locus-tag	class	description
FCN51_00005	ENOG4108UUM	single-stranded DNA-binding protein
FCN51_00060	ENOG4107QHF	type ii secretion system protein e
FCN51_00100	ENOG4105CZX	twitching motility protein
FCN51_00170	ENOG4105DC6	This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex (By similarity)
FCN51_00255	ENOG4105CDB	Required for chromosome condensation and partitioning (By similarity)
FCN51_00265	ENOG4105VDM	plasmid maintenance system antidote protein, xre family
FCN51_00320	ENOG4105C7H	Helicase, RecD TraA family
FCN51_00445	ENOG4105BZH	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
FCN51_00470	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)
FCN51_00540	ENOG4105XJC	Two component transcriptional regulator (Winged helix family
FCN51_00550	ENOG4105C4R	Atp-dependent dna helicase
FCN51_00645	ENOG4105K70	DNA-binding protein
FCN51_00655	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)
FCN51_00720	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)
FCN51_00740	ENOG4107RZZ	dna polymerase iii epsilon subunit
FCN51_00820	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
FCN51_00865	ENOG4105DE5	Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity (By similarity)
FCN51_00890	ENOG4105Y2X	UPF0335 protein
FCN51_00895	ENOG4105UT3	Methyl-accepting chemotaxis
FCN51_00900	ENOG4105BZE	flagellar hook protein, FlgE
FCN51_00905	ENOG4105D00	flagellar biosynthetic protein flhB
FCN51_00915	ENOG4105VS8	Flagellar biosynthetic protein fliq
FCN51_00935	ENOG4105SFI	flagellar basal-body rod protein
FCN51_00940	ENOG4108ZC9	flagellar basal-body rod protein flgc
FCN51_00945	ENOG4107W75	Flagellin
FCN51_00975	ENOG4105KTQ	flagellar basal-body rod protein
FCN51_00980	ENOG4105CGA	flagellar basal-body rod protein FlgG
FCN51_00990	ENOG4107W7W	Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation (By similarity)
FCN51_01010	ENOG4105C1F	The M ring may be actively involved in energy transduction (By similarity)
FCN51_01015	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)
FCN51_01025	ENOG4105DD5	Flagellar motor switch protein
FCN51_01035	ENOG4105CN7	Flagellar biosynthetic protein FliP
FCN51_01045	ENOG4105D7B	Flagellar biosynthesis protein flha
FCN51_01060	ENOG4105D92	Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation (By similarity)
FCN51_01065	ENOG41065XG	Chemotactic signal-response protein CheL
FCN51_01110	ENOG4107RD7	Flagellar Motor Protein, MotA
FCN51_01120	ENOG4105W00	Flagellar hook capping protein
FCN51_01240	ENOG4105EVE	HAD-superfamily hydrolase subfamily IA variant 3
FCN51_01405	ENOG4105GC4	N-4 methylation of cytosine
FCN51_01435	ENOG4105ENG	CRISPR-associated protein, Csy1 family
FCN51_01470	ENOG4105CQ3	Poorly processive error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by polIV. Exhibits no 3-5 exonuclease (proofreading) activity. May be involved in translesional synthesis in conjunction with the beta clamp from polIII (By similarity)
FCN51_01595	ENOG41060M0	Crispr-associated protein, cse4 family
FCN51_01615	ENOG4105C40	3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs (By similarity)
FCN51_01670	ENOG4105UT3	Methyl-accepting chemotaxis
FCN51_01695	ENOG4105CG5	Glycosyl transferase (Group 1
FCN51_01720	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)
FCN51_01730	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
FCN51_01750	ENOG4105CEC	DNA methylase N-4 N-6
FCN51_01765	ENOG4105M6W	Crispr-associated protein, Csy3 family
FCN51_01795	ENOG4105ENG	CRISPR-associated protein, Csy1 family
FCN51_01920	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)
FCN51_01950	ENOG4107QXV	Phosphate transporter
FCN51_02005	ENOG4107R2U	Catalyzes the formation of dTMP and tetrahydrofolate from dUMP and methylenetetrahydrofolate (By similarity)
FCN51_02015	ENOG4105D7V	transposase
FCN51_02070	ENOG4108Z4W	Probably deamidates glutamine residues to glutamate on methyl-accepting chemotaxis receptors (MCPs), playing an important role in chemotaxis (By similarity)
FCN51_02075	ENOG4108VYJ	response regulator receiver protein
FCN51_02080	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
FCN51_02085	ENOG4105BZU	Histidine kinase
FCN51_02090	ENOG4108V3W	Chemotaxis protein, CheW
FCN51_02095	ENOG4105CBS	Chea signal transduction histidine kinase
FCN51_02110	ENOG4105C8Q	Methyl-accepting chemotaxis
FCN51_02140	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FCN51_02145	ENOG4105CI4	it binds specifically double-stranded DNA at a 9 bp consensus (dnaA box) 5'-TTATC CA A CA A-3'. DnaA binds to ATP and to acidic phospholipids (By similarity)
FCN51_02155	ENOG4105C3X	it is required for DNA replication and normal SOS inducibility. RecF binds preferentially to single-stranded, linear DNA. It also seems to bind ATP (By similarity)
FCN51_02165	ENOG4105CXR	Phospho-2-dehydro-3-deoxyoctonate aldolase
FCN51_02170	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
FCN51_02180	ENOG4105CP7	Triose-phosphate isomerase
FCN51_02190	ENOG4105CRQ	synthase (Component I)
FCN51_02195	ENOG4105DDQ	anthranilate synthase
FCN51_02200	ENOG4107QYG	anthranilate phosphoribosyltransferase
FCN51_02205	ENOG4105DK0	Indole-3-glycerol phosphate synthase
FCN51_02210	ENOG4108YXW	Together with MoaA, is involved in the conversion of 5'- GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
FCN51_02215	ENOG4108JYK	Dehydrogenase
FCN51_02220	ENOG4105CPP	Dehydrogenase, E1 component
FCN51_02225	ENOG4105C7S	Dehydrogenase
FCN51_02230	ENOG4107QN2	dihydrolipoyl dehydrogenase
FCN51_02235	ENOG4105C0G	Catalyzes the radical-mediated insertion of two sulfur atoms into the C-6 and C-8 positions of the octanoyl moiety bound to the lipoyl domains of lipoate-dependent enzymes, thereby converting the octanoylated domains into lipoylated derivatives (By similarity)
FCN51_02250	ENOG4107TH8	cina domain protein
FCN51_02260	ENOG4106S48	Murein-degrading enzyme. May play a role in recycling of muropeptides during cell elongation and or cell division
FCN51_02265	ENOG4108ZCF	integral membrane protein
FCN51_02270	ENOG4105C83	adenylosuccinate lyase
FCN51_02275	ENOG4107QPR	SAICAR synthetase
FCN51_02280	ENOG4105VR9	phosphoribosylformylglycinamidine synthase
FCN51_02290	ENOG4105D21	Phosphoribosylformylglycinamidine synthase I
FCN51_02295	ENOG4107QIK	phosphoribosylformylglycinamidine synthase
FCN51_02320	ENOG4105CQX	Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol (By similarity)
FCN51_02330	ENOG4105IPI	Membrane
FCN51_02335	ENOG4105KHC	sulfurtransferase
FCN51_02340	ENOG4105C28	cystathionine
FCN51_02345	ENOG4105C0P	Mg chelatase subunit ChlI
FCN51_02350	ENOG4108JQ1	Dehydrogenase
FCN51_02360	ENOG4105XUA	cytochrome c
FCN51_02365	ENOG4105CET	Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria (By similarity)
FCN51_02370	ENOG4105CQC	Prephenate dehydratase
FCN51_02375	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
FCN51_02380	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
FCN51_02385	ENOG4105VEQ	Cold shock protein
FCN51_02415	ENOG4105CJF	Malonyl coA-acyl carrier protein transacylase
FCN51_02425	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
FCN51_02430	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
FCN51_02435	ENOG4105HHA	aminodeoxychorismate lyase
FCN51_02455	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)
FCN51_02460	ENOG4105D8A	3-Deoxy-D-manno-octulosonic-acid transferase
FCN51_02470	ENOG4105ET1	Component of the sulfite reductase complex that catalyzes the 6-electron reduction of sulfite to sulfide. This is one of several activities required for the biosynthesis of L- cysteine from sulfate (By similarity)
FCN51_02485	ENOG4105C11	sulfate adenylyltransferase), subunit 2
FCN51_02490	ENOG4105ET3	Reduction of activated sulfate into sulfite (By similarity)
FCN51_02500	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)
FCN51_02505	ENOG4107RJX	Catalyzes the conversion of 6-carboxy-5,6,7,8- tetrahydropterin (CPH4) to 7-carboxy-7-deazaguanine (CDG) (By similarity)
FCN51_02510	ENOG4105FD2	Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) (By similarity)
FCN51_02520	ENOG4105DWT	malate dehydrogenase (quinone)
FCN51_02525	ENOG4108Z9K	Osmotically inducible protein
FCN51_02530	ENOG4105D10	5-enolpyruvylshikimate-3-phosphate phospholyase
FCN51_02535	ENOG4105CSJ	Enoyl- acyl-carrier-protein reductase NADH
FCN51_02540	ENOG4108S7T	Catalyzes the oxidation of either pyridoxine 5'- phosphate (PNP) or pyridoxamine 5'-phosphate (PMP) into pyridoxal 5'-phosphate (PLP) (By similarity)
FCN51_02570	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
FCN51_02575	ENOG4105DZ1	carboxypeptidase
FCN51_02580	ENOG4105K6T	rare lipoprotein A
FCN51_02585	ENOG4105CVE	Lytic murein transglycosylase
FCN51_02600	ENOG4105CUB	amino acid
FCN51_02605	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
FCN51_02625	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)
FCN51_02635	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
FCN51_02640	ENOG4105CUT	histidyl-tRNA synthetase
FCN51_02645	ENOG4105C4E	Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate (By similarity)
FCN51_02655	ENOG4105EA8	2-Nitropropane dioxygenase
FCN51_02660	ENOG4105CFH	Aspartokinase
FCN51_02665	ENOG4107RFD	Non-specific O-methyltransferase that catalyzes the 2 O- methylation steps in the ubiquinone biosynthetic pathway (By similarity)
FCN51_02670	ENOG4105HHQ	6-phosphogluconolactonase (EC 3.1.1.31)
FCN51_02685	ENOG4105VW4	glutaredoxin 3
FCN51_02690	ENOG4105MJ2	Competence protein
FCN51_02695	ENOG4106T9E	Converts the free carboxyl group of a malonyl-thioester to its methyl ester by transfer of a methyl group from S-adenosyl- L-methionine (SAM). It allows to synthesize pimeloyl-ACP via the fatty acid synthetic pathway (By similarity)
FCN51_02700	ENOG4105CM1	Catalyzes, together with MoaC, the conversion of 5'-GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
FCN51_02720	ENOG4108BDP	Catalyzes the transfer of endogenously produced octanoic acid from octanoyl-acyl-carrier-protein onto the lipoyl domains of lipoate-dependent enzymes. Lipoyl-ACP can also act as a substrate although octanoyl-ACP is likely to be the physiological substrate (By similarity)
FCN51_02730	ENOG4105M85	Bola protein
FCN51_02735	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)
FCN51_02750	ENOG4105DY8	decarboxylase
FCN51_02755	ENOG4105DHU	Bile acid
FCN51_02770	ENOG4107NKQ	Flavinator of succinate dehydrogenase
FCN51_02775	ENOG4105CB5	ATP-dependent DNA helicase recG
FCN51_02785	ENOG4105CA8	Catalyzes the rearrangement of 1-deoxy-D-xylulose 5- phosphate (DXP) to produce the thiazole phosphate moiety of thiamine. Sulfur is provided by the thiocarboxylate moiety of the carrier protein ThiS. In vitro, sulfur can be provided by H(2)S (By similarity)
FCN51_02805	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
FCN51_02815	ENOG4105W0E	50S ribosomal protein L33
FCN51_02820	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
FCN51_02825	ENOG4105DS7	Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair (By similarity)
FCN51_02830	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)
FCN51_02840	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)
FCN51_02845	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)
FCN51_02850	ENOG4108ZAF	Molybdopterin
FCN51_02855	ENOG4105M00	molybdopterin converting factor, subunit 1
FCN51_02870	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)
FCN51_02875	ENOG4108IGT	Dipeptidase
FCN51_02890	ENOG4105CFU	surface antigen
FCN51_02900	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)
FCN51_02910	ENOG4105KGE	Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA (By similarity)
FCN51_02915	ENOG4105C37	(CBS) domain
FCN51_02920	ENOG4108R9S	DSBA oxidoreductase
FCN51_02945	ENOG4105EHE	chorismate mutase- prephenate dehydrogenase
FCN51_02950	ENOG4105M4E	phosphohistidine phosphatase, SixA
FCN51_02965	ENOG4107SW0	Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) (By similarity)
FCN51_02970	ENOG4105F03	Provides the (R)-glutamate required for cell wall biosynthesis (By similarity)
FCN51_02975	ENOG4105EAH	synthase
FCN51_02985	ENOG4105E05	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
FCN51_02990	ENOG4105BZH	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
FCN51_03005	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)
FCN51_03010	ENOG4107QT7	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)
FCN51_03020	ENOG4105M2E	Channel that opens in response to stretch forces in the membrane lipid bilayer. May participate in the regulation of osmotic pressure changes within the cell (By similarity)
FCN51_03025	ENOG41082FS	50S ribosomal protein L31
FCN51_03030	ENOG4108ZNX	Heat shock protein
FCN51_03050	ENOG4108UM6	Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) (By similarity)
FCN51_03055	ENOG4105CY8	phosphoribosylaminoimidazole carboxylase atpase subunit
FCN51_03060	ENOG4105W5Q	DNA repair protein (RadC
FCN51_03065	ENOG4105W5Q	DNA repair protein (RadC
FCN51_03070	ENOG4105C4R	Atp-dependent dna helicase
FCN51_03075	ENOG4107RQ5	Methylates ribosomal protein L11 (By similarity)
FCN51_03080	ENOG4105DC7	peptidase M24
FCN51_03085	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)
FCN51_03100	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)
FCN51_03135	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
FCN51_03140	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
FCN51_03145	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)
FCN51_03150	ENOG41082BR	50S ribosomal protein L35
FCN51_03155	ENOG4105DEI	Mannitol dehydrogenase
FCN51_03160	ENOG4105CE2	Aldehyde oxidase and xanthine dehydrogenase, molybdopterin binding
FCN51_03175	ENOG4105P9C	Participates in cysteine desulfuration mediated by SufS. Cysteine desulfuration mobilizes sulfur from L-cysteine to yield L-alanine and constitutes an essential step in sulfur metabolism for biosynthesis of a variety of sulfur-containing biomolecules. Functions as a sulfur acceptor for SufS, by mediating the direct transfer of the sulfur atom from the S-sulfanylcysteine of SufS, an intermediate product of cysteine desulfuration process (By similarity)
FCN51_03180	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)
FCN51_03185	ENOG4108R5P	Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery (By similarity)
FCN51_03210	ENOG4105CAK	Cell division ATP-binding protein ftsE
FCN51_03225	ENOG4105C4W	S-formylglutathione hydrolase
FCN51_03230	ENOG4105FFC	UPF0187 protein
FCN51_03235	ENOG4108VJ1	Transcriptional regulator (CarD family
FCN51_03240	ENOG4105RQ9	TPR repeat-containing protein
FCN51_03250	ENOG4105CU0	Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA (By similarity)
FCN51_03255	ENOG4105CBX	hi0933 family
FCN51_03265	ENOG4105K7U	Cell division inhibitor that blocks the formation of polar Z ring septums. Rapidly oscillates between the poles of the cell to destabilize FtsZ filaments that have formed before they mature into polar Z rings. Prevents FtsZ polymerization (By similarity)
FCN51_03270	ENOG4107QMS	site-determining protein
FCN51_03275	ENOG4105VJP	Prevents the cell division inhibition by proteins MinC and MinD at internal division sites while permitting inhibition at polar sites. This ensures cell division at the proper site by restricting the formation of a division septum at the midpoint of the long axis of the cell (By similarity)
FCN51_03280	ENOG4108WYP	Transcriptional regulator
FCN51_03285	ENOG4105BZ1	(ABC) transporter
FCN51_03305	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)
FCN51_03310	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)
FCN51_03315	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)
FCN51_03320	ENOG4105CV9	cyclopropane-fatty-acyl-phospholipid synthase
FCN51_03325	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
FCN51_03330	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)
FCN51_03335	ENOG4108ZDX	Binds together with S18 to 16S ribosomal RNA (By similarity)
FCN51_03345	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FCN51_03350	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)
FCN51_03360	ENOG4105C1M	carbamoyl-phosphate synthetase glutamine chain
FCN51_03365	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
FCN51_03370	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)
FCN51_03375	ENOG4105C7B	Threonine dehydratase
FCN51_03380	ENOG4105CJI	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
FCN51_03390	ENOG4105CN1	protease
FCN51_03400	ENOG4105EJF	Accelerates the degradation of transcripts by removing pyrophosphate from the 5'-end of triphosphorylated RNA, leading to a more labile monophosphorylated state that can stimulate subsequent ribonuclease cleavage (By similarity)
FCN51_03405	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
FCN51_03415	ENOG4105BZ1	(ABC) transporter
FCN51_03420	ENOG4105D4J	Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate
FCN51_03430	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
FCN51_03455	ENOG4105CEC	DNA methylase N-4 N-6
FCN51_03460	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
FCN51_03470	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
FCN51_03475	ENOG4105ENT	Efflux transporter rnd family, mfp subunit
FCN51_03480	ENOG4105BZS	acriflavin resistance protein
FCN51_03490	ENOG4105ENJ	RND efflux system, outer membrane lipoprotein
FCN51_03505	ENOG4105D7T	ABC transporter
FCN51_03510	ENOG4105EFS	Binding-protein-dependent transport systems, inner membrane component
FCN51_03520	ENOG4108ZT0	50S ribosomal protein l17
FCN51_03525	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
FCN51_03530	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)
FCN51_03535	ENOG4108Z04	Located at the top of the head of the 30S subunit, it contacts several helices of the 16S rRNA. In the 70S ribosome it contacts the 23S rRNA (bridge B1a) and protein L5 of the 50S subunit (bridge B1b), connecting the 2 subunits
FCN51_03540	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)
FCN51_03550	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
FCN51_03555	ENOG41084HQ	50S ribosomal protein L30
FCN51_03560	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)
FCN51_03565	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)
FCN51_03570	ENOG4108R5J	This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7 L12 stalk, and near the tRNA binding site of the peptidyltransferase center (By similarity)
FCN51_03575	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)
FCN51_03580	ENOG4105VBI	Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site (By similarity)
FCN51_03585	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
FCN51_03590	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
FCN51_03595	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
FCN51_03600	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
FCN51_03605	ENOG41083MP	50s ribosomal protein l29
FCN51_03610	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
FCN51_03615	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
FCN51_03620	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)
FCN51_03625	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
FCN51_03630	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
FCN51_03635	ENOG41080KG	One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome (By similarity)
FCN51_03640	ENOG4106U5A	One of the primary rRNA binding proteins, this protein initially binds near the 5'-end of the 23S rRNA. It is important during the early stages of 50S assembly. It makes multiple contacts with different domains of the 23S rRNA in the assembled 50S subunit and ribosome (By similarity)
FCN51_03645	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)
FCN51_03650	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
FCN51_03655	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
FCN51_03660	ENOG4108UHY	One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the head domain of the 30S subunit. Is located at the subunit interface close to the decoding center, probably blocks exit of the E-site tRNA (By similarity)
FCN51_03665	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)
FCN51_03670	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
FCN51_03675	ENOG4107QIH	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
FCN51_03680	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)
FCN51_03685	ENOG4108VZM	50s ribosomal protein L10
FCN51_03690	ENOG4105C64	Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release (By similarity)
FCN51_03695	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
FCN51_03700	ENOG4105ENJ	RND efflux system, outer membrane lipoprotein
FCN51_03730	ENOG4105CSH	Transporter
FCN51_03740	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
FCN51_03770	ENOG4108R4Z	Functions in the N-end rule pathway of protein degradation where it conjugates Leu, Phe and, less efficiently, Met from aminoacyl-tRNAs to the N-termini of proteins containing an N-terminal arginine or lysine (By similarity)
FCN51_03805	ENOG41060IM	Heme exporter protein
FCN51_03810	ENOG4108ZKK	Heme chaperone required for the biogenesis of c-type cytochromes. Transiently binds heme delivered by CcmC and transfers the heme to apo-cytochromes in a process facilitated by CcmF and CcmH (By similarity)
FCN51_03815	ENOG4105DA4	cytochrome c-type biogenesis protein
FCN51_03820	ENOG4107QX9	Thiol disulfide interChange protein
FCN51_03825	ENOG4105KWW	Biogenesis protein
FCN51_03850	ENOG4105DSW	Fusaric acid resistance protein
FCN51_03875	ENOG4105FDK	ABC transporter
FCN51_03895	ENOG4105CUU	Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) (By similarity)
FCN51_03905	ENOG4105CXB	phosphoribosylaminoimidazole synthetase
FCN51_03910	ENOG4108V3E	phosphoribosylglycinamide formyltransferase
FCN51_03915	ENOG4105CYJ	ribosomal RNA small subunit methyltransferase B
FCN51_03920	ENOG4105DJV	ribulose-phosphate 3-epimerase
FCN51_03945	ENOG4108ZQD	Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A (By similarity)
FCN51_03950	ENOG4105E2X	shikimate dehydrogenase
FCN51_03970	ENOG4105CH7	arginosuccinase
FCN51_03985	ENOG4105CMR	udp-glucose 4-epimerase
FCN51_03990	ENOG4108CHM	Preferentially cleaves peptide bonds on the carboxyl- terminal side of aspartate and glutamate. Along with other extracellular proteases it is involved in colonization and infection of human tissues. Required for proteolytic maturation of thiol protease SspB and inactivation of SspC, an inhibitor of SspB. It is the most important protease for degradation of fibronectin-binding protein (FnBP) and surface protein A, which are involved in adherence to host cells. May also protect bacteria against host defense mechanism by cleaving the immunoglobulin classes IgG, IgA and IgM. May be involved in the stability of secreted lipases
FCN51_04000	ENOG4105YVS	arsR family transcriptional regulator
FCN51_04005	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
FCN51_04010	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
FCN51_04050	ENOG4107RGH	Aldehyde dehydrogenase
FCN51_04060	ENOG4108RCM	Nitroreductase
FCN51_04080	ENOG4107RHB	Catalyzes the reversible phosphorylation of S-methyl-5'- thioadenosine (MTA) to adenine and 5-methylthioribose-1-phosphate. Involved in the breakdown of MTA, a major by-product of polyamine biosynthesis. Responsible for the first step in the methionine salvage pathway after MTA has been generated from S- adenosylmethionine. Has broad substrate specificity with 6- aminopurine nucleosides as preferred substrates (By similarity)
FCN51_04085	ENOG4105DJ5	Component of the ubiquinol-cytochrome c reductase complex (complex III or cytochrome b-c1 complex), which is a respiratory chain that generates an electrochemical potential coupled to ATP synthesis (By similarity)
FCN51_04090	ENOG4105DJ5	Component of the ubiquinol-cytochrome c reductase complex (complex III or cytochrome b-c1 complex), which is a respiratory chain that generates an electrochemical potential coupled to ATP synthesis (By similarity)
FCN51_04095	ENOG4105DBS	Key enzyme in heme biosynthesis. Catalyzes the oxidative decarboxylation of propionic acid side chains of rings A and B of coproporphyrinogen III (By similarity)
FCN51_04110	ENOG4105CA0	peroxidase
FCN51_04115	ENOG4105CEC	DNA methylase N-4 N-6
FCN51_04125	ENOG4105GCF	PGAM
FCN51_04130	ENOG4105IX2	One of the proteins required for the normal export of preproteins out of the cell cytoplasm. It is a molecular chaperone that binds to a subset of precursor proteins, maintaining them in a translocation-competent state. It also specifically binds to its receptor SecA (By similarity)
FCN51_04140	ENOG4105D6W	Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps (By similarity)
FCN51_04145	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)
FCN51_04150	ENOG4105D6S	protein involved in catabolism of external DNA
FCN51_04170	ENOG4105CEV	competence damage-inducible protein
FCN51_04175	ENOG4107QM9	Component of the acetyl coenzyme A carboxylase (ACC) complex. First, biotin carboxylase catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the carboxyltransferase to acetyl-CoA to form malonyl-CoA (By similarity)
FCN51_04180	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)
FCN51_04190	ENOG4105D49	3-dehydroquinate synthase
FCN51_04205	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)
FCN51_04210	ENOG41071I4	Phosphatidylserine decarboxylase proenzyme
FCN51_04215	ENOG4106PT6	cdpdiacylglycerol-serine O-phosphatidyltransferase
FCN51_04220	ENOG4105C47	NADH ubiquinone oxidoreductase 20 kda subunit
FCN51_04225	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)
FCN51_04270	ENOG4105C3E	May play a key role in the regulation of the intracellular concentration of adenosylhomocysteine (By similarity)
FCN51_04285	ENOG4107QN2	dihydrolipoyl dehydrogenase
FCN51_04290	ENOG4105C7S	Dehydrogenase
FCN51_04300	ENOG4105D6Z	AFG1 family ATPase
FCN51_04310	ENOG4105EGY	DNA internalization-related competence protein ComEC Rec2
FCN51_04315	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)
FCN51_04320	ENOG4105CXT	aspartate transcarbamylase
FCN51_04325	ENOG4105CD3	dihydroorotase
FCN51_04330	ENOG4105K7Z	Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP (By similarity)
FCN51_04335	ENOG4105C79	DNA protecting protein DprA
FCN51_04345	ENOG4105C40	3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs (By similarity)
FCN51_04350	ENOG4105CN1	protease
FCN51_04370	ENOG4108ZF1	Transcriptional regulator, BadM Rrf2 family
FCN51_04385	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)
FCN51_04390	ENOG4107AQZ	Membrane
FCN51_04395	ENOG4105C8S	subunit m
FCN51_04400	ENOG4105DC6	This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex (By similarity)
FCN51_04410	ENOG4105M02	This protein specifically catalyzes the removal of signal peptides from prolipoproteins (By similarity)
FCN51_04415	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)
FCN51_04420	ENOG4105DTN	riboflavin biosynthesis protein ribF
FCN51_04425	ENOG4106YVY	Bifunctional enzyme that catalyzes the enolization of 2,3-diketo-5-methylthiopentyl-1-phosphate (DK-MTP-1-P) into the intermediate 2-hydroxy-3-keto-5-methylthiopentenyl-1-phosphate (HK-MTPenyl-1-P), which is then dephosphorylated to form the acireductone 1,2-dihydroxy-3-keto-5-methylthiopentene (DHK-MTPene) (By similarity)
FCN51_04430	ENOG4108CAF	Catalyzes 2 different reactions between oxygene and the acireductone 1,2-dihydroxy-3-keto-5-methylthiopentene (DHK-MTPene) depending upon the metal bound in the active site. Fe-containing acireductone dioxygenase (Fe-ARD) produces formate and 2-keto-4- methylthiobutyrate (KMTB), the alpha-ketoacid precursor of methionine in the methionine recycle pathway. Ni-containing acireductone dioxygenase (Ni-ARD) produces methylthiopropionate, carbon monoxide and formate, and does not lie on the methionine recycle pathway (By similarity)
FCN51_04435	ENOG4107QY0	Catalyzes the dehydration of methylthioribulose-1- phosphate (MTRu-1-P) into 2,3-diketo-5-methylthiopentyl-1- phosphate (DK-MTP-1-P) (By similarity)
FCN51_04455	ENOG4105C8Y	Acetylornithine aminotransferase
FCN51_04460	ENOG4105DBV	ornithine carbamoyltransferase
FCN51_04480	ENOG4105CQ7	ATP-dependent helicase
FCN51_04490	ENOG4105CV8	reductase
FCN51_04500	ENOG4105BZ6	Presumably involved in the processing and regular turnover of intracellular proteins. Catalyzes the removal of unsubstituted N-terminal amino acids from various peptides (By similarity)
FCN51_04505	ENOG4108RNI	3'(2')5'-bisphosphate nucleotidase
FCN51_04510	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)
FCN51_04535	ENOG4108WBT	adenosyltransferase
FCN51_04565	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)
FCN51_04590	ENOG4105C85	amino acid
FCN51_04610	ENOG4107Y5K	Resolvase
FCN51_04640	ENOG4105CY3	ABC transporter, permease
FCN51_04645	ENOG4105DHJ	ABC, transporter
FCN51_04650	ENOG4105EGS	Mechanosensitive ion channel
FCN51_04665	ENOG4107SZR	mannose-6-phosphate isomerase
FCN51_04670	ENOG4105DW0	Catalyzes the ADP transfer to D-glycero-D-manno-heptose 1-phosphate, yielding ADP-D,D-heptose (By similarity)
FCN51_04675	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
FCN51_04690	ENOG4105C2N	RNA methyltransferase TrmH family group 3
FCN51_04700	ENOG4105C2X	Arabinose 5-phosphate isomerase
FCN51_04715	ENOG4108IUZ	ABC transporter
FCN51_04720	ENOG4105QVC	MOSC domain-containing protein
FCN51_04730	ENOG4107TNS	sigma 54 modulation protein ribosomal protein S30ea
FCN51_04740	ENOG4108ZNX	Heat shock protein
FCN51_04755	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)
FCN51_04760	ENOG4105DI7	Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs (By similarity)
FCN51_04770	ENOG4105C9Y	Catalyzes the hydrolysis of N-succinyl-L,L- diaminopimelic acid (SDAP), forming succinate and LL-2,6- diaminoheptanedioate (DAP), an intermediate involved in the bacterial biosynthesis of lysine and meso-diaminopimelic acid, an essential component of bacterial cell walls (By similarity)
FCN51_04775	ENOG4105DMJ	Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate (By similarity)
FCN51_04780	ENOG4105CAS	nag kinase
FCN51_04785	ENOG4105WHM	Necessary for normal cell division and for the maintenance of normal septation (By similarity)
FCN51_04790	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
FCN51_04795	ENOG41087PG	RNaseP catalyzes the removal of the 5'-leader sequence from pre-tRNA to produce the mature 5'-terminus. It can also cleave other RNA substrates such as 4.5S RNA. The protein component plays an auxiliary but essential role in vivo by binding to the 5'-leader sequence and broadening the substrate specificity of the ribozyme (By similarity)
FCN51_04800	ENOG4105VG0	50S ribosomal protein l34
FCN51_04810	ENOG4108UYE	Lactoylglutathione lyase
FCN51_04815	ENOG4105GYT	Protein of unknown function (DUF1009)
FCN51_04820	ENOG4105DAF	Involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
FCN51_04825	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)
FCN51_04830	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)
FCN51_04840	ENOG4105E1Z	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane
FCN51_04845	ENOG4105DZP	Membrane-associated zinc metalloprotease
FCN51_04850	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)
FCN51_04860	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
FCN51_04865	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)
FCN51_04870	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
FCN51_04880	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)
FCN51_04885	ENOG4105C3F	Signal peptidase i
FCN51_04890	ENOG4105KJV	Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein (By similarity)
FCN51_04895	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)
FCN51_04900	ENOG4105VFG	Promotes RNA polymerase assembly. Latches the N- and C- terminal regions of the beta' subunit thereby facilitating its interaction with the beta and alpha subunits (By similarity)
FCN51_04905	ENOG4105K8U	2-Amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase
FCN51_04915	ENOG4107B2H	carbonic anhydrase
FCN51_04925	ENOG4105C1J	atp-dependent rna helicase
FCN51_04930	ENOG4105DWV	Homoserine O-trans-acetylase
FCN51_04935	ENOG4105DWV	Homoserine O-trans-acetylase
FCN51_04940	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)
FCN51_04955	ENOG4105DZG	Dehydrogenase
FCN51_04965	ENOG4105C5F	glutamine synthetase
FCN51_04970	ENOG4108YZA	Nitrogen regulatory protein pii
FCN51_05000	ENOG4105CAY	ferredoxin--nadp reductase
FCN51_05005	ENOG4105MWK	D-amino acid dehydrogenase, small subunit
FCN51_05015	ENOG4105CI3	gtp-binding protein typa
FCN51_05035	ENOG4105CA9	Pyruvate kinase
FCN51_05045	ENOG4105D06	uba thif-type nad fad binding protein
FCN51_05070	ENOG4105EPD	Oligopeptide transporter, Opt family
FCN51_05085	ENOG4105EV9	Alpha Beta Hydrolase
FCN51_05090	ENOG4105DZ0	fad dependent oxidoreductase
FCN51_05095	ENOG4105PGM	cation diffusion facilitator family transporter
FCN51_05110	ENOG4105CKI	cobalamin synthesis protein
FCN51_05120	ENOG4105CEP	NADH dehydrogenase
FCN51_05135	ENOG4105VN1	Heat shock protein
FCN51_05140	ENOG4108EMS	branched-chain alpha-keto acid dehydrogenase subunit E2
FCN51_05145	ENOG4105CPP	Dehydrogenase, E1 component
FCN51_05150	ENOG4107R0V	Pyruvate dehydrogenase
FCN51_05160	ENOG4105CJ3	phosphate transporter
FCN51_05165	ENOG4105CSR	polyphosphate kinase 2
FCN51_05180	ENOG4105TW1	Carbohydrate-selective porin OprB
FCN51_05210	ENOG4105TPV	
FCN51_05230	ENOG4105C1G	acyl-Coa dehydrogenase
FCN51_05240	ENOG4108IIG	CoA transferase having broad substrate specificity for short-chain acyl-CoA thioesters with the activity decreasing when the length of the carboxylic acid chain exceeds four carbons (By similarity)
FCN51_05265	ENOG4105C9K	Endothelin-converting enzyme 1
FCN51_05305	ENOG4105EMU	Dehydrogenase
FCN51_05310	ENOG4105KPV	Transcriptional regulator
FCN51_05350	ENOG4105EEQ	Na H antiporter
FCN51_05470	ENOG4105C72	UPF0176 protein
FCN51_05605	ENOG4105E0K	tonB-dependent siderophore receptor
FCN51_05760	ENOG4105C26	Dehydrogenase
FCN51_05805	ENOG410630Q	Methylamine utilization
FCN51_05835	ENOG4105CSF	NADPH-dependent glycerol-3-phosphate dehydrogenase
FCN51_05865	ENOG4105E0X	reductase
FCN51_05870	ENOG4105CVP	deoxyribo-dipyrimidine photolyase
FCN51_05890	ENOG4105E15	Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate
FCN51_05895	ENOG4105RD7	BadF BadG BcrA BcrD
FCN51_05900	ENOG4105E2D	ec 3.2.1.52
FCN51_05905	ENOG4108IPX	Part of the ABC transporter complex HmuTUV involved in hemin import. Responsible for energy coupling to the transport system (By similarity)
FCN51_05910	ENOG4105EHG	Permease protein
FCN51_05920	ENOG4105D05	Receptor
FCN51_05925	ENOG4105EEQ	Na H antiporter
FCN51_05935	ENOG4105H9W	Short-chain dehydrogenase reductase Sdr
FCN51_05975	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
FCN51_06020	ENOG4105CTR	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
FCN51_06030	ENOG4108UN4	phage SPO1 DNA polymerase-related protein
FCN51_06035	ENOG4105E4C	Lytic transglycosylase catalytic
FCN51_06045	ENOG4105CM1	Catalyzes, together with MoaC, the conversion of 5'-GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
FCN51_06060	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)
FCN51_06080	ENOG410901P	UPF0249 protein
FCN51_06095	ENOG4105DHP	deoxycytidine triphosphate deaminase
FCN51_06100	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
FCN51_06115	ENOG4107QR9	Iron-sulfur cluster binding protein
FCN51_06120	ENOG4107R5T	Cysteine-rich domain
FCN51_06135	ENOG4105C7K	acetolactate synthase
FCN51_06155	ENOG4108UXA	Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA (By similarity)
FCN51_06165	ENOG4107WK2	Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) (By similarity)
FCN51_06170	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)
FCN51_06175	ENOG4105C3G	gtp-binding protein
FCN51_06180	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
FCN51_06195	ENOG4105C9M	aspartyl-trna synthetase
FCN51_06210	ENOG4105C88	aminopeptidase
FCN51_06225	ENOG4105JHE	Major Facilitator Superfamily
FCN51_06230	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)
FCN51_06235	ENOG4105CR4	methylisocitrate lyase
FCN51_06240	ENOG4105BZN	citrate synthase
FCN51_06245	ENOG4105DXD	2-methylcitrate dehydratase
FCN51_06275	ENOG4105EXC	Acyl-transferase
FCN51_06355	ENOG4105CJX	Molecular chaperone. Has ATPase activity (By similarity)
FCN51_06365	ENOG4105DXN	mazG family
FCN51_06370	ENOG4105C0N	N-acetylglutamate semialdehyde dehydrogenase
FCN51_06375	ENOG4105F6U	Short-chain dehydrogenase reductase Sdr
FCN51_06390	ENOG4105C42	Type I secretion membrane fusion protein (HlyD
FCN51_06400	ENOG4105D3Z	quinone oxidoreductase, yhdh yhfp family
FCN51_06405	ENOG4105C37	(CBS) domain
FCN51_06410	ENOG4105D6F	Phosphatase
FCN51_06430	ENOG4107QMV	Part of the ABC transporter complex PstSACB involved in phosphate import (By similarity)
FCN51_06435	ENOG4105BZU	Histidine kinase
FCN51_06440	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FCN51_06445	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
FCN51_06450	ENOG4105C49	Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine (By similarity)
FCN51_06460	ENOG4107EFR	Flavocytochrome c
FCN51_06465	ENOG4105F6H	The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate (By similarity)
FCN51_06470	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
FCN51_06475	ENOG4107QUT	magnesium and cobalt transport protein CorA
FCN51_06495	ENOG41090R7	Ferric uptake
FCN51_06505	ENOG4105CE8	Transfers the fatty acyl group on membrane lipoproteins (By similarity)
FCN51_06510	ENOG4108WRK	Transcriptional regulator
FCN51_06520	ENOG4107QIB	glycyl-tRNA synthetase, alpha subunit
FCN51_06525	ENOG4105C38	Glycyl-tRNA synthetase beta subunit
FCN51_06535	ENOG4105DXC	membrane
FCN51_06550	ENOG4105DC1	bifunctional purine biosynthesis protein purh
FCN51_06555	ENOG4105CZ1	Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA (By similarity)
FCN51_06560	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
FCN51_06565	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
FCN51_06570	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)
FCN51_06575	ENOG4105CFG	Acts as a chaperone (By similarity)
FCN51_06580	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
FCN51_06585	ENOG4105E3W	Two component transcriptional regulator (Winged helix family
FCN51_06590	ENOG4105EB3	Histidine kinase
FCN51_06600	ENOG4105C21	Displays ATPase and GTPase activities (By similarity)
FCN51_06605	ENOG4108UJU	UPF0301 protein
FCN51_06610	ENOG4105CSR	polyphosphate kinase 2
FCN51_06625	ENOG4105KAE	Involved in the modulation of the specificity of the ClpAP-mediated ATP-dependent protein degradation (By similarity)
FCN51_06630	ENOG4105DZ1	carboxypeptidase
FCN51_06635	ENOG4105CA1	Removes the N-terminal methionine from nascent proteins (By similarity)
FCN51_06645	ENOG4105CK3	Lysine 2,3-aminomutase YodO family protein
FCN51_06650	ENOG4105CAP	With EpmB is involved in the beta-lysylation step of the post-translational modification of translation elongation factor P (EF-P). Catalyzes the ATP-dependent activation of (R)-beta-lysine produced by EpmB, forming a lysyl-adenylate, from which the beta- lysyl moiety is then transferred to the epsilon-amino group of a conserved specific lysine residue in EF-P (By similarity)
FCN51_06670	ENOG4106HMZ	Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP) (By similarity)
FCN51_06675	ENOG4105EIE	fructose-bisphosphate aldolase
FCN51_06700	ENOG4105MK2	5-formyltetrahydrofolate cyclo-ligase
FCN51_06705	ENOG4105D48	metallophosphoesterase
FCN51_06720	ENOG4107QYT	Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor (By similarity)
FCN51_06735	ENOG4107SFH	ImpB mucB samB family
FCN51_06740	ENOG4105C85	amino acid
FCN51_06780	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)
FCN51_06790	ENOG4108FN7	Aldo keto reductase
FCN51_06805	ENOG410635M	Required for disulfide bond formation in some periplasmic proteins. Acts by oxidizing the DsbA protein (By similarity)
FCN51_06810	ENOG4105C1K	alpha-alpha-trehalose-phosphate synthase
FCN51_06815	ENOG4108K4C	ec 3.1.3.12
FCN51_06840	ENOG4107RTZ	reductase
FCN51_06855	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)
FCN51_06870	ENOG4108V1U	phospholipid-binding protein
FCN51_06880	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)
FCN51_06885	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)
FCN51_06890	ENOG4105EH2	Catalyzes the conversion of epoxyqueuosine (oQ) to queuosine (Q), which is a hypermodified base found in the wobble positions of tRNA(Asp), tRNA(Asn), tRNA(His) and tRNA(Tyr) (By similarity)
FCN51_06900	ENOG41066UG	Regulatory DnaK co-chaperone. Direct interaction between DnaK and DjlA is needed for the induction of the wcaABCDE operon, involved in the synthesis of a colanic acid polysaccharide capsule, possibly through activation of the RcsB RcsC phosphotransfer signaling pathway. The colanic acid capsule may help the bacterium survive conditions outside the host (By similarity)
FCN51_06915	ENOG4108YYQ	gCN5-related N-acetyltransferase
FCN51_06920	ENOG4105C5H	ABC transporter
FCN51_06930	ENOG4105F0N	pyrophosphate phospho-hydrolase
FCN51_06935	ENOG4105C8E	extradiol ring-cleavage dioxygenase class IIi protein subunit b
FCN51_06950	ENOG4108X7C	Antioxidant protein with alkyl hydroperoxidase activity. Required for the reduction of the AhpC active site cysteine residues and for the regeneration of the AhpC enzyme activity (By similarity)
FCN51_06955	ENOG4105D3R	alkyl hydroperoxide reductase
FCN51_06995	ENOG4105FBD	synthase
FCN51_07000	ENOG4105FE1	phytoene synthase
FCN51_07030	ENOG4105Y49	secretion protein, HlyD family
FCN51_07055	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
FCN51_07070	ENOG4108ZZ3	UPF0260 protein
FCN51_07145	ENOG4108IUZ	ABC transporter
FCN51_07150	ENOG4105C0Z	ABC transporter
FCN51_07170	ENOG4105BZU	Histidine kinase
FCN51_07180	ENOG4105DCY	Is an aliphatic amidase with a restricted substrate specificity, as it only hydrolyzes formamide (By similarity)
FCN51_07220	ENOG4105ENJ	RND efflux system, outer membrane lipoprotein
FCN51_07225	ENOG4105BZS	acriflavin resistance protein
FCN51_07230	ENOG4105C1P	efflux transporter, rnd family, mfp subunit
FCN51_07240	ENOG4107FQ9	ethanolamine ammonia-lyase
FCN51_07245	ENOG4105CPD	ethanolamine ammonia-lyase
FCN51_07250	ENOG4108R6W	Transcriptional regulator, ARAC family
FCN51_07255	ENOG4105DE7	Sulfate ABC transporter periplasmic sulfate-binding protein
FCN51_07270	ENOG4108I5D	sulfate abc transporter
FCN51_07275	ENOG4105ECW	sulfate abc transporter
FCN51_07280	ENOG4108IJ6	ABC transporter
FCN51_07285	ENOG4105C85	amino acid
FCN51_07305	ENOG4105ZIE	Exonuclease involved in the 3' processing of various precursor tRNAs. Initiates hydrolysis at the 3'-terminus of an RNA molecule and releases 5'-mononucleotides (By similarity)
FCN51_07310	ENOG4105CSD	Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1) (By similarity)
FCN51_07315	ENOG4107ZDE	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
FCN51_07320	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)
FCN51_07325	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)
FCN51_07330	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
FCN51_07335	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)
FCN51_07365	ENOG4107R1I	NAD-dependent malic enzyme
FCN51_07375	ENOG4108RHM	integral membrane protein
FCN51_07380	ENOG4105CYX	Short-chain dehydrogenase reductase Sdr
FCN51_07395	ENOG4105DP0	ferredoxin-NADP reductase
FCN51_07400	ENOG4105DC8	reductase
FCN51_07405	ENOG4105CD3	dihydroorotase
FCN51_07415	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
FCN51_07425	ENOG4105ESV	Glycosyl transferase, family 4
FCN51_07440	ENOG4105BZ6	Presumably involved in the processing and regular turnover of intracellular proteins. Catalyzes the removal of unsubstituted N-terminal amino acids from various peptides (By similarity)
FCN51_07460	ENOG41090KH	cytochrome o ubiquinol oxidase (subunit iv)
FCN51_07465	ENOG4105CCU	oxidase (Subunit III)
FCN51_07480	ENOG4105HFZ	Membrane
FCN51_07500	ENOG4108RG0	uracil-dna glycosylase
FCN51_07510	ENOG4105DSW	Fusaric acid resistance protein
FCN51_07515	ENOG4109003	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis (By similarity)
FCN51_07525	ENOG4105C2C	drug resistance transporter, Bcr CflA
FCN51_07535	ENOG4107TQK	Catalyzes the oxidation of the C8 methyl side group on heme O porphyrin ring into a formyl group (By similarity)
FCN51_07540	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)
FCN51_07560	ENOG4105CJN	penicillin-binding protein
FCN51_07565	ENOG4105CNI	cell division protein FtsW
FCN51_07605	ENOG4105CI8	Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons (By similarity)
FCN51_07610	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)
FCN51_07615	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)
FCN51_07630	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)
FCN51_07635	ENOG4105CAT	Cytidine monophosphate kinase
FCN51_07640	ENOG4105CMY	5-enolpyruvylshikimate-3-phosphate synthase
FCN51_07650	ENOG4105KRF	dihydroneopterin aldolase
FCN51_07655	ENOG4107EXU	Short-chain dehydrogenase reductase Sdr
FCN51_07660	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)
FCN51_07665	ENOG4105KDX	Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection (By similarity)
FCN51_07670	ENOG4107QMP	dna polymerase iii subunits gamma and tau
FCN51_07690	ENOG4105CE4	GlcNAc 6-P deacetylase
FCN51_07700	ENOG4105DJ9	glucan biosynthesis protein
FCN51_07705	ENOG4105F4R	Transcriptional regulator mode
FCN51_07720	ENOG4105CFB	Gamma-glutamyltranspeptidase (EC 2.3.2.2)
FCN51_07730	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)
FCN51_07750	ENOG4105BZA	Phosphoglycerate kinase
FCN51_07780	ENOG410612Q	succinate dehydrogenase (cytochrome b-556 subunit)
FCN51_07785	ENOG4105CM3	Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate (By similarity)
FCN51_07790	ENOG4108IIE	The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane (By similarity)
FCN51_07795	ENOG4105W8H	transhydrogenase (subunit alpha
FCN51_07800	ENOG4105C15	The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane (By similarity)
FCN51_07810	ENOG4105C26	Dehydrogenase
FCN51_07815	ENOG4107QM1	Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine (By similarity)
FCN51_07830	ENOG4105DVS	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
FCN51_07840	ENOG4105KEG	ribosomal-protein-alanine acetyltransferase
FCN51_07850	ENOG4108RDT	NADH dehydrogenase NAD(P)H nitroreductase)
FCN51_07880	ENOG4105K63	Thioredoxin
FCN51_07885	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)
FCN51_07890	ENOG4105W49	UPF0434 protein
FCN51_07900	ENOG4105CZQ	inner membrane transport protein YdhC
FCN51_07910	ENOG4108UPT	UPF0178 protein
FCN51_07920	ENOG4108UHJ	MAF-like protein
FCN51_07925	ENOG4105CFZ	Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III (By similarity)
FCN51_07930	ENOG4107S75	HAD-superfamily hydrolase subfamily IA variant 3
FCN51_07935	ENOG4108YXA	Membrane
FCN51_07950	ENOG4108URH	decarboxylase
FCN51_07970	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)
FCN51_07975	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)
FCN51_07980	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)
FCN51_07985	ENOG4107YTN	Specifically methylates the N7 position of guanine in position 527 of 16S rRNA (By similarity)
FCN51_08015	ENOG4105M0C	cytoplasmic protein
FCN51_08025	ENOG41069NU	Nitroreductase
FCN51_08030	ENOG4105K59	histidine triad (HIT) protein
FCN51_08035	ENOG4105KPZ	phosphoribosyl-atp pyrophosphatase
FCN51_08040	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)
FCN51_08045	ENOG4105CJV	Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase
FCN51_08050	ENOG4108UJE	IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisH subunit provides the glutamine amidotransferase activity that produces the ammonia necessary to HisF for the synthesis of IGP and AICAR (By similarity)
FCN51_08055	ENOG4105ECC	imidazole-glycerol-phosphate dehydratase
FCN51_08070	ENOG4107S6X	Glycosyl transferase, family 2
FCN51_08090	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)
FCN51_08110	ENOG4105II7	pyrroline-5-carboxylate reductase
FCN51_08140	ENOG4105D8X	mechanosensitive ion channel
FCN51_08150	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)
FCN51_08155	ENOG4105EIN	peptidylprolyl cis-trans isomerase
FCN51_08160	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
FCN51_08165	ENOG4105CDY	transcriptional regulatory protein
FCN51_08170	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)
FCN51_08175	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)
FCN51_08180	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)
FCN51_08185	ENOG4107YD3	Thioesterase
FCN51_08190	ENOG4105E02	MotA TolQ exbB proton channel
FCN51_08195	ENOG4108ZZF	transport protein (ExbD)
FCN51_08205	ENOG4107R6Y	Involved in the TonB-independent uptake of proteins (By similarity)
FCN51_08210	ENOG4105KCK	Peptidoglycan-associated lipoprotein
FCN51_08220	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)
FCN51_08225	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)
FCN51_08235	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
FCN51_08245	ENOG4108E87	P-loop hydrolase UPF0079
FCN51_08260	ENOG4105K63	Thioredoxin
FCN51_08270	ENOG4105DPM	folylpolyglutamate synthase Dihydrofolate synthase
FCN51_08280	ENOG4105C8N	cysteinyl-tRNA synthetase
FCN51_08290	ENOG4105DHZ	alpha beta
FCN51_08300	ENOG4105C3J	Cysteine desulfurase
FCN51_08310	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
FCN51_08320	ENOG4105E2K	Glycosyl transferase (Group 1
FCN51_08330	ENOG4105CNU	cell division protein FtsK
FCN51_08340	ENOG4108RT7	Glycosyl transferase, family 2
FCN51_08370	ENOG4108TGR	phosphatase
FCN51_08375	ENOG4105D1U	peptidase U62 modulator of DNA gyrase
FCN51_08380	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)
FCN51_08410	ENOG4108UUM	single-stranded DNA-binding protein
FCN51_08415	ENOG4106H78	methyltransferase
FCN51_08420	ENOG4105FE9	pseudouridine synthase
FCN51_08425	ENOG4108Z86	Glutamine amidotransferase
FCN51_08430	ENOG4108Z6B	deaminase
FCN51_08435	ENOG4105C0H	protease
FCN51_08440	ENOG4105DS0	Transcriptional regulator, Crp Fnr family
FCN51_08450	ENOG4105D4P	Coproporphyrinogen iii oxidase
FCN51_08460	ENOG4105DWH	electron transfer flavoprotein-ubiquinone oxidoreductase
FCN51_08465	ENOG4105TPV	
FCN51_08470	ENOG4105C10	Electron transfer flavoprotein
FCN51_08530	ENOG4105C8T	Leucyl-tRNA synthetase
FCN51_08535	ENOG4105TXM	Domain of unknown function (DUF3576)
FCN51_08555	ENOG4105CEN	a g-specific adenine glycosylase
FCN51_08560	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
FCN51_08565	ENOG4105CSM	endonuclease III
FCN51_08570	ENOG4105BZ1	(ABC) transporter
FCN51_08580	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)
FCN51_08585	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)
FCN51_08590	ENOG41080G2	Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) (By similarity)
FCN51_08595	ENOG4107ZJC	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
FCN51_08605	ENOG4108JPW	Aminotransferase
FCN51_08615	ENOG4105TW1	Carbohydrate-selective porin OprB
FCN51_08630	ENOG4105TW1	Carbohydrate-selective porin OprB
FCN51_08640	ENOG4105EKT	)-iron permease
FCN51_08655	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)
FCN51_08660	ENOG4105C54	Major Facilitator superfamily
FCN51_08665	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
FCN51_08670	ENOG4105KM4	Acetyl-CoA carboxylase, biotin carboxyl carrier protein
FCN51_08675	ENOG4108Z38	Catalyzes a trans-dehydration via an enolate intermediate (By similarity)
FCN51_08685	ENOG4107U9T	Pfam:Ribonuclease_BN
FCN51_08690	ENOG4105CU5	Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine (By similarity)
FCN51_08700	ENOG4105CA5	Required for the export of heme to the periplasm for the biogenesis of c-type cytochromes (By similarity)
FCN51_08705	ENOG4107EV4	once thought to export heme, this seems not to be the case, but its exact role is uncertain. Responsible for energy coupling to the transport system (By similarity)
FCN51_08710	ENOG4107QM5	aconitate hydratase
FCN51_08715	ENOG4105CDA	abc transporter atp-binding protein
FCN51_08725	ENOG4105EXG	Transcriptional regulator
FCN51_08735	ENOG4106JDQ	ATP-dependent Clp protease, Hsp 100, ATP-binding subunit ClpB
FCN51_08745	ENOG4105K7D	Required for maturation of 30S ribosomal subunits (By similarity)
FCN51_08760	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)
FCN51_08765	ENOG4107ZGG	Associates with free 30S ribosomal subunits (but not with 30S subunits that are part of 70S ribosomes or polysomes). Essential for efficient processing of 16S rRNA. May interact with the 5'-terminal helix region of 16S rRNA (By similarity)
FCN51_08775	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
FCN51_08780	ENOG4105MWK	D-amino acid dehydrogenase, small subunit
FCN51_08790	ENOG4109025	Glyoxalase Bleomycin resistance protein (Dioxygenase
FCN51_08795	ENOG4107GFK	fumarate
FCN51_08810	ENOG4107R2U	Catalyzes the formation of dTMP and tetrahydrofolate from dUMP and methylenetetrahydrofolate (By similarity)
FCN51_08850	ENOG4105EE6	Alcohol dehydrogenase zinc-binding domain protein
FCN51_08860	ENOG4105C01	Dihydroxy-acid dehydratase
FCN51_08865	ENOG4105C8U	phosphate abc transporter
FCN51_08870	ENOG4105E2Z	phosphate ABC transporter (Permease
FCN51_08875	ENOG4105BZY	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
FCN51_08895	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)
FCN51_08915	ENOG4105C1J	atp-dependent rna helicase
FCN51_08930	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)
FCN51_08935	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)
FCN51_08940	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)
FCN51_08945	ENOG4107PQ6	Inherit from NOG: atp synthase
FCN51_08970	ENOG4105CKK	Glycosyl transferase, family 2
FCN51_08975	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)
FCN51_08985	ENOG4105F1S	paraquat-inducible protein a
FCN51_08990	ENOG4105DY2	Paraquat-inducible protein b
FCN51_09000	ENOG4105CBA	glutamine phosphoribosylpyrophosphate amidotransferase
FCN51_09015	ENOG4105C3R	Methionine synthase
FCN51_09060	ENOG4105DY2	Paraquat-inducible protein b
FCN51_09065	ENOG4105DHJ	ABC, transporter
FCN51_09075	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
FCN51_09080	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
FCN51_09085	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
FCN51_09100	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)
FCN51_09105	ENOG4108ZEF	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate (By similarity)
FCN51_09120	ENOG4105EXG	Transcriptional regulator
FCN51_09130	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)
FCN51_09135	ENOG4105CCX	Catalyzes the production of spermidine from putrescine and decarboxylated S-adenosylmethionine (dcSAM), which serves as an aminopropyl donor (By similarity)
FCN51_09140	ENOG4105D43	The glycine cleavage system catalyzes the degradation of glycine (By similarity)
FCN51_09145	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)
FCN51_09150	ENOG4105CBI	The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor
FCN51_09170	ENOG4105XRQ	Xanthine dehydrogenase accessory factor
FCN51_09180	ENOG4105C5X	domain protein
FCN51_09230	ENOG4108VHT	MarR family transcriptional regulator
FCN51_09235	ENOG4105MSY	salicylate hydroxylase
FCN51_09240	ENOG4108XHQ	(2Fe-2S)-binding domain protein
FCN51_09245	ENOG4105CE2	Aldehyde oxidase and xanthine dehydrogenase, molybdopterin binding
FCN51_09255	ENOG4108UAU	isochorismatase
FCN51_09265	ENOG4105RE0	Asp Glu hydantoin racemase
FCN51_09270	ENOG4105CSP	Major Facilitator Superfamily
FCN51_09325	ENOG4105D3R	alkyl hydroperoxide reductase
FCN51_09335	ENOG4108R3E	Dna-3-methyladenine glycosylase i
FCN51_09345	ENOG4105KUZ	arsenate reductase
FCN51_09350	ENOG4108UQY	Iron-storage protein
FCN51_09380	ENOG4108M9X	Required for maturation of urease via the functional incorporation of the urease nickel metallocenter (By similarity)
FCN51_09385	ENOG4108YZ9	Urea amidohydrolase subunit gamma
FCN51_09390	ENOG4105KI2	Urea amidohydrolase subunit beta
FCN51_09395	ENOG4105CQM	Urea amidohydrolase subunit alpha
FCN51_09400	ENOG4105MMR	Involved in urease metallocenter assembly. Binds nickel. Probably functions as a nickel donor during metallocenter assembly (By similarity)
FCN51_09405	ENOG4108YH3	Required for maturation of urease via the functional incorporation of the urease nickel metallocenter (By similarity)
FCN51_09410	ENOG4105E8T	Facilitates the functional incorporation of the urease nickel metallocenter. This process requires GTP hydrolysis, probably effectuated by UreG (By similarity)
FCN51_09425	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FCN51_09430	ENOG4105BZU	Histidine kinase
FCN51_09440	ENOG4105C32	Amino acid ABC transporter (Permease)
FCN51_09450	ENOG4105C0Z	ABC transporter
FCN51_09455	ENOG4108IV0	ABC, transporter
FCN51_09475	ENOG4105CSA	Coproporphyrinogen iii oxidase
FCN51_09480	ENOG4105DFH	Transport of potassium into the cell (By similarity)
FCN51_09485	ENOG4105DFA	alanine racemase domain protein
FCN51_09490	ENOG4105CPQ	Dehydrogenase
FCN51_09495	ENOG4105CMQ	Chloride channel
FCN51_09515	ENOG4108Z67	carbohydrate kinase, thermoresistant glucokinase family
FCN51_09520	ENOG4105E66	phosphoriboisomerase A
FCN51_09525	ENOG4108Q79	6-phosphogluconolactonase (EC 3.1.1.31)
FCN51_09530	ENOG4108AZI	Catalyzes the hydrolysis of 4-amino-2-methyl-5- hydroxymethylpyrimidine pyrophosphate (HMP-PP) to 4-amino-2- methyl-5-hydroxymethylpyrimidine phosphate (HMP-P) (By similarity)
FCN51_09535	ENOG4108J5G	6-phosphogluconate dehydrogenase
FCN51_09540	ENOG4107QQX	Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway (By similarity)
FCN51_09555	ENOG4105CIH	Imidazole acetol-phosphate transaminase
FCN51_09570	ENOG4105KK4	UPF0060 membrane protein
FCN51_09595	ENOG4105DBW	Multi-copper polyphenol oxidoreductase laccase
FCN51_09605	ENOG4105C3B	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
FCN51_09620	ENOG4105DAA	L-lactate
FCN51_09625	ENOG4105E4C	Lytic transglycosylase catalytic
FCN51_09630	ENOG4107QNK	)-transporter
FCN51_09645	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
FCN51_09650	ENOG4105C6T	cysteine synthase
FCN51_09665	ENOG4105C35	Catalyzes the interconversion of methylthioribose-1- phosphate (MTR-1-P) into methylthioribulose-1-phosphate (MTRu-1-P) (By similarity)
FCN51_09680	ENOG4105MYN	Zinc uptake regulation protein
FCN51_09690	ENOG4105D5T	phosphonate abc transporter
FCN51_09695	ENOG4105FAV	ABC, transporter
FCN51_09700	ENOG4107YAQ	Catalyzes the reduction of FMN to FMNH2 which is used to reduce pyrimidine by RutA via the Rut pathway (By similarity)
FCN51_09705	ENOG4105CGU	Enoyl-CoA hydratase
FCN51_09710	ENOG4106HK8	GPR1 FUN34 yaaH family protein
FCN51_09715	ENOG4105DSW	Fusaric acid resistance protein
FCN51_09740	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)
FCN51_09750	ENOG41068B1	Cob-I-yrinic acid a,c-diamide adenosyltransferase
FCN51_09755	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)
FCN51_09760	ENOG4105E7Q	Cob(II)yrinic acid a,c-diamide reductase
FCN51_09770	ENOG4105EFT	decarboxylase
FCN51_09775	ENOG4108UHF	Joins Ado-cobinamide-GDP and alpha-ribazole to generate adenosylcobalamin (Ado-cobalamin) (By similarity)
FCN51_09780	ENOG4105CUP	Catalyzes the synthesis of alpha-ribazole-5'-phosphate from nicotinate mononucleotide (NAMN) and 5,6- dimethylbenzimidazole (DMB) (By similarity)
FCN51_09790	ENOG4105F27	Major Facilitator
FCN51_09825	ENOG4105CK2	sodium dicarboxylate symporter
FCN51_09845	ENOG4108ZZF	transport protein (ExbD)
FCN51_09855	ENOG4108IU3	tonb-dependent siderophore receptor
FCN51_09870	ENOG4107E2E	PKHD-type hydroxylase
FCN51_09885	ENOG4105C26	Dehydrogenase
FCN51_09890	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
FCN51_09895	ENOG4107TYH	extracellular solute-binding protein family 1
FCN51_09900	ENOG4105D81	ABC transporter, permease
FCN51_09905	ENOG4105NRK	Binding-protein-dependent transport systems, inner membrane component
FCN51_09920	ENOG4105JHE	Major Facilitator Superfamily
FCN51_09930	ENOG4105C26	Dehydrogenase
FCN51_09950	ENOG4108Q89	anthranilate 1,2-dioxygenase large subunit
FCN51_09960	ENOG4105CHR	reductase
FCN51_09975	ENOG4105MP9	class II Aldolase
FCN51_09980	ENOG4108VQN	4-hydroxyphenylacetate 3-monooxygenase reductase
FCN51_09985	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)
FCN51_09990	ENOG41090MY	MarR family Transcriptional regulator
FCN51_10005	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)
FCN51_10010	ENOG4105CQB	FAD linked oxidase domain protein
FCN51_10015	ENOG4105D01	(LipO)protein
FCN51_10020	ENOG4108JEI	Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system (By similarity)
FCN51_10025	ENOG4108UMI	ABC transporter, permease
FCN51_10035	ENOG41067QW	Transcriptional regulator
FCN51_10045	ENOG4105CF1	Alkylated DNA repair protein
FCN51_10070	ENOG4105ED7	Catalyzes the specific phosphorylation of 1,6-anhydro-N- acetylmuramic acid (anhMurNAc) with the simultaneous cleavage of the 1,6-anhydro ring, generating MurNAc-6-P. Is required for the utilization of anhMurNAc either imported from the medium or derived from its own cell wall murein, and thus plays a role in cell wall recycling (By similarity)
FCN51_10080	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)
FCN51_10085	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)
FCN51_10095	ENOG4105IX2	One of the proteins required for the normal export of preproteins out of the cell cytoplasm. It is a molecular chaperone that binds to a subset of precursor proteins, maintaining them in a translocation-competent state. It also specifically binds to its receptor SecA (By similarity)
FCN51_10105	ENOG4106EG9	Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) (By similarity)
FCN51_10110	ENOG4108ZGB	N-(5'-phosphoribosyl)anthranilate isomerase
FCN51_10125	ENOG4105EW8	cytosine purines, uracil, thiamine, allantoin permease
FCN51_10130	ENOG4105CD3	dihydroorotase
FCN51_10145	ENOG4105BZ8	glutamate synthase
FCN51_10150	ENOG4107SJI	Dehydrogenase
FCN51_10155	ENOG4105CE7	Amidase, hydantoinase carbamoylase family
FCN51_10170	ENOG41090U3	tautomerase
FCN51_10190	ENOG4105C85	amino acid
FCN51_10205	ENOG4105C4M	(Ubiquinol oxidase) subunit I
FCN51_10210	ENOG4105CFY	cytochrome d ubiquinol oxidase, subunit ii
FCN51_10220	ENOG4105CSH	Transporter
FCN51_10235	ENOG4105C2M	dna polymerase I
FCN51_10240	ENOG4105CM2	brancheD-chain amino acid aminotransferase
FCN51_10245	ENOG4105CNG	UPF0061 protein
FCN51_10250	ENOG4105E0A	ABC, transporter
FCN51_10255	ENOG4105EHG	Permease protein
FCN51_10270	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
FCN51_10275	ENOG4105CBT	Fructose-1,6-bisphosphatase
FCN51_10280	ENOG4105D6E	homoserine dehydrogenase
FCN51_10285	ENOG4105CHM	Aminotransferase
FCN51_10295	ENOG4108S10	Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins (By similarity)
FCN51_10305	ENOG4105EZY	Pyrroloquinoline quinone biosynthesis protein E
FCN51_10310	ENOG4105Z85	coenzyme PQQ synthesis
FCN51_10315	ENOG41086XE	Ring cyclization and eight-electron oxidation of 3a-(2- amino-2-carboxyethyl)-4,5-dioxo-4,5,6,7,8,9-hexahydroquinoline- 7,9-dicarboxylic-acid to PQQ (By similarity)
FCN51_10320	ENOG4105JIE	May be involved in the transport of PQQ or its precursor to the periplasm (By similarity)
FCN51_10345	ENOG4105CGK	Exodeoxyribonuclease III
FCN51_10350	ENOG4108YX9	iron--sulfur cluster insertion protein erpA
FCN51_10355	ENOG4105C4Q	deoxyguanosinetriphosphate triphosphohydrolase-like protein
FCN51_10360	ENOG4105C75	arginyL-tRNA synthetase
FCN51_10370	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)
FCN51_10375	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)
FCN51_10380	ENOG41081BE	Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. Together with TatC, TatB is part of a receptor directly interacting with Tat signal peptides. TatB may form an oligomeric binding site that transiently accommodates folded Tat precursor proteins before their translocation (By similarity)
FCN51_10385	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)
FCN51_10390	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)
FCN51_10400	ENOG4105CSG	Required to facilitate the formation of correct disulfide bonds in some periplasmic proteins and for the assembly of the periplasmic c-type cytochromes. Acts by transferring electrons from cytoplasmic thioredoxin to the periplasm. This transfer involves a cascade of disulfide bond formation and reduction steps (By similarity)
FCN51_10590	ENOG4108N0N	Phage Terminase Large Subunit
FCN51_10680	ENOG41068WC	Domain of unknown function (DUF955)
FCN51_10825	ENOG4105DSW	Fusaric acid resistance protein
FCN51_10830	ENOG4107RSM	transcriptional regulator
FCN51_10905	ENOG4105CYX	Short-chain dehydrogenase reductase Sdr
FCN51_10920	ENOG4105CXW	Synthesizes alpha-1,4-glucan chains using ADP-glucose (By similarity)
FCN51_10925	ENOG4105C9C	Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position (By similarity)
FCN51_10930	ENOG4105C9C	Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position (By similarity)
FCN51_10965	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
FCN51_10985	ENOG4107R7A	Allophanate hydrolase subunit 2
FCN51_10990	ENOG4105E7W	lamb ycsf family protein
FCN51_11035	ENOG4105CC0	LysR family Transcriptional regulator
FCN51_11040	ENOG4105EUB	pirin domain protein
FCN51_11045	ENOG4108YYH	Nadph-dependent fmn reductase
FCN51_11055	ENOG4105F27	Major Facilitator
FCN51_11060	ENOG4105C26	Dehydrogenase
FCN51_11070	ENOG4105CEP	NADH dehydrogenase
FCN51_11075	ENOG4108WUH	Transcriptional regulator, TetR family
FCN51_11090	ENOG4105D18	nicotinate-nucleotide pyrophosphorylase
FCN51_11115	ENOG4105CXG	d-lactate dehydrogenase
FCN51_11145	ENOG4105VYE	Inhibits all the catalytic activities of DNA gyrase by preventing its interaction with DNA. Acts by binding directly to the C-terminal domain of GyrB, which probably disrupts DNA binding by the gyrase (By similarity)
FCN51_11155	ENOG4108Z03	MAF-like protein
FCN51_11160	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)
FCN51_11165	ENOG4105CEK	Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine (By similarity)
FCN51_11170	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)
FCN51_11175	ENOG4105C03	ribonuclease
FCN51_11180	ENOG4108KNB	n-acetylmuramoyl-l-alanine amidase
FCN51_11225	ENOG4105C48	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
FCN51_11230	ENOG4105CUV	Homoserine Kinase
FCN51_11235	ENOG4108UMW	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
FCN51_11250	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)
FCN51_11270	ENOG4105C22	threonyL-tRNA synthetase
FCN51_11275	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)
FCN51_11285	ENOG41062D9	Histidine kinase
FCN51_11290	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FCN51_11300	ENOG4105C5H	ABC transporter
FCN51_11305	ENOG4108UGX	Major role in the synthesis of nucleoside triphosphates other than ATP. The ATP gamma phosphate is transferred to the NDP beta phosphate via a ping-pong mechanism, using a phosphorylated active-site intermediate (By similarity)
FCN51_11310	ENOG4105EPH	radical SAM domain protein
FCN51_11335	ENOG4106F3G	Catalyzes the tRNA-independent activation of glutamate in presence of ATP and the subsequent transfer of glutamate onto a tRNA(Asp). Glutamate is transferred on the 2-amino-5-(4,5- dihydroxy-2-cyclopenten-1-yl) moiety of the queuosine in the wobble position of the QUC anticodon (By similarity)
FCN51_11360	ENOG4105M4H	endoribonuclease L-psp
FCN51_11365	ENOG4107R03	Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate (By similarity)
FCN51_11375	ENOG4105CRQ	synthase (Component I)
FCN51_11400	ENOG4105CE9	30S ribosomal protein S2
FCN51_11405	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)
FCN51_11410	ENOG4107UIS	Involved in DNA repair and RecF pathway recombination (By similarity)
FCN51_11415	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)
FCN51_11420	ENOG4105DWA	May conjugate Arg from its aminoacyl-tRNA to the N- termini of proteins containing an N-terminal aspartate or glutamate
FCN51_11425	ENOG4105D52	delta-aminolevulinic acid dehydratase
FCN51_11430	ENOG4105CUB	amino acid
FCN51_11435	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)
FCN51_11440	ENOG4108Q6X	Aspartoacylase (EC 3.5.1.15)
FCN51_11455	ENOG4105C1J	atp-dependent rna helicase
FCN51_11470	ENOG4105EAC	phosphoserine phosphatase
FCN51_11475	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)
FCN51_11480	ENOG4105C7K	acetolactate synthase
FCN51_11485	ENOG4108ZP8	Acetolactate synthase small subunit
FCN51_11490	ENOG4105C6M	Alpha-keto-beta-hydroxylacyl reductoisomerase
FCN51_11500	ENOG4105E3B	Multicopper oxidase
FCN51_11510	ENOG4105C59	p-type ATPase
FCN51_11520	ENOG4108RWI	nicotinamidase
FCN51_11525	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)
FCN51_11540	ENOG4105C7V	phospho-2-dehydro-3-deoxyheptonate aldolase
FCN51_11560	ENOG4105CF9	Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation dephosphorylation (By similarity)
FCN51_11565	ENOG4108HRN	Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate (By similarity)
FCN51_11570	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)
FCN51_11575	ENOG4105C4F	May be involved in recombinational repair of damaged DNA (By similarity)
FCN51_11580	ENOG4106SNF	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane
FCN51_11585	ENOG4105C7C	involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
FCN51_11595	ENOG4105CIT	This protein may be involved in anomalous filament growth. May be a component of the septum (By similarity)
FCN51_11600	ENOG4108UFP	Essential cell division protein (By similarity)
FCN51_11605	ENOG4105CPF	Cell wall formation (By similarity)
FCN51_11610	ENOG4105D4A	Cell wall formation (By similarity)
FCN51_11615	ENOG4105DFU	Cell wall formation (By similarity)
FCN51_11630	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
FCN51_11635	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
FCN51_11645	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)
FCN51_11660	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
FCN51_11665	ENOG4107YUR	Cell division protein mraZ
FCN51_11685	ENOG4105D8W	glucose-6-phosphate 1-dehydrogenase
FCN51_11690	ENOG4105Y2X	UPF0335 protein
FCN51_11700	ENOG4105CGT	Catalyzes the transfer of a phosphate group to glutamate to form glutamate 5-phosphate which rapidly cyclizes to 5- oxoproline (By similarity)
FCN51_11705	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
FCN51_11710	ENOG4105K46	50S ribosomal protein l27
FCN51_11715	ENOG4105KK9	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
FCN51_11795	ENOG4105F6A	helicase
FCN51_11800	ENOG4105D85	methylase
FCN51_11805	ENOG4105DFP	Integrase
FCN51_11855	ENOG4108R5F	Component of the ubiquinol-cytochrome c reductase complex (complex III or cytochrome b-c1 complex), which is a respiratory chain that generates an electrochemical potential coupled to ATP synthesis (By similarity)
FCN51_11860	ENOG4105DJ5	Component of the ubiquinol-cytochrome c reductase complex (complex III or cytochrome b-c1 complex), which is a respiratory chain that generates an electrochemical potential coupled to ATP synthesis (By similarity)
FCN51_11865	ENOG4105DJ5	Component of the ubiquinol-cytochrome c reductase complex (complex III or cytochrome b-c1 complex), which is a respiratory chain that generates an electrochemical potential coupled to ATP synthesis (By similarity)
FCN51_11875	ENOG4108R6K	riboflavin synthase, subunit alpha
FCN51_11880	ENOG4105C66	Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate (By similarity)
FCN51_11885	ENOG4108UTT	Catalyzes the formation of 6,7-dimethyl-8- ribityllumazine by condensation of 5-amino-6-(D- ribitylamino)uracil with 3,4-dihydroxy-2-butanone 4-phosphate. This is the penultimate step in the biosynthesis of riboflavin (By similarity)
FCN51_11915	ENOG4105Y49	secretion protein, HlyD family
FCN51_11945	ENOG4108RIR	Molybdenum cofactor biosynthesis protein
FCN51_11955	ENOG4105EUJ	GTP cyclohydrolase i
FCN51_11960	ENOG4105NWN	ApaG protein
FCN51_11975	ENOG4105M6F	mutator MutT protein
FCN51_11990	ENOG4105VIE	preprotein translocase, subunit YajC
FCN51_11995	ENOG4105C25	Primosomal protein n'
FCN51_12000	ENOG4108IYT	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
FCN51_12020	ENOG4105BZU	Histidine kinase
FCN51_12060	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
FCN51_12065	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
FCN51_12080	ENOG4105DVT	helicase
FCN51_12085	ENOG4105ECY	inositol monophosphatase
FCN51_12090	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)
FCN51_12110	ENOG4105D7W	serine acetyltransferase
FCN51_12115	ENOG4108YZA	Nitrogen regulatory protein pii
FCN51_12120	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
FCN51_12135	ENOG4105CZ5	Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate (By similarity)
FCN51_12145	ENOG4105DYA	Acts on guanine, xanthine and to a lesser extent hypoxanthine (By similarity)
FCN51_12190	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)
FCN51_12215	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
FCN51_12220	ENOG4105KW8	RNA chaperone that binds small regulatory RNA (sRNAs) and mRNAs to facilitate mRNA translational regulation in response to envelope stress, environmental stress and changes in metabolite concentrations. Also binds with high specificity to tRNAs (By similarity)
FCN51_12225	ENOG4105C1N	GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis (By similarity)
FCN51_12240	ENOG4105CK4	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
FCN51_12265	ENOG4105CHH	sulfate transporter
FCN51_12270	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)
FCN51_12275	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
FCN51_12280	ENOG4106XY2	Folate-binding protein involved in regulating the level of ATP-DnaA and in the modification of some tRNAs. It is probably a key factor in regulatory networks that act via tRNA modification, such as initiation of chromosomal replication (By similarity)
FCN51_12285	ENOG4105CAQ	asparagine synthetase
FCN51_12290	ENOG4107TYR	Glycosyl Transferase
FCN51_12310	ENOG4105CNE	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane (By similarity)
FCN51_12315	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
FCN51_12325	ENOG4105D1K	glutamate--cysteine ligase
FCN51_12345	ENOG4105D1H	recombination factor protein RarA
FCN51_12350	ENOG4105EI2	Pseudouridine synthase
FCN51_12375	ENOG4105K5M	30s ribosomal protein S16
FCN51_12380	ENOG4108ZR6	An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Probably interacts with S19. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes (By similarity)
FCN51_12385	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
FCN51_12390	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)
FCN51_12395	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
FCN51_12400	ENOG4105MQS	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
FCN51_12405	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)
FCN51_12410	ENOG4105K5G	30S ribosomal protein S21
FCN51_12415	ENOG4108RBJ	Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions (By similarity)
FCN51_12425	ENOG41090HR	transcriptional regulator
FCN51_12430	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
FCN51_12435	ENOG4105E0F	Histidine kinase
FCN51_12450	ENOG41082R8	50S ribosomal protein l32
FCN51_12455	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)
FCN51_12460	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)
FCN51_12465	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)
FCN51_12470	ENOG4105WJX	transcriptional regulator MERR family
FCN51_12485	ENOG4105CJR	Integral membrane protein (MviN
FCN51_12495	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)
FCN51_12505	ENOG4108PZW	LysR family Transcriptional regulator
FCN51_12510	ENOG4105C3M	thioredoxin reductase
FCN51_12515	ENOG4105F7P	transcriptional regulator AsnC family
FCN51_12535	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)
FCN51_12540	ENOG4105BZ9	Cytochrome C oxidase, subunit I
FCN51_12545	ENOG4105F1R	Converts heme B (protoheme IX) to heme O by substitution of the vinyl group on carbon 2 of heme B porphyrin ring with a hydroxyethyl farnesyl side group (By similarity)
FCN51_12560	ENOG4105CMS	peptidase U62, modulator of DNA gyrase
FCN51_12565	ENOG4105C1V	Peptidase, M16
FCN51_12570	ENOG4105D98	threonine synthase
FCN51_12580	ENOG4105CTD	carboxy-peptidase
FCN51_12590	ENOG4105D86	that it carries out the mismatch recognition step. This protein has a weak ATPase activity (By similarity)
FCN51_12595	ENOG4105E1P	Modifies, by uridylylation or deuridylylation the PII (GlnB) regulatory protein (By similarity)
FCN51_12605	ENOG4108JJ7	ABC transporter
FCN51_12615	ENOG4105KDC	50s ribosomal protein l28
FCN51_12625	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)
FCN51_12635	ENOG4105CCA	Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle (By similarity)
FCN51_12640	ENOG4106BRA	Membrane
FCN51_12660	ENOG4105JRK	feS assembly protein SufD
FCN51_12665	ENOG4105C9B	Cysteine desulfurase
FCN51_12675	ENOG4105VG1	fes assembly suf system protein
FCN51_12680	ENOG4108YX9	iron--sulfur cluster insertion protein erpA
FCN51_12685	ENOG4107QS4	23S rRNA
FCN51_12690	ENOG4105C1J	atp-dependent rna helicase
FCN51_12700	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)
FCN51_12710	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
FCN51_12715	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)
FCN51_12720	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)
FCN51_12725	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)
FCN51_12730	ENOG4105K70	DNA-binding protein
FCN51_12750	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)
FCN51_12755	ENOG4105CYU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
FCN51_12760	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)
FCN51_12765	ENOG4105GKE	subunit e
FCN51_12770	ENOG4107QIZ	NADH dehydrogenase
FCN51_12780	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)
FCN51_12785	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)
FCN51_12790	ENOG4105DF2	NADH dehydrogenase subunit j
FCN51_12795	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)
FCN51_12800	ENOG4105D65	subunit l
FCN51_12805	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)
FCN51_12810	ENOG4105HJX	Biotin- acetyl-CoA-carboxylase ligase
FCN51_12815	ENOG4107QNB	Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis (By similarity)
FCN51_12825	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)
FCN51_12835	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)
FCN51_12855	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
FCN51_12860	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)
FCN51_12865	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)
FCN51_12890	ENOG41070EG	Hydrolyzes cAMP to 5'-AMP. Plays an important regulatory role in modulating the intracellular concentration of cAMP, thereby influencing cAMP-dependent processes (By similarity)
FCN51_12905	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)
FCN51_12915	ENOG4107RCI	amp-dependent synthetase and ligase
FCN51_13005	ENOG4108MIW	Induces the synthesis of acid phosphatase (AppA) and several other polypeptides (such as AppBC) during the deceleration phase of growth. It also acts as a transcriptional repressor for one group of proteins that are synthesized preferentially in exponential growth and for one group synthesized only in the stationary phase. Also involved in the stabilization of the sigma stress factor RpoS during stress conditions
FCN51_13030	ENOG4107SVC	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
FCN51_13040	ENOG41061A5	transposase
FCN51_13050	ENOG4105E5H	Transposase
FCN51_13075	ENOG4108HWB	Non-specific O-methyltransferase that catalyzes the 2 O- methylation steps in the ubiquinone biosynthetic pathway (By similarity)
FCN51_13120	ENOG4105ETX	regulatoR
FCN51_13125	ENOG4105DHQ	Histidine kinase
FCN51_13160	ENOG4108VN5	Inherit from COG: PepSY-associated TM helix
FCN51_13200	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
FCN51_13215	ENOG4105CHR	reductase
FCN51_13225	ENOG4105F6U	Short-chain dehydrogenase reductase Sdr
FCN51_13240	ENOG4105CFN	oxalyl-CoA decarboxylase
FCN51_13260	ENOG4108302	MgtC SapB transporter
FCN51_13270	ENOG4108Z9Z	response to DNA damage stimulus
FCN51_13280	ENOG4105DQ4	alcohol dehydrogenase
FCN51_13285	ENOG4105CHI	Involved in the active translocation of vitamin B12 (cyanocobalamin) across the outer membrane to the periplasmic space. It derives its energy for transport by interacting with the trans-periplasmic membrane protein TonB (By similarity)
FCN51_13295	ENOG4105DDW	LysR family Transcriptional regulator
FCN51_13300	ENOG4105C5H	ABC transporter
FCN51_13320	ENOG4108HWB	Non-specific O-methyltransferase that catalyzes the 2 O- methylation steps in the ubiquinone biosynthetic pathway (By similarity)
FCN51_13335	ENOG4105CEB	Aspartate aminotransferase
FCN51_13340	ENOG4105HDK	L-asparaginase
FCN51_13355	ENOG4108ESX	Receptor
FCN51_13360	ENOG4107E2E	PKHD-type hydroxylase
FCN51_13370	ENOG4108JJ9	ABC, transporter
FCN51_13375	ENOG4108JJ8	(ABC) transporter
FCN51_13380	ENOG4105C4M	(Ubiquinol oxidase) subunit I
FCN51_13385	ENOG4105CFY	cytochrome d ubiquinol oxidase, subunit ii
FCN51_13400	ENOG4105D64	Mechanosensitive ion channel
FCN51_13425	ENOG4108MI0	Resistance protein
FCN51_13430	ENOG4105J12	Multidrug resistance protein mdtN
FCN51_13445	ENOG4105NTW	Transcriptional regulator
FCN51_13460	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
FCN51_13505	ENOG4105EA8	2-Nitropropane dioxygenase
FCN51_13510	ENOG4108JQ7	(ABC) transporter
FCN51_13565	ENOG4105MZG	transcriptional modulator of maze toxin, mazf
FCN51_13570	ENOG4106A2Z	transcriptional regulator antitoxin, MazE
FCN51_13600	ENOG4105C4M	(Ubiquinol oxidase) subunit I
FCN51_13605	ENOG4105CFY	cytochrome d ubiquinol oxidase, subunit ii
FCN51_13670	ENOG4105C9Y	Catalyzes the hydrolysis of N-succinyl-L,L- diaminopimelic acid (SDAP), forming succinate and LL-2,6- diaminoheptanedioate (DAP), an intermediate involved in the bacterial biosynthesis of lysine and meso-diaminopimelic acid, an essential component of bacterial cell walls (By similarity)
FCN51_13680	ENOG4105ETS	cytosine purines uracil thiamine allantoin
FCN51_13690	ENOG4105C26	Dehydrogenase
FCN51_13695	ENOG4105H3G	oxidoreductase
FCN51_13715	ENOG4107QZF	nitrite reductase NADPH large subunit
FCN51_13735	ENOG4105DHQ	Histidine kinase
FCN51_13740	ENOG4105ETX	regulatoR
FCN51_13785	ENOG4105M0J	Toxic component of a toxin-antitoxin (TA) module. A
FCN51_13790	ENOG4105XMH	SpoVT AbrB domain protein
FCN51_13830	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
FCN51_13840	ENOG4105K4U	addiction module toxin, RelE StbE family
FCN51_13845	ENOG4105EEQ	Na H antiporter
FCN51_13855	ENOG41061A5	transposase
FCN51_13865	ENOG4105E5H	Transposase
FCN51_13895	ENOG4105K78	MarR family Transcriptional regulator
FCN51_13950	ENOG4108WUH	Transcriptional regulator, TetR family
FCN51_13955	ENOG4108I6A	alcohol dehydrogenase
FCN51_13960	ENOG4105C26	Dehydrogenase
FCN51_13985	ENOG41060A7	DNA polymerase beta domain protein region
FCN51_13995	ENOG4105CVR	type I restriction-modification system
FCN51_14020	ENOG4105H3G	oxidoreductase
FCN51_14025	ENOG4105W2W	Cytotoxic translational repressor of toxin-antitoxin stability system
FCN51_14040	ENOG4105DZ2	Transcriptional regulator
FCN51_14045	ENOG4105DSS	Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation (By similarity)
FCN51_14050	ENOG4105EQR	Transposase IS116 IS110 IS902
FCN51_14080	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)
FCN51_14115	ENOG4105CCI	Myosin-Cross-Reactive Antigen
FCN51_14125	ENOG4105K4U	addiction module toxin, RelE StbE family
FCN51_14170	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)
FCN51_14175	ENOG4105H3G	oxidoreductase
FCN51_14185	ENOG4108TJN	glycosyl transferase group 1
FCN51_14215	ENOG4107SQD	Transcriptional regulator, GntR family
FCN51_14225	ENOG4106NZI	LysR family Transcriptional regulator
FCN51_14320	ENOG4105K78	MarR family Transcriptional regulator