locus-tag	class	description
FVE67_00005	ENOG4108HRN	Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate (By similarity)
FVE67_00015	ENOG4105BZA	Phosphoglycerate kinase
FVE67_00030	ENOG4105CD5	CoA-binding domain protein
FVE67_00095	ENOG4105D5G	Transposase
FVE67_00115	ENOG4105CP7	Triose-phosphate isomerase
FVE67_00120	ENOG4105K4P	CoA-binding domain protein
FVE67_00125	ENOG4108KVX	Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpB that pull DNA away from mid-cell into both cell halves (By similarity)
FVE67_00135	ENOG4105KWU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
FVE67_00140	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)
FVE67_00145	ENOG4105CYU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
FVE67_00150	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)
FVE67_00155	ENOG4105CMZ	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient. This subunit may bind ubiquinone (By similarity)
FVE67_00160	ENOG4105P3U	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
FVE67_00165	ENOG4105DF2	NADH dehydrogenase subunit j
FVE67_00170	ENOG4105M5H	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
FVE67_00180	ENOG4105C8S	subunit m
FVE67_00185	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)
FVE67_00195	ENOG4105NTZ	Preprotein translocase subunit SecG
FVE67_00210	ENOG4108JB9	formate dehydrogenase
FVE67_00225	ENOG4105EYX	Acetyl-CoA decarbonylase synthase complex subunit gamma
FVE67_00230	ENOG4105E8X	CO dehydrogenase acetyl-CoA synthase complex beta subunit
FVE67_00235	ENOG4106HYN	CO dehydrogenase acetyl-CoA synthase delta subunit
FVE67_00270	ENOG4105CJG	carbon-monoxide dehydrogenase catalytic subunit
FVE67_00275	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)
FVE67_00280	ENOG4105CKU	formyltetrahydrofolate synthetase
FVE67_00295	ENOG4107ZC0	Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate (By similarity)
FVE67_00305	ENOG4105CMY	5-enolpyruvylshikimate-3-phosphate synthase
FVE67_00310	ENOG4105E2X	shikimate dehydrogenase
FVE67_00315	ENOG4105FF2	Type I DHQase
FVE67_00320	ENOG4105DC1	bifunctional purine biosynthesis protein purh
FVE67_00325	ENOG4105EZY	Pyrroloquinoline quinone biosynthesis protein E
FVE67_00335	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)
FVE67_00340	ENOG4105C25	Primosomal protein n'
FVE67_00345	ENOG4105C3Y	UTP-glucose-1-phosphate uridylyltransferase
FVE67_00355	ENOG4105CZX	twitching motility protein
FVE67_00360	ENOG4105CZX	twitching motility protein
FVE67_00365	ENOG4105CAK	Cell division ATP-binding protein ftsE
FVE67_00380	ENOG4105CN1	protease
FVE67_00385	ENOG4105PXI	polysaccharide deacetylase
FVE67_00390	ENOG4105VN1	Heat shock protein
FVE67_00395	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
FVE67_00405	ENOG41072GX	Peptidase M22 Glycoprotease
FVE67_00410	ENOG4105DZP	Membrane-associated zinc metalloprotease
FVE67_00415	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)
FVE67_00420	ENOG4105KNE	Phosphatidate cytidylyltransferase
FVE67_00425	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
FVE67_00430	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)
FVE67_00435	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
FVE67_00440	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)
FVE67_00445	ENOG4105CE9	30S ribosomal protein S2
FVE67_00450	ENOG4108RZE	Tetr family transcriptional regulator
FVE67_00470	ENOG4105BZJ	Electron transfer flavoprotein
FVE67_00475	ENOG4105C10	Electron transfer flavoprotein
FVE67_00495	ENOG41090P5	ferredoxin-like protein
FVE67_00505	ENOG4107X35	defense response to bacterium
FVE67_00510	ENOG4107XSR	periplasmic solute binding protein
FVE67_00515	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)
FVE67_00520	ENOG4105DAN	ATP-dependent protease
FVE67_00535	ENOG4105D8A	3-Deoxy-D-manno-octulosonic-acid transferase
FVE67_00545	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)
FVE67_00555	ENOG4105DZS	Phenylacetate-CoA ligase
FVE67_00560	ENOG4105C7Z	Conserved Protein
FVE67_00590	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)
FVE67_00600	ENOG4108Z4T	Peptidase M50
FVE67_00605	ENOG4105C31	Tryptophanyl-tRNA synthetase
FVE67_00610	ENOG4105PW4	Sugar fermentation stimulation protein homolog
FVE67_00615	ENOG4105C79	DNA protecting protein DprA
FVE67_00635	ENOG4105FD2	Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) (By similarity)
FVE67_00645	ENOG41071TK	Uncharacterised protein family (UPF0150)
FVE67_00650	ENOG4105C3E	May play a key role in the regulation of the intracellular concentration of adenosylhomocysteine (By similarity)
FVE67_00655	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
FVE67_00660	ENOG4108MYP	Catalyzes the irreversible beta-carboxylation of phosphoenolpyruvate (PEP) to form oxaloacetate (OAA), a four- carbon dicarboxylic acid source for the tricarboxylic acid cycle (By similarity)
FVE67_00665	ENOG4105E4Y	Endoribonuclease that initiates mRNA decay (By similarity)
FVE67_00670	ENOG4105C59	p-type ATPase
FVE67_00680	ENOG4105D64	Mechanosensitive ion channel
FVE67_00705	ENOG4105C83	adenylosuccinate lyase
FVE67_00710	ENOG4105M6F	mutator MutT protein
FVE67_00725	ENOG4108ZDX	Binds together with S18 to 16S ribosomal RNA (By similarity)
FVE67_00730	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)
FVE67_00735	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
FVE67_00740	ENOG4105CDU	Replicative dna helicase
FVE67_00745	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
FVE67_00755	ENOG4105C5R	Aminotransferase
FVE67_00760	ENOG4108ZF1	Transcriptional regulator, BadM Rrf2 family
FVE67_00770	ENOG4105DWV	Homoserine O-trans-acetylase
FVE67_00780	ENOG4105D7W	serine acetyltransferase
FVE67_00795	ENOG4105NBF	ammecr1 domain protein
FVE67_00800	ENOG4105DR5	peptidase
FVE67_00810	ENOG4105CSF	NADPH-dependent glycerol-3-phosphate dehydrogenase
FVE67_00850	ENOG4107QHF	type ii secretion system protein e
FVE67_00860	ENOG4105CZ1	Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA (By similarity)
FVE67_00875	ENOG4107QIK	phosphoribosylformylglycinamidine synthase
FVE67_00885	ENOG4105CG2	Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 (By similarity)
FVE67_00910	ENOG4108YZA	Nitrogen regulatory protein pii
FVE67_00915	ENOG4105E1P	Modifies, by uridylylation or deuridylylation the PII (GlnB) regulatory protein (By similarity)
FVE67_00930	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)
FVE67_00935	ENOG4105CBF	Catalyzes the synthesis of the hydroxymethylpyrimidine phosphate (HMP-P) moiety of thiamine from aminoimidazole ribotide (AIR) in a radical S-adenosyl-L-methionine (SAM)-dependent reaction (By similarity)
FVE67_00940	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)
FVE67_00955	ENOG4105ECW	sulfate abc transporter
FVE67_00965	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)
FVE67_00970	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)
FVE67_00980	ENOG41090JN	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)
FVE67_00985	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)
FVE67_00990	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)
FVE67_01010	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)
FVE67_01015	ENOG4105DVY	radical SAM domain protein
FVE67_01025	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
FVE67_01035	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
FVE67_01045	ENOG4105C5X	domain protein
FVE67_01050	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
FVE67_01055	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
FVE67_01060	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)
FVE67_01085	ENOG4105E26	Catalyzes the methyl esterification of L-isoaspartyl residues in peptides and proteins that result from spontaneous decomposition of normal L-aspartyl and L-asparaginyl residues. It plays a role in the repair and or degradation of damaged proteins (By similarity)
FVE67_01110	ENOG4105K63	Thioredoxin
FVE67_01115	ENOG4105DNJ	May play a role in the repair of endogenous alkylation damage (By similarity)
FVE67_01140	ENOG4105QA4	4Fe-4S Ferredoxin, iron-sulfur binding domain protein
FVE67_01145	ENOG4105C3J	Cysteine desulfurase
FVE67_01150	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
FVE67_01155	ENOG4105BZU	Histidine kinase
FVE67_01165	ENOG4107G9V	glycosyl transferase, family 39
FVE67_01175	ENOG4105CW3	Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway (By similarity)
FVE67_01180	ENOG4105CDH	Citrulline--aspartate ligase
FVE67_01185	ENOG4105EAH	synthase
FVE67_01200	ENOG41084CW	50S ribosomal protein L32
FVE67_01205	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)
FVE67_01210	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)
FVE67_01215	ENOG4105FE9	pseudouridine synthase
FVE67_01220	ENOG41074MP	UPF0103 Mediator of ErbB2-driven cell motility-containing protein
FVE67_01240	ENOG4107QSA	Oxaloacetate decarboxylase
FVE67_01245	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
FVE67_01250	ENOG4105EZI	multiple antibiotic resistance (MarC)-related protein
FVE67_01260	ENOG4105DVK	Precorrin-2 c20-methyltransferase
FVE67_01270	ENOG4108HRN	Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate (By similarity)
FVE67_01275	ENOG4105C3G	gtp-binding protein
FVE67_01285	ENOG4108V3W	Chemotaxis protein, CheW
FVE67_01290	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)
FVE67_01300	ENOG4105BZU	Histidine kinase
FVE67_01305	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
FVE67_01340	ENOG4108VYJ	response regulator receiver protein
FVE67_01345	ENOG4105DN4	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FVE67_01355	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
FVE67_01360	ENOG4105D7B	Flagellar biosynthesis protein flha
FVE67_01365	ENOG4105D00	flagellar biosynthetic protein flhB
FVE67_01370	ENOG4105D19	Role in flagellar biosynthesis (By similarity)
FVE67_01375	ENOG4105VS8	Flagellar biosynthetic protein fliq
FVE67_01380	ENOG4105CN7	Flagellar biosynthetic protein FliP
FVE67_01390	ENOG4105DD5	Flagellar motor switch protein
FVE67_01395	ENOG4105D24	FliM is one of three proteins (FliG, FliN, FliM) that forms the rotor-mounted switch complex (C ring), located at the base of the basal body. This complex interacts with the CheY and CheZ chemotaxis proteins, in addition to contacting components of the motor that determine the direction of flagellar rotation (By similarity)
FVE67_01400	ENOG4105X6C	Flagellar basal body-associated protein FliL
FVE67_01405	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)
FVE67_01410	ENOG4108UVJ	appr-1-p processing domain protein
FVE67_01425	ENOG4105C0Y	Responsible for the amidation of carboxylic groups at position A and C of either cobyrinic acid or hydrogenobrynic acid. NH(2) groups are provided by glutamine, and one molecule of ATP is hydrogenolyzed for each amidation (By similarity)
FVE67_01435	ENOG4107SFQ	iron-sulfur binding
FVE67_01465	ENOG4106EG9	Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) (By similarity)
FVE67_01470	ENOG4108Z11	Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes (By similarity)
FVE67_01475	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)
FVE67_01480	ENOG4105DVS	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
FVE67_01485	ENOG4105DR5	peptidase
FVE67_01490	ENOG41084DP	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
FVE67_01500	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)
FVE67_01505	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)
FVE67_01510	ENOG4108RIR	Molybdenum cofactor biosynthesis protein
FVE67_01515	ENOG4105D4F	Synthesizes selenophosphate from selenide and ATP (By similarity)
FVE67_01520	ENOG4105KJP	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
FVE67_01530	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)
FVE67_01565	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)
FVE67_01570	ENOG4105VIE	preprotein translocase, subunit YajC
FVE67_01575	ENOG4107QXI	Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs (By similarity)
FVE67_01585	ENOG4106KXD	ATP-dependent carboxylate-amine ligase (By similarity)
FVE67_01590	ENOG4107RM1	amidohydrolase
FVE67_01595	ENOG4105E4G	Type IV pilus
FVE67_01620	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)
FVE67_01625	ENOG4105C3F	Signal peptidase i
FVE67_01630	ENOG4107R6Y	Involved in the TonB-independent uptake of proteins (By similarity)
FVE67_01635	ENOG4105CXR	Phospho-2-dehydro-3-deoxyoctonate aldolase
FVE67_01640	ENOG41089BK	Glutamine amido-transferase
FVE67_01645	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)
FVE67_01650	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)
FVE67_01655	ENOG4105W5Q	DNA repair protein (RadC
FVE67_01660	ENOG4105C48	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
FVE67_01665	ENOG4108Z6B	deaminase
FVE67_01700	ENOG4105DCG	PHP domain protein
FVE67_01705	ENOG4105VSY	K01512 acylphosphatase EC 3.6.1.7
FVE67_01710	ENOG4105D42	Cleaves the N-terminal amino acid of tripeptides (By similarity)
FVE67_01715	ENOG4105MJ2	Competence protein
FVE67_01720	ENOG4105DW0	Catalyzes the ADP transfer to D-glycero-D-manno-heptose 1-phosphate, yielding ADP-D,D-heptose (By similarity)
FVE67_01740	ENOG4105CP9	extracellular ligand-binding receptor
FVE67_01745	ENOG4105C32	Amino acid ABC transporter (Permease)
FVE67_01750	ENOG4105CF8	branched-chain amino acid ABC transporter, permease
FVE67_01755	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)
FVE67_01765	ENOG4105CVE	Lytic murein transglycosylase
FVE67_01770	ENOG4105DJZ	UPF0182 protein
FVE67_01775	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
FVE67_01790	ENOG4105X0D	Fimbrial protein
FVE67_01795	ENOG4105D52	delta-aminolevulinic acid dehydratase
FVE67_01800	ENOG4105C6P	ATP-dependent serine protease that mediates the selective degradation of mutant and abnormal proteins as well as certain short-lived regulatory proteins. Required for cellular homeostasis and for survival from DNA damage and developmental changes induced by stress. Degrades polypeptides processively to yield small peptide fragments that are 5 to 10 amino acids long. Binds to DNA in a double-stranded, site-specific manner (By similarity)
FVE67_01815	ENOG4105C8V	SAICAR synthetase
FVE67_01820	ENOG4105FA0	parb-like partition protein
FVE67_01835	ENOG4105D1F	ATP-binding protein
FVE67_01840	ENOG4105DR4	Methyltransferase
FVE67_01845	ENOG4105EAU	Plays a role in nitrite reduction (By similarity)
FVE67_01860	ENOG4105CM3	Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate (By similarity)
FVE67_01865	ENOG4105CEY	Amp-dependent synthetase and ligase
FVE67_01870	ENOG4105CKF	membrane protein involved in aromatic hydrocarbon degradation
FVE67_01875	ENOG4105G5W	regulator Fur family
FVE67_01890	ENOG4105C0Y	Responsible for the amidation of carboxylic groups at position A and C of either cobyrinic acid or hydrogenobrynic acid. NH(2) groups are provided by glutamine, and one molecule of ATP is hydrogenolyzed for each amidation (By similarity)
FVE67_01925	ENOG4108JPM	phospho-2-dehydro-3-deoxyheptonate aldolase
FVE67_01930	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
FVE67_01940	ENOG41080R2	UPF0102 protein
FVE67_01950	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)
FVE67_01955	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
FVE67_01960	ENOG41080P6	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)
FVE67_01965	ENOG4105VB6	UPF0109 protein
FVE67_01970	ENOG4105K5M	30s ribosomal protein S16
FVE67_01985	ENOG4105BZH	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
FVE67_02005	ENOG4105C3B	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
FVE67_02020	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
FVE67_02045	ENOG4105BZ1	(ABC) transporter
FVE67_02050	ENOG4105D0M	Protease HtpX homolog
FVE67_02055	ENOG4105D0M	Protease HtpX homolog
FVE67_02060	ENOG4105CI8	Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons (By similarity)
FVE67_02065	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
FVE67_02070	ENOG4105CFG	Acts as a chaperone (By similarity)
FVE67_02080	ENOG4108HU6	Metal dependent phosphohydrolase
FVE67_02085	ENOG4105DC7	peptidase M24
FVE67_02105	ENOG4108R6G	acetyltransferase
FVE67_02120	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)
FVE67_02125	ENOG4105MA4	psp1 domain protein
FVE67_02140	ENOG4105D4M	Lactamase_B
FVE67_02155	ENOG4105DDK	oxidoreductase, beta subunit
FVE67_02160	ENOG4105D95	Oxidoreductase required for the transfer of electrons from pyruvate to flavodoxin (By similarity)
FVE67_02165	ENOG4105WGB	oxidoreductase, delta subunit
FVE67_02175	ENOG4105D5G	Transposase
FVE67_02185	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FVE67_02205	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)
FVE67_02235	ENOG4105QA4	4Fe-4S Ferredoxin, iron-sulfur binding domain protein
FVE67_02245	ENOG41076CZ	activating enzyme
FVE67_02255	ENOG4105CJD	(Anaerobic) ribonucleoside-triphosphate reductase
FVE67_02270	ENOG4105QA4	4Fe-4S Ferredoxin, iron-sulfur binding domain protein
FVE67_02285	ENOG4105C0Z	ABC transporter
FVE67_02290	ENOG4108IV0	ABC, transporter
FVE67_02295	ENOG4105DZS	Phenylacetate-CoA ligase
FVE67_02310	ENOG4105EM7	Selenocysteine-specific translation elongation factor
FVE67_02315	ENOG4105F03	Provides the (R)-glutamate required for cell wall biosynthesis (By similarity)
FVE67_02325	ENOG4107Z5K	Joins Ado-cobinamide-GDP and alpha-ribazole to generate adenosylcobalamin (Ado-cobalamin) (By similarity)
FVE67_02330	ENOG4105CUP	Catalyzes the synthesis of alpha-ribazole-5'-phosphate from nicotinate mononucleotide (NAMN) and 5,6- dimethylbenzimidazole (DMB) (By similarity)
FVE67_02335	ENOG4108Z03	MAF-like protein
FVE67_02340	ENOG4105F8V	Hydrolase, tatD family
FVE67_02345	ENOG4105CC5	ABC transporter
FVE67_02350	ENOG4105FDK	ABC transporter
FVE67_02355	ENOG4105DXN	mazG family
FVE67_02365	ENOG4105C8N	cysteinyl-tRNA synthetase
FVE67_02370	ENOG4107NFR	Fructose-1,6-bisphosphatase
FVE67_02375	ENOG4105VM1	flagellar
FVE67_02385	ENOG4108ZT0	50S ribosomal protein l17
FVE67_02390	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
FVE67_02395	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)
FVE67_02400	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)
FVE67_02410	ENOG41067V7	50S ribosomal protein L36
FVE67_02415	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)
FVE67_02425	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)
FVE67_02430	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)
FVE67_02435	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
FVE67_02440	ENOG4105VPB	50S ribosomal protein L30
FVE67_02445	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)
FVE67_02450	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)
FVE67_02460	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)
FVE67_02470	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
FVE67_02475	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
FVE67_02480	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
FVE67_02485	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
FVE67_02490	ENOG41082SA	50s ribosomal protein l29
FVE67_02495	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
FVE67_02505	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)
FVE67_02510	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
FVE67_02515	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
FVE67_02520	ENOG41080UE	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)
FVE67_02530	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)
FVE67_02535	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
FVE67_02540	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
FVE67_02545	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)
FVE67_02555	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)
FVE67_02565	ENOG4105C8J	)-transporter
FVE67_02575	ENOG4105D1H	recombination factor protein RarA
FVE67_02580	ENOG4105CEH	Catalyzes the synthesis of dihydrouridine a modified base found in the D-loop of most tRNAs (By similarity)
FVE67_02590	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)
FVE67_02600	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)
FVE67_02605	ENOG4105CIT	This protein may be involved in anomalous filament growth. May be a component of the septum (By similarity)
FVE67_02610	ENOG410812A	polypeptide-transport-associated domain protein, FtsQ-type
FVE67_02615	ENOG4105D4A	Cell wall formation (By similarity)
FVE67_02620	ENOG4105DFU	Cell wall formation (By similarity)
FVE67_02625	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)
FVE67_02630	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
FVE67_02635	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
FVE67_02640	ENOG4107EES	Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide the precursor of murein (By similarity)
FVE67_02645	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)
FVE67_02660	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
FVE67_02665	ENOG4108V6E	Cell division protein mraZ
FVE67_02670	ENOG4105HHA	aminodeoxychorismate lyase
FVE67_02695	ENOG4108VXP	Specifically catalyzes the dephosphorylation of 2- phosphoglycolate. Is involved in the dissimilation of the intracellular 2-phosphoglycolate formed during the DNA repair of 3'-phosphoglycolate ends, a major class of DNA lesions induced by oxidative stress (By similarity)
FVE67_02715	ENOG4108TVJ	Nitroreductase
FVE67_02725	ENOG4105CE8	Transfers the fatty acyl group on membrane lipoproteins (By similarity)
FVE67_02730	ENOG4108JU5	Magnesium and cobalt efflux protein
FVE67_02735	ENOG4108JUA	Transcriptional regulator
FVE67_02740	ENOG4105DJ0	Poly(A) Polymerase
FVE67_02755	ENOG4105CET	Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria (By similarity)
FVE67_02770	ENOG4105K64	Glycosyl transferase, family 2
FVE67_02775	ENOG4105C6P	ATP-dependent serine protease that mediates the selective degradation of mutant and abnormal proteins as well as certain short-lived regulatory proteins. Required for cellular homeostasis and for survival from DNA damage and developmental changes induced by stress. Degrades polypeptides processively to yield small peptide fragments that are 5 to 10 amino acids long. Binds to DNA in a double-stranded, site-specific manner (By similarity)
FVE67_02780	ENOG4105CB5	ATP-dependent DNA helicase recG
FVE67_02790	ENOG4108Z4W	Probably deamidates glutamine residues to glutamate on methyl-accepting chemotaxis receptors (MCPs), playing an important role in chemotaxis (By similarity)
FVE67_02800	ENOG4105CUY	Mechanosensitive ion channel
FVE67_02820	ENOG4105DKF	Catalyzes the radical-mediated transfer of the hydroxybenzyl group from 4-hydroxyphenylpyruvate (HPP) to 5-amino- 6-ribitylamino-2,4(1H,3H)-pyrimidinedione to form 7,8-didemethyl- 8-hydroxy-5-deazariboflavin (FO) (By similarity)
FVE67_02825	ENOG4107Y3Y	amidohydrolase
FVE67_02830	ENOG4105EV6	Pfam:DUF178
FVE67_02835	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)
FVE67_02840	ENOG4105CHM	Aminotransferase
FVE67_02845	ENOG4105CM1	Catalyzes, together with MoaC, the conversion of 5'-GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
FVE67_02875	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
FVE67_02880	ENOG41082DI	50s ribosomal protein l31
FVE67_02885	ENOG4105C4P	Facilitates transcription termination by a mechanism that involves Rho binding to the nascent RNA, activation of Rho's RNA-dependent ATPase activity, and release of the mRNA from the DNA template (By similarity)
FVE67_02890	ENOG4105CFY	cytochrome d ubiquinol oxidase, subunit ii
FVE67_02895	ENOG4105C4M	(Ubiquinol oxidase) subunit I
FVE67_02905	ENOG4105D98	threonine synthase
FVE67_02910	ENOG4105C8Q	Methyl-accepting chemotaxis
FVE67_02915	ENOG4107GFK	fumarate
FVE67_02930	ENOG4107YU2	histidine triad (hIT) protein
FVE67_02945	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)
FVE67_02950	ENOG4105CEH	Catalyzes the synthesis of dihydrouridine a modified base found in the D-loop of most tRNAs (By similarity)
FVE67_02970	ENOG4105D5G	Transposase
FVE67_02975	ENOG4107QR0	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
FVE67_02980	ENOG4107QIH	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
FVE67_02985	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)
FVE67_02990	ENOG4108VZM	50s ribosomal protein L10
FVE67_03005	ENOG4105E5V	Participates in transcription elongation, termination and antitermination (By similarity)
FVE67_03020	ENOG4105WDJ	50S ribosomal protein L33
FVE67_03025	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
FVE67_03055	ENOG4105EWK	phytoene
FVE67_03075	ENOG4107S4M	Sulfate adenylate transferase
FVE67_03080	ENOG41082CS	Transfers a GMP moiety from GTP to Mo-molybdopterin (Mo- MPT) cofactor (Moco or molybdenum cofactor) to form Mo- molybdopterin guanine dinucleotide (Mo-MGD) cofactor (By similarity)
FVE67_03085	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
FVE67_03105	ENOG4105GR3	Histidine kinase
FVE67_03110	ENOG4105CQS	hydrogenase expression formation protein HypD
FVE67_03120	ENOG4108317	Binds directly to 16S ribosomal RNA (By similarity)
FVE67_03140	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
FVE67_03145	ENOG4105CAJ	Catalyzes the last two sequential reactions in the de novo biosynthetic pathway for UDP-N-acetylglucosamine (UDP- GlcNAc). The C-terminal domain catalyzes the transfer of acetyl group from acetyl coenzyme A to glucosamine-1-phosphate (GlcN-1-P) to produce N-acetylglucosamine-1-phosphate (GlcNAc-1-P), which is converted into UDP-GlcNAc by the transfer of uridine 5- monophosphate (from uridine 5-triphosphate), a reaction catalyzed by the N-terminal domain (By similarity)
FVE67_03180	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)
FVE67_03185	ENOG4105VB5	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)
FVE67_03190	ENOG4105DWF	phosphomethylpyrimidine kinase
FVE67_03195	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)
FVE67_03200	ENOG4108Z7S	Single-stranded nucleic acid binding R3H domain-containing protein
FVE67_03205	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
FVE67_03210	ENOG4105VAS	Could be involved in insertion of integral membrane proteins into the membrane (By similarity)
FVE67_03215	ENOG41084AH	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)
FVE67_03220	ENOG41085QA	50S ribosomal protein l34
FVE67_03225	ENOG4105DK0	Indole-3-glycerol phosphate synthase
FVE67_03230	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
FVE67_03235	ENOG4105E21	Catalyzes the condensation of ATP and 5-phosphoribose 1- diphosphate to form N'-(5'-phosphoribosyl)-ATP (PR-ATP). Has a crucial role in the pathway because the rate of histidine biosynthesis seems to be controlled primarily by regulation of HisG enzymatic activity (By similarity)
FVE67_03240	ENOG4108PPB	Seems to be required for the assembly of the photosystem I complex (By similarity)
FVE67_03245	ENOG4105CYQ	Catalyzes the condensation of the acetyl group of acetyl-CoA with 3-methyl-2-oxobutanoate (2-oxoisovalerate) to form 3-carboxy-3-hydroxy-4-methylpentanoate (2-isopropylmalate) (By similarity)
FVE67_03250	ENOG4105C6M	Alpha-keto-beta-hydroxylacyl reductoisomerase
FVE67_03265	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
FVE67_03280	ENOG4105BZY	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
FVE67_03285	ENOG4105E2Z	phosphate ABC transporter (Permease
FVE67_03290	ENOG4105C8U	phosphate abc transporter
FVE67_03295	ENOG4107QMV	Part of the ABC transporter complex PstSACB involved in phosphate import (By similarity)
FVE67_03300	ENOG4105BZU	Histidine kinase
FVE67_03305	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FVE67_03310	ENOG41090R7	Ferric uptake
FVE67_03320	ENOG4105CE1	Ferrous iron transport protein b
FVE67_03325	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)
FVE67_03345	ENOG4108IAJ	Nad-dependent epimerase dehydratase
FVE67_03350	ENOG4108URP	Dtdp-4-dehydrorhamnose 3,5-epimerase
FVE67_03355	ENOG4105D5U	fad dependent oxidoreductase
FVE67_03440	ENOG4105DC1	bifunctional purine biosynthesis protein purh
FVE67_03455	ENOG4105ECC	imidazole-glycerol-phosphate dehydratase
FVE67_03465	ENOG4105CJV	Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase
FVE67_03470	ENOG4105C40	3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs (By similarity)
FVE67_03475	ENOG4105BZU	Histidine kinase
FVE67_03480	ENOG41062IR	nudix hydrolase
FVE67_03505	ENOG4105CBF	Catalyzes the synthesis of the hydroxymethylpyrimidine phosphate (HMP-P) moiety of thiamine from aminoimidazole ribotide (AIR) in a radical S-adenosyl-L-methionine (SAM)-dependent reaction (By similarity)
FVE67_03510	ENOG4108UK1	Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant (By similarity)
FVE67_03515	ENOG4105C9M	aspartyl-trna synthetase
FVE67_03520	ENOG4105C1K	alpha-alpha-trehalose-phosphate synthase
FVE67_03530	ENOG41088YS	Glycosyl transferase (Group 1
FVE67_03535	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)
FVE67_03540	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)
FVE67_03555	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
FVE67_03560	ENOG4105F6H	The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate (By similarity)
FVE67_03565	ENOG4105D49	3-dehydroquinate synthase
FVE67_03570	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)
FVE67_03575	ENOG4107UUG	Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins (By similarity)
FVE67_03590	ENOG4105C0H	protease
FVE67_03615	ENOG4107ZTM	Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1) (By similarity)
FVE67_03625	ENOG4105BZU	Histidine kinase
FVE67_03635	ENOG4105CHJ	isochorismatase hydrolase
FVE67_03640	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)
FVE67_03645	ENOG4105NDF	NAD-dependent protein deacetylase which modulates the activities of several enzymes which are inactive in their acetylated form. May also have NAD-dependent lysine demalonylase and desuccinylase activity (By similarity)
FVE67_03650	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)
FVE67_03665	ENOG4105D5G	Transposase
FVE67_03675	ENOG4108YZA	Nitrogen regulatory protein pii
FVE67_03685	ENOG4105D5G	Transposase
FVE67_03705	ENOG4105D6W	Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps (By similarity)
FVE67_03720	ENOG4105F55	Catalyzes the isomerization of sedoheptulose 7-phosphate in D-glycero-D-manno-heptose 7-phosphate (By similarity)
FVE67_03740	ENOG4105C6P	ATP-dependent serine protease that mediates the selective degradation of mutant and abnormal proteins as well as certain short-lived regulatory proteins. Required for cellular homeostasis and for survival from DNA damage and developmental changes induced by stress. Degrades polypeptides processively to yield small peptide fragments that are 5 to 10 amino acids long. Binds to DNA in a double-stranded, site-specific manner (By similarity)
FVE67_03745	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)
FVE67_03750	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)
FVE67_03755	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
FVE67_03770	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)
FVE67_03775	ENOG4108YZT	Adenosylcobinamide kinase
FVE67_03790	ENOG4106H78	methyltransferase
FVE67_03800	ENOG4105C5U	The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrA is an ATPase and a DNA-binding protein. A damage recognition complex composed of 2 UvrA and 2 UvrB subunits scans DNA for abnormalities. When the presence of a lesion has been verified by UvrB, the UvrA molecules dissociate (By similarity)
FVE67_03810	ENOG4105CB3	Required for the thiolation of cytidine in position 32 of tRNA, to form 2-thiocytidine (s(2)C32) (By similarity)
FVE67_03820	ENOG4107T5V	SNARE associated Golgi
FVE67_03825	ENOG4108ZGY	Transcriptional regulator (AsnC family)
FVE67_03830	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)
FVE67_03835	ENOG4105C4G	Synthesis of 3-octaprenyl-4-hydroxybenzoate (By similarity)
FVE67_03845	ENOG4108UMA	3-octaprenyl-4-hydroxybenzoate carboxy-lyase
FVE67_03850	ENOG4108UMW	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
FVE67_03860	ENOG4105CB8	Multifunctional enzyme that catalyzes the SAM-dependent methylation of uroporphyrinogen III at position C-2 and C-7 to form precorrin-2 and then position C-12 or C-18 to form trimethylpyrrocorphin 2. It also catalyzes the conversion of precorrin-2 into siroheme. This reaction consists of the NAD- dependent oxidation of precorrin-2 into sirohydrochlorin and its subsequent ferrochelation into siroheme (By similarity)
FVE67_03870	ENOG4108ZAI	phosphatidylglycerophosphatase a
FVE67_03875	ENOG4107TSX	ABC branched chain amino acid family transporter periplasmic ligand binding protein
FVE67_03885	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)
FVE67_03890	ENOG4105CNN	ABC, transporter
FVE67_03905	ENOG4108UMR	transcriptional regulator AsnC family
FVE67_03920	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
FVE67_03930	ENOG4108R86	Transcriptional regulator
FVE67_03935	ENOG4105CW7	secretion protein, HlyD family
FVE67_03935	ENOG4105CW7	secretion protein, HlyD family
FVE67_03940	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
FVE67_03955	ENOG4108ESY	Metal dependent phosphohydrolase
FVE67_03965	ENOG4105DI7	Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs (By similarity)
FVE67_03970	ENOG4105C0N	N-acetylglutamate semialdehyde dehydrogenase
FVE67_03975	ENOG4108UJD	30S ribosomal protein S9
FVE67_03980	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)
FVE67_03995	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
FVE67_04000	ENOG4108Y5D	Inherit from COG: cdp-diacylglycerol-glycerol-3-phosphate 3-phosphatidyltransferase
FVE67_04030	ENOG4105CJF	Malonyl coA-acyl carrier protein transacylase
FVE67_04035	ENOG4105KE9	The glycine cleavage system catalyzes the degradation of glycine. The H protein shuttles the methylamine group of glycine from the P protein to the T protein (By similarity)
FVE67_04055	ENOG4105DF0	Responsible for channeling the electrons from the oxidation of dihydroorotate from the FMN redox center in the PyrD type B subunit to the ultimate electron acceptor NAD( ) (By similarity)
FVE67_04060	ENOG4107RY0	Catalyzes the conversion of dihydroorotate to orotate (By similarity)
FVE67_04075	ENOG4105XA0	heptosyltransferase ii
FVE67_04080	ENOG4105C5U	The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrA is an ATPase and a DNA-binding protein. A damage recognition complex composed of 2 UvrA and 2 UvrB subunits scans DNA for abnormalities. When the presence of a lesion has been verified by UvrB, the UvrA molecules dissociate (By similarity)
FVE67_04110	ENOG4105BZU	Histidine kinase
FVE67_04135	ENOG4105CM2	brancheD-chain amino acid aminotransferase
FVE67_04140	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)
FVE67_04145	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)
FVE67_04150	ENOG4105CIZ	coA-substrate-specific enzyme activase
FVE67_04165	ENOG4107WJT	it plays a direct role in the translocation of protons across the membrane (By similarity)
FVE67_04170	ENOG4105VH4	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)
FVE67_04175	ENOG4105C0P	Mg chelatase subunit ChlI
FVE67_04180	ENOG4108VTU	Cdp-alcohol phosphatidyltransferase
FVE67_04185	ENOG4105CU0	Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA (By similarity)
FVE67_04215	ENOG4105D5G	Transposase
FVE67_04220	ENOG4105CIZ	coA-substrate-specific enzyme activase
FVE67_04230	ENOG4108YZA	Nitrogen regulatory protein pii
FVE67_04245	ENOG4105CY9	nitrogenase molybdenum-iron protein beta chain
FVE67_04255	ENOG4105CGC	Nitrogenase cofactor biosynthesis protein NifB
FVE67_04260	ENOG4108YZA	Nitrogen regulatory protein pii
FVE67_04265	ENOG4108YZA	Nitrogen regulatory protein pii
FVE67_04270	ENOG4105DSM	The key enzymatic reactions in nitrogen fixation are catalyzed by the nitrogenase complex, which has 2 components the iron protein and the molybdenum-iron protein (By similarity)
FVE67_04275	ENOG4107S73	homocitrate synthase
FVE67_04280	ENOG4108JUA	Transcriptional regulator
FVE67_04290	ENOG4105D5G	Transposase
FVE67_04315	ENOG4105BZU	Histidine kinase
FVE67_04320	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)
FVE67_04325	ENOG4105M02	This protein specifically catalyzes the removal of signal peptides from prolipoproteins (By similarity)
FVE67_04335	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
FVE67_04340	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
FVE67_04345	ENOG4105ERG	peptidase m48, ste24p
FVE67_04360	ENOG4105FA0	parb-like partition protein
FVE67_04365	ENOG4107QJE	Chromosome Partitioning Protein
FVE67_04370	ENOG4105BZU	Histidine kinase
FVE67_04385	ENOG4105K6T	rare lipoprotein A
FVE67_04390	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)
FVE67_04395	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)
FVE67_04400	ENOG4105C7C	involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
FVE67_04405	ENOG410801I	Peptidyl-prolyl cis-trans isomerase
FVE67_04415	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
FVE67_04420	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)
FVE67_04425	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)
FVE67_04430	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)
FVE67_04435	ENOG4105CDY	transcriptional regulatory protein
FVE67_04445	ENOG4107ZBH	radical SAM domain protein
FVE67_04455	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
FVE67_04460	ENOG4105MQS	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
FVE67_04470	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)
FVE67_04475	ENOG41074MP	UPF0103 Mediator of ErbB2-driven cell motility-containing protein
FVE67_04495	ENOG4105CJN	penicillin-binding protein
FVE67_04500	ENOG4105CNI	cell division protein FtsW
FVE67_04510	ENOG4105TYC	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)
FVE67_04515	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)
FVE67_04520	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
FVE67_04525	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)
FVE67_04530	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)
FVE67_04535	ENOG41082MC	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
FVE67_04555	ENOG4108M29	
FVE67_04560	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
FVE67_04570	ENOG4108R6K	riboflavin synthase, subunit alpha
FVE67_04575	ENOG4105K8I	Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpA that pull DNA away from mid-cell into both cell halves (By similarity)
FVE67_04590	ENOG4108UXA	Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA (By similarity)
FVE67_04595	ENOG4105C1Y	Converts seryl-tRNA(Sec) to selenocysteinyl-tRNA(Sec) required for selenoprotein biosynthesis (By similarity)
FVE67_04605	ENOG4105IES	Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA (By similarity)
FVE67_04620	ENOG4105BZ3	General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) (By similarity)
FVE67_04625	ENOG4105KRI	phosphocarrier protein (HPr
FVE67_04640	ENOG4105EHZ	conserved protein UCP016719
FVE67_04645	ENOG4105C5C	n-acetylmuramoyl-l-alanine amidase
FVE67_04650	ENOG4105D86	that it carries out the mismatch recognition step. This protein has a weak ATPase activity (By similarity)
FVE67_04655	ENOG4108Z1W	Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) (By similarity)
FVE67_04665	ENOG4105DX0	Hemolysin A
FVE67_04675	ENOG4105DZA	Converts GTP to 7,8-dihydroneopterin triphosphate (By similarity)
FVE67_04680	ENOG41080XS	Cobyrinic acid ac-diamide synthase
FVE67_04685	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)
FVE67_04690	ENOG4105C12	Phosphoribosylglycinamide synthetase
FVE67_04695	ENOG4105CU5	Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine (By similarity)
FVE67_04705	ENOG4105DDQ	anthranilate synthase
FVE67_04720	ENOG4105CD5	CoA-binding domain protein
FVE67_04725	ENOG4108UGV	hypoxanthine phosphoribosyltransferase
FVE67_04745	ENOG4105VFE	sira family
FVE67_04750	ENOG41066VF	YeeE YedE family protein
FVE67_04770	ENOG4108ZGB	N-(5'-phosphoribosyl)anthranilate isomerase
FVE67_04790	ENOG4105BZU	Histidine kinase
FVE67_04795	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
FVE67_04805	ENOG4105DTC	1-(5-phosphoribosyl)-5-amino-4-imidazole-carboxylate (air) carboxylase
FVE67_04845	ENOG4105E3S	small subunit
FVE67_04850	ENOG4105DPX	Hydrogenase, large subunit
FVE67_04860	ENOG4108USZ	hydrogenase
FVE67_04870	ENOG4105WMM	Probably plays a role in a hydrogenase nickel cofactor insertion step (By similarity)
FVE67_04885	ENOG4105CBM	Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 (By similarity)
FVE67_04890	ENOG4108Z2X	Catalyzes the pyruvoyl-dependent decarboxylation of aspartate to produce beta-alanine (By similarity)
FVE67_04895	ENOG4107R03	Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate (By similarity)
FVE67_04910	ENOG41080XS	Cobyrinic acid ac-diamide synthase
FVE67_04915	ENOG4105CYQ	Catalyzes the condensation of the acetyl group of acetyl-CoA with 3-methyl-2-oxobutanoate (2-oxoisovalerate) to form 3-carboxy-3-hydroxy-4-methylpentanoate (2-isopropylmalate) (By similarity)
FVE67_04920	ENOG4105CFH	Aspartokinase
FVE67_04925	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)
FVE67_04930	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)
FVE67_04935	ENOG4108UKJ	Cdp-alcohol phosphatidyltransferase
FVE67_04945	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)
FVE67_04950	ENOG4105VB9	50S ribosomal protein l28
FVE67_04955	ENOG4105E1Z	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane
FVE67_04960	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)
FVE67_04965	ENOG4105D60	lipoprotein releasing system transmembrane protein
FVE67_04970	ENOG4105CRK	lysyL-tRNA synthetase
FVE67_04985	ENOG4105ENA	helicase
FVE67_04990	ENOG4105C2X	Arabinose 5-phosphate isomerase
FVE67_04995	ENOG4108T7K	Acts as a flagellar brake, regulating swimming and swarming in a bis-(3'-5') cyclic diguanylic acid (c-di-GMP)- dependent manner. Increasing levels of c-di-GMP lead to decreased motility (By similarity)
FVE67_05010	ENOG4105D28	Specifically methylates the N7 position of a guanine in 16S rRNA (By similarity)
FVE67_05015	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
FVE67_05030	ENOG4107Y9E	nuclease
FVE67_05035	ENOG4105CQC	Prephenate dehydratase
FVE67_05055	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
FVE67_05060	ENOG4108194	Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis (By similarity)
FVE67_05065	ENOG4105EBE	Peptidase U61, LD-carboxypeptidase A
FVE67_05085	ENOG4105C4E	Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate (By similarity)
FVE67_05090	ENOG4105D5T	phosphonate abc transporter
FVE67_05100	ENOG4105CJI	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
FVE67_05105	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)
FVE67_05120	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)
FVE67_05130	ENOG4105C4R	Atp-dependent dna helicase
FVE67_05135	ENOG4108JJB	ABC transporter
FVE67_05145	ENOG4105EVY	Uses Mg-ATP and reduced ferredoxin to reduce ring D of protochlorophyllide (Pchlide) to form chlorophyllide a (Chlide). This reaction is light-independent (By similarity)
FVE67_05165	ENOG4105WPN	DNA integration recombination invertion protein
FVE67_05170	ENOG41061AI	Protein of unknown function (DUF2905)
FVE67_05175	ENOG4105BZU	Histidine kinase
FVE67_05185	ENOG4107RIU	May be involved in the formation or repair of Fe-S clusters present in iron-sulfur proteins (By similarity)
FVE67_05200	ENOG4105XA0	heptosyltransferase ii
FVE67_05205	ENOG4108ZI0	d,d-heptose 1,7-bisphosphate phosphatase
FVE67_05210	ENOG4105BZU	Histidine kinase
FVE67_05255	ENOG4105D1U	peptidase U62 modulator of DNA gyrase
FVE67_05275	ENOG4105D3H	Catalyzes the decarboxylation of 3-octaprenyl-4-hydroxy benzoate to 2-octaprenylphenol (By similarity)
FVE67_05290	ENOG4105CXB	phosphoribosylaminoimidazole synthetase
FVE67_05300	ENOG4105EYU	Glutamine amido-transferase
FVE67_05310	ENOG4107YD3	Thioesterase
FVE67_05315	ENOG41084JP	30S ribosomal protein S21
FVE67_05320	ENOG4105C98	muts2 protein
FVE67_05325	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)
FVE67_05330	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FVE67_05370	ENOG4105BZS	acriflavin resistance protein
FVE67_05390	ENOG4105EB3	Histidine kinase
FVE67_05395	ENOG4105ETX	regulatoR
FVE67_05400	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)
FVE67_05420	ENOG4105CKK	Glycosyl transferase, family 2
FVE67_05430	ENOG4107T8Q	Glycosyl transferase (Group 1
FVE67_05435	ENOG4105D5G	Transposase
FVE67_05460	ENOG4107SBE	Glycosyl transferase (Group 1
FVE67_05480	ENOG4105CYJ	ribosomal RNA small subunit methyltransferase B
FVE67_05490	ENOG4105N5T	Radical SAM Protein
FVE67_05495	ENOG4105CNU	cell division protein FtsK
FVE67_05500	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)
FVE67_05505	ENOG4105D0I	Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate (By similarity)
FVE67_05540	ENOG4105C8M	UPF0272 protein
FVE67_05550	ENOG4105CCW	damaged site, the DNA wraps around one UvrB monomer. DNA wrap is dependent on ATP binding by UvrB and probably causes local melting of the DNA helix, facilitating insertion of UvrB beta-hairpin between the DNA strands. Then UvrB probes one DNA strand for the presence of a lesion. If a lesion is found the UvrA subunits dissociate and the UvrB-DNA preincision complex is formed. This complex is subsequently bound by UvrC and the second UvrB is released. If no lesion is found, the DNA wraps around the other UvrB subunit that will check the other stand for damage (By similarity)
FVE67_05555	ENOG4107TH8	cina domain protein
FVE67_05585	ENOG4105CB3	Required for the thiolation of cytidine in position 32 of tRNA, to form 2-thiocytidine (s(2)C32) (By similarity)
FVE67_05590	ENOG4107S2Z	UPF0761 membrane protein
FVE67_05600	ENOG4105X3E	Catalyzes the decarboxylation of S-adenosylmethionine to S-adenosylmethioninamine (dcAdoMet), the propylamine donor required for the synthesis of the polyamines spermine and spermidine from the diamine putrescine (By similarity)
FVE67_05605	ENOG4105CCX	Catalyzes the production of spermidine from putrescine and decarboxylated S-adenosylmethionine (dcSAM), which serves as an aminopropyl donor (By similarity)
FVE67_05610	ENOG4105EYH	Exonuclease
FVE67_05615	ENOG4105W3S	hemerythrin-like, metal-binding protein
FVE67_05620	ENOG4107RFY	SbcCD D subunit
FVE67_05630	ENOG4105CD3	dihydroorotase
FVE67_05635	ENOG4105CXT	aspartate transcarbamylase
FVE67_05640	ENOG4105C0B	DNA polymerase III (alpha subunit)
FVE67_05645	ENOG4105C38	Glycyl-tRNA synthetase beta subunit
FVE67_05650	ENOG4107QIB	glycyl-tRNA synthetase, alpha subunit
FVE67_05660	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
FVE67_05670	ENOG4105C80	Catalyzes the reversible oxidation of malate to oxaloacetate (By similarity)
FVE67_05680	ENOG4105VEQ	Cold shock protein
FVE67_05685	ENOG4105CGT	Catalyzes the transfer of a phosphate group to glutamate to form glutamate 5-phosphate which rapidly cyclizes to 5- oxoproline (By similarity)
FVE67_05690	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
FVE67_05695	ENOG4105FF6	Modulates transcription in response to changes in cellular NADH NAD( ) redox state (By similarity)
FVE67_05700	ENOG4105C35	Catalyzes the interconversion of methylthioribose-1- phosphate (MTR-1-P) into methylthioribulose-1-phosphate (MTRu-1-P) (By similarity)
FVE67_05705	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)
FVE67_05710	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)
FVE67_05715	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)
FVE67_05720	ENOG4105D58	Diguanylate phosphodiesterase
FVE67_05725	ENOG4105DFU	Cell wall formation (By similarity)
FVE67_05730	ENOG4108R96	Methyltransferase, YaeB family
FVE67_05735	ENOG4105Y7X	Selectively cleaves double-stranded DNA at the second phosphodiester bond 3' to a deoxyinosine leaving behind the intact lesion on the nicked DNA. Acts in DNA repair (By similarity)
FVE67_05740	ENOG4105CE5	Catalyzes the formation of 4-diphosphocytidyl-2-C- methyl-D-erythritol from CTP and 2-C-methyl-D-erythritol 4- phosphate (MEP) (By similarity)
FVE67_05750	ENOG4107N1Q	ErfK YbiS YcfS YnhG family protein
FVE67_05755	ENOG4105C8N	cysteinyl-tRNA synthetase
FVE67_05775	ENOG4105CGK	Exodeoxyribonuclease III
FVE67_05780	ENOG4105CAY	ferredoxin--nadp reductase
FVE67_05785	ENOG41081QV	Universal stress protein
FVE67_05790	ENOG4105DB7	PHP domain protein
FVE67_05795	ENOG4105FE9	pseudouridine synthase
FVE67_05815	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
FVE67_05820	ENOG4105BZU	Histidine kinase
FVE67_05835	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)
FVE67_05840	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
FVE67_05850	ENOG4105DTN	riboflavin biosynthesis protein ribF
FVE67_05855	ENOG4105C1M	carbamoyl-phosphate synthetase glutamine chain
FVE67_05870	ENOG4105DVM	PP-loop domain protein
FVE67_05880	ENOG4105W87	Cbs domain
FVE67_05890	ENOG4105CUT	histidyl-tRNA synthetase
FVE67_05895	ENOG4105KJJ	Uncharacterized ACR, COG1993
FVE67_05900	ENOG4105WMR	Protein CrcB homolog
FVE67_05910	ENOG4107QYG	anthranilate phosphoribosyltransferase
FVE67_05920	ENOG4107ZYR	domain protein
FVE67_05935	ENOG41087NI	Sulfite exporter TauE/SafE
FVE67_05955	ENOG4105FE8	tRNA (Guanosine-2'-O-)-methyltransferase
FVE67_05960	ENOG4108W63	CRP FNR family transcriptional regulator
FVE67_05975	ENOG4108N6H	6-pyruvoyl tetrahydrobiopterin synthase
FVE67_05980	ENOG4107VRB	Catalyzes the conversion of 6-carboxy-5,6,7,8- tetrahydropterin (CPH4) to 7-carboxy-7-deazaguanine (CDG) (By similarity)
FVE67_05985	ENOG4105D22	carbon starvation protein
FVE67_05990	ENOG4107W7X	Aldolase
FVE67_05995	ENOG4105DQU	oxidoreductase, subunit beta
FVE67_06000	ENOG4105DI2	Pyruvate flavodoxin ferredoxin oxidoreductase domain protein
FVE67_06030	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)
FVE67_06035	ENOG4105E7H	involved in the assembly of LPS in the outer leaflet of the outer membrane. Determines N-hexane tolerance and is involved in outer membrane permeability. Essential for envelope biogenesis (By similarity)
FVE67_06045	ENOG41068B1	Cob-I-yrinic acid a,c-diamide adenosyltransferase
FVE67_06050	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)
FVE67_06055	ENOG410816I	Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection (By similarity)
FVE67_06060	ENOG4105C6E	dna polymerase iii
FVE67_06070	ENOG4105EZY	Pyrroloquinoline quinone biosynthesis protein E
FVE67_06085	ENOG4105EGS	Mechanosensitive ion channel
FVE67_06095	ENOG4105C03	ribonuclease
FVE67_06100	ENOG4105E8R	UPF0173 metal-dependent hydrolase
FVE67_06105	ENOG4107SDT	Homocitrate synthase
FVE67_06150	ENOG4105C4H	Specifically methylates the guanine in position 2445 (m2G2445) and the guanine in position 2069 (m7G2069) of 23S rRNA (By similarity)
FVE67_06155	ENOG4105DB1	molybdopterin oxidoreductase
FVE67_06160	ENOG4108KS2	transglutaminase domain protein
FVE67_06180	ENOG4107RYT	DNA ligase that seals nicks in double-stranded DNA during DNA replication, DNA recombination and DNA repair (By similarity)
FVE67_06190	ENOG4108JEB	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
FVE67_06195	ENOG4108QXE	glycerophosphoryl diester phosphodiesterase
FVE67_06200	ENOG4105C1X	Bifunctional enzyme with both catalase and broad- spectrum peroxidase activity (By similarity)
FVE67_06220	ENOG4107SBB	4-alpha-glucanotransferase (EC 2.4.1.25)
FVE67_06225	ENOG4107R91	Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position (By similarity)
FVE67_06230	ENOG4105CXW	Synthesizes alpha-1,4-glucan chains using ADP-glucose (By similarity)
FVE67_06240	ENOG4107R76	Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties (By similarity)
FVE67_06245	ENOG4105E4R	Precorrin-3B C17-methyltransferase
FVE67_06250	ENOG4105CIA	precorrin-4 C(11)-methyltransferase
FVE67_06255	ENOG4105CX4	Precorrin-6y C5,15-methyltransferase
FVE67_06260	ENOG4105EE8	May catalyze the methylation of C-1 in cobalt-precorrin- 5 and the subsequent extrusion of acetic acid from the resulting intermediate to form cobalt-precorrin-6A (By similarity)
FVE67_06265	ENOG41081F0	Precorrin-8x methylmutase
FVE67_06270	ENOG4108ESU	Part of the ABC transporter complex BtuCDF involved in vitamin B12 import. Involved in the translocation of the substrate across the membrane (By similarity)
FVE67_06275	ENOG4108IPX	Part of the ABC transporter complex HmuTUV involved in hemin import. Responsible for energy coupling to the transport system (By similarity)
FVE67_06290	ENOG4105C4N	this subunit has chaperone activity. The binding of ATP and its subsequent hydrolysis by HslU are essential for unfolding of protein substrates subsequently hydrolyzed by HslV. HslU recognizes the N-terminal part of its protein substrates and unfolds these before they are guided to HslV for hydrolysis (By similarity)
FVE67_06295	ENOG4108R5P	Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery (By similarity)
FVE67_06300	ENOG4108IYS	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
FVE67_06315	ENOG4108JQC	penicillin-binding protein 1A
FVE67_06325	ENOG4108YXI	Secondary thiamine-phosphate synthase enzyme
FVE67_06330	ENOG4108UUM	single-stranded DNA-binding protein
FVE67_06340	ENOG4105CRE	cytochrome C
FVE67_06345	ENOG4105BZS	acriflavin resistance protein
FVE67_06365	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FVE67_06385	ENOG4105FA2	dna polymerase iii
FVE67_06390	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
FVE67_06395	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)
FVE67_06400	ENOG4105D28	Specifically methylates the N7 position of a guanine in 16S rRNA (By similarity)
FVE67_06405	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
FVE67_06415	ENOG4105DSJ	YicC domain protein
FVE67_06425	ENOG4105KCK	Peptidoglycan-associated lipoprotein
FVE67_06435	ENOG4105CHC	glucokinase (EC 2.7.1.2)
FVE67_06440	ENOG4105K8N	protein family UPF0079, ATPase
FVE67_06445	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)
FVE67_06465	ENOG4108JQ7	(ABC) transporter
FVE67_06470	ENOG4105CKX	Catalyzes the conversion of 3'-phosphate to a 2',3'- cyclic phosphodiester at the end of RNA. The mechanism of action of the enzyme occurs in 3 steps (A) adenylation of the enzyme by ATP
FVE67_06480	ENOG4108PJD	permease
FVE67_06485	ENOG4105ECP	epimerase
FVE67_06490	ENOG4105CTQ	phosphohexokinase
FVE67_06505	ENOG4105C1G	acyl-Coa dehydrogenase
FVE67_06515	ENOG4105BZJ	Electron transfer flavoprotein
FVE67_06520	ENOG4105C10	Electron transfer flavoprotein
FVE67_06525	ENOG4105CHR	reductase
FVE67_06530	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
FVE67_06540	ENOG4108YZG	isomerase
FVE67_06545	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)
FVE67_06585	ENOG41080HT	Transcriptional regulator, arsr family
FVE67_06590	ENOG4105C8Y	Acetylornithine aminotransferase
FVE67_06595	ENOG41082X2	rubredoxin
FVE67_06610	ENOG41090A1	ferritin
FVE67_06615	ENOG4105E02	MotA TolQ exbB proton channel
FVE67_06620	ENOG4105E63	Pfam:DUF178
FVE67_06625	ENOG4108UIH	futalosine nucleosidase
FVE67_06630	ENOG4105D48	metallophosphoesterase
FVE67_06635	ENOG4105E4Y	Endoribonuclease that initiates mRNA decay (By similarity)
FVE67_06665	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)
FVE67_06675	ENOG4105KK9	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
FVE67_06680	ENOG4105K46	50S ribosomal protein l27
FVE67_06685	ENOG4108JA2	transcriptioN-repair coupling factor
FVE67_06700	ENOG410826D	Involved in DNA repair and RecF pathway recombination (By similarity)
FVE67_06705	ENOG4108URH	decarboxylase
FVE67_06715	ENOG4105E4C	Lytic transglycosylase catalytic
FVE67_06725	ENOG4105K8U	2-Amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase
FVE67_06730	ENOG4105CHM	Aminotransferase
FVE67_06775	ENOG4107U32	Beta-lactamase domain protein
FVE67_06785	ENOG4107S21	permease
FVE67_06815	ENOG4105BZS	acriflavin resistance protein
FVE67_06845	ENOG4105DRW	binding-protein-dependent transport systems inner membrane Component
FVE67_06855	ENOG4105QA4	4Fe-4S Ferredoxin, iron-sulfur binding domain protein
FVE67_06865	ENOG4105DB1	molybdopterin oxidoreductase
FVE67_06885	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
FVE67_06890	ENOG4105BZU	Histidine kinase
FVE67_06905	ENOG4107UKG	Glycosyl transferase, family 4
FVE67_06910	ENOG4105CQB	FAD linked oxidase domain protein
FVE67_06925	ENOG4105CPF	Cell wall formation (By similarity)
FVE67_06935	ENOG4105CEK	Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine (By similarity)
FVE67_06940	ENOG4108JVH	Protein of unknown function DUF43
FVE67_06945	ENOG4105D5G	Transposase
FVE67_06955	ENOG4105EYX	Acetyl-CoA decarbonylase synthase complex subunit gamma
FVE67_06975	ENOG4107RFD	Non-specific O-methyltransferase that catalyzes the 2 O- methylation steps in the ubiquinone biosynthetic pathway (By similarity)
FVE67_06990	ENOG410801E	Flagellar hook-associated 2 domain-containing protein
FVE67_06995	ENOG4105MQ3	flagellar protein FliS
FVE67_07010	ENOG4105E1Q	flagellar hook-associated protein
FVE67_07025	ENOG4105D92	Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation (By similarity)
FVE67_07030	ENOG4107W7W	Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation (By similarity)
FVE67_07040	ENOG4105CGA	flagellar basal-body rod protein FlgG
FVE67_07045	ENOG4108JQA	flagellar
FVE67_07070	ENOG4105CSA	Coproporphyrinogen iii oxidase
FVE67_07080	ENOG4105K7D	Required for maturation of 30S ribosomal subunits (By similarity)
FVE67_07085	ENOG4105CHV	Transcription elongation factor NusA
FVE67_07095	ENOG4107QHU	One of the essential components for the initiation of protein synthesis. Protects formylmethionyl-tRNA from spontaneous hydrolysis and promotes its binding to the 30S ribosomal subunits. Also involved in the hydrolysis of GTP during the formation of the 70S ribosomal complex (By similarity)
FVE67_07095	ENOG4107QHU	One of the essential components for the initiation of protein synthesis. Protects formylmethionyl-tRNA from spontaneous hydrolysis and promotes its binding to the 30S ribosomal subunits. Also involved in the hydrolysis of GTP during the formation of the 70S ribosomal complex (By similarity)
FVE67_07110	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
FVE67_07120	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
FVE67_07125	ENOG4105DBV	ornithine carbamoyltransferase
FVE67_07130	ENOG4105MK2	5-formyltetrahydrofolate cyclo-ligase
FVE67_07135	ENOG4107SVH	Potassium channel protein
FVE67_07140	ENOG4107QYV	phosphohexose isomerase
FVE67_07145	ENOG4105CAA	catalyzes amidations at positions B, D, E, and G on adenosylcobyrinic A,C-diamide. NH(2) groups are provided by glutamine, and one molecule of ATP is hydrogenolyzed for each amidation (By similarity)
FVE67_07170	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
FVE67_07190	ENOG4105W4M	Transport-associated protein
FVE67_07195	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)
FVE67_07205	ENOG4105DJQ	tetratricopeptide tpr_2 repeat protein
FVE67_07225	ENOG4105E2K	Glycosyl transferase (Group 1
FVE67_07235	ENOG4105C37	(CBS) domain
FVE67_07245	ENOG4105F4G	Membrane
FVE67_07250	ENOG4105ERD	Involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. Acts as DNA glycosylase that recognizes and removes damaged bases. Has a preference for oxidized purines, such as 7,8-dihydro-8-oxoguanine (8-oxoG). Has AP (apurinic apyrimidinic) lyase activity and introduces nicks in the DNA strand. Cleaves the DNA backbone by beta-delta elimination to generate a single-strand break at the site of the removed base with both 3'- and 5'-phosphates (By similarity)
FVE67_07270	ENOG4108F3G	Type I restriction-modification system, R subunit
FVE67_07310	ENOG4105ES5	Histidine kinase
FVE67_07315	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
FVE67_07330	ENOG4106K5Q	Modifies the topological state of DNA by introducing positive supercoils in an ATP-dependent process. It cleaves transiently a single DNA strand and remains covalently bound to the 5' DNA end through a tyrosine residue. May be involved in rewinding the DNA strands in the regions of the chromosome that have opened up to allow transcription or replication (By similarity)
FVE67_07335	ENOG4105EYX	Acetyl-CoA decarbonylase synthase complex subunit gamma
FVE67_07340	ENOG4108VJ1	Transcriptional regulator (CarD family
FVE67_07345	ENOG4105CTP	PilT protein domain protein
FVE67_07355	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)
FVE67_07365	ENOG4108JEI	Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system (By similarity)
FVE67_07370	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
FVE67_07385	ENOG41071I4	Phosphatidylserine decarboxylase proenzyme
FVE67_07390	ENOG4106PT6	cdpdiacylglycerol-serine O-phosphatidyltransferase
FVE67_07395	ENOG4105KC4	UPF0296 protein
FVE67_07400	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
FVE67_07405	ENOG4105C2N	RNA methyltransferase TrmH family group 3
FVE67_07410	ENOG4105D8A	3-Deoxy-D-manno-octulosonic-acid transferase
FVE67_07420	ENOG4105EK6	Transmembrane (T) component of an energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates (By similarity)
FVE67_07425	ENOG4107XQ1	cobalamin (vitamin B12) biosynthesis CbiM protein
FVE67_07440	ENOG4105CA0	peroxidase
FVE67_07460	ENOG4105D5G	Transposase
FVE67_07485	ENOG4107XUG	Specifically methylates the N7 position of a guanine in 16S rRNA (By similarity)
FVE67_07495	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
FVE67_07500	ENOG4108YXW	Together with MoaA, is involved in the conversion of 5'- GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
FVE67_07505	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)
FVE67_07510	ENOG41084BP	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)
FVE67_07515	ENOG41083MR	nifu domain-containing protein
FVE67_07520	ENOG4105C01	Dihydroxy-acid dehydratase
FVE67_07530	ENOG4105CY3	ABC transporter, permease
FVE67_07585	ENOG4105C75	arginyL-tRNA synthetase
FVE67_07605	ENOG4108Z0T	Part of a sulfur-relay system (By similarity)
FVE67_07620	ENOG4105CIH	Imidazole acetol-phosphate transaminase
FVE67_07630	ENOG4105C4Q	deoxyguanosinetriphosphate triphosphohydrolase-like protein
FVE67_07635	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)
FVE67_07640	ENOG4105CE6	Adenylation and deadenylation of glutamate--ammonia ligase (By similarity)
FVE67_07645	ENOG4105CRE	cytochrome C
FVE67_07660	ENOG4105CJ1	ABC, transporter
FVE67_07675	ENOG4105E3B	Multicopper oxidase
FVE67_07685	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)
FVE67_07700	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)
FVE67_07705	ENOG4107R5M	Catalyzes the transfer of a N-acetyl-glucosamine moiety to 1D-myo-inositol 3-phosphate to produce 1D-myo-inositol 2- acetamido-2-deoxy-glucopyranoside 3-phosphate in the mycothiol biosynthesis pathway (By similarity)
FVE67_07715	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)
FVE67_07725	ENOG4105GYT	Protein of unknown function (DUF1009)
FVE67_07730	ENOG4105DAF	Involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
FVE67_07735	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)
FVE67_07740	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)
FVE67_07745	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)
FVE67_07750	ENOG4105K70	DNA-binding protein
FVE67_07755	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
FVE67_07760	ENOG4105DW0	Catalyzes the ADP transfer to D-glycero-D-manno-heptose 1-phosphate, yielding ADP-D,D-heptose (By similarity)
FVE67_07765	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)
FVE67_07770	ENOG4105C4F	May be involved in recombinational repair of damaged DNA (By similarity)
FVE67_07785	ENOG4107S47	Specifically methylates the adenine in position 37 of tRNA(1)(Val) (anticodon cmo5UAC) (By similarity)
FVE67_07795	ENOG4107QKV	phosphomannomutase
FVE67_07800	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
FVE67_07815	ENOG4105D10	5-enolpyruvylshikimate-3-phosphate phospholyase
FVE67_07820	ENOG4105BZU	Histidine kinase
FVE67_07825	ENOG4105CJR	Integral membrane protein (MviN
FVE67_07830	ENOG4105C66	Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate (By similarity)
FVE67_07840	ENOG4105CPK	Glycosyl transferase (Group 1
FVE67_07845	ENOG4105M7K	Involved in the transcription termination process (By similarity)
FVE67_07850	ENOG4105DA5	(ABC) transporter
FVE67_07865	ENOG4107QHF	type ii secretion system protein e
FVE67_07875	ENOG4105CXV	gliding motility protein
FVE67_07885	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
FVE67_07890	ENOG4108NEV	two component transcriptional regulator, LytTR family
FVE67_07895	ENOG4105CBS	Chea signal transduction histidine kinase
FVE67_07900	ENOG4105CY1	sulfite reductase, dissimilatory-type alpha subunit
FVE67_07905	ENOG4105PJW	Sulfite reductase dissimilatory-type beta subunit
FVE67_07910	ENOG4105Z0W	Dissimilatory sulfite reductase D
FVE67_07920	ENOG4108S0S	Nucleotidyl transferase
FVE67_07925	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)
FVE67_07930	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)
FVE67_07940	ENOG4108ZP8	Acetolactate synthase small subunit
FVE67_07945	ENOG4105C7K	acetolactate synthase
FVE67_07955	ENOG4108ISE	4Fe-4S ferredoxin, iron-sulfur binding
FVE67_07975	ENOG4105CU5	Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine (By similarity)
FVE67_07980	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
FVE67_08010	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)
FVE67_08020	ENOG4105DFM	M18 family aminopeptidase
FVE67_08050	ENOG4107Z7S	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
FVE67_08055	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
FVE67_08065	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
FVE67_08075	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
FVE67_08095	ENOG4105DCU	2-hydroxyglutaryl-CoA dehydratase
FVE67_08130	ENOG4105WHM	Necessary for normal cell division and for the maintenance of normal septation (By similarity)
FVE67_08155	ENOG4105CRQ	synthase (Component I)
FVE67_08165	ENOG4107QX8	SPFH domain, Band 7 family protein
FVE67_08180	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)
FVE67_08185	ENOG4107SYB	Catalyzes the deamination of 5-methylthioadenosine and S-adenosyl-L-homocysteine into 5-methylthioinosine and S-inosyl-L- homocysteine, respectively. Is also able to deaminate adenosine (By similarity)
FVE67_08195	ENOG4105C0S	IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisF subunit catalyzes the cyclization activity that produces IGP and AICAR from PRFAR using the ammonia provided by the HisH subunit (By similarity)
FVE67_08200	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
FVE67_08210	ENOG4105F8C	transglutaminase domain-containing protein
FVE67_08215	ENOG4108NGH	radical SAM domain protein
FVE67_08220	ENOG4108V1J	Has antioxidant activity. Could remove peroxides or H(2)O(2) (By similarity)
FVE67_08230	ENOG41067SF	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)
FVE67_08235	ENOG4105C3M	thioredoxin reductase
FVE67_08240	ENOG4105D8I	Catalyzes the ATP-dependent transfer of a sulfur to tRNA to produce 4-thiouridine in position 8 of tRNAs, which functions as a near-UV photosensor. Also catalyzes the transfer of sulfur to the sulfur carrier protein ThiS, forming ThiS-thiocarboxylate. This is a step in the synthesis of thiazole, in the thiamine biosynthesis pathway. The sulfur is donated as persulfide by IscS (By similarity)
FVE67_08245	ENOG4107QI6	Cysteine desulfurase
FVE67_08255	ENOG4107QPA	Cleaves GlcNAc linked beta-1,4 to MurNAc tripeptides (By similarity)
FVE67_08260	ENOG4105DBD	Chaperone involved in the correct folding and assembly of outer membrane proteins. Recognizes specific patterns of aromatic residues and the orientation of their side chains, which are found more frequently in integral outer membrane proteins. May act in both early periplasmic and late outer membrane-associated steps of protein maturation (By similarity)
FVE67_08265	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
FVE67_08270	ENOG4105DH2	Converts cobyric acid to cobinamide by the addition of aminopropanol on the F carboxylic group (By similarity)
FVE67_08275	ENOG4105SG9	biopolymer transport protein, ExbD
FVE67_08290	ENOG4105CHM	Aminotransferase
FVE67_08300	ENOG4105EZI	multiple antibiotic resistance (MarC)-related protein
FVE67_08310	ENOG4105CKK	Glycosyl transferase, family 2
FVE67_08315	ENOG4108RAC	Rubrerythrin
FVE67_08330	ENOG4105C22	threonyL-tRNA synthetase
FVE67_08335	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)
FVE67_08340	ENOG41085CK	50S ribosomal protein L35
FVE67_08345	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)
FVE67_08350	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
FVE67_08355	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
FVE67_08360	ENOG4108ZUF	This protein is one of the two subunits of integration host factor, a specific DNA-binding protein that functions in genetic recombination as well as in transcriptional and translational control (By similarity)
FVE67_08370	ENOG4105MAX	Superoxide reductase
FVE67_08375	ENOG4105VCQ	rubredoxin
FVE67_08380	ENOG4105CNW	domain protein
FVE67_08395	ENOG4105C40	3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs (By similarity)
FVE67_08400	ENOG4105BZE	flagellar hook protein, FlgE
FVE67_08405	ENOG4105BZE	flagellar hook protein, FlgE
FVE67_08410	ENOG410822I	Flagellar hook capping protein
FVE67_08420	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
FVE67_08425	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)
FVE67_08430	ENOG4105MRR	Transcriptional regulator (By similarity)
FVE67_08440	ENOG4105C8Q	Methyl-accepting chemotaxis
FVE67_08455	ENOG4108UN4	phage SPO1 DNA polymerase-related protein
FVE67_08460	ENOG4108HMX	isocitrate dehydrogenase (NADP)
FVE67_08465	ENOG4105C8T	Leucyl-tRNA synthetase
FVE67_08475	ENOG4105CK3	Lysine 2,3-aminomutase YodO family protein
FVE67_08485	ENOG4105CK2	sodium dicarboxylate symporter
FVE67_08500	ENOG4105D5G	Transposase
FVE67_08520	ENOG4108W8W	CRISPR-associated RAMP protein, Csm3 family
FVE67_08530	ENOG4105G15	CRISPR-associated RAMP protein, Csm5 family
FVE67_08600	ENOG4108UN4	phage SPO1 DNA polymerase-related protein
FVE67_08620	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
FVE67_08635	ENOG4105CAS	nag kinase
FVE67_08640	ENOG4107YIW	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)
FVE67_08650	ENOG4105EJ7	Catalyzes the reduction of hydroxylamine to form NH(3) and H(2)O (By similarity)
FVE67_08655	ENOG4105D21	Phosphoribosylformylglycinamidine synthase I
FVE67_08660	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)
FVE67_08685	ENOG4105CS3	FliG is one of three proteins (FliG, FliN, FliM) that forms the rotor-mounted switch complex (C ring), located at the base of the basal body. This complex interacts with the CheY and CheZ chemotaxis proteins, in addition to contacting components of the motor that determine the direction of flagellar rotation (By similarity)
FVE67_08690	ENOG4105C1F	The M ring may be actively involved in energy transduction (By similarity)
FVE67_08695	ENOG4105VQ0	flagellar hook-basal body complex protein fliE
FVE67_08700	ENOG4108ZC9	flagellar basal-body rod protein flgc
FVE67_08705	ENOG4105K88	Structural component of flagellum, the bacterial motility apparatus. Part of the rod structure of flagellar basal body (By similarity)
FVE67_08725	ENOG4105D18	nicotinate-nucleotide pyrophosphorylase
FVE67_08730	ENOG4105IQJ	Involved in biosynthesis of the thiamine precursor thiazole (By similarity)
FVE67_08735	ENOG4105E2M	Manganese-dependent inorganic pyrophosphatase
FVE67_08745	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
FVE67_08765	ENOG4105DFA	alanine racemase domain protein
FVE67_08770	ENOG4108IYU	L-aspartate oxidase
FVE67_08775	ENOG4105E3H	phosphoglycerate mutase
FVE67_08780	ENOG41090X3	Peptidyl-prolyl cis-trans isomerase
FVE67_08790	ENOG4107SFQ	iron-sulfur binding
FVE67_08800	ENOG4108M19	cytochrome C
FVE67_08805	ENOG4105KNI	merR family transcriptional Regulator
FVE67_08815	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)
FVE67_08820	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)
FVE67_08825	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
FVE67_08835	ENOG4105DIW	FeS assembly protein SUFB
FVE67_08840	ENOG4105CIH	Imidazole acetol-phosphate transaminase
FVE67_08845	ENOG4105CAT	Cytidine monophosphate kinase
FVE67_08850	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)
FVE67_08860	ENOG41080YA	This protein is one of the two subunits of integration host factor, a specific DNA-binding protein that functions in genetic recombination as well as in transcriptional and translational control (By similarity)
FVE67_08865	ENOG4105CP4	Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth (By similarity)
FVE67_08875	ENOG4105DVC	DnaJ domain protein
FVE67_08880	ENOG4105EBH	Required during biogenesis of c-type cytochromes (cytochrome c6 and cytochrome f) at the step of heme attachment (By similarity)
FVE67_08885	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)
FVE67_08895	ENOG4105CYJ	ribosomal RNA small subunit methyltransferase B
FVE67_08900	ENOG4107XGZ	Hydrolase
FVE67_08905	ENOG4105VZ9	UPF0235 protein
FVE67_08935	ENOG4105VCQ	rubredoxin
FVE67_08945	ENOG4105VTS	DnaJ-like, subfamily C
FVE67_08965	ENOG4107UCJ	Catalyzes the synthesis of activated sulfate (By similarity)
FVE67_08990	ENOG4105C34	Pseudouridine synthase
FVE67_09005	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
FVE67_09010	ENOG4105BZU	Histidine kinase
FVE67_09020	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)
FVE67_09025	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)
FVE67_09035	ENOG4105C8B	TIGR00159 family
FVE67_09045	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
FVE67_09055	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)
FVE67_09060	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)
FVE67_09070	ENOG4105E14	MotA TolQ exbB proton channel
FVE67_09075	ENOG4105ER2	Ompa motb domain protein
FVE67_09085	ENOG4105CBM	Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 (By similarity)
FVE67_09095	ENOG4108Z4R	3-deoxy-d-manno-octulosonate 8-phosphate phosphatase
FVE67_09110	ENOG4108IUZ	ABC transporter
FVE67_09115	ENOG4105DTW	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FVE67_09120	ENOG41080QH	sigma 54 modulation protein ribosomal protein S30EA
FVE67_09125	ENOG4107RM2	PTS IIA-like nitrogen-regulatory protein PtsN
FVE67_09130	ENOG4105C21	Displays ATPase and GTPase activities (By similarity)
FVE67_09140	ENOG4105KEG	ribosomal-protein-alanine acetyltransferase