locus-tag	class	description
RGRSB_0002	ENOG4107QIX	Phosphoglucomutase (EC 5.4.2.2
RGRSB_0003	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
RGRSB_0004	ENOG4105KAN	Probably a ribosomal protein or a ribosome-associated protein (By similarity)
RGRSB_0005	ENOG4105KNM	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
RGRSB_0006	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)
RGRSB_0008	ENOG4105C9X	ppx gppa phosphatase
RGRSB_0017	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)
RGRSB_0018	ENOG4105CQR	helicase
RGRSB_0019	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
RGRSB_0021	ENOG4105CAA	catalyzes amidations at positions B, D, E, and G on adenosylcobyrinic A,C-diamide. NH(2) groups are provided by glutamine, and one molecule of ATP is hydrogenolyzed for each amidation (By similarity)
RGRSB_0030	ENOG4105C8M	UPF0272 protein
RGRSB_0031	ENOG4107RTD	sua5 ycio yrdc ywlc family protein
RGRSB_0034	ENOG4105C4W	S-formylglutathione hydrolase
RGRSB_0037	ENOG4108NWW	ferritin dps family protein
RGRSB_0038	ENOG4107QRP	cobalamin biosynthesis protein CobW
RGRSB_0039	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
RGRSB_0041	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)
RGRSB_0052	ENOG4105BZ1	(ABC) transporter
RGRSB_0054	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
RGRSB_0056	ENOG4106H78	methyltransferase
RGRSB_0057	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)
RGRSB_0064	ENOG4105SA9	Catalyzes the transfer of the L-Ara4N moiety of the glycolipid undecaprenyl phosphate-alpha-L-Ara4N to lipid A. The modified arabinose is attached to lipid A and is required for resistance to polymyxin and cationic antimicrobial peptides (By similarity)
RGRSB_0066	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
RGRSB_0068	ENOG4108WJV	had superfamily (subfamily IIIa) phosphatase
RGRSB_0075	ENOG4105D7N	magnesium and cobalt transport protein CorA
RGRSB_0080	ENOG41082B1	30S ribosomal protein S16
RGRSB_0082	ENOG4105C8S	subunit m
RGRSB_0083	ENOG4105EK6	Transmembrane (T) component of an energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates (By similarity)
RGRSB_0084	ENOG4108JJB	ABC transporter
RGRSB_0092	ENOG4105VN1	Heat shock protein
RGRSB_0097	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
RGRSB_0098	ENOG4105D0I	Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate (By similarity)
RGRSB_0099	ENOG4105E8R	UPF0173 metal-dependent hydrolase
RGRSB_0101	ENOG410682B	stage II sporulation protein
RGRSB_0104	ENOG4105CHH	sulfate transporter
RGRSB_0109	ENOG4105VFU	Rna-binding protein
RGRSB_0111	ENOG4105C9M	aspartyl-trna synthetase
RGRSB_0112	ENOG4105C26	Dehydrogenase
RGRSB_0114	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)
RGRSB_0116	ENOG4105CG3	alpha amylase, catalytic region
RGRSB_0117	ENOG4107ZYR	domain protein
RGRSB_0118	ENOG4105CZN	Potassium uptake protein
RGRSB_0119	ENOG4105JFG	SpoIID LytB domain protein
RGRSB_0121	ENOG4105WXN	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)
RGRSB_0126	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)
RGRSB_0127	ENOG4107T1U	Catalyzes the synthesis of activated sulfate (By similarity)
RGRSB_0128	ENOG4105CV1	Transketolase (EC 2.2.1.1)
RGRSB_0132	ENOG4105C7Z	Conserved Protein
RGRSB_0134	ENOG4107QQ4	Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans (By similarity)
RGRSB_0144	ENOG4105C0D	helicase
RGRSB_0149	ENOG4105D1D	Component of the cytochrome b6-f complex, which mediates electron transfer between photosystem II (PSII) and photosystem I (PSI), cyclic electron flow around PSI, and state transitions (By similarity)
RGRSB_0150	ENOG4105DQV	Component of the cytochrome b6-f complex, which mediates electron transfer between photosystem II (PSII) and photosystem I (PSI), cyclic electron flow around PSI, and state transitions (By similarity)
RGRSB_0154	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)
RGRSB_0159	ENOG4105C31	Tryptophanyl-tRNA synthetase
RGRSB_0167	ENOG4108UHE	carbonic anhydrase
RGRSB_0172	ENOG4105C5H	ABC transporter
RGRSB_0180	ENOG4105EXN	Sulfate transport protein CysZ
RGRSB_0182	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
RGRSB_0183	ENOG4105KC4	UPF0296 protein
RGRSB_0184	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
RGRSB_0185	ENOG4107QPD	alcohol dehydrogenase
RGRSB_0186	ENOG4105D17	glycoside hydrolase, family 3 domain protein
RGRSB_0187	ENOG41080JB	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)
RGRSB_0188	ENOG4105CJV	Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase
RGRSB_0189	ENOG41066AK	Catalyzes the formation of the isocyclic ring in chlorophyll biosynthesis. Mediates the cyclase reaction, which results in the formation of divinylprotochlorophyllide (Pchlide) characteristic of all chlorophylls from magnesium-protoporphyrin IX 13-monomethyl ester (MgPMME) (By similarity)
RGRSB_0191	ENOG4108R6K	riboflavin synthase, subunit alpha
RGRSB_0194	ENOG4105C8N	cysteinyl-tRNA synthetase
RGRSB_0196	ENOG4105CDA	abc transporter atp-binding protein
RGRSB_0198	ENOG4105EET	magnesium chelatase
RGRSB_0200	ENOG41083GQ	Protein CrcB homolog
RGRSB_0206	ENOG4108ZF3	Phosphatase
RGRSB_0208	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
RGRSB_0218	ENOG41074FZ	May increase the rate of spontaneous hydrolysis of aminoacrylate to malonic semialdehyde. Required to remove a toxic intermediate produce in the pyrimidine nitrogen degradation (By similarity)
RGRSB_0225	ENOG4107TK4	histidinol-phosphate phosphatase
RGRSB_0227	ENOG4105CMQ	Chloride channel
RGRSB_0229	ENOG4105EAG	UDP-N-acetylglucosamine 2-epimerase
RGRSB_0231	ENOG4108IUZ	ABC transporter
RGRSB_0233	ENOG4108IUW	ABC transporter
RGRSB_0236	ENOG4105CDY	transcriptional regulatory protein
RGRSB_0237	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)
RGRSB_0238	ENOG4105CCX	Catalyzes the production of spermidine from putrescine and decarboxylated S-adenosylmethionine (dcSAM), which serves as an aminopropyl donor (By similarity)
RGRSB_0239	ENOG4105E4R	Precorrin-3B C17-methyltransferase
RGRSB_0244	ENOG4108USA	electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon- concentration (By similarity)
RGRSB_0249	ENOG4109003	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis (By similarity)
RGRSB_0252	ENOG4105X3E	Catalyzes the decarboxylation of S-adenosylmethionine to S-adenosylmethioninamine (dcAdoMet), the propylamine donor required for the synthesis of the polyamines spermine and spermidine from the diamine putrescine (By similarity)
RGRSB_0255	ENOG4108JQ0	Key enzyme in the regulation of glycerol uptake and metabolism (By similarity)
RGRSB_0257	ENOG4105CNG	UPF0061 protein
RGRSB_0259	ENOG4105CJN	penicillin-binding protein
RGRSB_0263	ENOG4107SGM	protein serine threonine phosphatase
RGRSB_0264	ENOG4105CH7	arginosuccinase
RGRSB_0271	ENOG4105C15	The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane (By similarity)
RGRSB_0272	ENOG4105W8H	transhydrogenase (subunit alpha
RGRSB_0273	ENOG4108IIE	The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane (By similarity)
RGRSB_0274	ENOG4108S6J	ABC transporter, periplasmic molybdate-binding protein
RGRSB_0275	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
RGRSB_0277	ENOG4107N1Q	ErfK YbiS YcfS YnhG family protein
RGRSB_0280	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)
RGRSB_0285	ENOG4108PJD	permease
RGRSB_0288	ENOG4105EZ7	amino acid ABC transporter
RGRSB_0289	ENOG4107QXX	ABC transporter
RGRSB_0293	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
RGRSB_0294	ENOG4105EHU	Circadian clock protein KaiC
RGRSB_0295	ENOG4108ZGN	Component of the KaiABC clock protein complex, which constitutes the main circadian regulator in cyanobacteria. The KaiABC complex may act as a promoter-non-specific transcription regulator that represses transcription, possibly by acting on the state of chromosome compaction. In the complex, it decreases the phosphorylation status of KaiC. It has no effect on KaiC by itself, but instead needs the presence of both KaiA and KaiC, suggesting that it acts by antagonizing the interaction between KaiA and KaiC (By similarity)
RGRSB_0297	ENOG4105BZU	Histidine kinase
RGRSB_0300	ENOG4107U45	Cobalt transport protein
RGRSB_0302	ENOG4107EEN	Catalyzes the addition of meso-diaminopimelic acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan (By similarity)
RGRSB_0312	ENOG4105DSF	transport protein
RGRSB_0313	ENOG4105C8T	Leucyl-tRNA synthetase
RGRSB_0314	ENOG41084A0	50s ribosomal protein L35
RGRSB_0315	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)
RGRSB_0322	ENOG4105CH8	Succinyl-CoA ligase ADP-forming subunit alpha
RGRSB_0323	ENOG4105CMV	Succinyl-CoA synthetase subunit beta
RGRSB_0335	ENOG4105CHV	Transcription elongation factor NusA
RGRSB_0336	ENOG4107ZR3	Required for maturation of 30S ribosomal subunits (By similarity)
RGRSB_0339	ENOG4107RIQ	Sulfate adenylate transferase
RGRSB_0345	ENOG4105EB1	binding-protein-dependent transport systems inner membrane Component
RGRSB_0346	ENOG4105S9S	Binding-protein-dependent transport systems, inner membrane component
RGRSB_0347	ENOG4105EPJ	extracellular solute-binding protein family 1
RGRSB_0348	ENOG4108IJ9	(ABC) transporter
RGRSB_0350	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)
RGRSB_0354	ENOG4105C4E	Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate (By similarity)
RGRSB_0355	ENOG41084H8	Binds directly to 16S ribosomal RNA (By similarity)
RGRSB_0358	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
RGRSB_0364	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)
RGRSB_0371	ENOG4105BZN	citrate synthase
RGRSB_0372	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)
RGRSB_0374	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
RGRSB_0379	ENOG4108KNB	n-acetylmuramoyl-l-alanine amidase
RGRSB_0380	ENOG4105F03	Provides the (R)-glutamate required for cell wall biosynthesis (By similarity)
RGRSB_0383	ENOG4107Z9D	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
RGRSB_0386	ENOG4105X1F	electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon- concentration (By similarity)
RGRSB_0389	ENOG4105BZ4	penicillin-binding protein
RGRSB_0390	ENOG4105D5I	Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate (By similarity)
RGRSB_0392	ENOG4105BZU	Histidine kinase
RGRSB_0395	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
RGRSB_0402	ENOG4108R9R	May be involved in photosynthetic membrane biogenesis (By similarity)
RGRSB_0404	ENOG4108RNI	3'(2')5'-bisphosphate nucleotidase
RGRSB_0406	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)
RGRSB_0410	ENOG4105E66	phosphoriboisomerase A
RGRSB_0412	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)
RGRSB_0415	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)
RGRSB_0417	ENOG4107W5X	it plays a direct role in the translocation of protons across the membrane (By similarity)
RGRSB_0418	ENOG4105VH4	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)
RGRSB_0419	ENOG4105S30	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)
RGRSB_0420	ENOG4105VYJ	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)
RGRSB_0421	ENOG4105E3N	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)
RGRSB_0422	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
RGRSB_0423	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)
RGRSB_0425	ENOG4105FCI	Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate (By similarity)
RGRSB_0426	ENOG4107XHR	Involved in DNA repair and RecF pathway recombination (By similarity)
RGRSB_0428	ENOG4105CTK	cobaltochelatase, cobn subunit
RGRSB_0432	ENOG4105DC1	bifunctional purine biosynthesis protein purh
RGRSB_0433	ENOG4108JQC	penicillin-binding protein 1A
RGRSB_0436	ENOG4105D21	Phosphoribosylformylglycinamidine synthase I
RGRSB_0442	ENOG4108VEQ	Superoxide dismutase
RGRSB_0448	ENOG4108JYK	Dehydrogenase
RGRSB_0449	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)
RGRSB_0453	ENOG4107TTD	cytosine deaminase
RGRSB_0454	ENOG4105CIH	Imidazole acetol-phosphate transaminase
RGRSB_0455	ENOG4105CJX	Molecular chaperone. Has ATPase activity (By similarity)
RGRSB_0459	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)
RGRSB_0460	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)
RGRSB_0461	ENOG4105KZR	One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome (By similarity)
RGRSB_0462	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
RGRSB_0463	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
RGRSB_0464	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)
RGRSB_0465	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
RGRSB_0466	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
RGRSB_0467	ENOG410848H	50s ribosomal protein l29
RGRSB_0468	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
RGRSB_0469	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
RGRSB_0470	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
RGRSB_0471	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
RGRSB_0472	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)
RGRSB_0473	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)
RGRSB_0474	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)
RGRSB_0475	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)
RGRSB_0476	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
RGRSB_0480	ENOG41067V7	50S ribosomal protein L36
RGRSB_0481	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
RGRSB_0482	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)
RGRSB_0484	ENOG4108ZT0	50S ribosomal protein l17
RGRSB_0485	ENOG4105DI7	Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs (By similarity)
RGRSB_0486	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)
RGRSB_0487	ENOG4108UJD	30S ribosomal protein S9
RGRSB_0488	ENOG41082EV	50s ribosomal protein l31
RGRSB_0489	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
RGRSB_0491	ENOG4105PGM	cation diffusion facilitator family transporter
RGRSB_0493	ENOG4105ET3	Reduction of activated sulfate into sulfite (By similarity)
RGRSB_0495	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)
RGRSB_0496	ENOG4108VIA	integral membrane protein
RGRSB_0498	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)
RGRSB_0502	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
RGRSB_0503	ENOG4105DX0	Hemolysin A
RGRSB_0504	ENOG4105DSM	The key enzymatic reactions in nitrogen fixation are catalyzed by the nitrogenase complex, which has 2 components the iron protein and the molybdenum-iron protein (By similarity)
RGRSB_0505	ENOG4105C78	Uses Mg-ATP and reduced ferredoxin to reduce ring D of protochlorophyllide (Pchlide) to form chlorophyllide a (Chlide). This reaction is light-independent (By similarity)
RGRSB_0506	ENOG4105JFG	SpoIID LytB domain protein
RGRSB_0511	ENOG4107QI6	Cysteine desulfurase
RGRSB_0516	ENOG4107QMV	Part of the ABC transporter complex PstSACB involved in phosphate import (By similarity)
RGRSB_0517	ENOG4105C8U	phosphate abc transporter
RGRSB_0518	ENOG4105E2Z	phosphate ABC transporter (Permease
RGRSB_0521	ENOG4108K7V	UPF0284 protein
RGRSB_0525	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
RGRSB_0526	ENOG4107VQD	May catalyze the methylation of C-1 in cobalt-precorrin- 5 and the subsequent extrusion of acetic acid from the resulting intermediate to form cobalt-precorrin-6A (By similarity)
RGRSB_0527	ENOG4105C72	UPF0176 protein
RGRSB_0534	ENOG4108KMV	Glycosyl transferase (Group 1
RGRSB_0536	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)
RGRSB_0537	ENOG4105C35	Catalyzes the interconversion of methylthioribose-1- phosphate (MTR-1-P) into methylthioribulose-1-phosphate (MTRu-1-P) (By similarity)
RGRSB_0538	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)
RGRSB_0539	ENOG4105CJW	magnesium transporter
RGRSB_0544	ENOG4105ERH	Fumarylacetoacetate hydrolase
RGRSB_0545	ENOG41082BG	Binds together with S18 to 16S ribosomal RNA (By similarity)
RGRSB_0547	ENOG4108Z38	Catalyzes a trans-dehydration via an enolate intermediate (By similarity)
RGRSB_0548	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)
RGRSB_0550	ENOG4105C1B	dTDP-glucose 4-6-dehydratase
RGRSB_0555	ENOG4105CXT	aspartate transcarbamylase
RGRSB_0564	ENOG4105BZA	Phosphoglycerate kinase
RGRSB_0565	ENOG4105H0N	Participates in electron transfer between P700 and the cytochrome b6-f complex in photosystem I
RGRSB_0566	ENOG4105CHM	Aminotransferase
RGRSB_0568	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)
RGRSB_0570	ENOG4105CX4	Precorrin-6y C5,15-methyltransferase
RGRSB_0571	ENOG4105C6U	Exchanges the guanine residue with 7-aminomethyl-7- deazaguanine in tRNAs with GU(N) anticodons (tRNA-Asp, -Asn, -His and -Tyr). After this exchange, a cyclopentendiol moiety is attached to the 7-aminomethyl group of 7-deazaguanine, resulting in the hypermodified nucleoside queuosine (Q) (7-(((4,5-cis- dihydroxy-2-cyclopenten-1-yl)amino)methyl)-7-deazaguanosine) (By similarity)
RGRSB_0579	ENOG4105DXN	mazG family
RGRSB_0582	ENOG4105WMM	Probably plays a role in a hydrogenase nickel cofactor insertion step (By similarity)
RGRSB_0584	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
RGRSB_0585	ENOG4105DC6	This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex (By similarity)
RGRSB_0586	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
RGRSB_0591	ENOG4105BZU	Histidine kinase
RGRSB_0592	ENOG4107Z8Z	Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1) (By similarity)
RGRSB_0597	ENOG4105EBH	Required during biogenesis of c-type cytochromes (cytochrome c6 and cytochrome f) at the step of heme attachment (By similarity)
RGRSB_0601	ENOG4108V3E	phosphoribosylglycinamide formyltransferase
RGRSB_0608	ENOG4108JJB	ABC transporter
RGRSB_0615	ENOG4105VAS	Could be involved in insertion of integral membrane proteins into the membrane (By similarity)
RGRSB_0616	ENOG4105CJT	Mannose-1-phosphate guanylyltransferase
RGRSB_0619	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)
RGRSB_0621	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)
RGRSB_0631	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)
RGRSB_0633	ENOG4105DJZ	UPF0182 protein
RGRSB_0647	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
RGRSB_0654	ENOG4108IAJ	Nad-dependent epimerase dehydratase
RGRSB_0655	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
RGRSB_0656	ENOG4107VXZ	Hydrolase
RGRSB_0657	ENOG4105DR5	peptidase
RGRSB_0660	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
RGRSB_0662	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
RGRSB_0664	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)
RGRSB_0666	ENOG4105MK2	5-formyltetrahydrofolate cyclo-ligase
RGRSB_0671	ENOG4105CGK	Exodeoxyribonuclease III
RGRSB_0678	ENOG4105CTR	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
RGRSB_0681	ENOG4108Z08	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
RGRSB_0682	ENOG4107RAQ	aminopeptidase
RGRSB_0685	ENOG4108W6C	Dehydrogenase
RGRSB_0686	ENOG4105C6M	Alpha-keto-beta-hydroxylacyl reductoisomerase
RGRSB_0692	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
RGRSB_0695	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
RGRSB_0697	ENOG4107RJ1	sodium solute
RGRSB_0701	ENOG4105EMN	RNA polymerase sigma factor
RGRSB_0704	ENOG4108IQE	Amp-dependent synthetase and ligase
RGRSB_0707	ENOG4108UMW	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
RGRSB_0710	ENOG41084GG	50S ribosomal protein L33
RGRSB_0711	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)
RGRSB_0714	ENOG4105VUV	UPF0367 protein
RGRSB_0718	ENOG4105CVN	desaturase
RGRSB_0720	ENOG4108UV6	Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP) (By similarity)
RGRSB_0731	ENOG4108ZGB	N-(5'-phosphoribosyl)anthranilate isomerase
RGRSB_0736	ENOG4105DKJ	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
RGRSB_0739	ENOG4105EVY	Uses Mg-ATP and reduced ferredoxin to reduce ring D of protochlorophyllide (Pchlide) to form chlorophyllide a (Chlide). This reaction is light-independent (By similarity)
RGRSB_0740	ENOG4105XCI	PucC protein
RGRSB_0744	ENOG4106MP8	UPF0754 membrane protein
RGRSB_0745	ENOG4105CCA	Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle (By similarity)
RGRSB_0747	ENOG4105C6E	dna polymerase iii
RGRSB_0748	ENOG4106FN3	tellurium resistance protein
RGRSB_0750	ENOG4105HFZ	Membrane
RGRSB_0755	ENOG4105CG1	Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA (By similarity)
RGRSB_0756	ENOG4105F32	YngK protein
RGRSB_0757	ENOG41083EU	50s ribosomal protein l28
RGRSB_0758	ENOG4105CJT	Mannose-1-phosphate guanylyltransferase
RGRSB_0762	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)
RGRSB_0766	ENOG4107QZB	decarboxylase
RGRSB_0767	ENOG4105K70	DNA-binding protein
RGRSB_0768	ENOG41068B1	Cob-I-yrinic acid a,c-diamide adenosyltransferase
RGRSB_0770	ENOG4105WVZ	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
RGRSB_0773	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)
RGRSB_0777	ENOG4108ZI0	d,d-heptose 1,7-bisphosphate phosphatase
RGRSB_0778	ENOG4105F55	Catalyzes the isomerization of sedoheptulose 7-phosphate in D-glycero-D-manno-heptose 7-phosphate (By similarity)
RGRSB_0785	ENOG4105CDH	Citrulline--aspartate ligase
RGRSB_0786	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
RGRSB_0789	ENOG4108K5P	(LipO)protein
RGRSB_0796	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)
RGRSB_0805	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
RGRSB_0807	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)
RGRSB_0808	ENOG4105DAF	Involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
RGRSB_0811	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
RGRSB_0813	ENOG4105FD2	Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) (By similarity)
RGRSB_0822	ENOG4105E05	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
RGRSB_0829	ENOG4105C37	(CBS) domain
RGRSB_0832	ENOG4105EPH	radical SAM domain protein
RGRSB_0835	ENOG4108R4Z	Functions in the N-end rule pathway of protein degradation where it conjugates Leu, Phe and, less efficiently, Met from aminoacyl-tRNAs to the N-termini of proteins containing an N-terminal arginine or lysine (By similarity)
RGRSB_0836	ENOG41082AF	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)
RGRSB_0837	ENOG4108KGH	TRANSCRIPTIONal
RGRSB_0838	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)
RGRSB_0842	ENOG4105WVZ	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
RGRSB_0843	ENOG4108I0Q	anthranilate phosphoribosyltransferase
RGRSB_0845	ENOG4108UH8	Involved in the biosynthesis of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP), two major building blocks of isoprenoid compounds. Catalyzes the conversion of 4- diphosphocytidyl-2-C-methyl-D-erythritol 2-phosphate (CDP-ME2P) to 2-C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-CPP) with a corresponding release of cytidine 5-monophosphate (CMP) (By similarity)
RGRSB_0846	ENOG4105C5S	asparaginyl-tRNA synthetase
RGRSB_0848	ENOG4105E0X	reductase
RGRSB_0850	ENOG4105C38	Glycyl-tRNA synthetase beta subunit
RGRSB_0852	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)
RGRSB_0857	ENOG4107YU2	histidine triad (hIT) protein
RGRSB_0860	ENOG4105D0M	Protease HtpX homolog
RGRSB_0864	ENOG4105CKK	Glycosyl transferase, family 2
RGRSB_0872	ENOG4107R5M	Catalyzes the transfer of a N-acetyl-glucosamine moiety to 1D-myo-inositol 3-phosphate to produce 1D-myo-inositol 2- acetamido-2-deoxy-glucopyranoside 3-phosphate in the mycothiol biosynthesis pathway (By similarity)
RGRSB_0875	ENOG4107TYG	Oxidoreductase domain-containing protein
RGRSB_0880	ENOG4108N5B	2-phosphosulfolactate phosphatase
RGRSB_0882	ENOG4105C6H	Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction (By similarity)
RGRSB_0887	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)
RGRSB_0888	ENOG4105D6C	Part of the ABC transporter complex MacAB involved in macrolide export. Transmembrane domains (TMD) form a pore in the inner membrane and the ATP-binding domain (NBD) is responsible for energy generation (By similarity)
RGRSB_0889	ENOG4105CKJ	The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing (By similarity)
RGRSB_0891	ENOG4108HMW	glycyl-tRNA synthetase, alpha subunit
RGRSB_0894	ENOG4105FE8	tRNA (Guanosine-2'-O-)-methyltransferase
RGRSB_0900	ENOG4105CQC	Prephenate dehydratase
RGRSB_0903	ENOG4108ZQD	Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A (By similarity)
RGRSB_0905	ENOG4105C3J	Cysteine desulfurase
RGRSB_0910	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)
RGRSB_0912	ENOG4105DC8	reductase
RGRSB_0931	ENOG4105CE4	GlcNAc 6-P deacetylase
RGRSB_0932	ENOG4105DB7	PHP domain protein
RGRSB_0938	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)
RGRSB_0940	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
RGRSB_0941	ENOG4105C89	phosphohexose isomerase
RGRSB_0942	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)
RGRSB_0944	ENOG4105F3K	May play a role in DNA repair. It seems to be involved in an RecBC-independent recombinational process of DNA repair. It may act with RecF and RecO (By similarity)
RGRSB_0948	ENOG4105DR5	peptidase
RGRSB_0956	ENOG4105CD2	stage iii sporulation protein aa
RGRSB_0959	ENOG4105D49	3-dehydroquinate synthase
RGRSB_0964	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)
RGRSB_0965	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)
RGRSB_0966	ENOG4105M02	This protein specifically catalyzes the removal of signal peptides from prolipoproteins (By similarity)
RGRSB_0967	ENOG4107ZYJ	bioY protein
RGRSB_0968	ENOG4107QSQ	Catalyzes the conversion of dethiobiotin (DTB) to biotin by the insertion of a sulfur atom into dethiobiotin via a radical- based mechanism (By similarity)
RGRSB_0969	ENOG41090A4	Pterin carbinolamine dehydratase
RGRSB_0974	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)
RGRSB_0976	ENOG4107UAN	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)
RGRSB_0978	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)
RGRSB_0980	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
RGRSB_0981	ENOG41085RW	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)
RGRSB_0982	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)
RGRSB_0986	ENOG4107YBR	Specifically methylates the N7 position of a guanine in 16S rRNA (By similarity)
RGRSB_0987	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
RGRSB_0989	ENOG41083MR	nifu domain-containing protein
RGRSB_0990	ENOG4107U9H	DNA polymerase
RGRSB_0998	ENOG4105D5U	fad dependent oxidoreductase
RGRSB_1001	ENOG4105PW4	Sugar fermentation stimulation protein homolog
RGRSB_1003	ENOG41080W8	Cell division protein that is part of the divisome complex and is recruited early to the Z-ring. Probably stimulates Z-ring formation, perhaps through the cross-linking of FtsZ protofilaments. Its function overlaps with FtsA (By similarity)
RGRSB_1007	ENOG4107QSS	Involved in the synthesis of meso-diaminopimelate (m-DAP or DL-DAP), required for both lysine and peptidoglycan biosynthesis. Catalyzes the direct conversion of tetrahydrodipicolinate to LL-diaminopimelate, a reaction that requires three enzymes in E.coli (By similarity)
RGRSB_1016	ENOG4105D43	The glycine cleavage system catalyzes the degradation of glycine (By similarity)
RGRSB_1019	ENOG4108HRN	Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate (By similarity)
RGRSB_1020	ENOG4105C17	glyceraldehyde-3-phosphate dehydrogenase
RGRSB_1021	ENOG4107QRI	Phosphoketolase
RGRSB_1022	ENOG41086DT	Membrane protein of unknown function
RGRSB_1025	ENOG4105C3B	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
RGRSB_1029	ENOG4107QRG	dna polymerase iii
RGRSB_1031	ENOG4105C59	p-type ATPase
RGRSB_1038	ENOG4105CG3	alpha amylase, catalytic region
RGRSB_1040	ENOG4108KGH	TRANSCRIPTIONal
RGRSB_1044	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)
RGRSB_1048	ENOG4108RW0	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
RGRSB_1050	ENOG4105D10	5-enolpyruvylshikimate-3-phosphate phospholyase
RGRSB_1051	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)
RGRSB_1054	ENOG4105WVZ	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
RGRSB_1065	ENOG4105C0N	N-acetylglutamate semialdehyde dehydrogenase
RGRSB_1071	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)
RGRSB_1072	ENOG4105CE9	30S ribosomal protein S2
RGRSB_1076	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)
RGRSB_1079	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
RGRSB_1081	ENOG4108S7T	Catalyzes the oxidation of either pyridoxine 5'- phosphate (PNP) or pyridoxamine 5'-phosphate (PMP) into pyridoxal 5'-phosphate (PLP) (By similarity)
RGRSB_1086	ENOG4108MV2	Involved in light-induced Na( )-dependent proton extrusion. Also seems to be involved in CO(2) transport (By similarity)
RGRSB_1090	ENOG4105K8N	protein family UPF0079, ATPase
RGRSB_1094	ENOG4105DRP	amino acid AbC transporter
RGRSB_1097	ENOG4108UK2	deaminase
RGRSB_1098	ENOG4107ZFB	This enzyme is involved in nucleotide metabolism it produces dUMP, the immediate precursor of thymidine nucleotides and it decreases the intracellular concentration of dUTP so that uracil cannot be incorporated into DNA (By similarity)
RGRSB_1104	ENOG4107QIK	phosphoribosylformylglycinamidine synthase
RGRSB_1106	ENOG4105EYH	Exonuclease
RGRSB_1111	ENOG4105BZQ	cdp-diacylglycerol-glycerol-3-phosphate 3-phosphatidyltransferase
RGRSB_1112	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
RGRSB_1113	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
RGRSB_1114	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)
RGRSB_1115	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)
RGRSB_1116	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)
RGRSB_1119	ENOG4105CG2	Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 (By similarity)
RGRSB_1123	ENOG4108Z03	MAF-like protein
RGRSB_1129	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)
RGRSB_1130	ENOG4105ESV	Glycosyl transferase, family 4
RGRSB_1131	ENOG4105CCX	Catalyzes the production of spermidine from putrescine and decarboxylated S-adenosylmethionine (dcSAM), which serves as an aminopropyl donor (By similarity)
RGRSB_1133	ENOG4105DPM	folylpolyglutamate synthase Dihydrofolate synthase
RGRSB_1134	ENOG4107QRA	Extracellular solute-binding protein, family 5
RGRSB_1136	ENOG4108R0D	protein with myosin-like
RGRSB_1138	ENOG4105CSJ	Enoyl- acyl-carrier-protein reductase NADH
RGRSB_1146	ENOG4108JJB	ABC transporter
RGRSB_1153	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
RGRSB_1158	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
RGRSB_1165	ENOG4105EB3	Histidine kinase
RGRSB_1167	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
RGRSB_1175	ENOG4105CVB	Vitamin K epoxide reductase
RGRSB_1180	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)
RGRSB_1181	ENOG4105CRE	cytochrome C
RGRSB_1182	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
RGRSB_1183	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)
RGRSB_1184	ENOG4105KM4	Acetyl-CoA carboxylase, biotin carboxyl carrier protein
RGRSB_1190	ENOG4107Z8V	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)
RGRSB_1191	ENOG4105K64	Glycosyl transferase, family 2
RGRSB_1195	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)
RGRSB_1200	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)
RGRSB_1202	ENOG4105DDQ	anthranilate synthase
RGRSB_1206	ENOG4105DUM	transcriptional regulator, lysR family
RGRSB_1217	ENOG4108Q79	6-phosphogluconolactonase (EC 3.1.1.31)
RGRSB_1220	ENOG410803B	Involved in the transcription termination process (By similarity)
RGRSB_1228	ENOG4105CZI	D-fructose-1,6-bisphosphate 1-phosphohydrolase class 1
RGRSB_1230	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
RGRSB_1231	ENOG4107Y82	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)
RGRSB_1232	ENOG4105C75	arginyL-tRNA synthetase
RGRSB_1235	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)
RGRSB_1236	ENOG4108PWY	Carbohydrate-selective porin OprB
RGRSB_1237	ENOG4105FIK	Inherit from COG: dihydropteroate synthase
RGRSB_1239	ENOG4105CM1	Catalyzes, together with MoaC, the conversion of 5'-GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
RGRSB_1245	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)
RGRSB_1247	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)
RGRSB_1248	ENOG4105C5H	ABC transporter
RGRSB_1253	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
RGRSB_1258	ENOG4107WMZ	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)
RGRSB_1259	ENOG4105CPF	Cell wall formation (By similarity)
RGRSB_1268	ENOG4108JIC	nucleoside recognition domain protein
RGRSB_1273	ENOG4108HMX	isocitrate dehydrogenase (NADP)
RGRSB_1282	ENOG4107XW6	Cell division inhibitor that blocks the formation of polar Z ring septums. Rapidly oscillates between the poles of the cell to destabilize FtsZ filaments that have formed before they mature into polar Z rings. Prevents FtsZ polymerization (By similarity)
RGRSB_1290	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)
RGRSB_1293	ENOG4105EMU	Dehydrogenase
RGRSB_1294	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)
RGRSB_1297	ENOG4105C1V	Peptidase, M16
RGRSB_1299	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)
RGRSB_1300	ENOG4107Z3D	50S ribosomal protein l10
RGRSB_1301	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)
RGRSB_1302	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
RGRSB_1305	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)
RGRSB_1307	ENOG4105CHH	sulfate transporter
RGRSB_1308	ENOG4105CMR	udp-glucose 4-epimerase
RGRSB_1319	ENOG4105DVK	Precorrin-2 c20-methyltransferase
RGRSB_1320	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)
RGRSB_1322	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)
RGRSB_1324	ENOG4107QXI	Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs (By similarity)
RGRSB_1325	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)
RGRSB_1327	ENOG4105CXI	aluminum resistance protein
RGRSB_1331	ENOG4107S5Z	Catalyzes the transfer of endogenously produced octanoic acid from octanoyl-acyl-carrier-protein onto the lipoyl domain of GcvH, an intermediate carrier during protein lipoylation (By similarity)
RGRSB_1340	ENOG4105DFU	Cell wall formation (By similarity)
RGRSB_1345	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
RGRSB_1348	ENOG410902K	Involved in the modulation of the specificity of the ClpAP-mediated ATP-dependent protein degradation (By similarity)
RGRSB_1350	ENOG4105C5F	glutamine synthetase
RGRSB_1353	ENOG4105D43	The glycine cleavage system catalyzes the degradation of glycine (By similarity)
RGRSB_1355	ENOG4105DKQ	ROK family
RGRSB_1360	ENOG4105EPH	radical SAM domain protein
RGRSB_1361	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
RGRSB_1364	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
RGRSB_1370	ENOG4105CBM	Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 (By similarity)
RGRSB_1373	ENOG4105WH1	Two component transcriptional regulator luxr family
RGRSB_1374	ENOG4108JA5	May be involved in signal transduction. Participates in the KaiABC clock protein complex, which constitutes the main circadian regulator in cyanobacteria, via its interaction with KaiC. Required for robustness of the circadian rhythm of gene expression and is involved in clock outputs (By similarity)
RGRSB_1380	ENOG4105CZ5	Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate (By similarity)
RGRSB_1382	ENOG4105CIA	precorrin-4 C(11)-methyltransferase
RGRSB_1385	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)
RGRSB_1386	ENOG4105FDP	GntR family transcriptional regulator
RGRSB_1394	ENOG4108WT6	Carbon dioxide concentrating mechanism protein
RGRSB_1395	ENOG4105D65	subunit l
RGRSB_1396	ENOG4105C8S	subunit m
RGRSB_1397	ENOG4108IYU	L-aspartate oxidase
RGRSB_1399	ENOG4107Z12	Joins Ado-cobinamide-GDP and alpha-ribazole to generate adenosylcobalamin (Ado-cobalamin) (By similarity)
RGRSB_1402	ENOG4105CJN	penicillin-binding protein
RGRSB_1408	ENOG4105C01	Dihydroxy-acid dehydratase
RGRSB_1409	ENOG4107ZH9	Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis (By similarity)
RGRSB_1411	ENOG4106C1G	Component of the cytochrome b6-f complex, which mediates electron transfer between photosystem II (PSII) and photosystem I (PSI), cyclic electron flow around PSI, and state transitions (By similarity)
RGRSB_1412	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)
RGRSB_1414	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
RGRSB_1416	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)
RGRSB_1418	ENOG4105K46	50S ribosomal protein l27
RGRSB_1419	ENOG4105CMY	5-enolpyruvylshikimate-3-phosphate synthase
RGRSB_1422	ENOG4105CJI	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
RGRSB_1425	ENOG4105GHY	electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon- concentration (By similarity)
RGRSB_1430	ENOG4105DTC	1-(5-phosphoribosyl)-5-amino-4-imidazole-carboxylate (air) carboxylase
RGRSB_1431	ENOG4105KA4	The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing. RuvA stimulates, in the presence of DNA, the weak ATPase activity of RuvB (By similarity)
RGRSB_1433	ENOG4108T5I	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
RGRSB_1435	ENOG4105EGS	Mechanosensitive ion channel
RGRSB_1438	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)
RGRSB_1439	ENOG4108R6B	Component of the cytochrome b6-f complex, which mediates electron transfer between photosystem II (PSII) and photosystem I (PSI), cyclic electron flow around PSI, and state transitions (By similarity)
RGRSB_1440	ENOG4105F23	Fibronectin-binding protein
RGRSB_1443	ENOG4105BZ1	(ABC) transporter
RGRSB_1445	ENOG4105C59	p-type ATPase
RGRSB_1451	ENOG4105CJ1	ABC, transporter
RGRSB_1452	ENOG41081AP	Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) (By similarity)
RGRSB_1455	ENOG4107TS3	membrane protein, TerC
RGRSB_1456	ENOG4105D86	that it carries out the mismatch recognition step. This protein has a weak ATPase activity (By similarity)
RGRSB_1458	ENOG4105E15	Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate
RGRSB_1464	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
RGRSB_1466	ENOG4107QJE	Chromosome Partitioning Protein
RGRSB_1468	ENOG4108JA5	May be involved in signal transduction. Participates in the KaiABC clock protein complex, which constitutes the main circadian regulator in cyanobacteria, via its interaction with KaiC. Required for robustness of the circadian rhythm of gene expression and is involved in clock outputs (By similarity)
RGRSB_1469	ENOG4107RFW	hydrolase family 57
RGRSB_1471	ENOG4107TVC	Glycosyl transferase, family 2
RGRSB_1475	ENOG41065E1	Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) (By similarity)
RGRSB_1477	ENOG4105C9U	ATP-dependent DNA helicase RecQ
RGRSB_1478	ENOG4105CKK	Glycosyl transferase, family 2
RGRSB_1486	ENOG4105CP7	Triose-phosphate isomerase
RGRSB_1488	ENOG4105DP5	Catalyzes the biosynthesis of agmatine from arginine (By similarity)
RGRSB_1495	ENOG4105CFT	Part of the energy-coupling factor (ECF) transporter complex CbiMNOQ involved in cobalt import (By similarity)
RGRSB_1498	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)
RGRSB_1500	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)
RGRSB_1502	ENOG4105K63	Thioredoxin
RGRSB_1508	ENOG4105J3Z	Involved in the modulation of the specificity of the ClpAP-mediated ATP-dependent protein degradation (By similarity)
RGRSB_1509	ENOG4105CKA	Catalyzes the reversible isomerization-deamination of glucosamine 6-phosphate (GlcN6P) to form fructose 6-phosphate (Fru6P) and ammonium ion (By similarity)
RGRSB_1512	ENOG4105CUT	histidyl-tRNA synthetase
RGRSB_1514	ENOG4108Z6B	deaminase
RGRSB_1517	ENOG4105C8B	TIGR00159 family
RGRSB_1520	ENOG4105ERG	peptidase m48, ste24p
RGRSB_1523	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)
RGRSB_1525	ENOG4105CAT	Cytidine monophosphate kinase
RGRSB_1528	ENOG4105CKK	Glycosyl transferase, family 2
RGRSB_1529	ENOG41089I4	Inherit from COG: Glycosyl transferase, family 2
RGRSB_1531	ENOG4105ND9	Nitrogenase-associated protein
RGRSB_1535	ENOG4107S73	homocitrate synthase
RGRSB_1538	ENOG4105D7W	serine acetyltransferase
RGRSB_1541	ENOG4105C3J	Cysteine desulfurase
RGRSB_1542	ENOG4107RIU	May be involved in the formation or repair of Fe-S clusters present in iron-sulfur proteins (By similarity)
RGRSB_1543	ENOG4105DSM	The key enzymatic reactions in nitrogen fixation are catalyzed by the nitrogenase complex, which has 2 components the iron protein and the molybdenum-iron protein (By similarity)
RGRSB_1544	ENOG4105D0B	Nitrogenase protein alpha chain
RGRSB_1545	ENOG4105CY9	nitrogenase molybdenum-iron protein beta chain
RGRSB_1546	ENOG4105D0B	Nitrogenase protein alpha chain
RGRSB_1547	ENOG4105DK8	Nitrogenase molybdenum-iron cofactor biosynthesis protein NifN
RGRSB_1548	ENOG4108UR2	Nitrogen fixation protein NifX
RGRSB_1550	ENOG4105X87	nitrogen fixation
RGRSB_1551	ENOG4105R88	May protect the nitrogenase Fe-Mo protein from oxidative damage (By similarity)
RGRSB_1552	ENOG41081QJ	UBA THIF-type NAD FAD binding
RGRSB_1553	ENOG4105V5Z	Iron-sulfur cluster assembly accessory protein
RGRSB_1558	ENOG4105CE1	Ferrous iron transport protein b
RGRSB_1562	ENOG4105WCA	Ferredoxin
RGRSB_1567	ENOG4105CYU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
RGRSB_1568	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)
RGRSB_1569	ENOG4105KWU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
RGRSB_1572	ENOG4105D0M	Protease HtpX homolog
RGRSB_1574	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)
RGRSB_1575	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
RGRSB_1579	ENOG4106EG9	Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) (By similarity)
RGRSB_1582	ENOG4105C02	permease
RGRSB_1583	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
RGRSB_1586	ENOG4105CWT	An essential GTPase that binds both GDP and GTP, with rapid nucleotide exchange. Plays a role in 16S rRNA processing and 30S ribosomal subunit biogenesis and possibly also in cell cycle regulation and energy metabolism (By similarity)
RGRSB_1587	ENOG41080ZE	Adenylate cyclase
RGRSB_1592	ENOG4105E2N	Transfers and isomerizes the ribose moiety from AdoMet to the 7-aminomethyl group of 7-deazaguanine (preQ1-tRNA) to give epoxyqueuosine (oQ-tRNA) (By similarity)
RGRSB_1594	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)
RGRSB_1597	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)
RGRSB_1605	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)
RGRSB_1606	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)
RGRSB_1607	ENOG410667J	hydrolase
RGRSB_1608	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
RGRSB_1613	ENOG4105CT1	(ABC) transporter
RGRSB_1615	ENOG4107YD0	Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA (By similarity)
RGRSB_1616	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)
RGRSB_1617	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
RGRSB_1622	ENOG4105DQV	Component of the cytochrome b6-f complex, which mediates electron transfer between photosystem II (PSII) and photosystem I (PSI), cyclic electron flow around PSI, and state transitions (By similarity)
RGRSB_1630	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
RGRSB_1632	ENOG4105CWG	Catalyzes the last two steps in the biosynthesis of 5- methylaminomethyl-2-thiouridine (mnm(5)s(2)U) at the wobble position (U34) in tRNA. Catalyzes the FAD-dependent demodification of cmnm(5)s(2)U34 to nm(5)s(2)U34, followed by the transfer of a methyl group from S-adenosyl-L-methionine to nm(5)s(2)U34, to form mnm(5)s(2)U34 (By similarity)
RGRSB_1633	ENOG4108UK1	Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant (By similarity)
RGRSB_1634	ENOG4105CEV	competence damage-inducible protein
RGRSB_1636	ENOG4108PJD	permease
RGRSB_1638	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)
RGRSB_1641	ENOG4105CBD	Diacylglycerol kinase
RGRSB_1643	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)
RGRSB_1647	ENOG4105D9I	Responsible for the addition of glutamate residues to the C-terminus of ribosomal protein S6 (By similarity)
RGRSB_1649	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
RGRSB_1650	ENOG4105C1B	dTDP-glucose 4-6-dehydratase
RGRSB_1651	ENOG4105EY8	ABC transporter
RGRSB_1652	ENOG4105MFV	ABC-2 type transporter
RGRSB_1654	ENOG4105D0U	Arsenite-activated ATPase (ArsA)
RGRSB_1655	ENOG4105DB3	bacteriochlorophyll chlorophyll a synthase
RGRSB_1660	ENOG4108ZGN	Component of the KaiABC clock protein complex, which constitutes the main circadian regulator in cyanobacteria. The KaiABC complex may act as a promoter-non-specific transcription regulator that represses transcription, possibly by acting on the state of chromosome compaction. In the complex, it decreases the phosphorylation status of KaiC. It has no effect on KaiC by itself, but instead needs the presence of both KaiA and KaiC, suggesting that it acts by antagonizing the interaction between KaiA and KaiC (By similarity)
RGRSB_1661	ENOG4108JPM	phospho-2-dehydro-3-deoxyheptonate aldolase
RGRSB_1662	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
RGRSB_1669	ENOG4108Z11	Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes (By similarity)
RGRSB_1673	ENOG4105E4C	Lytic transglycosylase catalytic
RGRSB_1680	ENOG4107ETG	50S ribosomal protein L34
RGRSB_1681	ENOG4105UVI	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)
RGRSB_1686	ENOG4105C9S	Converts N-acetylmannosamine-6-phosphate (ManNAc-6-P) to N-acetylglucosamine-6-phosphate (GlcNAc-6-P) (By similarity)
RGRSB_1687	ENOG4105BZU	Histidine kinase
RGRSB_1688	ENOG4105CTK	cobaltochelatase, cobn subunit
RGRSB_1694	ENOG4105EEX	Two component transcriptional regulator (Winged helix family
RGRSB_1697	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
RGRSB_1699	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)
RGRSB_1703	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)
RGRSB_1705	ENOG4105C3G	gtp-binding protein
RGRSB_1711	ENOG4107RAJ	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
RGRSB_1715	ENOG4105C8A	Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP (By similarity)
RGRSB_1716	ENOG4105K70	DNA-binding protein
RGRSB_1718	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)
RGRSB_1720	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)
RGRSB_1722	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
RGRSB_1723	ENOG41068G9	50S ribosomal protein L32
RGRSB_1725	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)
RGRSB_1726	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)
RGRSB_1728	ENOG4108UHU	Aldolase
RGRSB_1730	ENOG4105CQS	hydrogenase expression formation protein HypD
RGRSB_1732	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)
RGRSB_1736	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
RGRSB_1737	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)
RGRSB_1738	ENOG4105C8V	SAICAR synthetase
RGRSB_1739	ENOG4105E1Z	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane
RGRSB_1740	ENOG4105C7C	involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
RGRSB_1744	ENOG410811H	Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine (By similarity)
RGRSB_1745	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)
RGRSB_1749	ENOG4105ETX	regulatoR
RGRSB_1754	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
RGRSB_1759	ENOG4108ZEF	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate (By similarity)
RGRSB_1760	ENOG4105D3Q	Sugar transferase
RGRSB_1761	ENOG4107R5M	Catalyzes the transfer of a N-acetyl-glucosamine moiety to 1D-myo-inositol 3-phosphate to produce 1D-myo-inositol 2- acetamido-2-deoxy-glucopyranoside 3-phosphate in the mycothiol biosynthesis pathway (By similarity)
RGRSB_1762	ENOG41080E3	single-stranded DNA-binding protein
RGRSB_1763	ENOG4105DFF	Rod shape-determining protein mreb
RGRSB_1764	ENOG4105N3I	Involved in formation and maintenance of cell shape (By similarity)
RGRSB_1772	ENOG4105CFZ	Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III (By similarity)
RGRSB_1773	ENOG4105D8X	mechanosensitive ion channel
RGRSB_1780	ENOG4105D7T	ABC transporter
RGRSB_1782	ENOG4107U7Q	Transfers the fatty acyl group on membrane lipoproteins (By similarity)
RGRSB_1783	ENOG4105DSE	periplasmic solute binding protein
RGRSB_1784	ENOG4105FDK	ABC transporter
RGRSB_1787	ENOG4105CKI	cobalamin synthesis protein
RGRSB_1788	ENOG4105CXN	decarboxylase
RGRSB_1792	ENOG4105CNI	cell division protein FtsW
RGRSB_1795	ENOG4105E67	Catalyzes the four-electron reduction of biliverdin IX- alpha (2-electron reduction at both the A and D rings)
RGRSB_1797	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
RGRSB_1798	ENOG4108JQC	penicillin-binding protein 1A
RGRSB_1801	ENOG4105C9Q	fumarate hydratase class II
RGRSB_1803	ENOG4105C3X	it is required for DNA replication and normal SOS inducibility. RecF binds preferentially to single-stranded, linear DNA. It also seems to bind ATP (By similarity)
RGRSB_1810	ENOG4105DKF	Catalyzes the radical-mediated transfer of the hydroxybenzyl group from 4-hydroxyphenylpyruvate (HPP) to 5-amino- 6-ribitylamino-2,4(1H,3H)-pyrimidinedione to form 7,8-didemethyl- 8-hydroxy-5-deazariboflavin (FO) (By similarity)
RGRSB_1811	ENOG4105C12	Phosphoribosylglycinamide synthetase
RGRSB_1819	ENOG4105CEP	NADH dehydrogenase
RGRSB_1821	ENOG4105DSF	transport protein
RGRSB_1825	ENOG4108YZ4	nudix hydrolase
RGRSB_1828	ENOG4105CJT	Mannose-1-phosphate guanylyltransferase
RGRSB_1831	ENOG4105C9W	Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity (By similarity)
RGRSB_1832	ENOG4108RSN	SNARE associated Golgi
RGRSB_1837	ENOG4105EWU	Squalene--hopene cyclase
RGRSB_1843	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)
RGRSB_1844	ENOG4105DRS	transport system, permease
RGRSB_1847	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
RGRSB_1857	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
RGRSB_1860	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)
RGRSB_1868	ENOG41080P6	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)
RGRSB_1869	ENOG4105E2X	shikimate dehydrogenase
RGRSB_1870	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)
RGRSB_1873	ENOG4105DPX	Hydrogenase, large subunit
RGRSB_1877	ENOG4105CW3	Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway (By similarity)
RGRSB_1882	ENOG4108EE5	Part of the ABC transporter complex MacAB involved in macrolide export. Transmembrane domains (TMD) form a pore in the inner membrane and the ATP-binding domain (NBD) is responsible for energy generation (By similarity)
RGRSB_1889	ENOG4105C68	Can catalyze the hydrolysis of ATP in the presence of single-stranded DNA, the ATP-dependent uptake of single-stranded DNA by duplex DNA, and the ATP-dependent hybridization of homologous single-stranded DNAs. It interacts with LexA causing its activation and leading to its autocatalytic cleavage (By similarity)
RGRSB_1891	ENOG410848W	30S ribosomal protein S21
RGRSB_1892	ENOG4105KHV	Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate (By similarity)
RGRSB_1894	ENOG4108IJ9	(ABC) transporter
RGRSB_1897	ENOG4105F6H	The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate (By similarity)
RGRSB_1899	ENOG4105BZ1	(ABC) transporter
RGRSB_1903	ENOG4105N7N	Pentapeptide repeat-containing protein
RGRSB_1906	ENOG4107UV6	ribonuclease Z
RGRSB_1909	ENOG4105DK0	Indole-3-glycerol phosphate synthase
RGRSB_1911	ENOG4107QYT	Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor (By similarity)
RGRSB_1913	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
RGRSB_1914	ENOG4108151	Beta-lactamase domain protein
RGRSB_1915	ENOG4108VCT	Sulfite exporter TauE/SafE
RGRSB_1918	ENOG4107QP0	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)
RGRSB_1919	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
RGRSB_1927	ENOG4105CBX	hi0933 family
RGRSB_1931	ENOG4105CGT	Catalyzes the transfer of a phosphate group to glutamate to form glutamate 5-phosphate which rapidly cyclizes to 5- oxoproline (By similarity)
RGRSB_1933	ENOG4106PVI	ATP-dependent carboxylate-amine ligase (By similarity)
RGRSB_1935	ENOG4105DR5	peptidase
RGRSB_1949	ENOG4105C37	(CBS) domain
RGRSB_1952	ENOG4105C72	UPF0176 protein
RGRSB_1954	ENOG4105CXB	phosphoribosylaminoimidazole synthetase
RGRSB_1955	ENOG4105C7E	Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) (By similarity)
RGRSB_1957	ENOG4105DF7	Catalyzes the radical-mediated transfer of the hydroxybenzyl group from 4-hydroxyphenylpyruvate (HPP) to 5-amino- 6-ribitylamino-2,4(1H,3H)-pyrimidinedione to form 7,8-didemethyl- 8-hydroxy-5-deazariboflavin (FO) (By similarity)