locus-tag	class	description
FA592_00105	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
FA592_00130	ENOG4108BGM	Quinol dehydrogenase periplasmic component
FA592_00140	ENOG4105DH2	Converts cobyric acid to cobinamide by the addition of aminopropanol on the F carboxylic group (By similarity)
FA592_00150	ENOG4108YZT	Adenosylcobinamide kinase
FA592_00170	ENOG4108UHF	Joins Ado-cobinamide-GDP and alpha-ribazole to generate adenosylcobalamin (Ado-cobalamin) (By similarity)
FA592_00180	ENOG4107PPM	cobalt chelatase
FA592_00185	ENOG4105EHG	Permease protein
FA592_00190	ENOG4105E0A	ABC, transporter
FA592_00200	ENOG41081F0	Precorrin-8x methylmutase
FA592_00205	ENOG4105EE8	May catalyze the methylation of C-1 in cobalt-precorrin- 5 and the subsequent extrusion of acetic acid from the resulting intermediate to form cobalt-precorrin-6A (By similarity)
FA592_00215	ENOG4107XSI	cobalt-precorrin-6y C15-methyltransferase
FA592_00220	ENOG4105DVK	Precorrin-2 c20-methyltransferase
FA592_00225	ENOG4105CIA	precorrin-4 C(11)-methyltransferase
FA592_00230	ENOG4108P62	biosynthesis protein (CbiG)
FA592_00235	ENOG4105E4R	Precorrin-3B C17-methyltransferase
FA592_00245	ENOG4108JTQ	reductase
FA592_00250	ENOG4105BZ1	(ABC) transporter
FA592_00255	ENOG4105C0Y	Responsible for the amidation of carboxylic groups at position A and C of either cobyrinic acid or hydrogenobrynic acid. NH(2) groups are provided by glutamine, and one molecule of ATP is hydrogenolyzed for each amidation (By similarity)
FA592_00265	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)
FA592_00270	ENOG4108IG5	Transcriptional regulator
FA592_00355	ENOG4105VTR	Integrase
FA592_00365	ENOG410841J	DNA-binding protein Hu
FA592_00375	ENOG4105CNU	cell division protein FtsK
FA592_00380	ENOG4107QIJ	Aconitate hydratase 2
FA592_00385	ENOG4108YZY	peptidylprolyl cis-trans isomerase
FA592_00390	ENOG4108HRN	Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate (By similarity)
FA592_00395	ENOG4105RW8	MltA-interacting MipA family protein
FA592_00405	ENOG4105C6X	Major Facilitator
FA592_00425	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
FA592_00430	ENOG4105C8Q	Methyl-accepting chemotaxis
FA592_00435	ENOG4105K4P	CoA-binding domain protein
FA592_00440	ENOG4105C7B	Threonine dehydratase
FA592_00450	ENOG4105CDA	abc transporter atp-binding protein
FA592_00455	ENOG4105DRP	amino acid AbC transporter
FA592_00460	ENOG4105EZ7	amino acid ABC transporter
FA592_00470	ENOG4105C7V	phospho-2-dehydro-3-deoxyheptonate aldolase
FA592_00485	ENOG4107T5V	SNARE associated Golgi
FA592_00490	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)
FA592_00495	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)
FA592_00500	ENOG4105CAY	ferredoxin--nadp reductase
FA592_00515	ENOG4105QTX	Pfam:UPF0153
FA592_00525	ENOG4105DK0	Indole-3-glycerol phosphate synthase
FA592_00535	ENOG4105CR7	Catalyzes the transfer of selenium from selenophosphate for conversion of 2-thiouridine to 2-selenouridine at the wobble position in tRNA (By similarity)
FA592_00540	ENOG4108JJB	ABC transporter
FA592_00555	ENOG4105CFT	Part of the energy-coupling factor (ECF) transporter complex CbiMNOQ involved in cobalt import (By similarity)
FA592_00560	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)
FA592_00565	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)
FA592_00580	ENOG4107SA8	fad-dependent pyridine nucleotide-disulfide oxidoreductase
FA592_00595	ENOG4105C7K	acetolactate synthase
FA592_00600	ENOG4108ZP8	Acetolactate synthase small subunit
FA592_00605	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)
FA592_00615	ENOG4105BZ8	glutamate synthase
FA592_00630	ENOG4108JUA	Transcriptional regulator
FA592_00640	ENOG4105CY9	nitrogenase molybdenum-iron protein beta chain
FA592_00645	ENOG4105SJ7	Fe-only nitrogenase subunit delta
FA592_00650	ENOG4107V0H	Nitrogenase protein alpha chain
FA592_00655	ENOG4105D7W	serine acetyltransferase
FA592_00660	ENOG4105DP5	Catalyzes the biosynthesis of agmatine from arginine (By similarity)
FA592_00665	ENOG4105CUT	histidyl-tRNA synthetase
FA592_00670	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
FA592_00675	ENOG4108ZEF	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate (By similarity)
FA592_00680	ENOG4108UMA	3-octaprenyl-4-hydroxybenzoate carboxy-lyase
FA592_00695	ENOG4105C8Q	Methyl-accepting chemotaxis
FA592_00700	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
FA592_00705	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
FA592_00720	ENOG4105DTC	1-(5-phosphoribosyl)-5-amino-4-imidazole-carboxylate (air) carboxylase
FA592_00725	ENOG4105DVM	PP-loop domain protein
FA592_00730	ENOG4105C8M	UPF0272 protein
FA592_00735	ENOG4105QUH	Domain of unknown function (DUF2088)
FA592_00740	ENOG4107GFK	fumarate
FA592_00760	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
FA592_00775	ENOG4105DKJ	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
FA592_00785	ENOG4108EU4	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)
FA592_00790	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)
FA592_00800	ENOG4105D49	3-dehydroquinate synthase
FA592_00810	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)
FA592_00835	ENOG4105DEN	Luciferase family
FA592_00840	ENOG4105FE9	pseudouridine synthase
FA592_00850	ENOG4105C7K	acetolactate synthase
FA592_00875	ENOG4108YXA	Membrane
FA592_00880	ENOG4107Z3H	Transcriptional regulator, TetR family
FA592_00915	ENOG4105C8Q	Methyl-accepting chemotaxis
FA592_00920	ENOG4108RAC	Rubrerythrin
FA592_00930	ENOG4105D3H	Catalyzes the decarboxylation of 3-octaprenyl-4-hydroxy benzoate to 2-octaprenylphenol (By similarity)
FA592_00935	ENOG4105D6W	Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps (By similarity)
FA592_00940	ENOG4105DRC	Na( ) H( ) antiporter that extrudes sodium in exchange for external protons (By similarity)
FA592_00945	ENOG4108YH1	overproduction of this protein in Escherichia coli inhibits the F plasmid-mediated exclusion of bacteriophage T7
FA592_00950	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)
FA592_00955	ENOG4105C7E	Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) (By similarity)
FA592_00960	ENOG4105EAH	synthase
FA592_00985	ENOG4105C6T	cysteine synthase
FA592_00990	ENOG4105BZU	Histidine kinase
FA592_00995	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)
FA592_01000	ENOG4108RIR	Molybdenum cofactor biosynthesis protein
FA592_01005	ENOG41084M5	Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid (By similarity)
FA592_01010	ENOG4105CEK	Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine (By similarity)
FA592_01020	ENOG4105D2N	Aldolase
FA592_01025	ENOG4105EIN	peptidylprolyl cis-trans isomerase
FA592_01030	ENOG4105CSM	endonuclease III
FA592_01040	ENOG4105CIN	aminoacyl-histidine dipeptidase
FA592_01050	ENOG4105PFA	Catalyzes the conversion of 5-hydroxyuridine (ho5U) to 5-methoxyuridine (mo5U) at position 34 in tRNA (By similarity)
FA592_01065	ENOG4105C4K	Nad synthetase
FA592_01070	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
FA592_01075	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)
FA592_01080	ENOG4105CAS	nag kinase
FA592_01085	ENOG4107QID	Threonine synthase
FA592_01090	ENOG4105CET	Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria (By similarity)
FA592_01100	ENOG4105CSR	polyphosphate kinase 2
FA592_01105	ENOG4105DHT	Metal Dependent Phosphohydrolase
FA592_01110	ENOG4105CFG	Acts as a chaperone (By similarity)
FA592_01115	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
FA592_01120	ENOG4108122	heat-inducible transcription repressor
FA592_01130	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
FA592_01135	ENOG4108ZF1	Transcriptional regulator, BadM Rrf2 family
FA592_01140	ENOG4105D7B	Flagellar biosynthesis protein flha
FA592_01145	ENOG4108KA0	Inherit from COG: Phosphoesterase, DHHA1
FA592_01155	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)
FA592_01160	ENOG410620I	Diguanylate cyclase
FA592_01165	ENOG4105DTN	riboflavin biosynthesis protein ribF
FA592_01175	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)
FA592_01180	ENOG4105EJ9	Membrane
FA592_01190	ENOG4105EEI	dihydropteroate synthase
FA592_01205	ENOG4105CFH	Aspartokinase
FA592_01210	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)
FA592_01215	ENOG4105CSA	Coproporphyrinogen iii oxidase
FA592_01220	ENOG4105CKD	glutathione-regulated potassium-efflux system protein
FA592_01225	ENOG4105KNI	merR family transcriptional Regulator
FA592_01230	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)
FA592_01260	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
FA592_01265	ENOG4105ZGC	lipoprotein carrier protein
FA592_01270	ENOG4105BZU	Histidine kinase
FA592_01275	ENOG4105DRC	Na( ) H( ) antiporter that extrudes sodium in exchange for external protons (By similarity)
FA592_01280	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)
FA592_01290	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
FA592_01295	ENOG4108512	Could be involved in insertion of integral membrane proteins into the membrane (By similarity)
FA592_01300	ENOG4105M7T	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)
FA592_01305	ENOG4105VG0	50S ribosomal protein l34
FA592_01335	ENOG4108YYX	Globally modulates RNA abundance by binding to RNase E (Rne) and regulating its endonucleolytic activity. Can modulate Rne action in a substrate-dependent manner by altering the composition of the degradosome. Modulates RNA-binding and helicase activities of the degradosome (By similarity)
FA592_01350	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
FA592_01355	ENOG4105CN1	protease
FA592_01365	ENOG4105VR9	phosphoribosylformylglycinamidine synthase
FA592_01370	ENOG4105D21	Phosphoribosylformylglycinamidine synthase I
FA592_01380	ENOG4105E9Q	Acyl-transferase
FA592_01385	ENOG4105CJX	Molecular chaperone. Has ATPase activity (By similarity)
FA592_01405	ENOG4105C7Z	Conserved Protein
FA592_01445	ENOG4107QUV	Domain protein
FA592_01465	ENOG4108V1J	Has antioxidant activity. Could remove peroxides or H(2)O(2) (By similarity)
FA592_01485	ENOG4105DHT	Metal Dependent Phosphohydrolase
FA592_01490	ENOG4105CGY	Dna recombination protein
FA592_01500	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
FA592_01510	ENOG4105EIN	peptidylprolyl cis-trans isomerase
FA592_01515	ENOG4105CIT	This protein may be involved in anomalous filament growth. May be a component of the septum (By similarity)
FA592_01520	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)
FA592_01535	ENOG4105D0M	Protease HtpX homolog
FA592_01545	ENOG4105C5H	ABC transporter
FA592_01550	ENOG4105C8Q	Methyl-accepting chemotaxis
FA592_01560	ENOG4105VG1	fes assembly suf system protein
FA592_01575	ENOG4105DC1	bifunctional purine biosynthesis protein purh
FA592_01590	ENOG4108S4H	thioesterase Superfamily protein
FA592_01595	ENOG41066UG	Regulatory DnaK co-chaperone. Direct interaction between DnaK and DjlA is needed for the induction of the wcaABCDE operon, involved in the synthesis of a colanic acid polysaccharide capsule, possibly through activation of the RcsB RcsC phosphotransfer signaling pathway. The colanic acid capsule may help the bacterium survive conditions outside the host (By similarity)
FA592_01600	ENOG4105C87	Aminotransferase class I and II
FA592_01620	ENOG4108URH	decarboxylase
FA592_01625	ENOG4107QWP	ABC-2 type transporter
FA592_01630	ENOG4107QWP	ABC-2 type transporter
FA592_01635	ENOG4105CJ1	ABC, transporter
FA592_01640	ENOG4105D0S	secretion protein (HlyD
FA592_01645	ENOG4107MVR	Transcriptional regulator
FA592_01660	ENOG4107QIK	phosphoribosylformylglycinamidine synthase
FA592_01665	ENOG4105BZU	Histidine kinase
FA592_01675	ENOG4105DCX	Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. Together with TatB, TatC is part of a receptor directly interacting with Tat signal peptides (By similarity)
FA592_01680	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)
FA592_01705	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
FA592_01710	ENOG4105BZU	Histidine kinase
FA592_01715	ENOG4105CY0	Metallo-Beta-Lactamase
FA592_01730	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)
FA592_01735	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)
FA592_01740	ENOG4105CZN	Potassium uptake protein
FA592_01745	ENOG4107ZYR	domain protein
FA592_01750	ENOG4105E0X	reductase
FA592_01765	ENOG4105MFX	4-diphosphocytidyl-2c-methyl-d-erythritol synthase
FA592_01770	ENOG4107P0T	Selenium-dependent molybdenum hydroxylase system protein, YqeB family
FA592_01775	ENOG4105DZS	Phenylacetate-CoA ligase
FA592_01790	ENOG41089UC	methyltransferase, type 11
FA592_01810	ENOG4105BZU	Histidine kinase
FA592_01855	ENOG4107WTJ	Methyl-accepting chemotaxis sensory transducer
FA592_01860	ENOG4108NIW	Leucine export protein LeuE
FA592_01865	ENOG4108594	Permease of the drug metabolite transporter
FA592_01870	ENOG4105C8Q	Methyl-accepting chemotaxis
FA592_01880	ENOG4105BZU	Histidine kinase
FA592_01885	ENOG4108YZA	Nitrogen regulatory protein pii
FA592_01900	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
FA592_01905	ENOG4105C38	Glycyl-tRNA synthetase beta subunit
FA592_01925	ENOG4105NBK	UPF0345 protein
FA592_01930	ENOG4105BZU	Histidine kinase
FA592_01935	ENOG4105CBX	hi0933 family
FA592_01945	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)
FA592_01950	ENOG4105CIY	formyltetrahydrofolate deformylase
FA592_01970	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)
FA592_01975	ENOG4105MQS	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
FA592_01990	ENOG4105CIG	ABC transporter
FA592_02010	ENOG4107R5R	arsenical pump membrane protein
FA592_02025	ENOG4105CGK	Exodeoxyribonuclease III
FA592_02040	ENOG4105C8Q	Methyl-accepting chemotaxis
FA592_02045	ENOG4105E09	nadh pyrophosphatase
FA592_02050	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)
FA592_02055	ENOG4105DQ2	Is probably involved in the electron transfer between its heme and the molybdenum cofactor of the reductase catalytic subunit YedY (By similarity)
FA592_02060	ENOG4108VSZ	Inherit from COG: ketosteroid isomerase-like protein
FA592_02075	ENOG4105C8Q	Methyl-accepting chemotaxis
FA592_02080	ENOG4108N3W	hemolysin secretion protein
FA592_02095	ENOG4108YYH	Nadph-dependent fmn reductase
FA592_02100	ENOG4108U5N	UPF0316 protein
FA592_02105	ENOG4105BZU	Histidine kinase
FA592_02120	ENOG4105C9U	ATP-dependent DNA helicase RecQ
FA592_02135	ENOG4105C1J	atp-dependent rna helicase
FA592_02180	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)
FA592_02185	ENOG4105CR4	methylisocitrate lyase
FA592_02190	ENOG4105BZN	citrate synthase
FA592_02195	ENOG4105DXD	2-methylcitrate dehydratase
FA592_02205	ENOG4108Z8G	Alkylphosphonate utilization operon protein PhnA
FA592_02215	ENOG4108UMN	azlc family
FA592_02220	ENOG4105CGA	flagellar basal-body rod protein FlgG
FA592_02225	ENOG4105CGA	flagellar basal-body rod protein FlgG
FA592_02230	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FA592_02240	ENOG4105KVH	Transcriptional regulator
FA592_02255	ENOG4105D7X	high-affinity nickel-transporter
FA592_02260	ENOG4105FDK	ABC transporter
FA592_02265	ENOG4105FAV	ABC, transporter
FA592_02285	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)
FA592_02290	ENOG4107QN1	sodium solute
FA592_02295	ENOG41062QD	Membrane
FA592_02300	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
FA592_02315	ENOG41076HS	cation diffusion facilitator family transporter
FA592_02320	ENOG4105CE1	Ferrous iron transport protein b
FA592_02325	ENOG4107K9B	ferrous iron transport protein
FA592_02350	ENOG4105X1Q	TOBE domain protein
FA592_02355	ENOG4107VIJ	nudix hydrolase
FA592_02360	ENOG4105D7N	magnesium and cobalt transport protein CorA
FA592_02365	ENOG4105DR5	peptidase
FA592_02370	ENOG4105MRU	Plasminogen-binding protein
FA592_02375	ENOG4105CQB	FAD linked oxidase domain protein
FA592_02380	ENOG4107S2Z	UPF0761 membrane protein
FA592_02390	ENOG4105CDU	Replicative dna helicase
FA592_02395	ENOG4105C4E	Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate (By similarity)
FA592_02400	ENOG4105C25	Primosomal protein n'
FA592_02430	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)
FA592_02440	ENOG4105CUU	Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) (By similarity)
FA592_02445	ENOG4108Z0R	Transferase
FA592_02450	ENOG4105DE5	Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity (By similarity)
FA592_02455	ENOG4108ZGB	N-(5'-phosphoribosyl)anthranilate isomerase
FA592_02460	ENOG4105DJV	ribulose-phosphate 3-epimerase
FA592_02465	ENOG4105VB9	50S ribosomal protein l28
FA592_02470	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)
FA592_02485	ENOG4105D48	metallophosphoesterase
FA592_02490	ENOG4108JA2	transcriptioN-repair coupling factor
FA592_02500	ENOG4105DR5	peptidase
FA592_02505	ENOG4105DPM	folylpolyglutamate synthase Dihydrofolate synthase
FA592_02510	ENOG4105BZU	Histidine kinase
FA592_02520	ENOG4105C8T	Leucyl-tRNA synthetase
FA592_02525	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)
FA592_02530	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)
FA592_02535	ENOG4105VIE	preprotein translocase, subunit YajC
FA592_02540	ENOG4105CE8	Transfers the fatty acyl group on membrane lipoproteins (By similarity)
FA592_02545	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
FA592_02555	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)
FA592_02565	ENOG4105KAE	Involved in the modulation of the specificity of the ClpAP-mediated ATP-dependent protein degradation (By similarity)
FA592_02580	ENOG4107Z7S	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
FA592_02585	ENOG41085EF	Carbon storage regulator
FA592_02590	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
FA592_02595	ENOG4105C4R	Atp-dependent dna helicase
FA592_02600	ENOG4105DUM	transcriptional regulator, lysR family
FA592_02630	ENOG4105CRQ	synthase (Component I)
FA592_02635	ENOG4105CXT	aspartate transcarbamylase
FA592_02645	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)
FA592_02675	ENOG4105V3S	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)
FA592_02680	ENOG4105VB6	UPF0109 protein
FA592_02690	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
FA592_02695	ENOG4105EI2	Pseudouridine synthase
FA592_02700	ENOG4105D8A	3-Deoxy-D-manno-octulosonic-acid transferase
FA592_02710	ENOG4105EGD	dinuclear metal center protein, YbgI family
FA592_02715	ENOG4107QIB	glycyl-tRNA synthetase, alpha subunit
FA592_02725	ENOG4108UM6	Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) (By similarity)
FA592_02730	ENOG4105CFP	Peptidase U32
FA592_02740	ENOG4107RVV	histidinol phosphate phosphatase, hisj family
FA592_02745	ENOG4105C5F	glutamine synthetase
FA592_02750	ENOG4108JQC	penicillin-binding protein 1A
FA592_02755	ENOG4108JQ6	ABC transporter
FA592_02760	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)
FA592_02765	ENOG4107YJQ	MAF-like protein
FA592_02775	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)
FA592_02800	ENOG4107EXU	Short-chain dehydrogenase reductase Sdr
FA592_02805	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
FA592_02810	ENOG4105DRI	Involved in the oxidation of myo-inositol (MI) to 2- keto-myo-inositol (2KMI or 2-inosose) (By similarity)
FA592_02815	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
FA592_02820	ENOG4105CJN	penicillin-binding protein
FA592_02830	ENOG4108ZC9	flagellar basal-body rod protein flgc
FA592_02835	ENOG4105K88	Structural component of flagellum, the bacterial motility apparatus. Part of the rod structure of flagellar basal body (By similarity)
FA592_02840	ENOG4105CNI	cell division protein FtsW
FA592_02875	ENOG4105HKU	nucleoside recognition domain-containing protein
FA592_02885	ENOG4108TVT	permease
FA592_02925	ENOG4105DDQ	anthranilate synthase
FA592_02940	ENOG4107EP5	CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Functions as a ssRNA-specific endoribonuclease (By similarity)
FA592_02950	ENOG4105DYN	CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Acts as a dsDNA endonuclease. May be involved in the integration of spacer DNA into the CRISPR cassette (By similarity)
FA592_03115	ENOG4108J8Q	Catalyzes the facilitated diffusion of 2-acyl-glycero-3- phosphoethanolamine (2-acyl-GPE) into the cell (By similarity)
FA592_03125	ENOG41082BM	Transcriptional regulator, arsr family
FA592_03140	ENOG4105CHY	citrate lyase, alpha
FA592_03145	ENOG4105CI0	Citrate lyase
FA592_03150	ENOG4105XGS	Covalent carrier of the coenzyme of citrate lyase (By similarity)
FA592_03155	ENOG4105DUA	(citrate (pro-3S)-lyase ligase
FA592_03165	ENOG4105D94	Major Facilitator Superfamily
FA592_03175	ENOG4105C7N	Xanthine uracil vitamin C permease
FA592_03180	ENOG4105DVY	radical SAM domain protein
FA592_03190	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)
FA592_03200	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
FA592_03210	ENOG4105E1P	Modifies, by uridylylation or deuridylylation the PII (GlnB) regulatory protein (By similarity)
FA592_03215	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
FA592_03220	ENOG4105BZU	Histidine kinase
FA592_03240	ENOG4105BZU	Histidine kinase
FA592_03250	ENOG4105EYW	Ion transport protein
FA592_03270	ENOG4105C5H	ABC transporter
FA592_03275	ENOG4105EQD	regulatoR
FA592_03285	ENOG4108RC0	Electron transport protein
FA592_03290	ENOG4105CJG	carbon-monoxide dehydrogenase catalytic subunit
FA592_03295	ENOG41080XS	Cobyrinic acid ac-diamide synthase
FA592_03300	ENOG4108MFN	small subunit of hydrogenase-3, iron-sulfur protein (part of formate hydrogenlyase (FHL) complex)
FA592_03310	ENOG4107TDF	Formate hydrogenlyase subunit 4
FA592_03315	ENOG4107WQX	hydrogenase 4 membrane subunit
FA592_03320	ENOG4108JPZ	Monovalent cation H antiporter subunit D
FA592_03325	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)
FA592_03335	ENOG4105C47	NADH ubiquinone oxidoreductase 20 kda subunit
FA592_03370	ENOG4105CUZ	uba thif-type nad fad binding protein
FA592_03385	ENOG4105EJ3	Catalyzes the conversion of the cyclic tetrahydrodipicolinate (THDP) into the acyclic N-succinyl-L-2- amino-6-oxopimelate using succinyl-CoA (By similarity)
FA592_03390	ENOG4105D1F	ATP-binding protein
FA592_03395	ENOG4108UH8	Involved in the biosynthesis of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP), two major building blocks of isoprenoid compounds. Catalyzes the conversion of 4- diphosphocytidyl-2-C-methyl-D-erythritol 2-phosphate (CDP-ME2P) to 2-C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-CPP) with a corresponding release of cytidine 5-monophosphate (CMP) (By similarity)
FA592_03415	ENOG4108YYC	ycei family
FA592_03420	ENOG4108ZK7	protein family UPF0029, Impact, N-terminal protein
FA592_03425	ENOG4108PQF	modD protein
FA592_03440	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
FA592_03445	ENOG4105E0C	molybdate abc transporter
FA592_03460	ENOG4105F4R	Transcriptional regulator mode
FA592_03465	ENOG4105DZ1	carboxypeptidase
FA592_03470	ENOG4105II7	pyrroline-5-carboxylate reductase
FA592_03475	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)
FA592_03480	ENOG4105C19	ABC transporter
FA592_03505	ENOG4105D64	Mechanosensitive ion channel
FA592_03510	ENOG4105BZU	Histidine kinase
FA592_03525	ENOG4105F5P	DNA-damage-inducible protein d
FA592_03635	ENOG4106EG9	Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) (By similarity)
FA592_03640	ENOG4105M7K	Involved in the transcription termination process (By similarity)
FA592_03645	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)
FA592_03655	ENOG4105CXR	Phospho-2-dehydro-3-deoxyoctonate aldolase
FA592_03660	ENOG4108JHT	EamA-like transporter family
FA592_03665	ENOG4105D64	Mechanosensitive ion channel
FA592_03670	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
FA592_03685	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)
FA592_03695	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)
FA592_03700	ENOG4106PT6	cdpdiacylglycerol-serine O-phosphatidyltransferase
FA592_03710	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)
FA592_03715	ENOG4107RQ5	Methylates ribosomal protein L11 (By similarity)
FA592_03720	ENOG4108VYJ	response regulator receiver protein
FA592_03725	ENOG4105CJV	Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase
FA592_03730	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)
FA592_03745	ENOG4105C5E	polysaccharide biosynthesis protein
FA592_03750	ENOG4105ESV	Glycosyl transferase, family 4
FA592_03760	ENOG4108RT7	Glycosyl transferase, family 2
FA592_03770	ENOG4105H63	Glycosyl transferase, family 2
FA592_03775	ENOG4108UW5	maltose o-acetyltransferase
FA592_03780	ENOG4107YYJ	Glycosyl transferase, family 2
FA592_03790	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
FA592_03800	ENOG4105C7K	acetolactate synthase
FA592_03805	ENOG4105FAW	cDP-glucose 4,6-dehydratase
FA592_03810	ENOG4105EJZ	Glucose-1-phosphate cytidylyltransferase
FA592_03820	ENOG4108URP	Dtdp-4-dehydrorhamnose 3,5-epimerase
FA592_03830	ENOG4105C1B	dTDP-glucose 4-6-dehydratase
FA592_03835	ENOG4108I19	Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis (By similarity)
FA592_03840	ENOG4107QKV	phosphomannomutase
FA592_03850	ENOG4105D16	lipopolysaccharide heptosyltransferase i
FA592_03865	ENOG4105XA0	heptosyltransferase ii
FA592_03885	ENOG4105F55	Catalyzes the isomerization of sedoheptulose 7-phosphate in D-glycero-D-manno-heptose 7-phosphate (By similarity)
FA592_03890	ENOG4105DW0	Catalyzes the ADP transfer to D-glycero-D-manno-heptose 1-phosphate, yielding ADP-D,D-heptose (By similarity)
FA592_03895	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)
FA592_03925	ENOG4105BZU	Histidine kinase
FA592_03930	ENOG4108PCN	EamA-like transporter family
FA592_03940	ENOG4105BZU	Histidine kinase
FA592_03945	ENOG4108V1J	Has antioxidant activity. Could remove peroxides or H(2)O(2) (By similarity)
FA592_03955	ENOG4105DBW	Multi-copper polyphenol oxidoreductase laccase
FA592_03960	ENOG4108R6K	riboflavin synthase, subunit alpha
FA592_03965	ENOG4105C8Q	Methyl-accepting chemotaxis
FA592_03970	ENOG4107R7A	Allophanate hydrolase subunit 2
FA592_03980	ENOG4105E7W	lamb ycsf family protein
FA592_03985	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)
FA592_03990	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)
FA592_03995	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)
FA592_04000	ENOG4105EIX	cytochrome c1
FA592_04010	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)
FA592_04015	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
FA592_04020	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
FA592_04025	ENOG4105CHR	reductase
FA592_04030	ENOG4105CJI	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
FA592_04040	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
FA592_04050	ENOG4105D3Q	Sugar transferase
FA592_04060	ENOG4108TJN	glycosyl transferase group 1
FA592_04065	ENOG4107TXM	Nad-dependent epimerase dehydratase
FA592_04070	ENOG4105C0K	Gdp-mannose 4,6-dehydratase
FA592_04085	ENOG4105CKK	Glycosyl transferase, family 2
FA592_04100	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
FA592_04105	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)
FA592_04125	ENOG4105C1B	dTDP-glucose 4-6-dehydratase
FA592_04130	ENOG4108I19	Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis (By similarity)
FA592_04155	ENOG4105EY8	ABC transporter
FA592_04165	ENOG4105CJT	Mannose-1-phosphate guanylyltransferase
FA592_04170	ENOG4105CMR	udp-glucose 4-epimerase
FA592_04175	ENOG4105DB1	molybdopterin oxidoreductase
FA592_04185	ENOG4105QA4	4Fe-4S Ferredoxin, iron-sulfur binding domain protein
FA592_04195	ENOG4105ETX	regulatoR
FA592_04200	ENOG4108KCW	iron-sulfur cluster binding
FA592_04210	ENOG4108N5C	SNARE associated Golgi protein-related protein
FA592_04215	ENOG4108M8H	domain protein
FA592_04235	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
FA592_04250	ENOG4105C1J	atp-dependent rna helicase
FA592_04255	ENOG4108UPT	UPF0178 protein
FA592_04260	ENOG4105CPC	Aldo Keto reductase
FA592_04265	ENOG4108RWP	Major Facilitator Superfamily protein
FA592_04270	ENOG4105CF7	AraC family transcriptional regulator
FA592_04285	ENOG4107QMV	Part of the ABC transporter complex PstSACB involved in phosphate import (By similarity)
FA592_04290	ENOG4105C8U	phosphate abc transporter
FA592_04295	ENOG4105E2Z	phosphate ABC transporter (Permease
FA592_04300	ENOG4105BZY	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
FA592_04310	ENOG4105C8E	extradiol ring-cleavage dioxygenase class IIi protein subunit b
FA592_04315	ENOG4108NVR	Methyl-accepting chemotaxis
FA592_04330	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
FA592_04340	ENOG4105NAU	thioesterase Superfamily protein
FA592_04360	ENOG4105KVH	Transcriptional regulator
FA592_04365	ENOG4108K2R	Glutathione-regulated potassium-efflux system ancillary protein
FA592_04370	ENOG4105BZU	Histidine kinase
FA592_04375	ENOG4105FD2	Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) (By similarity)
FA592_04380	ENOG4105EIZ	Catalyzes the conversion of 6-carboxy-5,6,7,8- tetrahydropterin (CPH4) to 7-carboxy-7-deazaguanine (CDG) (By similarity)
FA592_04425	ENOG4105C57	major facilitator superfamily
FA592_04430	ENOG4105ENJ	RND efflux system, outer membrane lipoprotein
FA592_04435	ENOG4105BZS	acriflavin resistance protein
FA592_04440	ENOG4105C1P	efflux transporter, rnd family, mfp subunit
FA592_04455	ENOG4108ZPB	UPF0306 protein
FA592_04460	ENOG4107QV7	Involved in the import of serine and threonine into the cell, with the concomitant import of sodium (symport system) (By similarity)
FA592_04490	ENOG4105D95	Oxidoreductase required for the transfer of electrons from pyruvate to flavodoxin (By similarity)
FA592_04500	ENOG4107QPK	)-transporter
FA592_04530	ENOG4105CF7	AraC family transcriptional regulator
FA592_04535	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
FA592_04555	ENOG4107QW4	alcohol dehydrogenase
FA592_04570	ENOG4108HH9	Catalyzes two reactions the first one is the production of beta-formyl glycinamide ribonucleotide (GAR) from formate, ATP and beta GAR
FA592_04585	ENOG4108UJD	30S ribosomal protein S9
FA592_04590	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)
FA592_04595	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
FA592_04635	ENOG4105EUH	cytochrome C oxidase, cbb3-type, subunit i
FA592_04640	ENOG4108RQS	Two component transcriptional regulator (Winged helix family
FA592_04655	ENOG4105C1M	carbamoyl-phosphate synthetase glutamine chain
FA592_04675	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
FA592_04680	ENOG4105CYE	ATP phosphoribosyltransferase regulatory subunit
FA592_04685	ENOG4107UUH	Aminotransferase
FA592_04690	ENOG4105C8Q	Methyl-accepting chemotaxis
FA592_04695	ENOG4105C8Q	Methyl-accepting chemotaxis
FA592_04700	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)
FA592_04715	ENOG4105C0H	protease
FA592_04720	ENOG41084FT	Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection (By similarity)
FA592_04725	ENOG4108Z2X	Catalyzes the pyruvoyl-dependent decarboxylation of aspartate to produce beta-alanine (By similarity)
FA592_04730	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)
FA592_04745	ENOG4108ZT0	50S ribosomal protein l17
FA592_04750	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
FA592_04760	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)
FA592_04765	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
FA592_04770	ENOG41067V7	50S ribosomal protein L36
FA592_04775	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)
FA592_04780	ENOG4105CA1	Removes the N-terminal methionine from nascent proteins (By similarity)
FA592_04785	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)
FA592_04790	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
FA592_04795	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)
FA592_04800	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)
FA592_04815	ENOG41082QR	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)
FA592_04820	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
FA592_04825	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
FA592_04830	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
FA592_04835	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
FA592_04840	ENOG41084HJ	50s ribosomal protein l29
FA592_04850	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
FA592_04855	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)
FA592_04860	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
FA592_04875	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)
FA592_04880	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)
FA592_04900	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
FA592_04905	ENOG4107SJW	iron permease, FTR1
FA592_04930	ENOG4108EE5	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)
FA592_04950	ENOG4105CE1	Ferrous iron transport protein b
FA592_04955	ENOG4105D10	5-enolpyruvylshikimate-3-phosphate phospholyase
FA592_04960	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)
FA592_04965	ENOG4108UMW	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
FA592_04975	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)
FA592_04980	ENOG4105CDH	Citrulline--aspartate ligase
FA592_04985	ENOG4107YTP	response regulator receiver protein
FA592_04995	ENOG4105BZU	Histidine kinase
FA592_05000	ENOG4105BZU	Histidine kinase
FA592_05005	ENOG4105BZU	Histidine kinase
FA592_05010	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
FA592_05015	ENOG4108Z4W	Probably deamidates glutamine residues to glutamate on methyl-accepting chemotaxis receptors (MCPs), playing an important role in chemotaxis (By similarity)
FA592_05040	ENOG4105BZU	Histidine kinase
FA592_05045	ENOG4105CBS	Chea signal transduction histidine kinase
FA592_05055	ENOG4105C8Q	Methyl-accepting chemotaxis
FA592_05060	ENOG4108V3W	Chemotaxis protein, CheW
FA592_05070	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)
FA592_05095	ENOG4105D7X	high-affinity nickel-transporter
FA592_05100	ENOG4105D7X	high-affinity nickel-transporter
FA592_05110	ENOG4108TGK	Low-potential electron donor to a number of redox enzymes (By similarity)
FA592_05120	ENOG4105N14	lysine exporter protein LysE YggA
FA592_05155	ENOG410829K	Lysine exporter protein (Lyse ygga)
FA592_05165	ENOG4105BZU	Histidine kinase
FA592_05170	ENOG4105FR1	rard protein
FA592_05180	ENOG41062D9	Histidine kinase
FA592_05185	ENOG4105DIJ	Phosphoethanolamine transferase
FA592_05195	ENOG4107XTP	(EAL) domain protein
FA592_05210	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
FA592_05215	ENOG4107RT4	flavin reductase domain protein
FA592_05220	ENOG4105DCU	2-hydroxyglutaryl-CoA dehydratase
FA592_05225	ENOG4105CIZ	coA-substrate-specific enzyme activase
FA592_05230	ENOG4105S10	periplasmic binding protein
FA592_05245	ENOG4108IJ0	Aspartate ammonia-lyase
FA592_05260	ENOG4105HDK	L-asparaginase
FA592_05265	ENOG4105BZU	Histidine kinase
FA592_05270	ENOG4105XJC	Two component transcriptional regulator (Winged helix family
FA592_05275	ENOG4105E8T	Facilitates the functional incorporation of the urease nickel metallocenter. This process requires GTP hydrolysis, probably effectuated by UreG (By similarity)
FA592_05290	ENOG4105CQM	Urea amidohydrolase subunit alpha
FA592_05295	ENOG4108YZ9	Urea amidohydrolase subunit gamma
FA592_05305	ENOG4108IV0	ABC, transporter
FA592_05310	ENOG4105C0Z	ABC transporter
FA592_05320	ENOG4105C32	Amino acid ABC transporter (Permease)
FA592_05335	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
FA592_05350	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
FA592_05390	ENOG4105EAB	amino acid AbC transporter
FA592_05395	ENOG4105E5Q	amino acid AbC transporter
FA592_05430	ENOG4105C52	Atpase, p-type (Transporting), had superfamily, subfamily ic
FA592_05470	ENOG4105D4F	Synthesizes selenophosphate from selenide and ATP (By similarity)
FA592_05475	ENOG4105VFE	sira family
FA592_05485	ENOG4105CHQ	Murein-degrading enzyme that degrades murein glycan strands and insoluble, high-molecular weight murein sacculi, with the concomitant formation of a 1,6-anhydromuramoyl product. Lytic transglycosylases (LTs) play an integral role in the metabolism of the peptidoglycan (PG) sacculus. Their lytic action creates space within the PG sacculus to allow for its expansion as well as for the insertion of various structures such as secretion systems and flagella (By similarity)
FA592_05490	ENOG4105BZU	Histidine kinase
FA592_05500	ENOG4105DXB	Major Facilitator superfamily
FA592_05525	ENOG41078M4	ABC transporter
FA592_05530	ENOG4107A5B	Binding-protein-dependent transport systems, inner membrane component
FA592_05535	ENOG4105C8W	ABC transporter
FA592_05545	ENOG4107H9G	Necessary for formate dehydrogenase activity (By similarity)
FA592_05555	ENOG4105QAX	Iron-sulfur
FA592_05580	ENOG4105E0A	ABC, transporter
FA592_05585	ENOG4105EHG	Permease protein
FA592_05590	ENOG4105S10	periplasmic binding protein
FA592_05595	ENOG4108M8W	Monooxygenase
FA592_05610	ENOG4105M15	transport protein ExbD
FA592_05615	ENOG4105M8K	biopolymer transport protein
FA592_05620	ENOG4105F4R	Transcriptional regulator mode
FA592_05640	ENOG4108BSC	Methyltransferase
FA592_05650	ENOG4108IJ6	ABC transporter
FA592_05655	ENOG4105ECW	sulfate abc transporter
FA592_05660	ENOG4107Z6A	sulfate abc transporter permease
FA592_05665	ENOG4105DE7	Sulfate ABC transporter periplasmic sulfate-binding protein
FA592_05670	ENOG4105WMR	Protein CrcB homolog
FA592_05710	ENOG4105QAX	Iron-sulfur
FA592_05740	ENOG4105C08	Histidine kinase
FA592_05750	ENOG4105C1Y	Converts seryl-tRNA(Sec) to selenocysteinyl-tRNA(Sec) required for selenoprotein biosynthesis (By similarity)
FA592_05755	ENOG4105EM7	Selenocysteine-specific translation elongation factor
FA592_05775	ENOG4105C2I	pirin domain protein
FA592_05825	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)
FA592_05830	ENOG4105CKK	Glycosyl transferase, family 2
FA592_05840	ENOG4105CHR	reductase
FA592_05860	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)
FA592_05895	ENOG4105C1J	atp-dependent rna helicase
FA592_05925	ENOG4108KS2	transglutaminase domain protein
FA592_05935	ENOG4105DVP	Adenine-specific
FA592_05940	ENOG4108VYJ	response regulator receiver protein
FA592_05960	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
FA592_05980	ENOG4108UMI	ABC transporter, permease
FA592_06025	ENOG4108NVR	Methyl-accepting chemotaxis
FA592_06030	ENOG4105E1F	short-chain dehydrogenase reductase
FA592_06045	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)
FA592_06055	ENOG4107RDB	Major Facilitator
FA592_06060	ENOG4105W39	Membrane
FA592_06075	ENOG4107QPK	)-transporter
FA592_06080	ENOG4105S10	periplasmic binding protein
FA592_06090	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
FA592_06095	ENOG4108ZEX	molybdopterin converting factor, subunit 2
FA592_06105	ENOG4107XTC	May be involved in the formation or repair of Fe-S clusters present in iron-sulfur proteins
FA592_06115	ENOG4108JIR	Flagellum-specific ATP synthase
FA592_06120	ENOG4105EUJ	GTP cyclohydrolase i
FA592_06130	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)
FA592_06145	ENOG4105C0P	Mg chelatase subunit ChlI
FA592_06150	ENOG4108ENG	carbohydrate kinase, YjeF related protein
FA592_06155	ENOG4108V3E	phosphoribosylglycinamide formyltransferase
FA592_06160	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)
FA592_06190	ENOG4105EYG	tyrosine recombinase. Not involved in the cutting and rejoining of the recombining DNA molecules on dif(SL) site (By similarity)
FA592_06275	ENOG4105BZS	acriflavin resistance protein
FA592_06280	ENOG4105BZS	acriflavin resistance protein
FA592_06285	ENOG4105ENJ	RND efflux system, outer membrane lipoprotein
FA592_06310	ENOG4105D1E	Undecaprenyl pyrophosphate phosphatase
FA592_06325	ENOG4105C26	Dehydrogenase
FA592_06340	ENOG4108JQ1	Dehydrogenase
FA592_06360	ENOG41061MD	high-affinity nickel-transporter
FA592_06365	ENOG4108N3W	hemolysin secretion protein
FA592_06390	ENOG4107QWP	ABC-2 type transporter
FA592_06395	ENOG4107QWP	ABC-2 type transporter
FA592_06400	ENOG4105CJ1	ABC, transporter
FA592_06405	ENOG4105D0S	secretion protein (HlyD
FA592_06415	ENOG4108DBC	nitroreductase
FA592_06460	ENOG4105I2S	Part of the ABC transporter complex hrt involved in hemin import. Responsible for the translocation of the substrate across the membrane (By similarity)
FA592_06465	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)
FA592_06475	ENOG4105D17	glycoside hydrolase, family 3 domain protein
FA592_06505	ENOG4108YYH	Nadph-dependent fmn reductase
FA592_06515	ENOG4108IXY	short-chain dehydrogenase reductase
FA592_06525	ENOG4108IJF	Heavy metal efflux pump, CzcA
FA592_06530	ENOG4105EP1	Efflux transporter rnd family, mfp subunit
FA592_06565	ENOG4105BZU	Histidine kinase
FA592_06585	ENOG4105ET3	Reduction of activated sulfate into sulfite (By similarity)
FA592_06590	ENOG4105C11	sulfate adenylyltransferase), subunit 2
FA592_06595	ENOG4105C3T	may be the GTPase, regulating ATP sulfurylase activity (By similarity)
FA592_06605	ENOG4105D06	uba thif-type nad fad binding protein
FA592_06615	ENOG4105ET1	Component of the sulfite reductase complex that catalyzes the 6-electron reduction of sulfite to sulfide. This is one of several activities required for the biosynthesis of L- cysteine from sulfate (By similarity)
FA592_06620	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)
FA592_06625	ENOG4105C28	cystathionine
FA592_06635	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
FA592_06655	ENOG4105BZU	Histidine kinase
FA592_06665	ENOG4108UXE	Protein tyrosine phosphatase
FA592_06675	ENOG4105EE5	Membrane protein terC
FA592_06680	ENOG4108XUR	Pfam:DUF178
FA592_06685	ENOG4105D82	Glutamate dehydrogenase
FA592_06690	ENOG4105CZ5	Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate (By similarity)
FA592_06695	ENOG4105C6K	Malic enzyme
FA592_06700	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)
FA592_06710	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
FA592_06715	ENOG4105KM4	Acetyl-CoA carboxylase, biotin carboxyl carrier protein
FA592_06720	ENOG4105DHP	deoxycytidine triphosphate deaminase
FA592_06740	ENOG4105DR4	Methyltransferase
FA592_06745	ENOG4107XM9	(LipO)protein
FA592_06760	ENOG4105C5E	polysaccharide biosynthesis protein
FA592_06765	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
FA592_06770	ENOG4105F0R	Cytidylyltransferase
FA592_06780	ENOG4105DVA	methyltransferase
FA592_06785	ENOG4105D2T	synthase
FA592_06790	ENOG4105VDT	-acetyltransferase
FA592_06820	ENOG4105C73	Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone (By similarity)
FA592_06825	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)
FA592_06830	ENOG4105BZN	citrate synthase
FA592_06845	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
FA592_06850	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)
FA592_06855	ENOG4105E63	Pfam:DUF178
FA592_06860	ENOG4105VS8	Flagellar biosynthetic protein fliq
FA592_06865	ENOG4105D4A	Cell wall formation (By similarity)
FA592_06870	ENOG4105CHR	reductase
FA592_06875	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)
FA592_06885	ENOG4105BZU	Histidine kinase
FA592_06905	ENOG4105DIN	metallophosphoesterase
FA592_06910	ENOG4105BZG	amino acid carrier protein
FA592_06915	ENOG4105C2W	permease
FA592_06920	ENOG4105CEA	Catalyzes the NADP-dependent rearrangement and reduction of 1-deoxy-D-xylulose-5-phosphate (DXP) to 2-C-methyl-D-erythritol 4-phosphate (MEP) (By similarity)
FA592_06925	ENOG4105KNE	Phosphatidate cytidylyltransferase
FA592_06945	ENOG4105K85	Involved in the cellular defense against the biological effects of O6-methylguanine (O6-MeG) in DNA. Repairs alkylated guanine in DNA by stoichiometrically transferring the alkyl group at the O-6 position to a cysteine residue in the enzyme. This is a suicide reaction the enzyme is irreversibly inactivated (By similarity)
FA592_06960	ENOG4107RU9	Transcriptional regulator, Crp Fnr family
FA592_06970	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
FA592_06975	ENOG41080AZ	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)
FA592_07010	ENOG4108YXW	Together with MoaA, is involved in the conversion of 5'- GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
FA592_07015	ENOG410885F	Protein of unknown function (DUF493)
FA592_07075	ENOG4105HFZ	Membrane
FA592_07090	ENOG4105D3S	4Fe-4S Ferredoxin, iron-sulfur binding domain protein
FA592_07095	ENOG4107QY8	reductase
FA592_07100	ENOG41082K6	Converts the free carboxyl group of a malonyl-thioester to its methyl ester by transfer of a methyl group from S-adenosyl- L-methionine (SAM). It allows to synthesize pimeloyl-ACP via the fatty acid synthetic pathway (By similarity)
FA592_07115	ENOG4105F8J	Adenylate Guanylate cyclase
FA592_07120	ENOG4105DHT	Metal Dependent Phosphohydrolase
FA592_07125	ENOG4105NU9	Preprotein translocase subunit SecG
FA592_07135	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)
FA592_07140	ENOG4107VCP	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)
FA592_07165	ENOG4108V0P	LemA family
FA592_07170	ENOG4105CI3	gtp-binding protein typa
FA592_07180	ENOG410822I	Flagellar hook capping protein
FA592_07185	ENOG4105BZE	flagellar hook protein, FlgE
FA592_07190	ENOG4105BZE	flagellar hook protein, FlgE
FA592_07195	ENOG41087GE	Catalyzes the formation of dTMP and tetrahydrofolate from dUMP and methylenetetrahydrofolate (By similarity)
FA592_07200	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)
FA592_07205	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)
FA592_07210	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)
FA592_07240	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)
FA592_07245	ENOG4105CEN	a g-specific adenine glycosylase
FA592_07250	ENOG4105C2C	drug resistance transporter, Bcr CflA
FA592_07265	ENOG4107GFK	fumarate
FA592_07305	ENOG4107SDU	Methyl-accepting chemotaxis
FA592_07325	ENOG4108W2Y	isochorismatase
FA592_07345	ENOG4105UEI	Transcriptional Regulator AraC Family
FA592_07355	ENOG41074MP	UPF0103 Mediator of ErbB2-driven cell motility-containing protein
FA592_07365	ENOG4105NBF	ammecr1 domain protein
FA592_07390	ENOG41063ZK	Transcriptional Regulator AraC Family
FA592_07400	ENOG4105IPS	esterase
FA592_07410	ENOG4108IEG	Formate dehydrogenase Alpha subunit
FA592_07440	ENOG4105C01	Dihydroxy-acid dehydratase
FA592_07445	ENOG41081FY	multiple antibiotic resistance (MarC)-related
FA592_07455	ENOG4105C3Y	UTP-glucose-1-phosphate uridylyltransferase
FA592_07465	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
FA592_07470	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)
FA592_07480	ENOG4105E05	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
FA592_07495	ENOG4105CJD	(Anaerobic) ribonucleoside-triphosphate reductase
FA592_07505	ENOG4105BZH	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
FA592_07510	ENOG4107QTF	adenylosuccinate lyase
FA592_07515	ENOG4105C34	Pseudouridine synthase
FA592_07520	ENOG4105FBJ	fumarylacetoacetate (faa) hydrolase
FA592_07525	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
FA592_07535	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)
FA592_07540	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)
FA592_07545	ENOG4105CN5	Metallo-Beta-Lactamase
FA592_07550	ENOG4105C2X	Arabinose 5-phosphate isomerase
FA592_07555	ENOG4105FE9	pseudouridine synthase
FA592_07580	ENOG4105VM1	flagellar
FA592_07600	ENOG4108ZQD	Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A (By similarity)
FA592_07605	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)
FA592_07615	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
FA592_07630	ENOG410813J	This protein specifically catalyzes the removal of signal peptides from prolipoproteins (By similarity)
FA592_07640	ENOG4105C22	threonyL-tRNA synthetase
FA592_07645	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)
FA592_07655	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)
FA592_07660	ENOG4105C58	cytochrome c oxidase accessory protein ccog
FA592_07670	ENOG41082DJ	30S ribosomal protein S21
FA592_07680	ENOG4108UHV	Lipoprotein
FA592_07685	ENOG4106032	Glutathionylspermidine synthase
FA592_07690	ENOG4105C5I	Dehydrogenase
FA592_07695	ENOG4108VPT	UPF0234 protein
FA592_07720	ENOG4105DIJ	Phosphoethanolamine transferase
FA592_07755	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FA592_07775	ENOG4105DHJ	ABC, transporter
FA592_07780	ENOG4105CY3	ABC transporter, permease
FA592_07795	ENOG41076UM	multiple antibiotic resistance (MarC)-related protein
FA592_07800	ENOG4105C8Q	Methyl-accepting chemotaxis
FA592_07810	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
FA592_07820	ENOG4108HWB	Non-specific O-methyltransferase that catalyzes the 2 O- methylation steps in the ubiquinone biosynthetic pathway (By similarity)
FA592_07830	ENOG4105BZU	Histidine kinase
FA592_07840	ENOG4108R5K	PPIases accelerate the folding of proteins (By similarity)
FA592_07845	ENOG4108YZA	Nitrogen regulatory protein pii
FA592_07855	ENOG4105CPC	Aldo Keto reductase
FA592_07865	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FA592_07880	ENOG4105E5Q	amino acid AbC transporter
FA592_07885	ENOG4106PMH	Extracellular solute-binding protein family 3
FA592_07920	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)
FA592_07930	ENOG4105CEY	Amp-dependent synthetase and ligase
FA592_07935	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)
FA592_07940	ENOG4105KWU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
FA592_07945	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)
FA592_07950	ENOG4105CYU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
FA592_07955	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)
FA592_07975	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)
FA592_07980	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)
FA592_07990	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)
FA592_07995	ENOG4105D65	subunit l
FA592_08000	ENOG4105C8S	subunit m
FA592_08015	ENOG4105C26	Dehydrogenase
FA592_08025	ENOG4105C4G	Synthesis of 3-octaprenyl-4-hydroxybenzoate (By similarity)
FA592_08040	ENOG4105C8Q	Methyl-accepting chemotaxis
FA592_08045	ENOG4107RHT	methyl-accepting chemotaxis sensory transducer with Pas Pac sensor
FA592_08065	ENOG4107YV6	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)
FA592_08070	ENOG41082DI	50s ribosomal protein l31
FA592_08080	ENOG4105C2N	RNA methyltransferase TrmH family group 3
FA592_08095	ENOG4105CHM	Aminotransferase
FA592_08100	ENOG4105D6E	homoserine dehydrogenase
FA592_08105	ENOG41082UM	UPF0102 protein
FA592_08110	ENOG4105K63	Thioredoxin
FA592_08115	ENOG4105C3M	thioredoxin reductase
FA592_08120	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
FA592_08130	ENOG4105N5T	Radical SAM Protein
FA592_08145	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
FA592_08155	ENOG4105CM2	brancheD-chain amino acid aminotransferase
FA592_08165	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
FA592_08170	ENOG4105XJC	Two component transcriptional regulator (Winged helix family
FA592_08180	ENOG4105WPN	DNA integration recombination invertion protein
FA592_08185	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)
FA592_08190	ENOG4105DAF	Involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
FA592_08195	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)
FA592_08210	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
FA592_08230	ENOG4105CUZ	uba thif-type nad fad binding protein
FA592_08235	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
FA592_08240	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)
FA592_08245	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)
FA592_08250	ENOG4105C0N	N-acetylglutamate semialdehyde dehydrogenase
FA592_08285	ENOG4105EAC	phosphoserine phosphatase
FA592_08295	ENOG4105CZX	twitching motility protein
FA592_08305	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
FA592_08315	ENOG4105CU5	Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine (By similarity)
FA592_08320	ENOG4105CQC	Prephenate dehydratase
FA592_08325	ENOG4105CIH	Imidazole acetol-phosphate transaminase
FA592_08330	ENOG4105C1F	The M ring may be actively involved in energy transduction (By similarity)
FA592_08335	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)
FA592_08345	ENOG4105C2V	Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) (By similarity)
FA592_08350	ENOG4105I3K	Ferric uptake regulator, Fur family
FA592_08355	ENOG4105D3R	alkyl hydroperoxide reductase
FA592_08360	ENOG4105C8Q	Methyl-accepting chemotaxis
FA592_08370	ENOG4108UGX	Major role in the synthesis of nucleoside triphosphates other than ATP. The ATP gamma phosphate is transferred to the NDP beta phosphate via a ping-pong mechanism, using a phosphorylated active-site intermediate (By similarity)
FA592_08385	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)
FA592_08390	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)
FA592_08395	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
FA592_08415	ENOG4107QVM	von Willebrand factor, type A
FA592_08435	ENOG4105E1Z	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane
FA592_08445	ENOG4105K5D	4fe-4S ferredoxin iroN-sulfur binding
FA592_08455	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FA592_08465	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)
FA592_08475	ENOG4105D18	nicotinate-nucleotide pyrophosphorylase
FA592_08480	ENOG4105D00	flagellar biosynthetic protein flhB
FA592_08495	ENOG4105VQJ	septum formation inhibitor
FA592_08530	ENOG4105K7D	Required for maturation of 30S ribosomal subunits (By similarity)
FA592_08535	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)
FA592_08560	ENOG4105BZU	Histidine kinase
FA592_08590	ENOG4105NQN	cytochrome C
FA592_08600	ENOG4105N5T	Radical SAM Protein
FA592_08605	ENOG4107QY8	reductase
FA592_08610	ENOG4105QA4	4Fe-4S Ferredoxin, iron-sulfur binding domain protein
FA592_08615	ENOG4105DVI	reductase, NrfD
FA592_08620	ENOG4105BZU	Histidine kinase
FA592_08625	ENOG4108J2R	molybdopterin oxidoreductase
FA592_08630	ENOG4105QA4	4Fe-4S Ferredoxin, iron-sulfur binding domain protein
FA592_08635	ENOG4105DVI	reductase, NrfD
FA592_08655	ENOG4105CSA	Coproporphyrinogen iii oxidase
FA592_08680	ENOG4105M15	transport protein ExbD
FA592_08685	ENOG4105M8K	biopolymer transport protein
FA592_08690	ENOG4105E2M	Manganese-dependent inorganic pyrophosphatase
FA592_08710	ENOG4105DVS	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
FA592_08725	ENOG4105CHQ	Murein-degrading enzyme that degrades murein glycan strands and insoluble, high-molecular weight murein sacculi, with the concomitant formation of a 1,6-anhydromuramoyl product. Lytic transglycosylases (LTs) play an integral role in the metabolism of the peptidoglycan (PG) sacculus. Their lytic action creates space within the PG sacculus to allow for its expansion as well as for the insertion of various structures such as secretion systems and flagella (By similarity)
FA592_08740	ENOG4105BZU	Histidine kinase
FA592_08745	ENOG4105EKD	Catalyzes the hydrolytic deamination of adenine to hypoxanthine. Plays an important role in the purine salvage pathway and in nitrogen catabolism (By similarity)
FA592_08750	ENOG4105CHR	reductase
FA592_08755	ENOG4105CF7	AraC family transcriptional regulator
FA592_08760	ENOG4107RDF	Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate (By similarity)
FA592_08765	ENOG4105DUM	transcriptional regulator, lysR family
FA592_08770	ENOG4105HMI	Membrane
FA592_08775	ENOG4108V06	Glutathione peroxidase
FA592_08780	ENOG4108JYZ	YitT family
FA592_08790	ENOG4107SYB	Catalyzes the deamination of 5-methylthioadenosine and S-adenosyl-L-homocysteine into 5-methylthioinosine and S-inosyl-L- homocysteine, respectively. Is also able to deaminate adenosine (By similarity)
FA592_08795	ENOG4108Z38	Catalyzes a trans-dehydration via an enolate intermediate (By similarity)
FA592_08800	ENOG4105DC7	peptidase M24
FA592_08805	ENOG4105K8U	2-Amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase
FA592_08810	ENOG4105FZW	flagellar biosynthesis regulator FlhF
FA592_08815	ENOG4107R21	site-determining protein
FA592_08825	ENOG4105DN4	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FA592_08830	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)
FA592_08835	ENOG4105DD5	Flagellar motor switch protein
FA592_08850	ENOG4105CKK	Glycosyl transferase, family 2
FA592_08860	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
FA592_08880	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
FA592_08885	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)
FA592_08890	ENOG4105MJ2	Competence protein
FA592_08930	ENOG4105CM3	Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate (By similarity)
FA592_08945	ENOG41082XB	radical SAM domain protein
FA592_08955	ENOG4105H1G	trap transporter solute receptor taxi family
FA592_08965	ENOG4105DFP	Integrase
FA592_09020	ENOG4105D01	(LipO)protein
FA592_09025	ENOG4108JEI	Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system (By similarity)
FA592_09030	ENOG4108UMI	ABC transporter, permease
FA592_09035	ENOG4105CJ3	phosphate transporter
FA592_09040	ENOG4105C80	Catalyzes the reversible oxidation of malate to oxaloacetate (By similarity)
FA592_09045	ENOG4107QRI	Phosphoketolase
FA592_09055	ENOG4106V2I	dimethylaminohydrolase
FA592_09090	ENOG4105BZU	Histidine kinase
FA592_09110	ENOG4105K63	Thioredoxin
FA592_09145	ENOG4105VYA	Uncharacterized conserved protein (DUF2132)
FA592_09150	ENOG4105EMU	Dehydrogenase
FA592_09160	ENOG4105C32	Amino acid ABC transporter (Permease)
FA592_09165	ENOG4105CF8	branched-chain amino acid ABC transporter, permease
FA592_09170	ENOG4105C0Z	ABC transporter
FA592_09175	ENOG4108IV0	ABC, transporter
FA592_09185	ENOG410802Z	Protein of unknown function (DUF328)
FA592_09230	ENOG4105E5V	Participates in transcription elongation, termination and antitermination (By similarity)
FA592_09235	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
FA592_09250	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)
FA592_09265	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)
FA592_09270	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)
FA592_09275	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)
FA592_09285	ENOG4105FDR	Membrane
FA592_09290	ENOG4105CV8	reductase
FA592_09300	ENOG4107QPK	)-transporter
FA592_09320	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FA592_09325	ENOG4105DEF	Extracellular solute-binding protein, family 5
FA592_09335	ENOG4105C8Q	Methyl-accepting chemotaxis
FA592_09340	ENOG4107RHT	methyl-accepting chemotaxis sensory transducer with Pas Pac sensor
FA592_09350	ENOG4108IEH	NADH dehydrogenase subunit g
FA592_09355	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)
FA592_09365	ENOG4107UFS	subunit j
FA592_09370	ENOG41080EA	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)
FA592_09375	ENOG4105D65	subunit l
FA592_09385	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)
FA592_09390	ENOG4105BZU	Histidine kinase
FA592_09415	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)
FA592_09420	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)
FA592_09425	ENOG4105KWU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
FA592_09440	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
FA592_09460	ENOG4105D28	Specifically methylates the N7 position of a guanine in 16S rRNA (By similarity)
FA592_09480	ENOG4105M2E	Channel that opens in response to stretch forces in the membrane lipid bilayer. May participate in the regulation of osmotic pressure changes within the cell (By similarity)
FA592_09490	ENOG4107T1C	Catalyzes the conversion of GTP to 2,5-diamino-6- ribosylamino-4(3H)-pyrimidinone 5'-phosphate (DARP), formate and pyrophosphate (By similarity)
FA592_09495	ENOG4105D52	delta-aminolevulinic acid dehydratase
FA592_09500	ENOG4105DBV	ornithine carbamoyltransferase
FA592_09505	ENOG4105T1H	UPF0763 protein
FA592_09510	ENOG4105D4P	Coproporphyrinogen iii oxidase
FA592_09515	ENOG4105CHG	glycolate oxidase (iron-sulfur subunit)
FA592_09530	ENOG4105K5B	UPF0225 protein
FA592_09545	ENOG4105BZU	Histidine kinase
FA592_09550	ENOG4105C3B	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
FA592_09555	ENOG4108S24	Fumarate reduCtase
FA592_09560	ENOG4105C00	Succinate dehydrogenase (Flavoprotein subunit)
FA592_09565	ENOG4105E33	succinate dehydrogenase
FA592_09575	ENOG410890F	Dynamin family
FA592_09580	ENOG4105F4G	Membrane
FA592_09585	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)
FA592_09590	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
FA592_09600	ENOG4105F6H	The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate (By similarity)
FA592_09615	ENOG4105CE9	30S ribosomal protein S2
FA592_09620	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)
FA592_09630	ENOG4105D19	Role in flagellar biosynthesis (By similarity)
FA592_09640	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
FA592_09650	ENOG4105C75	arginyL-tRNA synthetase
FA592_09660	ENOG4105BZU	Histidine kinase
FA592_09720	ENOG4105CP7	Triose-phosphate isomerase
FA592_09725	ENOG4105CSJ	Enoyl- acyl-carrier-protein reductase NADH
FA592_09735	ENOG4105CHV	Transcription elongation factor NusA
FA592_09745	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)
FA592_09770	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)
FA592_09775	ENOG4105CBM	Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 (By similarity)
FA592_09780	ENOG4107R03	Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate (By similarity)
FA592_09785	ENOG4105CG1	Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA (By similarity)
FA592_09810	ENOG4107QMP	dna polymerase iii subunits gamma and tau
FA592_09815	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)
FA592_09820	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
FA592_09850	ENOG4105CSR	polyphosphate kinase 2
FA592_09865	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)
FA592_09870	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)
FA592_09880	ENOG4108YXA	Membrane
FA592_09885	ENOG4105C1J	atp-dependent rna helicase
FA592_09890	ENOG4105DDY	UPF0142 protein ycaO
FA592_09910	ENOG410812K	response regulator receiver protein
FA592_09915	ENOG4105DR6	Trap dicarboxylate transporter, dctp subunit
FA592_09935	ENOG4105C32	Amino acid ABC transporter (Permease)
FA592_09945	ENOG4105C0Z	ABC transporter
FA592_09950	ENOG4108IV0	ABC, transporter
FA592_09955	ENOG4105CRE	cytochrome C
FA592_09995	ENOG4105CEV	competence damage-inducible protein
FA592_10000	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)
FA592_10005	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)
FA592_10010	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)
FA592_10015	ENOG4105DWV	Homoserine O-trans-acetylase
FA592_10030	ENOG4105D06	uba thif-type nad fad binding protein
FA592_10035	ENOG4107QSS	Involved in the synthesis of meso-diaminopimelate (m-DAP or DL-DAP), required for both lysine and peptidoglycan biosynthesis. Catalyzes the direct conversion of tetrahydrodipicolinate to LL-diaminopimelate, a reaction that requires three enzymes in E.coli (By similarity)
FA592_10050	ENOG4105C98	muts2 protein
FA592_10055	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)
FA592_10060	ENOG4105KME	endoribonuclease L-psp
FA592_10065	ENOG4107RSR	Malate quinone oxidoreductase
FA592_10085	ENOG4105CN1	protease
FA592_10100	ENOG4105CA9	Pyruvate kinase
FA592_10110	ENOG4105K46	50S ribosomal protein l27
FA592_10115	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
FA592_10120	ENOG4105CGT	Catalyzes the transfer of a phosphate group to glutamate to form glutamate 5-phosphate which rapidly cyclizes to 5- oxoproline (By similarity)
FA592_10125	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)
FA592_10135	ENOG4107QJE	Chromosome Partitioning Protein
FA592_10140	ENOG4105FA0	parb-like partition protein
FA592_10150	ENOG4105YF2	Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) (By similarity)
FA592_10155	ENOG4105PQH	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)
FA592_10160	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
FA592_10165	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)
FA592_10170	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)
FA592_10175	ENOG41082MC	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
FA592_10180	ENOG4105E02	MotA TolQ exbB proton channel
FA592_10185	ENOG4105M8F	Biopolymer transport protein exbD tolR
FA592_10195	ENOG4107R6Y	Involved in the TonB-independent uptake of proteins (By similarity)
FA592_10200	ENOG4105UYK	outer membrane protein a
FA592_10210	ENOG4108YZY	peptidylprolyl cis-trans isomerase
FA592_10220	ENOG4105CJF	Malonyl coA-acyl carrier protein transacylase
FA592_10225	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)
FA592_10230	ENOG4105CB3	Required for the thiolation of cytidine in position 32 of tRNA, to form 2-thiocytidine (s(2)C32) (By similarity)
FA592_10240	ENOG4105CBC	glutamate synthase
FA592_10245	ENOG4105BZ8	glutamate synthase
FA592_10255	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)
FA592_10260	ENOG4108UXA	Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA (By similarity)
FA592_10265	ENOG4105SCY	DNAK suppressor
FA592_10275	ENOG4105CEH	Catalyzes the synthesis of dihydrouridine a modified base found in the D-loop of most tRNAs (By similarity)
FA592_10295	ENOG4105DD5	Flagellar motor switch protein
FA592_10325	ENOG4105ND9	Nitrogenase-associated protein
FA592_10345	ENOG4105PYN	Pyridoxamine 5-phosphate oxidase-related
FA592_10355	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
FA592_10360	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)
FA592_10365	ENOG4105CBZ	Short-chain dehydrogenase reductase Sdr
FA592_10370	ENOG4105K56	Transcriptional regulator
FA592_10385	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)
FA592_10395	ENOG4105C85	amino acid
FA592_10400	ENOG4105HF0	Membrane
FA592_10405	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)
FA592_10410	ENOG4105CK2	sodium dicarboxylate symporter
FA592_10415	ENOG4105CK2	sodium dicarboxylate symporter
FA592_10425	ENOG4105C2M	dna polymerase I
FA592_10430	ENOG4108UI1	Probably functions as a manganese efflux pump (By similarity)
FA592_10450	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)
FA592_10470	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)
FA592_10475	ENOG4105BZU	Histidine kinase
FA592_10480	ENOG4105C8Q	Methyl-accepting chemotaxis
FA592_10485	ENOG4105CEY	Amp-dependent synthetase and ligase
FA592_10490	ENOG4105E2X	shikimate dehydrogenase
FA592_10495	ENOG4105CRQ	synthase (Component I)
FA592_10510	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)
FA592_10515	ENOG4105CRK	lysyL-tRNA synthetase
FA592_10530	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
FA592_10535	ENOG4105CZX	twitching motility protein
FA592_10540	ENOG410855J	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)
FA592_10560	ENOG4108VHG	Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis (By similarity)
FA592_10565	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)
FA592_10570	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
FA592_10575	ENOG4105BZU	Histidine kinase
FA592_10590	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)
FA592_10600	ENOG4108IYU	L-aspartate oxidase
FA592_10610	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
FA592_10630	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)
FA592_10635	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
FA592_10660	ENOG4105PV1	biotin lipoyl attachment domaiN-containing protein
FA592_10665	ENOG4105DJ1	Phosphoenolpyruvate Carboxylase
FA592_10670	ENOG4105CH7	arginosuccinase
FA592_10675	ENOG4105K59	histidine triad (HIT) protein
FA592_10680	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
FA592_10685	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
FA592_10690	ENOG4105CMY	5-enolpyruvylshikimate-3-phosphate synthase
FA592_10695	ENOG4105C48	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
FA592_10700	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)
FA592_10710	ENOG4108JQ1	Dehydrogenase
FA592_10720	ENOG4105ENT	Efflux transporter rnd family, mfp subunit
FA592_10730	ENOG4105BZS	acriflavin resistance protein
FA592_10740	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)
FA592_10745	ENOG4108NVR	Methyl-accepting chemotaxis
FA592_10765	ENOG4105D86	that it carries out the mismatch recognition step. This protein has a weak ATPase activity (By similarity)
FA592_10775	ENOG4105QNR	S1 RNA binding domain protein
FA592_10780	ENOG4105CBX	hi0933 family
FA592_10785	ENOG4105BZU	Histidine kinase
FA592_10790	ENOG4108YXA	Membrane
FA592_10795	ENOG4106492	Is required to sustain N(2)-dependent growth in the presence of low levels of carbon monoxide (CO). Probably acts by protecting the N(2) fixation ability of the nitrogenase complex, which is inactivated in the presence of CO (By similarity)
FA592_10805	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
FA592_10810	ENOG4105ENJ	RND efflux system, outer membrane lipoprotein
FA592_10835	ENOG4105ENT	Efflux transporter rnd family, mfp subunit
FA592_10840	ENOG4107RHT	methyl-accepting chemotaxis sensory transducer with Pas Pac sensor
FA592_10845	ENOG4105C8Q	Methyl-accepting chemotaxis
FA592_10855	ENOG4105C0B	DNA polymerase III (alpha subunit)
FA592_10870	ENOG41067MG	lrgb family
FA592_10880	ENOG4105DFH	Transport of potassium into the cell (By similarity)
FA592_10895	ENOG4105CNI	cell division protein FtsW
FA592_10900	ENOG4105C34	Pseudouridine synthase
FA592_10910	ENOG4105CZ1	Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA (By similarity)
FA592_10915	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)
FA592_10935	ENOG410692R	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)
FA592_10940	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)
FA592_10945	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)
FA592_10950	ENOG4105EA8	2-Nitropropane dioxygenase
FA592_10955	ENOG4105C5C	n-acetylmuramoyl-l-alanine amidase
FA592_10965	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)
FA592_10970	ENOG4105C9M	aspartyl-trna synthetase
FA592_10975	ENOG4105BZU	Histidine kinase
FA592_10985	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)
FA592_10990	ENOG4105C4F	May be involved in recombinational repair of damaged DNA (By similarity)
FA592_11000	ENOG4105F8V	Hydrolase, tatD family
FA592_11005	ENOG41068JE	domain protein
FA592_11010	ENOG4105K6T	rare lipoprotein A
FA592_11015	ENOG4105ECC	imidazole-glycerol-phosphate dehydratase
FA592_11020	ENOG4108Z4R	3-deoxy-d-manno-octulosonate 8-phosphate phosphatase
FA592_11035	ENOG4105WHM	Necessary for normal cell division and for the maintenance of normal septation (By similarity)
FA592_11050	ENOG4107RVG	penicillin-binding protein
FA592_11070	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)
FA592_11080	ENOG4105CZI	D-fructose-1,6-bisphosphate 1-phosphohydrolase class 1
FA592_11105	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)
FA592_11110	ENOG4105CX6	glutaminyL-tRNA synthetase
FA592_11150	ENOG4108W6G	cytochrome C
FA592_11155	ENOG4105EAU	Plays a role in nitrite reduction (By similarity)
FA592_11160	ENOG4105CRE	cytochrome C
FA592_11180	ENOG4105MJ9	esterase
FA592_11185	ENOG4108NIW	Leucine export protein LeuE
FA592_11190	ENOG4105CKK	Glycosyl transferase, family 2
FA592_11205	ENOG4108N5C	SNARE associated Golgi protein-related protein
FA592_11225	ENOG4105D8C	Channel that permits osmotically driven movement of water in both directions. It is involved in the osmoregulation and in the maintenance of cell turgor during volume expansion in rapidly growing cells. It mediates rapid entry or exit of water in response to abrupt changes in osmolarity (By similarity)
FA592_11235	ENOG4105EMK	carboxylate amino acid amine transporter
FA592_11270	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)
FA592_11280	ENOG4107QIW	Catalytic subunit of the periplasmic nitrate reductase (NAP). Only expressed at high levels during aerobic growth. NapAB complex receives electrons from the membrane-anchored tetraheme protein NapC, thus allowing electron flow between membrane and periplasm. Essential function for nitrate assimilation and may have a role in anaerobic metabolism (By similarity)
FA592_11285	ENOG4108BGM	Quinol dehydrogenase periplasmic component
FA592_11290	ENOG4105GXZ	Ferredoxin-type protein NapH
FA592_11295	ENOG4108ZMS	Electron transfer subunit of the periplasmic nitrate reductase complex NapAB (By similarity)
FA592_11300	ENOG4108ZNS	ferredoxin-type protein NapF
FA592_11330	ENOG4105VYW	UPF0251 protein
FA592_11350	ENOG4105C4M	(Ubiquinol oxidase) subunit I
FA592_11355	ENOG4105CFY	cytochrome d ubiquinol oxidase, subunit ii
FA592_11360	ENOG4105C3G	gtp-binding protein
FA592_11380	ENOG4105C3J	Cysteine desulfurase
FA592_11395	ENOG4105ETX	regulatoR
FA592_11410	ENOG4105VBD	cytochrome C, class I
FA592_11415	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)
FA592_11420	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)
FA592_11435	ENOG4105BZU	Histidine kinase
FA592_11445	ENOG4105C1J	atp-dependent rna helicase
FA592_11455	ENOG4105WWK	YheO domain protein
FA592_11460	ENOG4105CF3	3-Hydroxyisobutyrate dehydrogenase
FA592_11465	ENOG4108NVR	Methyl-accepting chemotaxis
FA592_11480	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)
FA592_11485	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)
FA592_11500	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
FA592_11505	ENOG4108N3W	hemolysin secretion protein
FA592_11515	ENOG4105CDY	transcriptional regulatory protein
FA592_11525	ENOG4105H1G	trap transporter solute receptor taxi family
FA592_11550	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
FA592_11555	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
FA592_11565	ENOG4105VTR	Integrase
FA592_11590	ENOG4105DFG	type I secretion outer membrane protein
FA592_11595	ENOG4108JJA	ABC, transporter
FA592_11680	ENOG4105DWK	Membrane
FA592_11685	ENOG4107XM3	UPF0442 protein
FA592_11690	ENOG4105C59	p-type ATPase
FA592_11710	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)
FA592_11715	ENOG4105K85	Involved in the cellular defense against the biological effects of O6-methylguanine (O6-MeG) in DNA. Repairs alkylated guanine in DNA by stoichiometrically transferring the alkyl group at the O-6 position to a cysteine residue in the enzyme. This is a suicide reaction the enzyme is irreversibly inactivated (By similarity)
FA592_11720	ENOG4105C8Q	Methyl-accepting chemotaxis
FA592_11725	ENOG4108UV6	Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP) (By similarity)
FA592_11740	ENOG4108UT2	hemolysin iii
FA592_11745	ENOG410829K	Lysine exporter protein (Lyse ygga)
FA592_11750	ENOG410631K	Membrane
FA592_11770	ENOG4105DE5	Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity (By similarity)
FA592_11795	ENOG4107QYE	Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation (By similarity)
FA592_11805	ENOG4105D0M	Protease HtpX homolog
FA592_11825	ENOG4105BZU	Histidine kinase
FA592_11830	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
FA592_11835	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)
FA592_11845	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
FA592_11850	ENOG4109003	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis (By similarity)
FA592_11860	ENOG4108YZG	isomerase
FA592_11865	ENOG4108Z4T	Peptidase M50
FA592_11870	ENOG4105C3F	Signal peptidase i
FA592_11875	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)
FA592_11885	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
FA592_11900	ENOG4105DKF	Catalyzes the radical-mediated transfer of the hydroxybenzyl group from 4-hydroxyphenylpyruvate (HPP) to 5-amino- 6-ribitylamino-2,4(1H,3H)-pyrimidinedione to form 7,8-didemethyl- 8-hydroxy-5-deazariboflavin (FO) (By similarity)
FA592_11910	ENOG4105CB5	ATP-dependent DNA helicase recG
FA592_11940	ENOG410821Z	Binds to the C-terminal region of flagellin, which is implicated in polymerization, and participates in the assembly of the flagellum (By similarity)
FA592_11945	ENOG410901F	(LipO)protein
FA592_11950	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)
FA592_11955	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)
FA592_11960	ENOG4108UUM	single-stranded DNA-binding protein
FA592_11970	ENOG4108VMB	DNA polymerase III subunit delta'
FA592_11975	ENOG4105C40	3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs (By similarity)
FA592_11990	ENOG4107QMS	site-determining protein
FA592_11995	ENOG41084TB	Prevents the cell division inhibition by proteins MinC and MinD at internal division sites while permitting inhibition at polar sites. This ensures cell division at the proper site by restricting the formation of a division septum at the midpoint of the long axis of the cell (By similarity)
FA592_12000	ENOG4105PXI	polysaccharide deacetylase
FA592_12010	ENOG4107TSN	permease
FA592_12015	ENOG4108UIN	ybak prolyl-trna synthetase associated region
FA592_12025	ENOG4105EJQ	L-serine dehydratase
FA592_12030	ENOG4105GSH	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
FA592_12035	ENOG4105EN6	Membrane
FA592_12040	ENOG4105C8Y	Acetylornithine aminotransferase
FA592_12055	ENOG410829W	Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein (By similarity)
FA592_12060	ENOG4105X6C	Flagellar basal body-associated protein FliL
FA592_12065	ENOG4105DNJ	May play a role in the repair of endogenous alkylation damage (By similarity)
FA592_12070	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)
FA592_12085	ENOG4105E4Y	Endoribonuclease that initiates mRNA decay (By similarity)
FA592_12090	ENOG4105BZ1	(ABC) transporter
FA592_12110	ENOG4105C09	Bile acid
FA592_12115	ENOG4108R5K	PPIases accelerate the folding of proteins (By similarity)
FA592_12125	ENOG4105XJC	Two component transcriptional regulator (Winged helix family
FA592_12140	ENOG4105BZU	Histidine kinase
FA592_12155	ENOG4108Z66	YbaK ebsC protein
FA592_12215	ENOG4107RN3	metallophosphoesterase
FA592_12250	ENOG4107XPZ	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)
FA592_12270	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)
FA592_12275	ENOG4105C0A	alcohol dehydrogenase
FA592_12280	ENOG4105BZU	Histidine kinase
FA592_12305	ENOG4108RBJ	Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions (By similarity)
FA592_12310	ENOG4107YD3	Thioesterase
FA592_12325	ENOG4108UN4	phage SPO1 DNA polymerase-related protein
FA592_12340	ENOG4107S73	homocitrate synthase
FA592_12350	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
FA592_12360	ENOG4105BZU	Histidine kinase
FA592_12375	ENOG4105CNW	domain protein
FA592_12390	ENOG4105D0B	Nitrogenase protein alpha chain
FA592_12400	ENOG4107EFR	Flavocytochrome c
FA592_12425	ENOG4108J5H	Homocysteine s-methyltransferase
FA592_12435	ENOG4105EGS	Mechanosensitive ion channel
FA592_12445	ENOG4108VQE	nitrogen fixation protein
FA592_12460	ENOG4105XV5	nifz family
FA592_12475	ENOG4105DTW	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FA592_12485	ENOG4108Z7F	N-acetyltransferase
FA592_12490	ENOG4105I9P	Metallothiol transferase which confers resistance to fosfomycin by catalyzing the addition of a thiol cofactor to fosfomycin. L-cysteine is probably the physiological thiol donor (By similarity)
FA592_12505	ENOG4105BZU	Histidine kinase
FA592_12525	ENOG4108VKG	metal-dependent hydrolase
FA592_12535	ENOG4105JAB	phenazine biosynthesis protein, phzf family
FA592_12540	ENOG4108594	Permease of the drug metabolite transporter
FA592_12545	ENOG4108W3Q	Transcriptional regulator
FA592_12575	ENOG4105BZU	Histidine kinase
FA592_12585	ENOG4105C1I	TRANSCRIPTIONAl REGULATOR GntR family
FA592_12600	ENOG4105BZU	Histidine kinase
FA592_12615	ENOG4105C8Q	Methyl-accepting chemotaxis
FA592_12635	ENOG4105RRV	Inherit from COG: copper resistance
FA592_12640	ENOG4105DSM	The key enzymatic reactions in nitrogen fixation are catalyzed by the nitrogenase complex, which has 2 components the iron protein and the molybdenum-iron protein (By similarity)
FA592_12660	ENOG41074H6	response regulator
FA592_12720	ENOG4105DGM	nitrilase cyanide hydratase and apolipoprotein n-acyltransferase
FA592_12740	ENOG4107SDU	Methyl-accepting chemotaxis
FA592_12750	ENOG4105BZ8	glutamate synthase
FA592_12755	ENOG4105WMM	Probably plays a role in a hydrogenase nickel cofactor insertion step (By similarity)
FA592_12760	ENOG4108XIB	electron transport protein ysaA
FA592_12765	ENOG4108HM5	NADH-ubiquinone oxidoreductase chain 49kDa
FA592_12770	ENOG4105CYU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
FA592_12780	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)
FA592_12810	ENOG4108YZY	peptidylprolyl cis-trans isomerase
FA592_12815	ENOG4107QZB	decarboxylase
FA592_12820	ENOG4105CKI	cobalamin synthesis protein
FA592_12825	ENOG4105VCD	cytoplasmic protein
FA592_12830	ENOG4105D22	carbon starvation protein
FA592_12840	ENOG4105C00	Succinate dehydrogenase (Flavoprotein subunit)
FA592_12845	ENOG41084IN	nitrogen fixation protein
FA592_12875	ENOG4105CG2	Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 (By similarity)
FA592_12880	ENOG4106NZV	Responsible for synthesis of pseudouridine from uracil- 13 in transfer RNAs (By similarity)
FA592_12895	ENOG4105BZU	Histidine kinase
FA592_12905	ENOG4105BZU	Histidine kinase
FA592_12920	ENOG4105C4U	4-methyl-5-beta-hydroxyethylthiazole kinase
FA592_12930	ENOG4105C8Q	Methyl-accepting chemotaxis
FA592_12945	ENOG4105C5H	ABC transporter
FA592_12950	ENOG4108SEK	ompa motb domain protein
FA592_12955	ENOG4105E14	MotA TolQ exbB proton channel
FA592_12960	ENOG4107XI7	Tetr family transcriptional regulator
FA592_12975	ENOG4105ENJ	RND efflux system, outer membrane lipoprotein
FA592_12990	ENOG4108RCM	Nitroreductase
FA592_12995	ENOG4105CVP	deoxyribo-dipyrimidine photolyase
FA592_13005	ENOG4108JQC	penicillin-binding protein 1A
FA592_13020	ENOG4105DZS	Phenylacetate-CoA ligase
FA592_13030	ENOG4105DZS	Phenylacetate-CoA ligase
FA592_13045	ENOG4108IA2	Sodium pantothenate symporter
FA592_13060	ENOG4107TPX	flagellar hook-associated
FA592_13075	ENOG4106H78	methyltransferase
FA592_13085	ENOG4105D92	Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation (By similarity)
FA592_13090	ENOG4105YKR	
FA592_13105	ENOG4105E1Q	flagellar hook-associated protein
FA592_13110	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
FA592_13120	ENOG4105CHH	sulfate transporter
FA592_13125	ENOG4105VSH	4-oxalocrotonate tautomerase
FA592_13130	ENOG4107WJT	it plays a direct role in the translocation of protons across the membrane (By similarity)
FA592_13140	ENOG4108UV6	Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP) (By similarity)
FA592_13155	ENOG4105D17	glycoside hydrolase, family 3 domain protein
FA592_13165	ENOG4105DI7	Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs (By similarity)
FA592_13175	ENOG4105EHH	Cleaves type-4 fimbrial leader sequence and methylates the N-terminal (generally Phe) residue (By similarity)
FA592_13190	ENOG4105CAJ	Catalyzes the last two sequential reactions in the de novo biosynthetic pathway for UDP-N-acetylglucosamine (UDP- GlcNAc). The C-terminal domain catalyzes the transfer of acetyl group from acetyl coenzyme A to glucosamine-1-phosphate (GlcN-1-P) to produce N-acetylglucosamine-1-phosphate (GlcNAc-1-P), which is converted into UDP-GlcNAc by the transfer of uridine 5- monophosphate (from uridine 5-triphosphate), a reaction catalyzed by the N-terminal domain (By similarity)
FA592_13195	ENOG4105CN7	Flagellar biosynthetic protein FliP
FA592_13200	ENOG4105DSB	aldose 1-epimerase
FA592_13205	ENOG4105NF4	modulator of drug activity
FA592_13220	ENOG4107PU6	Membrane
FA592_13225	ENOG4105CCT	upf0313 protein
FA592_13230	ENOG4107QP8	phosphohexose isomerase
FA592_13245	ENOG4105E3S	small subunit
FA592_13255	ENOG4105E3S	small subunit
FA592_13260	ENOG4105DPX	Hydrogenase, large subunit
FA592_13265	ENOG4105X7T	Ni Fe-hydrogenase, b-type cytochrome subunit
FA592_13270	ENOG4108USZ	hydrogenase
FA592_13275	ENOG4108P97	
FA592_13285	ENOG4105MRR	Transcriptional regulator (By similarity)
FA592_13295	ENOG4107RSS	Hydrogenase accessory protein HypB
FA592_13300	ENOG4105WRB	Hydrogenase assembly chaperone hypC hupF
FA592_13305	ENOG4105CQS	hydrogenase expression formation protein HypD
FA592_13310	ENOG4105C45	hydrogenase expression formation protein (HypE)
FA592_13315	ENOG4105WMM	Probably plays a role in a hydrogenase nickel cofactor insertion step (By similarity)
FA592_13320	ENOG4107TCE	N-acetyltransferase
FA592_13325	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)
FA592_13340	ENOG4105E9K	Isocitrate dehydrogenase
FA592_13345	ENOG4105C80	Catalyzes the reversible oxidation of malate to oxaloacetate (By similarity)
FA592_13350	ENOG4105CMV	Succinyl-CoA synthetase subunit beta
FA592_13355	ENOG4105CH8	Succinyl-CoA ligase ADP-forming subunit alpha
FA592_13365	ENOG4105DI2	Pyruvate flavodoxin ferredoxin oxidoreductase domain protein
FA592_13460	ENOG4105C9Q	fumarate hydratase class II
FA592_13485	ENOG4105CJ1	ABC, transporter
FA592_13490	ENOG4107QWP	ABC-2 type transporter
FA592_13495	ENOG4105CMI	transporter
FA592_13500	ENOG41081FY	multiple antibiotic resistance (MarC)-related
FA592_13520	ENOG4105DFA	alanine racemase domain protein
FA592_13525	ENOG4105DZP	Membrane-associated zinc metalloprotease
FA592_13530	ENOG4105BZQ	cdp-diacylglycerol-glycerol-3-phosphate 3-phosphatidyltransferase
FA592_13535	ENOG4105CAN	Short-chain dehydrogenase reductase Sdr
FA592_13540	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
FA592_13550	ENOG4107QYT	Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor (By similarity)
FA592_13555	ENOG4105BZ1	(ABC) transporter
FA592_13560	ENOG4105C8N	cysteinyl-tRNA synthetase
FA592_13565	ENOG4105CJR	Integral membrane protein (MviN
FA592_13575	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)
FA592_13600	ENOG4108EQQ	Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein (By similarity)
FA592_13605	ENOG4105C6K	Malic enzyme
FA592_13610	ENOG4105C6H	Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction (By similarity)
FA592_13615	ENOG4105KTH	gatB Yqey
FA592_13635	ENOG4107QHF	type ii secretion system protein e
FA592_13670	ENOG4105CWT	An essential GTPase that binds both GDP and GTP, with rapid nucleotide exchange. Plays a role in 16S rRNA processing and 30S ribosomal subunit biogenesis and possibly also in cell cycle regulation and energy metabolism (By similarity)
FA592_13675	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)
FA592_13680	ENOG4108R5P	Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery (By similarity)
FA592_13695	ENOG4105CDH	Citrulline--aspartate ligase
FA592_13700	ENOG410854I	s4 domain protein
FA592_13705	ENOG4107S1N	anthranilate phosphoribosyltransferase
FA592_13710	ENOG4105K8N	protein family UPF0079, ATPase
FA592_13715	ENOG4108IUZ	ABC transporter
FA592_13815	ENOG41084S7	Plasmid maintenance system antidote protein
FA592_13945	ENOG4108Q9H	CobQ/CobB/MinD/ParA nucleotide binding domain
FA592_13950	ENOG4107QJE	Chromosome Partitioning Protein
FA592_14040	ENOG4105CM6	amino acid regulated cytosolic protein
FA592_14045	ENOG4105CM6	amino acid regulated cytosolic protein
FA592_14050	ENOG4105C3F	Signal peptidase i