locus-tag	class	description
Rmag_0001	ENOG4105CI4	it binds specifically double-stranded DNA at a 9 bp consensus (dnaA box) 5'-TTATC CA A CA A-3'. DnaA binds to ATP and to acidic phospholipids (By similarity)
Rmag_0002	ENOG4105CZ8	DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity. The beta chain is required for initiation of replication once it is clamped onto DNA, it slides freely (bidirectional and ATP- independent) along duplex DNA (By similarity)
Rmag_0003	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)
Rmag_0005	ENOG4105C8T	Leucyl-tRNA synthetase
Rmag_0006	ENOG4107QYT	Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor (By similarity)
Rmag_0007	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)
Rmag_0008	ENOG4107MKT	Stringent starvation protein a
Rmag_0009	ENOG4105EIX	cytochrome c1
Rmag_0010	ENOG4105DJ5	Component of the ubiquinol-cytochrome c reductase complex (complex III or cytochrome b-c1 complex), which is a respiratory chain that generates an electrochemical potential coupled to ATP synthesis (By similarity)
Rmag_0011	ENOG4108R5F	Component of the ubiquinol-cytochrome c reductase complex (complex III or cytochrome b-c1 complex), which is a respiratory chain that generates an electrochemical potential coupled to ATP synthesis (By similarity)
Rmag_0013	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
Rmag_0014	ENOG4105ED7	Catalyzes the specific phosphorylation of 1,6-anhydro-N- acetylmuramic acid (anhMurNAc) with the simultaneous cleavage of the 1,6-anhydro ring, generating MurNAc-6-P. Is required for the utilization of anhMurNAc either imported from the medium or derived from its own cell wall murein, and thus plays a role in cell wall recycling (By similarity)
Rmag_0015	ENOG4105EKE	dihydroorotase
Rmag_0016	ENOG4105DTN	riboflavin biosynthesis protein ribF
Rmag_0018	ENOG4105CVG	Homoserine O-transsuccinylase
Rmag_0020	ENOG4105CHM	Aminotransferase
Rmag_0023	ENOG4105C8V	SAICAR synthetase
Rmag_0024	ENOG4105DR5	peptidase
Rmag_0025	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)
Rmag_0026	ENOG4105KNE	Phosphatidate cytidylyltransferase
Rmag_0027	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
Rmag_0028	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)
Rmag_0030	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)
Rmag_0035	ENOG4105BZ9	Cytochrome C oxidase, subunit I
Rmag_0037	ENOG4107QS1	Cytochrome C Oxidase, Subunit III
Rmag_0039	ENOG4105EUH	cytochrome C oxidase, cbb3-type, subunit i
Rmag_0041	ENOG4105D6P	C-type cytochrome. Part of the cbb3-type cytochrome c oxidase complex (By similarity)
Rmag_0043	ENOG4105CNU	cell division protein FtsK
Rmag_0044	ENOG4105C3M	thioredoxin reductase
Rmag_0045	ENOG4105CXT	aspartate transcarbamylase
Rmag_0047	ENOG4105CVE	Lytic murein transglycosylase
Rmag_0048	ENOG4105CJ2	(LipO)protein
Rmag_0050	ENOG4105WMR	Protein CrcB homolog
Rmag_0051	ENOG4105D7Z	glutathione synthase
Rmag_0052	ENOG4105K7D	Required for maturation of 30S ribosomal subunits (By similarity)
Rmag_0053	ENOG4105CHV	Transcription elongation factor NusA
Rmag_0054	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)
Rmag_0055	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)
Rmag_0056	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
Rmag_0057	ENOG4105C12	Phosphoribosylglycinamide synthetase
Rmag_0059	ENOG4105CU0	Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA (By similarity)
Rmag_0061	ENOG4108ZQD	Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A (By similarity)
Rmag_0062	ENOG4105CV1	Transketolase (EC 2.2.1.1)
Rmag_0063	ENOG4105C17	glyceraldehyde-3-phosphate dehydrogenase
Rmag_0065	ENOG4105BZA	Phosphoglycerate kinase
Rmag_0066	ENOG4105CA9	Pyruvate kinase
Rmag_0067	ENOG4105D2N	Aldolase
Rmag_0068	ENOG4107RE5	NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 (By similarity)
Rmag_0069	ENOG4105D28	Specifically methylates the N7 position of a guanine in 16S rRNA (By similarity)
Rmag_0071	ENOG4105F8V	Hydrolase, tatD family
Rmag_0072	ENOG4105EI2	Pseudouridine synthase
Rmag_0073	ENOG4105C4G	Synthesis of 3-octaprenyl-4-hydroxybenzoate (By similarity)
Rmag_0074	ENOG4105DMJ	Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate (By similarity)
Rmag_0077	ENOG4105FDK	ABC transporter
Rmag_0078	ENOG4105C2M	dna polymerase I
Rmag_0079	ENOG4105C75	arginyL-tRNA synthetase
Rmag_0080	ENOG4107R2I	The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination. The AddA nuclease domain is required for chi fragment generation
Rmag_0082	ENOG4107S5G	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)
Rmag_0085	ENOG4107RIQ	Sulfate adenylate transferase
Rmag_0090	ENOG4108YZY	peptidylprolyl cis-trans isomerase
Rmag_0092	ENOG4105EAY	pump that utilizes the energy of pyrophosphate hydrolysis as the driving force for
Rmag_0093	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)
Rmag_0094	ENOG4107R15	K00850 6-phosphofructokinase 1 EC 2.7.1.11
Rmag_0097	ENOG4105C8N	cysteinyl-tRNA synthetase
Rmag_0098	ENOG4105D3R	alkyl hydroperoxide reductase
Rmag_0099	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)
Rmag_0101	ENOG4107RK2	ADP-ribose diphosphatase NudE
Rmag_0103	ENOG4105CU5	Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine (By similarity)
Rmag_0105	ENOG4105D0V	Condensation of UDP-2,3-diacylglucosamine and 2,3- diacylglucosamine-1-phosphate to form lipid A disaccharide, a precursor of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
Rmag_0106	ENOG4105D18	nicotinate-nucleotide pyrophosphorylase
Rmag_0107	ENOG4108RNI	3'(2')5'-bisphosphate nucleotidase
Rmag_0108	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
Rmag_0109	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
Rmag_0110	ENOG4105CTR	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
Rmag_0111	ENOG4108RBP	3'-to-5' exoribonuclease specific for small oligoribonucleotides (By similarity)
Rmag_0112	ENOG4108I0Q	anthranilate phosphoribosyltransferase
Rmag_0113	ENOG4107RAQ	aminopeptidase
Rmag_0116	ENOG4105II7	pyrroline-5-carboxylate reductase
Rmag_0117	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)
Rmag_0118	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)
Rmag_0120	ENOG4105C25	Primosomal protein n'
Rmag_0121	ENOG4105KGE	Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA (By similarity)
Rmag_0122	ENOG4105D3U	Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine (By similarity)
Rmag_0123	ENOG4107QM9	Component of the acetyl coenzyme A carboxylase (ACC) complex. First, biotin carboxylase catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the carboxyltransferase to acetyl-CoA to form malonyl-CoA (By similarity)
Rmag_0124	ENOG4107IX6	phosphate transport regulator
Rmag_0125	ENOG4105CJ3	phosphate transporter
Rmag_0127	ENOG4105C1J	atp-dependent rna helicase
Rmag_0129	ENOG4105CK0	Membrane bOund o-acyl transferase mboat family protein
Rmag_0132	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)
Rmag_0133	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)
Rmag_0136	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)
Rmag_0137	ENOG4105EEI	dihydropteroate synthase
Rmag_0138	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
Rmag_0139	ENOG4105DGN	Electron transport complex
Rmag_0140	ENOG4108R3D	Electron transport complex
Rmag_0141	ENOG4107QTR	Required for nitrogen fixation. May be part of a membrane complex functioning as an intermediate in the electron transport to nitrogenase (By similarity)
Rmag_0142	ENOG4105D6A	Electron transport complex
Rmag_0143	ENOG4108UQQ	Electron transport complex
Rmag_0145	ENOG4105CH8	Succinyl-CoA ligase ADP-forming subunit alpha
Rmag_0146	ENOG4105CMV	Succinyl-CoA synthetase subunit beta
Rmag_0147	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)
Rmag_0148	ENOG4105CAP	With EpmB is involved in the beta-lysylation step of the post-translational modification of translation elongation factor P (EF-P). Catalyzes the ATP-dependent activation of (R)-beta-lysine produced by EpmB, forming a lysyl-adenylate, from which the beta- lysyl moiety is then transferred to the epsilon-amino group of a conserved specific lysine residue in EF-P (By similarity)
Rmag_0151	ENOG4105CDH	Citrulline--aspartate ligase
Rmag_0152	ENOG4105BZQ	cdp-diacylglycerol-glycerol-3-phosphate 3-phosphatidyltransferase
Rmag_0153	ENOG4108EQQ	Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein (By similarity)
Rmag_0156	ENOG4105CGH	5'-nucleotidase
Rmag_0158	ENOG4105C2X	Arabinose 5-phosphate isomerase
Rmag_0160	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)
Rmag_0161	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)
Rmag_0162	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)
Rmag_0163	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
Rmag_0164	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
Rmag_0165	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)
Rmag_0166	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)
Rmag_0167	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)
Rmag_0168	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
Rmag_0169	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
Rmag_0170	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)
Rmag_0171	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
Rmag_0172	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
Rmag_0174	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
Rmag_0175	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
Rmag_0176	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
Rmag_0177	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
Rmag_0178	ENOG4105VBI	Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site (By similarity)
Rmag_0179	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)
Rmag_0180	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)
Rmag_0181	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)
Rmag_0182	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)
Rmag_0183	ENOG4105VPB	50S ribosomal protein L30
Rmag_0184	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
Rmag_0185	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)
Rmag_0186	ENOG41067V7	50S ribosomal protein L36
Rmag_0187	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
Rmag_0188	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)
Rmag_0189	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)
Rmag_0190	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
Rmag_0191	ENOG4108ZT0	50S ribosomal protein l17
Rmag_0192	ENOG4105VCC	30S ribosomal protein S21
Rmag_0196	ENOG4105E0X	reductase
Rmag_0197	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
Rmag_0200	ENOG4105WHM	Necessary for normal cell division and for the maintenance of normal septation (By similarity)
Rmag_0203	ENOG4106RE7	Cytochrome
Rmag_0204	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
Rmag_0205	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)
Rmag_0206	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)
Rmag_0207	ENOG4105C1N	GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis (By similarity)
Rmag_0208	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)
Rmag_0209	ENOG4105CYJ	ribosomal RNA small subunit methyltransferase B
Rmag_0210	ENOG4105T95	Thiol disulfide interChange protein
Rmag_0211	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)
Rmag_0220	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
Rmag_0221	ENOG4107QRG	dna polymerase iii
Rmag_0222	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
Rmag_0224	ENOG4108ZCA	Inherit from COG: pyridine nucleotide-disulfide oxidoreductase
Rmag_0225	ENOG41082K8	Part of a sulfur-relay system required for 2-thiolation of 5-methylaminomethyl-2-thiouridine (mnm(5)s(2)U) at tRNA wobble positions. Interacts with IscS and stimulates its activity. Then, accepts a sulfur from IscS and transfers it in turn to TusD (By similarity)
Rmag_0227	ENOG4105E66	phosphoriboisomerase A
Rmag_0228	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)
Rmag_0232	ENOG4108DQ3	n-acetylglutamate synthase
Rmag_0233	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)
Rmag_0234	ENOG4105DFA	alanine racemase domain protein
Rmag_0236	ENOG4105D1U	peptidase U62 modulator of DNA gyrase
Rmag_0237	ENOG4105KWU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
Rmag_0238	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)
Rmag_0239	ENOG4105CYU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
Rmag_0240	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)
Rmag_0242	ENOG4107QIZ	NADH dehydrogenase
Rmag_0244	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)
Rmag_0245	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)
Rmag_0246	ENOG4105DF2	NADH dehydrogenase subunit j
Rmag_0247	ENOG41080EA	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)
Rmag_0249	ENOG4105C8S	subunit m
Rmag_0250	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)
Rmag_0255	ENOG4108JJ6	Type I secretion system ATPase
Rmag_0256	ENOG4105C42	Type I secretion membrane fusion protein (HlyD
Rmag_0257	ENOG4106T9E	Converts the free carboxyl group of a malonyl-thioester to its methyl ester by transfer of a methyl group from S-adenosyl- L-methionine (SAM). It allows to synthesize pimeloyl-ACP via the fatty acid synthetic pathway (By similarity)
Rmag_0259	ENOG4105PFA	Catalyzes the conversion of 5-hydroxyuridine (ho5U) to 5-methoxyuridine (mo5U) at position 34 in tRNA (By similarity)
Rmag_0261	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)
Rmag_0262	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
Rmag_0263	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)
Rmag_0265	ENOG4108V3E	phosphoribosylglycinamide formyltransferase
Rmag_0266	ENOG4105CXB	phosphoribosylaminoimidazole synthetase
Rmag_0267	ENOG4105BZQ	cdp-diacylglycerol-glycerol-3-phosphate 3-phosphatidyltransferase
Rmag_0268	ENOG4108KZ1	Mediates the interaction of DNA replication inititator protein DnaA with DNA polymerase subunit beta sliding clamp (dnaN). Stimulates hydrolysis of ATP-DnaA to ADP-DnaA, rendering DnaA inactive for reinititation, a process called regulatory inhibition of DnaA or RIDA (By similarity)
Rmag_0270	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)
Rmag_0271	ENOG4105EAC	phosphoserine phosphatase
Rmag_0272	ENOG4105DA4	cytochrome c-type biogenesis protein
Rmag_0274	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)
Rmag_0275	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
Rmag_0276	ENOG4108YZA	Nitrogen regulatory protein pii
Rmag_0277	ENOG4105BZU	Histidine kinase
Rmag_0278	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
Rmag_0280	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)
Rmag_0281	ENOG4108YZA	Nitrogen regulatory protein pii
Rmag_0283	ENOG41080XQ	Signal transduction protein with cbs domains
Rmag_0285	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)
Rmag_0286	ENOG4105X8U	Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. Together with TatC, TatB is part of a receptor directly interacting with Tat signal peptides. TatB may form an oligomeric binding site that transiently accommodates folded Tat precursor proteins before their translocation (By similarity)
Rmag_0287	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)
Rmag_0288	ENOG4105KPZ	phosphoribosyl-atp pyrophosphatase
Rmag_0289	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
Rmag_0293	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
Rmag_0294	ENOG4105D1S	lipid A biosynthesis
Rmag_0295	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)
Rmag_0296	ENOG4105CJN	penicillin-binding protein
Rmag_0298	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
Rmag_0302	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)
Rmag_0304	ENOG4105DZA	Converts GTP to 7,8-dihydroneopterin triphosphate (By similarity)
Rmag_0305	ENOG4105E99	Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) (By similarity)
Rmag_0306	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)
Rmag_0308	ENOG4107YWA	deoxycytidylate deaminase
Rmag_0309	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
Rmag_0310	ENOG4107XH4	PPIases accelerate the folding of proteins (By similarity)
Rmag_0311	ENOG4105K5D	4fe-4S ferredoxin iroN-sulfur binding
Rmag_0312	ENOG4105C5R	Aminotransferase
Rmag_0313	ENOG4105CQB	FAD linked oxidase domain protein
Rmag_0314	ENOG4105EU8	FAD linked oxidase domain protein
Rmag_0315	ENOG4105CHG	glycolate oxidase (iron-sulfur subunit)
Rmag_0318	ENOG4107QPA	Cleaves GlcNAc linked beta-1,4 to MurNAc tripeptides (By similarity)
Rmag_0320	ENOG4105C4R	Atp-dependent dna helicase
Rmag_0322	ENOG4105CK3	Lysine 2,3-aminomutase YodO family protein
Rmag_0323	ENOG4107QX9	Thiol disulfide interChange protein
Rmag_0327	ENOG4108Z1W	Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) (By similarity)
Rmag_0328	ENOG4108151	Beta-lactamase domain protein
Rmag_0329	ENOG4105C34	Pseudouridine synthase
Rmag_0332	ENOG4105ERD	Involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. Acts as DNA glycosylase that recognizes and removes damaged bases. Has a preference for oxidized purines, such as 7,8-dihydro-8-oxoguanine (8-oxoG). Has AP (apurinic apyrimidinic) lyase activity and introduces nicks in the DNA strand. Cleaves the DNA backbone by beta-delta elimination to generate a single-strand break at the site of the removed base with both 3'- and 5'-phosphates (By similarity)
Rmag_0336	ENOG4105DN9	Na H antiporter
Rmag_0337	ENOG4105CGM	Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis (By similarity)
Rmag_0338	ENOG4105C31	Tryptophanyl-tRNA synthetase
Rmag_0339	ENOG4105FE9	pseudouridine synthase
Rmag_0340	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)
Rmag_0341	ENOG4105D49	3-dehydroquinate synthase
Rmag_0343	ENOG41080G2	Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) (By similarity)
Rmag_0344	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)
Rmag_0345	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)
Rmag_0346	ENOG4105CNG	UPF0061 protein
Rmag_0347	ENOG4108Z4T	Peptidase M50
Rmag_0348	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)
Rmag_0349	ENOG4105DJ4	phosphatidylserine decarboxylase
Rmag_0350	ENOG4108JU6	CBS domain protein
Rmag_0351	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
Rmag_0352	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)
Rmag_0353	ENOG4105CFG	Acts as a chaperone (By similarity)
Rmag_0354	ENOG4108ZEF	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate (By similarity)
Rmag_0355	ENOG4106H78	methyltransferase
Rmag_0356	ENOG4105F0N	pyrophosphate phospho-hydrolase
Rmag_0361	ENOG4105ES5	Histidine kinase
Rmag_0362	ENOG4108ZXC	Two component transcriptional regulator, luxr family
Rmag_0363	ENOG4105C1A	potassium transporter peripheral membrane
Rmag_0364	ENOG4105D37	Low-affinity potassium transport system. Interacts with Trk system potassium uptake protein TrkA (By similarity)
Rmag_0365	ENOG4105DVT	helicase
Rmag_0366	ENOG4105EAH	synthase
Rmag_0367	ENOG4105F7M	Specifically methylates the uridine in position 2552 of 23S rRNA at the 2'-O position of the ribose in the fully assembled 50S ribosomal subunit (By similarity)
Rmag_0371	ENOG4105MQS	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
Rmag_0372	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
Rmag_0373	ENOG4105CAQ	asparagine synthetase
Rmag_0374	ENOG4108UMW	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
Rmag_0378	ENOG4108Z1B	Cyclase dehydrase
Rmag_0379	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
Rmag_0380	ENOG4105K70	DNA-binding protein
Rmag_0381	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)
Rmag_0382	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
Rmag_0384	ENOG4105C4E	Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate (By similarity)
Rmag_0386	ENOG4105C2V	Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) (By similarity)
Rmag_0387	ENOG4105CFP	Peptidase U32
Rmag_0388	ENOG4107Y49	methyltransferase
Rmag_0389	ENOG4105M2J	Glutaredoxin
Rmag_0392	ENOG4107QIK	phosphoribosylformylglycinamidine synthase
Rmag_0394	ENOG4105CDY	transcriptional regulatory protein
Rmag_0396	ENOG4105C9M	aspartyl-trna synthetase
Rmag_0398	ENOG4105CA1	Removes the N-terminal methionine from nascent proteins (By similarity)
Rmag_0399	ENOG4105D0M	Protease HtpX homolog
Rmag_0400	ENOG4108V0P	LemA family
Rmag_0404	ENOG4108JDX	DNA polymerase iii, epsilon subunit
Rmag_0405	ENOG4105VFG	Promotes RNA polymerase assembly. Latches the N- and C- terminal regions of the beta' subunit thereby facilitating its interaction with the beta and alpha subunits (By similarity)
Rmag_0409	ENOG4105D52	delta-aminolevulinic acid dehydratase
Rmag_0410	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)
Rmag_0411	ENOG4105D8A	3-Deoxy-D-manno-octulosonic-acid transferase
Rmag_0412	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
Rmag_0413	ENOG4105CGT	Catalyzes the transfer of a phosphate group to glutamate to form glutamate 5-phosphate which rapidly cyclizes to 5- oxoproline (By similarity)
Rmag_0414	ENOG4105K8U	2-Amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase
Rmag_0415	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
Rmag_0416	ENOG4108IAA	Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate (By similarity)
Rmag_0417	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)
Rmag_0419	ENOG4105CG2	Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 (By similarity)
Rmag_0420	ENOG4108V7X	Transcription factor that acts by binding directly to the RNA polymerase (RNAP). Required for negative regulation of rRNA expression and positive regulation of several amino acid biosynthesis promoters
Rmag_0421	ENOG4107S75	HAD-superfamily hydrolase subfamily IA variant 3
Rmag_0426	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)
Rmag_0427	ENOG4107VRB	Catalyzes the conversion of 6-carboxy-5,6,7,8- tetrahydropterin (CPH4) to 7-carboxy-7-deazaguanine (CDG) (By similarity)
Rmag_0430	ENOG4105D10	5-enolpyruvylshikimate-3-phosphate phospholyase
Rmag_0432	ENOG4106EG9	Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) (By similarity)
Rmag_0434	ENOG4108S7T	Catalyzes the oxidation of either pyridoxine 5'- phosphate (PNP) or pyridoxamine 5'-phosphate (PMP) into pyridoxal 5'-phosphate (PLP) (By similarity)
Rmag_0435	ENOG4105E2X	shikimate dehydrogenase
Rmag_0436	ENOG4105C03	ribonuclease
Rmag_0437	ENOG4108RKS	Short-chain dehydrogenase reductase Sdr
Rmag_0439	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
Rmag_0440	ENOG4105CD8	aminopeptidase N
Rmag_0441	ENOG4105CEV	competence damage-inducible protein
Rmag_0443	ENOG4105CIT	This protein may be involved in anomalous filament growth. May be a component of the septum (By similarity)
Rmag_0444	ENOG4105C7C	involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
Rmag_0445	ENOG4105C7K	acetolactate synthase
Rmag_0446	ENOG4108ZP8	Acetolactate synthase small subunit
Rmag_0447	ENOG4105C6M	Alpha-keto-beta-hydroxylacyl reductoisomerase
Rmag_0448	ENOG4106PT6	cdpdiacylglycerol-serine O-phosphatidyltransferase
Rmag_0449	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)
Rmag_0452	ENOG4105DBV	ornithine carbamoyltransferase
Rmag_0453	ENOG4105C8Y	Acetylornithine aminotransferase
Rmag_0454	ENOG41080QH	sigma 54 modulation protein ribosomal protein S30EA
Rmag_0455	ENOG4105CJW	magnesium transporter
Rmag_0456	ENOG4107QKV	phosphomannomutase
Rmag_0458	ENOG4105DAQ	Component of the pyruvate dehydrogenase (PDH) complex, that catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2) (By similarity)
Rmag_0461	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
Rmag_0462	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)
Rmag_0466	ENOG4107QMP	dna polymerase iii subunits gamma and tau
Rmag_0467	ENOG4108S0S	Nucleotidyl transferase
Rmag_0468	ENOG4105EHM	Aminoglycoside phosphotransferase
Rmag_0470	ENOG4105DZ1	carboxypeptidase
Rmag_0471	ENOG4105CNI	cell division protein FtsW
Rmag_0474	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)
Rmag_0476	ENOG4105K63	Thioredoxin
Rmag_0477	ENOG4105C4P	Facilitates transcription termination by a mechanism that involves Rho binding to the nascent RNA, activation of Rho's RNA-dependent ATPase activity, and release of the mRNA from the DNA template (By similarity)
Rmag_0479	ENOG4107YRI	Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1) (By similarity)
Rmag_0480	ENOG4105DJ0	Poly(A) Polymerase
Rmag_0481	ENOG41067QG	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
Rmag_0482	ENOG4105CTB	Polyprenyl synthetase
Rmag_0483	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)
Rmag_0484	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)
Rmag_0485	ENOG4105VGS	50s ribosomal protein l32
Rmag_0488	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)
Rmag_0489	ENOG4105CGY	Dna recombination protein
Rmag_0490	ENOG4105UBK	short-chain dehydrogenase reductase
Rmag_0491	ENOG4105ECY	inositol monophosphatase
Rmag_0493	ENOG4105CJX	Molecular chaperone. Has ATPase activity (By similarity)
Rmag_0495	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)
Rmag_0496	ENOG4105DBS	Key enzyme in heme biosynthesis. Catalyzes the oxidative decarboxylation of propionic acid side chains of rings A and B of coproporphyrinogen III (By similarity)
Rmag_0498	ENOG4105C5F	glutamine synthetase
Rmag_0499	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)
Rmag_0500	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)
Rmag_0501	ENOG4105CNI	cell division protein FtsW
Rmag_0502	ENOG4105C5H	ABC transporter
Rmag_0506	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)
Rmag_0507	ENOG4107YIM	Involved in the transcription termination process (By similarity)
Rmag_0509	ENOG4105K59	histidine triad (HIT) protein
Rmag_0510	ENOG4108UUM	single-stranded DNA-binding protein
Rmag_0511	ENOG4107RDB	Major Facilitator
Rmag_0513	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)
Rmag_0514	ENOG4105WVQ	Fe-S assembly protein IscX
Rmag_0515	ENOG4107R6Y	Involved in the TonB-independent uptake of proteins (By similarity)
Rmag_0516	ENOG4105KCK	Peptidoglycan-associated lipoprotein
Rmag_0519	ENOG4105EZI	multiple antibiotic resistance (MarC)-related protein
Rmag_0520	ENOG4105C4K	Nad synthetase
Rmag_0522	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
Rmag_0523	ENOG4105BZH	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
Rmag_0524	ENOG4105E05	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
Rmag_0527	ENOG4105DH5	Responsible for the end-turnover of tRNA specifically removes the terminal AMP residue from uncharged tRNA (tRNA-C-C-A). Also appears to be involved in tRNA biosynthesis (By similarity)
Rmag_0529	ENOG4105C01	Dihydroxy-acid dehydratase
Rmag_0530	ENOG4105C40	3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs (By similarity)
Rmag_0531	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
Rmag_0532	ENOG4105C49	Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine (By similarity)
Rmag_0533	ENOG4105EPW	hflc protein
Rmag_0534	ENOG4107QJR	hflk protein
Rmag_0535	ENOG4105E7H	involved in the assembly of LPS in the outer leaflet of the outer membrane. Determines N-hexane tolerance and is involved in outer membrane permeability. Essential for envelope biogenesis (By similarity)
Rmag_0537	ENOG4105C2N	RNA methyltransferase TrmH family group 3
Rmag_0538	ENOG4108I9X	Isocitrate lyase
Rmag_0542	ENOG4108BDP	Catalyzes the transfer of endogenously produced octanoic acid from octanoyl-acyl-carrier-protein onto the lipoyl domains of lipoate-dependent enzymes. Lipoyl-ACP can also act as a substrate although octanoyl-ACP is likely to be the physiological substrate (By similarity)
Rmag_0543	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)
Rmag_0546	ENOG4105CEZ	Catalyzes the NAD(P)-dependent oxidation of 4- (phosphohydroxy)-L-threonine (HTP) into 2-amino-3-oxo-4- (phosphohydroxy)butyric acid which spontaneously decarboxylates to form 3-amino-2-oxopropyl phosphate (AHAP) (By similarity)
Rmag_0547	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)
Rmag_0548	ENOG4105NWN	ApaG protein
Rmag_0549	ENOG4105DDT	Hydrolyzes diadenosine 5',5'''-P1,P4-tetraphosphate to yield ADP (By similarity)
Rmag_0550	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)
Rmag_0552	ENOG4105DZP	Membrane-associated zinc metalloprotease
Rmag_0553	ENOG4105E1Z	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane
Rmag_0554	ENOG4105D7M	Catalyzes the N-acylation of UDP-3-O-acylglucosamine using 3-hydroxyacyl-ACP as the acyl donor. Is involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
Rmag_0555	ENOG4108YXN	Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs (By similarity)
Rmag_0556	ENOG4105DAF	Involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
Rmag_0557	ENOG4105CJR	Integral membrane protein (MviN
Rmag_0558	ENOG4105KMG	Could be a mediator in iron transactions between iron acquisition and iron-requiring processes, such as synthesis and or repair of Fe-S clusters in biosynthetic enzymes (By similarity)
Rmag_0559	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
Rmag_0560	ENOG4105DEK	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
Rmag_0561	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
Rmag_0562	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
Rmag_0563	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)
Rmag_0564	ENOG4105FD2	Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) (By similarity)
Rmag_0565	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
Rmag_0566	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
Rmag_0568	ENOG4105DGW	oligopeptidase A
Rmag_0570	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)
Rmag_0571	ENOG4105D1F	ATP-binding protein
Rmag_0572	ENOG4108ZIT	Ferredoxin, 2FE-2S
Rmag_0573	ENOG4105C9I	Chaperone involved in the maturation of iron-sulfur cluster-containing proteins. Has a low intrinsic ATPase activity which is markedly stimulated by HscB
Rmag_0574	ENOG4108SWN	Co-chaperone involved in the maturation of iron-sulfur cluster-containing proteins. Seems to help targeting proteins to be folded toward HscA (By similarity)
Rmag_0575	ENOG4108Z4V	iron-sulfur cluster assembly
Rmag_0576	ENOG4107XTC	May be involved in the formation or repair of Fe-S clusters present in iron-sulfur proteins
Rmag_0577	ENOG4105C3J	Cysteine desulfurase
Rmag_0578	ENOG4108ZF1	Transcriptional regulator, BadM Rrf2 family
Rmag_0580	ENOG4105NWR	lipid A biosynthesis (Kdo)2-(Lauroyl)-lipid IVA acyltransferase
Rmag_0581	ENOG4105CB3	Required for the thiolation of cytidine in position 32 of tRNA, to form 2-thiocytidine (s(2)C32) (By similarity)
Rmag_0583	ENOG4105KHV	Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate (By similarity)
Rmag_0584	ENOG4105CM2	brancheD-chain amino acid aminotransferase
Rmag_0585	ENOG4105CFH	Aspartokinase
Rmag_0587	ENOG4105D0M	Protease HtpX homolog
Rmag_0589	ENOG4105E06	May play a role in 30S ribosomal subunit biogenesis. Unusual circulary permuted GTPase that catalyzes rapid hydrolysis of GTP with a slow catalytic turnover (By similarity)
Rmag_0591	ENOG41080YA	This protein is one of the two subunits of integration host factor, a specific DNA-binding protein that functions in genetic recombination as well as in transcriptional and translational control (By similarity)
Rmag_0592	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)
Rmag_0593	ENOG4105CAT	Cytidine monophosphate kinase
Rmag_0594	ENOG4105CRK	lysyL-tRNA synthetase
Rmag_0595	ENOG4105KWW	Biogenesis protein
Rmag_0596	ENOG4105C5H	ABC transporter
Rmag_0598	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)
Rmag_0600	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
Rmag_0601	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)
Rmag_0602	ENOG4105CEK	Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine (By similarity)
Rmag_0604	ENOG4105CB9	Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Binds to the hydrophobic signal sequence of the ribosome-nascent chain (RNC) as it emerges from the ribosomes. The SRP-RNC complex is then targeted to the cytoplasmic membrane where it interacts with the SRP receptor FtsY
Rmag_0606	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)
Rmag_0607	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
Rmag_0608	ENOG4108HWB	Non-specific O-methyltransferase that catalyzes the 2 O- methylation steps in the ubiquinone biosynthetic pathway (By similarity)
Rmag_0610	ENOG4105KJV	Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein (By similarity)
Rmag_0611	ENOG4105CSZ	Catalyzes the complicated ring closure reaction between the two acyclic compounds 1-deoxy-D-xylulose-5-phosphate (DXP) and 3-amino-2-oxopropyl phosphate (1-amino-acetone-3-phosphate or AAP) to form pyridoxine 5'-phosphate (PNP) and inorganic phosphate (By similarity)
Rmag_0614	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)
Rmag_0616	ENOG4105C0V	Provides the sole de novo source of dTMP for DNA biosynthesis (By similarity)
Rmag_0617	ENOG4105C3B	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
Rmag_0620	ENOG4105CN1	protease
Rmag_0621	ENOG4105C3F	Signal peptidase i
Rmag_0622	ENOG4108Z0T	Part of a sulfur-relay system (By similarity)
Rmag_0623	ENOG4105CMY	5-enolpyruvylshikimate-3-phosphate synthase
Rmag_0625	ENOG4105CIH	Imidazole acetol-phosphate transaminase
Rmag_0627	ENOG4108JQ1	Dehydrogenase
Rmag_0628	ENOG4107QM1	Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine (By similarity)
Rmag_0631	ENOG4108Z11	Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes (By similarity)
Rmag_0632	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)
Rmag_0635	ENOG4105D06	uba thif-type nad fad binding protein
Rmag_0636	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)
Rmag_0639	ENOG4105F4G	Membrane
Rmag_0641	ENOG4108ZUF	This protein is one of the two subunits of integration host factor, a specific DNA-binding protein that functions in genetic recombination as well as in transcriptional and translational control (By similarity)
Rmag_0642	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
Rmag_0643	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
Rmag_0645	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)
Rmag_0646	ENOG41082NX	50s ribosomal protein l35
Rmag_0647	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)
Rmag_0648	ENOG4105C22	threonyL-tRNA synthetase
Rmag_0649	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
Rmag_0651	ENOG4108DN8	FAD dependent oxidoreductase
Rmag_0652	ENOG4105M02	This protein specifically catalyzes the removal of signal peptides from prolipoproteins (By similarity)
Rmag_0654	ENOG4105CSJ	Enoyl- acyl-carrier-protein reductase NADH
Rmag_0656	ENOG4105EIN	peptidylprolyl cis-trans isomerase
Rmag_0659	ENOG4108ZKK	Heme chaperone required for the biogenesis of c-type cytochromes. Transiently binds heme delivered by CcmC and transfers the heme to apo-cytochromes in a process facilitated by CcmF and CcmH (By similarity)
Rmag_0661	ENOG41060IM	Heme exporter protein
Rmag_0662	ENOG41072GX	Peptidase M22 Glycoprotease
Rmag_0663	ENOG4105BZ4	penicillin-binding protein
Rmag_0664	ENOG4108ZDX	Binds together with S18 to 16S ribosomal RNA (By similarity)
Rmag_0665	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)
Rmag_0666	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
Rmag_0667	ENOG4105CDU	Replicative dna helicase
Rmag_0668	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
Rmag_0669	ENOG41070EG	Hydrolyzes cAMP to 5'-AMP. Plays an important regulatory role in modulating the intracellular concentration of cAMP, thereby influencing cAMP-dependent processes (By similarity)
Rmag_0671	ENOG4105CUT	histidyl-tRNA synthetase
Rmag_0673	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
Rmag_0674	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
Rmag_0676	ENOG4105BZ1	(ABC) transporter
Rmag_0677	ENOG4107QYG	anthranilate phosphoribosyltransferase
Rmag_0684	ENOG4105CJ0	Catalyzes the oxidation of erythronate-4-phosphate to 3- hydroxy-2-oxo-4-phosphonooxybutanoate (By similarity)
Rmag_0686	ENOG4105D9P	serine threonine protein kinase
Rmag_0687	ENOG4107R3J	Transporter
Rmag_0688	ENOG4108IFG	nitrite reductase, (NAD(P)H)
Rmag_0689	ENOG4108ZAF	Molybdopterin
Rmag_0690	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)
Rmag_0691	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
Rmag_0692	ENOG4108YXW	Together with MoaA, is involved in the conversion of 5'- GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
Rmag_0693	ENOG4105CM1	Catalyzes, together with MoaC, the conversion of 5'-GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
Rmag_0698	ENOG4108RIR	Molybdenum cofactor biosynthesis protein
Rmag_0701	ENOG4105DT1	RuBisCO catalyzes two reactions the carboxylation of D- ribulose 1,5-bisphosphate, the primary event in carbon dioxide fixation, as well as the oxidative fragmentation of the pentose substrate
Rmag_0704	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)
Rmag_0706	ENOG4107QKW	extracellular solute-binding protein family 1
Rmag_0707	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
Rmag_0708	ENOG4105E3B	Multicopper oxidase
Rmag_0714	ENOG41076HS	cation diffusion facilitator family transporter
Rmag_0716	ENOG41080RH	Thioredoxin
Rmag_0717	ENOG4105KUZ	arsenate reductase
Rmag_0721	ENOG4105C38	Glycyl-tRNA synthetase beta subunit
Rmag_0724	ENOG4105M8F	Biopolymer transport protein exbD tolR
Rmag_0725	ENOG4105E02	MotA TolQ exbB proton channel
Rmag_0730	ENOG4105C7E	Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) (By similarity)
Rmag_0731	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
Rmag_0732	ENOG4105FAV	ABC, transporter
Rmag_0733	ENOG41090R7	Ferric uptake
Rmag_0734	ENOG4105YRI	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane (By similarity)
Rmag_0736	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)
Rmag_0737	ENOG4105CA5	Required for the export of heme to the periplasm for the biogenesis of c-type cytochromes (By similarity)
Rmag_0738	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
Rmag_0739	ENOG4105C3E	May play a key role in the regulation of the intracellular concentration of adenosylhomocysteine (By similarity)
Rmag_0740	ENOG4107QIB	glycyl-tRNA synthetase, alpha subunit
Rmag_0741	ENOG4108UM1	dedA family
Rmag_0742	ENOG4105D64	Mechanosensitive ion channel
Rmag_0743	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)
Rmag_0747	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
Rmag_0748	ENOG41075W9	High frequency lysogenization protein HflD homolog
Rmag_0749	ENOG4105KQV	Binds directly to 16S ribosomal RNA (By similarity)
Rmag_0750	ENOG4105DVS	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
Rmag_0751	ENOG4105DR5	peptidase
Rmag_0755	ENOG4105CE5	Catalyzes the formation of 4-diphosphocytidyl-2-C- methyl-D-erythritol from CTP and 2-C-methyl-D-erythritol 4- phosphate (MEP) (By similarity)
Rmag_0756	ENOG41081M5	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)
Rmag_0757	ENOG4105DFU	Cell wall formation (By similarity)
Rmag_0759	ENOG4105CPF	Cell wall formation (By similarity)
Rmag_0762	ENOG4105E9H	Lytic Murein transglycosylase
Rmag_0763	ENOG4105M85	Bola protein
Rmag_0764	ENOG4108EX3	reductase
Rmag_0765	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)
Rmag_0766	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
Rmag_0767	ENOG4108MN8	Membrane
Rmag_0768	ENOG4105EJF	Accelerates the degradation of transcripts by removing pyrophosphate from the 5'-end of triphosphorylated RNA, leading to a more labile monophosphorylated state that can stimulate subsequent ribonuclease cleavage (By similarity)
Rmag_0769	ENOG4105D6E	homoserine dehydrogenase
Rmag_0772	ENOG4105C6T	cysteine synthase
Rmag_0774	ENOG4108YXA	Membrane
Rmag_0777	ENOG4105C1V	Peptidase, M16
Rmag_0781	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)
Rmag_0783	ENOG4105D6W	Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps (By similarity)
Rmag_0784	ENOG4105CH7	arginosuccinase
Rmag_0785	ENOG4105CAE	Modifies the free amino group of the aminoacyl moiety of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by (I) promoting its recognition by IF2 and (II) impairing its binding to EFTu-GTP (By similarity)
Rmag_0786	ENOG4108UIQ	Methylates the ribose at the nucleotide 34 wobble position in the two leucyl isoacceptors tRNA(Leu)(CmAA) and tRNA(Leu)(cmnm5UmAA). Catalyzes the methyl transfer from S- adenosyl-L-methionine to the 2'-OH of the wobble nucleotide (By similarity)
Rmag_0787	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
Rmag_0788	ENOG4105DZB	Electron transport complex
Rmag_0790	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)
Rmag_0793	ENOG4107GFK	fumarate
Rmag_0794	ENOG4105DFF	Rod shape-determining protein mreb
Rmag_0795	ENOG4105N3I	Involved in formation and maintenance of cell shape (By similarity)
Rmag_0797	ENOG4105CJN	penicillin-binding protein
Rmag_0799	ENOG4108JJ7	ABC transporter
Rmag_0800	ENOG4105D1W	Converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)- pyrimidinedione 5'-phosphate (By similarity)
Rmag_0801	ENOG4105CJS	Phosphopantothenoylcysteine decarboxylase
Rmag_0803	ENOG4105C0B	DNA polymerase III (alpha subunit)
Rmag_0805	ENOG41088H4	Diheme cytochrome SoxA (Sulfur oxidation)
Rmag_0809	ENOG4105CRQ	synthase (Component I)
Rmag_0810	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
Rmag_0811	ENOG4108IIJ	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
Rmag_0812	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)
Rmag_0813	ENOG4108VZM	50s ribosomal protein L10
Rmag_0814	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)
Rmag_0815	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
Rmag_0816	ENOG4105E5V	Participates in transcription elongation, termination and antitermination (By similarity)
Rmag_0817	ENOG4105PM1	preprotein translocase subunit SecE
Rmag_0818	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
Rmag_0819	ENOG4105C6K	Malic enzyme
Rmag_0821	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
Rmag_0822	ENOG4107YU2	histidine triad (hIT) protein
Rmag_0825	ENOG4108RDT	NADH dehydrogenase NAD(P)H nitroreductase)
Rmag_0826	ENOG4108RW0	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
Rmag_0828	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
Rmag_0831	ENOG4105CXR	Phospho-2-dehydro-3-deoxyoctonate aldolase
Rmag_0832	ENOG4105DK0	Indole-3-glycerol phosphate synthase
Rmag_0833	ENOG4108UKZ	OsmC family
Rmag_0834	ENOG4105CA8	Catalyzes the rearrangement of 1-deoxy-D-xylulose 5- phosphate (DXP) to produce the thiazole phosphate moiety of thiamine. Sulfur is provided by the thiocarboxylate moiety of the carrier protein ThiS. In vitro, sulfur can be provided by H(2)S (By similarity)
Rmag_0835	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)
Rmag_0836	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)
Rmag_0837	ENOG4108UM6	Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) (By similarity)
Rmag_0838	ENOG4105CY8	phosphoribosylaminoimidazole carboxylase atpase subunit
Rmag_0840	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)
Rmag_0841	ENOG4105CET	Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria (By similarity)
Rmag_0842	ENOG4105W49	UPF0434 protein
Rmag_0843	ENOG4105CHD	Transfers the gamma-phosphate of ATP to the 4'-position of a tetraacyldisaccharide 1-phosphate intermediate (termed DS-1- P) to form tetraacyldisaccharide 1,4'-bis-phosphate (lipid IVA) (By similarity)
Rmag_0844	ENOG4105D60	lipoprotein releasing system transmembrane protein
Rmag_0845	ENOG4105CQU	Part of the ABC transporter complex LolCDE involved in the translocation of mature outer membrane-directed lipoproteins, from the inner membrane to the periplasmic chaperone, LolA. Responsible for the formation of the LolA-lipoprotein complex in an ATP-dependent manner (By similarity)
Rmag_0846	ENOG4108Z2X	Catalyzes the pyruvoyl-dependent decarboxylation of aspartate to produce beta-alanine (By similarity)
Rmag_0847	ENOG4105D9Q	decarboxylase (Beta subunit)
Rmag_0848	ENOG4107QSA	Oxaloacetate decarboxylase
Rmag_0850	ENOG4105K9U	however, it seems to stimulate more or less all the activities of the other two initiation factors, IF-2 and IF-3 (By similarity)
Rmag_0851	ENOG4105SYT	Methylenetetrahydrofolate reductase
Rmag_0856	ENOG4105K8N	protein family UPF0079, ATPase
Rmag_0858	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)
Rmag_0860	ENOG4105QA4	4Fe-4S Ferredoxin, iron-sulfur binding domain protein
Rmag_0865	ENOG4108Z0T	Part of a sulfur-relay system (By similarity)
Rmag_0867	ENOG4108ZKU	Part of a sulfur-relay system required for 2-thiolation of 5-methylaminomethyl-2-thiouridine (mnm(5)s(2)U) at tRNA wobble positions (By similarity)
Rmag_0868	ENOG4108ZAT	Part of a sulfur-relay system required for 2-thiolation of 5-methylaminomethyl-2-thiouridine (mnm(5)s(2)U) at tRNA wobble positions. Accepts sulfur from TusA and transfers it in turn to TusE (By similarity)
Rmag_0869	ENOG4105PJW	Sulfite reductase dissimilatory-type beta subunit
Rmag_0870	ENOG4105CY1	sulfite reductase, dissimilatory-type alpha subunit
Rmag_0871	ENOG4105BZ8	glutamate synthase
Rmag_0872	ENOG4108YY1	This protein is located at the 30S-50S ribosomal subunit interface and may play a role in the structure and function of the aminoacyl-tRNA binding site (By similarity)
Rmag_0874	ENOG4108UKH	Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides (By similarity)
Rmag_0875	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
Rmag_0876	ENOG410903C	(LipO)protein
Rmag_0877	ENOG4105C1M	carbamoyl-phosphate synthetase glutamine chain
Rmag_0882	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)
Rmag_0883	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
Rmag_0884	ENOG4107QP8	phosphohexose isomerase
Rmag_0885	ENOG4105C3Y	UTP-glucose-1-phosphate uridylyltransferase
Rmag_0887	ENOG4105D3Q	Sugar transferase
Rmag_0889	ENOG4105ECJ	Glycosyl Transferase
Rmag_0890	ENOG4105CG5	Glycosyl transferase (Group 1
Rmag_0891	ENOG4105K64	Glycosyl transferase, family 2
Rmag_0892	ENOG4105KPE	licD family
Rmag_0902	ENOG4105C30	Nad-dependent epimerase dehydratase
Rmag_0903	ENOG4105C0K	Gdp-mannose 4,6-dehydratase
Rmag_0909	ENOG4105CX6	glutaminyL-tRNA synthetase
Rmag_0910	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
Rmag_0911	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
Rmag_0912	ENOG4105KAE	Involved in the modulation of the specificity of the ClpAP-mediated ATP-dependent protein degradation (By similarity)
Rmag_0913	ENOG4108K5H	permease YjgP YjgQ family protein
Rmag_0914	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
Rmag_0915	ENOG4108Z6B	deaminase
Rmag_0916	ENOG4105CHR	reductase
Rmag_0917	ENOG4105CJF	Malonyl coA-acyl carrier protein transacylase
Rmag_0918	ENOG4105K46	50S ribosomal protein l27
Rmag_0919	ENOG4105KK9	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
Rmag_0920	ENOG4108R5K	PPIases accelerate the folding of proteins (By similarity)
Rmag_0921	ENOG4105F10	Catalyzes the hydrolysis of the pyrophosphate bond of UDP-2,3-diacylglucosamine to yield 2,3-diacylglucosamine 1- phosphate (lipid X) and UMP (By similarity)
Rmag_0923	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)
Rmag_0924	ENOG4105D43	The glycine cleavage system catalyzes the degradation of glycine (By similarity)
Rmag_0925	ENOG4107835	probably involved in intracellular septation (By similarity)
Rmag_0927	ENOG4105KME	endoribonuclease L-psp
Rmag_0928	ENOG4105CB5	ATP-dependent DNA helicase recG
Rmag_0929	ENOG4105VEI	Removes the pyruvyl group from chorismate, with concomitant aromatization of the ring, to provide 4- hydroxybenzoate (4HB) for the ubiquinone pathway (By similarity)
Rmag_0930	ENOG4105DA6	Catalyzes the conversion of 5-methoxyuridine (mo5U) to uridine-5-oxyacetic acid (cmo5U) at position 34 in tRNA. May also participate in the methylation of uridine-5-oxyacetic acid (cmo5U) to uridine-5-oxyacetic acid methyl ester (mcmo5U) (By similarity)
Rmag_0931	ENOG4105DDQ	anthranilate synthase
Rmag_0932	ENOG41085GJ	domain protein
Rmag_0934	ENOG4105CSF	NADPH-dependent glycerol-3-phosphate dehydrogenase
Rmag_0935	ENOG4108UJD	30S ribosomal protein S9
Rmag_0936	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)
Rmag_0939	ENOG4108IFH	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
Rmag_0942	ENOG4105C1J	atp-dependent rna helicase
Rmag_0946	ENOG4105CJB	Exodeoxyribonuclease I
Rmag_0947	ENOG4105CSM	endonuclease III
Rmag_0949	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)
Rmag_0950	ENOG4105ECC	imidazole-glycerol-phosphate dehydratase
Rmag_0951	ENOG4105CM3	Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate (By similarity)
Rmag_0952	ENOG4107QNR	UPF0135 protein
Rmag_0953	ENOG4105CIH	Imidazole acetol-phosphate transaminase
Rmag_0954	ENOG4105DWF	phosphomethylpyrimidine kinase
Rmag_0956	ENOG4105K8U	2-Amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase
Rmag_0957	ENOG4105KKP	D-erythro-7,8-dihydroneopterin triphosphate 2'-epimerase
Rmag_0958	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)
Rmag_0960	ENOG4105E3A	(ABC) transporter
Rmag_0961	ENOG4105DA5	(ABC) transporter
Rmag_0962	ENOG4107QSN	dihydrolipoamide acetyltransferase
Rmag_0963	ENOG4107QN2	dihydrolipoyl dehydrogenase
Rmag_0964	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)
Rmag_0966	ENOG4108IYU	L-aspartate oxidase
Rmag_0968	ENOG4105VY0	Activates ribosomal RNA transcription. Plays a direct role in upstream activation of rRNA promoters (By similarity)
Rmag_0969	ENOG4105DC1	bifunctional purine biosynthesis protein purh
Rmag_0971	ENOG4105MK2	5-formyltetrahydrofolate cyclo-ligase
Rmag_0972	ENOG4105EAK	ubiquinone biosynthesis hydroxylase, ubiH ubiF VisC COQ6 family
Rmag_0973	ENOG4105CMS	peptidase U62, modulator of DNA gyrase
Rmag_0975	ENOG4108JU5	Magnesium and cobalt efflux protein
Rmag_0976	ENOG4105VDB	UPF0125 protein
Rmag_0977	ENOG4105CJV	Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase
Rmag_0980	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)
Rmag_0981	ENOG4108IUZ	ABC transporter
Rmag_0982	ENOG4105HJX	Biotin- acetyl-CoA-carboxylase ligase
Rmag_0983	ENOG41080IJ	Diacylglycerol kinase
Rmag_0984	ENOG4105DI7	Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs (By similarity)
Rmag_0985	ENOG4105DSS	Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation (By similarity)
Rmag_0986	ENOG4105DZ2	Transcriptional regulator
Rmag_0988	ENOG4107B2H	carbonic anhydrase
Rmag_0989	ENOG4108ZR6	An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Probably interacts with S19. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes (By similarity)
Rmag_0990	ENOG4105K5M	30s ribosomal protein S16
Rmag_0991	ENOG4107QTF	adenylosuccinate lyase
Rmag_0992	ENOG4107QIJ	Aconitate hydratase 2
Rmag_0993	ENOG4105W0E	50S ribosomal protein L33
Rmag_0994	ENOG4105KDC	50s ribosomal protein l28
Rmag_0995	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)
Rmag_0996	ENOG4105CGK	Exodeoxyribonuclease III
Rmag_0998	ENOG4108YH1	overproduction of this protein in Escherichia coli inhibits the F plasmid-mediated exclusion of bacteriophage T7
Rmag_0999	ENOG4105DPM	folylpolyglutamate synthase Dihydrofolate synthase
Rmag_1001	ENOG4105CBA	glutamine phosphoribosylpyrophosphate amidotransferase
Rmag_1002	ENOG4105C28	cystathionine
Rmag_1003	ENOG4108RKI	Necessary for the introduction of cis unsaturation into fatty acids. Catalyzes the dehydration of (3R)-3-hydroxydecanoyl- ACP to E-(2)-decenoyl-ACP and then its isomerization to Z-(3)- decenoyl-ACP. Can catalyze the dehydratase reaction for beta- hydroxyacyl-ACPs with saturated chain lengths up to 16 0, being most active on intermediate chain length (By similarity)
Rmag_1005	ENOG4107RAB	Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA (By similarity)
Rmag_1006	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)
Rmag_1007	ENOG4105VIE	preprotein translocase, subunit YajC
Rmag_1008	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)
Rmag_1009	ENOG4105CR7	Catalyzes the transfer of selenium from selenophosphate for conversion of 2-thiouridine to 2-selenouridine at the wobble position in tRNA (By similarity)
Rmag_1012	ENOG4105WH1	Two component transcriptional regulator luxr family
Rmag_1013	ENOG4105BZU	Histidine kinase
Rmag_1014	ENOG4105C1H	Exhibits a very high intrinsic GTPase hydrolysis rate. Involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA- cmnm(5)s(2)U34 (By similarity)
Rmag_1015	ENOG4105D9M	gamma-glutamylcysteine synthetase
Rmag_1016	ENOG4105M6F	mutator MutT protein
Rmag_1020	ENOG4108UHJ	MAF-like protein
Rmag_1021	ENOG4108JA2	transcriptioN-repair coupling factor
Rmag_1023	ENOG4105C48	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
Rmag_1024	ENOG4107QTG	Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl- CoA (By similarity)
Rmag_1025	ENOG4105F6H	The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate (By similarity)
Rmag_1026	ENOG4105CFZ	Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III (By similarity)
Rmag_1027	ENOG4105VFB	Binds the 23S rRNA (By similarity)
Rmag_1028	ENOG4105C59	p-type ATPase
Rmag_1030	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)
Rmag_1031	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
Rmag_1032	ENOG4108ZGB	N-(5'-phosphoribosyl)anthranilate isomerase
Rmag_1035	ENOG4108RPN	Protein smg homolog
Rmag_1037	ENOG4105VG0	50S ribosomal protein l34
Rmag_1038	ENOG4105NVJ	RNaseP catalyzes the removal of the 5'-leader sequence from pre-tRNA to produce the mature 5'-terminus. It can also cleave other RNA substrates such as 4.5S RNA. The protein component plays an auxiliary but essential role in vivo by binding to the 5'-leader sequence and broadening the substrate specificity of the ribozyme (By similarity)
Rmag_1039	ENOG4105VAS	Could be involved in insertion of integral membrane proteins into the membrane (By similarity)
Rmag_1040	ENOG4105DHW	Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins
Rmag_1042	ENOG4108VBV	N-Acetylmuramoyl-L-alanine amidase
Rmag_1043	ENOG4108Z4R	3-deoxy-d-manno-octulosonate 8-phosphate phosphatase
Rmag_1044	ENOG4105KNM	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
Rmag_1045	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)
Rmag_1046	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)
Rmag_1047	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
Rmag_1048	ENOG4107S15	F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation (By similarity)
Rmag_1049	ENOG4107Z6K	F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation (By similarity)
Rmag_1050	ENOG4105KY6	F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation (By similarity)
Rmag_1051	ENOG4105EE4	it plays a direct role in the translocation of protons across the membrane (By similarity)
Rmag_1053	ENOG4107SA8	fad-dependent pyridine nucleotide-disulfide oxidoreductase
Rmag_1054	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)
Rmag_1055	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
Rmag_1057	ENOG4105CSG	Required to facilitate the formation of correct disulfide bonds in some periplasmic proteins and for the assembly of the periplasmic c-type cytochromes. Acts by transferring electrons from cytoplasmic thioredoxin to the periplasm. This transfer involves a cascade of disulfide bond formation and reduction steps (By similarity)
Rmag_1058	ENOG4108Z38	Catalyzes a trans-dehydration via an enolate intermediate (By similarity)
Rmag_1059	ENOG4105KM4	Acetyl-CoA carboxylase, biotin carboxyl carrier protein
Rmag_1060	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
Rmag_1061	ENOG4105C0N	N-acetylglutamate semialdehyde dehydrogenase
Rmag_1062	ENOG4108YX9	iron--sulfur cluster insertion protein erpA
Rmag_1063	ENOG4105BZN	citrate synthase
Rmag_1064	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)
Rmag_1066	ENOG4105CNK	Required, probably indirectly, for the hydroxylation of 2-octaprenylphenol to 2-octaprenyl-6-hydroxy-phenol, the fourth step in ubiquinone biosynthesis (By similarity)
Rmag_1067	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)
Rmag_1068	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
Rmag_1069	ENOG4105C3G	gtp-binding protein
Rmag_1070	ENOG4105CJI	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
Rmag_1072	ENOG4105CE9	30S ribosomal protein S2
Rmag_1073	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)
Rmag_1075	ENOG4107EJC	Preprotein translocase subunit SecG
Rmag_1076	ENOG4105CP7	Triose-phosphate isomerase