locus-tag	class	description
FA584_RS00010	ENOG4107EFR	Flavocytochrome c
FA584_RS00060	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
FA584_RS00090	ENOG4108BGM	Quinol dehydrogenase periplasmic component
FA584_RS00100	ENOG4105DH2	Converts cobyric acid to cobinamide by the addition of aminopropanol on the F carboxylic group (By similarity)
FA584_RS00110	ENOG4108YZT	Adenosylcobinamide kinase
FA584_RS00130	ENOG4108UHF	Joins Ado-cobinamide-GDP and alpha-ribazole to generate adenosylcobalamin (Ado-cobalamin) (By similarity)
FA584_RS00140	ENOG4107PPM	cobalt chelatase
FA584_RS00145	ENOG4105EHG	Permease protein
FA584_RS00150	ENOG4105E0A	ABC, transporter
FA584_RS00160	ENOG41081F0	Precorrin-8x methylmutase
FA584_RS00165	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)
FA584_RS00175	ENOG4107XSI	cobalt-precorrin-6y C15-methyltransferase
FA584_RS00180	ENOG4105DVK	Precorrin-2 c20-methyltransferase
FA584_RS00185	ENOG4105CIA	precorrin-4 C(11)-methyltransferase
FA584_RS00190	ENOG4108P62	biosynthesis protein (CbiG)
FA584_RS00195	ENOG4105E4R	Precorrin-3B C17-methyltransferase
FA584_RS00205	ENOG4108JTQ	reductase
FA584_RS00210	ENOG4105BZ1	(ABC) transporter
FA584_RS00215	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)
FA584_RS00225	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)
FA584_RS00230	ENOG4108IG5	Transcriptional regulator
FA584_RS00370	ENOG4105VTR	Integrase
FA584_RS00380	ENOG410841J	DNA-binding protein Hu
FA584_RS00390	ENOG4105CNU	cell division protein FtsK
FA584_RS00395	ENOG4107QIJ	Aconitate hydratase 2
FA584_RS00400	ENOG4108YZY	peptidylprolyl cis-trans isomerase
FA584_RS00405	ENOG4108HRN	Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate (By similarity)
FA584_RS00410	ENOG4105RW8	MltA-interacting MipA family protein
FA584_RS00420	ENOG4105C6X	Major Facilitator
FA584_RS00440	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
FA584_RS00445	ENOG4105C8Q	Methyl-accepting chemotaxis
FA584_RS00450	ENOG4105K4P	CoA-binding domain protein
FA584_RS00455	ENOG4105C7B	Threonine dehydratase
FA584_RS00465	ENOG4105CDA	abc transporter atp-binding protein
FA584_RS00470	ENOG4105DRP	amino acid AbC transporter
FA584_RS00475	ENOG4105EZ7	amino acid ABC transporter
FA584_RS00500	ENOG4107T5V	SNARE associated Golgi
FA584_RS00505	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)
FA584_RS00510	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)
FA584_RS00515	ENOG4105CAY	ferredoxin--nadp reductase
FA584_RS00535	ENOG4105QTX	Pfam:UPF0153
FA584_RS00545	ENOG4105DK0	Indole-3-glycerol phosphate synthase
FA584_RS00555	ENOG4105CR7	Catalyzes the transfer of selenium from selenophosphate for conversion of 2-thiouridine to 2-selenouridine at the wobble position in tRNA (By similarity)
FA584_RS00560	ENOG4108JJB	ABC transporter
FA584_RS00575	ENOG4105CFT	Part of the energy-coupling factor (ECF) transporter complex CbiMNOQ involved in cobalt import (By similarity)
FA584_RS00580	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)
FA584_RS00585	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)
FA584_RS00600	ENOG4107SA8	fad-dependent pyridine nucleotide-disulfide oxidoreductase
FA584_RS00610	ENOG4105C7K	acetolactate synthase
FA584_RS00615	ENOG4108ZP8	Acetolactate synthase small subunit
FA584_RS00620	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)
FA584_RS00630	ENOG4105BZ8	glutamate synthase
FA584_RS00645	ENOG4108JUA	Transcriptional regulator
FA584_RS00655	ENOG4105CY9	nitrogenase molybdenum-iron protein beta chain
FA584_RS00660	ENOG4105SJ7	Fe-only nitrogenase subunit delta
FA584_RS00665	ENOG4107V0H	Nitrogenase protein alpha chain
FA584_RS00670	ENOG4105D7W	serine acetyltransferase
FA584_RS00675	ENOG4105DP5	Catalyzes the biosynthesis of agmatine from arginine (By similarity)
FA584_RS00680	ENOG4105CUT	histidyl-tRNA synthetase
FA584_RS00685	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
FA584_RS00690	ENOG4108ZEF	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate (By similarity)
FA584_RS00695	ENOG4108UMA	3-octaprenyl-4-hydroxybenzoate carboxy-lyase
FA584_RS00715	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
FA584_RS00720	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
FA584_RS00735	ENOG4105DTC	1-(5-phosphoribosyl)-5-amino-4-imidazole-carboxylate (air) carboxylase
FA584_RS00740	ENOG4105DVM	PP-loop domain protein
FA584_RS00745	ENOG4105C8M	UPF0272 protein
FA584_RS00750	ENOG4105QUH	Domain of unknown function (DUF2088)
FA584_RS00755	ENOG4107GFK	fumarate
FA584_RS00775	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
FA584_RS00790	ENOG4105DKJ	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
FA584_RS00800	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)
FA584_RS00805	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)
FA584_RS00815	ENOG4105D49	3-dehydroquinate synthase
FA584_RS00825	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)
FA584_RS00850	ENOG4105DEN	Luciferase family
FA584_RS00855	ENOG4105FE9	pseudouridine synthase
FA584_RS00865	ENOG4105C7K	acetolactate synthase
FA584_RS00890	ENOG4108YXA	Membrane
FA584_RS00895	ENOG4107Z3H	Transcriptional regulator, TetR family
FA584_RS00930	ENOG4105C8Q	Methyl-accepting chemotaxis
FA584_RS00935	ENOG4108RAC	Rubrerythrin
FA584_RS00945	ENOG4105D3H	Catalyzes the decarboxylation of 3-octaprenyl-4-hydroxy benzoate to 2-octaprenylphenol (By similarity)
FA584_RS00950	ENOG4105D6W	Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps (By similarity)
FA584_RS00955	ENOG4105DRC	Na( ) H( ) antiporter that extrudes sodium in exchange for external protons (By similarity)
FA584_RS00960	ENOG4108YH1	overproduction of this protein in Escherichia coli inhibits the F plasmid-mediated exclusion of bacteriophage T7
FA584_RS00965	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)
FA584_RS00970	ENOG4105C7E	Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) (By similarity)
FA584_RS00975	ENOG4105EAH	synthase
FA584_RS01000	ENOG4105C6T	cysteine synthase
FA584_RS01005	ENOG4105BZU	Histidine kinase
FA584_RS01010	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)
FA584_RS01015	ENOG4108RIR	Molybdenum cofactor biosynthesis protein
FA584_RS01020	ENOG41084M5	Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid (By similarity)
FA584_RS01025	ENOG4105CEK	Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine (By similarity)
FA584_RS01035	ENOG4105D2N	Aldolase
FA584_RS01045	ENOG4105CSM	endonuclease III
FA584_RS01055	ENOG4105CIN	aminoacyl-histidine dipeptidase
FA584_RS01080	ENOG4105C4K	Nad synthetase
FA584_RS01085	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
FA584_RS01090	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)
FA584_RS01095	ENOG4105CAS	nag kinase
FA584_RS01100	ENOG4107QID	Threonine synthase
FA584_RS01105	ENOG4105CET	Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria (By similarity)
FA584_RS01115	ENOG4105CSG	Required to facilitate the formation of correct disulfide bonds in some periplasmic proteins and for the assembly of the periplasmic c-type cytochromes. Acts by transferring electrons from cytoplasmic thioredoxin to the periplasm. This transfer involves a cascade of disulfide bond formation and reduction steps (By similarity)
FA584_RS01120	ENOG4105CSR	polyphosphate kinase 2
FA584_RS01125	ENOG4105DHT	Metal Dependent Phosphohydrolase
FA584_RS01130	ENOG4105CFG	Acts as a chaperone (By similarity)
FA584_RS01135	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
FA584_RS01140	ENOG4108122	heat-inducible transcription repressor
FA584_RS01155	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
FA584_RS01160	ENOG4108ZF1	Transcriptional regulator, BadM Rrf2 family
FA584_RS01165	ENOG4105D7B	Flagellar biosynthesis protein flha
FA584_RS01170	ENOG4108KA0	Inherit from COG: Phosphoesterase, DHHA1
FA584_RS01180	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)
FA584_RS01185	ENOG410620I	Diguanylate cyclase
FA584_RS01190	ENOG4105DTN	riboflavin biosynthesis protein ribF
FA584_RS01200	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)
FA584_RS01205	ENOG4105EJ9	Membrane
FA584_RS01215	ENOG4105EEI	dihydropteroate synthase
FA584_RS01230	ENOG4105CFH	Aspartokinase
FA584_RS01235	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)
FA584_RS01240	ENOG4105CSA	Coproporphyrinogen iii oxidase
FA584_RS01245	ENOG4105CKD	glutathione-regulated potassium-efflux system protein
FA584_RS01250	ENOG4105KNI	merR family transcriptional Regulator
FA584_RS01255	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)
FA584_RS01260	ENOG4105C0H	protease
FA584_RS01285	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
FA584_RS01290	ENOG4105ZGC	lipoprotein carrier protein
FA584_RS01295	ENOG4105BZU	Histidine kinase
FA584_RS01300	ENOG4105DRC	Na( ) H( ) antiporter that extrudes sodium in exchange for external protons (By similarity)
FA584_RS01305	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)
FA584_RS01315	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
FA584_RS01320	ENOG4108512	Could be involved in insertion of integral membrane proteins into the membrane (By similarity)
FA584_RS01325	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)
FA584_RS01330	ENOG4105VG0	50S ribosomal protein l34
FA584_RS01345	ENOG4105DJI	Methylaspartate mutase, E subunit
FA584_RS01360	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)
FA584_RS01375	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
FA584_RS01380	ENOG4105CN1	protease
FA584_RS01390	ENOG4105VR9	phosphoribosylformylglycinamidine synthase
FA584_RS01395	ENOG4105D21	Phosphoribosylformylglycinamidine synthase I
FA584_RS01405	ENOG4105E9Q	Acyl-transferase
FA584_RS01410	ENOG4105CJX	Molecular chaperone. Has ATPase activity (By similarity)
FA584_RS01430	ENOG4105C7Z	Conserved Protein
FA584_RS01435	ENOG41085GJ	domain protein
FA584_RS01470	ENOG4107QUV	Domain protein
FA584_RS01490	ENOG4108V1J	Has antioxidant activity. Could remove peroxides or H(2)O(2) (By similarity)
FA584_RS01510	ENOG4105DHT	Metal Dependent Phosphohydrolase
FA584_RS01515	ENOG4105CGY	Dna recombination protein
FA584_RS01525	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
FA584_RS01535	ENOG4105EIN	peptidylprolyl cis-trans isomerase
FA584_RS01540	ENOG4105CIT	This protein may be involved in anomalous filament growth. May be a component of the septum (By similarity)
FA584_RS01545	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)
FA584_RS01560	ENOG4105D0M	Protease HtpX homolog
FA584_RS01570	ENOG4105C5H	ABC transporter
FA584_RS01575	ENOG4105C8Q	Methyl-accepting chemotaxis
FA584_RS01585	ENOG4105VG1	fes assembly suf system protein
FA584_RS01600	ENOG4105DC1	bifunctional purine biosynthesis protein purh
FA584_RS01615	ENOG4108S4H	thioesterase Superfamily protein
FA584_RS01620	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)
FA584_RS01625	ENOG4105C87	Aminotransferase class I and II
FA584_RS01645	ENOG4108URH	decarboxylase
FA584_RS01650	ENOG4107QWP	ABC-2 type transporter
FA584_RS01655	ENOG4107QWP	ABC-2 type transporter
FA584_RS01665	ENOG4105D0S	secretion protein (HlyD
FA584_RS01670	ENOG4107MVR	Transcriptional regulator
FA584_RS01685	ENOG4107QIK	phosphoribosylformylglycinamidine synthase
FA584_RS01690	ENOG4105BZU	Histidine kinase
FA584_RS01700	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)
FA584_RS01705	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)
FA584_RS01730	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
FA584_RS01735	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
FA584_RS01740	ENOG4105BZU	Histidine kinase
FA584_RS01745	ENOG4105CY0	Metallo-Beta-Lactamase
FA584_RS01760	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)
FA584_RS01765	ENOG4105CZN	Potassium uptake protein
FA584_RS01770	ENOG4107ZYR	domain protein
FA584_RS01775	ENOG4105E0X	reductase
FA584_RS01790	ENOG4105MFX	4-diphosphocytidyl-2c-methyl-d-erythritol synthase
FA584_RS01795	ENOG4107P0T	Selenium-dependent molybdenum hydroxylase system protein, YqeB family
FA584_RS01800	ENOG4105DZS	Phenylacetate-CoA ligase
FA584_RS01815	ENOG41089UC	methyltransferase, type 11
FA584_RS01835	ENOG4105BZU	Histidine kinase
FA584_RS01880	ENOG4107WTJ	Methyl-accepting chemotaxis sensory transducer
FA584_RS01885	ENOG4108NIW	Leucine export protein LeuE
FA584_RS01890	ENOG4108594	Permease of the drug metabolite transporter
FA584_RS01905	ENOG4105BZU	Histidine kinase
FA584_RS01910	ENOG4108YZA	Nitrogen regulatory protein pii
FA584_RS01925	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
FA584_RS01930	ENOG4105C38	Glycyl-tRNA synthetase beta subunit
FA584_RS01950	ENOG4105NBK	UPF0345 protein
FA584_RS01955	ENOG4105BZU	Histidine kinase
FA584_RS01960	ENOG4105CBX	hi0933 family
FA584_RS01970	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)
FA584_RS01975	ENOG4105CIY	formyltetrahydrofolate deformylase
FA584_RS01980	ENOG4105D4J	Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate
FA584_RS01995	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)
FA584_RS02000	ENOG4105MQS	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
FA584_RS02015	ENOG4105CIG	ABC transporter
FA584_RS02035	ENOG4107R5R	arsenical pump membrane protein
FA584_RS02050	ENOG4105CGK	Exodeoxyribonuclease III
FA584_RS02070	ENOG4105E09	nadh pyrophosphatase
FA584_RS02075	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)
FA584_RS02080	ENOG4105DQ2	Is probably involved in the electron transfer between its heme and the molybdenum cofactor of the reductase catalytic subunit YedY (By similarity)
FA584_RS02085	ENOG4108VSZ	Inherit from COG: ketosteroid isomerase-like protein
FA584_RS02100	ENOG4105C8Q	Methyl-accepting chemotaxis
FA584_RS02115	ENOG4108YYH	Nadph-dependent fmn reductase
FA584_RS02120	ENOG4108U5N	UPF0316 protein
FA584_RS02125	ENOG4105BZU	Histidine kinase
FA584_RS02140	ENOG4105C9U	ATP-dependent DNA helicase RecQ
FA584_RS02155	ENOG4105C1J	atp-dependent rna helicase
FA584_RS02210	ENOG4105CR4	methylisocitrate lyase
FA584_RS02215	ENOG4105BZN	citrate synthase
FA584_RS02220	ENOG4105DXD	2-methylcitrate dehydratase
FA584_RS02230	ENOG4108Z8G	Alkylphosphonate utilization operon protein PhnA
FA584_RS02240	ENOG4108UMN	azlc family
FA584_RS02250	ENOG4105CGA	flagellar basal-body rod protein FlgG
FA584_RS02255	ENOG4105CGA	flagellar basal-body rod protein FlgG
FA584_RS02260	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FA584_RS02270	ENOG4105KVH	Transcriptional regulator
FA584_RS02285	ENOG4105D7X	high-affinity nickel-transporter
FA584_RS02290	ENOG4105FDK	ABC transporter
FA584_RS02295	ENOG4105FAV	ABC, transporter
FA584_RS02315	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)
FA584_RS02320	ENOG4107QN1	sodium solute
FA584_RS02325	ENOG41062QD	Membrane
FA584_RS02330	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
FA584_RS02345	ENOG41076HS	cation diffusion facilitator family transporter
FA584_RS02350	ENOG4105CE1	Ferrous iron transport protein b
FA584_RS02355	ENOG4107K9B	ferrous iron transport protein
FA584_RS02385	ENOG4105X1Q	TOBE domain protein
FA584_RS02390	ENOG4107VIJ	nudix hydrolase
FA584_RS02395	ENOG4105D7N	magnesium and cobalt transport protein CorA
FA584_RS02400	ENOG4105DR5	peptidase
FA584_RS02405	ENOG4105MRU	Plasminogen-binding protein
FA584_RS02410	ENOG4105CQB	FAD linked oxidase domain protein
FA584_RS02415	ENOG4107S2Z	UPF0761 membrane protein
FA584_RS02425	ENOG4105CDU	Replicative dna helicase
FA584_RS02430	ENOG4105C4E	Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate (By similarity)
FA584_RS02435	ENOG4105C25	Primosomal protein n'
FA584_RS02460	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)
FA584_RS02470	ENOG4105CUU	Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) (By similarity)
FA584_RS02475	ENOG4108Z0R	Transferase
FA584_RS02480	ENOG4105DE5	Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity (By similarity)
FA584_RS02485	ENOG4108ZGB	N-(5'-phosphoribosyl)anthranilate isomerase
FA584_RS02490	ENOG4105DJV	ribulose-phosphate 3-epimerase
FA584_RS02495	ENOG4105VB9	50S ribosomal protein l28
FA584_RS02500	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)
FA584_RS02515	ENOG4105D48	metallophosphoesterase
FA584_RS02520	ENOG4108JA2	transcriptioN-repair coupling factor
FA584_RS02530	ENOG4105DR5	peptidase
FA584_RS02535	ENOG4105DPM	folylpolyglutamate synthase Dihydrofolate synthase
FA584_RS02540	ENOG4105BZU	Histidine kinase
FA584_RS02550	ENOG4105C8T	Leucyl-tRNA synthetase
FA584_RS02555	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)
FA584_RS02560	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)
FA584_RS02565	ENOG4105VIE	preprotein translocase, subunit YajC
FA584_RS02570	ENOG4105CE8	Transfers the fatty acyl group on membrane lipoproteins (By similarity)
FA584_RS02575	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
FA584_RS02585	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)
FA584_RS02595	ENOG4105KAE	Involved in the modulation of the specificity of the ClpAP-mediated ATP-dependent protein degradation (By similarity)
FA584_RS02610	ENOG4107Z7S	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
FA584_RS02615	ENOG41085EF	Carbon storage regulator
FA584_RS02620	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
FA584_RS02625	ENOG4105C4R	Atp-dependent dna helicase
FA584_RS02630	ENOG4105DUM	transcriptional regulator, lysR family
FA584_RS02650	ENOG4105CRQ	synthase (Component I)
FA584_RS02655	ENOG4105CXT	aspartate transcarbamylase
FA584_RS02665	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)
FA584_RS02695	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)
FA584_RS02700	ENOG4105VB6	UPF0109 protein
FA584_RS02710	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
FA584_RS02715	ENOG4105EI2	Pseudouridine synthase
FA584_RS02720	ENOG4105D8A	3-Deoxy-D-manno-octulosonic-acid transferase
FA584_RS02730	ENOG4105EGD	dinuclear metal center protein, YbgI family
FA584_RS02735	ENOG4107QIB	glycyl-tRNA synthetase, alpha subunit
FA584_RS02745	ENOG4108UM6	Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) (By similarity)
FA584_RS02750	ENOG4105CFP	Peptidase U32
FA584_RS02760	ENOG4107RVV	histidinol phosphate phosphatase, hisj family
FA584_RS02765	ENOG4105C5F	glutamine synthetase
FA584_RS02770	ENOG4108JQC	penicillin-binding protein 1A
FA584_RS02775	ENOG4108JQ6	ABC transporter
FA584_RS02780	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)
FA584_RS02785	ENOG4107YJQ	MAF-like protein
FA584_RS02795	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)
FA584_RS02820	ENOG4107EXU	Short-chain dehydrogenase reductase Sdr
FA584_RS02825	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
FA584_RS02835	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
FA584_RS02840	ENOG4105CJN	penicillin-binding protein
FA584_RS02850	ENOG4108ZC9	flagellar basal-body rod protein flgc
FA584_RS02855	ENOG4105K88	Structural component of flagellum, the bacterial motility apparatus. Part of the rod structure of flagellar basal body (By similarity)
FA584_RS02860	ENOG4105CNI	cell division protein FtsW
FA584_RS02980	ENOG4105HKU	nucleoside recognition domain-containing protein
FA584_RS02990	ENOG4108TVT	permease
FA584_RS03055	ENOG4105DDQ	anthranilate synthase
FA584_RS03070	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)
FA584_RS03080	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)
FA584_RS03235	ENOG4108J8Q	Catalyzes the facilitated diffusion of 2-acyl-glycero-3- phosphoethanolamine (2-acyl-GPE) into the cell (By similarity)
FA584_RS03245	ENOG41082BM	Transcriptional regulator, arsr family
FA584_RS03260	ENOG4105CHY	citrate lyase, alpha
FA584_RS03265	ENOG4105CI0	Citrate lyase
FA584_RS03270	ENOG4105XGS	Covalent carrier of the coenzyme of citrate lyase (By similarity)
FA584_RS03275	ENOG4105DUA	(citrate (pro-3S)-lyase ligase
FA584_RS03285	ENOG4105D94	Major Facilitator Superfamily
FA584_RS03295	ENOG4105C7N	Xanthine uracil vitamin C permease
FA584_RS03300	ENOG4105DVY	radical SAM domain protein
FA584_RS03310	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)
FA584_RS03320	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
FA584_RS03330	ENOG4105E1P	Modifies, by uridylylation or deuridylylation the PII (GlnB) regulatory protein (By similarity)
FA584_RS03335	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
FA584_RS03340	ENOG4105BZU	Histidine kinase
FA584_RS03360	ENOG4105BZU	Histidine kinase
FA584_RS03370	ENOG4105EYW	Ion transport protein
FA584_RS03390	ENOG4105C5H	ABC transporter
FA584_RS03410	ENOG4108RC0	Electron transport protein
FA584_RS03415	ENOG4105CJG	carbon-monoxide dehydrogenase catalytic subunit
FA584_RS03420	ENOG41080XS	Cobyrinic acid ac-diamide synthase
FA584_RS03425	ENOG4108MFN	small subunit of hydrogenase-3, iron-sulfur protein (part of formate hydrogenlyase (FHL) complex)
FA584_RS03435	ENOG4107TDF	Formate hydrogenlyase subunit 4
FA584_RS03440	ENOG4107WQX	hydrogenase 4 membrane subunit
FA584_RS03445	ENOG4108JPZ	Monovalent cation H antiporter subunit D
FA584_RS03450	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)
FA584_RS03460	ENOG4105C47	NADH ubiquinone oxidoreductase 20 kda subunit
FA584_RS03495	ENOG4105CUZ	uba thif-type nad fad binding protein
FA584_RS03510	ENOG4105EJ3	Catalyzes the conversion of the cyclic tetrahydrodipicolinate (THDP) into the acyclic N-succinyl-L-2- amino-6-oxopimelate using succinyl-CoA (By similarity)
FA584_RS03515	ENOG4105D1F	ATP-binding protein
FA584_RS03520	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)
FA584_RS03540	ENOG4108YYC	ycei family
FA584_RS03545	ENOG4108ZK7	protein family UPF0029, Impact, N-terminal protein
FA584_RS03550	ENOG4108PQF	modD protein
FA584_RS03565	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
FA584_RS03570	ENOG4105E0C	molybdate abc transporter
FA584_RS03580	ENOG4108S6J	ABC transporter, periplasmic molybdate-binding protein
FA584_RS03585	ENOG4105F4R	Transcriptional regulator mode
FA584_RS03590	ENOG4105DZ1	carboxypeptidase
FA584_RS03595	ENOG4105II7	pyrroline-5-carboxylate reductase
FA584_RS03600	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)
FA584_RS03605	ENOG4105C19	ABC transporter
FA584_RS03625	ENOG4105D64	Mechanosensitive ion channel
FA584_RS03630	ENOG4105BZU	Histidine kinase
FA584_RS03645	ENOG4105F5P	DNA-damage-inducible protein d
FA584_RS03765	ENOG4106EG9	Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) (By similarity)
FA584_RS03770	ENOG4105M7K	Involved in the transcription termination process (By similarity)
FA584_RS03775	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)
FA584_RS03785	ENOG4105CXR	Phospho-2-dehydro-3-deoxyoctonate aldolase
FA584_RS03790	ENOG4108JHT	EamA-like transporter family
FA584_RS03795	ENOG4105D64	Mechanosensitive ion channel
FA584_RS03800	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
FA584_RS03815	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)
FA584_RS03825	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)
FA584_RS03830	ENOG4106PT6	cdpdiacylglycerol-serine O-phosphatidyltransferase
FA584_RS03840	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)
FA584_RS03845	ENOG4107RQ5	Methylates ribosomal protein L11 (By similarity)
FA584_RS03850	ENOG4108VYJ	response regulator receiver protein
FA584_RS03855	ENOG4105CJV	Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase
FA584_RS03860	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)
FA584_RS03880	ENOG4105ESV	Glycosyl transferase, family 4
FA584_RS03890	ENOG4108RT7	Glycosyl transferase, family 2
FA584_RS03900	ENOG4105H63	Glycosyl transferase, family 2
FA584_RS03905	ENOG4108UW5	maltose o-acetyltransferase
FA584_RS03910	ENOG4107YYJ	Glycosyl transferase, family 2
FA584_RS03920	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
FA584_RS03930	ENOG4105C7K	acetolactate synthase
FA584_RS03935	ENOG4105FAW	cDP-glucose 4,6-dehydratase
FA584_RS03940	ENOG4105EJZ	Glucose-1-phosphate cytidylyltransferase
FA584_RS03950	ENOG4108URP	Dtdp-4-dehydrorhamnose 3,5-epimerase
FA584_RS03960	ENOG4105C1B	dTDP-glucose 4-6-dehydratase
FA584_RS03965	ENOG4108I19	Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis (By similarity)
FA584_RS03970	ENOG4107QKV	phosphomannomutase
FA584_RS03980	ENOG4105D16	lipopolysaccharide heptosyltransferase i
FA584_RS03995	ENOG4105XA0	heptosyltransferase ii
FA584_RS04005	ENOG4105CND	Glycosyl transferase, family 2
FA584_RS04020	ENOG4105F55	Catalyzes the isomerization of sedoheptulose 7-phosphate in D-glycero-D-manno-heptose 7-phosphate (By similarity)
FA584_RS04025	ENOG4105DW0	Catalyzes the ADP transfer to D-glycero-D-manno-heptose 1-phosphate, yielding ADP-D,D-heptose (By similarity)
FA584_RS04030	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)
FA584_RS04055	ENOG4105C59	p-type ATPase
FA584_RS04065	ENOG4108PCN	EamA-like transporter family
FA584_RS04080	ENOG4105BZU	Histidine kinase
FA584_RS04085	ENOG4108V1J	Has antioxidant activity. Could remove peroxides or H(2)O(2) (By similarity)
FA584_RS04095	ENOG4105DBW	Multi-copper polyphenol oxidoreductase laccase
FA584_RS04100	ENOG4108R6K	riboflavin synthase, subunit alpha
FA584_RS04105	ENOG4105C8Q	Methyl-accepting chemotaxis
FA584_RS04110	ENOG4107R7A	Allophanate hydrolase subunit 2
FA584_RS04120	ENOG4105E7W	lamb ycsf family protein
FA584_RS04125	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)
FA584_RS04130	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)
FA584_RS04135	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)
FA584_RS04140	ENOG4105EIX	cytochrome c1
FA584_RS04150	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)
FA584_RS04155	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
FA584_RS04160	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
FA584_RS04165	ENOG4105CHR	reductase
FA584_RS04170	ENOG4105CJI	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
FA584_RS04180	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
FA584_RS04190	ENOG4105D3Q	Sugar transferase
FA584_RS04200	ENOG4108TJN	glycosyl transferase group 1
FA584_RS04205	ENOG4107TXM	Nad-dependent epimerase dehydratase
FA584_RS04210	ENOG4105C0K	Gdp-mannose 4,6-dehydratase
FA584_RS04230	ENOG4105CKK	Glycosyl transferase, family 2
FA584_RS04245	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
FA584_RS04250	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)
FA584_RS04270	ENOG4105C1B	dTDP-glucose 4-6-dehydratase
FA584_RS04275	ENOG4108I19	Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis (By similarity)
FA584_RS04290	ENOG4105EY8	ABC transporter
FA584_RS04300	ENOG4105CJT	Mannose-1-phosphate guanylyltransferase
FA584_RS04305	ENOG4105CMR	udp-glucose 4-epimerase
FA584_RS04310	ENOG4105DB1	molybdopterin oxidoreductase
FA584_RS04320	ENOG4105QA4	4Fe-4S Ferredoxin, iron-sulfur binding domain protein
FA584_RS04330	ENOG4105ETX	regulatoR
FA584_RS04335	ENOG4108KCW	iron-sulfur cluster binding
FA584_RS04345	ENOG4108N5C	SNARE associated Golgi protein-related protein
FA584_RS04350	ENOG4108M8H	domain protein
FA584_RS04370	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
FA584_RS04385	ENOG4105C1J	atp-dependent rna helicase
FA584_RS04390	ENOG4108UPT	UPF0178 protein
FA584_RS04395	ENOG4105CPC	Aldo Keto reductase
FA584_RS04400	ENOG4108RWP	Major Facilitator Superfamily protein
FA584_RS04405	ENOG4105CF7	AraC family transcriptional regulator
FA584_RS04420	ENOG4107QMV	Part of the ABC transporter complex PstSACB involved in phosphate import (By similarity)
FA584_RS04425	ENOG4105C8U	phosphate abc transporter
FA584_RS04430	ENOG4105E2Z	phosphate ABC transporter (Permease
FA584_RS04435	ENOG4105BZY	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
FA584_RS04445	ENOG4105C8E	extradiol ring-cleavage dioxygenase class IIi protein subunit b
FA584_RS04450	ENOG4108NVR	Methyl-accepting chemotaxis
FA584_RS04465	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
FA584_RS04475	ENOG4105NAU	thioesterase Superfamily protein
FA584_RS04495	ENOG4105KVH	Transcriptional regulator
FA584_RS04500	ENOG4108K2R	Glutathione-regulated potassium-efflux system ancillary protein
FA584_RS04505	ENOG4105BZU	Histidine kinase
FA584_RS04510	ENOG4105FD2	Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) (By similarity)
FA584_RS04515	ENOG4105EIZ	Catalyzes the conversion of 6-carboxy-5,6,7,8- tetrahydropterin (CPH4) to 7-carboxy-7-deazaguanine (CDG) (By similarity)
FA584_RS04565	ENOG4105C57	major facilitator superfamily
FA584_RS04570	ENOG4105ENJ	RND efflux system, outer membrane lipoprotein
FA584_RS04575	ENOG4105BZS	acriflavin resistance protein
FA584_RS04580	ENOG4105C1P	efflux transporter, rnd family, mfp subunit
FA584_RS04595	ENOG4108ZPB	UPF0306 protein
FA584_RS04600	ENOG4107QV7	Involved in the import of serine and threonine into the cell, with the concomitant import of sodium (symport system) (By similarity)
FA584_RS04630	ENOG4105D95	Oxidoreductase required for the transfer of electrons from pyruvate to flavodoxin (By similarity)
FA584_RS04640	ENOG4107QPK	)-transporter
FA584_RS04665	ENOG4108V1U	phospholipid-binding protein
FA584_RS04670	ENOG4105CF7	AraC family transcriptional regulator
FA584_RS04675	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
FA584_RS04695	ENOG4107QW4	alcohol dehydrogenase
FA584_RS04705	ENOG4107R4J	Chloride channel
FA584_RS04710	ENOG4108HH9	Catalyzes two reactions the first one is the production of beta-formyl glycinamide ribonucleotide (GAR) from formate, ATP and beta GAR
FA584_RS04725	ENOG4108UJD	30S ribosomal protein S9
FA584_RS04730	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)
FA584_RS04735	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
FA584_RS04775	ENOG4105EUH	cytochrome C oxidase, cbb3-type, subunit i
FA584_RS04780	ENOG4108RQS	Two component transcriptional regulator (Winged helix family
FA584_RS04795	ENOG4105C1M	carbamoyl-phosphate synthetase glutamine chain
FA584_RS04815	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
FA584_RS04820	ENOG4105CYE	ATP phosphoribosyltransferase regulatory subunit
FA584_RS04825	ENOG4107UUH	Aminotransferase
FA584_RS04830	ENOG4105C8Q	Methyl-accepting chemotaxis
FA584_RS04835	ENOG4105C8Q	Methyl-accepting chemotaxis
FA584_RS04840	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)
FA584_RS04855	ENOG4105C0H	protease
FA584_RS04860	ENOG41084FT	Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection (By similarity)
FA584_RS04865	ENOG4108Z2X	Catalyzes the pyruvoyl-dependent decarboxylation of aspartate to produce beta-alanine (By similarity)
FA584_RS04870	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)
FA584_RS04885	ENOG4108ZT0	50S ribosomal protein l17
FA584_RS04890	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
FA584_RS04900	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)
FA584_RS04905	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
FA584_RS04910	ENOG41067V7	50S ribosomal protein L36
FA584_RS04915	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)
FA584_RS04920	ENOG4105CA1	Removes the N-terminal methionine from nascent proteins (By similarity)
FA584_RS04925	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)
FA584_RS04930	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
FA584_RS04935	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)
FA584_RS04940	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)
FA584_RS04955	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)
FA584_RS04960	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
FA584_RS04965	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
FA584_RS04970	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
FA584_RS04975	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
FA584_RS04980	ENOG41084HJ	50s ribosomal protein l29
FA584_RS04990	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
FA584_RS04995	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)
FA584_RS05000	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
FA584_RS05015	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)
FA584_RS05020	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)
FA584_RS05040	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
FA584_RS05045	ENOG4107SJW	iron permease, FTR1
FA584_RS05070	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)
FA584_RS05090	ENOG4105CE1	Ferrous iron transport protein b
FA584_RS05095	ENOG4105D10	5-enolpyruvylshikimate-3-phosphate phospholyase
FA584_RS05100	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)
FA584_RS05105	ENOG4108UMW	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
FA584_RS05115	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)
FA584_RS05120	ENOG4105CDH	Citrulline--aspartate ligase
FA584_RS05125	ENOG4107YTP	response regulator receiver protein
FA584_RS05140	ENOG4105BZU	Histidine kinase
FA584_RS05145	ENOG4105BZU	Histidine kinase
FA584_RS05150	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
FA584_RS05155	ENOG4108Z4W	Probably deamidates glutamine residues to glutamate on methyl-accepting chemotaxis receptors (MCPs), playing an important role in chemotaxis (By similarity)
FA584_RS05185	ENOG4105BZU	Histidine kinase
FA584_RS05190	ENOG4105CBS	Chea signal transduction histidine kinase
FA584_RS05200	ENOG4105C8Q	Methyl-accepting chemotaxis
FA584_RS05205	ENOG4108V3W	Chemotaxis protein, CheW
FA584_RS05240	ENOG4105D7X	high-affinity nickel-transporter
FA584_RS05245	ENOG4105D7X	high-affinity nickel-transporter
FA584_RS05255	ENOG4108TGK	Low-potential electron donor to a number of redox enzymes (By similarity)
FA584_RS05265	ENOG4105N14	lysine exporter protein LysE YggA
FA584_RS05300	ENOG410829K	Lysine exporter protein (Lyse ygga)
FA584_RS05310	ENOG4105BZU	Histidine kinase
FA584_RS05315	ENOG4105FR1	rard protein
FA584_RS05325	ENOG41062D9	Histidine kinase
FA584_RS05330	ENOG4105DIJ	Phosphoethanolamine transferase
FA584_RS05340	ENOG4107XTP	(EAL) domain protein
FA584_RS05355	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
FA584_RS05360	ENOG4107RT4	flavin reductase domain protein
FA584_RS05365	ENOG4105DCU	2-hydroxyglutaryl-CoA dehydratase
FA584_RS05370	ENOG4105CIZ	coA-substrate-specific enzyme activase
FA584_RS05375	ENOG4105S10	periplasmic binding protein
FA584_RS05390	ENOG4108IJ0	Aspartate ammonia-lyase
FA584_RS05395	ENOG4108IJ0	Aspartate ammonia-lyase
FA584_RS05400	ENOG4105DS2	Anaerobic c4-dicarboxylate transporter
FA584_RS05405	ENOG4105HDK	L-asparaginase
FA584_RS05410	ENOG4105BZU	Histidine kinase
FA584_RS05415	ENOG4105XJC	Two component transcriptional regulator (Winged helix family
FA584_RS05420	ENOG4105E8T	Facilitates the functional incorporation of the urease nickel metallocenter. This process requires GTP hydrolysis, probably effectuated by UreG (By similarity)
FA584_RS05435	ENOG4105CQM	Urea amidohydrolase subunit alpha
FA584_RS05440	ENOG4108YZ9	Urea amidohydrolase subunit gamma
FA584_RS05450	ENOG4108IV0	ABC, transporter
FA584_RS05455	ENOG4105C0Z	ABC transporter
FA584_RS05465	ENOG4105C32	Amino acid ABC transporter (Permease)
FA584_RS05480	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
FA584_RS05495	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
FA584_RS05535	ENOG4105EAB	amino acid AbC transporter
FA584_RS05540	ENOG4105E5Q	amino acid AbC transporter
FA584_RS05575	ENOG4105C52	Atpase, p-type (Transporting), had superfamily, subfamily ic
FA584_RS05615	ENOG4105D4F	Synthesizes selenophosphate from selenide and ATP (By similarity)
FA584_RS05620	ENOG4105VFE	sira family
FA584_RS05630	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)
FA584_RS05635	ENOG4105BZU	Histidine kinase
FA584_RS05645	ENOG4105DXB	Major Facilitator superfamily
FA584_RS05670	ENOG41078M4	ABC transporter
FA584_RS05675	ENOG4107A5B	Binding-protein-dependent transport systems, inner membrane component
FA584_RS05680	ENOG4105C8W	ABC transporter
FA584_RS05700	ENOG4105QAX	Iron-sulfur
FA584_RS05725	ENOG4105E0A	ABC, transporter
FA584_RS05730	ENOG4105EHG	Permease protein
FA584_RS05735	ENOG4105S10	periplasmic binding protein
FA584_RS05740	ENOG4108M8W	Monooxygenase
FA584_RS05760	ENOG4105M15	transport protein ExbD
FA584_RS05765	ENOG4105M8K	biopolymer transport protein
FA584_RS05770	ENOG4105F4R	Transcriptional regulator mode
FA584_RS05795	ENOG4108BSC	Methyltransferase
FA584_RS05805	ENOG4108IJ6	ABC transporter
FA584_RS05810	ENOG4105ECW	sulfate abc transporter
FA584_RS05815	ENOG4107Z6A	sulfate abc transporter permease
FA584_RS05820	ENOG4105DE7	Sulfate ABC transporter periplasmic sulfate-binding protein
FA584_RS05825	ENOG4105WMR	Protein CrcB homolog
FA584_RS05860	ENOG4105QAX	Iron-sulfur
FA584_RS05890	ENOG4105C08	Histidine kinase
FA584_RS05900	ENOG4105C1Y	Converts seryl-tRNA(Sec) to selenocysteinyl-tRNA(Sec) required for selenoprotein biosynthesis (By similarity)
FA584_RS05905	ENOG4105EM7	Selenocysteine-specific translation elongation factor
FA584_RS05925	ENOG4105C2I	pirin domain protein
FA584_RS05975	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)
FA584_RS05980	ENOG4105CKK	Glycosyl transferase, family 2
FA584_RS05990	ENOG4105CHR	reductase
FA584_RS06010	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)
FA584_RS06045	ENOG4105C1J	atp-dependent rna helicase
FA584_RS06075	ENOG4108KS2	transglutaminase domain protein
FA584_RS06085	ENOG4105DVP	Adenine-specific
FA584_RS06090	ENOG4108VYJ	response regulator receiver protein
FA584_RS06110	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
FA584_RS06130	ENOG4108UMI	ABC transporter, permease
FA584_RS06175	ENOG4108NVR	Methyl-accepting chemotaxis
FA584_RS06180	ENOG4105E1F	short-chain dehydrogenase reductase
FA584_RS06195	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)
FA584_RS06205	ENOG4107RDB	Major Facilitator
FA584_RS06210	ENOG4105W39	Membrane
FA584_RS06225	ENOG4107QPK	)-transporter
FA584_RS06230	ENOG4105S10	periplasmic binding protein
FA584_RS06240	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
FA584_RS06245	ENOG4108ZEX	molybdopterin converting factor, subunit 2
FA584_RS06255	ENOG4107XTC	May be involved in the formation or repair of Fe-S clusters present in iron-sulfur proteins
FA584_RS06265	ENOG4108JIR	Flagellum-specific ATP synthase
FA584_RS06270	ENOG4105EUJ	GTP cyclohydrolase i
FA584_RS06280	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)
FA584_RS06295	ENOG4105C0P	Mg chelatase subunit ChlI
FA584_RS06300	ENOG4108ENG	carbohydrate kinase, YjeF related protein
FA584_RS06305	ENOG4108V3E	phosphoribosylglycinamide formyltransferase
FA584_RS06310	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)
FA584_RS06340	ENOG4105EYG	tyrosine recombinase. Not involved in the cutting and rejoining of the recombining DNA molecules on dif(SL) site (By similarity)
FA584_RS06415	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
FA584_RS06455	ENOG4105BZS	acriflavin resistance protein
FA584_RS06460	ENOG4105BZS	acriflavin resistance protein
FA584_RS06465	ENOG4105ENJ	RND efflux system, outer membrane lipoprotein
FA584_RS06490	ENOG4105D1E	Undecaprenyl pyrophosphate phosphatase
FA584_RS06505	ENOG4105C26	Dehydrogenase
FA584_RS06520	ENOG4108JQ1	Dehydrogenase
FA584_RS06545	ENOG4105C8Q	Methyl-accepting chemotaxis
FA584_RS06570	ENOG4107QWP	ABC-2 type transporter
FA584_RS06575	ENOG4107QWP	ABC-2 type transporter
FA584_RS06580	ENOG4105CJ1	ABC, transporter
FA584_RS06585	ENOG4105D0S	secretion protein (HlyD
FA584_RS06595	ENOG4108DBC	nitroreductase
FA584_RS06640	ENOG4105I2S	Part of the ABC transporter complex hrt involved in hemin import. Responsible for the translocation of the substrate across the membrane (By similarity)
FA584_RS06645	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)
FA584_RS06655	ENOG4105D17	glycoside hydrolase, family 3 domain protein
FA584_RS06685	ENOG4108YYH	Nadph-dependent fmn reductase
FA584_RS06695	ENOG4108IXY	short-chain dehydrogenase reductase
FA584_RS06705	ENOG4108IJF	Heavy metal efflux pump, CzcA
FA584_RS06710	ENOG4105EP1	Efflux transporter rnd family, mfp subunit
FA584_RS06735	ENOG4105BZU	Histidine kinase
FA584_RS06755	ENOG4105ET3	Reduction of activated sulfate into sulfite (By similarity)
FA584_RS06760	ENOG4105C11	sulfate adenylyltransferase), subunit 2
FA584_RS06765	ENOG4105C3T	may be the GTPase, regulating ATP sulfurylase activity (By similarity)
FA584_RS06775	ENOG4105D06	uba thif-type nad fad binding protein
FA584_RS06785	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)
FA584_RS06790	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)
FA584_RS06795	ENOG4105C28	cystathionine
FA584_RS06805	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
FA584_RS06825	ENOG4105BZU	Histidine kinase
FA584_RS06835	ENOG4108UXE	Protein tyrosine phosphatase
FA584_RS06845	ENOG4105EE5	Membrane protein terC
FA584_RS06850	ENOG4108XUR	Pfam:DUF178
FA584_RS06855	ENOG4105D82	Glutamate dehydrogenase
FA584_RS06860	ENOG4105CZ5	Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate (By similarity)
FA584_RS06865	ENOG4105C6K	Malic enzyme
FA584_RS06870	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)
FA584_RS06880	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
FA584_RS06885	ENOG4105KM4	Acetyl-CoA carboxylase, biotin carboxyl carrier protein
FA584_RS06890	ENOG4105DHP	deoxycytidine triphosphate deaminase
FA584_RS06910	ENOG4105DR4	Methyltransferase
FA584_RS06915	ENOG4107XM9	(LipO)protein
FA584_RS06930	ENOG4105C5E	polysaccharide biosynthesis protein
FA584_RS06935	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
FA584_RS06940	ENOG4105F0R	Cytidylyltransferase
FA584_RS06950	ENOG4105DVA	methyltransferase
FA584_RS06955	ENOG4105D2T	synthase
FA584_RS06960	ENOG4105VDT	-acetyltransferase
FA584_RS06990	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)
FA584_RS06995	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)
FA584_RS07000	ENOG4105BZN	citrate synthase
FA584_RS07015	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
FA584_RS07020	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)
FA584_RS07025	ENOG4105E63	Pfam:DUF178
FA584_RS07030	ENOG4105VS8	Flagellar biosynthetic protein fliq
FA584_RS07035	ENOG4105D4A	Cell wall formation (By similarity)
FA584_RS07040	ENOG4105CHR	reductase
FA584_RS07045	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)
FA584_RS07055	ENOG4105BZU	Histidine kinase
FA584_RS07075	ENOG4105DIN	metallophosphoesterase
FA584_RS07080	ENOG4105BZG	amino acid carrier protein
FA584_RS07085	ENOG4105C2W	permease
FA584_RS07090	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)
FA584_RS07095	ENOG4105KNE	Phosphatidate cytidylyltransferase
FA584_RS07110	ENOG4105BZW	Glycerate kinase
FA584_RS07115	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)
FA584_RS07130	ENOG4107RU9	Transcriptional regulator, Crp Fnr family
FA584_RS07140	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
FA584_RS07145	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)
FA584_RS07180	ENOG4108YXW	Together with MoaA, is involved in the conversion of 5'- GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
FA584_RS07185	ENOG410885F	Protein of unknown function (DUF493)
FA584_RS07245	ENOG4105HFZ	Membrane
FA584_RS07260	ENOG4105D3S	4Fe-4S Ferredoxin, iron-sulfur binding domain protein
FA584_RS07265	ENOG4107QY8	reductase
FA584_RS07270	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)
FA584_RS07285	ENOG4105F8J	Adenylate Guanylate cyclase
FA584_RS07290	ENOG4105DHT	Metal Dependent Phosphohydrolase
FA584_RS07295	ENOG4105NU9	Preprotein translocase subunit SecG
FA584_RS07305	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)
FA584_RS07310	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)
FA584_RS07335	ENOG4108V0P	LemA family
FA584_RS07340	ENOG4105CI3	gtp-binding protein typa
FA584_RS07350	ENOG410822I	Flagellar hook capping protein
FA584_RS07355	ENOG4105BZE	flagellar hook protein, FlgE
FA584_RS07360	ENOG4105BZE	flagellar hook protein, FlgE
FA584_RS07365	ENOG41087GE	Catalyzes the formation of dTMP and tetrahydrofolate from dUMP and methylenetetrahydrofolate (By similarity)
FA584_RS07370	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)
FA584_RS07375	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)
FA584_RS07380	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)
FA584_RS07385	ENOG4105C7D	DNA gyrase negatively supercoils closed circular double- stranded DNA in an ATP-dependent manner and also catalyzes the interconversion of other topological isomers of double-stranded DNA rings, including catenanes and knotted rings (By similarity)
FA584_RS07390	ENOG4108K0B	C-di-gmp phosphodiesterase
FA584_RS07395	ENOG4105CSD	Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1) (By similarity)
FA584_RS07410	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)
FA584_RS07415	ENOG4105CEN	a g-specific adenine glycosylase
FA584_RS07420	ENOG4105C2C	drug resistance transporter, Bcr CflA
FA584_RS07435	ENOG4107GFK	fumarate
FA584_RS07445	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
FA584_RS07450	ENOG4105MQS	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
FA584_RS07500	ENOG4105C8Q	Methyl-accepting chemotaxis
FA584_RS07520	ENOG4108W2Y	isochorismatase
FA584_RS07540	ENOG4105UEI	Transcriptional Regulator AraC Family
FA584_RS07550	ENOG41074MP	UPF0103 Mediator of ErbB2-driven cell motility-containing protein
FA584_RS07560	ENOG4105NBF	ammecr1 domain protein
FA584_RS07585	ENOG41063ZK	Transcriptional Regulator AraC Family
FA584_RS07595	ENOG4105IPS	esterase
FA584_RS07605	ENOG4108IEG	Formate dehydrogenase Alpha subunit
FA584_RS07635	ENOG4105C01	Dihydroxy-acid dehydratase
FA584_RS07640	ENOG41081FY	multiple antibiotic resistance (MarC)-related
FA584_RS07650	ENOG4105C3Y	UTP-glucose-1-phosphate uridylyltransferase
FA584_RS07660	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
FA584_RS07665	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)
FA584_RS07675	ENOG4105E05	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
FA584_RS07690	ENOG4105CJD	(Anaerobic) ribonucleoside-triphosphate reductase
FA584_RS07700	ENOG4105BZH	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
FA584_RS07705	ENOG4107QTF	adenylosuccinate lyase
FA584_RS07710	ENOG4105C34	Pseudouridine synthase
FA584_RS07715	ENOG4105FBJ	fumarylacetoacetate (faa) hydrolase
FA584_RS07720	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
FA584_RS07730	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)
FA584_RS07735	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)
FA584_RS07740	ENOG4105CN5	Metallo-Beta-Lactamase
FA584_RS07745	ENOG4105C2X	Arabinose 5-phosphate isomerase
FA584_RS07750	ENOG4105FE9	pseudouridine synthase
FA584_RS07755	ENOG4105D1H	recombination factor protein RarA
FA584_RS07765	ENOG4105VM1	flagellar
FA584_RS07785	ENOG4108ZQD	Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A (By similarity)
FA584_RS07790	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)
FA584_RS07800	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
FA584_RS07815	ENOG410813J	This protein specifically catalyzes the removal of signal peptides from prolipoproteins (By similarity)
FA584_RS07825	ENOG4105C22	threonyL-tRNA synthetase
FA584_RS07830	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)
FA584_RS07840	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)
FA584_RS07845	ENOG4105C58	cytochrome c oxidase accessory protein ccog
FA584_RS07855	ENOG41082DJ	30S ribosomal protein S21
FA584_RS07865	ENOG4108UHV	Lipoprotein
FA584_RS07870	ENOG4106032	Glutathionylspermidine synthase
FA584_RS07875	ENOG4105C5I	Dehydrogenase
FA584_RS07880	ENOG4108VPT	UPF0234 protein
FA584_RS07925	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FA584_RS07945	ENOG4105DHJ	ABC, transporter
FA584_RS07950	ENOG4105CY3	ABC transporter, permease
FA584_RS07965	ENOG41076UM	multiple antibiotic resistance (MarC)-related protein
FA584_RS07970	ENOG4105C8Q	Methyl-accepting chemotaxis
FA584_RS07980	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
FA584_RS07990	ENOG4108HWB	Non-specific O-methyltransferase that catalyzes the 2 O- methylation steps in the ubiquinone biosynthetic pathway (By similarity)
FA584_RS08000	ENOG4105BZU	Histidine kinase
FA584_RS08010	ENOG4108R5K	PPIases accelerate the folding of proteins (By similarity)
FA584_RS08015	ENOG4108YZA	Nitrogen regulatory protein pii
FA584_RS08025	ENOG4105CPC	Aldo Keto reductase
FA584_RS08035	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FA584_RS08075	ENOG4105E5Q	amino acid AbC transporter
FA584_RS08080	ENOG4106PMH	Extracellular solute-binding protein family 3
FA584_RS08115	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)
FA584_RS08125	ENOG4105CEY	Amp-dependent synthetase and ligase
FA584_RS08130	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)
FA584_RS08135	ENOG4105KWU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
FA584_RS08140	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)
FA584_RS08145	ENOG4105CYU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
FA584_RS08150	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)
FA584_RS08170	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)
FA584_RS08175	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)
FA584_RS08185	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)
FA584_RS08190	ENOG4105D65	subunit l
FA584_RS08195	ENOG4105C8S	subunit m
FA584_RS08200	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)
FA584_RS08210	ENOG4105C26	Dehydrogenase
FA584_RS08215	ENOG4105DKX	Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 in tRNAs that read codons beginning with uridine, leading to the formation of N6-(dimethylallyl)adenosine (i(6)A) (By similarity)
FA584_RS08220	ENOG4105C4G	Synthesis of 3-octaprenyl-4-hydroxybenzoate (By similarity)
FA584_RS08235	ENOG4105C8Q	Methyl-accepting chemotaxis
FA584_RS08240	ENOG4107RHT	methyl-accepting chemotaxis sensory transducer with Pas Pac sensor
FA584_RS08245	ENOG4105CM1	Catalyzes, together with MoaC, the conversion of 5'-GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
FA584_RS08250	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
FA584_RS08260	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)
FA584_RS08265	ENOG41082DI	50s ribosomal protein l31
FA584_RS08275	ENOG4105C2N	RNA methyltransferase TrmH family group 3
FA584_RS08290	ENOG4105CHM	Aminotransferase
FA584_RS08295	ENOG4105D6E	homoserine dehydrogenase
FA584_RS08300	ENOG41082UM	UPF0102 protein
FA584_RS08305	ENOG4105K63	Thioredoxin
FA584_RS08310	ENOG4105C3M	thioredoxin reductase
FA584_RS08315	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
FA584_RS08325	ENOG4105N5T	Radical SAM Protein
FA584_RS08340	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
FA584_RS08350	ENOG4105CM2	brancheD-chain amino acid aminotransferase
FA584_RS08360	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
FA584_RS08365	ENOG4105XJC	Two component transcriptional regulator (Winged helix family
FA584_RS08375	ENOG4105WPN	DNA integration recombination invertion protein
FA584_RS08380	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)
FA584_RS08385	ENOG4105DAF	Involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
FA584_RS08390	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)
FA584_RS08405	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
FA584_RS08425	ENOG4105CUZ	uba thif-type nad fad binding protein
FA584_RS08430	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
FA584_RS08435	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)
FA584_RS08440	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)
FA584_RS08445	ENOG4105C0N	N-acetylglutamate semialdehyde dehydrogenase
FA584_RS08480	ENOG4105EAC	phosphoserine phosphatase
FA584_RS08490	ENOG4105CZX	twitching motility protein
FA584_RS08500	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
FA584_RS08510	ENOG4105CU5	Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine (By similarity)
FA584_RS08515	ENOG4105CQC	Prephenate dehydratase
FA584_RS08520	ENOG4105CIH	Imidazole acetol-phosphate transaminase
FA584_RS08530	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)
FA584_RS08540	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)
FA584_RS08545	ENOG4105I3K	Ferric uptake regulator, Fur family
FA584_RS08550	ENOG4105D3R	alkyl hydroperoxide reductase
FA584_RS08565	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)
FA584_RS08580	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)
FA584_RS08585	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)
FA584_RS08590	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
FA584_RS08610	ENOG4107QVM	von Willebrand factor, type A
FA584_RS08625	ENOG4105E1Z	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane
FA584_RS08635	ENOG4105K5D	4fe-4S ferredoxin iroN-sulfur binding
FA584_RS08645	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FA584_RS08655	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)
FA584_RS08665	ENOG4105D18	nicotinate-nucleotide pyrophosphorylase
FA584_RS08670	ENOG4105D00	flagellar biosynthetic protein flhB
FA584_RS08685	ENOG4105VQJ	septum formation inhibitor
FA584_RS08700	ENOG4105D5I	Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate (By similarity)
FA584_RS08720	ENOG4105K7D	Required for maturation of 30S ribosomal subunits (By similarity)
FA584_RS08725	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)
FA584_RS08750	ENOG4105BZU	Histidine kinase
FA584_RS08780	ENOG4105NQN	cytochrome C
FA584_RS08790	ENOG4105N5T	Radical SAM Protein
FA584_RS08795	ENOG4107QY8	reductase
FA584_RS08800	ENOG4105QA4	4Fe-4S Ferredoxin, iron-sulfur binding domain protein
FA584_RS08805	ENOG4105DVI	reductase, NrfD
FA584_RS08810	ENOG4105BZU	Histidine kinase
FA584_RS08820	ENOG4105QA4	4Fe-4S Ferredoxin, iron-sulfur binding domain protein
FA584_RS08825	ENOG4105DVI	reductase, NrfD
FA584_RS08835	ENOG4105BZU	Histidine kinase
FA584_RS08845	ENOG4105CSA	Coproporphyrinogen iii oxidase
FA584_RS08870	ENOG4105M15	transport protein ExbD
FA584_RS08875	ENOG4105M8K	biopolymer transport protein
FA584_RS08880	ENOG4105E2M	Manganese-dependent inorganic pyrophosphatase
FA584_RS08900	ENOG4105DVS	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
FA584_RS08915	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)
FA584_RS08930	ENOG4105BZU	Histidine kinase
FA584_RS08935	ENOG4105EKD	Catalyzes the hydrolytic deamination of adenine to hypoxanthine. Plays an important role in the purine salvage pathway and in nitrogen catabolism (By similarity)
FA584_RS08940	ENOG4105CHR	reductase
FA584_RS08945	ENOG4105CF7	AraC family transcriptional regulator
FA584_RS08950	ENOG4107RDF	Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate (By similarity)
FA584_RS08955	ENOG4105DUM	transcriptional regulator, lysR family
FA584_RS08960	ENOG4105HMI	Membrane
FA584_RS08965	ENOG4108V06	Glutathione peroxidase
FA584_RS08970	ENOG4108JYZ	YitT family
FA584_RS08980	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)
FA584_RS08985	ENOG4108Z38	Catalyzes a trans-dehydration via an enolate intermediate (By similarity)
FA584_RS08990	ENOG4105DC7	peptidase M24
FA584_RS08995	ENOG4105K8U	2-Amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase
FA584_RS09000	ENOG4105FZW	flagellar biosynthesis regulator FlhF
FA584_RS09005	ENOG4107R21	site-determining protein
FA584_RS09015	ENOG4105DN4	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FA584_RS09020	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)
FA584_RS09025	ENOG4105DD5	Flagellar motor switch protein
FA584_RS09040	ENOG4105CKK	Glycosyl transferase, family 2
FA584_RS09050	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
FA584_RS09070	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
FA584_RS09075	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)
FA584_RS09080	ENOG4105MJ2	Competence protein
FA584_RS09120	ENOG4105CM3	Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate (By similarity)
FA584_RS09135	ENOG41082XB	radical SAM domain protein
FA584_RS09145	ENOG4105H1G	trap transporter solute receptor taxi family
FA584_RS09155	ENOG4105DFP	Integrase
FA584_RS09160	ENOG4105D85	methylase
FA584_RS09180	ENOG4107R3N	Filamentation induced by cAMP protein fic
FA584_RS09185	ENOG4105F6A	helicase
FA584_RS09190	ENOG4105ECI	YeeC-like protein
FA584_RS09240	ENOG4105D01	(LipO)protein
FA584_RS09245	ENOG4108JEI	Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system (By similarity)
FA584_RS09250	ENOG4108UMI	ABC transporter, permease
FA584_RS09255	ENOG4105CJ3	phosphate transporter
FA584_RS09260	ENOG4105C80	Catalyzes the reversible oxidation of malate to oxaloacetate (By similarity)
FA584_RS09265	ENOG4107QRI	Phosphoketolase
FA584_RS09275	ENOG4106V2I	dimethylaminohydrolase
FA584_RS09315	ENOG4105K63	Thioredoxin
FA584_RS09350	ENOG4105VYA	Uncharacterized conserved protein (DUF2132)
FA584_RS09355	ENOG4105EMU	Dehydrogenase
FA584_RS09360	ENOG4105CP9	extracellular ligand-binding receptor
FA584_RS09365	ENOG4105C32	Amino acid ABC transporter (Permease)
FA584_RS09370	ENOG4105CF8	branched-chain amino acid ABC transporter, permease
FA584_RS09375	ENOG4105C0Z	ABC transporter
FA584_RS09380	ENOG4108IV0	ABC, transporter
FA584_RS09390	ENOG410802Z	Protein of unknown function (DUF328)
FA584_RS09435	ENOG4105E5V	Participates in transcription elongation, termination and antitermination (By similarity)
FA584_RS09440	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
FA584_RS09455	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)
FA584_RS09470	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)
FA584_RS09475	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)
FA584_RS09480	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)
FA584_RS09490	ENOG4105FDR	Membrane
FA584_RS09495	ENOG4105CV8	reductase
FA584_RS09505	ENOG4107QPK	)-transporter
FA584_RS09525	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FA584_RS09530	ENOG4105DEF	Extracellular solute-binding protein, family 5
FA584_RS09540	ENOG4105C8Q	Methyl-accepting chemotaxis
FA584_RS09545	ENOG4107RHT	methyl-accepting chemotaxis sensory transducer with Pas Pac sensor
FA584_RS09555	ENOG4108IEH	NADH dehydrogenase subunit g
FA584_RS09560	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)
FA584_RS09570	ENOG4107UFS	subunit j
FA584_RS09575	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)
FA584_RS09580	ENOG4105D65	subunit l
FA584_RS09590	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)
FA584_RS09595	ENOG4105BZU	Histidine kinase
FA584_RS09620	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)
FA584_RS09625	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)
FA584_RS09630	ENOG4105KWU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
FA584_RS09645	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
FA584_RS09665	ENOG4105D28	Specifically methylates the N7 position of a guanine in 16S rRNA (By similarity)
FA584_RS09685	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)
FA584_RS09695	ENOG4107T1C	Catalyzes the conversion of GTP to 2,5-diamino-6- ribosylamino-4(3H)-pyrimidinone 5'-phosphate (DARP), formate and pyrophosphate (By similarity)
FA584_RS09700	ENOG4105D52	delta-aminolevulinic acid dehydratase
FA584_RS09705	ENOG4105DBV	ornithine carbamoyltransferase
FA584_RS09710	ENOG4105T1H	UPF0763 protein
FA584_RS09720	ENOG4105CHG	glycolate oxidase (iron-sulfur subunit)
FA584_RS09735	ENOG4105K5B	UPF0225 protein
FA584_RS09750	ENOG4105BZU	Histidine kinase
FA584_RS09755	ENOG4105C3B	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
FA584_RS09760	ENOG4108S24	Fumarate reduCtase
FA584_RS09765	ENOG4105C00	Succinate dehydrogenase (Flavoprotein subunit)
FA584_RS09770	ENOG4105E33	succinate dehydrogenase
FA584_RS09780	ENOG410890F	Dynamin family
FA584_RS09790	ENOG4105F4G	Membrane
FA584_RS09795	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)
FA584_RS09800	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
FA584_RS09810	ENOG4105F6H	The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate (By similarity)
FA584_RS09825	ENOG4105CE9	30S ribosomal protein S2
FA584_RS09830	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)
FA584_RS09840	ENOG4105D19	Role in flagellar biosynthesis (By similarity)
FA584_RS09850	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
FA584_RS09860	ENOG4105C75	arginyL-tRNA synthetase
FA584_RS09870	ENOG4105BZU	Histidine kinase
FA584_RS09920	ENOG4105CP7	Triose-phosphate isomerase
FA584_RS09925	ENOG4105CSJ	Enoyl- acyl-carrier-protein reductase NADH
FA584_RS09930	ENOG4108I5X	binding-protein-dependent transport systems inner membrane Component
FA584_RS09940	ENOG4105CHV	Transcription elongation factor NusA
FA584_RS09950	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)
FA584_RS09975	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)
FA584_RS09980	ENOG4105CBM	Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 (By similarity)
FA584_RS09985	ENOG4107R03	Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate (By similarity)
FA584_RS09990	ENOG4105CG1	Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA (By similarity)
FA584_RS10015	ENOG4107QMP	dna polymerase iii subunits gamma and tau
FA584_RS10020	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)
FA584_RS10025	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
FA584_RS10030	ENOG4105BZU	Histidine kinase
FA584_RS10035	ENOG4105EJ7	Catalyzes the reduction of hydroxylamine to form NH(3) and H(2)O (By similarity)
FA584_RS10040	ENOG4105QNF	Outer membrane lipoprotein
FA584_RS10055	ENOG4105CSR	polyphosphate kinase 2
FA584_RS10070	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)
FA584_RS10075	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)
FA584_RS10085	ENOG4108YXA	Membrane
FA584_RS10090	ENOG4105C1J	atp-dependent rna helicase
FA584_RS10095	ENOG4105DDY	UPF0142 protein ycaO
FA584_RS10115	ENOG410812K	response regulator receiver protein
FA584_RS10120	ENOG4105DR6	Trap dicarboxylate transporter, dctp subunit
FA584_RS10140	ENOG4105C32	Amino acid ABC transporter (Permease)
FA584_RS10145	ENOG4105CF8	branched-chain amino acid ABC transporter, permease
FA584_RS10150	ENOG4105C0Z	ABC transporter
FA584_RS10155	ENOG4108IV0	ABC, transporter
FA584_RS10160	ENOG4105CRE	cytochrome C
FA584_RS10200	ENOG4105CEV	competence damage-inducible protein
FA584_RS10205	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)
FA584_RS10215	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)
FA584_RS10220	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)
FA584_RS10225	ENOG4105DWV	Homoserine O-trans-acetylase
FA584_RS10240	ENOG4105D06	uba thif-type nad fad binding protein
FA584_RS10245	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)
FA584_RS10250	ENOG4105DFU	Cell wall formation (By similarity)
FA584_RS10260	ENOG4105C98	muts2 protein
FA584_RS10265	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)
FA584_RS10270	ENOG4105KME	endoribonuclease L-psp
FA584_RS10275	ENOG4107RSR	Malate quinone oxidoreductase
FA584_RS10295	ENOG4105CN1	protease
FA584_RS10310	ENOG4105CA9	Pyruvate kinase
FA584_RS10320	ENOG4105K46	50S ribosomal protein l27
FA584_RS10325	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
FA584_RS10330	ENOG4105CGT	Catalyzes the transfer of a phosphate group to glutamate to form glutamate 5-phosphate which rapidly cyclizes to 5- oxoproline (By similarity)
FA584_RS10335	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)
FA584_RS10345	ENOG4107QJE	Chromosome Partitioning Protein
FA584_RS10350	ENOG4105FA0	parb-like partition protein
FA584_RS10360	ENOG4105YF2	Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) (By similarity)
FA584_RS10365	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)
FA584_RS10370	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
FA584_RS10375	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)
FA584_RS10380	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)
FA584_RS10385	ENOG41082MC	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
FA584_RS10390	ENOG4105E02	MotA TolQ exbB proton channel
FA584_RS10395	ENOG4105M8F	Biopolymer transport protein exbD tolR
FA584_RS10405	ENOG4107R6Y	Involved in the TonB-independent uptake of proteins (By similarity)
FA584_RS10410	ENOG4105UYK	outer membrane protein a
FA584_RS10420	ENOG4108YZY	peptidylprolyl cis-trans isomerase
FA584_RS10430	ENOG4105CJF	Malonyl coA-acyl carrier protein transacylase
FA584_RS10435	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)
FA584_RS10440	ENOG4105CB3	Required for the thiolation of cytidine in position 32 of tRNA, to form 2-thiocytidine (s(2)C32) (By similarity)
FA584_RS10455	ENOG4105BZ8	glutamate synthase
FA584_RS10465	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)
FA584_RS10470	ENOG4108UXA	Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA (By similarity)
FA584_RS10475	ENOG4105SCY	DNAK suppressor
FA584_RS10485	ENOG4105CEH	Catalyzes the synthesis of dihydrouridine a modified base found in the D-loop of most tRNAs (By similarity)
FA584_RS10505	ENOG4105DD5	Flagellar motor switch protein
FA584_RS10535	ENOG4105ND9	Nitrogenase-associated protein
FA584_RS10555	ENOG4105PYN	Pyridoxamine 5-phosphate oxidase-related
FA584_RS10565	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
FA584_RS10570	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)
FA584_RS10575	ENOG4105CBZ	Short-chain dehydrogenase reductase Sdr
FA584_RS10580	ENOG4105K56	Transcriptional regulator
FA584_RS10595	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)
FA584_RS10605	ENOG4105C85	amino acid
FA584_RS10610	ENOG4105HF0	Membrane
FA584_RS10615	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)
FA584_RS10620	ENOG4105CK2	sodium dicarboxylate symporter
FA584_RS10625	ENOG4105CK2	sodium dicarboxylate symporter
FA584_RS10635	ENOG4105C2M	dna polymerase I
FA584_RS10640	ENOG4108UI1	Probably functions as a manganese efflux pump (By similarity)
FA584_RS10660	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)
FA584_RS10680	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)
FA584_RS10685	ENOG4105BZU	Histidine kinase
FA584_RS10690	ENOG4105C8Q	Methyl-accepting chemotaxis
FA584_RS10695	ENOG4105CEY	Amp-dependent synthetase and ligase
FA584_RS10700	ENOG4105E2X	shikimate dehydrogenase
FA584_RS10705	ENOG4105CRQ	synthase (Component I)
FA584_RS10720	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)
FA584_RS10725	ENOG4105CRK	lysyL-tRNA synthetase
FA584_RS10740	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
FA584_RS10745	ENOG4105CZX	twitching motility protein
FA584_RS10750	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)
FA584_RS10770	ENOG4108VHG	Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis (By similarity)
FA584_RS10775	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)
FA584_RS10780	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
FA584_RS10785	ENOG4105BZU	Histidine kinase
FA584_RS10800	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)
FA584_RS10810	ENOG4108IYU	L-aspartate oxidase
FA584_RS10820	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
FA584_RS10845	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
FA584_RS10865	ENOG4105PV1	biotin lipoyl attachment domaiN-containing protein
FA584_RS10870	ENOG4105DJ1	Phosphoenolpyruvate Carboxylase
FA584_RS10875	ENOG4105CH7	arginosuccinase
FA584_RS10880	ENOG4105K59	histidine triad (HIT) protein
FA584_RS10885	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
FA584_RS10890	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
FA584_RS10895	ENOG4105CMY	5-enolpyruvylshikimate-3-phosphate synthase
FA584_RS10900	ENOG4105C48	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
FA584_RS10905	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)
FA584_RS10915	ENOG4108JQ1	Dehydrogenase
FA584_RS10925	ENOG4105ENT	Efflux transporter rnd family, mfp subunit
FA584_RS10935	ENOG4105BZS	acriflavin resistance protein
FA584_RS10950	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)
FA584_RS10955	ENOG4105C8Q	Methyl-accepting chemotaxis
FA584_RS10980	ENOG4105D86	that it carries out the mismatch recognition step. This protein has a weak ATPase activity (By similarity)
FA584_RS10990	ENOG4105QNR	S1 RNA binding domain protein
FA584_RS10995	ENOG4105CBX	hi0933 family
FA584_RS11000	ENOG4105BZU	Histidine kinase
FA584_RS11005	ENOG4108YXA	Membrane
FA584_RS11010	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)
FA584_RS11020	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
FA584_RS11025	ENOG4105ENJ	RND efflux system, outer membrane lipoprotein
FA584_RS11050	ENOG4105ENT	Efflux transporter rnd family, mfp subunit
FA584_RS11055	ENOG4107RHT	methyl-accepting chemotaxis sensory transducer with Pas Pac sensor
FA584_RS11060	ENOG4105C8Q	Methyl-accepting chemotaxis
FA584_RS11070	ENOG4105C0B	DNA polymerase III (alpha subunit)
FA584_RS11085	ENOG41067MG	lrgb family
FA584_RS11095	ENOG4105DFH	Transport of potassium into the cell (By similarity)
FA584_RS11110	ENOG4105CNI	cell division protein FtsW
FA584_RS11115	ENOG4105C34	Pseudouridine synthase
FA584_RS11125	ENOG4105CZ1	Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA (By similarity)
FA584_RS11130	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)
FA584_RS11150	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)
FA584_RS11155	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)
FA584_RS11160	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)
FA584_RS11165	ENOG4105EA8	2-Nitropropane dioxygenase
FA584_RS11170	ENOG4105C5C	n-acetylmuramoyl-l-alanine amidase
FA584_RS11180	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)
FA584_RS11185	ENOG4105C9M	aspartyl-trna synthetase
FA584_RS11190	ENOG4105BZU	Histidine kinase
FA584_RS11200	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)
FA584_RS11205	ENOG4105C4F	May be involved in recombinational repair of damaged DNA (By similarity)
FA584_RS11215	ENOG4105F8V	Hydrolase, tatD family
FA584_RS11220	ENOG41068JE	domain protein
FA584_RS11225	ENOG4105K6T	rare lipoprotein A
FA584_RS11230	ENOG4105ECC	imidazole-glycerol-phosphate dehydratase
FA584_RS11235	ENOG4108Z4R	3-deoxy-d-manno-octulosonate 8-phosphate phosphatase
FA584_RS11250	ENOG4105WHM	Necessary for normal cell division and for the maintenance of normal septation (By similarity)
FA584_RS11265	ENOG4107RVG	penicillin-binding protein
FA584_RS11290	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)
FA584_RS11300	ENOG4105CZI	D-fructose-1,6-bisphosphate 1-phosphohydrolase class 1
FA584_RS11325	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)
FA584_RS11330	ENOG4105CX6	glutaminyL-tRNA synthetase
FA584_RS11355	ENOG4105CRE	cytochrome C
FA584_RS11375	ENOG4105MJ9	esterase
FA584_RS11380	ENOG4108NIW	Leucine export protein LeuE
FA584_RS11385	ENOG4105CKK	Glycosyl transferase, family 2
FA584_RS11400	ENOG4108N5C	SNARE associated Golgi protein-related protein
FA584_RS11425	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)
FA584_RS11435	ENOG4105EMK	carboxylate amino acid amine transporter
FA584_RS11470	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)
FA584_RS11480	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)
FA584_RS11485	ENOG4108BGM	Quinol dehydrogenase periplasmic component
FA584_RS11490	ENOG4105GXZ	Ferredoxin-type protein NapH
FA584_RS11495	ENOG4108ZMS	Electron transfer subunit of the periplasmic nitrate reductase complex NapAB (By similarity)
FA584_RS11500	ENOG4108ZNS	ferredoxin-type protein NapF
FA584_RS11530	ENOG4105VYW	UPF0251 protein
FA584_RS11550	ENOG4105C4M	(Ubiquinol oxidase) subunit I
FA584_RS11555	ENOG4105CFY	cytochrome d ubiquinol oxidase, subunit ii
FA584_RS11560	ENOG4105C3G	gtp-binding protein
FA584_RS11580	ENOG4105C3J	Cysteine desulfurase
FA584_RS11595	ENOG4105ETX	regulatoR
FA584_RS11610	ENOG4105VBD	cytochrome C, class I
FA584_RS11615	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)
FA584_RS11620	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)
FA584_RS11645	ENOG4105C1J	atp-dependent rna helicase
FA584_RS11660	ENOG4105CF3	3-Hydroxyisobutyrate dehydrogenase
FA584_RS11665	ENOG4108NVR	Methyl-accepting chemotaxis
FA584_RS11680	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)
FA584_RS11685	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)
FA584_RS11700	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
FA584_RS11715	ENOG4105CDY	transcriptional regulatory protein
FA584_RS11725	ENOG4105H1G	trap transporter solute receptor taxi family
FA584_RS11750	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
FA584_RS11755	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
FA584_RS11765	ENOG4105VTR	Integrase
FA584_RS11795	ENOG4105DVI	reductase, NrfD
FA584_RS11800	ENOG4105CRE	cytochrome C
FA584_RS11825	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)
FA584_RS11845	ENOG4105BZU	Histidine kinase
FA584_RS11850	ENOG4105DY9	regulatoR
FA584_RS11860	ENOG4105DFG	type I secretion outer membrane protein
FA584_RS11865	ENOG4108JJA	ABC, transporter
FA584_RS11955	ENOG4105DWK	Membrane
FA584_RS11960	ENOG4107XM3	UPF0442 protein
FA584_RS11965	ENOG4105C59	p-type ATPase
FA584_RS11985	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)
FA584_RS11990	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)
FA584_RS11995	ENOG4105C8Q	Methyl-accepting chemotaxis
FA584_RS12000	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)
FA584_RS12015	ENOG4108UT2	hemolysin iii
FA584_RS12020	ENOG410829K	Lysine exporter protein (Lyse ygga)
FA584_RS12025	ENOG410631K	Membrane
FA584_RS12045	ENOG4105DE5	Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity (By similarity)
FA584_RS12065	ENOG4105D6J	arsenicaL-resistance protein
FA584_RS12070	ENOG4107QYE	Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation (By similarity)
FA584_RS12080	ENOG4105D0M	Protease HtpX homolog
FA584_RS12100	ENOG4105BZU	Histidine kinase
FA584_RS12105	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
FA584_RS12110	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)
FA584_RS12120	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
FA584_RS12125	ENOG4109003	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis (By similarity)
FA584_RS12135	ENOG4108YZG	isomerase
FA584_RS12140	ENOG4108Z4T	Peptidase M50
FA584_RS12145	ENOG4105C3F	Signal peptidase i
FA584_RS12150	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)
FA584_RS12160	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
FA584_RS12175	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)
FA584_RS12185	ENOG4105CB5	ATP-dependent DNA helicase recG
FA584_RS12215	ENOG410821Z	Binds to the C-terminal region of flagellin, which is implicated in polymerization, and participates in the assembly of the flagellum (By similarity)
FA584_RS12220	ENOG410901F	(LipO)protein
FA584_RS12225	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)
FA584_RS12230	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)
FA584_RS12235	ENOG4108UUM	single-stranded DNA-binding protein
FA584_RS12245	ENOG4108VMB	DNA polymerase III subunit delta'
FA584_RS12250	ENOG4105C40	3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs (By similarity)
FA584_RS12265	ENOG4107QMS	site-determining protein
FA584_RS12270	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)
FA584_RS12275	ENOG4105PXI	polysaccharide deacetylase
FA584_RS12285	ENOG4107TSN	permease
FA584_RS12290	ENOG4108UIN	ybak prolyl-trna synthetase associated region
FA584_RS12300	ENOG4105EJQ	L-serine dehydratase
FA584_RS12305	ENOG4105GSH	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
FA584_RS12310	ENOG4105EN6	Membrane
FA584_RS12315	ENOG4105C8Y	Acetylornithine aminotransferase
FA584_RS12330	ENOG410829W	Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein (By similarity)
FA584_RS12335	ENOG4105X6C	Flagellar basal body-associated protein FliL
FA584_RS12340	ENOG4105DNJ	May play a role in the repair of endogenous alkylation damage (By similarity)
FA584_RS12345	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)
FA584_RS12360	ENOG4105E4Y	Endoribonuclease that initiates mRNA decay (By similarity)
FA584_RS12365	ENOG4105BZ1	(ABC) transporter
FA584_RS12385	ENOG4105C09	Bile acid
FA584_RS12390	ENOG4108R5K	PPIases accelerate the folding of proteins (By similarity)
FA584_RS12400	ENOG4105XJC	Two component transcriptional regulator (Winged helix family
FA584_RS12410	ENOG4105BZU	Histidine kinase
FA584_RS12415	ENOG4105BZU	Histidine kinase
FA584_RS12430	ENOG4108Z66	YbaK ebsC protein
FA584_RS12490	ENOG4107RN3	metallophosphoesterase
FA584_RS12525	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)
FA584_RS12545	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)
FA584_RS12550	ENOG4105C0A	alcohol dehydrogenase
FA584_RS12555	ENOG4105BZU	Histidine kinase
FA584_RS12580	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)
FA584_RS12585	ENOG4107YD3	Thioesterase
FA584_RS12600	ENOG4108UN4	phage SPO1 DNA polymerase-related protein
FA584_RS12615	ENOG4107S73	homocitrate synthase
FA584_RS12625	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
FA584_RS12635	ENOG4105BZU	Histidine kinase
FA584_RS12650	ENOG4105CNW	domain protein
FA584_RS12665	ENOG4105D0B	Nitrogenase protein alpha chain
FA584_RS12675	ENOG4107EFR	Flavocytochrome c
FA584_RS12710	ENOG4105EGS	Mechanosensitive ion channel
FA584_RS12720	ENOG4108VQE	nitrogen fixation protein
FA584_RS12725	ENOG4105MHQ	Low-potential electron donor to a number of redox enzymes (By similarity)
FA584_RS12735	ENOG4105XV5	nifz family
FA584_RS12750	ENOG4105DTW	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FA584_RS12760	ENOG4108Z7F	N-acetyltransferase
FA584_RS12765	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)
FA584_RS12780	ENOG4105BZU	Histidine kinase
FA584_RS12800	ENOG4108VKG	metal-dependent hydrolase
FA584_RS12810	ENOG4105JAB	phenazine biosynthesis protein, phzf family
FA584_RS12815	ENOG4108594	Permease of the drug metabolite transporter
FA584_RS12820	ENOG4108W3Q	Transcriptional regulator
FA584_RS12850	ENOG4105BZU	Histidine kinase
FA584_RS12860	ENOG4105C1I	TRANSCRIPTIONAl REGULATOR GntR family
FA584_RS12875	ENOG4105BZU	Histidine kinase
FA584_RS12890	ENOG4105C8Q	Methyl-accepting chemotaxis
FA584_RS12910	ENOG4105RRV	Inherit from COG: copper resistance
FA584_RS12915	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)
FA584_RS12935	ENOG41074H6	response regulator
FA584_RS12990	ENOG4105DGM	nitrilase cyanide hydratase and apolipoprotein n-acyltransferase
FA584_RS13010	ENOG4107SDU	Methyl-accepting chemotaxis
FA584_RS13020	ENOG4105BZ8	glutamate synthase
FA584_RS13025	ENOG4105WMM	Probably plays a role in a hydrogenase nickel cofactor insertion step (By similarity)
FA584_RS13030	ENOG4108XIB	electron transport protein ysaA
FA584_RS13035	ENOG4108HM5	NADH-ubiquinone oxidoreductase chain 49kDa
FA584_RS13040	ENOG4105CYU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
FA584_RS13050	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)
FA584_RS13085	ENOG4107QZB	decarboxylase
FA584_RS13090	ENOG4105CKI	cobalamin synthesis protein
FA584_RS13095	ENOG4105VCD	cytoplasmic protein
FA584_RS13100	ENOG4105D22	carbon starvation protein
FA584_RS13110	ENOG4105C00	Succinate dehydrogenase (Flavoprotein subunit)
FA584_RS13115	ENOG41084IN	nitrogen fixation protein
FA584_RS13145	ENOG4105CG2	Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 (By similarity)
FA584_RS13150	ENOG4106NZV	Responsible for synthesis of pseudouridine from uracil- 13 in transfer RNAs (By similarity)
FA584_RS13165	ENOG4105BZU	Histidine kinase
FA584_RS13175	ENOG4105BZU	Histidine kinase
FA584_RS13200	ENOG4105C8Q	Methyl-accepting chemotaxis
FA584_RS13215	ENOG4105C5H	ABC transporter
FA584_RS13220	ENOG4108SEK	ompa motb domain protein
FA584_RS13225	ENOG4105E14	MotA TolQ exbB proton channel
FA584_RS13230	ENOG4107XI7	Tetr family transcriptional regulator
FA584_RS13245	ENOG4105ENJ	RND efflux system, outer membrane lipoprotein
FA584_RS13260	ENOG4108RCM	Nitroreductase
FA584_RS13265	ENOG4105CVP	deoxyribo-dipyrimidine photolyase
FA584_RS13275	ENOG4108JQC	penicillin-binding protein 1A
FA584_RS13290	ENOG4105DZS	Phenylacetate-CoA ligase
FA584_RS13300	ENOG4105DZS	Phenylacetate-CoA ligase
FA584_RS13350	ENOG4106H78	methyltransferase
FA584_RS13360	ENOG4105D92	Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation (By similarity)
FA584_RS13365	ENOG4105YKR	
FA584_RS13380	ENOG4105E1Q	flagellar hook-associated protein
FA584_RS13385	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
FA584_RS13395	ENOG4105CHH	sulfate transporter
FA584_RS13400	ENOG4105VSH	4-oxalocrotonate tautomerase
FA584_RS13405	ENOG4107WJT	it plays a direct role in the translocation of protons across the membrane (By similarity)
FA584_RS13415	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)
FA584_RS13425	ENOG4105CSF	NADPH-dependent glycerol-3-phosphate dehydrogenase
FA584_RS13430	ENOG4105D17	glycoside hydrolase, family 3 domain protein
FA584_RS13440	ENOG4105DI7	Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs (By similarity)
FA584_RS13450	ENOG4105EHH	Cleaves type-4 fimbrial leader sequence and methylates the N-terminal (generally Phe) residue (By similarity)
FA584_RS13465	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)
FA584_RS13470	ENOG4105CN7	Flagellar biosynthetic protein FliP
FA584_RS13475	ENOG4105DSB	aldose 1-epimerase
FA584_RS13480	ENOG4105NF4	modulator of drug activity
FA584_RS13495	ENOG4107PU6	Membrane
FA584_RS13500	ENOG4105CCT	upf0313 protein
FA584_RS13505	ENOG4107QP8	phosphohexose isomerase
FA584_RS13520	ENOG4105E3S	small subunit
FA584_RS13530	ENOG4105E3S	small subunit
FA584_RS13535	ENOG4105DPX	Hydrogenase, large subunit
FA584_RS13540	ENOG4105X7T	Ni Fe-hydrogenase, b-type cytochrome subunit
FA584_RS13545	ENOG4108USZ	hydrogenase
FA584_RS13550	ENOG4108P97	
FA584_RS13560	ENOG4105MRR	Transcriptional regulator (By similarity)
FA584_RS13570	ENOG4107RSS	Hydrogenase accessory protein HypB
FA584_RS13575	ENOG4105WRB	Hydrogenase assembly chaperone hypC hupF
FA584_RS13580	ENOG4105CQS	hydrogenase expression formation protein HypD
FA584_RS13585	ENOG4105C45	hydrogenase expression formation protein (HypE)
FA584_RS13590	ENOG4105WMM	Probably plays a role in a hydrogenase nickel cofactor insertion step (By similarity)
FA584_RS13595	ENOG4107TCE	N-acetyltransferase
FA584_RS13600	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)
FA584_RS13615	ENOG4105E9K	Isocitrate dehydrogenase
FA584_RS13620	ENOG4105C80	Catalyzes the reversible oxidation of malate to oxaloacetate (By similarity)
FA584_RS13625	ENOG4105CMV	Succinyl-CoA synthetase subunit beta
FA584_RS13630	ENOG4105CH8	Succinyl-CoA ligase ADP-forming subunit alpha
FA584_RS13640	ENOG4105DI2	Pyruvate flavodoxin ferredoxin oxidoreductase domain protein
FA584_RS13765	ENOG4105CJ1	ABC, transporter
FA584_RS13770	ENOG4107QWP	ABC-2 type transporter
FA584_RS13775	ENOG4105CMI	transporter
FA584_RS13780	ENOG41081FY	multiple antibiotic resistance (MarC)-related
FA584_RS13800	ENOG4105DFA	alanine racemase domain protein
FA584_RS13805	ENOG4105DZP	Membrane-associated zinc metalloprotease
FA584_RS13810	ENOG4105BZQ	cdp-diacylglycerol-glycerol-3-phosphate 3-phosphatidyltransferase
FA584_RS13815	ENOG4105CAN	Short-chain dehydrogenase reductase Sdr
FA584_RS13820	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
FA584_RS13830	ENOG4107QYT	Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor (By similarity)
FA584_RS13835	ENOG4105BZ1	(ABC) transporter
FA584_RS13840	ENOG4105C8N	cysteinyl-tRNA synthetase
FA584_RS13845	ENOG4105CJR	Integral membrane protein (MviN
FA584_RS13855	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)
FA584_RS13860	ENOG4105CPF	Cell wall formation (By similarity)
FA584_RS13880	ENOG4108EQQ	Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein (By similarity)
FA584_RS13885	ENOG4105C6K	Malic enzyme
FA584_RS13890	ENOG4105C6H	Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction (By similarity)
FA584_RS13895	ENOG4105KTH	gatB Yqey
FA584_RS13915	ENOG4107QHF	type ii secretion system protein e
FA584_RS13950	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)
FA584_RS13955	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)
FA584_RS13960	ENOG4108R5P	Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery (By similarity)
FA584_RS13975	ENOG4105CDH	Citrulline--aspartate ligase
FA584_RS13980	ENOG410854I	s4 domain protein
FA584_RS13985	ENOG4107S1N	anthranilate phosphoribosyltransferase
FA584_RS13990	ENOG4105K8N	protein family UPF0079, ATPase
FA584_RS13995	ENOG4108IUZ	ABC transporter
FA584_RS14000	ENOG4105DTW	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FA584_RS14020	ENOG4105VTR	Integrase
FA584_RS14045	ENOG4105C8Q	Methyl-accepting chemotaxis
FA584_RS14050	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase