electron transport complex
FE785_06630	ENOG4105D6A	Electron transport complex
FE785_06635	ENOG4108UQQ	Electron transport complex
FE785_06640	ENOG4105DZB	Electron transport complex
FE785_06645	ENOG4105CSM	endonuclease III
FE785_06655	ENOG4108UMW	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
FE785_06660	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
FE785_06665	ENOG4105BZU	Histidine kinase
FE785_06670	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
FE785_06675	ENOG4105C1J	atp-dependent rna helicase
FE785_06700	ENOG4105DHT	Metal Dependent Phosphohydrolase
FE785_06705	ENOG4105BZU	Histidine kinase
FE785_06715	ENOG4105BZU	Histidine kinase
FE785_06730	ENOG41068B1	Cob-I-yrinic acid a,c-diamide adenosyltransferase
FE785_06735	ENOG4105JKQ	Part of the ABC transporter complex BtuCDF involved in vitamin B12 import. Binds vitamin B12 and delivers it to the periplasmic surface of BtuC (By similarity)
FE785_06745	ENOG4105CET	Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria (By similarity)
FE785_06750	ENOG4105W49	UPF0434 protein
FE785_06755	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)
FE785_06760	ENOG4108EQH	DNA internalization-related competence protein ComEC Rec2
FE785_06770	ENOG4105DAN	ATP-dependent protease
FE785_06795	ENOG4108RRZ	Transcription elongation factor GreB
FE785_06800	ENOG4105BZU	Histidine kinase
FE785_06815	ENOG4105CHF	Glutathione S-transferase
FE785_06820	ENOG4105BZU	Histidine kinase
FE785_06825	ENOG4105CQ7	ATP-dependent helicase
FE785_06835	ENOG4108YZY	peptidylprolyl cis-trans isomerase
FE785_06840	ENOG4107RZZ	dna polymerase iii epsilon subunit
FE785_06845	ENOG4108UMW	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
FE785_06855	ENOG4108RW0	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
FE785_06860	ENOG4105E9H	Lytic Murein transglycosylase
FE785_06865	ENOG4107SC1	transglycosylase
FE785_06870	ENOG4105C8N	cysteinyl-tRNA synthetase
FE785_06880	ENOG4108R5K	PPIases accelerate the folding of proteins (By similarity)
FE785_06885	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)
FE785_06895	ENOG4105CK2	sodium dicarboxylate symporter
FE785_06905	ENOG4108ZAI	phosphatidylglycerophosphatase a
FE785_06910	ENOG4105CDH	Citrulline--aspartate ligase
FE785_06915	ENOG4105DJ4	phosphatidylserine decarboxylase
FE785_06920	ENOG4108YZA	Nitrogen regulatory protein pii
FE785_06930	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
FE785_06935	ENOG4105CUX	Signal transduction histidine kinase
FE785_06955	ENOG4105CZ5	Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate (By similarity)
FE785_06980	ENOG4105KCK	Peptidoglycan-associated lipoprotein
FE785_06985	ENOG4107R6Y	Involved in the TonB-independent uptake of proteins (By similarity)
FE785_06995	ENOG4105M8F	Biopolymer transport protein exbD tolR
FE785_07000	ENOG4105E02	MotA TolQ exbB proton channel
FE785_07005	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)
FE785_07010	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)
FE785_07015	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)
FE785_07020	ENOG4105D0I	Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate (By similarity)
FE785_07025	ENOG4105C9M	aspartyl-trna synthetase
FE785_07035	ENOG4105EHH	Cleaves type-4 fimbrial leader sequence and methylates the N-terminal (generally Phe) residue (By similarity)
FE785_07045	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)
FE785_07050	ENOG4105CG2	Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 (By similarity)
FE785_07055	ENOG4107YIM	Involved in the transcription termination process (By similarity)
FE785_07060	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)
FE785_07075	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)
FE785_07080	ENOG4108Z11	Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes (By similarity)
FE785_07085	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)
FE785_07090	ENOG4105C5H	ABC transporter
FE785_07115	ENOG4105BZU	Histidine kinase
FE785_07130	ENOG4108ETH	Formylglycinamide ribotide synthetase
FE785_07140	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
FE785_07145	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
FE785_07150	ENOG4108IAB	Phoh family
FE785_07155	ENOG4105EGD	dinuclear metal center protein, YbgI family
FE785_07165	ENOG4105C8Q	Methyl-accepting chemotaxis
FE785_07170	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
FE785_07175	ENOG4105BZU	Histidine kinase
FE785_07185	ENOG4108V3W	Chemotaxis protein, CheW
FE785_07190	ENOG4108VYJ	response regulator receiver protein
FE785_07200	ENOG4105D00	flagellar biosynthetic protein flhB
FE785_07205	ENOG4108V3W	Chemotaxis protein, CheW
FE785_07210	ENOG4105CBS	Chea signal transduction histidine kinase
FE785_07215	ENOG4108KCC	Plays an important role in bacterial chemotaxis signal transduction pathway by accelerating the dephosphorylation of phosphorylated CheY (CheY-P) (By similarity)
FE785_07220	ENOG4108VYJ	response regulator receiver protein
FE785_07225	ENOG4105DN4	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FE785_07230	ENOG4107R21	site-determining protein
FE785_07235	ENOG4105FZW	flagellar biosynthesis regulator FlhF
FE785_07240	ENOG4105D7B	Flagellar biosynthesis protein flha
FE785_07245	ENOG4105D00	flagellar biosynthetic protein flhB
FE785_07250	ENOG4105D19	Role in flagellar biosynthesis (By similarity)
FE785_07255	ENOG4105VS8	Flagellar biosynthetic protein fliq
FE785_07260	ENOG4105CN7	Flagellar biosynthetic protein FliP
FE785_07265	ENOG4105VTB	flagellar biosynthesis protein fliO
FE785_07270	ENOG4105DD5	Flagellar motor switch protein
FE785_07275	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)
FE785_07285	ENOG4105ER2	Ompa motb domain protein
FE785_07290	ENOG4107RD7	Flagellar Motor Protein, MotA
FE785_07295	ENOG4108NVR	Methyl-accepting chemotaxis
FE785_07310	ENOG4108JIR	Flagellum-specific ATP synthase
FE785_07320	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)
FE785_07325	ENOG4105C1F	The M ring may be actively involved in energy transduction (By similarity)
FE785_07330	ENOG4105X6K	flagellar hook-basal body complex protein fliE
FE785_07335	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
FE785_07340	ENOG4105BZU	Histidine kinase
FE785_07345	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
FE785_07355	ENOG4105MQ3	flagellar protein FliS
FE785_07360	ENOG410804A	Flagellar hook-associated 2 domain-containing protein
FE785_07375	ENOG4105I03	Flagellin
FE785_07380	ENOG4105I03	Flagellin
FE785_07385	ENOG4105I03	Flagellin
FE785_07390	ENOG4105I03	Flagellin
FE785_07400	ENOG4105F0R	Cytidylyltransferase
FE785_07430	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)
FE785_07445	ENOG4107SE4	UDP-N-acetylglucosamine 2-epimerase
FE785_07450	ENOG4105D2T	synthase
FE785_07460	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
FE785_07465	ENOG4108IAJ	Nad-dependent epimerase dehydratase
FE785_07470	ENOG4106S48	Murein-degrading enzyme. May play a role in recycling of muropeptides during cell elongation and or cell division
FE785_07490	ENOG4105D92	Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation (By similarity)
FE785_07495	ENOG4107W7W	Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation (By similarity)
FE785_07500	ENOG4105CGA	flagellar basal-body rod protein FlgG
FE785_07505	ENOG4105CGA	flagellar basal-body rod protein FlgG
FE785_07510	ENOG4105BZE	flagellar hook protein, FlgE
FE785_07515	ENOG410822I	Flagellar hook capping protein
FE785_07520	ENOG4108ZC9	flagellar basal-body rod protein flgc
FE785_07525	ENOG4105K88	Structural component of flagellum, the bacterial motility apparatus. Part of the rod structure of flagellar basal body (By similarity)
FE785_07535	ENOG4107R88	Chemotaxis protein (CheV)
FE785_07585	ENOG4105CD8	aminopeptidase N
FE785_07590	ENOG4105KCK	Peptidoglycan-associated lipoprotein
FE785_07595	ENOG4105DS0	Transcriptional regulator, Crp Fnr family
FE785_07600	ENOG4108RVA	ribokinase
FE785_07605	ENOG4105C2N	RNA methyltransferase TrmH family group 3
FE785_07610	ENOG4105C40	3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs (By similarity)
FE785_07615	ENOG4106S48	Murein-degrading enzyme. May play a role in recycling of muropeptides during cell elongation and or cell division
FE785_07620	ENOG4105D8I	Catalyzes the ATP-dependent transfer of a sulfur to tRNA to produce 4-thiouridine in position 8 of tRNAs, which functions as a near-UV photosensor. Also catalyzes the transfer of sulfur to the sulfur carrier protein ThiS, forming ThiS-thiocarboxylate. This is a step in the synthesis of thiazole, in the thiamine biosynthesis pathway. The sulfur is donated as persulfide by IscS (By similarity)
FE785_07630	ENOG4105CZI	D-fructose-1,6-bisphosphate 1-phosphohydrolase class 1
FE785_07635	ENOG4105F0N	pyrophosphate phospho-hydrolase
FE785_07645	ENOG4108Z2X	Catalyzes the pyruvoyl-dependent decarboxylation of aspartate to produce beta-alanine (By similarity)
FE785_07650	ENOG4106VK6	Flagellar motor protein
FE785_07660	ENOG4107R03	Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate (By similarity)
FE785_07665	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
FE785_07670	ENOG4105K8U	2-Amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase
FE785_07675	ENOG4105DJ0	Poly(A) Polymerase
FE785_07685	ENOG4105C31	Tryptophanyl-tRNA synthetase
FE785_07695	ENOG4105CHH	sulfate transporter
FE785_07700	ENOG4105BZU	Histidine kinase
FE785_07705	ENOG4105NBK	UPF0345 protein
FE785_07725	ENOG4105D10	5-enolpyruvylshikimate-3-phosphate phospholyase
FE785_07740	ENOG4105BZU	Histidine kinase
FE785_07745	ENOG4105BZU	Histidine kinase
FE785_07750	ENOG4108UHE	carbonic anhydrase
FE785_07755	ENOG4105C76	Specifically methylates the 50S ribosomal protein L3 on a specific glutamine residue (By similarity)
FE785_07760	ENOG4108RIR	Molybdenum cofactor biosynthesis protein
FE785_07765	ENOG4105C6P	ATP-dependent serine protease that mediates the selective degradation of mutant and abnormal proteins as well as certain short-lived regulatory proteins. Required for cellular homeostasis and for survival from DNA damage and developmental changes induced by stress. Degrades polypeptides processively to yield small peptide fragments that are 5 to 10 amino acids long. Binds to DNA in a double-stranded, site-specific manner (By similarity)
FE785_07770	ENOG4105C8Q	Methyl-accepting chemotaxis
FE785_07775	ENOG4108UJV	acyl-CoA thioesterase i
FE785_07780	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)
FE785_07855	ENOG4105ENJ	RND efflux system, outer membrane lipoprotein
FE785_07880	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)
FE785_07885	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
FE785_07890	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
FE785_07895	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)
FE785_07900	ENOG41082NX	50s ribosomal protein l35
FE785_07905	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)
FE785_07910	ENOG4105C22	threonyL-tRNA synthetase
FE785_07920	ENOG4105D05	Receptor
FE785_07940	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)
FE785_07955	ENOG4105BZU	Histidine kinase
FE785_07980	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)
FE785_07985	ENOG4105C6M	Alpha-keto-beta-hydroxylacyl reductoisomerase
FE785_07990	ENOG4108ZP8	Acetolactate synthase small subunit
FE785_07995	ENOG4105C7K	acetolactate synthase
FE785_08000	ENOG4108RBP	3'-to-5' exoribonuclease specific for small oligoribonucleotides (By similarity)
FE785_08005	ENOG4105D0M	Protease HtpX homolog
FE785_08010	ENOG41090A4	Pterin carbinolamine dehydratase
FE785_08015	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)
FE785_08020	ENOG4105Z6S	cytochrome C, class I
FE785_08025	ENOG4106RE7	Cytochrome
FE785_08035	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
FE785_08040	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)
FE785_08045	ENOG4105N21	Membrane
FE785_08050	ENOG4105CUT	histidyl-tRNA synthetase
FE785_08060	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
FE785_08070	ENOG4108Z4V	iron-sulfur cluster assembly
FE785_08075	ENOG4108ZF1	Transcriptional regulator, BadM Rrf2 family
FE785_08090	ENOG4105ECY	inositol monophosphatase
FE785_08095	ENOG4105KEG	ribosomal-protein-alanine acetyltransferase
FE785_08105	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)
FE785_08110	ENOG4106PT6	cdpdiacylglycerol-serine O-phosphatidyltransferase
FE785_08115	ENOG4108ZCA	Inherit from COG: pyridine nucleotide-disulfide oxidoreductase
FE785_08120	ENOG4105VFE	sira family
FE785_08125	ENOG4105ERG	peptidase m48, ste24p
FE785_08145	ENOG41088H4	Diheme cytochrome SoxA (Sulfur oxidation)
FE785_08155	ENOG4105C01	Dihydroxy-acid dehydratase
FE785_08165	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)
FE785_08175	ENOG4105M2J	Glutaredoxin
FE785_08180	ENOG4105CAQ	asparagine synthetase
FE785_08190	ENOG4105BZU	Histidine kinase
FE785_08195	ENOG4108ZQD	Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A (By similarity)
FE785_08200	ENOG4105M6F	mutator MutT protein
FE785_08205	ENOG4105CIH	Imidazole acetol-phosphate transaminase
FE785_08210	ENOG4105C5V	Catalyzes two activities which are involved in the cyclic version of arginine biosynthesis the synthesis of N- acetylglutamate from glutamate and acetyl-CoA as the acetyl donor, and of ornithine by transacetylation between N(2)-acetylornithine and glutamate (By similarity)
FE785_08215	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
FE785_08225	ENOG4105C7C	involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
FE785_08230	ENOG4105CIT	This protein may be involved in anomalous filament growth. May be a component of the septum (By similarity)
FE785_08235	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)
FE785_08240	ENOG4105CPF	Cell wall formation (By similarity)
FE785_08245	ENOG4105DFU	Cell wall formation (By similarity)
FE785_08260	ENOG4105JRK	feS assembly protein SufD
FE785_08265	ENOG4105C3K	feS assembly ATPase SufC
FE785_08270	ENOG4105DIW	FeS assembly protein SUFB
FE785_08280	ENOG4105NXV	High-affinity zinc uptake system protein
FE785_08285	ENOG4105FDK	ABC transporter
FE785_08290	ENOG4105FAV	ABC, transporter
FE785_08300	ENOG4105C0V	Provides the sole de novo source of dTMP for DNA biosynthesis (By similarity)
FE785_08305	ENOG4105C3B	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
FE785_08315	ENOG41061TZ	Short-chain dehydrogenase reductase Sdr
FE785_08320	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)
FE785_08325	ENOG4105CNI	cell division protein FtsW
FE785_08330	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
FE785_08335	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
FE785_08340	ENOG4108EQQ	Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein (By similarity)
FE785_08345	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)
FE785_08350	ENOG4105CJN	penicillin-binding protein
FE785_08360	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)
FE785_08365	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
FE785_08370	ENOG4108V6E	Cell division protein mraZ
FE785_08390	ENOG4105FFN	Specifically methylates the guanosine in position 1516 of 16S rRNA (By similarity)
FE785_08400	ENOG4105CU0	Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA (By similarity)
FE785_08410	ENOG41082RQ	UPF0102 protein
FE785_08425	ENOG4107R2I	The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination. The AddA nuclease domain is required for chi fragment generation
FE785_08440	ENOG4105EI2	Pseudouridine synthase
FE785_08450	ENOG4105DE5	Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity (By similarity)
FE785_08465	ENOG4105EN6	Membrane
FE785_08470	ENOG4105CFB	Gamma-glutamyltranspeptidase (EC 2.3.2.2)
FE785_08485	ENOG4107UUG	Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins (By similarity)
FE785_08495	ENOG4106UJV	Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its allylic isomer, dimethylallyl diphosphate (DMAPP) (By similarity)
FE785_08500	ENOG4105F99	Hydroxymethylglutaryl-CoA synthase
FE785_08505	ENOG4105D5I	Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate (By similarity)
FE785_08520	ENOG4105KB2	stringent starvation protein b
FE785_08525	ENOG4107MKT	Stringent starvation protein a
FE785_08530	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)
FE785_08535	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)
FE785_08540	ENOG4105CK3	Lysine 2,3-aminomutase YodO family protein
FE785_08555	ENOG4106YN8	Prenyltransferase
FE785_08585	ENOG4105CKK	Glycosyl transferase, family 2
FE785_08600	ENOG4105CGY	Dna recombination protein
FE785_08620	ENOG4105D7Q	type ii secretion system
FE785_08625	ENOG4107QHF	type ii secretion system protein e
FE785_08635	ENOG4105GVR	general secretion pathway protein D
FE785_08675	ENOG4105C03	ribonuclease
FE785_08680	ENOG4108Z03	MAF-like protein
FE785_08690	ENOG4105CQB	FAD linked oxidase domain protein
FE785_08715	ENOG4105D16	lipopolysaccharide heptosyltransferase i
FE785_08720	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)
FE785_08730	ENOG4105BZ1	(ABC) transporter
FE785_08735	ENOG4105NWR	lipid A biosynthesis (Kdo)2-(Lauroyl)-lipid IVA acyltransferase
FE785_08745	ENOG4105CM2	brancheD-chain amino acid aminotransferase
FE785_08750	ENOG4105C8Y	Acetylornithine aminotransferase
FE785_08755	ENOG4105DBV	ornithine carbamoyltransferase
FE785_08760	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)
FE785_08765	ENOG4105KDX	Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection (By similarity)
FE785_08770	ENOG4107QMP	dna polymerase iii subunits gamma and tau
FE785_08790	ENOG4108KB1	transcriptional regulator, arac family
FE785_08845	ENOG4105DHZ	alpha beta
FE785_08850	ENOG4105CJ0	Catalyzes the oxidation of erythronate-4-phosphate to 3- hydroxy-2-oxo-4-phosphonooxybutanoate (By similarity)
FE785_08855	ENOG4105UUH	Domain of unknown function DUF302 
FE785_08875	ENOG4105CDV	Ompa motb domain protein
FE785_08905	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)
FE785_08910	ENOG4108Z38	Catalyzes a trans-dehydration via an enolate intermediate (By similarity)
FE785_08915	ENOG4105KM4	Acetyl-CoA carboxylase, biotin carboxyl carrier protein
FE785_08920	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
FE785_08925	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
FE785_08930	ENOG4105CEH	Catalyzes the synthesis of dihydrouridine a modified base found in the D-loop of most tRNAs (By similarity)
FE785_08935	ENOG4105VY0	Activates ribosomal RNA transcription. Plays a direct role in upstream activation of rRNA promoters (By similarity)
FE785_08940	ENOG4105DC1	bifunctional purine biosynthesis protein purh
FE785_08955	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
FE785_08965	ENOG4105D4P	Coproporphyrinogen iii oxidase
FE785_08970	ENOG4105FSR	swimming returnes to normal when residues 206-207 are both mutated to Ala. Overexpression also leads to a reduction in flagellar abundance and a 20-fold increase in c-di- GMP levels in vivo. Required for aminoglycoside-mediated induction of biofilm formation, it also plays a lesser role in biofilm production in response to other classes of translation inhibitors. The c-di-GMP produced by this enzyme up-regulates poly-GlcNAc production as well as the biofilm synthesis protein PgaD, although c-di-GMP is probably not the main inducing principle. Cyclic-di- GMP is a second messenger which controls cell surface-associated traits in bacteria
FE785_08975	ENOG4105C4H	Specifically methylates the guanine in position 2445 (m2G2445) and the guanine in position 2069 (m7G2069) of 23S rRNA (By similarity)
FE785_08980	ENOG4105CVE	Lytic murein transglycosylase
FE785_08995	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)
FE785_09010	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)
FE785_09020	ENOG4105M02	This protein specifically catalyzes the removal of signal peptides from prolipoproteins (By similarity)
FE785_09025	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)
FE785_09030	ENOG4105DTN	riboflavin biosynthesis protein ribF
FE785_09035	ENOG4105CJR	Integral membrane protein (MviN
FE785_09045	ENOG4105VCH	membrane
FE785_09050	ENOG4105KQV	Binds directly to 16S ribosomal RNA (By similarity)
FE785_09055	ENOG4108UXA	Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA (By similarity)
FE785_09060	ENOG4105KEM	Functions as a ribosomal silencing factor. Interacts with ribosomal protein L14 (rplN), blocking formation of intersubunit bridge B8. Prevents association of the 30S and 50S ribosomal subunits and the formation of functional ribosomes, thus repressing translation (By similarity)
FE785_09065	ENOG4108Z1W	Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) (By similarity)
FE785_09070	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)
FE785_09085	ENOG4105C8T	Leucyl-tRNA synthetase
FE785_09095	ENOG4105CE8	Transfers the fatty acyl group on membrane lipoproteins (By similarity)
FE785_09100	ENOG4108JU5	Magnesium and cobalt efflux protein
FE785_09105	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)
FE785_09110	ENOG4105C9A	Phoh family
FE785_09115	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)
FE785_09135	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FE785_09140	ENOG4108VAU	general secretion pathway protein G
FE785_09180	ENOG4108UJD	30S ribosomal protein S9
FE785_09185	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)
FE785_09200	ENOG4105F4R	Transcriptional regulator mode
FE785_09205	ENOG4105BZU	Histidine kinase
FE785_09215	ENOG4105BZH	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
FE785_09220	ENOG4108RNI	3'(2')5'-bisphosphate nucleotidase
FE785_09225	ENOG4107RK2	ADP-ribose diphosphatase NudE
FE785_09230	ENOG4107Y3D	HAD-superfamily hydrolase subfamily IA variant 3
FE785_09235	ENOG4105FQ6	thiopurine methyltransferase
FE785_09245	ENOG4105IH7	synthase
FE785_09250	ENOG4105C5H	ABC transporter
FE785_09255	ENOG4105E05	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
FE785_09260	ENOG4105C8Q	Methyl-accepting chemotaxis
FE785_09270	ENOG4108AEY	RNA polymerase sigma factor
FE785_09275	ENOG4108IPX	Part of the ABC transporter complex HmuTUV involved in hemin import. Responsible for energy coupling to the transport system (By similarity)
FE785_09280	ENOG4105EHG	Permease protein
FE785_09285	ENOG4107S2Z	UPF0761 membrane protein
FE785_09300	ENOG4105E18	UPF0276 protein
FE785_09310	ENOG4107S0N	DJ-1 family
FE785_09315	ENOG4105CN1	protease
FE785_09320	ENOG41080HT	Transcriptional regulator, arsr family
FE785_09335	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FE785_09340	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)
FE785_09345	ENOG4105KTH	gatB Yqey
FE785_09350	ENOG4105VCC	30S ribosomal protein S21
FE785_09355	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)
FE785_09360	ENOG4105K7Z	Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP (By similarity)
FE785_09385	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
FE785_09390	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)
FE785_09395	ENOG4105CY8	phosphoribosylaminoimidazole carboxylase atpase subunit
FE785_09400	ENOG4108UM6	Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) (By similarity)
FE785_09410	ENOG4105BZU	Histidine kinase
FE785_09420	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
FE785_09425	ENOG4105SYT	Methylenetetrahydrofolate reductase
FE785_09430	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)
FE785_09440	ENOG4105D7Z	glutathione synthase
FE785_09450	ENOG4108UJU	UPF0301 protein
FE785_09455	ENOG4107Y66	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
FE785_09460	ENOG4108UK1	Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant (By similarity)
FE785_09465	ENOG4105CXT	aspartate transcarbamylase
FE785_09470	ENOG4105CD3	dihydroorotase
FE785_09485	ENOG4105CSR	polyphosphate kinase 2
FE785_09490	ENOG4105DFA	alanine racemase domain protein
FE785_09500	ENOG4105II7	pyrroline-5-carboxylate reductase
FE785_09505	ENOG4108VIA	integral membrane protein
FE785_09510	ENOG4105DWV	Homoserine O-trans-acetylase
FE785_09515	ENOG4105DWV	Homoserine O-trans-acetylase
FE785_09520	ENOG4105BZU	Histidine kinase
FE785_09550	ENOG4106CJB	Phospholipase Carboxylesterase
FE785_09560	ENOG4105CU5	Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine (By similarity)
FE785_09570	ENOG4105DR4	Methyltransferase
FE785_09575	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)
FE785_09580	ENOG4105BZU	Histidine kinase
FE785_09585	ENOG4105KT5	UmuD protein
FE785_09590	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)
FE785_09600	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
FE785_09605	ENOG4105BZU	Histidine kinase
FE785_09610	ENOG410642E	Short chain dehydrogenase
FE785_09615	ENOG4107RSR	Malate quinone oxidoreductase
FE785_09620	ENOG4105CKI	cobalamin synthesis protein
FE785_09625	ENOG4105DZA	Converts GTP to 7,8-dihydroneopterin triphosphate (By similarity)
FE785_09635	ENOG4105F4G	Membrane
FE785_09640	ENOG4105EWT	decarboxylase family
FE785_09645	ENOG4105C1J	atp-dependent rna helicase
FE785_09660	ENOG4105D58	Diguanylate phosphodiesterase
FE785_09665	ENOG4105CD3	dihydroorotase
FE785_09675	ENOG4105BZU	Histidine kinase
FE785_09680	ENOG4105VAS	Could be involved in insertion of integral membrane proteins into the membrane (By similarity)
FE785_09690	ENOG4105C9X	ppx gppa phosphatase
FE785_09695	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)
FE785_09705	ENOG4105EFU	Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin (By similarity)
FE785_09710	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)
FE785_09720	ENOG4105CDV	Ompa motb domain protein
FE785_09750	ENOG4105EGS	Mechanosensitive ion channel
FE785_09755	ENOG4105D64	Mechanosensitive ion channel
FE785_09760	ENOG4105CAS	nag kinase
FE785_09765	ENOG4108VPT	UPF0234 protein
FE785_09770	ENOG4105CHM	Aminotransferase
FE785_09775	ENOG4105BZU	Histidine kinase
FE785_09780	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)
FE785_09785	ENOG4105BZG	amino acid carrier protein
FE785_09790	ENOG4105CJS	Phosphopantothenoylcysteine decarboxylase
FE785_09800	ENOG4105W5Q	DNA repair protein (RadC
FE785_09805	ENOG4105KDC	50s ribosomal protein l28
FE785_09810	ENOG4105W0E	50S ribosomal protein L33
FE785_09820	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)
FE785_09830	ENOG4105CGB	Part of the ABC transporter complex ModABC involved in molybdenum import. Responsible for energy coupling to the transport system (By similarity)
FE785_09835	ENOG4105E0C	molybdate abc transporter
FE785_09840	ENOG4108S6J	ABC transporter, periplasmic molybdate-binding protein
FE785_09845	ENOG4105F4R	Transcriptional regulator mode
FE785_09860	ENOG4108ZEF	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate (By similarity)
FE785_09865	ENOG4106H78	methyltransferase
FE785_09870	ENOG4105QNR	S1 RNA binding domain protein
FE785_09875	ENOG4105BZU	Histidine kinase
FE785_09890	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)
FE785_09910	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)
FE785_09920	ENOG4108194	Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis (By similarity)
FE785_09950	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)
FE785_09955	ENOG4107RY0	Catalyzes the conversion of dihydroorotate to orotate (By similarity)
FE785_09960	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)
FE785_09965	ENOG4105CSF	NADPH-dependent glycerol-3-phosphate dehydrogenase
FE785_09970	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)
FE785_09975	ENOG4105VW4	glutaredoxin 3
FE785_09985	ENOG4105CJI	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
FE785_09990	ENOG4105CBC	glutamate synthase
FE785_09995	ENOG4105BZ8	glutamate synthase
FE785_10005	ENOG4105EZI	multiple antibiotic resistance (MarC)-related protein
FE785_10025	ENOG4105BZU	Histidine kinase
FE785_10030	ENOG4105RK9	auxin efflux carrier
FE785_10035	ENOG4107QHI	-hydrogenase
FE785_10040	ENOG4105DMT	epimerase dehydratase
FE785_10055	ENOG4105CHR	reductase
FE785_10060	ENOG4105BZU	Histidine kinase
FE785_10065	ENOG4105C5I	Dehydrogenase
FE785_10070	ENOG4105BZU	Histidine kinase
FE785_10075	ENOG4105CH5	extracellular solute-binding protein, family 7
FE785_10080	ENOG4105C8Q	Methyl-accepting chemotaxis
FE785_10090	ENOG4105D05	Receptor
FE785_10100	ENOG4107QIX	Phosphoglucomutase (EC 5.4.2.2
FE785_10115	ENOG41083J0	(ABC) transporter
FE785_10120	ENOG4105C4R	Atp-dependent dna helicase
FE785_10125	ENOG4105K63	Thioredoxin
FE785_10130	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)
FE785_10135	ENOG4105NRA	50s ribosomal protein l31 type b
FE785_10145	ENOG4105CFZ	Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III (By similarity)
FE785_10150	ENOG4105D58	Diguanylate phosphodiesterase
FE785_10155	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)
FE785_10160	ENOG4105CEN	a g-specific adenine glycosylase
FE785_10165	ENOG4105CZ1	Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA (By similarity)
FE785_10175	ENOG4105CSA	Coproporphyrinogen iii oxidase
FE785_10185	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)
FE785_10190	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)
FE785_10195	ENOG4105DSJ	YicC domain protein
FE785_10205	ENOG4108JQC	penicillin-binding protein 1A
FE785_10215	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)
FE785_10220	ENOG4105BZU	Histidine kinase
FE785_10225	ENOG4105CKD	glutathione-regulated potassium-efflux system protein
FE785_10250	ENOG4105F5W	AtP-binding protein
FE785_10260	ENOG4105C59	p-type ATPase
FE785_10270	ENOG4107STQ	Multicopper oxidase
FE785_10275	ENOG4105D6P	C-type cytochrome. Part of the cbb3-type cytochrome c oxidase complex (By similarity)
FE785_10310	ENOG4106063	Acetyl-CoA carboxylase biotin carboxyl carrier protein subunit
FE785_10325	ENOG41082YX	Transcriptional regulator, arsr family
FE785_10335	ENOG4105CUC	YeeE YedE family protein
FE785_10340	ENOG4107TPS	domain protein
FE785_10345	ENOG4105C57	major facilitator superfamily
FE785_10390	ENOG4105VTR	Integrase
FE785_10415	ENOG4108Q79	6-phosphogluconolactonase (EC 3.1.1.31)
FE785_10435	ENOG4105C3Q	Glycosyl transferase, family 2
FE785_10440	ENOG4108ZFX	Mannosyl-3-phosphoglycerate phosphatase
FE785_10445	ENOG4106762	Involved in the synthesis of autoinducer 2 (AI-2) which is secreted by bacteria and is used to communicate both the cell density and the metabolic potential of the environment. The regulation of gene expression in response to changes in cell density is called quorum sensing. Catalyzes the transformation of S-ribosylhomocysteine (RHC) to homocysteine (HC) and 4,5- dihydroxy-2,3-pentadione (DPD) (By similarity)
FE785_10450	ENOG4105DUF	Catalyzes the irreversible cleavage of the glycosidic bond in both 5'-methylthioadenosine (MTA) and S- adenosylhomocysteine (SAH AdoHcy) to adenine and the corresponding thioribose, 5'-methylthioribose and S-ribosylhomocysteine, respectively (By similarity)
FE785_10455	ENOG4108R5S	membrane
FE785_10460	ENOG4105BZU	Histidine kinase
FE785_10465	ENOG4108HH9	Catalyzes two reactions the first one is the production of beta-formyl glycinamide ribonucleotide (GAR) from formate, ATP and beta GAR
FE785_10475	ENOG4105DEK	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FE785_10480	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
FE785_10485	ENOG4105DSB	aldose 1-epimerase
FE785_10490	ENOG4105D49	3-dehydroquinate synthase
FE785_10495	ENOG4105KHV	Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate (By similarity)
FE785_10500	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
FE785_10505	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
FE785_10510	ENOG4107RJC	Iron-containing alcohol dehydrogenase
FE785_10515	ENOG4105CET	Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria (By similarity)
FE785_10525	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)
FE785_10535	ENOG4105KME	endoribonuclease L-psp
FE785_10545	ENOG4105CB5	ATP-dependent DNA helicase recG
FE785_10550	ENOG4108ESY	Metal dependent phosphohydrolase
FE785_10555	ENOG4105VEI	Removes the pyruvyl group from chorismate, with concomitant aromatization of the ring, to provide 4- hydroxybenzoate (4HB) for the ubiquinone pathway (By similarity)
FE785_10560	ENOG4108NVR	Methyl-accepting chemotaxis
FE785_10575	ENOG4105C4G	Synthesis of 3-octaprenyl-4-hydroxybenzoate (By similarity)
FE785_10590	ENOG4105KNM	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
FE785_10595	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)
FE785_10600	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)
FE785_10605	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
FE785_10610	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)
FE785_10615	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)
FE785_10620	ENOG41081A3	ATP synthase f0, c subunit
FE785_10625	ENOG4105EE4	it plays a direct role in the translocation of protons across the membrane (By similarity)
FE785_10645	ENOG4107QJE	Chromosome Partitioning Protein
FE785_10650	ENOG4105D28	Specifically methylates the N7 position of a guanine in 16S rRNA (By similarity)
FE785_10655	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)
FE785_10670	ENOG4108IJ7	Glycine betaine
FE785_10675	ENOG4108HQS	Glycine betaine
FE785_10680	ENOG4105GIJ	Glycine betaine
FE785_10695	ENOG4107R1K	Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1) (By similarity)
FE785_10740	ENOG4108ZK7	protein family UPF0029, Impact, N-terminal protein
FE785_10750	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)
FE785_10760	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
FE785_10765	ENOG4105NVJ	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)
FE785_10770	ENOG4105VG0	50S ribosomal protein l34
FE785_10780	ENOG4105BZU	Histidine kinase
FE785_10785	ENOG4105HF0	Membrane