locus-tag	class	description
IMCC26256_111	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)
IMCC26256_111000	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)
IMCC26256_111001	ENOG4108Z08	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
IMCC26256_111002	ENOG4105HHA	aminodeoxychorismate lyase
IMCC26256_111003	ENOG4105E2X	shikimate dehydrogenase
IMCC26256_111005	ENOG4107QHF	type ii secretion system protein e
IMCC26256_111006	ENOG4105CZX	twitching motility protein
IMCC26256_111010	ENOG4106855	Competence protein
IMCC26256_111016	ENOG4105D10	5-enolpyruvylshikimate-3-phosphate phospholyase
IMCC26256_111017	ENOG4105KHV	Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate (By similarity)
IMCC26256_111018	ENOG4105D49	3-dehydroquinate synthase
IMCC26256_111019	ENOG4108Z38	Catalyzes a trans-dehydration via an enolate intermediate (By similarity)
IMCC26256_111020	ENOG4105DC7	peptidase M24
IMCC26256_111021	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)
IMCC26256_111022	ENOG410803B	Involved in the transcription termination process (By similarity)
IMCC26256_111025	ENOG4108UK1	Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant (By similarity)
IMCC26256_111026	ENOG4105CXT	aspartate transcarbamylase
IMCC26256_111027	ENOG4105CD3	dihydroorotase
IMCC26256_111028	ENOG4105C1M	carbamoyl-phosphate synthetase glutamine chain
IMCC26256_111029	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
IMCC26256_11103	ENOG4105CEC	DNA methylase N-4 N-6
IMCC26256_111030	ENOG4107RY0	Catalyzes the conversion of dihydroorotate to orotate (By similarity)
IMCC26256_111031	ENOG4106EG9	Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) (By similarity)
IMCC26256_111033	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
IMCC26256_111034	ENOG4105MTQ	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)
IMCC26256_111036	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
IMCC26256_111038	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)
IMCC26256_111039	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)
IMCC26256_111040	ENOG4105CYJ	ribosomal RNA small subunit methyltransferase B
IMCC26256_111043	ENOG4108YXW	Together with MoaA, is involved in the conversion of 5'- GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
IMCC26256_111045	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)
IMCC26256_111046	ENOG4108R6K	riboflavin synthase, subunit alpha
IMCC26256_111047	ENOG4105C66	Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate (By similarity)
IMCC26256_111048	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)
IMCC26256_111049	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)
IMCC26256_111052	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)
IMCC26256_111053	ENOG41084BS	50S ribosomal protein L35
IMCC26256_111054	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)
IMCC26256_111056	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
IMCC26256_111057	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
IMCC26256_111058	ENOG4105C0N	N-acetylglutamate semialdehyde dehydrogenase
IMCC26256_111059	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)
IMCC26256_111060	ENOG4105CAS	nag kinase
IMCC26256_111061	ENOG4105C8Y	Acetylornithine aminotransferase
IMCC26256_111062	ENOG4105DBV	ornithine carbamoyltransferase
IMCC26256_111063	ENOG4105XBY	Regulates arginine biosynthesis genes (By similarity)
IMCC26256_111064	ENOG4105CDH	Citrulline--aspartate ligase
IMCC26256_111065	ENOG4105CH7	arginosuccinase
IMCC26256_111066	ENOG4106A3M	Cytochrome p-450
IMCC26256_111067	ENOG4108JQC	penicillin-binding protein 1A
IMCC26256_111068	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)
IMCC26256_111075	ENOG4105EXC	Acyl-transferase
IMCC26256_111078	ENOG4108HWB	Non-specific O-methyltransferase that catalyzes the 2 O- methylation steps in the ubiquinone biosynthetic pathway (By similarity)
IMCC26256_111088	ENOG4105DI2	Pyruvate flavodoxin ferredoxin oxidoreductase domain protein
IMCC26256_111089	ENOG4105DQU	oxidoreductase, subunit beta
IMCC26256_111094	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)
IMCC26256_111095	ENOG4105C4F	May be involved in recombinational repair of damaged DNA (By similarity)
IMCC26256_11110	ENOG4105VM8	Could accelerate the degradation of some genes transcripts potentially through selective RNA binding (By similarity)
IMCC26256_111101	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
IMCC26256_111104	ENOG4108Z4T	Peptidase M50
IMCC26256_111106	ENOG4105C31	Tryptophanyl-tRNA synthetase
IMCC26256_111108	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)
IMCC26256_111109	ENOG4105FE9	pseudouridine synthase
IMCC26256_111112	ENOG4105CMY	5-enolpyruvylshikimate-3-phosphate synthase
IMCC26256_111115	ENOG4105C48	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
IMCC26256_111117	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
IMCC26256_111118	ENOG4107QX3	carboxylase
IMCC26256_111120	ENOG4106A3M	Cytochrome p-450
IMCC26256_111126	ENOG4105BZQ	cdp-diacylglycerol-glycerol-3-phosphate 3-phosphatidyltransferase
IMCC26256_111127	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)
IMCC26256_111128	ENOG4108UW8	fha domain-containing protein
IMCC26256_11113	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)
IMCC26256_111132	ENOG4105D43	The glycine cleavage system catalyzes the degradation of glycine (By similarity)
IMCC26256_111133	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
IMCC26256_111137	ENOG4105CE8	Transfers the fatty acyl group on membrane lipoproteins (By similarity)
IMCC26256_111139	ENOG4108P8V	Thymidylate synthase complementing protein ThyX
IMCC26256_111143	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)
IMCC26256_111144	ENOG41067S4	Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. TatA could form the protein-conducting channel of the Tat system (By similarity)
IMCC26256_111152	ENOG4105DVV	Catalyzes the covalent attachment of the prokaryotic ubiquitin-like protein modifier Pup to the proteasomal substrate proteins, thereby targeting them for proteasomal degradation. This tagging system is termed pupylation. The ligation reaction involves the side-chain carboxylate of the C-terminal glutamate of Pup and the side-chain amino group of a substrate lysine (By similarity)
IMCC26256_111153	ENOG4105F7N	Component of the proteasome core, a large protease complex with broad specificity involved in protein degradation (By similarity)
IMCC26256_111154	ENOG4105KPK	Component of the proteasome core, a large protease complex with broad specificity involved in protein degradation (By similarity)
IMCC26256_111156	ENOG4105E5F	proteasome
IMCC26256_111157	ENOG4105DHM	ATPase which is responsible for recognizing, binding, unfolding and translocation of pupylated proteins into the bacterial 20S proteasome core particle. May be essential for opening the gate of the 20S proteasome via an interaction with its C-terminus, thereby allowing substrate entry and access to the site of proteolysis. Thus, the C-termini of the proteasomal ATPase may function like a 'key in a lock' to induce gate opening and therefore regulate proteolysis (By similarity)
IMCC26256_111163	ENOG4105CB3	Required for the thiolation of cytidine in position 32 of tRNA, to form 2-thiocytidine (s(2)C32) (By similarity)
IMCC26256_111173	ENOG4105CV1	Transketolase (EC 2.2.1.1)
IMCC26256_111174	ENOG4107QQX	Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway (By similarity)
IMCC26256_111175	ENOG4105DKF	Catalyzes the radical-mediated transfer of the hydroxybenzyl group from 4-hydroxyphenylpyruvate (HPP) to 5-amino- 6-ribitylamino-2,4(1H,3H)-pyrimidinedione to form 7,8-didemethyl- 8-hydroxy-5-deazariboflavin (FO) (By similarity)
IMCC26256_111179	ENOG4108JWX	
IMCC26256_111180	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
IMCC26256_111181	ENOG4105F1R	Converts heme B (protoheme IX) to heme O by substitution of the vinyl group on carbon 2 of heme B porphyrin ring with a hydroxyethyl farnesyl side group (By similarity)
IMCC26256_111182	ENOG4107QXG	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
IMCC26256_111187	ENOG4105CC9	acyl-Coa dehydrogenase
IMCC26256_111190	ENOG4105BZU	Histidine kinase
IMCC26256_111193	ENOG4105CC9	acyl-Coa dehydrogenase
IMCC26256_111197	ENOG4107SGF	Catalyzes the oxidation of the C8 methyl side group on heme O porphyrin ring into a formyl group (By similarity)
IMCC26256_1112	ENOG4108KQJ	Type 11 methyltransferase
IMCC26256_111200	ENOG4105CJP	fad dependent oxidoreductase
IMCC26256_111203	ENOG4105D8C	Channel that permits osmotically driven movement of water in both directions. It is involved in the osmoregulation and in the maintenance of cell turgor during volume expansion in rapidly growing cells. It mediates rapid entry or exit of water in response to abrupt changes in osmolarity (By similarity)
IMCC26256_111213	ENOG4108JQ7	(ABC) transporter
IMCC26256_111214	ENOG4105C3U	ABC transporter
IMCC26256_111215	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
IMCC26256_111219	ENOG4105CP7	Triose-phosphate isomerase
IMCC26256_111220	ENOG4105BZA	Phosphoglycerate kinase
IMCC26256_111221	ENOG4105C17	glyceraldehyde-3-phosphate dehydrogenase
IMCC26256_111222	ENOG4105C21	Displays ATPase and GTPase activities (By similarity)
IMCC26256_111223	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)
IMCC26256_111224	ENOG4105D0I	Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate (By similarity)
IMCC26256_111225	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)
IMCC26256_111226	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)
IMCC26256_111227	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)
IMCC26256_111228	ENOG4108ZQD	Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A (By similarity)
IMCC26256_111229	ENOG4105WH1	Two component transcriptional regulator luxr family
IMCC26256_111231	ENOG4108HWB	Non-specific O-methyltransferase that catalyzes the 2 O- methylation steps in the ubiquinone biosynthetic pathway (By similarity)
IMCC26256_111235	ENOG4105C1G	acyl-Coa dehydrogenase
IMCC26256_111238	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
IMCC26256_111243	ENOG4105F6H	The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate (By similarity)
IMCC26256_111245	ENOG4108ZGB	N-(5'-phosphoribosyl)anthranilate isomerase
IMCC26256_111246	ENOG4105DK0	Indole-3-glycerol phosphate synthase
IMCC26256_111247	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)
IMCC26256_111248	ENOG4105CRQ	synthase (Component I)
IMCC26256_111249	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
IMCC26256_11125	ENOG4108J2R	molybdopterin oxidoreductase
IMCC26256_111252	ENOG4105CJV	Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase
IMCC26256_111253	ENOG4105ECC	imidazole-glycerol-phosphate dehydratase
IMCC26256_111254	ENOG4105CIH	Imidazole acetol-phosphate transaminase
IMCC26256_111255	ENOG4105CEK	Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine (By similarity)
IMCC26256_111258	ENOG4108RTV	Catalyzes the transfer of acetyl from acetyl-CoA to desacetylmycothiol (Cys-GlcN-Ins) to form mycothiol (By similarity)
IMCC26256_111259	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
IMCC26256_11126	ENOG4105EXC	Acyl-transferase
IMCC26256_111262	ENOG4105C7Z	Conserved Protein
IMCC26256_111264	ENOG4106A3M	Cytochrome p-450
IMCC26256_11127	ENOG4107RBB	ABC transporter, permease
IMCC26256_111273	ENOG4105BZU	Histidine kinase
IMCC26256_11128	ENOG4105D6C	Part of the ABC transporter complex MacAB involved in macrolide export. Transmembrane domains (TMD) form a pore in the inner membrane and the ATP-binding domain (NBD) is responsible for energy generation (By similarity)
IMCC26256_111283	ENOG4105DNJ	May play a role in the repair of endogenous alkylation damage (By similarity)
IMCC26256_111289	ENOG4105FBW	Monooxygenase
IMCC26256_111290	ENOG4107ZFB	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)
IMCC26256_111291	ENOG4107TSN	permease
IMCC26256_111294	ENOG4105C11	sulfate adenylyltransferase), subunit 2
IMCC26256_111297	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)
IMCC26256_111300	ENOG4106N3V	dolichyl-phosphate beta-D-mannosyltransferase (EC 2.4.1.83)
IMCC26256_111309	ENOG4107TK4	histidinol-phosphate phosphatase
IMCC26256_11131	ENOG4105E6M	Sulphatase-modifying factor protein
IMCC26256_111310	ENOG4105CHU	acetyl-coa acetyltransferase
IMCC26256_111312	ENOG4107B57	rieske 2fe-2S domain-containing protein
IMCC26256_111314	ENOG4107RPC	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
IMCC26256_111315	ENOG4105C9X	ppx gppa phosphatase
IMCC26256_111318	ENOG4105BZU	Histidine kinase
IMCC26256_111319	ENOG4107QX3	carboxylase
IMCC26256_111320	ENOG4105D2B	acyl-CoA dehydrogenase
IMCC26256_111321	ENOG4105CC9	acyl-Coa dehydrogenase
IMCC26256_111322	ENOG4105M2Z	protein tyrosine serine phosphatase
IMCC26256_111325	ENOG4105C26	Dehydrogenase
IMCC26256_111327	ENOG41061TZ	Short-chain dehydrogenase reductase Sdr
IMCC26256_111329	ENOG4108Z86	Glutamine amidotransferase
IMCC26256_111330	ENOG4107R6G	Catalyzes the S-adenosylmethionine monomethyl esterification of trans-aconitate (By similarity)
IMCC26256_111331	ENOG4108QIU	Dehydrogenase
IMCC26256_111333	ENOG4105CEY	Amp-dependent synthetase and ligase
IMCC26256_111334	ENOG41061TZ	Short-chain dehydrogenase reductase Sdr
IMCC26256_111335	ENOG4105CEY	Amp-dependent synthetase and ligase
IMCC26256_111341	ENOG4105D4R	Catalyzes the desulfonation of aliphatic sulfonates (By similarity)
IMCC26256_111345	ENOG4105CEY	Amp-dependent synthetase and ligase
IMCC26256_111347	ENOG4105CEY	Amp-dependent synthetase and ligase
IMCC26256_111348	ENOG4105DYT	3-hydroxyacyl-CoA dehydrogenase
IMCC26256_111349	ENOG4105CF8	branched-chain amino acid ABC transporter, permease
IMCC26256_111350	ENOG4108IV0	ABC, transporter
IMCC26256_111353	ENOG4105EVB	acetyltransferase
IMCC26256_111355	ENOG4105CHU	acetyl-coa acetyltransferase
IMCC26256_111356	ENOG4108Z0R	Transferase
IMCC26256_111360	ENOG4105EBR	Carboxylesterase
IMCC26256_111362	ENOG41061TZ	Short-chain dehydrogenase reductase Sdr
IMCC26256_111363	ENOG4105CHR	reductase
IMCC26256_111365	ENOG4105DYW	oxidoreductase
IMCC26256_111367	ENOG4105CC9	acyl-Coa dehydrogenase
IMCC26256_111370	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)
IMCC26256_111372	ENOG4105CBC	glutamate synthase
IMCC26256_111373	ENOG4105C1G	acyl-Coa dehydrogenase
IMCC26256_111377	ENOG410846T	CoA-transferase family III
IMCC26256_111381	ENOG4105IQ5	FAD linked oxidase domain protein
IMCC26256_111383	ENOG41083B3	HAD-superfamily subfamily IB hydrolase
IMCC26256_111385	ENOG4107QIW	Catalytic subunit of the periplasmic nitrate reductase (NAP). Only expressed at high levels during aerobic growth. NapAB complex receives electrons from the membrane-anchored tetraheme protein NapC, thus allowing electron flow between membrane and periplasm. Essential function for nitrate assimilation and may have a role in anaerobic metabolism (By similarity)
IMCC26256_111386	ENOG4108RW0	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
IMCC26256_111387	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)
IMCC26256_11139	ENOG4107TBN	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
IMCC26256_111396	ENOG4105DB9	Binding-protein-dependent transport systems inner membrane component
IMCC26256_111398	ENOG4105C10	Electron transfer flavoprotein
IMCC26256_11140	ENOG4105D6C	Part of the ABC transporter complex MacAB involved in macrolide export. Transmembrane domains (TMD) form a pore in the inner membrane and the ATP-binding domain (NBD) is responsible for energy generation (By similarity)
IMCC26256_111403	ENOG4105D8C	Channel that permits osmotically driven movement of water in both directions. It is involved in the osmoregulation and in the maintenance of cell turgor during volume expansion in rapidly growing cells. It mediates rapid entry or exit of water in response to abrupt changes in osmolarity (By similarity)
IMCC26256_111409	ENOG4108I0Q	anthranilate phosphoribosyltransferase
IMCC26256_11141	ENOG4107R34	abc transporter permease protein
IMCC26256_111410	ENOG4105K51	Acts as a transcriptional regulator. Probably redox- responsive. The apo- but not holo-form probably binds DNA (By similarity)
IMCC26256_111414	ENOG410684T	prevent-host-death family
IMCC26256_111415	ENOG4105VG9	Plasmid stabilization system
IMCC26256_11142	ENOG4108UM6	Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) (By similarity)
IMCC26256_111429	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)
IMCC26256_11143	ENOG4105EA8	2-Nitropropane dioxygenase
IMCC26256_111430	ENOG4105CVJ	phosphoglycerate mutase
IMCC26256_111432	ENOG4105CVJ	phosphoglycerate mutase
IMCC26256_111434	ENOG4108JQC	penicillin-binding protein 1A
IMCC26256_11144	ENOG4105C0K	Gdp-mannose 4,6-dehydratase
IMCC26256_111446	ENOG4105ECY	inositol monophosphatase
IMCC26256_111447	ENOG4105ECY	inositol monophosphatase
IMCC26256_111448	ENOG4107QKC	Oxidoreductase alpha (molybdopterin) subunit
IMCC26256_111449	ENOG4107H9G	Necessary for formate dehydrogenase activity (By similarity)
IMCC26256_111452	ENOG4105KZX	Pterin carbinolamine dehydratase
IMCC26256_111453	ENOG4105RX7	peptidase S8 and S53, subtilisin, kexin, sedolisin
IMCC26256_111459	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
IMCC26256_111460	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)
IMCC26256_111461	ENOG4105C4Q	deoxyguanosinetriphosphate triphosphohydrolase-like protein
IMCC26256_111462	ENOG4108HRN	Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate (By similarity)
IMCC26256_111463	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)
IMCC26256_111464	ENOG4105D9H	Catalyzes the attachment of glycine to tRNA(Gly) (By similarity)
IMCC26256_111465	ENOG4106DBE	Involved in DNA repair and RecF pathway recombination (By similarity)
IMCC26256_111466	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
IMCC26256_111471	ENOG4105CCU	oxidase (Subunit III)
IMCC26256_111473	ENOG4105CV4	Subunits I and II form the functional core of the enzyme complex. Electrons originating in cytochrome c are transferred via heme a and Cu(A) to the binuclear center formed by heme a3 and Cu(B) (By similarity)
IMCC26256_111474	ENOG4105CWT	An essential GTPase that binds both GDP and GTP, with rapid nucleotide exchange. Plays a role in 16S rRNA processing and 30S ribosomal subunit biogenesis and possibly also in cell cycle regulation and energy metabolism (By similarity)
IMCC26256_111476	ENOG4107VNR	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)
IMCC26256_111479	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)
IMCC26256_111480	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)
IMCC26256_111481	ENOG4105CI8	Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons (By similarity)
IMCC26256_111483	ENOG4105D2B	acyl-CoA dehydrogenase
IMCC26256_111484	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)
IMCC26256_111485	ENOG4105KQV	Binds directly to 16S ribosomal RNA (By similarity)
IMCC26256_111489	ENOG41083P1	competence protein ComEA helix-hairpin-helix repeat protein
IMCC26256_111490	ENOG4105C8T	Leucyl-tRNA synthetase
IMCC26256_111492	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)
IMCC26256_111493	ENOG4105CBG	Sulfatase
IMCC26256_111495	ENOG4105C1X	Bifunctional enzyme with both catalase and broad- spectrum peroxidase activity (By similarity)
IMCC26256_111496	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)
IMCC26256_111497	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)
IMCC26256_111498	ENOG4105KEM	Functions as a ribosomal silencing factor. Interacts with ribosomal protein L14 (rplN), blocking formation of intersubunit bridge B8. Prevents association of the 30S and 50S ribosomal subunits and the formation of functional ribosomes, thus repressing translation (By similarity)
IMCC26256_11150	ENOG4107R4J	Chloride channel
IMCC26256_111500	ENOG4108Z1W	Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) (By similarity)
IMCC26256_111502	ENOG4105CVP	deoxyribo-dipyrimidine photolyase
IMCC26256_111503	ENOG4108RTV	Catalyzes the transfer of acetyl from acetyl-CoA to desacetylmycothiol (Cys-GlcN-Ins) to form mycothiol (By similarity)
IMCC26256_111505	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
IMCC26256_111506	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)
IMCC26256_111507	ENOG4105CGT	Catalyzes the transfer of a phosphate group to glutamate to form glutamate 5-phosphate which rapidly cyclizes to 5- oxoproline (By similarity)
IMCC26256_111508	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
IMCC26256_111509	ENOG4105K46	50S ribosomal protein l27
IMCC26256_111510	ENOG410826X	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
IMCC26256_111511	ENOG4105C03	ribonuclease
IMCC26256_111515	ENOG4105CNI	cell division protein FtsW
IMCC26256_111520	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)
IMCC26256_111521	ENOG4105DPM	folylpolyglutamate synthase Dihydrofolate synthase
IMCC26256_111522	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)
IMCC26256_111523	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)
IMCC26256_111524	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)
IMCC26256_111525	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
IMCC26256_111526	ENOG4105CMR	udp-glucose 4-epimerase
IMCC26256_111530	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)
IMCC26256_111531	ENOG4105C79	DNA protecting protein DprA
IMCC26256_11154	ENOG4105SYT	Methylenetetrahydrofolate reductase
IMCC26256_111541	ENOG4107QK4	glycoside hydrolase, family 3 domain protein
IMCC26256_111542	ENOG4105EXC	Acyl-transferase
IMCC26256_111550	ENOG4105BZU	Histidine kinase
IMCC26256_111556	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
IMCC26256_111557	ENOG4105CHR	reductase
IMCC26256_111563	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)
IMCC26256_111564	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)
IMCC26256_111565	ENOG4108RQ5	Beta-lactamase domain-containing protein
IMCC26256_111566	ENOG4105F03	Provides the (R)-glutamate required for cell wall biosynthesis (By similarity)
IMCC26256_111567	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)
IMCC26256_111573	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
IMCC26256_111576	ENOG4105D9F	endo-1,4-beta-xylanase (EC 3.2.1.8)
IMCC26256_11158	ENOG4108Z6B	deaminase
IMCC26256_111583	ENOG4108IXY	short-chain dehydrogenase reductase
IMCC26256_111585	ENOG4105CC9	acyl-Coa dehydrogenase
IMCC26256_111586	ENOG4105EV8	ectoine hydroxylase
IMCC26256_111590	ENOG4105CPC	Aldo Keto reductase
IMCC26256_111595	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
IMCC26256_111598	ENOG4105C29	acyl-CoA thioesterase
IMCC26256_111600	ENOG4105EXC	Acyl-transferase
IMCC26256_111601	ENOG4108HW8	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)
IMCC26256_111602	ENOG4108UJU	UPF0301 protein
IMCC26256_111603	ENOG4105CSR	polyphosphate kinase 2
IMCC26256_111610	ENOG4105CJ1	ABC, transporter
IMCC26256_111615	ENOG4105CJH	Alcohol dehydrogenase zinc-binding domain protein
IMCC26256_111618	ENOG4105EUB	pirin domain protein
IMCC26256_11162	ENOG410816I	Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection (By similarity)
IMCC26256_111621	ENOG41067SE	Tetr family transcriptional regulator
IMCC26256_111623	ENOG4108RAV	Conserved protein
IMCC26256_111626	ENOG4105D3R	alkyl hydroperoxide reductase
IMCC26256_111627	ENOG4108K5P	(LipO)protein
IMCC26256_111628	ENOG4105CRP	Part of the ABC transporter FtsEX involved in
IMCC26256_111629	ENOG4105CAK	Cell division ATP-binding protein ftsE
IMCC26256_11163	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)
IMCC26256_111630	ENOG4105CG1	Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA (By similarity)
IMCC26256_111631	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
IMCC26256_111633	ENOG4105MJ2	Competence protein
IMCC26256_111634	ENOG4105C3E	May play a key role in the regulation of the intracellular concentration of adenosylhomocysteine (By similarity)
IMCC26256_111635	ENOG41086CI	Bifunctional phosphoglucose phosphomannose isomerase
IMCC26256_111637	ENOG4107QKV	phosphomannomutase
IMCC26256_11164	ENOG4105DWV	Homoserine O-trans-acetylase
IMCC26256_111641	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)
IMCC26256_111646	ENOG4105EIH	LPPG Fo 2-phospho-L-lactate transferase
IMCC26256_111647	ENOG41088YA	Catalyzes the GTP-dependent successive addition of two or more gamma-linked L-glutamates to the L-lactyl phosphodiester of 7,8-didemethyl-8-hydroxy-5-deazariboflavin (F420-0) to form coenzyme F420-0-glutamyl-glutamate (F420-2) or polyglutamated F420 derivatives (By similarity)
IMCC26256_111648	ENOG41088YA	Catalyzes the GTP-dependent successive addition of two or more gamma-linked L-glutamates to the L-lactyl phosphodiester of 7,8-didemethyl-8-hydroxy-5-deazariboflavin (F420-0) to form coenzyme F420-0-glutamyl-glutamate (F420-2) or polyglutamated F420 derivatives (By similarity)
IMCC26256_111649	ENOG4108S0S	Nucleotidyl transferase
IMCC26256_111653	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
IMCC26256_111654	ENOG4108KGH	TRANSCRIPTIONal
IMCC26256_111655	ENOG4105CRQ	synthase (Component I)
IMCC26256_111658	ENOG4108JIK	carboxylase
IMCC26256_111662	ENOG4105E39	Enoyl-CoA hydratase
IMCC26256_111665	ENOG41083MR	nifu domain-containing protein
IMCC26256_111666	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
IMCC26256_111667	ENOG4105E39	Enoyl-CoA hydratase
IMCC26256_111669	ENOG4107RE3	peptidase, S41
IMCC26256_111670	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)
IMCC26256_111671	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)
IMCC26256_111676	ENOG4105CHR	reductase
IMCC26256_111678	ENOG4105KNM	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
IMCC26256_111679	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)
IMCC26256_111680	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)
IMCC26256_111682	ENOG4108T62	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)
IMCC26256_111683	ENOG4107ZFM	Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) (By similarity)
IMCC26256_111684	ENOG4105ZA1	atp synthase
IMCC26256_111685	ENOG4107UH5	it plays a direct role in the translocation of protons across the membrane (By similarity)
IMCC26256_111688	ENOG4105ESV	Glycosyl transferase, family 4
IMCC26256_111689	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)
IMCC26256_111690	ENOG4108YZG	isomerase
IMCC26256_111691	ENOG4105CPK	Glycosyl transferase (Group 1
IMCC26256_111692	ENOG4105CXW	Synthesizes alpha-1,4-glucan chains using ADP-glucose (By similarity)
IMCC26256_111693	ENOG4108TJN	glycosyl transferase group 1
IMCC26256_111695	ENOG4108QV3	biosynthesis protein
IMCC26256_111697	ENOG4105D3Q	Sugar transferase
IMCC26256_111705	ENOG4105BZ1	(ABC) transporter
IMCC26256_111707	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
IMCC26256_11171	ENOG4105D8K	carboxyl transferase
IMCC26256_111710	ENOG4105VFB	Binds the 23S rRNA (By similarity)
IMCC26256_111712	ENOG4105E3H	phosphoglycerate mutase
IMCC26256_111714	ENOG4105EMU	Dehydrogenase
IMCC26256_111715	ENOG4107R5I	Catalyzes the gamma-elimination of phosphate from L- phosphohomoserine and the beta-addition of water to produce L- threonine (By similarity)
IMCC26256_111716	ENOG4105D6E	homoserine dehydrogenase
IMCC26256_111718	ENOG4105C75	arginyL-tRNA synthetase
IMCC26256_111719	ENOG4105BZU	Histidine kinase
IMCC26256_111721	ENOG4105CHR	reductase
IMCC26256_111724	ENOG4105C9U	ATP-dependent DNA helicase RecQ
IMCC26256_111730	ENOG4105C9U	ATP-dependent DNA helicase RecQ
IMCC26256_111734	ENOG4105C25	Primosomal protein n'
IMCC26256_11174	ENOG4105C04	l-carnitine dehydratase bile acid-inducible protein F
IMCC26256_111741	ENOG4105BZK	Transcription regulator that activates transcription by stimulating RNA polymerase (RNAP) recycling in case of stress conditions such as supercoiled DNA or high salt concentrations. Probably acts by releasing the RNAP, when it is trapped or immobilized on tightly supercoiled DNA. Does not activate transcription on linear DNA. Probably not involved in DNA repair (By similarity)
IMCC26256_111747	ENOG41061TZ	Short-chain dehydrogenase reductase Sdr
IMCC26256_111748	ENOG4108VC7	Protein of unknown function (DUF2587)
IMCC26256_111749	ENOG4105C7V	phospho-2-dehydro-3-deoxyheptonate aldolase
IMCC26256_111750	ENOG4105C57	major facilitator superfamily
IMCC26256_111751	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
IMCC26256_111752	ENOG41087NI	Sulfite exporter TauE/SafE
IMCC26256_111753	ENOG4109050	May catalyze the ATP-dependent phosphorylation of lipids other than diacylglycerol (DAG)
IMCC26256_111755	ENOG4105KRM	Acts as a transcriptional regulator. Probably redox- responsive. The apo- but not holo-form probably binds DNA (By similarity)
IMCC26256_111761	ENOG4105D1F	ATP-binding protein
IMCC26256_111762	ENOG41082BM	Transcriptional regulator, arsr family
IMCC26256_111763	ENOG4107QI6	Cysteine desulfurase
IMCC26256_111767	ENOG4108I0Z	Aconitate hydratase
IMCC26256_111768	ENOG4107XH4	PPIases accelerate the folding of proteins (By similarity)
IMCC26256_111771	ENOG4107QX9	Thiol disulfide interChange protein
IMCC26256_111772	ENOG4105DA4	cytochrome c-type biogenesis protein
IMCC26256_111775	ENOG41060IM	Heme exporter protein
IMCC26256_111777	ENOG4107EV4	once thought to export heme, this seems not to be the case, but its exact role is uncertain. Responsible for energy coupling to the transport system (By similarity)
IMCC26256_111778	ENOG4108Z6X	(sortase) family
IMCC26256_11178	ENOG4105RFZ	Methylmalonyl-coA mutase
IMCC26256_111780	ENOG4106063	Acetyl-CoA carboxylase biotin carboxyl carrier protein subunit
IMCC26256_111781	ENOG4106YT9	Enoyl-CoA hydratase
IMCC26256_111784	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
IMCC26256_11179	ENOG4105DYT	3-hydroxyacyl-CoA dehydrogenase
IMCC26256_111790	ENOG4105CPC	Aldo Keto reductase
IMCC26256_111796	ENOG4105DSY	exodeoxyribonuclease V, gamma
IMCC26256_111797	ENOG4107QKA	exodeoxyribonuclease V beta
IMCC26256_111798	ENOG4105C7H	Helicase, RecD TraA family
IMCC26256_111799	ENOG4105CWG	Catalyzes the last two steps in the biosynthesis of 5- methylaminomethyl-2-thiouridine (mnm(5)s(2)U) at the wobble position (U34) in tRNA. Catalyzes the FAD-dependent demodification of cmnm(5)s(2)U34 to nm(5)s(2)U34, followed by the transfer of a methyl group from S-adenosyl-L-methionine to nm(5)s(2)U34, to form mnm(5)s(2)U34 (By similarity)
IMCC26256_1118	ENOG41068W2	Cytochrome p-450
IMCC26256_111800	ENOG4107SFI	Major Facilitator superfamily
IMCC26256_111802	ENOG4107FQX	Alpha-acetolactate decarboxylase
IMCC26256_111805	ENOG4108NA0	Uncharacterized conserved protein (COG2071)
IMCC26256_11181	ENOG4108R5K	PPIases accelerate the folding of proteins (By similarity)
IMCC26256_111823	ENOG4105C1J	atp-dependent rna helicase
IMCC26256_11183	ENOG4105CFH	Aspartokinase
IMCC26256_111833	ENOG4105C1G	acyl-Coa dehydrogenase
IMCC26256_11184	ENOG4105CM3	Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate (By similarity)
IMCC26256_111842	ENOG4105CHU	acetyl-coa acetyltransferase
IMCC26256_111843	ENOG4105C1G	acyl-Coa dehydrogenase
IMCC26256_111844	ENOG4105CC9	acyl-Coa dehydrogenase
IMCC26256_111845	ENOG4105BZU	Histidine kinase
IMCC26256_111846	ENOG41080W3	amp-dependent synthetase and ligase
IMCC26256_111849	ENOG4105EA8	2-Nitropropane dioxygenase
IMCC26256_111852	ENOG4106YT9	Enoyl-CoA hydratase
IMCC26256_111854	ENOG4105CHR	reductase
IMCC26256_111855	ENOG4105CC9	acyl-Coa dehydrogenase
IMCC26256_111857	ENOG41079Y2	Catalyzes the coenzyme F420-dependent oxidation of glucose 6-phosphate (G6P) to 6-phosphogluconolactone
IMCC26256_111859	ENOG4105FJ0	thiamine
IMCC26256_111860	ENOG4105C4Y	ABC transporter
IMCC26256_111861	ENOG4106SMU	thiamine transporter membrane protein
IMCC26256_111862	ENOG4108UCS	ABC, transporter
IMCC26256_111863	ENOG4105E0X	reductase
IMCC26256_111864	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
IMCC26256_111865	ENOG4105EB3	Histidine kinase
IMCC26256_111866	ENOG4105C66	Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate (By similarity)
IMCC26256_111870	ENOG4108S7T	Catalyzes the oxidation of either pyridoxine 5'- phosphate (PNP) or pyridoxamine 5'-phosphate (PMP) into pyridoxal 5'-phosphate (PLP) (By similarity)
IMCC26256_111872	ENOG4105C1G	acyl-Coa dehydrogenase
IMCC26256_111874	ENOG4105CEY	Amp-dependent synthetase and ligase
IMCC26256_111882	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)
IMCC26256_111888	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)
IMCC26256_111889	ENOG4105E4F	Isochorismate synthase
IMCC26256_11189	ENOG4107QMS	site-determining protein
IMCC26256_111891	ENOG4105C4A	Catalyzes the thiamine diphosphate-dependent decarboxylation of 2-oxoglutarate and the subsequent addition of the resulting succinic semialdehyde-thiamine pyrophosphate anion to isochorismate to yield 2-succinyl-5-enolpyruvyl-6-hydroxy-3- cyclohexene-1-carboxylate (SEPHCHC) (By similarity)
IMCC26256_111903	ENOG4108ZP8	Acetolactate synthase small subunit
IMCC26256_111905	ENOG4105CRK	lysyL-tRNA synthetase
IMCC26256_111906	ENOG4105C01	Dihydroxy-acid dehydratase
IMCC26256_111909	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)
IMCC26256_111910	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)
IMCC26256_111911	ENOG41081AP	Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) (By similarity)
IMCC26256_111915	ENOG4105KF3	Short-chain dehydrogenase reductase Sdr
IMCC26256_111916	ENOG4108DT4	serine threonine protein kinase
IMCC26256_111920	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)
IMCC26256_111924	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
IMCC26256_111928	ENOG4105D5P	Methylmalonyl-coA mutase
IMCC26256_111929	ENOG4105NDF	NAD-dependent protein deacetylase which modulates the activities of several enzymes which are inactive in their acetylated form. May also have NAD-dependent lysine demalonylase and desuccinylase activity (By similarity)
IMCC26256_111930	ENOG4105D06	uba thif-type nad fad binding protein
IMCC26256_111932	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)
IMCC26256_111934	ENOG4105C3R	Methionine synthase
IMCC26256_111937	ENOG4107V9E	glucose-1-phosphate thymidylyltransferase
IMCC26256_11194	ENOG4105D1F	ATP-binding protein
IMCC26256_111943	ENOG4105EY8	ABC transporter
IMCC26256_111946	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)
IMCC26256_111948	ENOG4107QN2	dihydrolipoyl dehydrogenase
IMCC26256_11195	ENOG4108YX9	iron--sulfur cluster insertion protein erpA
IMCC26256_111950	ENOG4105CPK	Glycosyl transferase (Group 1
IMCC26256_111951	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)
IMCC26256_111952	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)
IMCC26256_111953	ENOG4105CMR	udp-glucose 4-epimerase
IMCC26256_111957	ENOG4105C1G	acyl-Coa dehydrogenase
IMCC26256_111958	ENOG4105CC9	acyl-Coa dehydrogenase
IMCC26256_111959	ENOG4107VMB	Beta-lactamase domain protein
IMCC26256_111960	ENOG4105C3K	feS assembly ATPase SufC
IMCC26256_111961	ENOG4105C9B	Cysteine desulfurase
IMCC26256_111962	ENOG4108UNV	SUF system FeS assembly protein, NifU family
IMCC26256_111966	ENOG4105C3K	feS assembly ATPase SufC
IMCC26256_111968	ENOG4105JRK	feS assembly protein SufD
IMCC26256_111969	ENOG4105DIW	FeS assembly protein SUFB
IMCC26256_111970	ENOG4105DJZ	UPF0182 protein
IMCC26256_111974	ENOG4105DFF	Rod shape-determining protein mreb
IMCC26256_111976	ENOG4108ZAF	Molybdopterin
IMCC26256_111981	ENOG4107ZXU	DSBA oxidoreductase
IMCC26256_111982	ENOG4108N0W	Major Facilitator superfamily
IMCC26256_111983	ENOG4105CUU	Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) (By similarity)
IMCC26256_111986	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
IMCC26256_111988	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
IMCC26256_11199	ENOG4105KME	endoribonuclease L-psp
IMCC26256_111990	ENOG4105BZY	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
IMCC26256_111991	ENOG4105E2Z	phosphate ABC transporter (Permease
IMCC26256_111992	ENOG4105C8U	phosphate abc transporter
IMCC26256_111993	ENOG4107QMV	Part of the ABC transporter complex PstSACB involved in phosphate import (By similarity)
IMCC26256_111994	ENOG4108UTW	Plays a role in the regulation of phosphate uptake
IMCC26256_111997	ENOG41062D9	Histidine kinase
IMCC26256_111998	ENOG4105ETX	regulatoR
IMCC26256_112	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)
IMCC26256_112001	ENOG4105K51	Acts as a transcriptional regulator. Probably redox- responsive. The apo- but not holo-form probably binds DNA (By similarity)
IMCC26256_112004	ENOG4105DU6	RNA polymerase
IMCC26256_112008	ENOG4105K51	Acts as a transcriptional regulator. Probably redox- responsive. The apo- but not holo-form probably binds DNA (By similarity)
IMCC26256_11201	ENOG4107NHD	transcriptional regulator
IMCC26256_112010	ENOG4108UVJ	appr-1-p processing domain protein
IMCC26256_112012	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
IMCC26256_112014	ENOG4107KWJ	von Willebrand factor, type A
IMCC26256_112016	ENOG4105CS2	ec 3.2.1.21
IMCC26256_112020	ENOG4105E33	succinate dehydrogenase
IMCC26256_112029	ENOG4105C6V	Glycerol-3-phosphate dehydrogenase
IMCC26256_112031	ENOG4107QVN	Key enzyme in the regulation of glycerol uptake and metabolism (By similarity)
IMCC26256_112035	ENOG4108YIQ	Alpha beta hydrolase
IMCC26256_112036	ENOG4105K85	Involved in the cellular defense against the biological effects of O6-methylguanine (O6-MeG) in DNA. Repairs alkylated guanine in DNA by stoichiometrically transferring the alkyl group at the O-6 position to a cysteine residue in the enzyme. This is a suicide reaction the enzyme is irreversibly inactivated (By similarity)
IMCC26256_112037	ENOG4105D9Z	Catalyzes the reversible oxidation of malate to oxaloacetate (By similarity)
IMCC26256_112039	ENOG4108HMX	isocitrate dehydrogenase (NADP)
IMCC26256_112041	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)
IMCC26256_112042	ENOG4105DC1	bifunctional purine biosynthesis protein purh
IMCC26256_112044	ENOG4105CH8	Succinyl-CoA ligase ADP-forming subunit alpha
IMCC26256_112045	ENOG4105CMV	Succinyl-CoA synthetase subunit beta
IMCC26256_112046	ENOG4105D5P	Methylmalonyl-coA mutase
IMCC26256_112048	ENOG4105C4R	Atp-dependent dna helicase
IMCC26256_112050	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
IMCC26256_112051	ENOG4107QVP	Dehydrogenase
IMCC26256_112052	ENOG4105P8F	nudix hydrolase
IMCC26256_112056	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
IMCC26256_112057	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)
IMCC26256_112060	ENOG4108097	ATP-binding protein
IMCC26256_112061	ENOG4108UN4	phage SPO1 DNA polymerase-related protein
IMCC26256_112062	ENOG4107S9D	Alpha beta hydrolase
IMCC26256_112063	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
IMCC26256_112064	ENOG4105CJW	magnesium transporter
IMCC26256_112065	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)
IMCC26256_112066	ENOG41082V8	Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein (By similarity)
IMCC26256_112067	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
IMCC26256_112068	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
IMCC26256_112069	ENOG4108UJD	30S ribosomal protein S9
IMCC26256_11207	ENOG4105FR1	rard protein
IMCC26256_112070	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)
IMCC26256_112075	ENOG4105CK0	Membrane bOund o-acyl transferase mboat family protein
IMCC26256_112077	ENOG4105DI7	Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs (By similarity)
IMCC26256_112078	ENOG4108ZT0	50S ribosomal protein l17
IMCC26256_112079	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
IMCC26256_11208	ENOG41061ZR	Transcriptional regulator
IMCC26256_112080	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)
IMCC26256_112081	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)
IMCC26256_11209	ENOG4105C4K	Nad synthetase
IMCC26256_112091	ENOG4107QQG	Dehydrogenase
IMCC26256_112096	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)
IMCC26256_112106	ENOG4105EY8	ABC transporter
IMCC26256_112107	ENOG4105K64	Glycosyl transferase, family 2
IMCC26256_112115	ENOG4107R8N	Glycosyl transferase, family 2
IMCC26256_112119	ENOG4105D7W	serine acetyltransferase
IMCC26256_112120	ENOG4107T8Q	Glycosyl transferase (Group 1
IMCC26256_112124	ENOG4105CGN	Glycosyl transferase (Group 1
IMCC26256_112125	ENOG41080E2	ribosomal-protein-alanine acetyltransferase
IMCC26256_112126	ENOG4105ESV	Glycosyl transferase, family 4
IMCC26256_112127	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
IMCC26256_112131	ENOG4105CA1	Removes the N-terminal methionine from nascent proteins (By similarity)
IMCC26256_112132	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)
IMCC26256_112133	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)
IMCC26256_112134	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
IMCC26256_112135	ENOG410849U	50S ribosomal protein L30
IMCC26256_112136	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)
IMCC26256_112137	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)
IMCC26256_112138	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)
IMCC26256_112139	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)
IMCC26256_112140	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
IMCC26256_112141	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
IMCC26256_112142	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
IMCC26256_112143	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
IMCC26256_112144	ENOG41082SA	50s ribosomal protein l29
IMCC26256_112145	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
IMCC26256_112146	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
IMCC26256_112147	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)
IMCC26256_112148	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
IMCC26256_112149	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
IMCC26256_11215	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
IMCC26256_112150	ENOG4105KZR	One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome (By similarity)
IMCC26256_112151	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)
IMCC26256_112152	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)
IMCC26256_112154	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
IMCC26256_112155	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)
IMCC26256_112156	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)
IMCC26256_112157	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)
IMCC26256_112158	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
IMCC26256_112159	ENOG4108IIJ	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
IMCC26256_112160	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)
IMCC26256_112161	ENOG4108VZM	50s ribosomal protein L10
IMCC26256_112162	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)
IMCC26256_112163	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
IMCC26256_112164	ENOG4105E5V	Participates in transcription elongation, termination and antitermination (By similarity)
IMCC26256_112167	ENOG4105WDJ	50S ribosomal protein L33
IMCC26256_112168	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
IMCC26256_112174	ENOG4108VPT	UPF0234 protein
IMCC26256_112177	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)
IMCC26256_112179	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)
IMCC26256_112180	ENOG4105C8S	subunit m
IMCC26256_112181	ENOG4105D65	subunit l
IMCC26256_112182	ENOG41082X4	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)
IMCC26256_112183	ENOG4105DF2	NADH dehydrogenase subunit j
IMCC26256_112184	ENOG4108M11	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)
IMCC26256_112185	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)
IMCC26256_112186	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)
IMCC26256_112187	ENOG4105CYU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
IMCC26256_112188	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)
IMCC26256_112189	ENOG4105KWU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
IMCC26256_112191	ENOG4105C8S	subunit m
IMCC26256_112192	ENOG4105D65	subunit l
IMCC26256_112193	ENOG4105M5H	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
IMCC26256_112194	ENOG4105DF2	NADH dehydrogenase subunit j
IMCC26256_112195	ENOG4105P3U	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
IMCC26256_112196	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)
IMCC26256_112197	ENOG4108IEH	NADH dehydrogenase subunit g
IMCC26256_112198	ENOG4107QIZ	NADH dehydrogenase
IMCC26256_112200	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)
IMCC26256_112201	ENOG4105CYU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
IMCC26256_112202	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)
IMCC26256_112203	ENOG4105KWU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
IMCC26256_112204	ENOG4105P52	geranylgeranyl reductase
IMCC26256_112215	ENOG41061MV	Arylsulfatase
IMCC26256_112217	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
IMCC26256_112218	ENOG4105D52	delta-aminolevulinic acid dehydratase
IMCC26256_112220	ENOG4105D6W	Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps (By similarity)
IMCC26256_112221	ENOG4105C7E	Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) (By similarity)
IMCC26256_112222	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)
IMCC26256_112224	ENOG4105CEY	Amp-dependent synthetase and ligase
IMCC26256_112234	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)
IMCC26256_11224	ENOG4108I5C	dEAD DEAH box helicase
IMCC26256_112240	ENOG41090R7	Ferric uptake
IMCC26256_112244	ENOG4105DSE	periplasmic solute binding protein
IMCC26256_112245	ENOG4105FDK	ABC transporter
IMCC26256_112246	ENOG4107VVP	(ABC) transporter
IMCC26256_112248	ENOG4105C26	Dehydrogenase
IMCC26256_112249	ENOG4105D38	putrescine abc transporter
IMCC26256_11225	ENOG4108KGH	TRANSCRIPTIONal
IMCC26256_112250	ENOG4105F38	ABC transporter, permease
IMCC26256_112253	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
IMCC26256_112254	ENOG4105C26	Dehydrogenase
IMCC26256_112257	ENOG4108JPX	Catalyzes the transfer of the alpha-amino group from S- adenosyl-L-methionine (SAM) to 7-keto-8-aminopelargonic acid (KAPA) to form 7,8-diaminopelargonic acid (DAPA). It is the only animotransferase known to utilize SAM as an amino donor (By similarity)
IMCC26256_112258	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)
IMCC26256_112259	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)
IMCC26256_112261	ENOG4108JPX	Catalyzes the transfer of the alpha-amino group from S- adenosyl-L-methionine (SAM) to 7-keto-8-aminopelargonic acid (KAPA) to form 7,8-diaminopelargonic acid (DAPA). It is the only animotransferase known to utilize SAM as an amino donor (By similarity)
IMCC26256_112263	ENOG4105VM8	Could accelerate the degradation of some genes transcripts potentially through selective RNA binding (By similarity)
IMCC26256_11227	ENOG4107VEG	TrkA-N domain protein
IMCC26256_112272	ENOG4105BZY	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
IMCC26256_112273	ENOG4105E2Z	phosphate ABC transporter (Permease
IMCC26256_112286	ENOG4107R5W	Monooxygenase
IMCC26256_112287	ENOG4105CXB	phosphoribosylaminoimidazole synthetase
IMCC26256_112289	ENOG4107UCJ	Catalyzes the synthesis of activated sulfate (By similarity)
IMCC26256_112290	ENOG4107QIK	phosphoribosylformylglycinamidine synthase
IMCC26256_112293	ENOG4105D21	Phosphoribosylformylglycinamidine synthase I
IMCC26256_112294	ENOG4108A1T	Phosphoribosylformylglycinamidine synthase, purS
IMCC26256_112295	ENOG4105C8V	SAICAR synthetase
IMCC26256_112296	ENOG4105C83	adenylosuccinate lyase
IMCC26256_112298	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
IMCC26256_112299	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
IMCC26256_11230	ENOG4105C0X	amino acid
IMCC26256_112300	ENOG4105KNI	merR family transcriptional Regulator
IMCC26256_112301	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)
IMCC26256_112302	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
IMCC26256_112303	ENOG4105CFG	Acts as a chaperone (By similarity)
IMCC26256_112304	ENOG4105EYW	Ion transport protein
IMCC26256_112305	ENOG4105DF6	Fe-S oxidoreductase
IMCC26256_112306	ENOG4105DHP	deoxycytidine triphosphate deaminase
IMCC26256_112307	ENOG4105T0Z	Conserved Protein
IMCC26256_11231	ENOG4105EAY	pump that utilizes the energy of pyrophosphate hydrolysis as the driving force for
IMCC26256_112310	ENOG4105CCX	Catalyzes the production of spermidine from putrescine and decarboxylated S-adenosylmethionine (dcSAM), which serves as an aminopropyl donor (By similarity)
IMCC26256_112311	ENOG4105XPP	Protein of unknown function (DUF1275)
IMCC26256_112318	ENOG4105ETX	regulatoR
IMCC26256_11232	ENOG4105DQR	SNARE associated Golgi
IMCC26256_112324	ENOG4105CDU	Replicative dna helicase
IMCC26256_112325	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
IMCC26256_112326	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)
IMCC26256_112328	ENOG410829C	Binds together with S18 to 16S ribosomal RNA (By similarity)
IMCC26256_11233	ENOG4105C73	Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone (By similarity)
IMCC26256_112330	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
IMCC26256_112334	ENOG4105CZA	synthase
IMCC26256_112335	ENOG4108MIC	Mg-protoporphyrin IX methyl transferase
IMCC26256_112336	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
IMCC26256_112337	ENOG4105CZX	twitching motility protein
IMCC26256_112340	ENOG4105CJR	Integral membrane protein (MviN
IMCC26256_112341	ENOG4105EPR	degv family
IMCC26256_112344	ENOG4105C3M	thioredoxin reductase
IMCC26256_112345	ENOG4105C3M	thioredoxin reductase
IMCC26256_112346	ENOG4108E1C	hydrolase
IMCC26256_112348	ENOG4107QJE	Chromosome Partitioning Protein
IMCC26256_112349	ENOG4107YBR	Specifically methylates the N7 position of a guanine in 16S rRNA (By similarity)
IMCC26256_11235	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
IMCC26256_11236	ENOG4107QRG	dna polymerase iii
IMCC26256_11239	ENOG4105EMN	RNA polymerase sigma factor
IMCC26256_11242	ENOG4107RD1	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)
IMCC26256_11243	ENOG4108UGV	hypoxanthine phosphoribosyltransferase
IMCC26256_11244	ENOG4105EUJ	GTP cyclohydrolase i
IMCC26256_11245	ENOG4105EEI	dihydropteroate synthase
IMCC26256_11247	ENOG4105KRF	dihydroneopterin aldolase
IMCC26256_11250	ENOG4108IAA	Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate (By similarity)
IMCC26256_11251	ENOG4108IYU	L-aspartate oxidase
IMCC26256_11252	ENOG4105D18	nicotinate-nucleotide pyrophosphorylase
IMCC26256_11253	ENOG4105CGM	Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis (By similarity)
IMCC26256_11254	ENOG4105CRK	lysyL-tRNA synthetase
IMCC26256_11256	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
IMCC26256_11258	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)
IMCC26256_11259	ENOG4105DNJ	May play a role in the repair of endogenous alkylation damage (By similarity)
IMCC26256_11260	ENOG4105E59	Participates in a DNA-damage check-point. DisA forms globular foci that rapidly scan along the chromosomes searching for lesions (By similarity)
IMCC26256_11263	ENOG4108VJ1	Transcriptional regulator (CarD family
IMCC26256_11264	ENOG4105CTP	PilT protein domain protein
IMCC26256_11265	ENOG4108EM8	Bifunctional enzyme that catalyzes the formation of 4- diphosphocytidyl-2-C-methyl-D-erythritol from CTP and 2-C-methyl- D-erythritol 4-phosphate (MEP) (IspD), and 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) (IspF) (By similarity)
IMCC26256_11266	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)
IMCC26256_11267	ENOG4105C8N	cysteinyl-tRNA synthetase
IMCC26256_11268	ENOG4105C2N	RNA methyltransferase TrmH family group 3
IMCC26256_11272	ENOG4105BZW	Glycerate kinase
IMCC26256_11273	ENOG4105C3Q	Glycosyl transferase, family 2
IMCC26256_11275	ENOG4108IYI	Catalyzes the gamma-elimination of phosphate from L- phosphohomoserine and the beta-addition of water to produce L- threonine (By similarity)
IMCC26256_11283	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
IMCC26256_11285	ENOG4107JTW	chlorite dismutase
IMCC26256_11289	ENOG4105BZU	Histidine kinase
IMCC26256_11292	ENOG4105E1P	Modifies, by uridylylation or deuridylylation the PII (GlnB) regulatory protein (By similarity)
IMCC26256_11296	ENOG4108RW0	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
IMCC26256_11297	ENOG4105C9Y	Catalyzes the hydrolysis of N-succinyl-L,L- diaminopimelic acid (SDAP), forming succinate and LL-2,6- diaminoheptanedioate (DAP), an intermediate involved in the bacterial biosynthesis of lysine and meso-diaminopimelic acid, an essential component of bacterial cell walls (By similarity)
IMCC26256_113	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)
IMCC26256_11301	ENOG4107RSM	transcriptional regulator
IMCC26256_11307	ENOG4105D1U	peptidase U62 modulator of DNA gyrase
IMCC26256_11308	ENOG4105CMS	peptidase U62, modulator of DNA gyrase
IMCC26256_11309	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
IMCC26256_11312	ENOG4105K7Z	Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP (By similarity)
IMCC26256_11313	ENOG4105C3Y	UTP-glucose-1-phosphate uridylyltransferase
IMCC26256_11314	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
IMCC26256_11315	ENOG4105CM1	Catalyzes, together with MoaC, the conversion of 5'-GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
IMCC26256_11316	ENOG4108YXW	Together with MoaA, is involved in the conversion of 5'- GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
IMCC26256_1132	ENOG4105EXX	Deoxyribodipyrimidine photolyase-related protein
IMCC26256_11322	ENOG4107RUK	Involved in iron-sulfur cluster biogenesis. Binds a 4Fe- 4S cluster, can transfer this cluster to apoproteins, and thereby intervenes in the maturation of Fe S proteins. Could also act as a scaffold chaperone for damaged Fe S proteins (By similarity)
IMCC26256_11330	ENOG4105CUB	amino acid
IMCC26256_11332	ENOG4105CP9	extracellular ligand-binding receptor
IMCC26256_11337	ENOG4107G87	m6 family metalloprotease domain protein
IMCC26256_11338	ENOG4107TFB	basic membrane
IMCC26256_11353	ENOG4105CC9	acyl-Coa dehydrogenase
IMCC26256_11354	ENOG4107R5B	glutamine synthetase
IMCC26256_11355	ENOG4107QRH	Arylsulfatase (Ec 3.1.6.1)
IMCC26256_11356	ENOG4105FBW	Monooxygenase
IMCC26256_11362	ENOG4105CGN	Glycosyl transferase (Group 1
IMCC26256_11363	ENOG4108SHN	Glycosyl transferase, family 2
IMCC26256_11368	ENOG4107BJW	polysaccharide deacetylase
IMCC26256_11375	ENOG4107R8H	Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine (By similarity)
IMCC26256_11377	ENOG4105E39	Enoyl-CoA hydratase
IMCC26256_11378	ENOG4105C3G	gtp-binding protein
IMCC26256_1138	ENOG4105DYT	3-hydroxyacyl-CoA dehydrogenase
IMCC26256_11381	ENOG4105KRN	Transcriptional regulator, abrb family
IMCC26256_11382	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)
IMCC26256_11383	ENOG4105F8V	Hydrolase, tatD family
IMCC26256_11384	ENOG4105K6T	rare lipoprotein A
IMCC26256_11386	ENOG4105CTR	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
IMCC26256_11388	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)
IMCC26256_11389	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
IMCC26256_11390	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)
IMCC26256_11391	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
IMCC26256_11393	ENOG4107UUG	Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins (By similarity)
IMCC26256_11394	ENOG4108IY2	MazG family
IMCC26256_11396	ENOG4105PDP	Short chain dehydrogenase
IMCC26256_11397	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
IMCC26256_1140	ENOG4105F2C	Acetyl-CoA acetyltransferase
IMCC26256_11401	ENOG4105C5R	Aminotransferase
IMCC26256_11403	ENOG4105D9U	N-acetyltransferase
IMCC26256_11411	ENOG4105DYW	oxidoreductase
IMCC26256_11412	ENOG4105K63	Thioredoxin
IMCC26256_11418	ENOG4105CI0	Citrate lyase
IMCC26256_11419	ENOG4105C1G	acyl-Coa dehydrogenase
IMCC26256_11421	ENOG4105BZ1	(ABC) transporter
IMCC26256_11422	ENOG4105C1G	acyl-Coa dehydrogenase
IMCC26256_11424	ENOG4105DJG	MaoC domain protein dehydratase
IMCC26256_11427	ENOG4105CJ1	ABC, transporter
IMCC26256_11429	ENOG4107XDQ	Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA (By similarity)
IMCC26256_1143	ENOG4105DDQ	anthranilate synthase
IMCC26256_11430	ENOG4105MXW	flavin reductase domain protein, FMN-binding
IMCC26256_11433	ENOG4105BZ1	(ABC) transporter
IMCC26256_11434	ENOG4105BZ1	(ABC) transporter
IMCC26256_11436	ENOG4105BZ1	(ABC) transporter
IMCC26256_1144	ENOG4105D9P	serine threonine protein kinase
IMCC26256_11441	ENOG4107QIV	Cytochrome c biogenesis protein
IMCC26256_11448	ENOG4105CBG	Sulfatase
IMCC26256_1145	ENOG4105CJN	penicillin-binding protein
IMCC26256_11450	ENOG4105EUZ	Beta-lactamase domain protein
IMCC26256_11452	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
IMCC26256_11453	ENOG4105CEY	Amp-dependent synthetase and ligase
IMCC26256_11457	ENOG4105CI2	imidazolone-5-propionate hydrolase
IMCC26256_11458	ENOG4107QRP	cobalamin biosynthesis protein CobW
IMCC26256_11464	ENOG4105C52	Atpase, p-type (Transporting), had superfamily, subfamily ic
IMCC26256_11468	ENOG4105EYH	Exonuclease
IMCC26256_1147	ENOG4108ZF3	Phosphatase
IMCC26256_11483	ENOG4107CN4	Pfam:PhdYeFM
IMCC26256_1149	ENOG4105IDI	abc transporter atp-binding protein
IMCC26256_11492	ENOG4108V1T	peptidylprolyl cis-trans isomerase
IMCC26256_115	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)
IMCC26256_11510	ENOG4105CEY	Amp-dependent synthetase and ligase
IMCC26256_11512	ENOG4107SIQ	Naphthoate synthase
IMCC26256_11513	ENOG4105BZU	Histidine kinase
IMCC26256_11514	ENOG4105VEQ	Cold shock protein
IMCC26256_11515	ENOG4105DTQ	mandelate racemase muconate lactonizing
IMCC26256_1152	ENOG410839S	Toxic component of a toxin-antitoxin (TA) module (By similarity)
IMCC26256_11522	ENOG4105CBG	Sulfatase
IMCC26256_11525	ENOG4105C04	l-carnitine dehydratase bile acid-inducible protein F
IMCC26256_11526	ENOG4105DBE	peroxidase
IMCC26256_11529	ENOG4107XDQ	Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA (By similarity)
IMCC26256_11530	ENOG4108J2P	Alpha beta hydrolase fold
IMCC26256_11540	ENOG4105CPC	Aldo Keto reductase
IMCC26256_11541	ENOG4105HMD	
IMCC26256_11549	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)
IMCC26256_11552	ENOG4108KR4	dihydrodipicolinate reductase
IMCC26256_11556	ENOG4105DRC	Na( ) H( ) antiporter that extrudes sodium in exchange for external protons (By similarity)
IMCC26256_11557	ENOG4107QRH	Arylsulfatase (Ec 3.1.6.1)
IMCC26256_11566	ENOG4105KF3	Short-chain dehydrogenase reductase Sdr
IMCC26256_11567	ENOG4105CNT	hydrolase family 2
IMCC26256_11568	ENOG4105CHU	acetyl-coa acetyltransferase
IMCC26256_11572	ENOG4108J2P	Alpha beta hydrolase fold
IMCC26256_11586	ENOG4105C0D	helicase
IMCC26256_11588	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)
IMCC26256_11591	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)
IMCC26256_116	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)
IMCC26256_11601	ENOG4105CHR	reductase
IMCC26256_11606	ENOG4108YZA	Nitrogen regulatory protein pii
IMCC26256_11607	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
IMCC26256_11608	ENOG4105CJ1	ABC, transporter
IMCC26256_11612	ENOG4105MC2	DSBA oxidoreductase
IMCC26256_11613	ENOG41065RQ	ADP-ribosylation crystallin J1
IMCC26256_11614	ENOG4105CGD	Nad-dependent epimerase dehydratase
IMCC26256_11615	ENOG4108J2P	Alpha beta hydrolase fold
IMCC26256_11622	ENOG4105RX7	peptidase S8 and S53, subtilisin, kexin, sedolisin
IMCC26256_11623	ENOG4105BZU	Histidine kinase
IMCC26256_11625	ENOG4106YT9	Enoyl-CoA hydratase
IMCC26256_11640	ENOG4105CHR	reductase
IMCC26256_11646	ENOG4105D4R	Catalyzes the desulfonation of aliphatic sulfonates (By similarity)
IMCC26256_11647	ENOG4105DRI	Involved in the oxidation of myo-inositol (MI) to 2- keto-myo-inositol (2KMI or 2-inosose) (By similarity)
IMCC26256_11653	ENOG4105EWK	phytoene
IMCC26256_11658	ENOG4105CHR	reductase
IMCC26256_11659	ENOG4105C1J	atp-dependent rna helicase
IMCC26256_1166	ENOG4105DU0	nucleoside hydrolase
IMCC26256_11663	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)
IMCC26256_11666	ENOG4107QXN	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)
IMCC26256_11668	ENOG4105MQS	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
IMCC26256_11669	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
IMCC26256_1167	ENOG4108RVA	ribokinase
IMCC26256_11673	ENOG4107YD5	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)
IMCC26256_11674	ENOG4108IV0	ABC, transporter
IMCC26256_11675	ENOG4105C0Z	ABC transporter
IMCC26256_11676	ENOG4105CF8	branched-chain amino acid ABC transporter, permease
IMCC26256_11679	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)
IMCC26256_11680	ENOG4105CM2	brancheD-chain amino acid aminotransferase
IMCC26256_11681	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)
IMCC26256_11683	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)
IMCC26256_11689	ENOG4105K70	DNA-binding protein
IMCC26256_11691	ENOG4107W19	lmbE family
IMCC26256_11694	ENOG4105CSF	NADPH-dependent glycerol-3-phosphate dehydrogenase
IMCC26256_11696	ENOG4105C8I	hydrolase, family 38
IMCC26256_11700	ENOG41067KJ	GYD family
IMCC26256_11702	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
IMCC26256_11708	ENOG4105C0B	DNA polymerase III (alpha subunit)
IMCC26256_11709	ENOG4105BZU	Histidine kinase
IMCC26256_11711	ENOG41073R8	VanW family
IMCC26256_11712	ENOG4105CC9	acyl-Coa dehydrogenase
IMCC26256_11713	ENOG4105T1M	mycothiol conjugate amidase mca
IMCC26256_11715	ENOG4105F2C	Acetyl-CoA acetyltransferase
IMCC26256_11726	ENOG4108S01	response regulator
IMCC26256_11729	ENOG4105C1G	acyl-Coa dehydrogenase
IMCC26256_11732	ENOG4105C10	Electron transfer flavoprotein
IMCC26256_11735	ENOG4105CGK	Exodeoxyribonuclease III
IMCC26256_11739	ENOG4105C04	l-carnitine dehydratase bile acid-inducible protein F
IMCC26256_11742	ENOG4105CY8	phosphoribosylaminoimidazole carboxylase atpase subunit
IMCC26256_11749	ENOG4107R49	K07407 alpha-galactosidase EC 3.2.1.22
IMCC26256_11750	ENOG4105CRD	Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) (By similarity)
IMCC26256_11751	ENOG4105F0Z	galactose-1-phosphate uridylyltransferase
IMCC26256_11755	ENOG4105CEY	Amp-dependent synthetase and ligase
IMCC26256_11757	ENOG4105CPF	Cell wall formation (By similarity)
IMCC26256_11758	ENOG4105C0M	Catalyzes the conversion of oxaloacetate (OAA) to phosphoenolpyruvate (PEP), the rate-limiting step in the metabolic pathway that produces glucose from lactate and other precursors derived from the citric acid cycle (By similarity)
IMCC26256_11760	ENOG4105VB9	50S ribosomal protein l28
IMCC26256_11761	ENOG4105DP4	dak2 domain fusion protein ylov
IMCC26256_11763	ENOG4106H78	methyltransferase
IMCC26256_11764	ENOG4108ZEF	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate (By similarity)
IMCC26256_11767	ENOG41085U1	50S ribosomal protein L32
IMCC26256_11768	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)
IMCC26256_11769	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
IMCC26256_11770	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)
IMCC26256_11772	ENOG4105VSY	K01512 acylphosphatase EC 3.6.1.7
IMCC26256_11774	ENOG4105D8X	mechanosensitive ion channel
IMCC26256_11777	ENOG4105K5M	30s ribosomal protein S16
IMCC26256_11779	ENOG4107XUM	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)
IMCC26256_11780	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
IMCC26256_11783	ENOG41080R2	UPF0102 protein
IMCC26256_11785	ENOG4105E39	Enoyl-CoA hydratase
IMCC26256_11787	ENOG4105C79	DNA protecting protein DprA
IMCC26256_11788	ENOG4105C0P	Mg chelatase subunit ChlI
IMCC26256_11789	ENOG4108IYT	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
IMCC26256_11790	ENOG4105DN4	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
IMCC26256_11792	ENOG4105CE9	30S ribosomal protein S2
IMCC26256_11793	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)
IMCC26256_11794	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
IMCC26256_11795	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)
IMCC26256_11796	ENOG4105KNE	Phosphatidate cytidylyltransferase
IMCC26256_11797	ENOG4105CEA	Catalyzes the NADP-dependent rearrangement and reduction of 1-deoxy-D-xylulose-5-phosphate (DXP) to 2-C-methyl-D-erythritol 4-phosphate (MEP) (By similarity)
IMCC26256_11799	ENOG4105C4E	Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate (By similarity)
IMCC26256_1180	ENOG4106N3V	dolichyl-phosphate beta-D-mannosyltransferase (EC 2.4.1.83)
IMCC26256_11802	ENOG4105ET3	Reduction of activated sulfate into sulfite (By similarity)
IMCC26256_11803	ENOG4105ET1	Component of the sulfite reductase complex that catalyzes the 6-electron reduction of sulfite to sulfide. This is one of several activities required for the biosynthesis of L- cysteine from sulfate (By similarity)
IMCC26256_11806	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)
IMCC26256_11809	ENOG4107Z1I	Required for maturation of 30S ribosomal subunits (By similarity)
IMCC26256_11810	ENOG4105CHV	Transcription elongation factor NusA
IMCC26256_11811	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)
IMCC26256_11811	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)
IMCC26256_11812	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)
IMCC26256_11814	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
IMCC26256_11815	ENOG4105DTN	riboflavin biosynthesis protein ribF
IMCC26256_11816	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
IMCC26256_11817	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
IMCC26256_11818	ENOG4105C1V	Peptidase, M16
IMCC26256_11819	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
IMCC26256_11822	ENOG41067SE	Tetr family transcriptional regulator
IMCC26256_11824	ENOG4105CN5	Metallo-Beta-Lactamase
IMCC26256_11826	ENOG4107QZI	cell division protein FtsK
IMCC26256_11827	ENOG4105CBM	Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 (By similarity)
IMCC26256_11829	ENOG4105CEV	competence damage-inducible protein
IMCC26256_11831	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)
IMCC26256_11833	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)
IMCC26256_11836	ENOG4105C1N	GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis (By similarity)
IMCC26256_11839	ENOG4105DMJ	Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate (By similarity)
IMCC26256_1184	ENOG4105CS9	pantothenic acid kinase
IMCC26256_11843	ENOG4108Z11	Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes (By similarity)
IMCC26256_11844	ENOG4105BZH	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
IMCC26256_11849	ENOG4108KN0	Choline kinase
IMCC26256_11856	ENOG4108V06	Glutathione peroxidase
IMCC26256_11857	ENOG4105CI3	gtp-binding protein typa
IMCC26256_11858	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
IMCC26256_1186	ENOG4105C89	phosphohexose isomerase
IMCC26256_11860	ENOG4105NYX	DNA-binding protein
IMCC26256_11861	ENOG4105CHR	reductase
IMCC26256_11865	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
IMCC26256_1187	ENOG4105CQC	Prephenate dehydratase
IMCC26256_11875	ENOG4105C9Q	fumarate hydratase class II
IMCC26256_11876	ENOG4107FW0	short-chain dehydrogenase reductase
IMCC26256_11878	ENOG4105C3U	ABC transporter
IMCC26256_11879	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
IMCC26256_1188	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)
IMCC26256_11881	ENOG4105DEF	Extracellular solute-binding protein, family 5
IMCC26256_11885	ENOG4108KZ5	Catalyzes the deacetylation of 1D-myo-inositol 2- acetamido-2-deoxy-alpha-D-glucopyranoside (GlcNAc-Ins) in the mycothiol biosynthesis pathway (By similarity)
IMCC26256_11887	ENOG4105KF3	Short-chain dehydrogenase reductase Sdr
IMCC26256_11890	ENOG4105C26	Dehydrogenase
IMCC26256_11894	ENOG4106A3M	Cytochrome p-450
IMCC26256_11897	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)
IMCC26256_1190	ENOG4105X7H	acyl-CoA dehydrogenase
IMCC26256_11900	ENOG4105W1Y	Transcriptional regulator
IMCC26256_11902	ENOG4105CGU	Enoyl-CoA hydratase
IMCC26256_11904	ENOG4108EQM	faD-dependent pyridine nucleotide-disulfide oxidoreductase
IMCC26256_11905	ENOG4105JNK	Glycosyl transferase (Group 1
IMCC26256_11909	ENOG4105DKQ	ROK family
IMCC26256_1191	ENOG4108KC2	acyl-Coa dehydrogenase
IMCC26256_11910	ENOG41079Y2	Catalyzes the coenzyme F420-dependent oxidation of glucose 6-phosphate (G6P) to 6-phosphogluconolactone
IMCC26256_11915	ENOG4105E39	Enoyl-CoA hydratase
IMCC26256_11916	ENOG4106A3M	Cytochrome p-450
IMCC26256_11919	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)
IMCC26256_1192	ENOG4105CG3	alpha amylase, catalytic region
IMCC26256_11924	ENOG4105C0Z	ABC transporter
IMCC26256_11925	ENOG4108IV0	ABC, transporter
IMCC26256_11927	ENOG4105CHM	Aminotransferase
IMCC26256_11930	ENOG4107QVN	Key enzyme in the regulation of glycerol uptake and metabolism (By similarity)
IMCC26256_11932	ENOG4105C29	acyl-CoA thioesterase
IMCC26256_11934	ENOG4105EFU	Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin (By similarity)
IMCC26256_11938	ENOG4105CQ3	Poorly processive error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by polIV. Exhibits no 3-5 exonuclease (proofreading) activity. May be involved in translesional synthesis in conjunction with the beta clamp from polIII (By similarity)
IMCC26256_11942	ENOG4108V6E	Cell division protein mraZ
IMCC26256_11943	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
IMCC26256_11946	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)
IMCC26256_11948	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
IMCC26256_11949	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
IMCC26256_11950	ENOG4105CNI	cell division protein FtsW
IMCC26256_11951	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)
IMCC26256_11952	ENOG4105DFU	Cell wall formation (By similarity)
IMCC26256_11953	ENOG4105D4A	Cell wall formation (By similarity)
IMCC26256_11954	ENOG4105ME9	cell division protein FtsQ
IMCC26256_11955	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)
IMCC26256_11956	ENOG4105DBW	Multi-copper polyphenol oxidoreductase laccase
IMCC26256_11957	ENOG4105DFA	alanine racemase domain protein
IMCC26256_11958	ENOG4105VR5	Cell division protein that is part of the divisome complex and is recruited early to the Z-ring. Probably stimulates Z-ring formation, perhaps through the cross-linking of FtsZ protofilaments. Its function overlaps with FtsA (By similarity)
IMCC26256_11959	ENOG4108VIA	integral membrane protein
IMCC26256_1196	ENOG4105C5I	Dehydrogenase
IMCC26256_11961	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)
IMCC26256_11962	ENOG4105SCY	DNAK suppressor
IMCC26256_11964	ENOG4105C34	Pseudouridine synthase
IMCC26256_11969	ENOG4105EB3	Histidine kinase
IMCC26256_11974	ENOG4105C8N	cysteinyl-tRNA synthetase
IMCC26256_11975	ENOG4105C22	threonyL-tRNA synthetase
IMCC26256_11979	ENOG4107YQ3	lipid a biosynthesis lauroyl acyltransferase
IMCC26256_1198	ENOG4106YT9	Enoyl-CoA hydratase
IMCC26256_11980	ENOG4105E2K	Glycosyl transferase (Group 1
IMCC26256_11981	ENOG4108V0P	LemA family
IMCC26256_11982	ENOG4105D0M	Protease HtpX homolog
IMCC26256_11983	ENOG4108R5T	secreted protein
IMCC26256_11985	ENOG4108UHX	Involved in the hydrolysis of glutamine to glutamate and ammonia. Channels an ammonia molecule to PdxS (By similarity)
IMCC26256_11986	ENOG4105CDY	transcriptional regulatory protein
IMCC26256_11987	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
IMCC26256_11988	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)
IMCC26256_11989	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)
IMCC26256_11990	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)
IMCC26256_11991	ENOG4105VIE	preprotein translocase, subunit YajC
IMCC26256_11992	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)
IMCC26256_11993	ENOG4107RTU	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)
IMCC26256_11994	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)
IMCC26256_11995	ENOG4105CUT	histidyl-tRNA synthetase
IMCC26256_11996	ENOG4105C9M	aspartyl-trna synthetase