locus-tag	class	description
Mevan_0001	ENOG4105VCQ	rubredoxin
Mevan_0002	ENOG4105ECC	imidazole-glycerol-phosphate dehydratase
Mevan_0004	ENOG4105E4Z	Catalyzes the stereoinversion of LL-2,6- diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso- DAP), a precursor of L-lysine and an essential component of the bacterial peptidoglycan (By similarity)
Mevan_0012	ENOG4108UM1	dedA family
Mevan_0015	ENOG4105IES	Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA (By similarity)
Mevan_0020	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
Mevan_0021	ENOG4105CR7	Catalyzes the transfer of selenium from selenophosphate for conversion of 2-thiouridine to 2-selenouridine at the wobble position in tRNA (By similarity)
Mevan_0022	ENOG4105CR7	Catalyzes the transfer of selenium from selenophosphate for conversion of 2-thiouridine to 2-selenouridine at the wobble position in tRNA (By similarity)
Mevan_0023	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)
Mevan_0027	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
Mevan_0028	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
Mevan_0031	ENOG4105G01	cobalamin (vitamin B12) biosynthesis CbiM protein
Mevan_0040	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)
Mevan_0044	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)
Mevan_0046	ENOG4105D1X	Specifically dimethylates two adjacent adenosines (A1518 and A1519) in the loop of a conserved hairpin near the 3'-end of 16S rRNA in the 30S particle. May play a critical role in biogenesis of 30S subunits (By similarity)
Mevan_0048	ENOG4105D6W	Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps (By similarity)
Mevan_0049	ENOG4107RBB	ABC transporter, permease
Mevan_0051	ENOG4108Z6B	deaminase
Mevan_0055	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)
Mevan_0060	ENOG4105D0B	Nitrogenase protein alpha chain
Mevan_0061	ENOG4105CY9	nitrogenase molybdenum-iron protein beta chain
Mevan_0062	ENOG4105D0B	Nitrogenase protein alpha chain
Mevan_0063	ENOG4108YZA	Nitrogen regulatory protein pii
Mevan_0064	ENOG4108YZA	Nitrogen regulatory protein pii
Mevan_0065	ENOG4105DSM	The key enzymatic reactions in nitrogen fixation are catalyzed by the nitrogenase complex, which has 2 components the iron protein and the molybdenum-iron protein (By similarity)
Mevan_0067	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)
Mevan_0068	ENOG4105EWK	phytoene
Mevan_0075	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)
Mevan_0093	ENOG4105CFG	Acts as a chaperone (By similarity)
Mevan_0122	ENOG4105MJ2	Competence protein
Mevan_0124	ENOG4107SV1	subunit D
Mevan_0125	ENOG4105EET	magnesium chelatase
Mevan_0126	ENOG4105CTK	cobaltochelatase, cobn subunit
Mevan_0128	ENOG4105E0A	ABC, transporter
Mevan_0130	ENOG4105EHG	Permease protein
Mevan_0138	ENOG4108V3W	Chemotaxis protein, CheW
Mevan_0142	ENOG4105BZU	Histidine kinase
Mevan_0143	ENOG4105C0A	alcohol dehydrogenase
Mevan_0144	ENOG4105BZU	Histidine kinase
Mevan_0147	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)
Mevan_0151	ENOG4105C3M	thioredoxin reductase
Mevan_0157	ENOG4105CH8	Succinyl-CoA ligase ADP-forming subunit alpha
Mevan_0158	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)
Mevan_0162	ENOG4105C26	Dehydrogenase
Mevan_0169	ENOG4105CB3	Required for the thiolation of cytidine in position 32 of tRNA, to form 2-thiocytidine (s(2)C32) (By similarity)
Mevan_0170	ENOG4105C8N	cysteinyl-tRNA synthetase
Mevan_0172	ENOG4105DWV	Homoserine O-trans-acetylase
Mevan_0173	ENOG4107QI6	Cysteine desulfurase
Mevan_0174	ENOG4107RIU	May be involved in the formation or repair of Fe-S clusters present in iron-sulfur proteins (By similarity)
Mevan_0175	ENOG4105CB3	Required for the thiolation of cytidine in position 32 of tRNA, to form 2-thiocytidine (s(2)C32) (By similarity)
Mevan_0177	ENOG4105D7W	serine acetyltransferase
Mevan_0178	ENOG4105C6T	cysteine synthase
Mevan_0182	ENOG4105DBV	ornithine carbamoyltransferase
Mevan_0183	ENOG4107Y49	methyltransferase
Mevan_0198	ENOG4105EAG	UDP-N-acetylglucosamine 2-epimerase
Mevan_0199	ENOG4105CPK	Glycosyl transferase (Group 1
Mevan_0201	ENOG4105CGN	Glycosyl transferase (Group 1
Mevan_0207	ENOG4108V2W	Carbonate dehydratase
Mevan_0211	ENOG4105CAQ	asparagine synthetase
Mevan_0212	ENOG4105DF0	Responsible for channeling the electrons from the oxidation of dihydroorotate from the FMN redox center in the PyrD type B subunit to the ultimate electron acceptor NAD( ) (By similarity)
Mevan_0213	ENOG4105C3E	May play a key role in the regulation of the intracellular concentration of adenosylhomocysteine (By similarity)
Mevan_0216	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
Mevan_0218	ENOG4108V3W	Chemotaxis protein, CheW
Mevan_0219	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
Mevan_0220	ENOG4105CBS	Chea signal transduction histidine kinase
Mevan_0221	ENOG4108Z4W	Probably deamidates glutamine residues to glutamate on methyl-accepting chemotaxis receptors (MCPs), playing an important role in chemotaxis (By similarity)
Mevan_0224	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
Mevan_0225	ENOG41083C3	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
Mevan_0229	ENOG4105DYN	CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Acts as a dsDNA endonuclease. May be involved in the integration of spacer DNA into the CRISPR cassette (By similarity)
Mevan_0236	ENOG4105E4R	Precorrin-3B C17-methyltransferase
Mevan_0238	ENOG4105DH2	Converts cobyric acid to cobinamide by the addition of aminopropanol on the F carboxylic group (By similarity)
Mevan_0242	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)
Mevan_0243	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)
Mevan_0246	ENOG4105DW0	Catalyzes the ADP transfer to D-glycero-D-manno-heptose 1-phosphate, yielding ADP-D,D-heptose (By similarity)
Mevan_0251	ENOG4107XPA	Joins Ado-cobinamide-GDP and alpha-ribazole to generate adenosylcobalamin (Ado-cobalamin) (By similarity)
Mevan_0253	ENOG4105E2X	shikimate dehydrogenase
Mevan_0256	ENOG4107YTP	response regulator receiver protein
Mevan_0259	ENOG4105BZU	Histidine kinase
Mevan_0262	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)
Mevan_0270	ENOG4107Z3H	Transcriptional regulator, TetR family
Mevan_0271	ENOG4105ENX	hydrolase
Mevan_0274	ENOG4105C8M	UPF0272 protein
Mevan_0276	ENOG4105CPC	Aldo Keto reductase
Mevan_0277	ENOG4105DTC	1-(5-phosphoribosyl)-5-amino-4-imidazole-carboxylate (air) carboxylase
Mevan_0282	ENOG4108IG5	Transcriptional regulator
Mevan_0283	ENOG4105EAB	amino acid AbC transporter
Mevan_0289	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)
Mevan_0291	ENOG4105CEK	Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine (By similarity)
Mevan_0293	ENOG4107T0X	DNA ligase
Mevan_0294	ENOG4105C83	adenylosuccinate lyase
Mevan_0295	ENOG4105NTK	Transcriptional repressor Mpra
Mevan_0303	ENOG41080XS	Cobyrinic acid ac-diamide synthase
Mevan_0305	ENOG4105BZ8	glutamate synthase
Mevan_0306	ENOG4105EYX	Acetyl-CoA decarbonylase synthase complex subunit gamma
Mevan_0308	ENOG41080XS	Cobyrinic acid ac-diamide synthase
Mevan_0309	ENOG4105E8X	CO dehydrogenase acetyl-CoA synthase complex beta subunit
Mevan_0313	ENOG4105D1X	Specifically dimethylates two adjacent adenosines (A1518 and A1519) in the loop of a conserved hairpin near the 3'-end of 16S rRNA in the 30S particle. May play a critical role in biogenesis of 30S subunits (By similarity)
Mevan_0317	ENOG4105DTC	1-(5-phosphoribosyl)-5-amino-4-imidazole-carboxylate (air) carboxylase
Mevan_0328	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
Mevan_0329	ENOG4108ZGB	N-(5'-phosphoribosyl)anthranilate isomerase
Mevan_0330	ENOG4105DDQ	anthranilate synthase
Mevan_0331	ENOG4105CRQ	synthase (Component I)
Mevan_0337	ENOG4108YBP	pseudouridine synthase
Mevan_0338	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)
Mevan_0339	ENOG4105CGK	Exodeoxyribonuclease III
Mevan_0341	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
Mevan_0347	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)
Mevan_0350	ENOG4105C75	arginyL-tRNA synthetase
Mevan_0357	ENOG410805Y	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
Mevan_0360	ENOG4108UXA	Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA (By similarity)
Mevan_0363	ENOG41085E0	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)
Mevan_0367	ENOG4108JIQ	Produces ATP from ADP in the presence of a proton gradient across the membrane. The V-type alpha chain is a catalytic subunit (By similarity)
Mevan_0368	ENOG4108JIP	Produces ATP from ADP in the presence of a proton gradient across the membrane. The V-type beta chain is a regulatory subunit (By similarity)
Mevan_0369	ENOG4105M56	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
Mevan_0374	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
Mevan_0376	ENOG41086B8	CoB-CoM heterodisulfide reductase
Mevan_0382	ENOG4105C8N	cysteinyl-tRNA synthetase
Mevan_0383	ENOG4108ZK7	protein family UPF0029, Impact, N-terminal protein
Mevan_0385	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)
Mevan_0390	ENOG4105E33	succinate dehydrogenase
Mevan_0392	ENOG4105D07	Signal peptide peptidase, SppA
Mevan_0399	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)
Mevan_0400	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
Mevan_0408	ENOG4107Z5F	Aminotransferase class IV
Mevan_0415	ENOG4105C1B	dTDP-glucose 4-6-dehydratase
Mevan_0416	ENOG4105C3Y	UTP-glucose-1-phosphate uridylyltransferase
Mevan_0419	ENOG4108HRN	Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate (By similarity)
Mevan_0421	ENOG4105C8U	phosphate abc transporter
Mevan_0422	ENOG4105E2Z	phosphate ABC transporter (Permease
Mevan_0423	ENOG4105BZY	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
Mevan_0426	ENOG4105C8Y	Acetylornithine aminotransferase
Mevan_0427	ENOG4107RZC	phospholipase d
Mevan_0429	ENOG4108R9M	Involved in allosteric regulation of aspartate carbamoyltransferase (By similarity)
Mevan_0430	ENOG4105CMV	Succinyl-CoA synthetase subunit beta
Mevan_0438	ENOG4108IUS	Transketolase
Mevan_0439	ENOG4105DJV	ribulose-phosphate 3-epimerase
Mevan_0440	ENOG4108HHA	Transketolase
Mevan_0441	ENOG4105CN9	Peptidase m42 family protein
Mevan_0444	ENOG4105BZU	Histidine kinase
Mevan_0445	ENOG4105C3G	gtp-binding protein
Mevan_0447	ENOG4105CG2	Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 (By similarity)
Mevan_0449	ENOG4105CYJ	ribosomal RNA small subunit methyltransferase B
Mevan_0451	ENOG4108R5K	PPIases accelerate the folding of proteins (By similarity)
Mevan_0452	ENOG4108YXI	Secondary thiamine-phosphate synthase enzyme
Mevan_0455	ENOG4105DG4	malate L-lactate dehydrogenase
Mevan_0456	ENOG4105CNW	domain protein
Mevan_0457	ENOG4105CNW	domain protein
Mevan_0458	ENOG4105KY8	Rubrerythrin
Mevan_0461	ENOG4108UV6	Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP) (By similarity)
Mevan_0463	ENOG4107QRT	dEAD DEAH box helicase
Mevan_0466	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
Mevan_0467	ENOG4107QMS	site-determining protein
Mevan_0471	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
Mevan_0473	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)
Mevan_0475	ENOG41086B8	CoB-CoM heterodisulfide reductase
Mevan_0477	ENOG4105MAX	Superoxide reductase
Mevan_0482	ENOG4105CNW	domain protein
Mevan_0483	ENOG4108531	cuta1 divalent ion tolerance protein
Mevan_0487	ENOG4105CJS	Phosphopantothenoylcysteine decarboxylase
Mevan_0488	ENOG4105C3K	feS assembly ATPase SufC
Mevan_0489	ENOG4105DIW	FeS assembly protein SUFB
Mevan_0490	ENOG4105CKK	Glycosyl transferase, family 2
Mevan_0491	ENOG4106PT6	cdpdiacylglycerol-serine O-phosphatidyltransferase
Mevan_0492	ENOG4105D3R	alkyl hydroperoxide reductase
Mevan_0498	ENOG4105EHG	Permease protein
Mevan_0499	ENOG4108HWH	(ABC) transporter
Mevan_0501	ENOG4108USZ	hydrogenase
Mevan_0502	ENOG4105C6P	ATP-dependent serine protease that mediates the selective degradation of mutant and abnormal proteins as well as certain short-lived regulatory proteins. Required for cellular homeostasis and for survival from DNA damage and developmental changes induced by stress. Degrades polypeptides processively to yield small peptide fragments that are 5 to 10 amino acids long. Binds to DNA in a double-stranded, site-specific manner (By similarity)
Mevan_0503	ENOG4107W7X	Aldolase
Mevan_0505	ENOG4105E66	phosphoriboisomerase A
Mevan_0506	ENOG4108YZY	peptidylprolyl cis-trans isomerase
Mevan_0507	ENOG41068T5	Catalyzes the hydrolysis of methenyl-H(4)MPT( ) to 5- formyl-H(4)MPT (By similarity)
Mevan_0512	ENOG4105EUS	Binding-protein-dependent transport systems, inner membrane component
Mevan_0514	ENOG4108UTW	Plays a role in the regulation of phosphate uptake
Mevan_0515	ENOG4105CU5	Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine (By similarity)
Mevan_0518	ENOG4105EE8	May catalyze the methylation of C-1 in cobalt-precorrin- 5 and the subsequent extrusion of acetic acid from the resulting intermediate to form cobalt-precorrin-6A (By similarity)
Mevan_0519	ENOG4105DC7	peptidase M24
Mevan_0520	ENOG4105CMY	5-enolpyruvylshikimate-3-phosphate synthase
Mevan_0521	ENOG4105C5F	glutamine synthetase
Mevan_0523	ENOG4105EM7	Selenocysteine-specific translation elongation factor
Mevan_0527	ENOG4105CHU	acetyl-coa acetyltransferase
Mevan_0530	ENOG4105CAA	catalyzes amidations at positions B, D, E, and G on adenosylcobyrinic A,C-diamide. NH(2) groups are provided by glutamine, and one molecule of ATP is hydrogenolyzed for each amidation (By similarity)
Mevan_0534	ENOG4105DVT	helicase
Mevan_0535	ENOG4107R76	Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties (By similarity)
Mevan_0536	ENOG4105E26	Catalyzes the methyl esterification of L-isoaspartyl residues in peptides and proteins that result from spontaneous decomposition of normal L-aspartyl and L-asparaginyl residues. It plays a role in the repair and or degradation of damaged proteins (By similarity)
Mevan_0540	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)
Mevan_0544	ENOG4105D18	nicotinate-nucleotide pyrophosphorylase
Mevan_0546	ENOG4107R56	PP-loop domain protein
Mevan_0547	ENOG4107H9G	Necessary for formate dehydrogenase activity (By similarity)
Mevan_0548	ENOG4105D06	uba thif-type nad fad binding protein
Mevan_0549	ENOG4108ZAF	Molybdopterin
Mevan_0552	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)
Mevan_0562	ENOG4105DCC	Formylmethanofuran dehydrogenase subunit A
Mevan_0565	ENOG41080XP	Cbs domain
Mevan_0566	ENOG41080XP	Cbs domain
Mevan_0568	ENOG4105CXB	phosphoribosylaminoimidazole synthetase
Mevan_0571	ENOG4105D52	delta-aminolevulinic acid dehydratase
Mevan_0572	ENOG4107QZF	nitrite reductase NADPH large subunit
Mevan_0578	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)
Mevan_0579	ENOG4105HDK	L-asparaginase
Mevan_0582	ENOG4108VA3	3-hexulose-6-phosphate synthase
Mevan_0584	ENOG4105DI2	Pyruvate flavodoxin ferredoxin oxidoreductase domain protein
Mevan_0589	ENOG4105KJJ	Uncharacterized ACR, COG1993
Mevan_0590	ENOG4105WMR	Protein CrcB homolog
Mevan_0598	ENOG4105D3H	Catalyzes the decarboxylation of 3-octaprenyl-4-hydroxy benzoate to 2-octaprenylphenol (By similarity)
Mevan_0600	ENOG4105WHM	Necessary for normal cell division and for the maintenance of normal septation (By similarity)
Mevan_0604	ENOG4105CXW	Synthesizes alpha-1,4-glucan chains using ADP-glucose (By similarity)
Mevan_0605	ENOG4105C89	phosphohexose isomerase
Mevan_0609	ENOG4108V2W	Carbonate dehydratase
Mevan_0611	ENOG4105TMB	Formate nitrite transporter
Mevan_0613	ENOG4105BZU	Histidine kinase
Mevan_0614	ENOG4105E3W	Two component transcriptional regulator (Winged helix family
Mevan_0617	ENOG4105DR4	Methyltransferase
Mevan_0618	ENOG4105CW3	Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway (By similarity)
Mevan_0626	ENOG4105DDK	oxidoreductase, beta subunit
Mevan_0629	ENOG4105DK7	lysyl-tRNA synthetase
Mevan_0630	ENOG4108Z04	Located at the top of the head of the 30S subunit, it contacts several helices of the 16S rRNA. In the 70S ribosome it contacts the 23S rRNA (bridge B1a) and protein L5 of the 50S subunit (bridge B1b), connecting the 2 subunits
Mevan_0631	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)
Mevan_0632	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)
Mevan_0634	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
Mevan_0635	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)
Mevan_0639	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
Mevan_0641	ENOG4105WRB	Hydrogenase assembly chaperone hypC hupF
Mevan_0643	ENOG4107QN2	dihydrolipoyl dehydrogenase
Mevan_0645	ENOG4105C9W	Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity (By similarity)
Mevan_0647	ENOG4105EM7	Selenocysteine-specific translation elongation factor
Mevan_0650	ENOG4105EQY	Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif (By similarity)
Mevan_0652	ENOG4107WZZ	SMC domain protein
Mevan_0656	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
Mevan_0659	ENOG4105WCJ	ec 1.1.1.193
Mevan_0660	ENOG4105C4K	Nad synthetase
Mevan_0661	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)
Mevan_0663	ENOG4105IQJ	Involved in biosynthesis of the thiamine precursor thiazole (By similarity)
Mevan_0664	ENOG4105D8I	Catalyzes the ATP-dependent transfer of a sulfur to tRNA to produce 4-thiouridine in position 8 of tRNAs, which functions as a near-UV photosensor. Also catalyzes the transfer of sulfur to the sulfur carrier protein ThiS, forming ThiS-thiocarboxylate. This is a step in the synthesis of thiazole, in the thiamine biosynthesis pathway. The sulfur is donated as persulfide by IscS (By similarity)
Mevan_0666	ENOG4105CB3	Required for the thiolation of cytidine in position 32 of tRNA, to form 2-thiocytidine (s(2)C32) (By similarity)
Mevan_0669	ENOG4105CP4	Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth (By similarity)
Mevan_0672	ENOG4108IIJ	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
Mevan_0673	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
Mevan_0674	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
Mevan_0676	ENOG4105CHV	Transcription elongation factor NusA
Mevan_0678	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)
Mevan_0679	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)
Mevan_0680	ENOG4105C3T	may be the GTPase, regulating ATP sulfurylase activity (By similarity)
Mevan_0681	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
Mevan_0682	ENOG4107QKV	phosphomannomutase
Mevan_0684	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
Mevan_0685	ENOG41066UU	tRNA (Adenine-N1-)-methyltransferase
Mevan_0689	ENOG4105C0V	Provides the sole de novo source of dTMP for DNA biosynthesis (By similarity)
Mevan_0691	ENOG4105CY0	Metallo-Beta-Lactamase
Mevan_0694	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)
Mevan_0697	ENOG41074MP	UPF0103 Mediator of ErbB2-driven cell motility-containing protein
Mevan_0702	ENOG4107QK3	aspartate-semialdehyde dehydrogenase (EC 1.2.1.11
Mevan_0707	ENOG4105CHM	Aminotransferase
Mevan_0708	ENOG4105CDB	Required for chromosome condensation and partitioning (By similarity)
Mevan_0709	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)
Mevan_0710	ENOG4105CGT	Catalyzes the transfer of a phosphate group to glutamate to form glutamate 5-phosphate which rapidly cyclizes to 5- oxoproline (By similarity)
Mevan_0714	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)
Mevan_0715	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
Mevan_0716	ENOG41082SA	50s ribosomal protein l29
Mevan_0719	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
Mevan_0720	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
Mevan_0721	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
Mevan_0723	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
Mevan_0725	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)
Mevan_0726	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)
Mevan_0729	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)
Mevan_0730	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)
Mevan_0732	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
Mevan_0733	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)
Mevan_0734	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
Mevan_0737	ENOG4105DHP	deoxycytidine triphosphate deaminase
Mevan_0738	ENOG4105CAG	UPF0210 protein
Mevan_0741	ENOG4105D37	Low-affinity potassium transport system. Interacts with Trk system potassium uptake protein TrkA (By similarity)
Mevan_0743	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
Mevan_0744	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
Mevan_0747	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)
Mevan_0749	ENOG4105K4I	Scp-like extracellular
Mevan_0750	ENOG4105E3H	phosphoglycerate mutase
Mevan_0754	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
Mevan_0756	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
Mevan_0772	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)
Mevan_0773	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)
Mevan_0777	ENOG4105CP4	Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth (By similarity)
Mevan_0779	ENOG4105SC1	monovalent cation H antiporter subunit E
Mevan_0782	ENOG4108T9Q	UPF0278 protein
Mevan_0784	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)
Mevan_0787	ENOG4105C0Y	Responsible for the amidation of carboxylic groups at position A and C of either cobyrinic acid or hydrogenobrynic acid. NH(2) groups are provided by glutamine, and one molecule of ATP is hydrogenolyzed for each amidation (By similarity)
Mevan_0789	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
Mevan_0790	ENOG4105CFT	Part of the energy-coupling factor (ECF) transporter complex CbiMNOQ involved in cobalt import (By similarity)
Mevan_0794	ENOG4108RIR	Molybdenum cofactor biosynthesis protein
Mevan_0797	ENOG4105D1U	peptidase U62 modulator of DNA gyrase
Mevan_0798	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)
Mevan_0800	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)
Mevan_0801	ENOG41065E1	Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) (By similarity)
Mevan_0804	ENOG4105N5T	Radical SAM Protein
Mevan_0809	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)
Mevan_0810	ENOG4108RE9	Phosphodiesterase
Mevan_0811	ENOG4105BZ8	glutamate synthase
Mevan_0812	ENOG4108MFN	small subunit of hydrogenase-3, iron-sulfur protein (part of formate hydrogenlyase (FHL) complex)
Mevan_0813	ENOG4105DDK	oxidoreductase, beta subunit
Mevan_0814	ENOG4105D95	Oxidoreductase required for the transfer of electrons from pyruvate to flavodoxin (By similarity)
Mevan_0816	ENOG4105EJ5	oxidoreductase gamma subunit
Mevan_0817	ENOG4108JYZ	YitT family
Mevan_0823	ENOG4105BZG	amino acid carrier protein
Mevan_0824	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
Mevan_0827	ENOG4105EHE	chorismate mutase- prephenate dehydrogenase
Mevan_0828	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
Mevan_0829	ENOG4108KVX	Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpB that pull DNA away from mid-cell into both cell halves (By similarity)
Mevan_0831	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
Mevan_0832	ENOG4108I5D	sulfate abc transporter
Mevan_0836	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)
Mevan_0837	ENOG4107QT7	Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA (By similarity)
Mevan_0839	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)
Mevan_0840	ENOG4105CHM	Aminotransferase
Mevan_0841	ENOG4105CQC	Prephenate dehydratase
Mevan_0845	ENOG4105BZA	Phosphoglycerate kinase
Mevan_0859	ENOG41080KG	One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome (By similarity)
Mevan_0860	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
Mevan_0861	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
Mevan_0866	ENOG4108UMA	3-octaprenyl-4-hydroxybenzoate carboxy-lyase
Mevan_0880	ENOG4108QZ0	Tetrahydromethanopterin S-methyltransferase (EC 2.1.1.86)
Mevan_0883	ENOG4105F8V	Hydrolase, tatD family
Mevan_0885	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)
Mevan_0886	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)
Mevan_0887	ENOG4108W8G	Catalyzes the transformation of pimelate into pimeloyl- CoA with concomitant hydrolysis of ATP to AMP (By similarity)
Mevan_0895	ENOG4105X3E	Catalyzes the decarboxylation of S-adenosylmethionine to S-adenosylmethioninamine (dcAdoMet), the propylamine donor required for the synthesis of the polyamines spermine and spermidine from the diamine putrescine (By similarity)
Mevan_0896	ENOG4105CCX	Catalyzes the production of spermidine from putrescine and decarboxylated S-adenosylmethionine (dcSAM), which serves as an aminopropyl donor (By similarity)
Mevan_0897	ENOG4105CYW	agmatinase
Mevan_0899	ENOG41060GT	Translocates 4-amino-4-deoxy-L-arabinose- phosphoundecaprenol (alpha-L-Ara4N-phosphoundecaprenol) from the cytoplasmic to the periplasmic side of the inner membrane (By similarity)
Mevan_0901	ENOG4105C1M	carbamoyl-phosphate synthetase glutamine chain
Mevan_0903	ENOG4108P62	biosynthesis protein (CbiG)
Mevan_0904	ENOG4105C31	Tryptophanyl-tRNA synthetase
Mevan_0911	ENOG4105C1A	potassium transporter peripheral membrane
Mevan_0913	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
Mevan_0916	ENOG4105CA9	Pyruvate kinase
Mevan_0917	ENOG4105CJS	Phosphopantothenoylcysteine decarboxylase
Mevan_0919	ENOG4105FIE	Catalyzes the transfer of a formyl group from 5-formyl tetrahydromethanopterin (5-formyl-H(4)MPT) to methanofuran (MFR) so as to produce formylmethanofuran (formyl-MFR) and tetrahydromethanopterin (H(4)MPT) (By similarity)
Mevan_0924	ENOG4105CUT	histidyl-tRNA synthetase
Mevan_0925	ENOG4105VG1	fes assembly suf system protein
Mevan_0926	ENOG4105C5S	asparaginyl-tRNA synthetase
Mevan_0927	ENOG4105C35	Catalyzes the interconversion of methylthioribose-1- phosphate (MTR-1-P) into methylthioribulose-1-phosphate (MTRu-1-P) (By similarity)
Mevan_0928	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
Mevan_0931	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)
Mevan_0937	ENOG4108JPZ	Monovalent cation H antiporter subunit D
Mevan_0938	ENOG4105MKQ	Monovalent cation H antiporter subunit C
Mevan_0939	ENOG4108JEI	Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system (By similarity)
Mevan_0941	ENOG4105K63	Thioredoxin
Mevan_0944	ENOG4107ZCS	Phosphomethylpyrimidine kinase
Mevan_0945	ENOG4105DZH	s-adenosylmethionine synthetase (EC 2.5.1.6)
Mevan_0946	ENOG4105C8X	One of the components of the high-affinity ATP-driven potassium transport (or KDP) system, which catalyzes the hydrolysis of ATP coupled with the exchange of hydrogen and potassium ions (By similarity)
Mevan_0947	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
Mevan_0952	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)
Mevan_0954	ENOG41066FR	extracellular solute-binding protein
Mevan_0956	ENOG4108UHX	Involved in the hydrolysis of glutamine to glutamate and ammonia. Channels an ammonia molecule to PdxS (By similarity)
Mevan_0957	ENOG4108JVH	Protein of unknown function DUF43
Mevan_0959	ENOG4105CXT	aspartate transcarbamylase
Mevan_0962	ENOG4105CIA	precorrin-4 C(11)-methyltransferase
Mevan_0980	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
Mevan_0981	ENOG4105ET3	Reduction of activated sulfate into sulfite (By similarity)
Mevan_0988	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
Mevan_0991	ENOG4105DTI	Phosphonopyruvate decarboxylase
Mevan_0997	ENOG4105E3S	small subunit
Mevan_1002	ENOG4108IA2	Sodium pantothenate symporter
Mevan_1004	ENOG4105D6E	homoserine dehydrogenase
Mevan_1009	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
Mevan_1014	ENOG4105DUM	transcriptional regulator, lysR family
Mevan_1017	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
Mevan_1019	ENOG4105E26	Catalyzes the methyl esterification of L-isoaspartyl residues in peptides and proteins that result from spontaneous decomposition of normal L-aspartyl and L-asparaginyl residues. It plays a role in the repair and or degradation of damaged proteins (By similarity)
Mevan_1025	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)
Mevan_1031	ENOG4105DZA	Converts GTP to 7,8-dihydroneopterin triphosphate (By similarity)
Mevan_1032	ENOG4105CPF	Cell wall formation (By similarity)
Mevan_1058	ENOG4106UJV	Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its allylic isomer, dimethylallyl diphosphate (DMAPP) (By similarity)
Mevan_1062	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)
Mevan_1064	ENOG4108Z0R	Transferase
Mevan_1065	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)
Mevan_1066	ENOG4105KPZ	phosphoribosyl-atp pyrophosphatase
Mevan_1067	ENOG4105CP4	Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth (By similarity)
Mevan_1072	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)
Mevan_1078	ENOG4105CAS	nag kinase
Mevan_1079	ENOG4108YZA	Nitrogen regulatory protein pii
Mevan_1081	ENOG4108YZA	Nitrogen regulatory protein pii
Mevan_1082	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)
Mevan_1089	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
Mevan_1091	ENOG4107QP2	Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) (By similarity)
Mevan_1092	ENOG4105EYU	Glutamine amido-transferase
Mevan_1093	ENOG4105CBC	glutamate synthase
Mevan_1100	ENOG4105C7E	Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) (By similarity)
Mevan_1102	ENOG4107RA4	Glycosyl transferase (Group 1
Mevan_1108	ENOG4105C1I	TRANSCRIPTIONAl REGULATOR GntR family
Mevan_1109	ENOG4108JCI	Transcriptional regulator
Mevan_1111	ENOG4105C6X	Major Facilitator
Mevan_1112	ENOG4105E26	Catalyzes the methyl esterification of L-isoaspartyl residues in peptides and proteins that result from spontaneous decomposition of normal L-aspartyl and L-asparaginyl residues. It plays a role in the repair and or degradation of damaged proteins (By similarity)
Mevan_1113	ENOG4105CD9	Involved in the production of pyridoxal phosphate, probably by incorporating ammonia into the pyridine ring (By similarity)
Mevan_1117	ENOG4105E3H	phosphoglycerate mutase
Mevan_1121	ENOG4105C0N	N-acetylglutamate semialdehyde dehydrogenase
Mevan_1123	ENOG4108RW0	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
Mevan_1124	ENOG4105HJX	Biotin- acetyl-CoA-carboxylase ligase
Mevan_1128	ENOG4108HH9	Catalyzes two reactions the first one is the production of beta-formyl glycinamide ribonucleotide (GAR) from formate, ATP and beta GAR
Mevan_1136	ENOG4105CVK	Glutamate decarboxylase
Mevan_1137	ENOG4105CM2	brancheD-chain amino acid aminotransferase
Mevan_1138	ENOG4105CP4	Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth (By similarity)
Mevan_1140	ENOG4108IYI	Catalyzes the gamma-elimination of phosphate from L- phosphohomoserine and the beta-addition of water to produce L- threonine (By similarity)
Mevan_1141	ENOG4105MQS	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
Mevan_1149	ENOG4105ERH	Fumarylacetoacetate hydrolase
Mevan_1150	ENOG4109003	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis (By similarity)
Mevan_1151	ENOG4105EWK	phytoene
Mevan_1154	ENOG4105C4H	Specifically methylates the guanine in position 2445 (m2G2445) and the guanine in position 2069 (m7G2069) of 23S rRNA (By similarity)
Mevan_1157	ENOG4107QWE	)-transporter
Mevan_1158	ENOG4107SDT	Homocitrate synthase
Mevan_1163	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
Mevan_1166	ENOG4108N5B	2-phosphosulfolactate phosphatase
Mevan_1168	ENOG4105D0U	Arsenite-activated ATPase (ArsA)
Mevan_1171	ENOG4105UQX	Mate efflux family protein
Mevan_1178	ENOG4105DCI	Phosphohydrolase
Mevan_1180	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)
Mevan_1182	ENOG4105D21	Phosphoribosylformylglycinamidine synthase I
Mevan_1183	ENOG4107QIK	phosphoribosylformylglycinamidine synthase
Mevan_1185	ENOG4105C66	Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate (By similarity)
Mevan_1187	ENOG4105CB1	The purine nucleoside phosphorylases catalyze the phosphorolytic breakdown of the N-glycosidic bond in the beta- (deoxy)ribonucleoside molecules, with the formation of the corresponding free purine bases and pentose-1-phosphate (By similarity)
Mevan_1188	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)
Mevan_1189	ENOG4105CBF	Catalyzes the synthesis of the hydroxymethylpyrimidine phosphate (HMP-P) moiety of thiamine from aminoimidazole ribotide (AIR) in a radical S-adenosyl-L-methionine (SAM)-dependent reaction (By similarity)
Mevan_1192	ENOG410642S	Nicotianamine synthase protein
Mevan_1194	ENOG4105CE1	Ferrous iron transport protein b
Mevan_1195	ENOG4105CK3	Lysine 2,3-aminomutase YodO family protein
Mevan_1197	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)
Mevan_1201	ENOG4105MRR	Transcriptional regulator (By similarity)
Mevan_1207	ENOG4106NZV	Responsible for synthesis of pseudouridine from uracil- 13 in transfer RNAs (By similarity)
Mevan_1208	ENOG4105CH7	arginosuccinase
Mevan_1215	ENOG4106M32	3-dehydroquinate synthase
Mevan_1218	ENOG4105DI2	Pyruvate flavodoxin ferredoxin oxidoreductase domain protein
Mevan_1221	ENOG4105CKD	glutathione-regulated potassium-efflux system protein
Mevan_1227	ENOG4105D9H	Catalyzes the attachment of glycine to tRNA(Gly) (By similarity)
Mevan_1229	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)
Mevan_1231	ENOG4105C59	p-type ATPase
Mevan_1233	ENOG4105E2M	Manganese-dependent inorganic pyrophosphatase
Mevan_1237	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
Mevan_1240	ENOG4105FD2	Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) (By similarity)
Mevan_1241	ENOG4105CJD	(Anaerobic) ribonucleoside-triphosphate reductase
Mevan_1242	ENOG4108K3F	N(2),N(2)-dimethylguanosine tRNA methyltransferase
Mevan_1266	ENOG4105CD5	CoA-binding domain protein
Mevan_1267	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)
Mevan_1269	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)
Mevan_1273	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)
Mevan_1276	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)
Mevan_1277	ENOG4105D64	Mechanosensitive ion channel
Mevan_1278	ENOG41081FY	multiple antibiotic resistance (MarC)-related
Mevan_1281	ENOG4105C8M	UPF0272 protein
Mevan_1282	ENOG4108R3D	Electron transport complex
Mevan_1284	ENOG4108JEI	Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system (By similarity)
Mevan_1285	ENOG41061P3	phosphosulfolactate synthase
Mevan_1286	ENOG4105C45	hydrogenase expression formation protein (HypE)
Mevan_1289	ENOG4105CP4	Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth (By similarity)
Mevan_1291	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
Mevan_1293	ENOG4108UM6	Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) (By similarity)
Mevan_1295	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)
Mevan_1296	ENOG4107EEM	One of the essential components for the initiation of protein synthesis. Protects formylmethionyl-tRNA from spontaneous hydrolysis and promotes its binding to the 30S ribosomal subunits. Also involved in the hydrolysis of GTP during the formation of the 70S ribosomal complex (By similarity)
Mevan_1299	ENOG4105CP4	Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth (By similarity)
Mevan_1300	ENOG4105CQS	hydrogenase expression formation protein HypD
Mevan_1306	ENOG4105D5I	Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate (By similarity)
Mevan_1312	ENOG4105WMM	Probably plays a role in a hydrogenase nickel cofactor insertion step (By similarity)
Mevan_1313	ENOG41082X2	rubredoxin
Mevan_1315	ENOG4105C7Z	Conserved Protein
Mevan_1316	ENOG4105DQU	oxidoreductase, subunit beta
Mevan_1325	ENOG4105DZS	Phenylacetate-CoA ligase
Mevan_1328	ENOG4107NFR	Fructose-1,6-bisphosphatase
Mevan_1329	ENOG4105C01	Dihydroxy-acid dehydratase
Mevan_1331	ENOG4105D5I	Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate (By similarity)
Mevan_1333	ENOG4105D1H	recombination factor protein RarA
Mevan_1341	ENOG41081F0	Precorrin-8x methylmutase
Mevan_1342	ENOG4105K59	histidine triad (HIT) protein
Mevan_1349	ENOG4108K7V	UPF0284 protein
Mevan_1350	ENOG4107QSA	Oxaloacetate decarboxylase
Mevan_1351	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
Mevan_1355	ENOG4105CVA	phosphate
Mevan_1356	ENOG4105DCU	2-hydroxyglutaryl-CoA dehydratase
Mevan_1357	ENOG4106HK8	GPR1 FUN34 yaaH family protein
Mevan_1358	ENOG4105CIZ	coA-substrate-specific enzyme activase
Mevan_1359	ENOG4105EN6	Membrane
Mevan_1362	ENOG4108T9Q	UPF0278 protein
Mevan_1363	ENOG4105CM1	Catalyzes, together with MoaC, the conversion of 5'-GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
Mevan_1366	ENOG41080U2	Amidohydrolase family
Mevan_1368	ENOG4105MQS	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
Mevan_1372	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
Mevan_1375	ENOG4105P52	geranylgeranyl reductase
Mevan_1378	ENOG4105C5R	Aminotransferase
Mevan_1379	ENOG4107QNG	Phosphoribosylglycinamide synthetase
Mevan_1383	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
Mevan_1384	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)
Mevan_1386	ENOG4105D0M	Protease HtpX homolog
Mevan_1388	ENOG4105DSS	Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation (By similarity)
Mevan_1390	ENOG4107XMU	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
Mevan_1392	ENOG4105EIH	LPPG Fo 2-phospho-L-lactate transferase
Mevan_1395	ENOG41080XP	Cbs domain
Mevan_1398	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
Mevan_1400	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)
Mevan_1403	ENOG4105C22	threonyL-tRNA synthetase
Mevan_1404	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)
Mevan_1407	ENOG4105CP4	Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth (By similarity)
Mevan_1417	ENOG4105F8V	Hydrolase, tatD family
Mevan_1421	ENOG4105D9I	Responsible for the addition of glutamate residues to the C-terminus of ribosomal protein S6 (By similarity)
Mevan_1422	ENOG4106KXD	ATP-dependent carboxylate-amine ligase (By similarity)
Mevan_1424	ENOG4107RY0	Catalyzes the conversion of dihydroorotate to orotate (By similarity)
Mevan_1425	ENOG4105CAV	thus facilitating recognition of the initiation point. It is needed to translate mRNA with a short Shine-Dalgarno (SD) purine-rich sequence (By similarity)
Mevan_1436	ENOG4107RKG	DJ-1/PfpI family
Mevan_1442	ENOG4105CEY	Amp-dependent synthetase and ligase
Mevan_1447	ENOG4105C6R	Transfers a GMP moiety from GTP to Mo-molybdopterin (Mo- MPT) cofactor (Moco or molybdenum cofactor) to form Mo- molybdopterin guanine dinucleotide (Mo-MGD) cofactor (By similarity)
Mevan_1449	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
Mevan_1453	ENOG4105EIZ	Catalyzes the conversion of 6-carboxy-5,6,7,8- tetrahydropterin (CPH4) to 7-carboxy-7-deazaguanine (CDG) (By similarity)
Mevan_1454	ENOG4105CJW	magnesium transporter
Mevan_1464	ENOG4107QMS	site-determining protein
Mevan_1466	ENOG4105F4P	)-transporter
Mevan_1470	ENOG4105E3H	phosphoglycerate mutase
Mevan_1471	ENOG4108JTQ	reductase
Mevan_1482	ENOG4105C6U	Exchanges the guanine residue with 7-aminomethyl-7- deazaguanine in tRNAs with GU(N) anticodons (tRNA-Asp, -Asn, -His and -Tyr). After this exchange, a cyclopentendiol moiety is attached to the 7-aminomethyl group of 7-deazaguanine, resulting in the hypermodified nucleoside queuosine (Q) (7-(((4,5-cis- dihydroxy-2-cyclopenten-1-yl)amino)methyl)-7-deazaguanosine) (By similarity)
Mevan_1484	ENOG41081HM	2'-5' rna ligase
Mevan_1486	ENOG4107FQX	Alpha-acetolactate decarboxylase
Mevan_1488	ENOG4106NZV	Responsible for synthesis of pseudouridine from uracil- 13 in transfer RNAs (By similarity)
Mevan_1489	ENOG4105CRK	lysyL-tRNA synthetase
Mevan_1493	ENOG4108IJ8	ABC transporter
Mevan_1495	ENOG4108KD5	ADP-ribosylation crystallin J1
Mevan_1499	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)
Mevan_1505	ENOG4105CP7	Triose-phosphate isomerase
Mevan_1506	ENOG41061GT	Aldolase
Mevan_1509	ENOG4105CCP	Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Acts as a receptor for the complex formed by the signal recognition particle (SRP) and the ribosome-nascent chain (RNC)
Mevan_1512	ENOG4105CZ5	Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate (By similarity)
Mevan_1513	ENOG4107S6Z	Na H antiporter
Mevan_1517	ENOG4105VZ8	Transcriptional regulator
Mevan_1519	ENOG4108JZF	Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid (By similarity)
Mevan_1524	ENOG4105CE9	30S ribosomal protein S2
Mevan_1531	ENOG4109003	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis (By similarity)
Mevan_1532	ENOG4105CFP	Peptidase U32
Mevan_1533	ENOG4105CGC	Nitrogenase cofactor biosynthesis protein NifB
Mevan_1534	ENOG4105VUC	UPF0237 protein
Mevan_1538	ENOG4105C6M	Alpha-keto-beta-hydroxylacyl reductoisomerase
Mevan_1540	ENOG4105C09	Bile acid
Mevan_1542	ENOG4108ZP8	Acetolactate synthase small subunit
Mevan_1543	ENOG4105C7K	acetolactate synthase
Mevan_1545	ENOG4105CKX	Catalyzes the conversion of 3'-phosphate to a 2',3'- cyclic phosphodiester at the end of RNA. The mechanism of action of the enzyme occurs in 3 steps (A) adenylation of the enzyme by ATP
Mevan_1548	ENOG4105C80	Catalyzes the reversible oxidation of malate to oxaloacetate (By similarity)
Mevan_1556	ENOG4107R37	Glutamate dehydrogenase
Mevan_1562	ENOG410600Z	Regulatory protein MarR
Mevan_1563	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)
Mevan_1564	ENOG4107RBB	ABC transporter, permease
Mevan_1565	ENOG4108RAC	Rubrerythrin
Mevan_1569	ENOG4105CE1	Ferrous iron transport protein b
Mevan_1570	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
Mevan_1571	ENOG4105C7N	Xanthine uracil vitamin C permease
Mevan_1572	ENOG4105CY0	Metallo-Beta-Lactamase
Mevan_1573	ENOG4105KPK	Component of the proteasome core, a large protease complex with broad specificity involved in protein degradation (By similarity)
Mevan_1574	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)
Mevan_1575	ENOG4105C8T	Leucyl-tRNA synthetase
Mevan_1577	ENOG4105UQX	Mate efflux family protein
Mevan_1580	ENOG4105D9I	Responsible for the addition of glutamate residues to the C-terminus of ribosomal protein S6 (By similarity)
Mevan_1583	ENOG4105EAG	UDP-N-acetylglucosamine 2-epimerase
Mevan_1587	ENOG4105D7N	magnesium and cobalt transport protein CorA
Mevan_1590	ENOG4105DZS	Phenylacetate-CoA ligase
Mevan_1594	ENOG4105MRR	Transcriptional regulator (By similarity)
Mevan_1595	ENOG4105EJ7	Catalyzes the reduction of hydroxylamine to form NH(3) and H(2)O (By similarity)
Mevan_1599	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)
Mevan_1600	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)
Mevan_1601	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)
Mevan_1604	ENOG4105C3S	Mate efflux family protein
Mevan_1608	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
Mevan_1611	ENOG4105N14	lysine exporter protein LysE YggA
Mevan_1612	ENOG4105E0X	reductase
Mevan_1616	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
Mevan_1622	ENOG4108B1Q	Ribonuclease
Mevan_1623	ENOG4105DCU	2-hydroxyglutaryl-CoA dehydratase
Mevan_1624	ENOG4105K8R	UPF0145 protein
Mevan_1628	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)
Mevan_1629	ENOG4105C1J	atp-dependent rna helicase
Mevan_1633	ENOG4105NI8	Cytosine-specific methyltransferase
Mevan_1647	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)
Mevan_1662	ENOG4105DCC	Formylmethanofuran dehydrogenase subunit A
Mevan_1665	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
Mevan_1666	ENOG4108S6J	ABC transporter, periplasmic molybdate-binding protein
Mevan_1667	ENOG4105E0C	molybdate abc transporter
Mevan_1668	ENOG4108XG4	DNA-binding transcriptional regulator
Mevan_1669	ENOG4105EYF	MMPL domain protein
Mevan_1676	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)
Mevan_1678	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)
Mevan_1683	ENOG4105D6J	arsenicaL-resistance protein
Mevan_1686	ENOG4105CHH	sulfate transporter
Mevan_1689	ENOG4105D64	Mechanosensitive ion channel
Mevan_1691	ENOG4105CSM	endonuclease III
Mevan_1693	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)
Mevan_1694	ENOG4105C8V	SAICAR synthetase
Mevan_1695	ENOG4105EAC	phosphoserine phosphatase
Mevan_1699	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
Mevan_1700	ENOG4105NBF	ammecr1 domain protein