locus-tag	class	description
FAI40_00005	ENOG4105CI4	it binds specifically double-stranded DNA at a 9 bp consensus (dnaA box) 5'-TTATC CA A CA A-3'. DnaA binds to ATP and to acidic phospholipids (By similarity)
FAI40_00010	ENOG4105CZ8	DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity. The beta chain is required for initiation of replication once it is clamped onto DNA, it slides freely (bidirectional and ATP- independent) along duplex DNA (By similarity)
FAI40_00015	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)
FAI40_00020	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)
FAI40_00030	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
FAI40_00045	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
FAI40_00055	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
FAI40_00090	ENOG4105HHA	aminodeoxychorismate lyase
FAI40_00095	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
FAI40_00100	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
FAI40_00110	ENOG4105CJF	Malonyl coA-acyl carrier protein transacylase
FAI40_00115	ENOG4105C9K	Endothelin-converting enzyme 1
FAI40_00120	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)
FAI40_00165	ENOG4105H9W	Short-chain dehydrogenase reductase Sdr
FAI40_00175	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)
FAI40_00185	ENOG4105KGE	Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA (By similarity)
FAI40_00190	ENOG4107RCQ	(CBS) domain
FAI40_00195	ENOG4108R9S	DSBA oxidoreductase
FAI40_00200	ENOG4107SW0	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)
FAI40_00205	ENOG4105F03	Provides the (R)-glutamate required for cell wall biosynthesis (By similarity)
FAI40_00210	ENOG4105EAH	synthase
FAI40_00215	ENOG4105E05	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
FAI40_00220	ENOG4105BZH	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
FAI40_00225	ENOG4105CSJ	Enoyl- acyl-carrier-protein reductase NADH
FAI40_00230	ENOG4108S7T	Catalyzes the oxidation of either pyridoxine 5'- phosphate (PNP) or pyridoxamine 5'-phosphate (PMP) into pyridoxal 5'-phosphate (PLP) (By similarity)
FAI40_00240	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)
FAI40_00255	ENOG4105CU0	Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA (By similarity)
FAI40_00260	ENOG4107Y7W	Participates in the translocation of lipoproteins from the inner membrane to the outer membrane. Only forms a complex with a lipoprotein if the residue after the N-terminal Cys is not an aspartate (The Asp acts as a targeting signal to indicate that the lipoprotein should stay in the inner membrane) (By similarity)
FAI40_00275	ENOG4105C4G	Synthesis of 3-octaprenyl-4-hydroxybenzoate (By similarity)
FAI40_00280	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
FAI40_00285	ENOG4105CNE	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane (By similarity)
FAI40_00295	ENOG4105CD3	dihydroorotase
FAI40_00300	ENOG4105XA0	heptosyltransferase ii
FAI40_00310	ENOG4108ZQD	Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A (By similarity)
FAI40_00325	ENOG4105F8V	Hydrolase, tatD family
FAI40_00330	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)
FAI40_00335	ENOG4107QMP	dna polymerase iii subunits gamma and tau
FAI40_00340	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
FAI40_00345	ENOG4105DZ1	carboxypeptidase
FAI40_00365	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
FAI40_00380	ENOG4105EQY	Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif (By similarity)
FAI40_00385	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
FAI40_00390	ENOG4105CUT	histidyl-tRNA synthetase
FAI40_00395	ENOG4105C4E	Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate (By similarity)
FAI40_00405	ENOG4107QWG	2-Nitropropane dioxygenase
FAI40_00410	ENOG4105CFH	Aspartokinase
FAI40_00415	ENOG4107RFD	Non-specific O-methyltransferase that catalyzes the 2 O- methylation steps in the ubiquinone biosynthetic pathway (By similarity)
FAI40_00450	ENOG4108BDP	Catalyzes the transfer of endogenously produced octanoic acid from octanoyl-acyl-carrier-protein onto the lipoyl domains of lipoate-dependent enzymes. Lipoyl-ACP can also act as a substrate although octanoyl-ACP is likely to be the physiological substrate (By similarity)
FAI40_00475	ENOG4105C0B	DNA polymerase III (alpha subunit)
FAI40_00480	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)
FAI40_00485	ENOG4105D60	lipoprotein releasing system transmembrane protein
FAI40_00490	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)
FAI40_00500	ENOG4107QNB	Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis (By similarity)
FAI40_00515	ENOG4105K70	DNA-binding protein
FAI40_00525	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)
FAI40_00530	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)
FAI40_00535	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
FAI40_00550	ENOG4105C1J	atp-dependent rna helicase
FAI40_00560	ENOG4105VG1	fes assembly suf system protein
FAI40_00565	ENOG4105C9B	Cysteine desulfurase
FAI40_00570	ENOG4105JRK	feS assembly protein SufD
FAI40_00575	ENOG4105C3K	feS assembly ATPase SufC
FAI40_00590	ENOG4106BRA	Membrane
FAI40_00590	ENOG4106BRA	Membrane
FAI40_00600	ENOG4108RWI	nicotinamidase
FAI40_00605	ENOG4105CHM	Aminotransferase
FAI40_00615	ENOG4105KK9	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
FAI40_00620	ENOG4105K46	50S ribosomal protein l27
FAI40_00625	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
FAI40_00630	ENOG4105Y2X	UPF0335 protein
FAI40_00635	ENOG4105D8W	glucose-6-phosphate 1-dehydrogenase
FAI40_00645	ENOG4107YUR	Cell division protein mraZ
FAI40_00650	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
FAI40_00665	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)
FAI40_00675	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
FAI40_00680	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
FAI40_00690	ENOG4105DVQ	Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II) (By similarity)
FAI40_00695	ENOG4105DFU	Cell wall formation (By similarity)
FAI40_00700	ENOG4105D4A	Cell wall formation (By similarity)
FAI40_00705	ENOG4105CPF	Cell wall formation (By similarity)
FAI40_00710	ENOG4108UFP	Essential cell division protein (By similarity)
FAI40_00715	ENOG4105CIT	This protein may be involved in anomalous filament growth. May be a component of the septum (By similarity)
FAI40_00720	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)
FAI40_00730	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)
FAI40_00735	ENOG4105C7C	involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
FAI40_00740	ENOG4106SNF	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane
FAI40_00745	ENOG4105C4F	May be involved in recombinational repair of damaged DNA (By similarity)
FAI40_00750	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)
FAI40_00755	ENOG4105C37	(CBS) domain
FAI40_00770	ENOG4108Z8G	Alkylphosphonate utilization operon protein PhnA
FAI40_00800	ENOG4105DYA	Acts on guanine, xanthine and to a lesser extent hypoxanthine (By similarity)
FAI40_00835	ENOG4107QXP	Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine (By similarity)
FAI40_00840	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)
FAI40_00845	ENOG4105CGT	Catalyzes the transfer of a phosphate group to glutamate to form glutamate 5-phosphate which rapidly cyclizes to 5- oxoproline (By similarity)
FAI40_00850	ENOG4108ZCF	integral membrane protein
FAI40_00855	ENOG4105DKJ	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
FAI40_00890	ENOG4105C1J	atp-dependent rna helicase
FAI40_00895	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)
FAI40_00905	ENOG4105D52	delta-aminolevulinic acid dehydratase
FAI40_00910	ENOG41082FP	UPF0102 protein
FAI40_00935	ENOG4107QPR	SAICAR synthetase
FAI40_00945	ENOG4108ZCF	integral membrane protein
FAI40_00955	ENOG4105C0G	Catalyzes the radical-mediated insertion of two sulfur atoms into the C-6 and C-8 positions of the octanoyl moiety bound to the lipoyl domains of lipoate-dependent enzymes, thereby converting the octanoylated domains into lipoylated derivatives (By similarity)
FAI40_00975	ENOG4108JYK	Dehydrogenase
FAI40_00985	ENOG4105CP7	Triose-phosphate isomerase
FAI40_00995	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
FAI40_01000	ENOG4105CXR	Phospho-2-dehydro-3-deoxyoctonate aldolase
FAI40_01015	ENOG4105W0E	50S ribosomal protein L33
FAI40_01030	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)
FAI40_01040	ENOG4105CYJ	ribosomal RNA small subunit methyltransferase B
FAI40_01065	ENOG4105CHR	reductase
FAI40_01075	ENOG4105CG2	Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 (By similarity)
FAI40_01080	ENOG4107XZX	Involved in the transcription termination process (By similarity)
FAI40_01095	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)
FAI40_01100	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)
FAI40_01110	ENOG41082FS	50S ribosomal protein L31
FAI40_01120	ENOG4105C4R	Atp-dependent dna helicase
FAI40_01125	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
FAI40_01135	ENOG4105DC7	peptidase M24
FAI40_01155	ENOG4105D06	uba thif-type nad fad binding protein
FAI40_01165	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)
FAI40_01170	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)
FAI40_01180	ENOG4106EG9	Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) (By similarity)
FAI40_01195	ENOG4105CSH	Transporter
FAI40_01210	ENOG4105PDP	Short chain dehydrogenase
FAI40_01250	ENOG4105DZG	Dehydrogenase
FAI40_01260	ENOG4105CP7	Triose-phosphate isomerase
FAI40_01270	ENOG4105C5H	ABC transporter
FAI40_01280	ENOG4105C1J	atp-dependent rna helicase
FAI40_01290	ENOG4105CHT	Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) (By similarity)
FAI40_01295	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)
FAI40_01300	ENOG41080G2	Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) (By similarity)
FAI40_01305	ENOG4107ZJC	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
FAI40_01310	ENOG4105PGM	cation diffusion facilitator family transporter
FAI40_01320	ENOG4108FN7	Aldo keto reductase
FAI40_01330	ENOG4105ENJ	RND efflux system, outer membrane lipoprotein
FAI40_01335	ENOG4108IG5	Transcriptional regulator
FAI40_01340	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
FAI40_01345	ENOG4105CW7	secretion protein, HlyD family
FAI40_01350	ENOG4105CYJ	ribosomal RNA small subunit methyltransferase B
FAI40_01355	ENOG4105DFA	alanine racemase domain protein
FAI40_01360	ENOG4105CSA	Coproporphyrinogen iii oxidase
FAI40_01370	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
FAI40_01375	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
FAI40_01380	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
FAI40_01385	ENOG4107ZGG	Associates with free 30S ribosomal subunits (but not with 30S subunits that are part of 70S ribosomes or polysomes). Essential for efficient processing of 16S rRNA. May interact with the 5'-terminal helix region of 16S rRNA (By similarity)
FAI40_01405	ENOG4105K7D	Required for maturation of 30S ribosomal subunits (By similarity)
FAI40_01420	ENOG4105E5Q	amino acid AbC transporter
FAI40_01425	ENOG4105CDA	abc transporter atp-binding protein
FAI40_01430	ENOG4107EV4	once thought to export heme, this seems not to be the case, but its exact role is uncertain. Responsible for energy coupling to the transport system (By similarity)
FAI40_01435	ENOG4105CA5	Required for the export of heme to the periplasm for the biogenesis of c-type cytochromes (By similarity)
FAI40_01440	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
FAI40_01445	ENOG4105KM4	Acetyl-CoA carboxylase, biotin carboxyl carrier protein
FAI40_01465	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)
FAI40_01470	ENOG4105CXT	aspartate transcarbamylase
FAI40_01475	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)
FAI40_01480	ENOG4105C79	DNA protecting protein DprA
FAI40_01505	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)
FAI40_01595	ENOG4105WR6	Phage protein, GP46
FAI40_01830	ENOG4108R5K	PPIases accelerate the folding of proteins (By similarity)
FAI40_01835	ENOG4108ZEF	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate (By similarity)
FAI40_01840	ENOG4105C24	DNA gyrase negatively supercoils closed circular double- stranded DNA in an ATP-dependent manner and also catalyzes the interconversion of other topological isomers of double-stranded DNA rings, including catenanes and knotted rings (By similarity)
FAI40_01850	ENOG4107QSV	RmuC domain protein
FAI40_01860	ENOG4105DIJ	Phosphoethanolamine transferase
FAI40_01865	ENOG4105DIJ	Phosphoethanolamine transferase
FAI40_01915	ENOG4108K3A	Glutathione S-transferase
FAI40_01920	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)
FAI40_01950	ENOG4105D48	metallophosphoesterase
FAI40_01955	ENOG4105MK2	5-formyltetrahydrofolate cyclo-ligase
FAI40_01990	ENOG4105CK3	Lysine 2,3-aminomutase YodO family protein
FAI40_01995	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)
FAI40_02000	ENOG4105ECY	inositol monophosphatase
FAI40_02010	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)
FAI40_02020	ENOG4105C7N	Xanthine uracil vitamin C permease
FAI40_02035	ENOG4105CTB	Polyprenyl synthetase
FAI40_02040	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)
FAI40_02045	ENOG4105DX0	Hemolysin A
FAI40_02050	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
FAI40_02060	ENOG4108V1T	peptidylprolyl cis-trans isomerase
FAI40_02065	ENOG4105C31	Tryptophanyl-tRNA synthetase
FAI40_02070	ENOG4107R5R	arsenical pump membrane protein
FAI40_02080	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)
FAI40_02085	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
FAI40_02090	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
FAI40_02095	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)
FAI40_02100	ENOG41082BR	50S ribosomal protein L35
FAI40_02130	ENOG41071I4	Phosphatidylserine decarboxylase proenzyme
FAI40_02150	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)
FAI40_02155	ENOG4108RNI	3'(2')5'-bisphosphate nucleotidase
FAI40_02160	ENOG4105EK0	Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine (By similarity)
FAI40_02185	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)
FAI40_02195	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
FAI40_02200	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)
FAI40_02205	ENOG4108ZDX	Binds together with S18 to 16S ribosomal RNA (By similarity)
FAI40_02215	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FAI40_02220	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)
FAI40_02230	ENOG4105C1M	carbamoyl-phosphate synthetase glutamine chain
FAI40_02235	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
FAI40_02240	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)
FAI40_02245	ENOG4105CJI	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
FAI40_02265	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
FAI40_02280	ENOG4105CN1	protease
FAI40_02285	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)
FAI40_02290	ENOG4105BZ1	(ABC) transporter
FAI40_02295	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
FAI40_02310	ENOG4105CEC	DNA methylase N-4 N-6
FAI40_02315	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
FAI40_02340	ENOG4108ZT0	50S ribosomal protein l17
FAI40_02345	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
FAI40_02350	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)
FAI40_02355	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
FAI40_02360	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)
FAI40_02365	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)
FAI40_02370	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
FAI40_02375	ENOG4105VPB	50S ribosomal protein L30
FAI40_02380	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)
FAI40_02385	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)
FAI40_02390	ENOG4108R5J	This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7 L12 stalk, and near the tRNA binding site of the peptidyltransferase center (By similarity)
FAI40_02395	ENOG4108UJY	One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit (By similarity)
FAI40_02400	ENOG4105VBI	Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site (By similarity)
FAI40_02405	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
FAI40_02410	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
FAI40_02415	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
FAI40_02420	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
FAI40_02430	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
FAI40_02435	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
FAI40_02440	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)
FAI40_02445	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
FAI40_02450	ENOG4105CFD	One of the primary rRNA binding proteins. Required for association of the 30S and 50S subunits to form the 70S ribosome, for tRNA binding and peptide bond formation. It has been suggested to have peptidyltransferase activity
FAI40_02455	ENOG41080KG	One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome (By similarity)
FAI40_02460	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)
FAI40_02465	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)
FAI40_02470	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
FAI40_02475	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
FAI40_02480	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)
FAI40_02485	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)
FAI40_02490	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
FAI40_02495	ENOG4107QIH	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
FAI40_02500	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)
FAI40_02505	ENOG4108VZM	50s ribosomal protein L10
FAI40_02510	ENOG4105C64	Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release (By similarity)
FAI40_02515	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
FAI40_02520	ENOG4105K7U	Cell division inhibitor that blocks the formation of polar Z ring septums. Rapidly oscillates between the poles of the cell to destabilize FtsZ filaments that have formed before they mature into polar Z rings. Prevents FtsZ polymerization (By similarity)
FAI40_02525	ENOG4107QMS	site-determining protein
FAI40_02530	ENOG4105VJP	Prevents the cell division inhibition by proteins MinC and MinD at internal division sites while permitting inhibition at polar sites. This ensures cell division at the proper site by restricting the formation of a division septum at the midpoint of the long axis of the cell (By similarity)
FAI40_02545	ENOG4105C8T	Leucyl-tRNA synthetase
FAI40_02550	ENOG4105TXM	Domain of unknown function (DUF3576)
FAI40_02575	ENOG4108ZGC	gaf domain protein
FAI40_02605	ENOG4107RY0	Catalyzes the conversion of dihydroorotate to orotate (By similarity)
FAI40_02610	ENOG4105DEI	Mannitol dehydrogenase
FAI40_02615	ENOG4108Z67	carbohydrate kinase, thermoresistant glucokinase family
FAI40_02625	ENOG4105CUV	Homoserine Kinase
FAI40_02635	ENOG4105C1J	atp-dependent rna helicase
FAI40_02645	ENOG4105ECI	YeeC-like protein
FAI40_02650	ENOG4105F6A	helicase
FAI40_02660	ENOG4105D85	methylase
FAI40_02680	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)
FAI40_02685	ENOG4105C0H	protease
FAI40_02690	ENOG4108Z6B	deaminase
FAI40_02695	ENOG4105FE9	pseudouridine synthase
FAI40_02700	ENOG4106H78	methyltransferase
FAI40_02710	ENOG4105C34	Pseudouridine synthase
FAI40_02720	ENOG4105D0A	hydroxylase
FAI40_02735	ENOG4105K59	histidine triad (HIT) protein
FAI40_02775	ENOG4106E1W	protein with protein kinase and helix-hairpin-helix DNA-binding
FAI40_02785	ENOG4108M24	von Willebrand factor, type A
FAI40_02790	ENOG4105EKD	Catalyzes the hydrolytic deamination of adenine to hypoxanthine. Plays an important role in the purine salvage pathway and in nitrogen catabolism (By similarity)
FAI40_02805	ENOG4105FNP	Molybdopterin-guanine dinucleotide biosynthesis protein b
FAI40_02825	ENOG4105EMU	Dehydrogenase
FAI40_02830	ENOG4105C5I	Dehydrogenase
FAI40_02840	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)
FAI40_02845	ENOG4105C8S	subunit m
FAI40_02850	ENOG4105D65	subunit l
FAI40_02855	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)
FAI40_02860	ENOG4107UFS	subunit j
FAI40_02875	ENOG4107R0R	NADH dehydrogenase subunit g
FAI40_02880	ENOG4107QIZ	NADH dehydrogenase
FAI40_02885	ENOG4105GKE	subunit e
FAI40_02890	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)
FAI40_02895	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)
FAI40_02900	ENOG4105KWU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
FAI40_02925	ENOG4105C2N	RNA methyltransferase TrmH family group 3
FAI40_02930	ENOG4108RCM	Nitroreductase
FAI40_02945	ENOG4105DEK	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FAI40_02960	ENOG4105BZA	Phosphoglycerate kinase
FAI40_02965	ENOG4105C17	glyceraldehyde-3-phosphate dehydrogenase
FAI40_03000	ENOG4105DFP	Integrase
FAI40_03115	ENOG4108V7X	Transcription factor that acts by binding directly to the RNA polymerase (RNAP). Required for negative regulation of rRNA expression and positive regulation of several amino acid biosynthesis promoters
FAI40_03125	ENOG4105CM1	Catalyzes, together with MoaC, the conversion of 5'-GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
FAI40_03145	ENOG410901P	UPF0249 protein
FAI40_03175	ENOG4105WPN	DNA integration recombination invertion protein
FAI40_03185	ENOG4105ZIE	Exonuclease involved in the 3' processing of various precursor tRNAs. Initiates hydrolysis at the 3'-terminus of an RNA molecule and releases 5'-mononucleotides (By similarity)
FAI40_03190	ENOG4105K63	Thioredoxin
FAI40_03195	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
FAI40_03200	ENOG4105C5N	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
FAI40_03220	ENOG4108E87	P-loop hydrolase UPF0079
FAI40_03225	ENOG4105CAY	ferredoxin--nadp reductase
FAI40_03230	ENOG4108Z7F	N-acetyltransferase
FAI40_03235	ENOG4105CHR	reductase
FAI40_03285	ENOG4105CI3	gtp-binding protein typa
FAI40_03290	ENOG4105CSD	Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1) (By similarity)
FAI40_03310	ENOG4105CKK	Glycosyl transferase, family 2
FAI40_03350	ENOG4108S55	polysaccharide biosynthesis protein
FAI40_03355	ENOG4105C26	Dehydrogenase
FAI40_03360	ENOG4105WMR	Protein CrcB homolog
FAI40_03375	ENOG4105DIJ	Phosphoethanolamine transferase
FAI40_03380	ENOG4105DIJ	Phosphoethanolamine transferase
FAI40_03385	ENOG4105CBD	Diacylglycerol kinase
FAI40_03420	ENOG4108UYE	Lactoylglutathione lyase
FAI40_03490	ENOG4105CHH	sulfate transporter
FAI40_03540	ENOG4105EQ2	LysR family Transcriptional regulator
FAI40_03545	ENOG4105ENX	hydrolase
FAI40_03555	ENOG4105C45	hydrogenase expression formation protein (HypE)
FAI40_03560	ENOG4105CQS	hydrogenase expression formation protein HypD
FAI40_03570	ENOG4107RSS	Hydrogenase accessory protein HypB
FAI40_03580	ENOG410816D	Probably plays a role in a hydrogenase nickel cofactor insertion step (By similarity)
FAI40_03585	ENOG4108MFN	small subunit of hydrogenase-3, iron-sulfur protein (part of formate hydrogenlyase (FHL) complex)
FAI40_03590	ENOG4107R30	NADH dehydrogenase
FAI40_03595	ENOG4107TDF	Formate hydrogenlyase subunit 4
FAI40_03600	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)
FAI40_03610	ENOG4105C47	NADH ubiquinone oxidoreductase 20 kda subunit
FAI40_03615	ENOG4105I6X	formate hydrogenlyase maturation
FAI40_03620	ENOG4108MG9	hydrogenase 3 maturation protease
FAI40_03625	ENOG4108RC0	Electron transport protein
FAI40_03630	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)
FAI40_03635	ENOG4105C8H	hydrogenase maturation protein Hypf
FAI40_03690	ENOG4105C5W	Aldolase
FAI40_03710	ENOG4108Z1K	This enzyme is involved in nucleotide metabolism it produces dUMP, the immediate precursor of thymidine nucleotides and it decreases the intracellular concentration of dUTP so that uracil cannot be incorporated into DNA (By similarity)
FAI40_03805	ENOG4105CPQ	Dehydrogenase
FAI40_03840	ENOG4105DRC	Na( ) H( ) antiporter that extrudes sodium in exchange for external protons (By similarity)
FAI40_03845	ENOG4107R3N	Filamentation induced by cAMP protein fic
FAI40_04095	ENOG4105DZR	Type I site-specific deoxyribonuclease
FAI40_04105	ENOG4107XZC	Restriction modification system DNA (Specificity
FAI40_04210	ENOG4105CPQ	Dehydrogenase
FAI40_04215	ENOG4105CYX	Short-chain dehydrogenase reductase Sdr
FAI40_04275	ENOG4105CPC	Aldo Keto reductase
FAI40_04520	ENOG4108RDD	Activation of anaerobic ribonucleoside-triphosphate reductase under anaerobic conditions by generation of an organic free radical, using S-adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine (By similarity)
FAI40_04525	ENOG4105CJD	(Anaerobic) ribonucleoside-triphosphate reductase
FAI40_04630	ENOG4105TW1	Carbohydrate-selective porin OprB
FAI40_04865	ENOG4108I6A	alcohol dehydrogenase
FAI40_04890	ENOG4105FBQ	ATPase associated with various cellular activities aaa_5
FAI40_04905	ENOG4107R4J	Chloride channel
FAI40_04910	ENOG4108V62	Rhodanese domain protein
FAI40_04920	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
FAI40_04925	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)
FAI40_04930	ENOG4105CFB	Gamma-glutamyltranspeptidase (EC 2.3.2.2)
FAI40_04980	ENOG4107QMH	DNA methylase
FAI40_04990	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)
FAI40_04995	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)
FAI40_05010	ENOG4105K63	Thioredoxin
FAI40_05020	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)
FAI40_05025	ENOG4107YTN	Specifically methylates the N7 position of guanine in position 527 of 16S rRNA (By similarity)
FAI40_05030	ENOG4107QJE	Chromosome Partitioning Protein
FAI40_05035	ENOG4105FA0	parb-like partition protein
FAI40_05050	ENOG4105M0C	cytoplasmic protein
FAI40_05060	ENOG41090A4	Pterin carbinolamine dehydratase
FAI40_05065	ENOG4105MIR	Phenylalanine 4-monooxygenase
FAI40_05070	ENOG4105CYX	Short-chain dehydrogenase reductase Sdr
FAI40_05080	ENOG4107SBE	Glycosyl transferase (Group 1
FAI40_05085	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)
FAI40_05090	ENOG4108R6K	riboflavin synthase, subunit alpha
FAI40_05095	ENOG4105C66	Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate (By similarity)
FAI40_05100	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)
FAI40_05115	ENOG4108S10	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)
FAI40_05135	ENOG4105C3S	Mate efflux family protein
FAI40_05150	ENOG4108YXA	Membrane
FAI40_05155	ENOG4105MN5	HAD-superfamily hydrolase subfamily IA variant 3
FAI40_05160	ENOG4105CFZ	Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III (By similarity)
FAI40_05165	ENOG4108UHJ	MAF-like protein
FAI40_05215	ENOG4108Y1S	CRISPR-associated protein, Csy4 family
FAI40_05220	ENOG4105KK4	UPF0060 membrane protein
FAI40_05225	ENOG4105C4Q	deoxyguanosinetriphosphate triphosphohydrolase-like protein
FAI40_05285	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)
FAI40_05305	ENOG4108Z1K	This enzyme is involved in nucleotide metabolism it produces dUMP, the immediate precursor of thymidine nucleotides and it decreases the intracellular concentration of dUTP so that uracil cannot be incorporated into DNA (By similarity)
FAI40_05330	ENOG4107XAN	XdhC and CoxI family
FAI40_05335	ENOG4108IYT	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)
FAI40_05340	ENOG4105C25	Primosomal protein n'
FAI40_05345	ENOG4108UUM	single-stranded DNA-binding protein
FAI40_05360	ENOG4105FD2	Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) (By similarity)
FAI40_05365	ENOG4105CJJ	Is involved in NO detoxification in an aerobic process, termed nitric oxide dioxygenase (NOD) reaction that utilizes O(2) and NAD(P)H to convert NO to nitrate, which protects the bacterium from various noxious nitrogen compounds. Therefore, plays a central role in the inducible response to nitrosative stress (By similarity)
FAI40_05375	ENOG4107RJX	Catalyzes the conversion of 6-carboxy-5,6,7,8- tetrahydropterin (CPH4) to 7-carboxy-7-deazaguanine (CDG) (By similarity)
FAI40_05385	ENOG4105CH6	catalase
FAI40_05390	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
FAI40_05405	ENOG4105DHJ	ABC, transporter
FAI40_05425	ENOG4105MRR	Transcriptional regulator (By similarity)
FAI40_05440	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
FAI40_05445	ENOG4105CJM	Binding-protein-dependent transport systems, inner membrane component
FAI40_05450	ENOG4107RNA	Nickel ABC transporter, periplasmic nickel-binding protein
FAI40_05475	ENOG4108JJ9	ABC, transporter
FAI40_05480	ENOG4108JJ8	(ABC) transporter
FAI40_05485	ENOG4105C4M	(Ubiquinol oxidase) subunit I
FAI40_05490	ENOG4105CFY	cytochrome d ubiquinol oxidase, subunit ii
FAI40_05505	ENOG4105K8U	2-Amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase
FAI40_05510	ENOG4105EEI	dihydropteroate synthase
FAI40_05520	ENOG4105KPY	Small multidrug resistance protein
FAI40_05545	ENOG4108MUZ	hydrolase
FAI40_05580	ENOG4105CJX	Molecular chaperone. Has ATPase activity (By similarity)
FAI40_05595	ENOG4105C26	Dehydrogenase
FAI40_05635	ENOG4105CIG	ABC transporter
FAI40_05650	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
FAI40_05670	ENOG4105C7P	2-oxoglutarate dehydrogenase, E1
FAI40_05695	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)
FAI40_05700	ENOG4105DPM	folylpolyglutamate synthase Dihydrofolate synthase
FAI40_05720	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)
FAI40_05725	ENOG4105ED0	Phosphorolytic exoribonuclease that removes nucleotide residues following the -CCA terminus of tRNA and adds nucleotides to the ends of RNA molecules by using nucleoside diphosphates as substrates (By similarity)
FAI40_05735	ENOG4108JQC	penicillin-binding protein 1A
FAI40_05755	ENOG4105M8F	Biopolymer transport protein exbD tolR
FAI40_05770	ENOG4105D8X	mechanosensitive ion channel
FAI40_05775	ENOG4105DHU	Bile acid
FAI40_05780	ENOG4105CEN	a g-specific adenine glycosylase
FAI40_05790	ENOG4105EAC	phosphoserine phosphatase
FAI40_05795	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)
FAI40_05800	ENOG4105C6M	Alpha-keto-beta-hydroxylacyl reductoisomerase
FAI40_05805	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
FAI40_05815	ENOG4105DKQ	ROK family
FAI40_05825	ENOG4108JQ1	Dehydrogenase
FAI40_05830	ENOG4107QM1	Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine (By similarity)
FAI40_05840	ENOG4105D03	DNA-3-methyladenine glycosylase II
FAI40_05845	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)
FAI40_05850	ENOG4108Z03	MAF-like protein
FAI40_05860	ENOG4105VYE	Inhibits all the catalytic activities of DNA gyrase by preventing its interaction with DNA. Acts by binding directly to the C-terminal domain of GyrB, which probably disrupts DNA binding by the gyrase (By similarity)
FAI40_05870	ENOG4105DZR	Type I site-specific deoxyribonuclease
FAI40_05885	ENOG4105CV8	reductase
FAI40_05905	ENOG4105EAF	CDP-diacylglycerol pyrophosphatase (EC 3.6.1.26)
FAI40_05985	ENOG4108V7B	Catalyzes the reaction of cyanate with bicarbonate to produce ammonia and carbon dioxide (By similarity)
FAI40_05990	ENOG4105M78	Catalyzes, although with low efficiency, the sulfur transfer reaction from thiosulfate to cyanide (By similarity)
FAI40_06010	ENOG4105F1S	paraquat-inducible protein a
FAI40_06015	ENOG4105DY2	Paraquat-inducible protein b
FAI40_06025	ENOG4107H9G	Necessary for formate dehydrogenase activity (By similarity)
FAI40_06055	ENOG4105E3N	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)
FAI40_06060	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
FAI40_06065	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)
FAI40_06070	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)
FAI40_06075	ENOG4107ZDE	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
FAI40_06165	ENOG4105II7	pyrroline-5-carboxylate reductase
FAI40_06175	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)
FAI40_06180	ENOG4105C3B	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
FAI40_06185	ENOG4105DBW	Multi-copper polyphenol oxidoreductase laccase
FAI40_06200	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
FAI40_06215	ENOG4107WK2	Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) (By similarity)
FAI40_06220	ENOG4107WK2	Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) (By similarity)
FAI40_06225	ENOG4105KEM	Functions as a ribosomal silencing factor. Interacts with ribosomal protein L14 (rplN), blocking formation of intersubunit bridge B8. Prevents association of the 30S and 50S ribosomal subunits and the formation of functional ribosomes, thus repressing translation (By similarity)
FAI40_06230	ENOG4108UXA	Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA (By similarity)
FAI40_06310	ENOG4105II7	pyrroline-5-carboxylate reductase
FAI40_06320	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)
FAI40_06325	ENOG4105C3B	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
FAI40_06330	ENOG4105DBW	Multi-copper polyphenol oxidoreductase laccase
FAI40_06340	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
FAI40_06345	ENOG4105C3G	gtp-binding protein
FAI40_06350	ENOG4107WK2	Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) (By similarity)
FAI40_06355	ENOG4105KEM	Functions as a ribosomal silencing factor. Interacts with ribosomal protein L14 (rplN), blocking formation of intersubunit bridge B8. Prevents association of the 30S and 50S ribosomal subunits and the formation of functional ribosomes, thus repressing translation (By similarity)
FAI40_06360	ENOG4108UXA	Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA (By similarity)
FAI40_06370	ENOG4105C5X	domain protein
FAI40_06430	ENOG4105KAE	Involved in the modulation of the specificity of the ClpAP-mediated ATP-dependent protein degradation (By similarity)
FAI40_06435	ENOG4105DZ1	carboxypeptidase
FAI40_06440	ENOG4105CA1	Removes the N-terminal methionine from nascent proteins (By similarity)
FAI40_06445	ENOG4105CFB	Gamma-glutamyltranspeptidase (EC 2.3.2.2)
FAI40_06455	ENOG4107QMP	dna polymerase iii subunits gamma and tau
FAI40_06460	ENOG4105KDX	Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection (By similarity)
FAI40_06465	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)
FAI40_06470	ENOG4105CYX	Short-chain dehydrogenase reductase Sdr
FAI40_06480	ENOG4105CAT	Cytidine monophosphate kinase
FAI40_06485	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)
FAI40_06490	ENOG4105EZR	dyp-type peroxidase family protein
FAI40_06520	ENOG4105DMF	Dehydrogenase
FAI40_06525	ENOG4108UMI	ABC transporter, permease
FAI40_06535	ENOG4105D01	(LipO)protein
FAI40_06540	ENOG4105CUB	amino acid
FAI40_06555	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)
FAI40_06560	ENOG4105C22	threonyL-tRNA synthetase
FAI40_06570	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
FAI40_06575	ENOG4105C21	Displays ATPase and GTPase activities (By similarity)
FAI40_06580	ENOG4105EGS	Mechanosensitive ion channel
FAI40_06595	ENOG4105ES5	Histidine kinase
FAI40_06600	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
FAI40_06605	ENOG4105KW8	RNA chaperone that binds small regulatory RNA (sRNAs) and mRNAs to facilitate mRNA translational regulation in response to envelope stress, environmental stress and changes in metabolite concentrations. Also binds with high specificity to tRNAs (By similarity)
FAI40_06610	ENOG4105C1N	GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis (By similarity)
FAI40_06620	ENOG4108IQD	Involved in the biosynthesis of D-alanyl-lipoteichoic acid (LTA). Catalyzes an ATP-dependent two-step reaction where it forms a high energy D-alanyl AMP intermediate and transfers the alanyl residues from AMP to Dcp (By similarity)
FAI40_06635	ENOG4107RCI	amp-dependent synthetase and ligase
FAI40_06665	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)
FAI40_06670	ENOG4108UJD	30S ribosomal protein S9
FAI40_06675	ENOG4105CM2	brancheD-chain amino acid aminotransferase
FAI40_06685	ENOG4105CM1	Catalyzes, together with MoaC, the conversion of 5'-GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
FAI40_06690	ENOG4108YXW	Together with MoaA, is involved in the conversion of 5'- GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
FAI40_06720	ENOG4108ZZ3	UPF0260 protein
FAI40_06735	ENOG4105Y49	secretion protein, HlyD family
FAI40_06740	ENOG4105ENJ	RND efflux system, outer membrane lipoprotein
FAI40_06755	ENOG4105TW1	Carbohydrate-selective porin OprB
FAI40_06760	ENOG4105TW1	Carbohydrate-selective porin OprB
FAI40_06780	ENOG41089I4	Inherit from COG: Glycosyl transferase, family 2
FAI40_06840	ENOG4108YZ9	Urea amidohydrolase subunit gamma
FAI40_06850	ENOG4105CQM	Urea amidohydrolase subunit alpha
FAI40_06855	ENOG4108VDS	Involved in urease metallocenter assembly. Binds nickel. Probably functions as a nickel donor during metallocenter assembly (By similarity)
FAI40_06860	ENOG4107Z51	Required for maturation of urease via the functional incorporation of the urease nickel metallocenter (By similarity)
FAI40_06865	ENOG4105E8T	Facilitates the functional incorporation of the urease nickel metallocenter. This process requires GTP hydrolysis, probably effectuated by UreG (By similarity)
FAI40_06870	ENOG4108XNJ	Required for maturation of urease via the functional incorporation of the urease nickel metallocenter (By similarity)
FAI40_06890	ENOG4105CCF	Lysine exporter protein (Lyse ygga)
FAI40_06905	ENOG4105DS1	cytochrome b561
FAI40_06915	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)
FAI40_06920	ENOG410626R	Converts the free carboxyl group of a malonyl-thioester to its methyl ester by transfer of a methyl group from S-adenosyl- L-methionine (SAM). It allows to synthesize pimeloyl-ACP via the fatty acid synthetic pathway (By similarity)
FAI40_06930	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)
FAI40_06935	ENOG4108JPX	Catalyzes the transfer of the alpha-amino group from S- adenosyl-L-methionine (SAM) to 7-keto-8-aminopelargonic acid (KAPA) to form 7,8-diaminopelargonic acid (DAPA). It is the only animotransferase known to utilize SAM as an amino donor (By similarity)
FAI40_06945	ENOG4108JJA	ABC, transporter
FAI40_06980	ENOG4105CV9	cyclopropane-fatty-acyl-phospholipid synthase
FAI40_06990	ENOG4105C8U	phosphate abc transporter
FAI40_06995	ENOG4105E2Z	phosphate ABC transporter (Permease
FAI40_07000	ENOG4105BZY	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
FAI40_07005	ENOG4108UTW	Plays a role in the regulation of phosphate uptake
FAI40_07010	ENOG4105C85	amino acid
FAI40_07015	ENOG4105C85	amino acid
FAI40_07020	ENOG4105C1P	efflux transporter, rnd family, mfp subunit
FAI40_07025	ENOG4105BZS	acriflavin resistance protein
FAI40_07045	ENOG4105VSH	4-oxalocrotonate tautomerase
FAI40_07075	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)
FAI40_07080	ENOG4105DHZ	alpha beta
FAI40_07085	ENOG4105C3J	Cysteine desulfurase
FAI40_07090	ENOG4105C3J	Cysteine desulfurase
FAI40_07100	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
FAI40_07110	ENOG4108JU3	Alkyl hydroperoxide reductase
FAI40_07170	ENOG4105C3E	May play a key role in the regulation of the intracellular concentration of adenosylhomocysteine (By similarity)
FAI40_07190	ENOG4105DWY	Agmatine deiminase
FAI40_07195	ENOG4105C2I	pirin domain protein
FAI40_07215	ENOG4105DR1	Catalyzes the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. Together with NAD(P)HX epimerase, which catalyzes the epimerization of the S- and R-forms, the enzyme allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration (By similarity)
FAI40_07250	ENOG4105C5F	glutamine synthetase
FAI40_07255	ENOG4105DRC	Na( ) H( ) antiporter that extrudes sodium in exchange for external protons (By similarity)
FAI40_07260	ENOG4105CVJ	phosphoglycerate mutase
FAI40_07265	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
FAI40_07290	ENOG4105NF4	modulator of drug activity
FAI40_07300	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
FAI40_07315	ENOG4105C10	Electron transfer flavoprotein
FAI40_07320	ENOG4105TPV	
FAI40_07325	ENOG4105DWH	electron transfer flavoprotein-ubiquinone oxidoreductase
FAI40_07330	ENOG4105CZ1	Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA (By similarity)
FAI40_07335	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
FAI40_07340	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
FAI40_07345	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)
FAI40_07350	ENOG4105CFG	Acts as a chaperone (By similarity)
FAI40_07370	ENOG4105DHP	deoxycytidine triphosphate deaminase
FAI40_07375	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
FAI40_07380	ENOG4108URH	decarboxylase
FAI40_07395	ENOG4105C2C	drug resistance transporter, Bcr CflA
FAI40_07400	ENOG4109003	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis (By similarity)
FAI40_07420	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
FAI40_07425	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)
FAI40_07430	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)
FAI40_07435	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)
FAI40_07440	ENOG4105C1J	atp-dependent rna helicase
FAI40_07445	ENOG4108UJU	UPF0301 protein
FAI40_07450	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
FAI40_07495	ENOG4105C1X	Bifunctional enzyme with both catalase and broad- spectrum peroxidase activity (By similarity)
FAI40_07500	ENOG4108RU0	short-chain dehydrogenase reductase
FAI40_07520	ENOG4105CK0	Membrane bOund o-acyl transferase mboat family protein
FAI40_07565	ENOG4105F4C	Redox regulated molecular chaperone. Protects both thermally unfolding and oxidatively damaged proteins from irreversible aggregation. Plays an important role in the bacterial defense system toward oxidative stress (By similarity)
FAI40_07570	ENOG4105C8Y	Acetylornithine aminotransferase
FAI40_07580	ENOG41067S4	Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. TatA could form the protein-conducting channel of the Tat system (By similarity)
FAI40_07585	ENOG4105DTN	riboflavin biosynthesis protein ribF
FAI40_07590	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)
FAI40_07595	ENOG4105M02	This protein specifically catalyzes the removal of signal peptides from prolipoproteins (By similarity)
FAI40_07605	ENOG4105DC6	This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex (By similarity)
FAI40_07615	ENOG4105E4C	Lytic transglycosylase catalytic
FAI40_07625	ENOG4108KK1	membrane protein AbrB duplication
FAI40_07635	ENOG4105DW0	Catalyzes the ADP transfer to D-glycero-D-manno-heptose 1-phosphate, yielding ADP-D,D-heptose (By similarity)
FAI40_07640	ENOG4107SZR	mannose-6-phosphate isomerase
FAI40_07650	ENOG4107R2U	Catalyzes the formation of dTMP and tetrahydrofolate from dUMP and methylenetetrahydrofolate (By similarity)
FAI40_07660	ENOG4108RDT	NADH dehydrogenase NAD(P)H nitroreductase)
FAI40_07665	ENOG41072GX	Peptidase M22 Glycoprotease
FAI40_07680	ENOG41090R7	Ferric uptake
FAI40_07690	ENOG4105CE8	Transfers the fatty acyl group on membrane lipoproteins (By similarity)
FAI40_07720	ENOG4105W49	UPF0434 protein
FAI40_07765	ENOG4105IPI	Membrane
FAI40_07770	ENOG4105F0N	pyrophosphate phospho-hydrolase
FAI40_07780	ENOG4105C5H	ABC transporter
FAI40_07790	ENOG4105C0N	N-acetylglutamate semialdehyde dehydrogenase
FAI40_07825	ENOG4108I19	Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis (By similarity)
FAI40_07850	ENOG4108MG3	formate dehydrogenase
FAI40_07855	ENOG4105QA4	4Fe-4S Ferredoxin, iron-sulfur binding domain protein
FAI40_07860	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)
FAI40_07875	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)
FAI40_07880	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)
FAI40_07885	ENOG4107QM5	aconitate hydratase
FAI40_07895	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)
FAI40_07945	ENOG4105MDH	Antioxidant protein with alkyl hydroperoxidase activity. Required for the reduction of the AhpC active site cysteine residues and for the regeneration of the AhpC enzyme activity (By similarity)
FAI40_07960	ENOG4105EJC	lysr family transcriptional regulator
FAI40_07965	ENOG4107QPD	alcohol dehydrogenase
FAI40_07990	ENOG4105CXG	d-lactate dehydrogenase
FAI40_07995	ENOG4105EE6	Alcohol dehydrogenase zinc-binding domain protein
FAI40_08010	ENOG4105CSH	Transporter
FAI40_08045	ENOG4105FA0	parb-like partition protein
FAI40_08130	ENOG4108DT4	serine threonine protein kinase
FAI40_08145	ENOG4105ER2	Ompa motb domain protein
FAI40_08240	ENOG4108RCM	Nitroreductase
FAI40_08245	ENOG4105C84	Histidine ammonia-lyase
FAI40_08270	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)
FAI40_08285	ENOG4105VXN	addiction module toxin, RelE StbE family
FAI40_08390	ENOG4108YZA	Nitrogen regulatory protein pii
FAI40_08400	ENOG4105BZU	Histidine kinase
FAI40_08405	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
FAI40_08410	ENOG4105K5M	30s ribosomal protein S16
FAI40_08415	ENOG4108ZR6	An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Probably interacts with S19. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes (By similarity)
FAI40_08420	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
FAI40_08425	ENOG4108YY1	This protein is located at the 30S-50S ribosomal subunit interface and may play a role in the structure and function of the aminoacyl-tRNA binding site (By similarity)
FAI40_08455	ENOG4105EPD	Oligopeptide transporter, Opt family
FAI40_08475	ENOG4105C48	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
FAI40_08480	ENOG4108UMW	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
FAI40_08605	ENOG4105CUB	amino acid
FAI40_08615	ENOG4105C6T	cysteine synthase
FAI40_08620	ENOG4105D7W	serine acetyltransferase
FAI40_08675	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)
FAI40_08685	ENOG4107R1I	NAD-dependent malic enzyme
FAI40_08695	ENOG4105KWW	Biogenesis protein
FAI40_08705	ENOG4105DA4	cytochrome c-type biogenesis protein
FAI40_08710	ENOG4108ZKK	Heme chaperone required for the biogenesis of c-type cytochromes. Transiently binds heme delivered by CcmC and transfers the heme to apo-cytochromes in a process facilitated by CcmF and CcmH (By similarity)
FAI40_08720	ENOG41060IM	Heme exporter protein
FAI40_08745	ENOG4105D1H	recombination factor protein RarA
FAI40_08750	ENOG4105EI2	Pseudouridine synthase
FAI40_08760	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)
FAI40_08775	ENOG4105D4P	Coproporphyrinogen iii oxidase
FAI40_08780	ENOG4105CKK	Glycosyl transferase, family 2
FAI40_08820	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)
FAI40_08855	ENOG4105YK5	50S ribosomal protein L36
FAI40_08885	ENOG4107RTZ	reductase
FAI40_08895	ENOG4105EE4	it plays a direct role in the translocation of protons across the membrane (By similarity)
FAI40_08900	ENOG41085US	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)
FAI40_08910	ENOG4108733	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)
FAI40_08920	ENOG4105SA9	Catalyzes the transfer of the L-Ara4N moiety of the glycolipid undecaprenyl phosphate-alpha-L-Ara4N to lipid A. The modified arabinose is attached to lipid A and is required for resistance to polymyxin and cationic antimicrobial peptides (By similarity)
FAI40_08935	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)
FAI40_08940	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)
FAI40_08960	ENOG4105ENN	converts alpha-aldose to the beta-anomer. It is active on D-glucose, L-arabinose, D-xylose, D-galactose, maltose and lactose (By similarity)
FAI40_08965	ENOG4105D0A	hydroxylase
FAI40_08970	ENOG4105CTR	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
FAI40_08995	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)
FAI40_09005	ENOG4105C5I	Dehydrogenase
FAI40_09010	ENOG4105KJF	protein tyrosine phosphatase
FAI40_09025	ENOG4105KPV	Transcriptional regulator
FAI40_09040	ENOG4105CEP	NADH dehydrogenase
FAI40_09045	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)
FAI40_09050	ENOG4105EIN	peptidylprolyl cis-trans isomerase
FAI40_09055	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
FAI40_09060	ENOG4105CDY	transcriptional regulatory protein
FAI40_09065	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)
FAI40_09070	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)
FAI40_09075	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)
FAI40_09080	ENOG4107YD3	Thioesterase
FAI40_09085	ENOG4105E02	MotA TolQ exbB proton channel
FAI40_09090	ENOG4108ZZF	transport protein (ExbD)
FAI40_09100	ENOG4107R6Y	Involved in the TonB-independent uptake of proteins (By similarity)
FAI40_09105	ENOG4105KCK	Peptidoglycan-associated lipoprotein
FAI40_09115	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)
FAI40_09120	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)
FAI40_09125	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
FAI40_09130	ENOG4105CV1	Transketolase (EC 2.2.1.1)
FAI40_09135	ENOG4107QYV	phosphohexose isomerase
FAI40_09140	ENOG4108J5G	6-phosphogluconate dehydrogenase
FAI40_09145	ENOG4108Q79	6-phosphogluconolactonase (EC 3.1.1.31)
FAI40_09150	ENOG4105E66	phosphoriboisomerase A
FAI40_09155	ENOG4107R03	Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate (By similarity)
FAI40_09180	ENOG4105DWF	phosphomethylpyrimidine kinase
FAI40_09185	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)
FAI40_09190	ENOG4105C4U	4-methyl-5-beta-hydroxyethylthiazole kinase
FAI40_09205	ENOG4105DVS	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
FAI40_09210	ENOG4105C03	ribonuclease
FAI40_09215	ENOG4105C5C	n-acetylmuramoyl-l-alanine amidase
FAI40_09235	ENOG4105CJN	penicillin-binding protein
FAI40_09240	ENOG4105CNI	cell division protein FtsW
FAI40_09245	ENOG4107RA9	decarboxylase
FAI40_09250	ENOG4107RA9	decarboxylase
FAI40_09255	ENOG4105C38	Glycyl-tRNA synthetase beta subunit
FAI40_09260	ENOG4107QIB	glycyl-tRNA synthetase, alpha subunit
FAI40_09270	ENOG4105C9M	aspartyl-trna synthetase
FAI40_09290	ENOG4105CGK	Exodeoxyribonuclease III
FAI40_09295	ENOG4108YX9	iron--sulfur cluster insertion protein erpA
FAI40_09300	ENOG4105C75	arginyL-tRNA synthetase
FAI40_09310	ENOG41081BE	Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. Together with TatC, TatB is part of a receptor directly interacting with Tat signal peptides. TatB may form an oligomeric binding site that transiently accommodates folded Tat precursor proteins before their translocation (By similarity)
FAI40_09315	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)
FAI40_09320	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)
FAI40_09345	ENOG4105DP0	ferredoxin-NADP reductase
FAI40_09350	ENOG4105DC8	reductase
FAI40_09375	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)
FAI40_09395	ENOG4105C8N	cysteinyl-tRNA synthetase
FAI40_09400	ENOG4107QI1	Mate efflux family protein
FAI40_09405	ENOG4105F27	Major Facilitator
FAI40_09410	ENOG4105G6W	One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the body of the 30S subunit (By similarity)
FAI40_09415	ENOG4105C8A	Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP (By similarity)
FAI40_09425	ENOG4107B2H	carbonic anhydrase
FAI40_09430	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)
FAI40_09440	ENOG4105C13	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
FAI40_09445	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)
FAI40_09450	ENOG4108I62	cina-like protein
FAI40_09455	ENOG4105M6F	mutator MutT protein
FAI40_09470	ENOG4105VFG	Promotes RNA polymerase assembly. Latches the N- and C- terminal regions of the beta' subunit thereby facilitating its interaction with the beta and alpha subunits (By similarity)
FAI40_09475	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)
FAI40_09480	ENOG4105KJV	Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein (By similarity)
FAI40_09485	ENOG4105C3F	Signal peptidase i
FAI40_09490	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)
FAI40_09495	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)
FAI40_09500	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
FAI40_09505	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)
FAI40_09510	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
FAI40_09515	ENOG4105KNE	Phosphatidate cytidylyltransferase
FAI40_09520	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)
FAI40_09525	ENOG4105DZP	Membrane-associated zinc metalloprotease
FAI40_09530	ENOG4105E1Z	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane
FAI40_09540	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)
FAI40_09545	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)
FAI40_09550	ENOG4105DAF	Involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
FAI40_09560	ENOG41084B3	50S ribosomal protein l34
FAI40_09565	ENOG41087PG	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)
FAI40_09570	ENOG4105VAS	Could be involved in insertion of integral membrane proteins into the membrane (By similarity)
FAI40_09575	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
FAI40_09580	ENOG4105WHM	Necessary for normal cell division and for the maintenance of normal septation (By similarity)
FAI40_09585	ENOG4105CAS	nag kinase
FAI40_09590	ENOG4105DMJ	Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate (By similarity)
FAI40_09595	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)
FAI40_09605	ENOG4105DI7	Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs (By similarity)
FAI40_09610	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)
FAI40_09615	ENOG4108Z02	Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions (By similarity)
FAI40_09620	ENOG4108IUZ	ABC transporter
FAI40_09635	ENOG4105C2X	Arabinose 5-phosphate isomerase
FAI40_09655	ENOG4105CNK	Required, probably indirectly, for the hydroxylation of 2-octaprenylphenol to 2-octaprenyl-6-hydroxy-phenol, the fourth step in ubiquinone biosynthesis (By similarity)
FAI40_09665	ENOG4108RRZ	Transcription elongation factor GreB
FAI40_09670	ENOG4105D7Z	glutathione synthase
FAI40_09675	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)
FAI40_09680	ENOG4108J6I	peptidase, M16
FAI40_09685	ENOG4105E1P	Modifies, by uridylylation or deuridylylation the PII (GlnB) regulatory protein (By similarity)
FAI40_09690	ENOG4105D86	that it carries out the mismatch recognition step. This protein has a weak ATPase activity (By similarity)
FAI40_09700	ENOG4105CSF	NADPH-dependent glycerol-3-phosphate dehydrogenase
FAI40_09705	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)
FAI40_09720	ENOG4105IX2	One of the proteins required for the normal export of preproteins out of the cell cytoplasm. It is a molecular chaperone that binds to a subset of precursor proteins, maintaining them in a translocation-competent state. It also specifically binds to its receptor SecA (By similarity)
FAI40_09740	ENOG4105EHG	Permease protein
FAI40_09745	ENOG4105E0A	ABC, transporter
FAI40_09750	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
FAI40_09755	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
FAI40_09765	ENOG4105DK7	lysyl-tRNA synthetase
FAI40_09775	ENOG4105HFZ	Membrane
FAI40_09785	ENOG4105ESV	Glycosyl transferase, family 4
FAI40_09795	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
FAI40_09800	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)
FAI40_09830	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
FAI40_09840	ENOG4105CA9	Pyruvate kinase
FAI40_09865	ENOG4105FE1	phytoene synthase
FAI40_09870	ENOG4107S11	squalene-associated FAD-dependent desaturase
FAI40_09885	ENOG4105CE9	30S ribosomal protein S2
FAI40_09890	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)
FAI40_09895	ENOG4107UIS	Involved in DNA repair and RecF pathway recombination (By similarity)
FAI40_09900	ENOG4105C24	DNA gyrase negatively supercoils closed circular double- stranded DNA in an ATP-dependent manner and also catalyzes the interconversion of other topological isomers of double-stranded DNA rings, including catenanes and knotted rings (By similarity)
FAI40_09905	ENOG4105CQX	Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol (By similarity)
FAI40_09915	ENOG4105C0P	Mg chelatase subunit ChlI
FAI40_09920	ENOG4105CET	Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria (By similarity)
FAI40_09925	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
FAI40_09930	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
FAI40_09935	ENOG4105VEQ	Cold shock protein
FAI40_09940	ENOG4105CB5	ATP-dependent DNA helicase recG
FAI40_09945	ENOG4108JA2	transcriptioN-repair coupling factor
FAI40_09950	ENOG4105F7M	Specifically methylates the uridine in position 2552 of 23S rRNA at the 2'-O position of the ribose in the fully assembled 50S ribosomal subunit (By similarity)
FAI40_10140	ENOG4105Y2X	UPF0335 protein
FAI40_10250	ENOG4105DFP	Integrase
FAI40_10265	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)
FAI40_10270	ENOG4105C3M	thioredoxin reductase
FAI40_10280	ENOG4105K5G	30S ribosomal protein S21
FAI40_10295	ENOG41082R8	50S ribosomal protein l32
FAI40_10300	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)
FAI40_10305	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)
FAI40_10325	ENOG4105KDC	50s ribosomal protein l28
FAI40_10330	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)
FAI40_10335	ENOG4105CJS	Phosphopantothenoylcysteine decarboxylase
FAI40_10340	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)
FAI40_10345	ENOG4105KQV	Binds directly to 16S ribosomal RNA (By similarity)
FAI40_10420	ENOG4105VUH	addiction module killer protein