locus-tag	class	description
Anamo_0001	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)
Anamo_0002	ENOG4105CZ8	DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity. The beta chain is required for initiation of replication once it is clamped onto DNA, it slides freely (bidirectional and ATP- independent) along duplex DNA (By similarity)
Anamo_0003	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)
Anamo_0004	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)
Anamo_0007	ENOG4108YZ8	Superoxide reductase
Anamo_0009	ENOG4105BZU	Histidine kinase
Anamo_0010	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
Anamo_0011	ENOG4108UTW	Plays a role in the regulation of phosphate uptake
Anamo_0012	ENOG4105BZY	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
Anamo_0013	ENOG4105E2Z	phosphate ABC transporter (Permease
Anamo_0014	ENOG4105C8U	phosphate abc transporter
Anamo_0015	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)
Anamo_0016	ENOG4108K0D	peptidase, M48
Anamo_0017	ENOG41074CX	linocin_m18 bacteriocin protein
Anamo_0019	ENOG4107Y9U	Membrane
Anamo_0020	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)
Anamo_0021	ENOG4108RTV	Catalyzes the transfer of acetyl from acetyl-CoA to desacetylmycothiol (Cys-GlcN-Ins) to form mycothiol (By similarity)
Anamo_0022	ENOG4107R4N	Cell wall formation (By similarity)
Anamo_0025	ENOG4107QIZ	NADH dehydrogenase
Anamo_0030	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)
Anamo_0031	ENOG4105C8Q	Methyl-accepting chemotaxis
Anamo_0033	ENOG4105C7B	Threonine dehydratase
Anamo_0034	ENOG4105EWC	Purine nucleoside phosphorylase
Anamo_0035	ENOG4108RCM	Nitroreductase
Anamo_0037	ENOG4105ERH	Fumarylacetoacetate hydrolase
Anamo_0039	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)
Anamo_0041	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
Anamo_0042	ENOG4107R2I	The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination. The AddA nuclease domain is required for chi fragment generation
Anamo_0045	ENOG4105EAM	Na Pi-cotransporter
Anamo_0046	ENOG4108UTW	Plays a role in the regulation of phosphate uptake
Anamo_0047	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)
Anamo_0048	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
Anamo_0049	ENOG4108IPJ	Membrane
Anamo_0050	ENOG4108RAC	Rubrerythrin
Anamo_0052	ENOG4108JQ7	(ABC) transporter
Anamo_0053	ENOG4105C3U	ABC transporter
Anamo_0054	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
Anamo_0056	ENOG4105DEF	Extracellular solute-binding protein, family 5
Anamo_0057	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
Anamo_0058	ENOG4105CIZ	coA-substrate-specific enzyme activase
Anamo_0059	ENOG4108Z3G	3H domain protein
Anamo_0062	ENOG4105II7	pyrroline-5-carboxylate reductase
Anamo_0063	ENOG4105VSY	K01512 acylphosphatase EC 3.6.1.7
Anamo_0064	ENOG4105CSF	NADPH-dependent glycerol-3-phosphate dehydrogenase
Anamo_0065	ENOG4108R3D	Electron transport complex
Anamo_0066	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
Anamo_0071	ENOG4105DCG	PHP domain protein
Anamo_0073	ENOG410902H	NADH dehydrogenase (Ubiquinone), 24 kDa subunit
Anamo_0074	ENOG4107QIZ	NADH dehydrogenase
Anamo_0076	ENOG4105QAX	Iron-sulfur
Anamo_0077	ENOG4105WE2	aldehyde ferredoxin oxidoreductase
Anamo_0078	ENOG41076HS	cation diffusion facilitator family transporter
Anamo_0081	ENOG4105BZU	Histidine kinase
Anamo_0084	ENOG4108IV0	ABC, transporter
Anamo_0085	ENOG4105C0Z	ABC transporter
Anamo_0087	ENOG4105C32	Amino acid ABC transporter (Permease)
Anamo_0088	ENOG4105CP9	extracellular ligand-binding receptor
Anamo_0089	ENOG4108RMU	ferritin dps family protein
Anamo_0090	ENOG4108HRN	Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate (By similarity)
Anamo_0092	ENOG4108Z5K	methylglyoxal synthase
Anamo_0093	ENOG4107R4J	Chloride channel
Anamo_0094	ENOG4105CU5	Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine (By similarity)
Anamo_0095	ENOG4105WE2	aldehyde ferredoxin oxidoreductase
Anamo_0100	ENOG4105DR5	peptidase
Anamo_0101	ENOG4105D8C	Channel that permits osmotically driven movement of water in both directions. It is involved in the osmoregulation and in the maintenance of cell turgor during volume expansion in rapidly growing cells. It mediates rapid entry or exit of water in response to abrupt changes in osmolarity (By similarity)
Anamo_0106	ENOG4105EQN	UPF0261 protein
Anamo_0107	ENOG4107W7X	Aldolase
Anamo_0108	ENOG4105C2F	Histidine kinase
Anamo_0109	ENOG4105WH1	Two component transcriptional regulator luxr family
Anamo_0110	ENOG4105M3W	utilization protein
Anamo_0111	ENOG4106S4J	ethanolamine utilization protein EutP
Anamo_0112	ENOG4105KNY	Microcompartments protein
Anamo_0113	ENOG4105EHR	propanediol utilization protein pduB
Anamo_0115	ENOG4105YCI	dehydratase medium subunit
Anamo_0116	ENOG4108ZFT	Dehydratase small subunit
Anamo_0117	ENOG41084PW	diol glycerol dehydratase reactivating factor large subunit
Anamo_0119	ENOG4105KNY	Microcompartments protein
Anamo_0120	ENOG4105KNY	Microcompartments protein
Anamo_0121	ENOG4108VPX	Involved in 1,2-propanediol (1,2-PD) degradation by catalyzing the conversion of propanoyl-CoA to propanoyl-phosphate (By similarity)
Anamo_0122	ENOG4107RWI	ethanolamine utilization protein eutJ
Anamo_0126	ENOG4108WBT	adenosyltransferase
Anamo_0127	ENOG4108EKI	Dehydrogenase
Anamo_0128	ENOG4107QTR	Required for nitrogen fixation. May be part of a membrane complex functioning as an intermediate in the electron transport to nitrogenase (By similarity)
Anamo_0129	ENOG4108WT6	Carbon dioxide concentrating mechanism protein
Anamo_0130	ENOG4105DCT	glycerol dehydrogenase
Anamo_0132	ENOG4108UIC	UPF0340 protein
Anamo_0134	ENOG4107QK8	The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor
Anamo_0135	ENOG4107RGW	The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor
Anamo_0136	ENOG4105I3K	Ferric uptake regulator, Fur family
Anamo_0137	ENOG4105CJ1	ABC, transporter
Anamo_0143	ENOG4105EHG	Permease protein
Anamo_0144	ENOG4105E0A	ABC, transporter
Anamo_0147	ENOG4105D1F	ATP-binding protein
Anamo_0148	ENOG4108ZP8	Acetolactate synthase small subunit
Anamo_0149	ENOG4105C6M	Alpha-keto-beta-hydroxylacyl reductoisomerase
Anamo_0150	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)
Anamo_0151	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)
Anamo_0152	ENOG4105C7K	acetolactate synthase
Anamo_0157	ENOG4105K95	(LipO)protein
Anamo_0158	ENOG4108IJ8	ABC transporter
Anamo_0159	ENOG4105E90	ABC transporter
Anamo_0161	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)
Anamo_0163	ENOG4105EJQ	L-serine dehydratase
Anamo_0164	ENOG4107U53	septum site-determining protein minD
Anamo_0165	ENOG4105C8Q	Methyl-accepting chemotaxis
Anamo_0167	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)
Anamo_0168	ENOG41071I4	Phosphatidylserine decarboxylase proenzyme
Anamo_0169	ENOG4106PT6	cdpdiacylglycerol-serine O-phosphatidyltransferase
Anamo_0170	ENOG4105CK2	sodium dicarboxylate symporter
Anamo_0172	ENOG4109015	Biopolymer transport protein exbD tolR
Anamo_0173	ENOG4105JKQ	Part of the ABC transporter complex BtuCDF involved in vitamin B12 import. Binds vitamin B12 and delivers it to the periplasmic surface of BtuC (By similarity)
Anamo_0177	ENOG4105Y36	Binding-protein-dependent transport systems, inner membrane component
Anamo_0178	ENOG4105D7T	ABC transporter
Anamo_0179	ENOG4108IJ6	ABC transporter
Anamo_0180	ENOG4105E0C	molybdate abc transporter
Anamo_0194	ENOG4105CHR	reductase
Anamo_0195	ENOG4105D78	K07001 NTE family protein
Anamo_0198	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
Anamo_0199	ENOG4105WDJ	50S ribosomal protein L33
Anamo_0201	ENOG41062BN	Preprotein translocase SecE subunit
Anamo_0202	ENOG4105E5V	Participates in transcription elongation, termination and antitermination (By similarity)
Anamo_0203	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
Anamo_0204	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)
Anamo_0205	ENOG4108VZM	50s ribosomal protein L10
Anamo_0206	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)
Anamo_0207	ENOG4105Y7X	Selectively cleaves double-stranded DNA at the second phosphodiester bond 3' to a deoxyinosine leaving behind the intact lesion on the nicked DNA. Acts in DNA repair (By similarity)
Anamo_0208	ENOG4105DHP	deoxycytidine triphosphate deaminase
Anamo_0210	ENOG4105C3R	Methionine synthase
Anamo_0211	ENOG4105SYT	Methylenetetrahydrofolate reductase
Anamo_0214	ENOG4105DWV	Homoserine O-trans-acetylase
Anamo_0221	ENOG4108UMW	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
Anamo_0223	ENOG4105CW7	secretion protein, HlyD family
Anamo_0224	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
Anamo_0225	ENOG4105IQJ	Involved in biosynthesis of the thiamine precursor thiazole (By similarity)
Anamo_0228	ENOG4105DI2	Pyruvate flavodoxin ferredoxin oxidoreductase domain protein
Anamo_0229	ENOG4105DQU	oxidoreductase, subunit beta
Anamo_0232	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)
Anamo_0233	ENOG4108Z0Z	intracellular protease Pfpi family
Anamo_0236	ENOG4105DKQ	ROK family
Anamo_0245	ENOG4105C9W	Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity (By similarity)
Anamo_0246	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
Anamo_0248	ENOG4105VM1	flagellar
Anamo_0249	ENOG41080R2	UPF0102 protein
Anamo_0250	ENOG4105C0P	Mg chelatase subunit ChlI
Anamo_0252	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)
Anamo_0253	ENOG4108FW6	Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs (By similarity)
Anamo_0254	ENOG4108IYS	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
Anamo_0255	ENOG4108R5P	Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery (By similarity)
Anamo_0256	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)
Anamo_0258	ENOG4105Q75	Structural component of flagellum, the bacterial motility apparatus. Part of the rod structure of flagellar basal body (By similarity)
Anamo_0259	ENOG4108ZC9	flagellar basal-body rod protein flgc
Anamo_0260	ENOG4105VQ0	flagellar hook-basal body complex protein fliE
Anamo_0261	ENOG4105C1F	The M ring may be actively involved in energy transduction (By similarity)
Anamo_0262	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)
Anamo_0266	ENOG4105E4C	Lytic transglycosylase catalytic
Anamo_0270	ENOG4105BZE	flagellar hook protein, FlgE
Anamo_0272	ENOG4105E14	MotA TolQ exbB proton channel
Anamo_0273	ENOG4106VK6	Flagellar motor protein
Anamo_0275	ENOG4105D24	FliM is one of three proteins (FliG, FliN, FliM) that forms the rotor-mounted switch complex (C ring), located at the base of the basal body. This complex interacts with the CheY and CheZ chemotaxis proteins, in addition to contacting components of the motor that determine the direction of flagellar rotation (By similarity)
Anamo_0276	ENOG4105DD5	Flagellar motor switch protein
Anamo_0277	ENOG4107YTP	response regulator receiver protein
Anamo_0279	ENOG4105CN7	Flagellar biosynthetic protein FliP
Anamo_0280	ENOG4105VS8	Flagellar biosynthetic protein fliq
Anamo_0281	ENOG4105D19	Role in flagellar biosynthesis (By similarity)
Anamo_0282	ENOG4105D00	flagellar biosynthetic protein flhB
Anamo_0283	ENOG4105D7B	Flagellar biosynthesis protein flha
Anamo_0284	ENOG4105FZW	flagellar biosynthesis regulator FlhF
Anamo_0287	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
Anamo_0288	ENOG4105CBS	Chea signal transduction histidine kinase
Anamo_0289	ENOG4107PHP	CheC --inhibitor of MCP methylation
Anamo_0290	ENOG4108Z4W	Probably deamidates glutamine residues to glutamate on methyl-accepting chemotaxis receptors (MCPs), playing an important role in chemotaxis (By similarity)
Anamo_0292	ENOG4105DN4	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
Anamo_0297	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
Anamo_0300	ENOG4105CH7	arginosuccinase
Anamo_0304	ENOG4105W5T	Binds to the C-terminal region of flagellin, which is implicated in polymerization, and participates in the assembly of the flagellum (By similarity)
Anamo_0305	ENOG410862U	Carbon storage regulator
Anamo_0306	ENOG4105CVJ	phosphoglycerate mutase
Anamo_0307	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
Anamo_0309	ENOG4105E1Z	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane
Anamo_0311	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)
Anamo_0312	ENOG4105C7C	involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
Anamo_0313	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)
Anamo_0314	ENOG4105DAF	Involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
Anamo_0315	ENOG4108Z4R	3-deoxy-d-manno-octulosonate 8-phosphate phosphatase
Anamo_0317	ENOG4105GYT	Protein of unknown function (DUF1009)
Anamo_0318	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)
Anamo_0320	ENOG4105BZ1	(ABC) transporter
Anamo_0321	ENOG4105EAM	Na Pi-cotransporter
Anamo_0322	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)
Anamo_0323	ENOG4105CET	Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria (By similarity)
Anamo_0324	ENOG4105CXR	Phospho-2-dehydro-3-deoxyoctonate aldolase
Anamo_0325	ENOG4105C2X	Arabinose 5-phosphate isomerase
Anamo_0326	ENOG4105D8A	3-Deoxy-D-manno-octulosonic-acid transferase
Anamo_0327	ENOG4105C0A	alcohol dehydrogenase
Anamo_0328	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
Anamo_0331	ENOG4105D22	carbon starvation protein
Anamo_0333	ENOG4105D0U	Arsenite-activated ATPase (ArsA)
Anamo_0335	ENOG4108UQV	Membrane
Anamo_0336	ENOG4107R91	Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position (By similarity)
Anamo_0339	ENOG4105K8U	2-Amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase
Anamo_0342	ENOG4105CI8	Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons (By similarity)
Anamo_0343	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
Anamo_0344	ENOG4105CFG	Acts as a chaperone (By similarity)
Anamo_0345	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)
Anamo_0348	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)
Anamo_0349	ENOG4108JVH	Protein of unknown function DUF43
Anamo_0350	ENOG4105CFG	Acts as a chaperone (By similarity)
Anamo_0351	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)
Anamo_0352	ENOG4107YU2	histidine triad (hIT) protein
Anamo_0354	ENOG4108Z11	Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes (By similarity)
Anamo_0357	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)
Anamo_0359	ENOG4105C32	Amino acid ABC transporter (Permease)
Anamo_0360	ENOG4105CF8	branched-chain amino acid ABC transporter, permease
Anamo_0361	ENOG4105C0Z	ABC transporter
Anamo_0362	ENOG4108IV0	ABC, transporter
Anamo_0363	ENOG4105BZQ	cdp-diacylglycerol-glycerol-3-phosphate 3-phosphatidyltransferase
Anamo_0364	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)
Anamo_0365	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
Anamo_0367	ENOG4105C75	arginyL-tRNA synthetase
Anamo_0370	ENOG410829C	Binds together with S18 to 16S ribosomal RNA (By similarity)
Anamo_0371	ENOG4107XMK	single-stranded DNA-binding protein
Anamo_0372	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)
Anamo_0374	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
Anamo_0375	ENOG4105CDU	Replicative dna helicase
Anamo_0376	ENOG4105I3N	Conserved Protein
Anamo_0377	ENOG4107ZIF	6-carboxy-5,6,7,8-tetrahydropterin synthase
Anamo_0378	ENOG4108JQ1	Dehydrogenase
Anamo_0380	ENOG4105BZH	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
Anamo_0382	ENOG4105DFA	alanine racemase domain protein
Anamo_0384	ENOG4105MMF	Cell division protein DIVIVA
Anamo_0386	ENOG4105C8J	)-transporter
Anamo_0387	ENOG4105C8J	)-transporter
Anamo_0389	ENOG4105E4Y	Endoribonuclease that initiates mRNA decay (By similarity)
Anamo_0390	ENOG4105D48	metallophosphoesterase
Anamo_0391	ENOG4105WRB	Hydrogenase assembly chaperone hypC hupF
Anamo_0393	ENOG4105C45	hydrogenase expression formation protein (HypE)
Anamo_0397	ENOG4105EZ5	reductase
Anamo_0398	ENOG4105Q1T	In the first step of glycine, betaine and sarcosine reductases, the substrate is bound to component PB via a Schiff base intermediate. Then the PB-activated substrate is nucleophilically attacked by the selenol anion of component PA to transform it to a carboxymethylated selenoether and the respective amine. By action of component PC, acetyl phosphate is formed, leaving component PA in its oxidized state. Finally component PA becomes reduced by the thioredoxin system to start a new catalytic cycle of reductive deamination
Anamo_0399	ENOG4105Q1T	In the first step of glycine, betaine and sarcosine reductases, the substrate is bound to component PB via a Schiff base intermediate. Then the PB-activated substrate is nucleophilically attacked by the selenol anion of component PA to transform it to a carboxymethylated selenoether and the respective amine. By action of component PC, acetyl phosphate is formed, leaving component PA in its oxidized state. Finally component PA becomes reduced by the thioredoxin system to start a new catalytic cycle of reductive deamination
Anamo_0403	ENOG4105BZG	amino acid carrier protein
Anamo_0404	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
Anamo_0406	ENOG4105C1J	atp-dependent rna helicase
Anamo_0408	ENOG4108HHA	Transketolase
Anamo_0409	ENOG41066UU	tRNA (Adenine-N1-)-methyltransferase
Anamo_0410	ENOG4105WPN	DNA integration recombination invertion protein
Anamo_0411	ENOG4105D4F	Synthesizes selenophosphate from selenide and ATP (By similarity)
Anamo_0412	ENOG4105VCQ	rubredoxin
Anamo_0413	ENOG4108IYI	Catalyzes the gamma-elimination of phosphate from L- phosphohomoserine and the beta-addition of water to produce L- threonine (By similarity)
Anamo_0414	ENOG4105D5I	Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate (By similarity)
Anamo_0415	ENOG4105CFH	Aspartokinase
Anamo_0416	ENOG4105CM3	Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate (By similarity)
Anamo_0418	ENOG4108IUZ	ABC transporter
Anamo_0420	ENOG4105CJR	Integral membrane protein (MviN
Anamo_0421	ENOG4105F4C	Redox regulated molecular chaperone. Protects both thermally unfolding and oxidatively damaged proteins from irreversible aggregation. Plays an important role in the bacterial defense system toward oxidative stress (By similarity)
Anamo_0423	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)
Anamo_0424	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
Anamo_0425	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
Anamo_0426	ENOG4105DTC	1-(5-phosphoribosyl)-5-amino-4-imidazole-carboxylate (air) carboxylase
Anamo_0427	ENOG4105C40	3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs (By similarity)
Anamo_0428	ENOG4105F4G	Membrane
Anamo_0430	ENOG4105EAY	pump that utilizes the energy of pyrophosphate hydrolysis as the driving force for
Anamo_0431	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)
Anamo_0432	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
Anamo_0434	ENOG41082I2	s4 domain protein
Anamo_0435	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
Anamo_0436	ENOG4105FF6	Modulates transcription in response to changes in cellular NADH NAD( ) redox state (By similarity)
Anamo_0438	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)
Anamo_0439	ENOG4108JIS	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)
Anamo_0441	ENOG4105CM1	Catalyzes, together with MoaC, the conversion of 5'-GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
Anamo_0443	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
Anamo_0445	ENOG4108YYA	Hydrolyzes D-tyrosyl-tRNA(Tyr) into D-tyrosine and free tRNA(Tyr). Could be a defense mechanism against a harmful effect of D-tyrosine (By similarity)
Anamo_0446	ENOG4108JMX	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
Anamo_0447	ENOG4105DFF	Rod shape-determining protein mreb
Anamo_0450	ENOG4105CJN	penicillin-binding protein
Anamo_0453	ENOG41083CN	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)
Anamo_0454	ENOG4105CNI	cell division protein FtsW
Anamo_0457	ENOG4105C03	ribonuclease
Anamo_0459	ENOG4107S47	Specifically methylates the adenine in position 37 of tRNA(1)(Val) (anticodon cmo5UAC) (By similarity)
Anamo_0460	ENOG4105CU0	Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA (By similarity)
Anamo_0461	ENOG4105CKH	Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation (By similarity)
Anamo_0462	ENOG4105F8V	Hydrolase, tatD family
Anamo_0463	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)
Anamo_0464	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)
Anamo_0466	ENOG4108IIJ	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
Anamo_0467	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
Anamo_0469	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)
Anamo_0470	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)
Anamo_0471	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)
Anamo_0472	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
Anamo_0473	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
Anamo_0474	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)
Anamo_0475	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)
Anamo_0476	ENOG4105KZR	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)
Anamo_0477	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
Anamo_0478	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
Anamo_0479	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)
Anamo_0480	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
Anamo_0481	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
Anamo_0482	ENOG41082SA	50s ribosomal protein l29
Anamo_0483	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
Anamo_0484	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
Anamo_0485	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
Anamo_0486	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
Anamo_0487	ENOG41082QR	Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site (By similarity)
Anamo_0488	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)
Anamo_0489	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)
Anamo_0490	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)
Anamo_0491	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)
Anamo_0492	ENOG4105VPB	50S ribosomal protein L30
Anamo_0493	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
Anamo_0494	ENOG4105CGG	The central subunit of the protein translocation channel SecYEG. Consists of two halves formed by TMs 1-5 and 6-10. These two domains form a lateral gate at the front which open onto the bilayer between TMs 2 and 7, and are clamped together by SecE at the back. The channel is closed by both a pore ring composed of hydrophobic SecY resides and a short helix (helix 2A) on the extracellular side of the membrane which forms a plug. The plug probably moves laterally to allow the channel to open. The ring and the pore may move independently (By similarity)
Anamo_0495	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)
Anamo_0498	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)
Anamo_0499	ENOG41067V7	50S ribosomal protein L36
Anamo_0500	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
Anamo_0501	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)
Anamo_0502	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)
Anamo_0503	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
Anamo_0504	ENOG4108ZT0	50S ribosomal protein l17
Anamo_0505	ENOG4108JJB	ABC transporter
Anamo_0506	ENOG4108JJB	ABC transporter
Anamo_0507	ENOG4105EK6	Transmembrane (T) component of an energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates (By similarity)
Anamo_0508	ENOG4105DI7	Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs (By similarity)
Anamo_0509	ENOG4105DFF	Rod shape-determining protein mreb
Anamo_0510	ENOG4105CGA	flagellar basal-body rod protein FlgG
Anamo_0511	ENOG4105CGA	flagellar basal-body rod protein FlgG
Anamo_0513	ENOG4107W7W	Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation (By similarity)
Anamo_0514	ENOG4105D92	Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation (By similarity)
Anamo_0518	ENOG4108R0D	protein with myosin-like
Anamo_0520	ENOG4108RTV	Catalyzes the transfer of acetyl from acetyl-CoA to desacetylmycothiol (Cys-GlcN-Ins) to form mycothiol (By similarity)
Anamo_0521	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
Anamo_0526	ENOG4105I03	Flagellin
Anamo_0532	ENOG4108HWB	Non-specific O-methyltransferase that catalyzes the 2 O- methylation steps in the ubiquinone biosynthetic pathway (By similarity)
Anamo_0533	ENOG4105C5E	polysaccharide biosynthesis protein
Anamo_0534	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
Anamo_0535	ENOG4107TY6	Acylneuraminate cytidylyltransferase
Anamo_0538	ENOG4105D2T	synthase
Anamo_0543	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)
Anamo_0544	ENOG4105D64	Mechanosensitive ion channel
Anamo_0546	ENOG4105C87	Aminotransferase class I and II
Anamo_0553	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
Anamo_0554	ENOG4108Z03	MAF-like protein
Anamo_0557	ENOG4108HHA	Transketolase
Anamo_0558	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)
Anamo_0559	ENOG4105CAK	Cell division ATP-binding protein ftsE
Anamo_0560	ENOG4107RYD	Part of the ABC transporter FtsEX involved in cellular division (By similarity)
Anamo_0561	ENOG4105DR5	peptidase
Anamo_0562	ENOG4105CN1	protease
Anamo_0564	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
Anamo_0568	ENOG4107TAE	Glycosyl transferase (Group 1
Anamo_0569	ENOG4105K64	Glycosyl transferase, family 2
Anamo_0570	ENOG4105XA0	heptosyltransferase ii
Anamo_0571	ENOG4105CPK	Glycosyl transferase (Group 1
Anamo_0572	ENOG4105ZU5	s-layer protein
Anamo_0574	ENOG4105CTQ	phosphohexokinase
Anamo_0584	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
Anamo_0585	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)
Anamo_0586	ENOG4105CJV	Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase
Anamo_0587	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)
Anamo_0588	ENOG4105ECC	imidazole-glycerol-phosphate dehydratase
Anamo_0589	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)
Anamo_0590	ENOG4108IQ6	Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine (By similarity)
Anamo_0591	ENOG4105DNJ	May play a role in the repair of endogenous alkylation damage (By similarity)
Anamo_0593	ENOG4107QX8	SPFH domain, Band 7 family protein
Anamo_0594	ENOG4105C8T	Leucyl-tRNA synthetase
Anamo_0596	ENOG410857I	Binds directly to 16S ribosomal RNA (By similarity)
Anamo_0598	ENOG41087VS	50S ribosomal protein l34
Anamo_0600	ENOG4105VAS	Could be involved in insertion of integral membrane proteins into the membrane (By similarity)
Anamo_0601	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
Anamo_0603	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
Anamo_0604	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
Anamo_0605	ENOG4108Z1K	This enzyme is involved in nucleotide metabolism it produces dUMP, the immediate precursor of thymidine nucleotides and it decreases the intracellular concentration of dUTP so that uracil cannot be incorporated into DNA (By similarity)
Anamo_0606	ENOG4105CZ1	Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA (By similarity)
Anamo_0608	ENOG4108ZEF	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate (By similarity)
Anamo_0609	ENOG4105CDE	UPF0348 protein
Anamo_0610	ENOG4105C6H	Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction (By similarity)
Anamo_0611	ENOG4108K9K	Uncharacterised protein family (UPF0236)
Anamo_0613	ENOG410855N	50S ribosomal protein L32
Anamo_0614	ENOG4108VVV	Transcriptional factor involved in regulation of membrane lipid biosynthesis by repressing genes involved in fatty acid and phospholipid metabolism (By similarity)
Anamo_0615	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)
Anamo_0616	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)
Anamo_0617	ENOG4105EA8	2-Nitropropane dioxygenase
Anamo_0618	ENOG4105CJF	Malonyl coA-acyl carrier protein transacylase
Anamo_0619	ENOG4105CHR	reductase
Anamo_0620	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
Anamo_0624	ENOG4105CXT	aspartate transcarbamylase
Anamo_0625	ENOG4105CD3	dihydroorotase
Anamo_0626	ENOG4105DF0	Responsible for channeling the electrons from the oxidation of dihydroorotate from the FMN redox center in the PyrD type B subunit to the ultimate electron acceptor NAD( ) (By similarity)
Anamo_0627	ENOG4107QYT	Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor (By similarity)
Anamo_0629	ENOG4107QV3	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)
Anamo_0632	ENOG4105HJX	Biotin- acetyl-CoA-carboxylase ligase
Anamo_0636	ENOG4105DHJ	ABC, transporter
Anamo_0638	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
Anamo_0641	ENOG4105MA4	psp1 domain protein
Anamo_0642	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)
Anamo_0645	ENOG4105C83	adenylosuccinate lyase
Anamo_0647	ENOG4105CKU	formyltetrahydrofolate synthetase
Anamo_0652	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
Anamo_0653	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)
Anamo_0654	ENOG4105C3M	thioredoxin reductase
Anamo_0656	ENOG4105CP4	Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth (By similarity)
Anamo_0657	ENOG4107WAU	Protein tyrosine phosphatase
Anamo_0660	ENOG4105D0M	Protease HtpX homolog
Anamo_0661	ENOG4105C6E	dna polymerase iii
Anamo_0662	ENOG4105C0B	DNA polymerase III (alpha subunit)
Anamo_0663	ENOG4105CA9	Pyruvate kinase
Anamo_0665	ENOG4105EFU	Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin (By similarity)
Anamo_0666	ENOG4106M28	alanine racemase domain protein
Anamo_0667	ENOG4105C8B	TIGR00159 family
Anamo_0669	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
Anamo_0670	ENOG4105C3Y	UTP-glucose-1-phosphate uridylyltransferase
Anamo_0672	ENOG4105N80	Ferric uptake regulator, Fur family
Anamo_0674	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)
Anamo_0675	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
Anamo_0676	ENOG4105KW6	This is one of the proteins that binds to the 5S RNA in the ribosome where it forms part of the central protuberance (By similarity)
Anamo_0677	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
Anamo_0678	ENOG4108JA2	transcriptioN-repair coupling factor
Anamo_0679	ENOG4105DXN	mazG family
Anamo_0680	ENOG4107QSA	Oxaloacetate decarboxylase
Anamo_0683	ENOG4105CTJ	Metal Dependent Phosphohydrolase
Anamo_0685	ENOG4108JU6	CBS domain protein
Anamo_0687	ENOG4108HMW	glycyl-tRNA synthetase, alpha subunit
Anamo_0688	ENOG4105C38	Glycyl-tRNA synthetase beta subunit
Anamo_0689	ENOG4105CF9	Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation dephosphorylation (By similarity)
Anamo_0690	ENOG4105C4Q	deoxyguanosinetriphosphate triphosphohydrolase-like protein
Anamo_0691	ENOG4108JQC	penicillin-binding protein 1A
Anamo_0693	ENOG4105CCX	Catalyzes the production of spermidine from putrescine and decarboxylated S-adenosylmethionine (dcSAM), which serves as an aminopropyl donor (By similarity)
Anamo_0694	ENOG4105CYW	agmatinase
Anamo_0695	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)
Anamo_0697	ENOG4105DBV	ornithine carbamoyltransferase
Anamo_0698	ENOG4105MRR	Transcriptional regulator (By similarity)
Anamo_0701	ENOG4107RA1	nh(3)-dependent nad( ) synthetase
Anamo_0702	ENOG4105CDY	transcriptional regulatory protein
Anamo_0704	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)
Anamo_0705	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)
Anamo_0707	ENOG4105JFG	SpoIID LytB domain protein
Anamo_0708	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)
Anamo_0709	ENOG4105NBF	ammecr1 domain protein
Anamo_0711	ENOG4105C84	Histidine ammonia-lyase
Anamo_0712	ENOG4105CCS	Glutamate formiminotransferase
Anamo_0713	ENOG4105CI2	imidazolone-5-propionate hydrolase
Anamo_0716	ENOG41082V8	Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein (By similarity)
Anamo_0717	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)
Anamo_0718	ENOG4105K8N	protein family UPF0079, ATPase
Anamo_0719	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)
Anamo_0721	ENOG4105DI2	Pyruvate flavodoxin ferredoxin oxidoreductase domain protein
Anamo_0722	ENOG4105DQU	oxidoreductase, subunit beta
Anamo_0724	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
Anamo_0726	ENOG4105VUF	Transcriptional regulator
Anamo_0732	ENOG41082EK	Restriction modification system DNA (Specificity
Anamo_0733	ENOG4105DZR	Type I site-specific deoxyribonuclease
Anamo_0736	ENOG4108UMN	azlc family
Anamo_0745	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)
Anamo_0748	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
Anamo_0749	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)
Anamo_0750	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)
Anamo_0751	ENOG4105CA4	amino acids such as threonine, to avoid such errors, it has a posttransfer editing activity that hydrolyzes mischarged Thr-tRNA(Val) in a tRNA-dependent manner (By similarity)
Anamo_0757	ENOG4105DJT	lAO AO transport system ATPase
Anamo_0758	ENOG4105CZ5	Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate (By similarity)
Anamo_0759	ENOG4105ESV	Glycosyl transferase, family 4
Anamo_0760	ENOG4105EAG	UDP-N-acetylglucosamine 2-epimerase
Anamo_0761	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
Anamo_0762	ENOG4105CIH	Imidazole acetol-phosphate transaminase
Anamo_0764	ENOG4108UN4	phage SPO1 DNA polymerase-related protein
Anamo_0765	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
Anamo_0766	ENOG4105KNE	Phosphatidate cytidylyltransferase
Anamo_0767	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)
Anamo_0769	ENOG4105C4E	Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate (By similarity)
Anamo_0770	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)
Anamo_0774	ENOG4105M7K	Involved in the transcription termination process (By similarity)
Anamo_0775	ENOG4105DVS	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
Anamo_0777	ENOG4105C3E	May play a key role in the regulation of the intracellular concentration of adenosylhomocysteine (By similarity)
Anamo_0778	ENOG4105D6T	Catalyzes the deamination of 5-methylthioadenosine and S-adenosyl-L-homocysteine into 5-methylthioinosine and S-inosyl-L- homocysteine, respectively. Is also able to deaminate adenosine (By similarity)
Anamo_0779	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)
Anamo_0780	ENOG4108Z08	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
Anamo_0781	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)
Anamo_0782	ENOG4105C48	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
Anamo_0783	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)
Anamo_0784	ENOG4108Z02	Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions (By similarity)
Anamo_0785	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)
Anamo_0787	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)
Anamo_0791	ENOG4108YZ4	nudix hydrolase
Anamo_0792	ENOG4108IYS	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
Anamo_0793	ENOG4105CZG	Phosphotransfer between the C1 and C5 carbon atoms of pentose (By similarity)
Anamo_0794	ENOG4105CB1	The purine nucleoside phosphorylases catalyze the phosphorolytic breakdown of the N-glycosidic bond in the beta- (deoxy)ribonucleoside molecules, with the formation of the corresponding free purine bases and pentose-1-phosphate (By similarity)
Anamo_0798	ENOG4105C8N	cysteinyl-tRNA synthetase
Anamo_0799	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)
Anamo_0800	ENOG4105D1W	Converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)- pyrimidinedione 5'-phosphate (By similarity)
Anamo_0801	ENOG4108R6K	riboflavin synthase, subunit alpha
Anamo_0802	ENOG4105C66	Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate (By similarity)
Anamo_0803	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)
Anamo_0804	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)
Anamo_0809	ENOG4105EBX	v-type atpase
Anamo_0814	ENOG4108JIQ	Produces ATP from ADP in the presence of a proton gradient across the membrane. The V-type alpha chain is a catalytic subunit (By similarity)
Anamo_0815	ENOG4108JIP	Produces ATP from ADP in the presence of a proton gradient across the membrane. The V-type beta chain is a regulatory subunit (By similarity)
Anamo_0817	ENOG410816I	Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection (By similarity)
Anamo_0818	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)
Anamo_0819	ENOG4105CTP	PilT protein domain protein
Anamo_0820	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)
Anamo_0822	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)
Anamo_0823	ENOG4105CP4	Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth (By similarity)
Anamo_0824	ENOG4105VEQ	Cold shock protein
Anamo_0826	ENOG41068B1	Cob-I-yrinic acid a,c-diamide adenosyltransferase
Anamo_0828	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
Anamo_0833	ENOG4105KGF	protein, YerC YecD
Anamo_0834	ENOG4105CIH	Imidazole acetol-phosphate transaminase
Anamo_0840	ENOG4108UGV	hypoxanthine phosphoribosyltransferase
Anamo_0841	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)
Anamo_0842	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)
Anamo_0843	ENOG4105C5U	The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrA is an ATPase and a DNA-binding protein. A damage recognition complex composed of 2 UvrA and 2 UvrB subunits scans DNA for abnormalities. When the presence of a lesion has been verified by UvrB, the UvrA molecules dissociate (By similarity)
Anamo_0846	ENOG4105D1U	peptidase U62 modulator of DNA gyrase
Anamo_0847	ENOG4105CNU	cell division protein FtsK
Anamo_0851	ENOG4105CTB	Polyprenyl synthetase
Anamo_0852	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)
Anamo_0853	ENOG4105DX0	Hemolysin A
Anamo_0854	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)
Anamo_0855	ENOG4105C4F	May be involved in recombinational repair of damaged DNA (By similarity)
Anamo_0856	ENOG4105KK9	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
Anamo_0858	ENOG4105K46	50S ribosomal protein l27
Anamo_0859	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
Anamo_0860	ENOG4108Z1W	Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) (By similarity)
Anamo_0861	ENOG4108KGH	TRANSCRIPTIONal
Anamo_0863	ENOG4105CP7	Triose-phosphate isomerase
Anamo_0864	ENOG4105BZA	Phosphoglycerate kinase
Anamo_0866	ENOG4105CIE	May be required for sporulation (By similarity)
Anamo_0867	ENOG4105CHW	UPF0052 protein
Anamo_0868	ENOG4105C21	Displays ATPase and GTPase activities (By similarity)
Anamo_0869	ENOG4108RIR	Molybdenum cofactor biosynthesis protein
Anamo_0870	ENOG4108YXW	Together with MoaA, is involved in the conversion of 5'- GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
Anamo_0871	ENOG4105CM1	Catalyzes, together with MoaC, the conversion of 5'-GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
Anamo_0872	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
Anamo_0873	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
Anamo_0875	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)
Anamo_0876	ENOG4105CDK	Essential cell division protein that forms a contractile ring structure (Z ring) at the future cell division site. The regulation of the ring assembly controls the timing and the location of cell division. One of the functions of the FtsZ ring is to recruit other cell division proteins to the septum to produce a new cell wall between the dividing cells. Binds GTP and shows GTPase activity (By similarity)
Anamo_0877	ENOG4105CIT	This protein may be involved in anomalous filament growth. May be a component of the septum (By similarity)
Anamo_0879	ENOG4105DFU	Cell wall formation (By similarity)
Anamo_0880	ENOG4105DVQ	Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II) (By similarity)
Anamo_0881	ENOG4105CNI	cell division protein FtsW
Anamo_0882	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
Anamo_0884	ENOG4107EES	Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide the precursor of murein (By similarity)
Anamo_0885	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)
Anamo_0886	ENOG4105CJN	penicillin-binding protein
Anamo_0888	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
Anamo_0889	ENOG4108V6E	Cell division protein mraZ
Anamo_0891	ENOG4105BZU	Histidine kinase
Anamo_0892	ENOG4105M56	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
Anamo_0894	ENOG4108JIQ	Produces ATP from ADP in the presence of a proton gradient across the membrane. The V-type alpha chain is a catalytic subunit (By similarity)
Anamo_0902	ENOG4105C98	muts2 protein
Anamo_0906	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
Anamo_0907	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
Anamo_0909	ENOG4105CZN	Potassium uptake protein
Anamo_0910	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)
Anamo_0911	ENOG41084MZ	50S ribosomal protein L35
Anamo_0912	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)
Anamo_0913	ENOG4105C22	threonyL-tRNA synthetase
Anamo_0915	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)
Anamo_0924	ENOG4105CB3	Required for the thiolation of cytidine in position 32 of tRNA, to form 2-thiocytidine (s(2)C32) (By similarity)
Anamo_0928	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)
Anamo_0931	ENOG4105E26	Catalyzes the methyl esterification of L-isoaspartyl residues in peptides and proteins that result from spontaneous decomposition of normal L-aspartyl and L-asparaginyl residues. It plays a role in the repair and or degradation of damaged proteins (By similarity)
Anamo_0940	ENOG4105DTN	riboflavin biosynthesis protein ribF
Anamo_0941	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
Anamo_0943	ENOG41085VJ	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)
Anamo_0944	ENOG4105W7A	Protein of unknown function (DUF503)
Anamo_0945	ENOG4107EEM	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)
Anamo_0946	ENOG4105VZN	Nucleic-acid-binding protein implicated in transcription termination
Anamo_0947	ENOG4105CHV	Transcription elongation factor NusA
Anamo_0948	ENOG4105K7D	Required for maturation of 30S ribosomal subunits (By similarity)
Anamo_0951	ENOG4105C25	Primosomal protein n'
Anamo_0952	ENOG4105CJS	Phosphopantothenoylcysteine decarboxylase
Anamo_0953	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)
Anamo_0954	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
Anamo_0955	ENOG4105KC4	UPF0296 protein
Anamo_0956	ENOG4105DSJ	YicC domain protein
Anamo_0957	ENOG4105C1N	GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis (By similarity)
Anamo_0960	ENOG4108HU6	Metal dependent phosphohydrolase
Anamo_0961	ENOG4105FE9	pseudouridine synthase
Anamo_0962	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)
Anamo_0963	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)
Anamo_0964	ENOG4105C31	Tryptophanyl-tRNA synthetase
Anamo_0965	ENOG4105EGD	dinuclear metal center protein, YbgI family
Anamo_0967	ENOG41084T3	4fe-4S ferredoxin iron-sulfur binding domain-containing protein
Anamo_0968	ENOG4105DFT	pur operon repressor
Anamo_0970	ENOG4105CID	antiterminator
Anamo_0971	ENOG4105CI1	PTS System
Anamo_0973	ENOG4108V1U	phospholipid-binding protein
Anamo_0974	ENOG4108IV0	ABC, transporter
Anamo_0975	ENOG4105C0Z	ABC transporter
Anamo_0976	ENOG4105C32	Amino acid ABC transporter (Permease)
Anamo_0978	ENOG4105CFH	Aspartokinase
Anamo_0979	ENOG4105DMJ	Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate (By similarity)
Anamo_0980	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
Anamo_0981	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
Anamo_0984	ENOG4107QUV	Domain protein
Anamo_0986	ENOG4108KB0	deacetylase
Anamo_0987	ENOG4105C8Y	Acetylornithine aminotransferase
Anamo_0988	ENOG4107U4Q	acetylglutamate kinase
Anamo_0989	ENOG4105C0N	N-acetylglutamate semialdehyde dehydrogenase
Anamo_0990	ENOG4105D9I	Responsible for the addition of glutamate residues to the C-terminus of ribosomal protein S6 (By similarity)
Anamo_0991	ENOG4106928	lysine biosynthesis protein LysW
Anamo_0992	ENOG4105CFC	Transporter
Anamo_0993	ENOG4105CH2	amidohydrolase
Anamo_0995	ENOG4105CJM	Binding-protein-dependent transport systems, inner membrane component
Anamo_0996	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
Anamo_0998	ENOG4108JQ7	(ABC) transporter
Anamo_0999	ENOG4105C4Y	ABC transporter
Anamo_1000	ENOG4107RCV	ABC transporter, permease
Anamo_1001	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
Anamo_1004	ENOG4105CUB	amino acid
Anamo_1006	ENOG4105EM7	Selenocysteine-specific translation elongation factor
Anamo_1011	ENOG4108RWI	nicotinamidase
Anamo_1013	ENOG4105CSA	Coproporphyrinogen iii oxidase
Anamo_1014	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)
Anamo_1020	ENOG4105DJ9	glucan biosynthesis protein
Anamo_1021	ENOG4105C3A	Involved in the biosynthesis of osmoregulated periplasmic glucans (OPGs) (By similarity)
Anamo_1024	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
Anamo_1029	ENOG4105D6T	Catalyzes the deamination of 5-methylthioadenosine and S-adenosyl-L-homocysteine into 5-methylthioinosine and S-inosyl-L- homocysteine, respectively. Is also able to deaminate adenosine (By similarity)
Anamo_1034	ENOG4105D37	Low-affinity potassium transport system. Interacts with Trk system potassium uptake protein TrkA (By similarity)
Anamo_1035	ENOG4105C1A	potassium transporter peripheral membrane
Anamo_1036	ENOG4107RB3	L-asparaginase
Anamo_1038	ENOG4105D22	carbon starvation protein
Anamo_1040	ENOG4105D0U	Arsenite-activated ATPase (ArsA)
Anamo_1042	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
Anamo_1044	ENOG4105C94	Transporter
Anamo_1047	ENOG4105Q1T	In the first step of glycine, betaine and sarcosine reductases, the substrate is bound to component PB via a Schiff base intermediate. Then the PB-activated substrate is nucleophilically attacked by the selenol anion of component PA to transform it to a carboxymethylated selenoether and the respective amine. By action of component PC, acetyl phosphate is formed, leaving component PA in its oxidized state. Finally component PA becomes reduced by the thioredoxin system to start a new catalytic cycle of reductive deamination
Anamo_1048	ENOG4105Q1T	In the first step of glycine, betaine and sarcosine reductases, the substrate is bound to component PB via a Schiff base intermediate. Then the PB-activated substrate is nucleophilically attacked by the selenol anion of component PA to transform it to a carboxymethylated selenoether and the respective amine. By action of component PC, acetyl phosphate is formed, leaving component PA in its oxidized state. Finally component PA becomes reduced by the thioredoxin system to start a new catalytic cycle of reductive deamination
Anamo_1050	ENOG4105BZU	Histidine kinase
Anamo_1052	ENOG4105CM1	Catalyzes, together with MoaC, the conversion of 5'-GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
Anamo_1060	ENOG4105CH2	amidohydrolase
Anamo_1061	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)
Anamo_1062	ENOG4105EBE	Peptidase U61, LD-carboxypeptidase A
Anamo_1063	ENOG4105CSD	Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1) (By similarity)
Anamo_1065	ENOG4105TMB	Formate nitrite transporter
Anamo_1067	ENOG4108Z66	YbaK ebsC protein
Anamo_1068	ENOG4105E4C	Lytic transglycosylase catalytic
Anamo_1072	ENOG4105CV8	reductase
Anamo_1074	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
Anamo_1078	ENOG4107BVJ	4,5-dihydroxyphthalate decarboxylase
Anamo_1080	ENOG4105E8R	UPF0173 metal-dependent hydrolase
Anamo_1083	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
Anamo_1085	ENOG4105F38	ABC transporter, permease
Anamo_1091	ENOG4105CN9	Peptidase m42 family protein
Anamo_1092	ENOG4105CN9	Peptidase m42 family protein
Anamo_1093	ENOG4105CN9	Peptidase m42 family protein
Anamo_1097	ENOG4108V3G	Catalyzes the reductive cleavage of azo bond in aromatic azo compounds to the corresponding amines. Requires NADH, but not NADPH, as an electron donor for its activity (By similarity)
Anamo_1098	ENOG4105DFD	Na H antiporter
Anamo_1099	ENOG4105DYB	Isoaspartyl dipeptidase
Anamo_1102	ENOG4107XBN	GntR Family Transcriptional Regulator
Anamo_1103	ENOG4105CG6	trap dicarboxylate transporter dctm subunit
Anamo_1106	ENOG4105CHZ	Catalyzes the dehydration of D-mannonate (By similarity)
Anamo_1107	ENOG4105DEI	Mannitol dehydrogenase
Anamo_1109	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)
Anamo_1111	ENOG4107S5Z	Catalyzes the transfer of endogenously produced octanoic acid from octanoyl-acyl-carrier-protein onto the lipoyl domain of GcvH, an intermediate carrier during protein lipoylation (By similarity)
Anamo_1114	ENOG4105C8Q	Methyl-accepting chemotaxis
Anamo_1116	ENOG4105CXY	transporter
Anamo_1118	ENOG4105E09	nadh pyrophosphatase
Anamo_1119	ENOG4108UVJ	appr-1-p processing domain protein
Anamo_1124	ENOG4105CKA	Catalyzes the reversible isomerization-deamination of glucosamine 6-phosphate (GlcN6P) to form fructose 6-phosphate (Fru6P) and ammonium ion (By similarity)
Anamo_1132	ENOG4107H9G	Necessary for formate dehydrogenase activity (By similarity)
Anamo_1134	ENOG4105D9I	Responsible for the addition of glutamate residues to the C-terminus of ribosomal protein S6 (By similarity)
Anamo_1135	ENOG41068T5	Catalyzes the hydrolysis of methenyl-H(4)MPT( ) to 5- formyl-H(4)MPT (By similarity)
Anamo_1137	ENOG4108N3W	hemolysin secretion protein
Anamo_1138	ENOG4105FIE	Catalyzes the transfer of a formyl group from 5-formyl tetrahydromethanopterin (5-formyl-H(4)MPT) to methanofuran (MFR) so as to produce formylmethanofuran (formyl-MFR) and tetrahydromethanopterin (H(4)MPT) (By similarity)
Anamo_1143	ENOG4105DCC	Formylmethanofuran dehydrogenase subunit A
Anamo_1147	ENOG4108N1H	methylenetetrahydrofolate dehydrogenase (NADP(
Anamo_1149	ENOG4105C6R	Transfers a GMP moiety from GTP to Mo-molybdopterin (Mo- MPT) cofactor (Moco or molybdenum cofactor) to form Mo- molybdopterin guanine dinucleotide (Mo-MGD) cofactor (By similarity)
Anamo_1159	ENOG4105CG6	trap dicarboxylate transporter dctm subunit
Anamo_1161	ENOG4105DR6	Trap dicarboxylate transporter, dctp subunit
Anamo_1165	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
Anamo_1167	ENOG4105VXN	addiction module toxin, RelE StbE family
Anamo_1172	ENOG4105C10	Electron transfer flavoprotein
Anamo_1173	ENOG4105BZJ	Electron transfer flavoprotein
Anamo_1174	ENOG4105CQB	FAD linked oxidase domain protein
Anamo_1182	ENOG4105MZG	transcriptional modulator of maze toxin, mazf
Anamo_1184	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
Anamo_1186	ENOG4105W2C	Glycosyl transferase
Anamo_1187	ENOG4105EAG	UDP-N-acetylglucosamine 2-epimerase
Anamo_1188	ENOG4107T8Q	Glycosyl transferase (Group 1
Anamo_1193	ENOG4107R5M	Catalyzes the transfer of a N-acetyl-glucosamine moiety to 1D-myo-inositol 3-phosphate to produce 1D-myo-inositol 2- acetamido-2-deoxy-glucopyranoside 3-phosphate in the mycothiol biosynthesis pathway (By similarity)
Anamo_1199	ENOG4105J5G	Transferase hexapeptide repeat containing protein
Anamo_1201	ENOG4107QQG	Dehydrogenase
Anamo_1223	ENOG4105D3Q	Sugar transferase
Anamo_1228	ENOG4107ZIM	Dtdp-4-dehydrorhamnose 3,5-epimerase
Anamo_1231	ENOG4105C1B	dTDP-glucose 4-6-dehydratase
Anamo_1232	ENOG4105DBZ	Dtdp-4-dehydrorhamnose reductase
Anamo_1233	ENOG4108MX3	Polysaccharide Biosynthesis Protein
Anamo_1237	ENOG41089UC	methyltransferase, type 11
Anamo_1240	ENOG4105EZ5	reductase
Anamo_1241	ENOG4107VHA	regulatoR
Anamo_1245	ENOG4107REC	cytoplasmic protein
Anamo_1250	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
Anamo_1252	ENOG4107UUY	ec 2.7.1.11
Anamo_1256	ENOG4105I9Z	UPF0264 protein
Anamo_1257	ENOG4105CJV	Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase
Anamo_1258	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)
Anamo_1259	ENOG4107QKR	Dehydrogenase
Anamo_1260	ENOG4106Z86	ATP-nad acox kinase
Anamo_1261	ENOG4105CHR	reductase
Anamo_1264	ENOG4107RUY	(E1 component), alpha subunit
Anamo_1265	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)
Anamo_1267	ENOG4107QJT	sodium dicarboxylate symporter
Anamo_1268	ENOG4105CJW	magnesium transporter
Anamo_1269	ENOG4105DFD	Na H antiporter
Anamo_1272	ENOG4106PMH	Extracellular solute-binding protein family 3
Anamo_1273	ENOG4105E5Q	amino acid AbC transporter
Anamo_1275	ENOG4105E5Q	amino acid AbC transporter
Anamo_1276	ENOG4107258	Transcriptional regulator
Anamo_1277	ENOG4105CGP	Urocanate hydratase
Anamo_1278	ENOG4105DWD	nucleoside recognition domain protein
Anamo_1280	ENOG4105PUK	Membrane
Anamo_1284	ENOG4105DR6	Trap dicarboxylate transporter, dctp subunit
Anamo_1285	ENOG4105CG6	trap dicarboxylate transporter dctm subunit
Anamo_1286	ENOG4105XDZ	Tripartite ATP-independent periplasmic transporter
Anamo_1288	ENOG4105E2X	shikimate dehydrogenase
Anamo_1289	ENOG4107SG5	Dehydrogenase
Anamo_1290	ENOG4105CBH	Hydroxymethylglutaryl-CoA lyase
Anamo_1292	ENOG4105FF2	Type I DHQase
Anamo_1293	ENOG41069M3	Transcriptional regulator
Anamo_1302	ENOG4105MQS	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
Anamo_1303	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
Anamo_1313	ENOG4105D1Z	hydroxypyruvate reductase
Anamo_1314	ENOG4105C0A	alcohol dehydrogenase
Anamo_1315	ENOG4105CN9	Peptidase m42 family protein
Anamo_1320	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
Anamo_1322	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)
Anamo_1323	ENOG4107S2N	Type III effector Hrp-dependent
Anamo_1324	ENOG4105CAX	The 2-keto-3-deoxygluconate permease transports the degraded pectin products into the bacterial cell, where they serve as carbon and energy sources. This is a hydrogen coupled transport system (By similarity)
Anamo_1325	ENOG4105CTX	dehydratase
Anamo_1326	ENOG4105CTX	dehydratase
Anamo_1328	ENOG4105CHM	Aminotransferase
Anamo_1329	ENOG4105C01	Dihydroxy-acid dehydratase
Anamo_1330	ENOG4105C6Z	Gluconate
Anamo_1331	ENOG4107HP6	Transcriptional regulator
Anamo_1336	ENOG4105D21	Phosphoribosylformylglycinamidine synthase I
Anamo_1337	ENOG4107QIK	phosphoribosylformylglycinamidine synthase
Anamo_1339	ENOG4105CXB	phosphoribosylaminoimidazole synthetase
Anamo_1340	ENOG4108V3E	phosphoribosylglycinamide formyltransferase
Anamo_1341	ENOG4105DC1	bifunctional purine biosynthesis protein purh
Anamo_1342	ENOG4107QNG	Phosphoribosylglycinamide synthetase
Anamo_1343	ENOG4105C7N	Xanthine uracil vitamin C permease
Anamo_1346	ENOG4105CE2	Aldehyde oxidase and xanthine dehydrogenase, molybdopterin binding
Anamo_1348	ENOG4105C7W	Xanthine dehydrogenase
Anamo_1351	ENOG4105D6T	Catalyzes the deamination of 5-methylthioadenosine and S-adenosyl-L-homocysteine into 5-methylthioinosine and S-inosyl-L- homocysteine, respectively. Is also able to deaminate adenosine (By similarity)
Anamo_1354	ENOG4105DQW	permease for cytosine purines, uracil, thiamine, allantoin
Anamo_1357	ENOG4105CE2	Aldehyde oxidase and xanthine dehydrogenase, molybdopterin binding
Anamo_1358	ENOG4107QYT	Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor (By similarity)
Anamo_1359	ENOG4105DBV	ornithine carbamoyltransferase
Anamo_1360	ENOG4107S4Y	M20 DapE family protein YgeY
Anamo_1364	ENOG4105DND	Transcriptional regulator
Anamo_1365	ENOG4108UM6	Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) (By similarity)
Anamo_1366	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)
Anamo_1368	ENOG4105FCI	Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate (By similarity)
Anamo_1371	ENOG4105CDH	Citrulline--aspartate ligase
Anamo_1372	ENOG4105C6K	Malic enzyme
Anamo_1373	ENOG4105QUH	Domain of unknown function (DUF2088)
Anamo_1376	ENOG4105JN3	extra-cytoplasmic solute receptor family protein
Anamo_1377	ENOG4105MQS	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
Anamo_1378	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
Anamo_1384	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)
Anamo_1385	ENOG4105DZW	Dipeptidase
Anamo_1390	ENOG4105DZW	Dipeptidase
Anamo_1391	ENOG4108WYP	Transcriptional regulator
Anamo_1393	ENOG4107RIU	May be involved in the formation or repair of Fe-S clusters present in iron-sulfur proteins (By similarity)
Anamo_1395	ENOG4105DDK	oxidoreductase, beta subunit
Anamo_1396	ENOG4105D95	Oxidoreductase required for the transfer of electrons from pyruvate to flavodoxin (By similarity)
Anamo_1397	ENOG4107XUH	ferredoxin (flavodoxin) oxidoreductase
Anamo_1401	ENOG4106XMA	In vivo, quickly hydrolyzes the ureidoacrylate peracid to avoid toxicity, but can also hydrolyzes ureidoacrylate that is formed spontaneously from ureidoacrylate peracid. One of the products of hydrolysis, carbamate, hydrolyzes spontaneously, thereby releasing one of the pyrimidine rings nitrogen atoms as ammonia and one of its carbons as CO2 (By similarity)
Anamo_1402	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)
Anamo_1404	ENOG4105CFB	Gamma-glutamyltranspeptidase (EC 2.3.2.2)
Anamo_1408	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
Anamo_1409	ENOG4108Z4T	Peptidase M50
Anamo_1411	ENOG4108ZQD	Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A (By similarity)
Anamo_1413	ENOG4107RSS	Hydrogenase accessory protein HypB
Anamo_1414	ENOG4105WMM	Probably plays a role in a hydrogenase nickel cofactor insertion step (By similarity)
Anamo_1415	ENOG4105MS2	ribosomal subunit Interface protein
Anamo_1418	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)
Anamo_1419	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
Anamo_1420	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)
Anamo_1421	ENOG4105CE9	30S ribosomal protein S2
Anamo_1422	ENOG4105VPX	protein, conserved in bacteria
Anamo_1426	ENOG4108Z6B	deaminase
Anamo_1429	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)
Anamo_1432	ENOG4105C84	Histidine ammonia-lyase
Anamo_1434	ENOG4105C7W	Xanthine dehydrogenase
Anamo_1437	ENOG4105K95	(LipO)protein
Anamo_1444	ENOG4105C2M	dna polymerase I
Anamo_1445	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)
Anamo_1446	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)
Anamo_1447	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)
Anamo_1448	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)
Anamo_1449	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)
Anamo_1450	ENOG4105C47	NADH ubiquinone oxidoreductase 20 kda subunit
Anamo_1452	ENOG4105D65	subunit l
Anamo_1453	ENOG4108ZE9	Monovalent cation H antiporter subunit C
Anamo_1455	ENOG4105D65	subunit l
Anamo_1459	ENOG4105SC1	monovalent cation H antiporter subunit E
Anamo_1461	ENOG4105CJ1	ABC, transporter
Anamo_1463	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
Anamo_1466	ENOG4105QA4	4Fe-4S Ferredoxin, iron-sulfur binding domain protein
Anamo_1467	ENOG4105WE2	aldehyde ferredoxin oxidoreductase
Anamo_1469	ENOG4105DFD	Na H antiporter
Anamo_1474	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)
Anamo_1477	ENOG4108ZI0	d,d-heptose 1,7-bisphosphate phosphatase
Anamo_1479	ENOG4105C0K	Gdp-mannose 4,6-dehydratase
Anamo_1481	ENOG4105F55	Catalyzes the isomerization of sedoheptulose 7-phosphate in D-glycero-D-manno-heptose 7-phosphate (By similarity)
Anamo_1483	ENOG4105DTS	flagellar hook-associated
Anamo_1487	ENOG4107RGW	The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor
Anamo_1488	ENOG4107QK8	The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor
Anamo_1489	ENOG4105DRR	Transcriptional regulator, GntR family
Anamo_1490	ENOG4105CB3	Required for the thiolation of cytidine in position 32 of tRNA, to form 2-thiocytidine (s(2)C32) (By similarity)
Anamo_1492	ENOG4105DIW	FeS assembly protein SUFB
Anamo_1493	ENOG4105C3K	feS assembly ATPase SufC
Anamo_1494	ENOG4107QP8	phosphohexose isomerase
Anamo_1496	ENOG410902H	NADH dehydrogenase (Ubiquinone), 24 kDa subunit
Anamo_1497	ENOG4107QIZ	NADH dehydrogenase
Anamo_1499	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)
Anamo_1500	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)
Anamo_1501	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)
Anamo_1502	ENOG41081AP	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)
Anamo_1503	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)
Anamo_1504	ENOG4105CRK	lysyL-tRNA synthetase
Anamo_1507	ENOG4108EQH	DNA internalization-related competence protein ComEC Rec2
Anamo_1509	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)
Anamo_1510	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)
Anamo_1511	ENOG4105CPF	Cell wall formation (By similarity)
Anamo_1517	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
Anamo_1518	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
Anamo_1519	ENOG4108K5P	(LipO)protein
Anamo_1520	ENOG4105C4P	Facilitates transcription termination by a mechanism that involves Rho binding to the nascent RNA, activation of Rho's RNA-dependent ATPase activity, and release of the mRNA from the DNA template (By similarity)
Anamo_1521	ENOG4105CW3	Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway (By similarity)
Anamo_1525	ENOG4108YZP	cobalt ABC transporter, inner membrane subunit CbiQ
Anamo_1527	ENOG4107XQ1	cobalamin (vitamin B12) biosynthesis CbiM protein
Anamo_1530	ENOG4105CEM	UPF0597 protein
Anamo_1536	ENOG4105DFD	Na H antiporter
Anamo_1539	ENOG41066A3	ATP guanido phosphotransferase
Anamo_1542	ENOG4108UI1	Probably functions as a manganese efflux pump (By similarity)
Anamo_1543	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)
Anamo_1544	ENOG4105CD5	CoA-binding domain protein
Anamo_1546	ENOG4108K9K	Uncharacterised protein family (UPF0236)
Anamo_1547	ENOG4105CD3	dihydroorotase
Anamo_1548	ENOG4105EXW	epimerase dehydratase
Anamo_1549	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)
Anamo_1550	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
Anamo_1551	ENOG4107Z8R	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)
Anamo_1552	ENOG41084QK	UPF0109 protein
Anamo_1553	ENOG4105K5M	30s ribosomal protein S16
Anamo_1556	ENOG4105C5I	Dehydrogenase
Anamo_1557	ENOG4105CH2	amidohydrolase
Anamo_1560	ENOG4108IAA	Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate (By similarity)
Anamo_1561	ENOG4105C7N	Xanthine uracil vitamin C permease
Anamo_1562	ENOG4105CPN	adenine deaminase
Anamo_1564	ENOG4108IV0	ABC, transporter
Anamo_1565	ENOG4105C0Z	ABC transporter
Anamo_1567	ENOG4105C32	Amino acid ABC transporter (Permease)
Anamo_1570	ENOG4107QMW	pyridine nucleotide-disulfide oxidoreductase
Anamo_1572	ENOG4105BZU	Histidine kinase
Anamo_1574	ENOG4105CVA	phosphate
Anamo_1575	ENOG4105DWD	nucleoside recognition domain protein
Anamo_1576	ENOG4105WE2	aldehyde ferredoxin oxidoreductase
Anamo_1584	ENOG41088YS	Glycosyl transferase (Group 1
Anamo_1586	ENOG4105C1K	alpha-alpha-trehalose-phosphate synthase
Anamo_1587	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)
Anamo_1588	ENOG4108KF8	Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid (By similarity)
Anamo_1589	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
Anamo_1592	ENOG4105CQP	nitrilase cyanide hydratase and apolipoprotein n-acyltransferase
Anamo_1593	ENOG4105D6U	Sodium Glutamate Symporter
Anamo_1594	ENOG4105K95	(LipO)protein
Anamo_1595	ENOG4105C9B	Cysteine desulfurase
Anamo_1596	ENOG4105DC7	peptidase M24
Anamo_1597	ENOG4105K95	(LipO)protein
Anamo_1598	ENOG4108ME1	Peptidase M55 D-aminopeptidase
Anamo_1599	ENOG4105DYN	CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Acts as a dsDNA endonuclease. May be involved in the integration of spacer DNA into the CRISPR cassette (By similarity)
Anamo_1607	ENOG4105K95	(LipO)protein
Anamo_1610	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
Anamo_1611	ENOG4105C0H	protease
Anamo_1613	ENOG4107EJG	GntR family transcriptional regulator
Anamo_1617	ENOG4105EZ5	reductase
Anamo_1621	ENOG4105CG6	trap dicarboxylate transporter dctm subunit
Anamo_1623	ENOG4105EJQ	L-serine dehydratase
Anamo_1624	ENOG4105D6U	Sodium Glutamate Symporter
Anamo_1627	ENOG4105E8R	UPF0173 metal-dependent hydrolase
Anamo_1630	ENOG4105C9M	aspartyl-trna synthetase
Anamo_1631	ENOG4105CUT	histidyl-tRNA synthetase
Anamo_1632	ENOG4105MCT	stage V sporulation protein S
Anamo_1636	ENOG4105VEQ	Cold shock protein
Anamo_1637	ENOG4108Z7R	Chaperone CsaA
Anamo_1642	ENOG4105D0M	Protease HtpX homolog
Anamo_1643	ENOG4108UV6	Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP) (By similarity)
Anamo_1644	ENOG4105C4U	4-methyl-5-beta-hydroxyethylthiazole kinase
Anamo_1646	ENOG4105C3G	gtp-binding protein
Anamo_1647	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)
Anamo_1650	ENOG4105CE1	Ferrous iron transport protein b
Anamo_1651	ENOG4108IPX	Part of the ABC transporter complex HmuTUV involved in hemin import. Responsible for energy coupling to the transport system (By similarity)
Anamo_1652	ENOG4105EHG	Permease protein
Anamo_1653	ENOG4105ETE	Transcriptional regulator (LacI family
Anamo_1659	ENOG4107A5B	Binding-protein-dependent transport systems, inner membrane component
Anamo_1660	ENOG4105C8W	ABC transporter
Anamo_1662	ENOG4108IA2	Sodium pantothenate symporter
Anamo_1663	ENOG4105RG0	Membrane
Anamo_1664	ENOG4105C01	Dihydroxy-acid dehydratase
Anamo_1668	ENOG4105CI3	gtp-binding protein typa
Anamo_1678	ENOG4107QIZ	NADH dehydrogenase
Anamo_1680	ENOG4105BZU	Histidine kinase
Anamo_1687	ENOG4107R76	Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties (By similarity)
Anamo_1688	ENOG4105CXW	Synthesizes alpha-1,4-glucan chains using ADP-glucose (By similarity)
Anamo_1689	ENOG4107QQ4	Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans (By similarity)
Anamo_1691	ENOG4108N5B	2-phosphosulfolactate phosphatase
Anamo_1692	ENOG4105BZ3	General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) (By similarity)
Anamo_1694	ENOG4105EHH	Cleaves type-4 fimbrial leader sequence and methylates the N-terminal (generally Phe) residue (By similarity)
Anamo_1701	ENOG4105BZG	amino acid carrier protein
Anamo_1703	ENOG4105C5R	Aminotransferase
Anamo_1707	ENOG4105DJY	efflux transporter, rnd family, mfp subunit
Anamo_1710	ENOG4108UJD	30S ribosomal protein S9
Anamo_1711	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)
Anamo_1714	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)
Anamo_1716	ENOG4105C5C	n-acetylmuramoyl-l-alanine amidase
Anamo_1719	ENOG4105DB7	PHP domain protein
Anamo_1720	ENOG4108V3W	Chemotaxis protein, CheW
Anamo_1721	ENOG4108RE9	Phosphodiesterase
Anamo_1722	ENOG4105D6E	homoserine dehydrogenase
Anamo_1728	ENOG4105KRI	phosphocarrier protein (HPr
Anamo_1730	ENOG4105BZ8	glutamate synthase
Anamo_1732	ENOG4108JQ0	Key enzyme in the regulation of glycerol uptake and metabolism (By similarity)
Anamo_1735	ENOG4105CMT	Dihydroxyacetone kinase
Anamo_1738	ENOG4105D1S	lipid A biosynthesis
Anamo_1739	ENOG4105X1Q	TOBE domain protein
Anamo_1740	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)
Anamo_1742	ENOG4108U5N	UPF0316 protein
Anamo_1744	ENOG4105WH1	Two component transcriptional regulator luxr family
Anamo_1746	ENOG4105EYH	Exonuclease
Anamo_1750	ENOG4107R88	Chemotaxis protein (CheV)
Anamo_1751	ENOG4107SBB	4-alpha-glucanotransferase (EC 2.4.1.25)
Anamo_1752	ENOG4105D95	Oxidoreductase required for the transfer of electrons from pyruvate to flavodoxin (By similarity)
Anamo_1753	ENOG4108HRN	Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate (By similarity)
Anamo_1756	ENOG4105MQS	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
Anamo_1757	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
Anamo_1759	ENOG4105UQX	Mate efflux family protein
Anamo_1760	ENOG4105EJ7	Catalyzes the reduction of hydroxylamine to form NH(3) and H(2)O (By similarity)
Anamo_1762	ENOG4105UFH	BadM Rrf2 family transcriptional regulator
Anamo_1765	ENOG4105VCQ	rubredoxin
Anamo_1766	ENOG4105DZ0	fad dependent oxidoreductase
Anamo_1767	ENOG4105NDF	NAD-dependent protein deacetylase which modulates the activities of several enzymes which are inactive in their acetylated form. May also have NAD-dependent lysine demalonylase and desuccinylase activity (By similarity)
Anamo_1771	ENOG4107P0T	Selenium-dependent molybdenum hydroxylase system protein, YqeB family
Anamo_1772	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)
Anamo_1777	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)
Anamo_1778	ENOG4105M7V	2'-5' rna ligase
Anamo_1779	ENOG4105CEV	competence damage-inducible protein
Anamo_1780	ENOG4108ZAI	phosphatidylglycerophosphatase a
Anamo_1781	ENOG4105CBM	Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 (By similarity)
Anamo_1783	ENOG4105DJV	ribulose-phosphate 3-epimerase
Anamo_1785	ENOG4105CYJ	ribosomal RNA small subunit methyltransferase B
Anamo_1789	ENOG4108WYP	Transcriptional regulator
Anamo_1791	ENOG4105C1I	TRANSCRIPTIONAl REGULATOR GntR family
Anamo_1793	ENOG4105DW0	Catalyzes the ADP transfer to D-glycero-D-manno-heptose 1-phosphate, yielding ADP-D,D-heptose (By similarity)
Anamo_1794	ENOG4105CEY	Amp-dependent synthetase and ligase
Anamo_1798	ENOG4105C34	Pseudouridine synthase
Anamo_1801	ENOG4105E3H	phosphoglycerate mutase
Anamo_1802	ENOG4105C1I	TRANSCRIPTIONAl REGULATOR GntR family
Anamo_1803	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)
Anamo_1805	ENOG4105C6X	Major Facilitator
Anamo_1806	ENOG4105CRQ	synthase (Component I)
Anamo_1808	ENOG4105DK0	Indole-3-glycerol phosphate synthase
Anamo_1809	ENOG4108ZGB	N-(5'-phosphoribosyl)anthranilate isomerase
Anamo_1810	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
Anamo_1811	ENOG4105F6H	The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate (By similarity)
Anamo_1812	ENOG4105CFM	UPF0317 protein
Anamo_1813	ENOG4105E7W	lamb ycsf family protein
Anamo_1815	ENOG4105P4J	Allophanate hydrolase, subunit 1
Anamo_1816	ENOG4105C5A	transporter
Anamo_1818	ENOG4107R1M	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) (By similarity)
Anamo_1821	ENOG4108I5C	dEAD DEAH box helicase
Anamo_1828	ENOG4105CMG	Carbohydrate kinase
Anamo_1829	ENOG4105C01	Dihydroxy-acid dehydratase
Anamo_1832	ENOG4108XRC	Protein of unknown function (DUF458) 
Anamo_1834	ENOG4105DPN	Oligoendopeptidase f
Anamo_1839	ENOG4105D6E	homoserine dehydrogenase
Anamo_1840	ENOG4108UHU	Aldolase
Anamo_1842	ENOG4105DR6	Trap dicarboxylate transporter, dctp subunit
Anamo_1844	ENOG4105CG6	trap dicarboxylate transporter dctm subunit
Anamo_1846	ENOG4107QZW	Altronate oxidoreductase
Anamo_1847	ENOG4105CTX	dehydratase
Anamo_1848	ENOG4107HP6	Transcriptional regulator
Anamo_1849	ENOG4105C8J	)-transporter
Anamo_1851	ENOG4105C6T	cysteine synthase
Anamo_1852	ENOG4105D7W	serine acetyltransferase
Anamo_1855	ENOG4105CKM	Branched-chain carboxylic acid kinase
Anamo_1856	ENOG4107RE7	phosphate butyryltransferase
Anamo_1857	ENOG4107RE7	phosphate butyryltransferase
Anamo_1858	ENOG4105CKM	Branched-chain carboxylic acid kinase
Anamo_1859	ENOG4105CM2	brancheD-chain amino acid aminotransferase
Anamo_1863	ENOG4105CPF	Cell wall formation (By similarity)
Anamo_1865	ENOG41082BV	acetyltransferase
Anamo_1867	ENOG41065RQ	ADP-ribosylation crystallin J1
Anamo_1873	ENOG4105C0D	helicase
Anamo_1879	ENOG4105BZU	Histidine kinase
Anamo_1880	ENOG4105ETX	regulatoR
Anamo_1881	ENOG4105CKK	Glycosyl transferase, family 2
Anamo_1883	ENOG4105C1B	dTDP-glucose 4-6-dehydratase
Anamo_1884	ENOG4105CKK	Glycosyl transferase, family 2
Anamo_1886	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)
Anamo_1887	ENOG4105E98	transcriptional regulator DeoR family
Anamo_1888	ENOG4105DE4	1-phosphofructokinase
Anamo_1889	ENOG4105DM4	PTS System
Anamo_1890	ENOG4105DM4	PTS System
Anamo_1892	ENOG4108IJ7	Glycine betaine
Anamo_1893	ENOG4108HQS	Glycine betaine
Anamo_1895	ENOG4105DIN	metallophosphoesterase
Anamo_1900	ENOG4107RGW	The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor
Anamo_1901	ENOG4107QK8	The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor
Anamo_1902	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)
Anamo_1904	ENOG4108JIP	Produces ATP from ADP in the presence of a proton gradient across the membrane. The V-type beta chain is a regulatory subunit (By similarity)
Anamo_1905	ENOG4108JIQ	Produces ATP from ADP in the presence of a proton gradient across the membrane. The V-type alpha chain is a catalytic subunit (By similarity)
Anamo_1908	ENOG410839E	ATP synthase, F0 subunit c
Anamo_1912	ENOG4106C6A	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
Anamo_1913	ENOG4105DC8	reductase
Anamo_1915	ENOG4105CPN	adenine deaminase
Anamo_1917	ENOG4108RW0	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
Anamo_1919	ENOG4107KMQ	bfd domain protein (2fe-2s)-binding domain protein
Anamo_1921	ENOG4108JU3	Alkyl hydroperoxide reductase
Anamo_1922	ENOG4105D43	The glycine cleavage system catalyzes the degradation of glycine (By similarity)
Anamo_1924	ENOG4105C8J	)-transporter
Anamo_1931	ENOG4105ZU5	s-layer protein
Anamo_1934	ENOG4105DC7	peptidase M24
Anamo_1937	ENOG4107RID	5-oxoprolinase (ATP-hydrolyzing)
Anamo_1942	ENOG4105G9B	Transcriptional regulator
Anamo_1949	ENOG4107QSE	Dipeptidase
Anamo_1950	ENOG4105CTU	Proline racemase
Anamo_1951	ENOG4105F1A	Pyruvate formate-lyase
Anamo_1952	ENOG4105C6N	Formate acetyltransferase
Anamo_1954	ENOG4105D7N	magnesium and cobalt transport protein CorA
Anamo_1959	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
Anamo_1961	ENOG4105DEF	Extracellular solute-binding protein, family 5
Anamo_1962	ENOG4108JQ7	(ABC) transporter
Anamo_1963	ENOG4105C3U	ABC transporter
Anamo_1965	ENOG4107R7I	amino acid
Anamo_1966	ENOG4105WE2	aldehyde ferredoxin oxidoreductase
Anamo_1967	ENOG4108XIB	electron transport protein ysaA
Anamo_1968	ENOG4105DR6	Trap dicarboxylate transporter, dctp subunit
Anamo_1969	ENOG4105CG6	trap dicarboxylate transporter dctm subunit
Anamo_1970	ENOG4105CG6	trap dicarboxylate transporter dctm subunit
Anamo_1975	ENOG4105DR6	Trap dicarboxylate transporter, dctp subunit
Anamo_1978	ENOG4105QUH	Domain of unknown function (DUF2088)
Anamo_1980	ENOG4105DR6	Trap dicarboxylate transporter, dctp subunit
Anamo_1983	ENOG4108JPM	phospho-2-dehydro-3-deoxyheptonate aldolase
Anamo_1985	ENOG4105CMY	5-enolpyruvylshikimate-3-phosphate synthase
Anamo_1986	ENOG4105D10	5-enolpyruvylshikimate-3-phosphate phospholyase
Anamo_1987	ENOG4105D49	3-dehydroquinate synthase
Anamo_1990	ENOG4108I5D	sulfate abc transporter
Anamo_1991	ENOG4105C4Y	ABC transporter
Anamo_1992	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
Anamo_1994	ENOG4105D38	putrescine abc transporter
Anamo_1996	ENOG4105D1F	ATP-binding protein
Anamo_2011	ENOG4105CZX	twitching motility protein
Anamo_2012	ENOG4107QHF	type ii secretion system protein e
Anamo_2013	ENOG4108IV0	ABC, transporter
Anamo_2014	ENOG4105C0Z	ABC transporter
Anamo_2015	ENOG4105CF8	branched-chain amino acid ABC transporter, permease
Anamo_2016	ENOG4105C32	Amino acid ABC transporter (Permease)
Anamo_2018	ENOG4108YXI	Secondary thiamine-phosphate synthase enzyme
Anamo_2021	ENOG4108EE5	Part of the ABC transporter complex MacAB involved in macrolide export. Transmembrane domains (TMD) form a pore in the inner membrane and the ATP-binding domain (NBD) is responsible for energy generation (By similarity)
Anamo_2022	ENOG4105D6C	Part of the ABC transporter complex MacAB involved in macrolide export. Transmembrane domains (TMD) form a pore in the inner membrane and the ATP-binding domain (NBD) is responsible for energy generation (By similarity)
Anamo_2023	ENOG4105DJY	efflux transporter, rnd family, mfp subunit
Anamo_2025	ENOG4105C1I	TRANSCRIPTIONAl REGULATOR GntR family
Anamo_2026	ENOG4107NFR	Fructose-1,6-bisphosphatase
Anamo_2027	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
Anamo_2030	ENOG4105DE9	3-keto-5-aminohexanoate cleavage enzyme
Anamo_2031	ENOG41073TP	transcriptional regulator
Anamo_2032	ENOG4105CG6	trap dicarboxylate transporter dctm subunit
Anamo_2034	ENOG4105DR6	Trap dicarboxylate transporter, dctp subunit
Anamo_2036	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)
Anamo_2038	ENOG4106DSS	Tartrate dehydratase subunit alpha
Anamo_2039	ENOG4105D9Q	decarboxylase (Beta subunit)
Anamo_2040	ENOG4108JIJ	Catalyzes a 2-step reaction, involving the ATP-dependent carboxylation of the covalently attached biotin in the first step and the transfer of the carboxyl group to pyruvate in the second (By similarity)
Anamo_2042	ENOG4107QX3	carboxylase
Anamo_2043	ENOG4108ZVT	methylmalonyl-coA epimerase
Anamo_2044	ENOG4105D5P	Methylmalonyl-coA mutase
Anamo_2047	ENOG4105CNW	domain protein
Anamo_2049	ENOG4105D82	Glutamate dehydrogenase
Anamo_2050	ENOG4105ETU	transcriptional activator (TenA
Anamo_2052	ENOG4105PW4	Sugar fermentation stimulation protein homolog
Anamo_2054	ENOG4105UIB	(ABC) transporter
Anamo_2055	ENOG4108JQ9	ABC transporter
Anamo_2057	ENOG4105DYA	Acts on guanine, xanthine and to a lesser extent hypoxanthine (By similarity)
Anamo_2058	ENOG4105VKD	bioY protein
Anamo_2059	ENOG4108ZK7	protein family UPF0029, Impact, N-terminal protein
Anamo_2061	ENOG41090R7	Ferric uptake
Anamo_2063	ENOG4105FDK	ABC transporter
Anamo_2066	ENOG4107S21	permease
Anamo_2068	ENOG4108K9K	Uncharacterised protein family (UPF0236)
Anamo_2070	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
Anamo_2071	ENOG4105C3U	ABC transporter
Anamo_2072	ENOG4108JQ7	(ABC) transporter
Anamo_2073	ENOG4105DYB	Isoaspartyl dipeptidase
Anamo_2077	ENOG4105CVJ	phosphoglycerate mutase
Anamo_2078	ENOG4105CHR	reductase
Anamo_2081	ENOG4107QJE	Chromosome Partitioning Protein
Anamo_2082	ENOG4105D28	Specifically methylates the N7 position of a guanine in 16S rRNA (By similarity)
Anamo_2088	ENOG4105CY0	Metallo-Beta-Lactamase
Anamo_2090	ENOG4107QXG	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
Anamo_2091	ENOG4107QIV	Cytochrome c biogenesis protein
Anamo_2092	ENOG4108JQ7	(ABC) transporter
Anamo_2093	ENOG4105C3U	ABC transporter
Anamo_2094	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
Anamo_2095	ENOG4105CJM	Binding-protein-dependent transport systems, inner membrane component
Anamo_2096	ENOG4105DEF	Extracellular solute-binding protein, family 5
Anamo_2097	ENOG4105C8M	UPF0272 protein
Anamo_2101	ENOG4105CPI	Metal Dependent Phosphohydrolase
Anamo_2102	ENOG4108K7V	UPF0284 protein
Anamo_2104	ENOG4108UHF	Joins Ado-cobinamide-GDP and alpha-ribazole to generate adenosylcobalamin (Ado-cobalamin) (By similarity)
Anamo_2105	ENOG4105J7I	hydrolase