locus-tag	class	description
TK90_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)
TK90_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)
TK90_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)
TK90_0004	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)
TK90_0006	ENOG4105DGW	oligopeptidase A
TK90_0007	ENOG4105CGK	Exodeoxyribonuclease III
TK90_0008	ENOG4105D3H	Catalyzes the decarboxylation of 3-octaprenyl-4-hydroxy benzoate to 2-octaprenylphenol (By similarity)
TK90_0010	ENOG4108EX3	reductase
TK90_0011	ENOG41076E6	Uroporphyrinogen-III Synthase
TK90_0012	ENOG4105D6W	Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps (By similarity)
TK90_0013	ENOG4108NEV	two component transcriptional regulator, LytTR family
TK90_0015	ENOG4105CH7	arginosuccinase
TK90_0017	ENOG4105CNG	UPF0061 protein
TK90_0019	ENOG4105CHH	sulfate transporter
TK90_0021	ENOG4105CHB	tonB-dependent Receptor
TK90_0023	ENOG4105C94	Transporter
TK90_0025	ENOG41067TZ	transcriptional regulator, MarR family
TK90_0027	ENOG4105CE7	Amidase, hydantoinase carbamoylase family
TK90_0028	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)
TK90_0031	ENOG4105CXT	aspartate transcarbamylase
TK90_0032	ENOG4105CAQ	asparagine synthetase
TK90_0034	ENOG4105BZU	Histidine kinase
TK90_0036	ENOG4105C7K	acetolactate synthase
TK90_0038	ENOG4105CRE	cytochrome C
TK90_0039	ENOG4105EBH	Required during biogenesis of c-type cytochromes (cytochrome c6 and cytochrome f) at the step of heme attachment (By similarity)
TK90_0040	ENOG4106RE7	Cytochrome
TK90_0041	ENOG4105WHM	Necessary for normal cell division and for the maintenance of normal septation (By similarity)
TK90_0044	ENOG4105C2M	dna polymerase I
TK90_0045	ENOG4108URH	decarboxylase
TK90_0049	ENOG4105CUX	Signal transduction histidine kinase
TK90_0050	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
TK90_0051	ENOG4107RY0	Catalyzes the conversion of dihydroorotate to orotate (By similarity)
TK90_0052	ENOG4108UIQ	Methylates the ribose at the nucleotide 34 wobble position in the two leucyl isoacceptors tRNA(Leu)(CmAA) and tRNA(Leu)(cmnm5UmAA). Catalyzes the methyl transfer from S- adenosyl-L-methionine to the 2'-OH of the wobble nucleotide (By similarity)
TK90_0054	ENOG4107R15	K00850 6-phosphofructokinase 1 EC 2.7.1.11
TK90_0055	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)
TK90_0057	ENOG4108KDI	dmso reductase anchor subunit
TK90_0058	ENOG4105QA4	4Fe-4S Ferredoxin, iron-sulfur binding domain protein
TK90_0059	ENOG4105DB1	molybdopterin oxidoreductase
TK90_0062	ENOG4107RIQ	Sulfate adenylate transferase
TK90_0067	ENOG4108YZY	peptidylprolyl cis-trans isomerase
TK90_0070	ENOG4105CGK	Exodeoxyribonuclease III
TK90_0071	ENOG4107QP2	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)
TK90_0076	ENOG4105F2I	Transposase
TK90_0077	ENOG4108UQS	dipeptidase
TK90_0079	ENOG4105C5I	Dehydrogenase
TK90_0084	ENOG4105CZI	D-fructose-1,6-bisphosphate 1-phosphohydrolase class 1
TK90_0085	ENOG4105CTQ	phosphohexokinase
TK90_0091	ENOG4108ZEF	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate (By similarity)
TK90_0092	ENOG4105K5D	4fe-4S ferredoxin iroN-sulfur binding
TK90_0094	ENOG4105KQV	Binds directly to 16S ribosomal RNA (By similarity)
TK90_0096	ENOG4105C4R	Atp-dependent dna helicase
TK90_0097	ENOG4105C7P	2-oxoglutarate dehydrogenase, E1
TK90_0098	ENOG4105C7S	Dehydrogenase
TK90_0100	ENOG4105BZU	Histidine kinase
TK90_0101	ENOG4105CNK	Required, probably indirectly, for the hydroxylation of 2-octaprenylphenol to 2-octaprenyl-6-hydroxy-phenol, the fourth step in ubiquinone biosynthesis (By similarity)
TK90_0103	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)
TK90_0115	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)
TK90_0116	ENOG4108R5P	Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery (By similarity)
TK90_0117	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)
TK90_0119	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)
TK90_0121	ENOG4105CU5	Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine (By similarity)
TK90_0125	ENOG4105ECC	imidazole-glycerol-phosphate dehydratase
TK90_0126	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)
TK90_0127	ENOG4105CJV	Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase
TK90_0128	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)
TK90_0129	ENOG4105KPZ	phosphoribosyl-atp pyrophosphatase
TK90_0130	ENOG4105WKS	Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. TatA could form the protein-conducting channel of the Tat system (By similarity)
TK90_0131	ENOG4105X8U	Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. Together with TatC, TatB is part of a receptor directly interacting with Tat signal peptides. TatB may form an oligomeric binding site that transiently accommodates folded Tat precursor proteins before their translocation (By similarity)
TK90_0132	ENOG4105DCX	Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. Together with TatB, TatC is part of a receptor directly interacting with Tat signal peptides (By similarity)
TK90_0133	ENOG4105CJI	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
TK90_0138	ENOG4105BZU	Histidine kinase
TK90_0140	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)
TK90_0141	ENOG4107IX6	phosphate transport regulator
TK90_0142	ENOG4105CJ3	phosphate transporter
TK90_0143	ENOG4105CM1	Catalyzes, together with MoaC, the conversion of 5'-GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
TK90_0144	ENOG4105DB1	molybdopterin oxidoreductase
TK90_0145	ENOG4105QA4	4Fe-4S Ferredoxin, iron-sulfur binding domain protein
TK90_0146	ENOG4108KDI	dmso reductase anchor subunit
TK90_0149	ENOG4105Z6S	cytochrome C, class I
TK90_0150	ENOG4105C0P	Mg chelatase subunit ChlI
TK90_0151	ENOG4105W0Z	cytoplasmic protein
TK90_0154	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)
TK90_0156	ENOG4105D3C	The physiological role of BioH is to remove the methyl group introduced by BioC when the pimeloyl moiety is complete. It allows to synthesize pimeloyl-ACP via the fatty acid synthetic pathway through the hydrolysis of the ester bonds of pimeloyl-ACP esters (By similarity)
TK90_0157	ENOG4106T9E	Converts the free carboxyl group of a malonyl-thioester to its methyl ester by transfer of a methyl group from S-adenosyl- L-methionine (SAM). It allows to synthesize pimeloyl-ACP via the fatty acid synthetic pathway (By similarity)
TK90_0158	ENOG4105EUH	cytochrome C oxidase, cbb3-type, subunit i
TK90_0162	ENOG4105C58	cytochrome c oxidase accessory protein ccog
TK90_0167	ENOG4105DEK	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
TK90_0168	ENOG4105CRP	Part of the ABC transporter FtsEX involved in
TK90_0169	ENOG4105CAK	Cell division ATP-binding protein ftsE
TK90_0170	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)
TK90_0177	ENOG4105C12	Phosphoribosylglycinamide synthetase
TK90_0178	ENOG4105DC1	bifunctional purine biosynthesis protein purh
TK90_0181	ENOG4105DWA	May conjugate Arg from its aminoacyl-tRNA to the N- termini of proteins containing an N-terminal aspartate or glutamate
TK90_0182	ENOG4105C3R	Methionine synthase
TK90_0185	ENOG4105CAS	nag kinase
TK90_0187	ENOG4107RQ2	Cytochrome c oxidase, subunit I
TK90_0190	ENOG4108EGH	Is involved in NO detoxification in an aerobic process, termed nitric oxide dioxygenase (NOD) reaction that utilizes O(2) and NAD(P)H to convert NO to nitrate, which protects the bacterium from various noxious nitrogen compounds. Therefore, plays a central role in the inducible response to nitrosative stress (By similarity)
TK90_0191	ENOG4108Z86	Glutamine amidotransferase
TK90_0193	ENOG4107ZVW	dihydroneopterin aldolase
TK90_0195	ENOG4108YZA	Nitrogen regulatory protein pii
TK90_0197	ENOG4105E2Y	ABC, transporter
TK90_0201	ENOG4105CCX	Catalyzes the production of spermidine from putrescine and decarboxylated S-adenosylmethionine (dcSAM), which serves as an aminopropyl donor (By similarity)
TK90_0202	ENOG4105DP5	Catalyzes the biosynthesis of agmatine from arginine (By similarity)
TK90_0203	ENOG4105VNG	YcgL domain-containing protein
TK90_0224	ENOG4105VDM	plasmid maintenance system antidote protein, xre family
TK90_0225	ENOG4107QX9	Thiol disulfide interChange protein
TK90_0227	ENOG4105D0I	Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate (By similarity)
TK90_0233	ENOG4105DP0	ferredoxin-NADP reductase
TK90_0236	ENOG4107S7U	Sulfide dehydrogenase
TK90_0242	ENOG4105XJC	Two component transcriptional regulator (Winged helix family
TK90_0243	ENOG4105E0F	Histidine kinase
TK90_0244	ENOG4105MWK	D-amino acid dehydrogenase, small subunit
TK90_0245	ENOG4105CQ7	ATP-dependent helicase
TK90_0247	ENOG4105C75	arginyL-tRNA synthetase
TK90_0248	ENOG4105C25	Primosomal protein n'
TK90_0249	ENOG4105C15	The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane (By similarity)
TK90_0250	ENOG4105W8H	transhydrogenase (subunit alpha
TK90_0251	ENOG4108IIE	The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane (By similarity)
TK90_0253	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
TK90_0254	ENOG4105CEV	competence damage-inducible protein
TK90_0256	ENOG4105BZH	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
TK90_0264	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)
TK90_0265	ENOG4105CBC	glutamate synthase
TK90_0267	ENOG4105C4Q	deoxyguanosinetriphosphate triphosphohydrolase-like protein
TK90_0268	ENOG4105D49	3-dehydroquinate synthase
TK90_0269	ENOG4105VCC	30S ribosomal protein S21
TK90_0271	ENOG4105BZ8	glutamate synthase
TK90_0272	ENOG4105CFZ	Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III (By similarity)
TK90_0274	ENOG4108JQC	penicillin-binding protein 1A
TK90_0279	ENOG4105E4G	Type IV pilus
TK90_0280	ENOG4105KHV	Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate (By similarity)
TK90_0284	ENOG4108IFH	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
TK90_0285	ENOG4105CSG	Required to facilitate the formation of correct disulfide bonds in some periplasmic proteins and for the assembly of the periplasmic c-type cytochromes. Acts by transferring electrons from cytoplasmic thioredoxin to the periplasm. This transfer involves a cascade of disulfide bond formation and reduction steps (By similarity)
TK90_0290	ENOG4108YH1	overproduction of this protein in Escherichia coli inhibits the F plasmid-mediated exclusion of bacteriophage T7
TK90_0291	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
TK90_0292	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
TK90_0293	ENOG4105UYK	outer membrane protein a
TK90_0295	ENOG4105MA0	exported protein
TK90_0296	ENOG4105CFU	surface antigen
TK90_0297	ENOG4108UCS	ABC, transporter
TK90_0298	ENOG4107QVT	Binding-protein-dependent transport systems, inner membrane component
TK90_0300	ENOG4105CE6	Adenylation and deadenylation of glutamate--ammonia ligase (By similarity)
TK90_0301	ENOG4105CM2	brancheD-chain amino acid aminotransferase
TK90_0303	ENOG4105DW0	Catalyzes the ADP transfer to D-glycero-D-manno-heptose 1-phosphate, yielding ADP-D,D-heptose (By similarity)
TK90_0304	ENOG4105CUI	Catalyzes the interconversion between ADP-D-glycero- beta-D-manno-heptose and ADP-L-glycero-beta-D-manno-heptose via an epimerization at carbon 6 of the heptose (By similarity)
TK90_0307	ENOG4105DKP	glycosyl transferase, family 9
TK90_0308	ENOG4105D1S	lipid A biosynthesis
TK90_0310	ENOG4105BZ1	(ABC) transporter
TK90_0313	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)
TK90_0316	ENOG4105D9P	serine threonine protein kinase
TK90_0318	ENOG4107543	(lipo)polysaccharide
TK90_0319	ENOG4107RJ7	Glycosyl transferase (Group 1
TK90_0320	ENOG4105XA0	heptosyltransferase ii
TK90_0321	ENOG4105F55	Catalyzes the isomerization of sedoheptulose 7-phosphate in D-glycero-D-manno-heptose 7-phosphate (By similarity)
TK90_0322	ENOG4108ZI0	d,d-heptose 1,7-bisphosphate phosphatase
TK90_0323	ENOG4105D8A	3-Deoxy-D-manno-octulosonic-acid transferase
TK90_0324	ENOG4105GPY	SprT protein
TK90_0326	ENOG4105ZIE	Exonuclease involved in the 3' processing of various precursor tRNAs. Initiates hydrolysis at the 3'-terminus of an RNA molecule and releases 5'-mononucleotides (By similarity)
TK90_0328	ENOG4105VQ7	Rod shape-determining protein MreD
TK90_0329	ENOG4105N3I	Involved in formation and maintenance of cell shape (By similarity)
TK90_0330	ENOG4105DFF	Rod shape-determining protein mreb
TK90_0331	ENOG41080G2	Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) (By similarity)
TK90_0332	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)
TK90_0333	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)
TK90_0334	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)
TK90_0336	ENOG4105D06	uba thif-type nad fad binding protein
TK90_0339	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)
TK90_0340	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
TK90_0341	ENOG4105C7E	Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) (By similarity)
TK90_0342	ENOG4105DJQ	tetratricopeptide tpr_2 repeat protein
TK90_0343	ENOG4105C1U	Plays a critical role in the incorporation of lipoproteins in the outer membrane after they are released by the LolA protein (By similarity)
TK90_0344	ENOG4105CTR	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
TK90_0345	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
TK90_0346	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)
TK90_0347	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
TK90_0348	ENOG4105C3G	gtp-binding protein
TK90_0349	ENOG4105M2J	Glutaredoxin
TK90_0350	ENOG4105DH5	Responsible for the end-turnover of tRNA specifically removes the terminal AMP residue from uncharged tRNA (tRNA-C-C-A). Also appears to be involved in tRNA biosynthesis (By similarity)
TK90_0351	ENOG4105DAQ	Component of the pyruvate dehydrogenase (PDH) complex, that catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2) (By similarity)
TK90_0352	ENOG4107QSN	dihydrolipoamide acetyltransferase
TK90_0353	ENOG4107QN2	dihydrolipoyl dehydrogenase
TK90_0355	ENOG4105CDH	Citrulline--aspartate ligase
TK90_0356	ENOG4105BZU	Histidine kinase
TK90_0357	ENOG410903C	(LipO)protein
TK90_0359	ENOG4105DFU	Cell wall formation (By similarity)
TK90_0360	ENOG4108UMA	3-octaprenyl-4-hydroxybenzoate carboxy-lyase
TK90_0362	ENOG41080RH	Thioredoxin
TK90_0365	ENOG4105C2X	Arabinose 5-phosphate isomerase
TK90_0366	ENOG4108Z4R	3-deoxy-d-manno-octulosonate 8-phosphate phosphatase
TK90_0369	ENOG4108IUZ	ABC transporter
TK90_0370	ENOG4105DTW	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
TK90_0371	ENOG41080QH	sigma 54 modulation protein ribosomal protein S30EA
TK90_0372	ENOG4107RM2	PTS IIA-like nitrogen-regulatory protein PtsN
TK90_0374	ENOG4105C21	Displays ATPase and GTPase activities (By similarity)
TK90_0376	ENOG41080Z8	PHOSPHOCARRIER protein
TK90_0377	ENOG4105CIH	Imidazole acetol-phosphate transaminase
TK90_0378	ENOG4105CEK	Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine (By similarity)
TK90_0379	ENOG4105E99	Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) (By similarity)
TK90_0380	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)
TK90_0381	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
TK90_0383	ENOG4105E3I	toluene tolerance
TK90_0384	ENOG4107PE3	Mammalian cell entry related domain protein
TK90_0385	ENOG4105CY3	ABC transporter, permease
TK90_0386	ENOG4105DHJ	ABC, transporter
TK90_0390	ENOG4105HF0	Membrane
TK90_0391	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
TK90_0392	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)
TK90_0393	ENOG4105DWF	phosphomethylpyrimidine kinase
TK90_0396	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)
TK90_0397	ENOG4108HRM	phosphoenolpyruvate--protein phosphotransferase
TK90_0400	ENOG4105C0N	N-acetylglutamate semialdehyde dehydrogenase
TK90_0403	ENOG4108YX9	iron--sulfur cluster insertion protein erpA
TK90_0404	ENOG4105ED7	Catalyzes the specific phosphorylation of 1,6-anhydro-N- acetylmuramic acid (anhMurNAc) with the simultaneous cleavage of the 1,6-anhydro ring, generating MurNAc-6-P. Is required for the utilization of anhMurNAc either imported from the medium or derived from its own cell wall murein, and thus plays a role in cell wall recycling (By similarity)
TK90_0405	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)
TK90_0408	ENOG4105Q2H	domain protein
TK90_0409	ENOG4105GJM	(LipO)protein
TK90_0410	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
TK90_0412	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
TK90_0413	ENOG4108IAB	Phoh family
TK90_0415	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)
TK90_0416	ENOG4105CTB	Polyprenyl synthetase
TK90_0417	ENOG410868T	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
TK90_0418	ENOG4108RAC	Rubrerythrin
TK90_0423	ENOG4105DNJ	May play a role in the repair of endogenous alkylation damage (By similarity)
TK90_0424	ENOG4108JU6	CBS domain protein
TK90_0425	ENOG4106KVJ	cytochrome C assembly protein
TK90_0426	ENOG4105CB9	Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Binds to the hydrophobic signal sequence of the ribosome-nascent chain (RNC) as it emerges from the ribosomes. The SRP-RNC complex is then targeted to the cytoplasmic membrane where it interacts with the SRP receptor FtsY
TK90_0427	ENOG4105K5M	30s ribosomal protein S16
TK90_0428	ENOG4108ZR6	An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Probably interacts with S19. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes (By similarity)
TK90_0429	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
TK90_0430	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)
TK90_0433	ENOG4108XRS	Monoheme cytochrome SoxX (Sulfur oxidation)
TK90_0434	ENOG4108XRS	Monoheme cytochrome SoxX (Sulfur oxidation)
TK90_0435	ENOG4105CJX	Molecular chaperone. Has ATPase activity (By similarity)
TK90_0436	ENOG4108YZY	peptidylprolyl cis-trans isomerase
TK90_0443	ENOG4108UQY	Iron-storage protein
TK90_0453	ENOG4108ZZ3	UPF0260 protein
TK90_0456	ENOG4105C4F	May be involved in recombinational repair of damaged DNA (By similarity)
TK90_0457	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)
TK90_0458	ENOG4105CI8	Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons (By similarity)
TK90_0459	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
TK90_0460	ENOG4105CFG	Acts as a chaperone (By similarity)
TK90_0461	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)
TK90_0462	ENOG4105BZU	Histidine kinase
TK90_0464	ENOG4105CK3	Lysine 2,3-aminomutase YodO family protein
TK90_0465	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)
TK90_0466	ENOG4105CAP	With EpmB is involved in the beta-lysylation step of the post-translational modification of translation elongation factor P (EF-P). Catalyzes the ATP-dependent activation of (R)-beta-lysine produced by EpmB, forming a lysyl-adenylate, from which the beta- lysyl moiety is then transferred to the epsilon-amino group of a conserved specific lysine residue in EF-P (By similarity)
TK90_0467	ENOG4106HRJ	d-alanyl-d-alanine carboxypeptidase
TK90_0472	ENOG4105C2D	reductase
TK90_0475	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
TK90_0479	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)
TK90_0482	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
TK90_0484	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)
TK90_0485	ENOG4108535	NAD dependent epimerase/dehydratase family
TK90_0486	ENOG4105K5B	UPF0225 protein
TK90_0488	ENOG4105DP0	ferredoxin-NADP reductase
TK90_0489	ENOG4105BZU	Histidine kinase
TK90_0490	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)
TK90_0491	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)
TK90_0492	ENOG4105K8N	protein family UPF0079, ATPase
TK90_0493	ENOG4105C5C	n-acetylmuramoyl-l-alanine amidase
TK90_0494	ENOG4105DC6	This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex (By similarity)
TK90_0495	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)
TK90_0496	ENOG4105KW8	RNA chaperone that binds small regulatory RNA (sRNAs) and mRNAs to facilitate mRNA translational regulation in response to envelope stress, environmental stress and changes in metabolite concentrations. Also binds with high specificity to tRNAs (By similarity)
TK90_0497	ENOG4105C1N	GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis (By similarity)
TK90_0498	ENOG4105E9H	Lytic Murein transglycosylase
TK90_0500	ENOG4108UMW	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
TK90_0501	ENOG4108JDX	DNA polymerase iii, epsilon subunit
TK90_0503	ENOG4105C90	Catalyzes the attachment of proline to tRNA(Pro) in a two-step reaction proline is first activated by ATP to form Pro- AMP and then transferred to the acceptor end of tRNA(Pro). As ProRS can inadvertently accommodate and process non-cognate amino acids such as alanine and cysteine, to avoid such errors it has two additional distinct editing activities against alanine. One activity is designated as 'pretransfer' editing and involves the tRNA(Pro)-independent hydrolysis of activated Ala-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Ala-tRNA(Pro). The misacylated Cys- tRNA(Pro) is not edited by ProRS (By similarity)
TK90_0506	ENOG4105BZS	acriflavin resistance protein
TK90_0510	ENOG4105E1F	short-chain dehydrogenase reductase
TK90_0514	ENOG4105C9M	aspartyl-trna synthetase
TK90_0517	ENOG4105BZU	Histidine kinase
TK90_0521	ENOG4105BZU	Histidine kinase
TK90_0529	ENOG4105BZU	Histidine kinase
TK90_0530	ENOG4105BZU	Histidine kinase
TK90_0531	ENOG4105CQX	Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol (By similarity)
TK90_0532	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)
TK90_0533	ENOG4105BZU	Histidine kinase
TK90_0535	ENOG4105D0M	Protease HtpX homolog
TK90_0536	ENOG4105C5X	domain protein
TK90_0537	ENOG4105BZU	Histidine kinase
TK90_0541	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)
TK90_0542	ENOG4108UJD	30S ribosomal protein S9
TK90_0545	ENOG4105CHG	glycolate oxidase (iron-sulfur subunit)
TK90_0548	ENOG4105E66	phosphoriboisomerase A
TK90_0549	ENOG4105C7B	Threonine dehydratase
TK90_0550	ENOG4107QN2	dihydrolipoyl dehydrogenase
TK90_0552	ENOG4108V3E	phosphoribosylglycinamide formyltransferase
TK90_0553	ENOG4105CXB	phosphoribosylaminoimidazole synthetase
TK90_0555	ENOG4105C02	permease
TK90_0556	ENOG4108KZ1	Mediates the interaction of DNA replication inititator protein DnaA with DNA polymerase subunit beta sliding clamp (dnaN). Stimulates hydrolysis of ATP-DnaA to ADP-DnaA, rendering DnaA inactive for reinititation, a process called regulatory inhibition of DnaA or RIDA (By similarity)
TK90_0558	ENOG4105CS1	NAD(P)H quinone oxidoreductase
TK90_0559	ENOG4105K89	arsenate reductase
TK90_0560	ENOG4105VSY	K01512 acylphosphatase EC 3.6.1.7
TK90_0561	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)
TK90_0562	ENOG4107YD3	Thioesterase
TK90_0563	ENOG4105E02	MotA TolQ exbB proton channel
TK90_0564	ENOG4105M8F	Biopolymer transport protein exbD tolR
TK90_0566	ENOG4107R6Y	Involved in the TonB-independent uptake of proteins (By similarity)
TK90_0567	ENOG4105KCK	Peptidoglycan-associated lipoprotein
TK90_0569	ENOG4107VRB	Catalyzes the conversion of 6-carboxy-5,6,7,8- tetrahydropterin (CPH4) to 7-carboxy-7-deazaguanine (CDG) (By similarity)
TK90_0570	ENOG4105FD2	Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) (By similarity)
TK90_0571	ENOG4105CUC	YeeE YedE family protein
TK90_0572	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
TK90_0573	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)
TK90_0574	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)
TK90_0575	ENOG4105C6P	ATP-dependent serine protease that mediates the selective degradation of mutant and abnormal proteins as well as certain short-lived regulatory proteins. Required for cellular homeostasis and for survival from DNA damage and developmental changes induced by stress. Degrades polypeptides processively to yield small peptide fragments that are 5 to 10 amino acids long. Binds to DNA in a double-stranded, site-specific manner (By similarity)
TK90_0576	ENOG4105K70	DNA-binding protein
TK90_0577	ENOG4105ER2	Ompa motb domain protein
TK90_0578	ENOG4107RD7	Flagellar Motor Protein, MotA
TK90_0580	ENOG4107RHT	methyl-accepting chemotaxis sensory transducer with Pas Pac sensor
TK90_0582	ENOG4105C4E	Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate (By similarity)
TK90_0587	ENOG41081FY	multiple antibiotic resistance (MarC)-related
TK90_0588	ENOG4105C6T	cysteine synthase
TK90_0590	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
TK90_0594	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)
TK90_0595	ENOG4105W49	UPF0434 protein
TK90_0596	ENOG4105CET	Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria (By similarity)
TK90_0597	ENOG4105EIN	peptidylprolyl cis-trans isomerase
TK90_0598	ENOG4105CSJ	Enoyl- acyl-carrier-protein reductase NADH
TK90_0601	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
TK90_0602	ENOG4108JQ5	ABC transporter
TK90_0603	ENOG4105CN0	Catalyzes the oxidation of 5,10- methylenetetrahydrofolate to 5,10-methenyltetrahydrofolate and then the hydrolysis of 5,10-methenyltetrahydrofolate to 10- formyltetrahydrofolate (By similarity)
TK90_0604	ENOG4105BZU	Histidine kinase
TK90_0609	ENOG4105D3Q	Sugar transferase
TK90_0610	ENOG4105CGN	Glycosyl transferase (Group 1
TK90_0611	ENOG4107QQG	Dehydrogenase
TK90_0617	ENOG4105BZ1	(ABC) transporter
TK90_0619	ENOG4105DAY	polysaccharide export protein
TK90_0620	ENOG4105KJF	protein tyrosine phosphatase
TK90_0622	ENOG4105E3R	(LipO)protein
TK90_0628	ENOG4105ERG	peptidase m48, ste24p
TK90_0630	ENOG41082J7	Rhodanese domain protein
TK90_0631	ENOG41082K8	Part of a sulfur-relay system required for 2-thiolation of 5-methylaminomethyl-2-thiouridine (mnm(5)s(2)U) at tRNA wobble positions. Interacts with IscS and stimulates its activity. Then, accepts a sulfur from IscS and transfers it in turn to TusD (By similarity)
TK90_0637	ENOG41086B8	CoB-CoM heterodisulfide reductase
TK90_0638	ENOG4105RQ5	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)
TK90_0640	ENOG4105PHD	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)
TK90_0642	ENOG4105DF9	Lipoate-protein, ligase
TK90_0644	ENOG4105CZF	Catalyzes the conversion of dethiobiotin (DTB) to biotin by the insertion of a sulfur atom into dethiobiotin via a radical- based mechanism (By similarity)
TK90_0652	ENOG4105FAE	von Willebrand factor, type A
TK90_0653	ENOG4105DGU	Histone deacetylase
TK90_0656	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
TK90_0658	ENOG4105D1H	recombination factor protein RarA
TK90_0667	ENOG4105D7T	ABC transporter
TK90_0668	ENOG4108IFG	nitrite reductase, (NAD(P)H)
TK90_0669	ENOG4105KH3	nitrite reductase (NAD(P)h) small subunit
TK90_0671	ENOG4105CB8	Multifunctional enzyme that catalyzes the SAM-dependent methylation of uroporphyrinogen III at position C-2 and C-7 to form precorrin-2 and then position C-12 or C-18 to form trimethylpyrrocorphin 2. It also catalyzes the conversion of precorrin-2 into siroheme. This reaction consists of the NAD- dependent oxidation of precorrin-2 into sirohydrochlorin and its subsequent ferrochelation into siroheme (By similarity)
TK90_0673	ENOG4108IQE	Amp-dependent synthetase and ligase
TK90_0676	ENOG4105C8N	cysteinyl-tRNA synthetase
TK90_0677	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
TK90_0678	ENOG4105BZU	Histidine kinase
TK90_0679	ENOG4108UXN	response regulator
TK90_0680	ENOG4105BZU	Histidine kinase
TK90_0682	ENOG4105EJ9	Membrane
TK90_0683	ENOG4105CKI	cobalamin synthesis protein
TK90_0688	ENOG4105C4H	Specifically methylates the guanine in position 2445 (m2G2445) and the guanine in position 2069 (m7G2069) of 23S rRNA (By similarity)
TK90_0690	ENOG4105CJ1	ABC, transporter
TK90_0693	ENOG4105CF3	3-Hydroxyisobutyrate dehydrogenase
TK90_0694	ENOG4105K3M	)-transporter
TK90_0695	ENOG4105CHQ	Murein-degrading enzyme that degrades murein glycan strands and insoluble, high-molecular weight murein sacculi, with the concomitant formation of a 1,6-anhydromuramoyl product. Lytic transglycosylases (LTs) play an integral role in the metabolism of the peptidoglycan (PG) sacculus. Their lytic action creates space within the PG sacculus to allow for its expansion as well as for the insertion of various structures such as secretion systems and flagella (By similarity)
TK90_0698	ENOG4105C1M	carbamoyl-phosphate synthetase glutamine chain
TK90_0699	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
TK90_0700	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)
TK90_0701	ENOG4105HBR	Rna-binding protein
TK90_0702	ENOG4105F7M	Specifically methylates the uridine in position 2552 of 23S rRNA at the 2'-O position of the ribose in the fully assembled 50S ribosomal subunit (By similarity)
TK90_0703	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)
TK90_0704	ENOG4105EEI	dihydropteroate synthase
TK90_0705	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
TK90_0706	ENOG4105CP7	Triose-phosphate isomerase
TK90_0707	ENOG4107EJC	Preprotein translocase subunit SecG
TK90_0708	ENOG4105KWU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
TK90_0709	ENOG4105ES3	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
TK90_0710	ENOG4105CYU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
TK90_0711	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)
TK90_0713	ENOG4107QIZ	NADH dehydrogenase
TK90_0714	ENOG4107R0R	NADH dehydrogenase subunit g
TK90_0715	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)
TK90_0716	ENOG41081XG	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)
TK90_0717	ENOG4105DF2	NADH dehydrogenase subunit j
TK90_0718	ENOG41080FQ	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)
TK90_0720	ENOG4105C8S	subunit m
TK90_0721	ENOG4105CNR	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
TK90_0723	ENOG4105K7D	Required for maturation of 30S ribosomal subunits (By similarity)
TK90_0724	ENOG4105CHV	Transcription elongation factor NusA
TK90_0725	ENOG4107QHU	One of the essential components for the initiation of protein synthesis. Protects formylmethionyl-tRNA from spontaneous hydrolysis and promotes its binding to the 30S ribosomal subunits. Also involved in the hydrolysis of GTP during the formation of the 70S ribosomal complex (By similarity)
TK90_0726	ENOG4105KG7	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)
TK90_0727	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
TK90_0728	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
TK90_0729	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
TK90_0730	ENOG4107UX3	phosphatidylethanolamine N-methyltransferase
TK90_0731	ENOG4108UGX	Major role in the synthesis of nucleoside triphosphates other than ATP. The ATP gamma phosphate is transferred to the NDP beta phosphate via a ping-pong mechanism, using a phosphorylated active-site intermediate (By similarity)
TK90_0732	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
TK90_0735	ENOG4105CUT	histidyl-tRNA synthetase
TK90_0737	ENOG4105CNE	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane (By similarity)
TK90_0738	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
TK90_0739	ENOG4105CHM	Aminotransferase
TK90_0741	ENOG4105C8J	)-transporter
TK90_0742	ENOG4107QIX	Phosphoglucomutase (EC 5.4.2.2
TK90_0744	ENOG4108RKI	Necessary for the introduction of cis unsaturation into fatty acids. Catalyzes the dehydration of (3R)-3-hydroxydecanoyl- ACP to E-(2)-decenoyl-ACP and then its isomerization to Z-(3)- decenoyl-ACP. Can catalyze the dehydratase reaction for beta- hydroxyacyl-ACPs with saturated chain lengths up to 16 0, being most active on intermediate chain length (By similarity)
TK90_0748	ENOG4105D65	subunit l
TK90_0749	ENOG4105HC0	Na H antiporter
TK90_0750	ENOG4105MKQ	Monovalent cation H antiporter subunit C
TK90_0751	ENOG4108JPZ	Monovalent cation H antiporter subunit D
TK90_0752	ENOG4105SC1	monovalent cation H antiporter subunit E
TK90_0753	ENOG41080TA	Multiple resistance and ph regulation protein f
TK90_0754	ENOG4105KJM	monovalent cation h antiporter subunit g
TK90_0756	ENOG41080HT	Transcriptional regulator, arsr family
TK90_0757	ENOG4107TPS	domain protein
TK90_0761	ENOG4107S90	membrAne
TK90_0765	ENOG4108YYC	ycei family
TK90_0769	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)
TK90_0776	ENOG4108ZCA	Inherit from COG: pyridine nucleotide-disulfide oxidoreductase
TK90_0782	ENOG4105MK2	5-formyltetrahydrofolate cyclo-ligase
TK90_0784	ENOG4105C98	muts2 protein
TK90_0788	ENOG4105CV9	cyclopropane-fatty-acyl-phospholipid synthase
TK90_0791	ENOG4108WBT	adenosyltransferase
TK90_0795	ENOG41068B1	Cob-I-yrinic acid a,c-diamide adenosyltransferase
TK90_0796	ENOG4105C0Y	Responsible for the amidation of carboxylic groups at position A and C of either cobyrinic acid or hydrogenobrynic acid. NH(2) groups are provided by glutamine, and one molecule of ATP is hydrogenolyzed for each amidation (By similarity)
TK90_0797	ENOG4105CB8	Multifunctional enzyme that catalyzes the SAM-dependent methylation of uroporphyrinogen III at position C-2 and C-7 to form precorrin-2 and then position C-12 or C-18 to form trimethylpyrrocorphin 2. It also catalyzes the conversion of precorrin-2 into siroheme. This reaction consists of the NAD- dependent oxidation of precorrin-2 into sirohydrochlorin and its subsequent ferrochelation into siroheme (By similarity)
TK90_0798	ENOG4105EE8	May catalyze the methylation of C-1 in cobalt-precorrin- 5 and the subsequent extrusion of acetic acid from the resulting intermediate to form cobalt-precorrin-6A (By similarity)
TK90_0799	ENOG4105DA5	(ABC) transporter
TK90_0800	ENOG4105E3A	(ABC) transporter
TK90_0802	ENOG41081F0	Precorrin-8x methylmutase
TK90_0803	ENOG4105DVK	Precorrin-2 c20-methyltransferase
TK90_0812	ENOG4105CA0	peroxidase
TK90_0814	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)
TK90_0816	ENOG4107SM8	Adenylate Guanylate cyclase
TK90_0820	ENOG4105CVP	deoxyribo-dipyrimidine photolyase
TK90_0821	ENOG4105EXX	Deoxyribodipyrimidine photolyase-related protein
TK90_0822	ENOG4108XDN	Transcriptional regulator
TK90_0823	ENOG4105C7Z	Conserved Protein
TK90_0826	ENOG4105ECY	inositol monophosphatase
TK90_0828	ENOG4105D7W	serine acetyltransferase
TK90_0829	ENOG4108ZF1	Transcriptional regulator, BadM Rrf2 family
TK90_0830	ENOG4105C3J	Cysteine desulfurase
TK90_0831	ENOG4107XTC	May be involved in the formation or repair of Fe-S clusters present in iron-sulfur proteins
TK90_0832	ENOG4108Z4V	iron-sulfur cluster assembly
TK90_0833	ENOG4108SWN	Co-chaperone involved in the maturation of iron-sulfur cluster-containing proteins. Seems to help targeting proteins to be folded toward HscA (By similarity)
TK90_0834	ENOG4105C9I	Chaperone involved in the maturation of iron-sulfur cluster-containing proteins. Has a low intrinsic ATPase activity which is markedly stimulated by HscB
TK90_0835	ENOG4108ZIT	Ferredoxin, 2FE-2S
TK90_0836	ENOG4105WVQ	Fe-S assembly protein IscX
TK90_0837	ENOG4108JJ7	ABC transporter
TK90_0838	ENOG4106TD9	Diguanylate cyclase
TK90_0839	ENOG4105C9U	ATP-dependent DNA helicase RecQ
TK90_0843	ENOG4105DQW	permease for cytosine purines, uracil, thiamine, allantoin
TK90_0848	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
TK90_0849	ENOG4105BZU	Histidine kinase
TK90_0851	ENOG4106F3G	Catalyzes the tRNA-independent activation of glutamate in presence of ATP and the subsequent transfer of glutamate onto a tRNA(Asp). Glutamate is transferred on the 2-amino-5-(4,5- dihydroxy-2-cyclopenten-1-yl) moiety of the queuosine in the wobble position of the QUC anticodon (By similarity)
TK90_0852	ENOG4108V7X	Transcription factor that acts by binding directly to the RNA polymerase (RNAP). Required for negative regulation of rRNA expression and positive regulation of several amino acid biosynthesis promoters
TK90_0853	ENOG4107S75	HAD-superfamily hydrolase subfamily IA variant 3
TK90_0856	ENOG4105ENT	Efflux transporter rnd family, mfp subunit
TK90_0857	ENOG4105BZS	acriflavin resistance protein
TK90_0858	ENOG4105DT1	RuBisCO catalyzes two reactions the carboxylation of D- ribulose 1,5-bisphosphate, the primary event in carbon dioxide fixation, as well as the oxidative fragmentation of the pentose substrate
TK90_0859	ENOG4108VFZ	ribulose bisphosphate carboxylase, small
TK90_0864	ENOG4105KNY	Microcompartments protein
TK90_0865	ENOG4105KNY	Microcompartments protein
TK90_0866	ENOG4105KNY	Microcompartments protein
TK90_0867	ENOG4108UQY	Iron-storage protein
TK90_0868	ENOG41090A4	Pterin carbinolamine dehydratase
TK90_0869	ENOG4107QJE	Chromosome Partitioning Protein
TK90_0872	ENOG4105FAE	von Willebrand factor, type A
TK90_0873	ENOG4105DUM	transcriptional regulator, lysR family
TK90_0877	ENOG4105C5H	ABC transporter
TK90_0879	ENOG4105EVH	UPF0753 protein
TK90_0884	ENOG41082CG	Protein CrcB homolog
TK90_0885	ENOG41084I6	Protein CrcB homolog
TK90_0886	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)
TK90_0889	ENOG41087PB	Frataxin-like domain
TK90_0890	ENOG4105M08	Membrane
TK90_0893	ENOG4105FFN	Specifically methylates the guanosine in position 1516 of 16S rRNA (By similarity)
TK90_0895	ENOG4105C5I	Dehydrogenase
TK90_0896	ENOG4108MN8	Membrane
TK90_0901	ENOG4105D8X	mechanosensitive ion channel
TK90_0902	ENOG4108VKV	Monofunctional biosynthetic peptidoglycan transglycosylase
TK90_0906	ENOG4105CQX	Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol (By similarity)
TK90_0909	ENOG4105E27	serine threonine protein kinase
TK90_0912	ENOG4105C22	threonyL-tRNA synthetase
TK90_0913	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)
TK90_0914	ENOG41082NX	50s ribosomal protein l35
TK90_0915	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)
TK90_0916	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
TK90_0917	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
TK90_0918	ENOG4108ZUF	This protein is one of the two subunits of integration host factor, a specific DNA-binding protein that functions in genetic recombination as well as in transcriptional and translational control (By similarity)
TK90_0920	ENOG4108T7K	Acts as a flagellar brake, regulating swimming and swarming in a bis-(3'-5') cyclic diguanylic acid (c-di-GMP)- dependent manner. Increasing levels of c-di-GMP lead to decreased motility (By similarity)
TK90_0924	ENOG4107R88	Chemotaxis protein (CheV)
TK90_0925	ENOG4105BZU	Histidine kinase
TK90_0926	ENOG4105K88	Structural component of flagellum, the bacterial motility apparatus. Part of the rod structure of flagellar basal body (By similarity)
TK90_0927	ENOG4108ZC9	flagellar basal-body rod protein flgc
TK90_0928	ENOG4105W00	Flagellar hook capping protein
TK90_0929	ENOG4105BZE	flagellar hook protein, FlgE
TK90_0930	ENOG4108KPB	Flagellar basal-body rod protein FlgF
TK90_0931	ENOG4105CGA	flagellar basal-body rod protein FlgG
TK90_0932	ENOG4107W7W	Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation (By similarity)
TK90_0933	ENOG4105D92	Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation (By similarity)
TK90_0934	ENOG4108ZW7	flagellar rod assembly protein muramidase flgj
TK90_0936	ENOG4105DTJ	flagellar hook-associated protein
TK90_0940	ENOG4108V75	Glutamine amidotransferase
TK90_0941	ENOG41067HS	methyltransferase
TK90_0942	ENOG410902C	phosphohistidine phosphatase, SixA
TK90_0943	ENOG4105C9X	ppx gppa phosphatase
TK90_0944	ENOG4105CUU	Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) (By similarity)
TK90_0945	ENOG4105DBV	ornithine carbamoyltransferase
TK90_0946	ENOG4105C8Y	Acetylornithine aminotransferase
TK90_0947	ENOG4105CK4	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
TK90_0948	ENOG4105C8P	)-transporter
TK90_0949	ENOG4105C8Q	Methyl-accepting chemotaxis
TK90_0953	ENOG4108UTW	Plays a role in the regulation of phosphate uptake
TK90_0954	ENOG4105BZY	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
TK90_0955	ENOG4105C8U	phosphate abc transporter
TK90_0956	ENOG4105C8U	phosphate abc transporter
TK90_0958	ENOG4105BZU	Histidine kinase
TK90_0959	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
TK90_0961	ENOG4108V7B	Catalyzes the reaction of cyanate with bicarbonate to produce ammonia and carbon dioxide (By similarity)
TK90_0962	ENOG4105D7T	ABC transporter
TK90_0964	ENOG4105I5W	Transporter
TK90_0965	ENOG4108JUA	Transcriptional regulator
TK90_0967	ENOG4105I5W	Transporter
TK90_0968	ENOG4105D7T	ABC transporter
TK90_0972	ENOG4107QZF	nitrite reductase NADPH large subunit
TK90_0975	ENOG4105E4C	Lytic transglycosylase catalytic
TK90_0977	ENOG4108194	Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis (By similarity)
TK90_0983	ENOG4105CRK	lysyL-tRNA synthetase
TK90_0987	ENOG4105BZU	Histidine kinase
TK90_0996	ENOG4105BZU	Histidine kinase
TK90_0997	ENOG4105CQB	FAD linked oxidase domain protein
TK90_0999	ENOG4108JPZ	Monovalent cation H antiporter subunit D
TK90_1000	ENOG4108JPZ	Monovalent cation H antiporter subunit D
TK90_1001	ENOG4105CNR	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
TK90_1004	ENOG4105KJM	monovalent cation h antiporter subunit g
TK90_1009	ENOG41083B3	HAD-superfamily subfamily IB hydrolase
TK90_1013	ENOG4106YN8	Prenyltransferase
TK90_1023	ENOG4108Z4U	Ferredoxin
TK90_1024	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)
TK90_1026	ENOG4105BZU	Histidine kinase
TK90_1027	ENOG4105BZU	Histidine kinase
TK90_1028	ENOG4105C1J	atp-dependent rna helicase
TK90_1029	ENOG4108NVR	Methyl-accepting chemotaxis
TK90_1030	ENOG4105KUZ	arsenate reductase
TK90_1031	ENOG4105DMJ	Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate (By similarity)
TK90_1032	ENOG4105CIH	Imidazole acetol-phosphate transaminase
TK90_1035	ENOG41082J7	Rhodanese domain protein
TK90_1040	ENOG410838F	Glycosyl transferase family 2
TK90_1041	ENOG41082J7	Rhodanese domain protein
TK90_1043	ENOG4108151	Beta-lactamase domain protein
TK90_1046	ENOG4105C1J	atp-dependent rna helicase
TK90_1050	ENOG4108R4Z	Functions in the N-end rule pathway of protein degradation where it conjugates Leu, Phe and, less efficiently, Met from aminoacyl-tRNAs to the N-termini of proteins containing an N-terminal arginine or lysine (By similarity)
TK90_1052	ENOG4105CWR	In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance (By similarity)
TK90_1055	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)
TK90_1056	ENOG4105VZ9	UPF0235 protein
TK90_1057	ENOG4105EKE	dihydroorotase
TK90_1059	ENOG4108UVJ	appr-1-p processing domain protein
TK90_1065	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
TK90_1066	ENOG4105CV6	ABC transporter, permease
TK90_1067	ENOG4108I0Y	(ABC) transporter
TK90_1068	ENOG4108UJV	acyl-CoA thioesterase i
TK90_1071	ENOG4106VK6	Flagellar motor protein
TK90_1072	ENOG4105E14	MotA TolQ exbB proton channel
TK90_1073	ENOG4108V0P	LemA family
TK90_1074	ENOG4105D0M	Protease HtpX homolog
TK90_1077	ENOG4105DR5	peptidase
TK90_1078	ENOG4105E3A	(ABC) transporter
TK90_1079	ENOG4105DA5	(ABC) transporter
TK90_1080	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)
TK90_1086	ENOG4105EIF	outer membrane protein W
TK90_1091	ENOG4105BZU	Histidine kinase
TK90_1093	ENOG4107QKV	phosphomannomutase
TK90_1094	ENOG4105CJT	Mannose-1-phosphate guanylyltransferase
TK90_1095	ENOG4105C0B	DNA polymerase III (alpha subunit)
TK90_1105	ENOG41082AG	Plasmid maintenance system antidote protein
TK90_1107	ENOG4108RAV	Conserved protein
TK90_1110	ENOG4105F2I	Transposase
TK90_1119	ENOG4105BZU	Histidine kinase
TK90_1120	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)
TK90_1138	ENOG4105CMM	transposase
TK90_1143	ENOG4107R08	Integrase
TK90_1146	ENOG4107RZC	phospholipase d
TK90_1148	ENOG41085PJ	rdd domain containing protein
TK90_1149	ENOG4107R1Y	fructose-bisphosphate aldolase
TK90_1150	ENOG4105CGH	5'-nucleotidase
TK90_1151	ENOG4105EZ6	Catalyzes the 2'-O-methylation at nucleotide C2498 in 23S rRNA (By similarity)
TK90_1153	ENOG4108ETH	Formylglycinamide ribotide synthetase
TK90_1155	ENOG4108JUA	Transcriptional regulator
TK90_1156	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
TK90_1158	ENOG4105C1F	The M ring may be actively involved in energy transduction (By similarity)
TK90_1159	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)
TK90_1161	ENOG4108JIR	Flagellum-specific ATP synthase
TK90_1163	ENOG4105WF4	Flagellar hook-length control protein
TK90_1165	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)
TK90_1166	ENOG4105DD5	Flagellar motor switch protein
TK90_1167	ENOG4105VTB	flagellar biosynthesis protein fliO
TK90_1168	ENOG4105CN7	Flagellar biosynthetic protein FliP
TK90_1169	ENOG4105VS8	Flagellar biosynthetic protein fliq
TK90_1170	ENOG4105D19	Role in flagellar biosynthesis (By similarity)
TK90_1171	ENOG4105D00	flagellar biosynthetic protein flhB
TK90_1172	ENOG4105D7B	Flagellar biosynthesis protein flha
TK90_1173	ENOG4105FZW	flagellar biosynthesis regulator FlhF
TK90_1175	ENOG4105DN4	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
TK90_1176	ENOG4108VYJ	response regulator receiver protein
TK90_1177	ENOG4108KCC	Plays an important role in bacterial chemotaxis signal transduction pathway by accelerating the dephosphorylation of phosphorylated CheY (CheY-P) (By similarity)
TK90_1178	ENOG4105CBS	Chea signal transduction histidine kinase
TK90_1179	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
TK90_1180	ENOG4105E14	MotA TolQ exbB proton channel
TK90_1181	ENOG4105ER2	Ompa motb domain protein
TK90_1182	ENOG4107QJE	Chromosome Partitioning Protein
TK90_1184	ENOG4108V3W	Chemotaxis protein, CheW
TK90_1187	ENOG4105VM1	flagellar
TK90_1190	ENOG4105C03	ribonuclease
TK90_1191	ENOG4105EI2	Pseudouridine synthase
TK90_1192	ENOG4108VXP	Specifically catalyzes the dephosphorylation of 2- phosphoglycolate. Is involved in the dissimilation of the intracellular 2-phosphoglycolate formed during the DNA repair of 3'-phosphoglycolate ends, a major class of DNA lesions induced by oxidative stress (By similarity)
TK90_1195	ENOG4108JA2	transcriptioN-repair coupling factor
TK90_1197	ENOG4105DWY	Agmatine deiminase
TK90_1199	ENOG4105D60	lipoprotein releasing system transmembrane protein
TK90_1200	ENOG4105CQU	Part of the ABC transporter complex LolCDE involved in the translocation of mature outer membrane-directed lipoproteins, from the inner membrane to the periplasmic chaperone, LolA. Responsible for the formation of the LolA-lipoprotein complex in an ATP-dependent manner (By similarity)
TK90_1202	ENOG4108EQH	DNA internalization-related competence protein ComEC Rec2
TK90_1203	ENOG4105C35	Catalyzes the interconversion of methylthioribose-1- phosphate (MTR-1-P) into methylthioribulose-1-phosphate (MTRu-1-P) (By similarity)
TK90_1204	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)
TK90_1205	ENOG4107QM1	Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine (By similarity)
TK90_1206	ENOG4108JQ1	Dehydrogenase
TK90_1207	ENOG4105CQC	Prephenate dehydratase
TK90_1208	ENOG4105CIH	Imidazole acetol-phosphate transaminase
TK90_1210	ENOG4105CMY	5-enolpyruvylshikimate-3-phosphate synthase
TK90_1212	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)
TK90_1213	ENOG41080YA	This protein is one of the two subunits of integration host factor, a specific DNA-binding protein that functions in genetic recombination as well as in transcriptional and translational control (By similarity)
TK90_1216	ENOG4105CFV	Tetratricopeptide repeat protein
TK90_1217	ENOG4106EG9	Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) (By similarity)
TK90_1218	ENOG4105KQC	Competence protein
TK90_1219	ENOG4105C3Y	UTP-glucose-1-phosphate uridylyltransferase
TK90_1221	ENOG4105C01	Dihydroxy-acid dehydratase
TK90_1223	ENOG4105E09	nadh pyrophosphatase
TK90_1224	ENOG4107W7X	Aldolase
TK90_1225	ENOG4105T86	cytochrome C
TK90_1226	ENOG4105CE2	Aldehyde oxidase and xanthine dehydrogenase, molybdopterin binding
TK90_1232	ENOG4105CDU	Replicative dna helicase
TK90_1241	ENOG4105CHM	Aminotransferase
TK90_1242	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)
TK90_1243	ENOG4107QPA	Cleaves GlcNAc linked beta-1,4 to MurNAc tripeptides (By similarity)
TK90_1245	ENOG4108UGV	hypoxanthine phosphoribosyltransferase
TK90_1246	ENOG4107RHB	Catalyzes the reversible phosphorylation of S-methyl-5'- thioadenosine (MTA) to adenine and 5-methylthioribose-1-phosphate. Involved in the breakdown of MTA, a major by-product of polyamine biosynthesis. Responsible for the first step in the methionine salvage pathway after MTA has been generated from S- adenosylmethionine. Has broad substrate specificity with 6- aminopurine nucleosides as preferred substrates (By similarity)
TK90_1248	ENOG41086KC	Transcriptional regulator
TK90_1250	ENOG4107791	aminotransferase class V
TK90_1252	ENOG4107QRG	dna polymerase iii
TK90_1253	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
TK90_1254	ENOG4105HHA	aminodeoxychorismate lyase
TK90_1257	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
TK90_1258	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
TK90_1259	ENOG4105CHR	reductase
TK90_1260	ENOG4105CJF	Malonyl coA-acyl carrier protein transacylase
TK90_1261	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)
TK90_1262	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
TK90_1263	ENOG4105KAE	Involved in the modulation of the specificity of the ClpAP-mediated ATP-dependent protein degradation (By similarity)
TK90_1266	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
TK90_1267	ENOG41075W9	High frequency lysogenization protein HflD homolog
TK90_1268	ENOG4107QM5	aconitate hydratase
TK90_1271	ENOG4105BZU	Histidine kinase
TK90_1272	ENOG4105C9Q	fumarate hydratase class II
TK90_1273	ENOG4107QTF	adenylosuccinate lyase
TK90_1274	ENOG4105EZE	Cupin 4 family protein
TK90_1275	ENOG4105CEH	Catalyzes the synthesis of dihydrouridine a modified base found in the D-loop of most tRNAs (By similarity)
TK90_1278	ENOG4107T1C	Catalyzes the conversion of GTP to 2,5-diamino-6- ribosylamino-4(3H)-pyrimidinone 5'-phosphate (DARP), formate and pyrophosphate (By similarity)
TK90_1279	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)
TK90_1281	ENOG4105D6E	homoserine dehydrogenase
TK90_1282	ENOG4105CHM	Aminotransferase
TK90_1284	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
TK90_1285	ENOG4108K5P	(LipO)protein
TK90_1286	ENOG4108UM1	dedA family
TK90_1287	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)
TK90_1288	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
TK90_1289	ENOG4105C98	muts2 protein
TK90_1292	ENOG4105BZU	Histidine kinase
TK90_1293	ENOG4106NZV	Responsible for synthesis of pseudouridine from uracil- 13 in transfer RNAs (By similarity)
TK90_1294	ENOG41072GX	Peptidase M22 Glycoprotease
TK90_1295	ENOG4105DVT	helicase
TK90_1297	ENOG4105BZ4	penicillin-binding protein
TK90_1300	ENOG4105K4H	Nlp p60 protein
TK90_1302	ENOG4107RAB	Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA (By similarity)
TK90_1303	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)
TK90_1304	ENOG4105VIE	preprotein translocase, subunit YajC
TK90_1305	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)
TK90_1306	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)
TK90_1314	ENOG4105CQF	Transcriptional regulator
TK90_1316	ENOG4108JJA	ABC, transporter
TK90_1317	ENOG4108Z6B	deaminase
TK90_1318	ENOG4108V06	Glutathione peroxidase
TK90_1321	ENOG4105DHJ	ABC, transporter
TK90_1322	ENOG4105CY3	ABC transporter, permease
TK90_1323	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
TK90_1325	ENOG4105F8C	transglutaminase domain-containing protein
TK90_1326	ENOG4108ZF1	Transcriptional regulator, BadM Rrf2 family
TK90_1327	ENOG4108PXI	ErfK YbiS YcfS YnhG
TK90_1328	ENOG4105CBA	glutamine phosphoribosylpyrophosphate amidotransferase
TK90_1329	ENOG4105E96	Colicin v production protein
TK90_1331	ENOG4105DPM	folylpolyglutamate synthase Dihydrofolate synthase
TK90_1332	ENOG4107QTG	Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl- CoA (By similarity)
TK90_1333	ENOG4105F6H	The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate (By similarity)
TK90_1334	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
TK90_1336	ENOG4108ZGB	N-(5'-phosphoribosyl)anthranilate isomerase
TK90_1337	ENOG4105DI7	Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs (By similarity)
TK90_1340	ENOG4105CM3	Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate (By similarity)
TK90_1341	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)
TK90_1343	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
TK90_1345	ENOG4108MP6	LysR family Transcriptional regulator
TK90_1347	ENOG4105C17	glyceraldehyde-3-phosphate dehydrogenase
TK90_1348	ENOG4105KAV	tspo and mbr like protein
TK90_1356	ENOG4105BZU	Histidine kinase
TK90_1357	ENOG4105DEN	Luciferase family
TK90_1358	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
TK90_1359	ENOG4105KSC	Transcriptional regulator, TraR DksA family
TK90_1364	ENOG4108V5V	Serine Threonine protein kinase
TK90_1369	ENOG4105D44	asparaginase
TK90_1370	ENOG4105EKD	Catalyzes the hydrolytic deamination of adenine to hypoxanthine. Plays an important role in the purine salvage pathway and in nitrogen catabolism (By similarity)
TK90_1372	ENOG4106TD9	Diguanylate cyclase
TK90_1378	ENOG4107QHF	type ii secretion system protein e
TK90_1379	ENOG4105D3Z	quinone oxidoreductase, yhdh yhfp family
TK90_1381	ENOG4107SEY	Conserved Protein
TK90_1382	ENOG4105D78	K07001 NTE family protein
TK90_1387	ENOG4105BZU	Histidine kinase
TK90_1391	ENOG4105VDW	Csbd family
TK90_1396	ENOG4105DAA	L-lactate
TK90_1402	ENOG4107SDU	Methyl-accepting chemotaxis
TK90_1403	ENOG4108NJZ	Sensory box GGDEF EAL domain protein
TK90_1408	ENOG4105DYS	nad(p)h dehydrogenase (quinone)
TK90_1412	ENOG4108UGV	hypoxanthine phosphoribosyltransferase
TK90_1419	ENOG4105EAY	pump that utilizes the energy of pyrophosphate hydrolysis as the driving force for
TK90_1420	ENOG41083IP	HIT family
TK90_1426	ENOG4105BZU	Histidine kinase
TK90_1427	ENOG4108ISG	Major Facilitator
TK90_1441	ENOG4105E05	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
TK90_1442	ENOG4105BZH	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
TK90_1443	ENOG4105C3M	thioredoxin reductase
TK90_1446	ENOG4105MQ3	flagellar protein FliS
TK90_1447	ENOG4105DTS	flagellar hook-associated
TK90_1449	ENOG41063QE	flagellar protein FlaG
TK90_1452	ENOG4105GN9	Joins Ado-cobinamide-GDP and alpha-ribazole to generate adenosylcobalamin (Ado-cobalamin) (By similarity)
TK90_1454	ENOG4105CUP	Catalyzes the synthesis of alpha-ribazole-5'-phosphate from nicotinate mononucleotide (NAMN) and 5,6- dimethylbenzimidazole (DMB) (By similarity)
TK90_1455	ENOG4108YZT	Adenosylcobinamide kinase
TK90_1456	ENOG4105CAA	catalyzes amidations at positions B, D, E, and G on adenosylcobyrinic A,C-diamide. NH(2) groups are provided by glutamine, and one molecule of ATP is hydrogenolyzed for each amidation (By similarity)
TK90_1457	ENOG4105EFT	decarboxylase
TK90_1458	ENOG4105DH2	Converts cobyric acid to cobinamide by the addition of aminopropanol on the F carboxylic group (By similarity)
TK90_1459	ENOG4105E7Q	Cob(II)yrinic acid a,c-diamide reductase
TK90_1460	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)
TK90_1461	ENOG4105EHG	Permease protein
TK90_1462	ENOG4105E0A	ABC, transporter
TK90_1464	ENOG4105EUB	pirin domain protein
TK90_1465	ENOG4107QVN	Key enzyme in the regulation of glycerol uptake and metabolism (By similarity)
TK90_1467	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)
TK90_1468	ENOG4105CE5	Catalyzes the formation of 4-diphosphocytidyl-2-C- methyl-D-erythritol from CTP and 2-C-methyl-D-erythritol 4- phosphate (MEP) (By similarity)
TK90_1469	ENOG4105XX3	Essential cell division protein. May link together the upstream cell division proteins, which are predominantly cytoplasmic, with the downstream cell division proteins, which are predominantly periplasmic (By similarity)
TK90_1470	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
TK90_1471	ENOG4105CXR	Phospho-2-dehydro-3-deoxyoctonate aldolase
TK90_1472	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
TK90_1474	ENOG4106TD9	Diguanylate cyclase
TK90_1478	ENOG4105D3U	Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine (By similarity)
TK90_1479	ENOG4107QM9	Component of the acetyl coenzyme A carboxylase (ACC) complex. First, biotin carboxylase catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the carboxyltransferase to acetyl-CoA to form malonyl-CoA (By similarity)
TK90_1480	ENOG4105C0B	DNA polymerase III (alpha subunit)
TK90_1481	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
TK90_1482	ENOG4105CK5	oxidoreductase
TK90_1484	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)
TK90_1485	ENOG4105DAF	Involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
TK90_1486	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)
TK90_1489	ENOG4105E1Z	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane
TK90_1490	ENOG4105DZP	Membrane-associated zinc metalloprotease
TK90_1492	ENOG4105KNE	Phosphatidate cytidylyltransferase
TK90_1493	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
TK90_1494	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)
TK90_1495	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
TK90_1496	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)
TK90_1497	ENOG4105CE9	30S ribosomal protein S2
TK90_1498	ENOG4105CA1	Removes the N-terminal methionine from nascent proteins (By similarity)
TK90_1499	ENOG4105E1P	Modifies, by uridylylation or deuridylylation the PII (GlnB) regulatory protein (By similarity)
TK90_1505	ENOG4105CS1	NAD(P)H quinone oxidoreductase
TK90_1506	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)
TK90_1507	ENOG4108HWB	Non-specific O-methyltransferase that catalyzes the 2 O- methylation steps in the ubiquinone biosynthetic pathway (By similarity)
TK90_1508	ENOG4108VXP	Specifically catalyzes the dephosphorylation of 2- phosphoglycolate. Is involved in the dissimilation of the intracellular 2-phosphoglycolate formed during the DNA repair of 3'-phosphoglycolate ends, a major class of DNA lesions induced by oxidative stress (By similarity)
TK90_1510	ENOG4105FE1	phytoene synthase
TK90_1511	ENOG4105D4P	Coproporphyrinogen iii oxidase
TK90_1513	ENOG4107S11	squalene-associated FAD-dependent desaturase
TK90_1515	ENOG4105CCT	upf0313 protein
TK90_1518	ENOG4105CBC	glutamate synthase
TK90_1519	ENOG4108S7T	Catalyzes the oxidation of either pyridoxine 5'- phosphate (PNP) or pyridoxamine 5'-phosphate (PMP) into pyridoxal 5'-phosphate (PLP) (By similarity)
TK90_1521	ENOG4105GRZ	Ycii-related protein
TK90_1525	ENOG4105KCV	RNA signal recognition particle 4.5S RNA
TK90_1526	ENOG4105CHP	RNA polymerase
TK90_1527	ENOG4107SBB	4-alpha-glucanotransferase (EC 2.4.1.25)
TK90_1529	ENOG4107QQ4	Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans (By similarity)
TK90_1530	ENOG4105C9C	Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position (By similarity)
TK90_1533	ENOG4105M0J	Toxic component of a toxin-antitoxin (TA) module. A
TK90_1539	ENOG4105D3Q	Sugar transferase
TK90_1549	ENOG4107QRS	glycosyltransferase group 2 family protein
TK90_1550	ENOG4107QQG	Dehydrogenase
TK90_1561	ENOG4105F2I	Transposase
TK90_1575	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)
TK90_1577	ENOG4105CDB	Required for chromosome condensation and partitioning (By similarity)
TK90_1578	ENOG4107YRI	Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1) (By similarity)
TK90_1579	ENOG4107S5T	Carbohydrate kinase
TK90_1581	ENOG4105EXN	Sulfate transport protein CysZ
TK90_1582	ENOG4105EN6	Membrane
TK90_1586	ENOG4105VQD	rieske 2fe-2S domain-containing protein
TK90_1589	ENOG4108UPT	UPF0178 protein
TK90_1593	ENOG4105BZU	Histidine kinase
TK90_1594	ENOG4105BZU	Histidine kinase
TK90_1596	ENOG4105C6Z	Gluconate
TK90_1597	ENOG4105BZQ	cdp-diacylglycerol-glycerol-3-phosphate 3-phosphatidyltransferase
TK90_1598	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)
TK90_1599	ENOG4105E50	uracil-dna glycosylase
TK90_1600	ENOG41080ZE	Adenylate cyclase
TK90_1601	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)
TK90_1602	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)
TK90_1603	ENOG4105VGS	50s ribosomal protein l32
TK90_1605	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
TK90_1606	ENOG4107QSA	Oxaloacetate decarboxylase
TK90_1607	ENOG4108UHJ	MAF-like protein
TK90_1608	ENOG41082YX	Transcriptional regulator, arsr family
TK90_1612	ENOG4105VM8	Could accelerate the degradation of some genes transcripts potentially through selective RNA binding (By similarity)
TK90_1613	ENOG4105CFH	Aspartokinase
TK90_1614	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)
TK90_1616	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)
TK90_1617	ENOG4107TH8	cina domain protein
TK90_1619	ENOG4105D86	that it carries out the mismatch recognition step. This protein has a weak ATPase activity (By similarity)
TK90_1623	ENOG4107QYX	exodeoxyribonuclease v alpha
TK90_1624	ENOG4107QKA	exodeoxyribonuclease V beta
TK90_1625	ENOG4105DSY	exodeoxyribonuclease V, gamma
TK90_1626	ENOG4105D9N	nucleoside
TK90_1627	ENOG4108S6J	ABC transporter, periplasmic molybdate-binding protein
TK90_1628	ENOG4105E0C	molybdate abc transporter
TK90_1629	ENOG4105CGB	Part of the ABC transporter complex ModABC involved in molybdenum import. Responsible for energy coupling to the transport system (By similarity)
TK90_1633	ENOG41082AG	Plasmid maintenance system antidote protein
TK90_1637	ENOG4108F3G	Type I restriction-modification system, R subunit
TK90_1643	ENOG4105ECQ	AraC Family Transcriptional Regulator
TK90_1648	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)
TK90_1650	ENOG4105VCH	membrane
TK90_1652	ENOG4105CEI	nitrite reductase
TK90_1655	ENOG4105M2E	Channel that opens in response to stretch forces in the membrane lipid bilayer. May participate in the regulation of osmotic pressure changes within the cell (By similarity)
TK90_1658	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)
TK90_1663	ENOG4105BZU	Histidine kinase
TK90_1667	ENOG4105BZU	Histidine kinase
TK90_1668	ENOG4105N1F	Hnh endonuclease
TK90_1678	ENOG4108ZAI	phosphatidylglycerophosphatase a
TK90_1679	ENOG4105CG2	Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 (By similarity)
TK90_1680	ENOG4107YIM	Involved in the transcription termination process (By similarity)
TK90_1681	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)
TK90_1683	ENOG4105CCD	The exact function is not known. Can catalyze the reduction of a variety of substrates like dimethyl sulfoxide, trimethylamine N-oxide, phenylmethyl sulfoxide and L-methionine sulfoxide. Cannot reduce cyclic N-oxides. Shows no activity as sulfite oxidase (By similarity)
TK90_1685	ENOG4108UK5	Transposase
TK90_1689	ENOG4105CQU	Part of the ABC transporter complex LolCDE involved in the translocation of mature outer membrane-directed lipoproteins, from the inner membrane to the periplasmic chaperone, LolA. Responsible for the formation of the LolA-lipoprotein complex in an ATP-dependent manner (By similarity)
TK90_1690	ENOG4105CJW	magnesium transporter
TK90_1691	ENOG4105CJW	magnesium transporter
TK90_1708	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)
TK90_1709	ENOG4108XM1	transcriptional regulator AsnC family
TK90_1710	ENOG4105FAV	ABC, transporter
TK90_1711	ENOG4105FDK	ABC transporter
TK90_1712	ENOG4105NXV	High-affinity zinc uptake system protein
TK90_1714	ENOG4105BZU	Histidine kinase
TK90_1715	ENOG4105BZU	Histidine kinase
TK90_1716	ENOG4105CBI	The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor
TK90_1717	ENOG4108V1J	Has antioxidant activity. Could remove peroxides or H(2)O(2) (By similarity)
TK90_1718	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
TK90_1719	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)
TK90_1720	ENOG4105D43	The glycine cleavage system catalyzes the degradation of glycine (By similarity)
TK90_1722	ENOG4105BZG	amino acid carrier protein
TK90_1723	ENOG4105D18	nicotinate-nucleotide pyrophosphorylase
TK90_1724	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)
TK90_1725	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)
TK90_1726	ENOG4105C31	Tryptophanyl-tRNA synthetase
TK90_1728	ENOG4107RTD	sua5 ycio yrdc ywlc family protein
TK90_1729	ENOG4105K9H	YciI-like protein
TK90_1730	ENOG4107TF3	peptidylprolyl cis-trans isomerase
TK90_1735	ENOG4105CSM	endonuclease III
TK90_1740	ENOG4105D10	5-enolpyruvylshikimate-3-phosphate phospholyase
TK90_1743	ENOG4105NXH	GreA GreB family elongation factor
TK90_1744	ENOG41085GJ	domain protein
TK90_1746	ENOG4105RQ5	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)
TK90_1750	ENOG4105BZU	Histidine kinase
TK90_1753	ENOG4105FE9	pseudouridine synthase
TK90_1754	ENOG4108RIR	Molybdenum cofactor biosynthesis protein
TK90_1757	ENOG4107RSM	transcriptional regulator
TK90_1759	ENOG4105ERU	peptidase
TK90_1765	ENOG4105D9I	Responsible for the addition of glutamate residues to the C-terminus of ribosomal protein S6 (By similarity)
TK90_1766	ENOG4105D9I	Responsible for the addition of glutamate residues to the C-terminus of ribosomal protein S6 (By similarity)
TK90_1768	ENOG4105KJP	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
TK90_1770	ENOG4105CPW	cytochrome b561
TK90_1771	ENOG4105DFC	had-superfamily hydrolase, subfamily ia, variant
TK90_1772	ENOG4108YZN	class I peptide chain release factor
TK90_1774	ENOG4105C8A	Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP (By similarity)
TK90_1776	ENOG41080E2	ribosomal-protein-alanine acetyltransferase
TK90_1777	ENOG4108UN4	phage SPO1 DNA polymerase-related protein
TK90_1778	ENOG4106PT6	cdpdiacylglycerol-serine O-phosphatidyltransferase
TK90_1779	ENOG41071I4	Phosphatidylserine decarboxylase proenzyme
TK90_1780	ENOG4105C6M	Alpha-keto-beta-hydroxylacyl reductoisomerase
TK90_1781	ENOG4108ZP8	Acetolactate synthase small subunit
TK90_1782	ENOG4105C7K	acetolactate synthase
TK90_1785	ENOG4105DHP	deoxycytidine triphosphate deaminase
TK90_1787	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)
TK90_1788	ENOG4107QY0	Catalyzes the dehydration of methylthioribulose-1- phosphate (MTRu-1-P) into 2,3-diketo-5-methylthiopentyl-1- phosphate (DK-MTP-1-P) (By similarity)
TK90_1790	ENOG4105DGN	Electron transport complex
TK90_1791	ENOG4108R3D	Electron transport complex
TK90_1793	ENOG4105D6A	Electron transport complex
TK90_1795	ENOG4105DZB	Electron transport complex
TK90_1798	ENOG4105C2W	permease
TK90_1799	ENOG4105EUJ	GTP cyclohydrolase i
TK90_1801	ENOG4108V06	Glutathione peroxidase
TK90_1814	ENOG4108Z9W	Outer membrane porin
TK90_1819	ENOG4105D0A	hydroxylase
TK90_1820	ENOG4105D0A	hydroxylase
TK90_1821	ENOG4107RAQ	aminopeptidase
TK90_1825	ENOG4105W8B	Activator of cell division through the inhibition of FtsZ GTPase activity, therefore promoting FtsZ assembly into bundles of protofilaments necessary for the formation of the division Z ring. It is recruited early at mid-cell but it is not essential for cell division (By similarity)
TK90_1826	ENOG4107Y7W	Participates in the translocation of lipoproteins from the inner membrane to the outer membrane. Only forms a complex with a lipoprotein if the residue after the N-terminal Cys is not an aspartate (The Asp acts as a targeting signal to indicate that the lipoprotein should stay in the inner membrane) (By similarity)
TK90_1827	ENOG4105CNU	cell division protein FtsK
TK90_1831	ENOG4105C3N	Participates in control of cell volume in low-osmolarity conditions (By similarity)
TK90_1832	ENOG4105DS7	Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair (By similarity)
TK90_1833	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)
TK90_1836	ENOG4105VJP	Prevents the cell division inhibition by proteins MinC and MinD at internal division sites while permitting inhibition at polar sites. This ensures cell division at the proper site by restricting the formation of a division septum at the midpoint of the long axis of the cell (By similarity)
TK90_1837	ENOG4107QMS	site-determining protein
TK90_1838	ENOG4105K7U	Cell division inhibitor that blocks the formation of polar Z ring septums. Rapidly oscillates between the poles of the cell to destabilize FtsZ filaments that have formed before they mature into polar Z rings. Prevents FtsZ polymerization (By similarity)
TK90_1840	ENOG4105CV9	cyclopropane-fatty-acyl-phospholipid synthase
TK90_1844	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
TK90_1845	ENOG4105C76	Specifically methylates the 50S ribosomal protein L3 on a specific glutamine residue (By similarity)
TK90_1846	ENOG4105DJ4	phosphatidylserine decarboxylase
TK90_1847	ENOG4108RBP	3'-to-5' exoribonuclease specific for small oligoribonucleotides (By similarity)
TK90_1849	ENOG41090A4	Pterin carbinolamine dehydratase
TK90_1850	ENOG4105E06	May play a role in 30S ribosomal subunit biogenesis. Unusual circulary permuted GTPase that catalyzes rapid hydrolysis of GTP with a slow catalytic turnover (By similarity)
TK90_1852	ENOG4107YU2	histidine triad (hIT) protein
TK90_1853	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)
TK90_1854	ENOG4105KDX	Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection (By similarity)
TK90_1855	ENOG4107QMP	dna polymerase iii subunits gamma and tau
TK90_1856	ENOG4105EHV	domain protein
TK90_1860	ENOG4105VDW	Csbd family
TK90_1863	ENOG4105C2X	Arabinose 5-phosphate isomerase
TK90_1865	ENOG4107QN1	sodium solute
TK90_1868	ENOG4108IQF	Catalyzes the conversion of acetate into acetyl-CoA (AcCoA), an essential intermediate at the junction of anabolic and catabolic pathways. AcsA undergoes a two-step reaction. In the first half reaction, AcsA combines acetate with ATP to form acetyl-adenylate (AcAMP) intermediate. In the second half reaction, it can then transfer the acetyl group from AcAMP to the sulfhydryl group of CoA, forming the product AcCoA (By similarity)
TK90_1869	ENOG4105F4R	Transcriptional regulator mode
TK90_1870	ENOG4105BZU	Histidine kinase
TK90_1873	ENOG41083UI	stage II sporulation protein
TK90_1875	ENOG41083MR	nifu domain-containing protein
TK90_1876	ENOG4105Y75	tpr repeat protein
TK90_1877	ENOG4105E33	succinate dehydrogenase
TK90_1879	ENOG4105N1I	succinate dehydrogenase, hydrophobic membrane anchor protein
TK90_1881	ENOG4106XY2	Folate-binding protein involved in regulating the level of ATP-DnaA and in the modification of some tRNAs. It is probably a key factor in regulatory networks that act via tRNA modification, such as initiation of chromosomal replication (By similarity)
TK90_1883	ENOG4105C66	Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate (By similarity)
TK90_1885	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)
TK90_1886	ENOG4108Z11	Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes (By similarity)
TK90_1887	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)
TK90_1893	ENOG4105EU8	FAD linked oxidase domain protein
TK90_1894	ENOG4105CHG	glycolate oxidase (iron-sulfur subunit)
TK90_1895	ENOG4105C5R	Aminotransferase
TK90_1902	ENOG4105C7Z	Conserved Protein
TK90_1903	ENOG4105C3B	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
TK90_1904	ENOG4105C0V	Provides the sole de novo source of dTMP for DNA biosynthesis (By similarity)
TK90_1906	ENOG4105CY0	Metallo-Beta-Lactamase
TK90_1909	ENOG4108T9Q	UPF0278 protein
TK90_1912	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
TK90_1913	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)
TK90_1915	ENOG4105DVS	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
TK90_1916	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)
TK90_1917	ENOG4108R5K	PPIases accelerate the folding of proteins (By similarity)
TK90_1918	ENOG4105F10	Catalyzes the hydrolysis of the pyrophosphate bond of UDP-2,3-diacylglucosamine to yield 2,3-diacylglucosamine 1- phosphate (lipid X) and UMP (By similarity)
TK90_1922	ENOG41067SE	Tetr family transcriptional regulator
TK90_1923	ENOG4105ED9	Protein of unknown function (DUF455)
TK90_1925	ENOG4105C59	p-type ATPase
TK90_1928	ENOG4105CQX	Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol (By similarity)
TK90_1929	ENOG4105C28	cystathionine
TK90_1930	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
TK90_1931	ENOG4105CDU	Replicative dna helicase
TK90_1932	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
TK90_1934	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)
TK90_1935	ENOG4108ZDX	Binds together with S18 to 16S ribosomal RNA (By similarity)
TK90_1937	ENOG4105C2N	RNA methyltransferase TrmH family group 3
TK90_1938	ENOG4105C40	3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs (By similarity)
TK90_1939	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
TK90_1940	ENOG4105C49	Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine (By similarity)
TK90_1941	ENOG4105EPW	hflc protein
TK90_1942	ENOG4107QJR	hflk protein
TK90_1943	ENOG4105KJV	Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein (By similarity)
TK90_1944	ENOG4105CSZ	Catalyzes the complicated ring closure reaction between the two acyclic compounds 1-deoxy-D-xylulose-5-phosphate (DXP) and 3-amino-2-oxopropyl phosphate (1-amino-acetone-3-phosphate or AAP) to form pyridoxine 5'-phosphate (PNP) and inorganic phosphate (By similarity)
TK90_1945	ENOG41071DT	Involved in DNA repair and RecF pathway recombination (By similarity)
TK90_1947	ENOG4108ZBM	Digests double-stranded RNA. Involved in the processing of primary rRNA transcript to yield the immediate precursors to the large and small rRNAs (23S and 16S). Also processes some mRNAs, and tRNAs when they are encoded in the rRNA operon (By similarity)
TK90_1949	ENOG4105C3F	Signal peptidase i
TK90_1950	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)
TK90_1952	ENOG4105C0H	protease
TK90_1954	ENOG4105VQK	sigma E regulatory protein, MucB RseB
TK90_1956	ENOG4105EMN	RNA polymerase sigma factor
TK90_1957	ENOG4108IYU	L-aspartate oxidase
TK90_1958	ENOG4108EGH	Is involved in NO detoxification in an aerobic process, termed nitric oxide dioxygenase (NOD) reaction that utilizes O(2) and NAD(P)H to convert NO to nitrate, which protects the bacterium from various noxious nitrogen compounds. Therefore, plays a central role in the inducible response to nitrosative stress (By similarity)
TK90_1959	ENOG4105DXN	mazG family
TK90_1960	ENOG4107S76	domain protein
TK90_1966	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)
TK90_1967	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)
TK90_1968	ENOG4108Z43	UPF0250 protein
TK90_1969	ENOG4105F0I	Aminotransferase
TK90_1970	ENOG4105DZ1	carboxypeptidase
TK90_1972	ENOG4105CVE	Lytic murein transglycosylase
TK90_1973	ENOG4105CNI	cell division protein FtsW
TK90_1974	ENOG4105CJN	penicillin-binding protein
TK90_1975	ENOG4105F0N	pyrophosphate phospho-hydrolase
TK90_1976	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)
TK90_1977	ENOG4105E7H	involved in the assembly of LPS in the outer leaflet of the outer membrane. Determines N-hexane tolerance and is involved in outer membrane permeability. Essential for envelope biogenesis (By similarity)
TK90_1978	ENOG4105DBD	Chaperone involved in the correct folding and assembly of outer membrane proteins. Recognizes specific patterns of aromatic residues and the orientation of their side chains, which are found more frequently in integral outer membrane proteins. May act in both early periplasmic and late outer membrane-associated steps of protein maturation (By similarity)
TK90_1979	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)
TK90_1980	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)
TK90_1981	ENOG4105CHC	glucokinase (EC 2.7.1.2)
TK90_1982	ENOG4105NWN	ApaG protein
TK90_1983	ENOG4105DDT	Hydrolyzes diadenosine 5',5'''-P1,P4-tetraphosphate to yield ADP (By similarity)
TK90_1984	ENOG4105CMS	peptidase U62, modulator of DNA gyrase
TK90_1986	ENOG4105D1U	peptidase U62 modulator of DNA gyrase
TK90_1989	ENOG4105C03	ribonuclease
TK90_1993	ENOG4105DUM	transcriptional regulator, lysR family
TK90_1994	ENOG4105BZU	Histidine kinase
TK90_1995	ENOG4105KDC	50s ribosomal protein l28
TK90_1996	ENOG4105W0E	50S ribosomal protein L33
TK90_2000	ENOG4105ERD	Involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. Acts as DNA glycosylase that recognizes and removes damaged bases. Has a preference for oxidized purines, such as 7,8-dihydro-8-oxoguanine (8-oxoG). Has AP (apurinic apyrimidinic) lyase activity and introduces nicks in the DNA strand. Cleaves the DNA backbone by beta-delta elimination to generate a single-strand break at the site of the removed base with both 3'- and 5'-phosphates (By similarity)
TK90_2001	ENOG4105CWR	In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance (By similarity)
TK90_2002	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)
TK90_2003	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
TK90_2004	ENOG4105EAH	synthase
TK90_2005	ENOG4105KK9	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
TK90_2006	ENOG4105K46	50S ribosomal protein l27
TK90_2007	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
TK90_2008	ENOG4105CGT	Catalyzes the transfer of a phosphate group to glutamate to form glutamate 5-phosphate which rapidly cyclizes to 5- oxoproline (By similarity)
TK90_2009	ENOG4105KME	endoribonuclease L-psp
TK90_2010	ENOG4105CB5	ATP-dependent DNA helicase recG
TK90_2011	ENOG4105Y3U	Transglycosylase-associated protein
TK90_2013	ENOG4105CKF	membrane protein involved in aromatic hydrocarbon degradation
TK90_2016	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)
TK90_2017	ENOG4105NHU	Nuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves the cruciform structure in supercoiled DNA by nicking to strands with the same polarity at sites symmetrically opposed at the junction in the homologous arms and leaves a 5'-terminal phosphate and a 3'-terminal hydroxyl group (By similarity)
TK90_2018	ENOG4105CDY	transcriptional regulatory protein
TK90_2019	ENOG4107S0N	DJ-1 family
TK90_2020	ENOG4105CN1	protease
TK90_2021	ENOG41063SB	peptidase
TK90_2022	ENOG41080HT	Transcriptional regulator, arsr family
TK90_2023	ENOG4105C72	UPF0176 protein
TK90_2024	ENOG4105VW4	glutaredoxin 3
TK90_2025	ENOG4105IX2	One of the proteins required for the normal export of preproteins out of the cell cytoplasm. It is a molecular chaperone that binds to a subset of precursor proteins, maintaining them in a translocation-competent state. It also specifically binds to its receptor SecA (By similarity)
TK90_2026	ENOG4105CSF	NADPH-dependent glycerol-3-phosphate dehydrogenase
TK90_2032	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
TK90_2033	ENOG4105DBW	Multi-copper polyphenol oxidoreductase laccase
TK90_2034	ENOG4105C34	Pseudouridine synthase
TK90_2035	ENOG4106SNF	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane
TK90_2036	ENOG4108YZA	Nitrogen regulatory protein pii
TK90_2037	ENOG4105EQR	Transposase IS116 IS110 IS902
TK90_2038	ENOG4105C4K	Nad synthetase
TK90_2040	ENOG4105CMV	Succinyl-CoA synthetase subunit beta
TK90_2041	ENOG4108Z2X	Catalyzes the pyruvoyl-dependent decarboxylation of aspartate to produce beta-alanine (By similarity)
TK90_2042	ENOG4108IAA	Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate (By similarity)
TK90_2043	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
TK90_2045	ENOG4105K8U	2-Amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase
TK90_2046	ENOG4105DJ0	Poly(A) Polymerase
TK90_2048	ENOG4105VEJ	Heat shock protein
TK90_2050	ENOG41090R7	Ferric uptake
TK90_2051	ENOG4105YRI	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane (By similarity)
TK90_2052	ENOG4105VDB	UPF0125 protein
TK90_2053	ENOG4108Z1B	Cyclase dehydrase
TK90_2054	ENOG4105C8J	)-transporter
TK90_2055	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
TK90_2059	ENOG4105C02	permease
TK90_2061	ENOG4105CQ7	ATP-dependent helicase
TK90_2064	ENOG4105CQU	Part of the ABC transporter complex LolCDE involved in the translocation of mature outer membrane-directed lipoproteins, from the inner membrane to the periplasmic chaperone, LolA. Responsible for the formation of the LolA-lipoprotein complex in an ATP-dependent manner (By similarity)
TK90_2066	ENOG4105EQR	Transposase IS116 IS110 IS902
TK90_2074	ENOG4105D7N	magnesium and cobalt transport protein CorA
TK90_2075	ENOG4105C1X	Bifunctional enzyme with both catalase and broad- spectrum peroxidase activity (By similarity)
TK90_2079	ENOG4105EZI	multiple antibiotic resistance (MarC)-related protein
TK90_2085	ENOG4105CC0	LysR family Transcriptional regulator
TK90_2086	ENOG4108VGI	doxx family
TK90_2089	ENOG4105EUB	pirin domain protein
TK90_2092	ENOG4105ERG	peptidase m48, ste24p
TK90_2094	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
TK90_2101	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)
TK90_2102	ENOG4105K63	Thioredoxin
TK90_2103	ENOG4105T95	Thiol disulfide interChange protein
TK90_2104	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)
TK90_2107	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)
TK90_2108	ENOG4105FNP	Molybdopterin-guanine dinucleotide biosynthesis protein b
TK90_2109	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
TK90_2114	ENOG4108M8S	permease YjgP YjgQ family protein
TK90_2115	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)
TK90_2119	ENOG4107QP8	phosphohexose isomerase
TK90_2120	ENOG4105CXW	Synthesizes alpha-1,4-glucan chains using ADP-glucose (By similarity)
TK90_2121	ENOG4105CCA	Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle (By similarity)
TK90_2123	ENOG4107TUY	Histidine kinase
TK90_2124	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
TK90_2125	ENOG4108Z03	MAF-like protein
TK90_2126	ENOG4108UXA	Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA (By similarity)
TK90_2128	ENOG4108Z1W	Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) (By similarity)
TK90_2129	ENOG4105C2S	Catalyzes the NADPH dependent reduction of L-gamma- glutamyl 5-phosphate into L-glutamate 5-semialdehyde and phosphate. The product spontaneously undergoes cyclization to form 1-pyrroline-5-carboxylate (By similarity)
TK90_2132	ENOG4105C8T	Leucyl-tRNA synthetase
TK90_2135	ENOG4105CE8	Transfers the fatty acyl group on membrane lipoproteins (By similarity)
TK90_2136	ENOG4108JU5	Magnesium and cobalt efflux protein
TK90_2137	ENOG4105KGE	Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA (By similarity)
TK90_2138	ENOG4105C9A	Phoh family
TK90_2139	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)
TK90_2140	ENOG4108UUM	single-stranded DNA-binding protein
TK90_2141	ENOG4107RDB	Major Facilitator
TK90_2142	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)
TK90_2143	ENOG4108ZT0	50S ribosomal protein l17
TK90_2144	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
TK90_2145	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)
TK90_2146	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)
TK90_2147	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
TK90_2148	ENOG41067V7	50S ribosomal protein L36
TK90_2149	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)
TK90_2150	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
TK90_2151	ENOG4105VPB	50S ribosomal protein L30
TK90_2152	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)
TK90_2153	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)
TK90_2154	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)
TK90_2155	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)
TK90_2156	ENOG4105VBI	Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site (By similarity)
TK90_2157	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
TK90_2158	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
TK90_2159	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
TK90_2160	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
TK90_2162	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
TK90_2163	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
TK90_2164	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)
TK90_2165	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
TK90_2166	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
TK90_2167	ENOG41080KG	One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome (By similarity)
TK90_2168	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)
TK90_2169	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)
TK90_2170	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
TK90_2171	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
TK90_2172	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)
TK90_2173	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)
TK90_2174	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)
TK90_2175	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
TK90_2176	ENOG4108IIJ	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
TK90_2177	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)
TK90_2178	ENOG4108VZM	50s ribosomal protein L10
TK90_2179	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)
TK90_2180	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
TK90_2181	ENOG4105E5V	Participates in transcription elongation, termination and antitermination (By similarity)
TK90_2182	ENOG4105PM1	preprotein translocase subunit SecE
TK90_2183	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
TK90_2184	ENOG4107QHF	type ii secretion system protein e
TK90_2187	ENOG4108ZQD	Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A (By similarity)
TK90_2188	ENOG4105DHA	Cell division factor that enhances FtsZ-ring assembly. Directly interacts with FtsZ and promotes bundling of FtsZ protofilaments, with a reduction in FtsZ GTPase activity (By similarity)
TK90_2189	ENOG4105M6F	mutator MutT protein
TK90_2190	ENOG4105C5V	Catalyzes two activities which are involved in the cyclic version of arginine biosynthesis the synthesis of N- acetylglutamate from glutamate and acetyl-CoA as the acetyl donor, and of ornithine by transacetylation between N(2)-acetylornithine and glutamate (By similarity)
TK90_2191	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
TK90_2194	ENOG4105C7C	involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
TK90_2195	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)
TK90_2196	ENOG4105CIT	This protein may be involved in anomalous filament growth. May be a component of the septum (By similarity)
TK90_2197	ENOG4105K7E	Essential cell division protein. May link together the upstream cell division proteins, which are predominantly cytoplasmic, with the downstream cell division proteins, which are predominantly periplasmic. May control correct divisome assembly (By similarity)
TK90_2198	ENOG4105CPF	Cell wall formation (By similarity)
TK90_2199	ENOG4105D4A	Cell wall formation (By similarity)
TK90_2200	ENOG4105DFU	Cell wall formation (By similarity)
TK90_2201	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)
TK90_2202	ENOG4105CNI	cell division protein FtsW
TK90_2203	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
TK90_2204	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
TK90_2205	ENOG4108EQQ	Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein (By similarity)
TK90_2206	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)
TK90_2207	ENOG4105CJN	penicillin-binding protein
TK90_2208	ENOG41063Y6	Essential cell division protein. May link together the upstream cell division proteins, which are predominantly cytoplasmic, with the downstream cell division proteins, which are predominantly periplasmic (By similarity)
TK90_2209	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
TK90_2210	ENOG4108V6E	Cell division protein mraZ
TK90_2211	ENOG4105CU0	Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA (By similarity)
TK90_2212	ENOG4105E1C	Regulator of peptidoglycan synthesis that is essential for the function of penicillin-binding protein 1A (PBP1a) (By similarity)
TK90_2213	ENOG41082RQ	UPF0102 protein
TK90_2214	ENOG4105CQB	FAD linked oxidase domain protein
TK90_2215	ENOG4105KB2	stringent starvation protein b
TK90_2216	ENOG4107MKT	Stringent starvation protein a
TK90_2217	ENOG4105EIX	cytochrome c1
TK90_2218	ENOG4105DJ5	Component of the ubiquinol-cytochrome c reductase complex (complex III or cytochrome b-c1 complex), which is a respiratory chain that generates an electrochemical potential coupled to ATP synthesis (By similarity)
TK90_2219	ENOG4108R5F	Component of the ubiquinol-cytochrome c reductase complex (complex III or cytochrome b-c1 complex), which is a respiratory chain that generates an electrochemical potential coupled to ATP synthesis (By similarity)
TK90_2220	ENOG4107QNR	UPF0135 protein
TK90_2221	ENOG4105C0H	protease
TK90_2227	ENOG4105CD8	aminopeptidase N
TK90_2228	ENOG4105F8V	Hydrolase, tatD family
TK90_2231	ENOG4105W2W	Cytotoxic translational repressor of toxin-antitoxin stability system
TK90_2232	ENOG4105D9I	Responsible for the addition of glutamate residues to the C-terminus of ribosomal protein S6 (By similarity)
TK90_2237	ENOG4105M85	Bola protein
TK90_2240	ENOG4107QRT	dEAD DEAH box helicase
TK90_2242	ENOG4105KM4	Acetyl-CoA carboxylase, biotin carboxyl carrier protein
TK90_2243	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
TK90_2244	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
TK90_2246	ENOG4105CEH	Catalyzes the synthesis of dihydrouridine a modified base found in the D-loop of most tRNAs (By similarity)
TK90_2248	ENOG4107TK4	histidinol-phosphate phosphatase
TK90_2254	ENOG4105C4R	Atp-dependent dna helicase
TK90_2255	ENOG4105C3N	Participates in control of cell volume in low-osmolarity conditions (By similarity)
TK90_2259	ENOG4105CJS	Phosphopantothenoylcysteine decarboxylase
TK90_2260	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)
TK90_2261	ENOG4107QXP	Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine (By similarity)
TK90_2262	ENOG4105D8V	Glucose sorbosone dehydrogenase
TK90_2264	ENOG4105NWR	lipid A biosynthesis (Kdo)2-(Lauroyl)-lipid IVA acyltransferase
TK90_2266	ENOG4105D37	Low-affinity potassium transport system. Interacts with Trk system potassium uptake protein TrkA (By similarity)
TK90_2267	ENOG4105C1A	potassium transporter peripheral membrane
TK90_2268	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
TK90_2269	ENOG4105ES5	Histidine kinase
TK90_2271	ENOG4105CYJ	ribosomal RNA small subunit methyltransferase B
TK90_2272	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)
TK90_2273	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)
TK90_2275	ENOG4105C79	DNA protecting protein DprA
TK90_2276	ENOG4108RPN	Protein smg homolog
TK90_2278	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)
TK90_2279	ENOG4105DBS	Key enzyme in heme biosynthesis. Catalyzes the oxidative decarboxylation of propionic acid side chains of rings A and B of coproporphyrinogen III (By similarity)
TK90_2280	ENOG4105D52	delta-aminolevulinic acid dehydratase
TK90_2281	ENOG4105E2X	shikimate dehydrogenase
TK90_2282	ENOG4108ZG0	Ompa motb domain protein
TK90_2283	ENOG4105C4G	Synthesis of 3-octaprenyl-4-hydroxybenzoate (By similarity)
TK90_2284	ENOG4105MJ2	Competence protein
TK90_2286	ENOG4105CZF	Catalyzes the conversion of dethiobiotin (DTB) to biotin by the insertion of a sulfur atom into dethiobiotin via a radical- based mechanism (By similarity)
TK90_2288	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)
TK90_2290	ENOG4105DHF	Membrane
TK90_2291	ENOG4105W5Q	DNA repair protein (RadC
TK90_2292	ENOG4105C01	Dihydroxy-acid dehydratase
TK90_2295	ENOG4107QZM	n-acetylglutamate synthase
TK90_2297	ENOG4108V7X	Transcription factor that acts by binding directly to the RNA polymerase (RNAP). Required for negative regulation of rRNA expression and positive regulation of several amino acid biosynthesis promoters
TK90_2298	ENOG41070EG	Hydrolyzes cAMP to 5'-AMP. Plays an important regulatory role in modulating the intracellular concentration of cAMP, thereby influencing cAMP-dependent processes (By similarity)
TK90_2299	ENOG4105EHM	Aminoglycoside phosphotransferase
TK90_2300	ENOG4108S0S	Nucleotidyl transferase
TK90_2311	ENOG4108S0N	Oxygenase that introduces the hydroxyl group at carbon five of 2-nonaprenyl-3-methyl-6-methoxy-1,4-benzoquinol resulting in the formation of 2-nonaprenyl-3-methyl-5-hydroxy-6-methoxy-1,4- benzoquinol (By similarity)
TK90_2312	ENOG4105Q84	sucrose synthase
TK90_2318	ENOG4105BZU	Histidine kinase
TK90_2319	ENOG4105E0X	reductase
TK90_2320	ENOG4105DXI	Major Facilitator superfamily
TK90_2321	ENOG4105BZS	acriflavin resistance protein
TK90_2322	ENOG4105ENT	Efflux transporter rnd family, mfp subunit
TK90_2323	ENOG4105CHF	Glutathione S-transferase
TK90_2324	ENOG4105D9M	gamma-glutamylcysteine synthetase
TK90_2325	ENOG4107FQX	Alpha-acetolactate decarboxylase
TK90_2327	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)
TK90_2338	ENOG4105C5H	ABC transporter
TK90_2339	ENOG4105BZU	Histidine kinase
TK90_2340	ENOG4105C5Q	Transcriptional regulator
TK90_2342	ENOG4105ECY	inositol monophosphatase
TK90_2343	ENOG4105F8J	Adenylate Guanylate cyclase
TK90_2346	ENOG4105EE6	Alcohol dehydrogenase zinc-binding domain protein
TK90_2351	ENOG4108ZXC	Two component transcriptional regulator, luxr family
TK90_2352	ENOG4105DGM	nitrilase cyanide hydratase and apolipoprotein n-acyltransferase
TK90_2355	ENOG4105FDS	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)
TK90_2356	ENOG4108UKZ	OsmC family
TK90_2357	ENOG4107RYR	Transcriptional regulator, Crp Fnr family
TK90_2358	ENOG4105DK0	Indole-3-glycerol phosphate synthase
TK90_2359	ENOG4108I0Q	anthranilate phosphoribosyltransferase
TK90_2360	ENOG4105C2C	drug resistance transporter, Bcr CflA
TK90_2361	ENOG4105DDQ	anthranilate synthase
TK90_2362	ENOG4105CRQ	synthase (Component I)
TK90_2363	ENOG4108VXP	Specifically catalyzes the dephosphorylation of 2- phosphoglycolate. Is involved in the dissimilation of the intracellular 2-phosphoglycolate formed during the DNA repair of 3'-phosphoglycolate ends, a major class of DNA lesions induced by oxidative stress (By similarity)
TK90_2367	ENOG4107Y49	methyltransferase
TK90_2368	ENOG4105CY8	phosphoribosylaminoimidazole carboxylase atpase subunit
TK90_2369	ENOG4108UM6	Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) (By similarity)
TK90_2373	ENOG4107SC1	transglycosylase
TK90_2374	ENOG4108R99	pseudouridine synthase
TK90_2376	ENOG4105C2M	dna polymerase I
TK90_2377	ENOG4105C80	Catalyzes the reversible oxidation of malate to oxaloacetate (By similarity)
TK90_2378	ENOG4105C6K	Malic enzyme
TK90_2379	ENOG4105ERG	peptidase m48, ste24p
TK90_2381	ENOG4105VFB	Binds the 23S rRNA (By similarity)
TK90_2382	ENOG4105CBM	Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 (By similarity)
TK90_2383	ENOG4105C8V	SAICAR synthetase
TK90_2384	ENOG4105E78	Catalyzes a mechanistically unusual reaction, the ATP- dependent insertion of CO2 between the N7 and N8 nitrogen atoms of 7,8-diaminopelargonic acid (DAPA) to form an ureido ring (By similarity)
TK90_2386	ENOG4105D2N	Aldolase
TK90_2387	ENOG4105CA9	Pyruvate kinase
TK90_2388	ENOG4105BZA	Phosphoglycerate kinase
TK90_2389	ENOG4105C17	glyceraldehyde-3-phosphate dehydrogenase
TK90_2390	ENOG4105CV1	Transketolase (EC 2.2.1.1)
TK90_2391	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
TK90_2392	ENOG4105C3E	May play a key role in the regulation of the intracellular concentration of adenosylhomocysteine (By similarity)
TK90_2393	ENOG4105SYT	Methylenetetrahydrofolate reductase
TK90_2394	ENOG4105QF0	Specifically methylates the N3 position of the uracil ring of uridine 1498 (m3U1498) in 16S rRNA. Acts on the fully assembled 30S ribosomal subunit (By similarity)
TK90_2396	ENOG4105CBS	Chea signal transduction histidine kinase
TK90_2397	ENOG4105C8Q	Methyl-accepting chemotaxis
TK90_2398	ENOG4105YVF	chew protein
TK90_2399	ENOG4105M3Z	response regulator
TK90_2400	ENOG4108UNF	response regulator
TK90_2401	ENOG4105D7Z	glutathione synthase
TK90_2402	ENOG41081YB	ApbE family
TK90_2406	ENOG4108UJU	UPF0301 protein
TK90_2407	ENOG4107Y66	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
TK90_2409	ENOG4105CXT	aspartate transcarbamylase
TK90_2410	ENOG4105CD3	dihydroorotase
TK90_2411	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)
TK90_2412	ENOG4105CZX	twitching motility protein
TK90_2413	ENOG4105CZX	twitching motility protein
TK90_2414	ENOG4105CZX	twitching motility protein
TK90_2415	ENOG4105DFA	alanine racemase domain protein
TK90_2416	ENOG4105II7	pyrroline-5-carboxylate reductase
TK90_2417	ENOG4108RNI	3'(2')5'-bisphosphate nucleotidase
TK90_2418	ENOG4107RK2	ADP-ribose diphosphatase NudE
TK90_2420	ENOG4107Y3D	HAD-superfamily hydrolase subfamily IA variant 3
TK90_2426	ENOG4108VIA	integral membrane protein
TK90_2427	ENOG4105CF9	Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation dephosphorylation (By similarity)
TK90_2428	ENOG4108HRN	Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate (By similarity)
TK90_2429	ENOG4105D9I	Responsible for the addition of glutamate residues to the C-terminus of ribosomal protein S6 (By similarity)
TK90_2432	ENOG4105MYN	Zinc uptake regulation protein
TK90_2436	ENOG4105FDK	ABC transporter
TK90_2439	ENOG4105DZA	Converts GTP to 7,8-dihydroneopterin triphosphate (By similarity)
TK90_2440	ENOG4108V7X	Transcription factor that acts by binding directly to the RNA polymerase (RNAP). Required for negative regulation of rRNA expression and positive regulation of several amino acid biosynthesis promoters
TK90_2441	ENOG4105CKI	cobalamin synthesis protein
TK90_2453	ENOG4105C26	Dehydrogenase
TK90_2455	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
TK90_2456	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)
TK90_2457	ENOG4105DFG	type I secretion outer membrane protein
TK90_2463	ENOG4105CZ1	Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA (By similarity)
TK90_2464	ENOG4105CA8	Catalyzes the rearrangement of 1-deoxy-D-xylulose 5- phosphate (DXP) to produce the thiazole phosphate moiety of thiamine. Sulfur is provided by the thiocarboxylate moiety of the carrier protein ThiS. In vitro, sulfur can be provided by H(2)S (By similarity)
TK90_2465	ENOG4105CA8	Catalyzes the rearrangement of 1-deoxy-D-xylulose 5- phosphate (DXP) to produce the thiazole phosphate moiety of thiamine. Sulfur is provided by the thiocarboxylate moiety of the carrier protein ThiS. In vitro, sulfur can be provided by H(2)S (By similarity)
TK90_2466	ENOG41090R7	Ferric uptake
TK90_2467	ENOG4105C1J	atp-dependent rna helicase
TK90_2468	ENOG4105K63	Thioredoxin
TK90_2469	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)
TK90_2472	ENOG4105CSA	Coproporphyrinogen iii oxidase
TK90_2473	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)
TK90_2474	ENOG4105ED0	Phosphorolytic exoribonuclease that removes nucleotide residues following the -CCA terminus of tRNA and adds nucleotides to the ends of RNA molecules by using nucleoside diphosphates as substrates (By similarity)
TK90_2475	ENOG4105DSJ	YicC domain protein
TK90_2477	ENOG4105VN1	Heat shock protein
TK90_2479	ENOG4105C0H	protease
TK90_2480	ENOG4108ZAF	Molybdopterin
TK90_2481	ENOG4105M00	molybdopterin converting factor, subunit 1
TK90_2482	ENOG4108YXW	Together with MoaA, is involved in the conversion of 5'- GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
TK90_2484	ENOG4105CEN	a g-specific adenine glycosylase
TK90_2485	ENOG4105KMG	Could be a mediator in iron transactions between iron acquisition and iron-requiring processes, such as synthesis and or repair of Fe-S clusters in biosynthetic enzymes (By similarity)
TK90_2486	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)
TK90_2491	ENOG4105M6F	mutator MutT protein
TK90_2492	ENOG4105CFI	type iii restriction protein res subunit
TK90_2497	ENOG4105BZU	Histidine kinase
TK90_2498	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
TK90_2500	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)
TK90_2507	ENOG4108QV3	biosynthesis protein
TK90_2515	ENOG4105CAQ	asparagine synthetase
TK90_2517	ENOG4108PQP	glycosyl transferase group 1
TK90_2518	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)
TK90_2519	ENOG4105DZS	Phenylacetate-CoA ligase
TK90_2521	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
TK90_2524	ENOG4108SHN	Glycosyl transferase, family 2
TK90_2527	ENOG4105BZ1	(ABC) transporter
TK90_2529	ENOG4105CEY	Amp-dependent synthetase and ligase
TK90_2542	ENOG4105EAG	UDP-N-acetylglucosamine 2-epimerase
TK90_2543	ENOG4107QQG	Dehydrogenase
TK90_2546	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)
TK90_2553	ENOG4105C48	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
TK90_2554	ENOG41090X3	Peptidyl-prolyl cis-trans isomerase
TK90_2555	ENOG4105M02	This protein specifically catalyzes the removal of signal peptides from prolipoproteins (By similarity)
TK90_2556	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)
TK90_2557	ENOG4105DTN	riboflavin biosynthesis protein ribF
TK90_2558	ENOG4105CJR	Integral membrane protein (MviN
TK90_2559	ENOG4105VEQ	Cold shock protein
TK90_2561	ENOG4105E0I	Catalyzes the formation of N(4)-acetylcytidine (ac(4)C) at the wobble position of tRNA(Met), by using acetyl-CoA as an acetyl donor and ATP (or GTP) (By similarity)
TK90_2562	ENOG4105C8Q	Methyl-accepting chemotaxis
TK90_2563	ENOG4105C5H	ABC transporter
TK90_2564	ENOG4107YZX	Universal stress protein
TK90_2569	ENOG4105CPC	Aldo Keto reductase
TK90_2570	ENOG4105EYA	deoxyribonuclease
TK90_2571	ENOG4105CUZ	uba thif-type nad fad binding protein
TK90_2574	ENOG4105C38	Glycyl-tRNA synthetase beta subunit
TK90_2575	ENOG4108HMW	glycyl-tRNA synthetase, alpha subunit
TK90_2577	ENOG4105C5F	glutamine synthetase
TK90_2579	ENOG4105CB3	Required for the thiolation of cytidine in position 32 of tRNA, to form 2-thiocytidine (s(2)C32) (By similarity)
TK90_2582	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)
TK90_2584	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
TK90_2585	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)
TK90_2586	ENOG4105KNM	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
TK90_2587	ENOG4105C4J	Produces ATP from ADP in the presence of a proton gradient across the membrane. The catalytic sites are hosted primarily by the beta subunits (By similarity)
TK90_2588	ENOG4105J80	Produces ATP from ADP in the presence of a proton gradient across the membrane. The gamma chain is believed to be important in regulating ATPase activity and the flow of protons through the CF(0) complex (By similarity)
TK90_2589	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
TK90_2590	ENOG4107S15	F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation (By similarity)
TK90_2591	ENOG4107Z6K	F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation (By similarity)
TK90_2592	ENOG4105KY6	F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation (By similarity)
TK90_2593	ENOG4107RAZ	it plays a direct role in the translocation of protons across the membrane (By similarity)
TK90_2595	ENOG4105FA0	parb-like partition protein
TK90_2596	ENOG4107QJE	Chromosome Partitioning Protein
TK90_2597	ENOG4105D28	Specifically methylates the N7 position of a guanine in 16S rRNA (By similarity)
TK90_2598	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)
TK90_2599	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)
TK90_2600	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
TK90_2601	ENOG4105VAS	Could be involved in insertion of integral membrane proteins into the membrane (By similarity)
TK90_2602	ENOG4105NVJ	RNaseP catalyzes the removal of the 5'-leader sequence from pre-tRNA to produce the mature 5'-terminus. It can also cleave other RNA substrates such as 4.5S RNA. The protein component plays an auxiliary but essential role in vivo by binding to the 5'-leader sequence and broadening the substrate specificity of the ribozyme (By similarity)
TK90_2603	ENOG4105VG0	50S ribosomal protein l34
TK90_2647	ENOG4108ESY	Metal dependent phosphohydrolase
TK90_2687	ENOG4105BZU	Histidine kinase
TK90_2689	ENOG4105D7V	transposase
TK90_2695	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)
TK90_2717	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)
TK90_2753	ENOG41090GG	peptidase S8 and S53, subtilisin, kexin, sedolisin
TK90_2756	ENOG4107QX8	SPFH domain, Band 7 family protein
TK90_2768	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)
TK90_2770	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)
TK90_2775	ENOG4105FA0	parb-like partition protein
TK90_2792	ENOG4105CFI	type iii restriction protein res subunit
TK90_2808	ENOG4105BZU	Histidine kinase
TK90_2811	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
TK90_2813	ENOG4105CB5	ATP-dependent DNA helicase recG
TK90_2827	ENOG4106S48	Murein-degrading enzyme. May play a role in recycling of muropeptides during cell elongation and or cell division
TK90_2833	ENOG4107QHF	type ii secretion system protein e
TK90_2840	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)
TK90_2844	ENOG4105VM8	Could accelerate the degradation of some genes transcripts potentially through selective RNA binding (By similarity)
TK90_2848	ENOG4105C4R	Atp-dependent dna helicase
TK90_2855	ENOG4107QHF	type ii secretion system protein e
TK90_2860	ENOG4107QHF	type ii secretion system protein e
TK90_2866	ENOG4105BZU	Histidine kinase
TK90_2879	ENOG4107SKI	cobyrinic Acid a,c-diamide synthase