locus-tag	class	description
G6N82_00040	ENOG4105D74	hydrolase
G6N82_00065	ENOG4105BZU	Histidine kinase
G6N82_00070	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)
G6N82_00095	ENOG4106SNF	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane
G6N82_00100	ENOG4105DRC	Na( ) H( ) antiporter that extrudes sodium in exchange for external protons (By similarity)
G6N82_00140	ENOG4105GRZ	Ycii-related protein
G6N82_00145	ENOG4105CHP	RNA polymerase
G6N82_00155	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
G6N82_00165	ENOG4105CHR	reductase
G6N82_00180	ENOG410612Q	succinate dehydrogenase (cytochrome b-556 subunit)
G6N82_00190	ENOG4105C00	Succinate dehydrogenase (Flavoprotein subunit)
G6N82_00220	ENOG4108R5K	PPIases accelerate the folding of proteins (By similarity)
G6N82_00255	ENOG4105CYJ	ribosomal RNA small subunit methyltransferase B
G6N82_00265	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)
G6N82_00275	ENOG4105DI2	Pyruvate flavodoxin ferredoxin oxidoreductase domain protein
G6N82_00290	ENOG4105CVP	deoxyribo-dipyrimidine photolyase
G6N82_00305	ENOG4105PDP	Short chain dehydrogenase
G6N82_00310	ENOG4105CBA	glutamine phosphoribosylpyrophosphate amidotransferase
G6N82_00315	ENOG4105D60	lipoprotein releasing system transmembrane protein
G6N82_00320	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)
G6N82_00330	ENOG4108V06	Glutathione peroxidase
G6N82_00345	ENOG4105CEY	Amp-dependent synthetase and ligase
G6N82_00375	ENOG4108RIR	Molybdenum cofactor biosynthesis protein
G6N82_00380	ENOG4107SC1	transglycosylase
G6N82_00390	ENOG4105DWH	electron transfer flavoprotein-ubiquinone oxidoreductase
G6N82_00395	ENOG4105CTR	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
G6N82_00405	ENOG4105C01	Dihydroxy-acid dehydratase
G6N82_00410	ENOG4105DR1	Catalyzes the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. Together with NAD(P)HX epimerase, which catalyzes the epimerization of the S- and R-forms, the enzyme allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration (By similarity)
G6N82_00420	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
G6N82_00425	ENOG4105CEY	Amp-dependent synthetase and ligase
G6N82_00440	ENOG4105D6Z	AFG1 family ATPase
G6N82_00480	ENOG4105C03	ribonuclease
G6N82_00485	ENOG4105C5C	n-acetylmuramoyl-l-alanine amidase
G6N82_00490	ENOG4108JQC	penicillin-binding protein 1A
G6N82_00495	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
G6N82_00500	ENOG4105CG1	Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA (By similarity)
G6N82_00510	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)
G6N82_00520	ENOG4105CSJ	Enoyl- acyl-carrier-protein reductase NADH
G6N82_00555	ENOG4105CHU	acetyl-coa acetyltransferase
G6N82_00560	ENOG4107RGH	Aldehyde dehydrogenase
G6N82_00565	ENOG4105KWU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
G6N82_00570	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)
G6N82_00575	ENOG4105CYU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
G6N82_00580	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)
G6N82_00595	ENOG4107QIZ	NADH dehydrogenase
G6N82_00605	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)
G6N82_00610	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)
G6N82_00615	ENOG4105DF2	NADH dehydrogenase subunit j
G6N82_00620	ENOG4105M5H	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
G6N82_00625	ENOG4105D65	subunit l
G6N82_00630	ENOG4105C8S	subunit m
G6N82_00635	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)
G6N82_00640	ENOG4105HJX	Biotin- acetyl-CoA-carboxylase ligase
G6N82_00645	ENOG4107QNB	Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis (By similarity)
G6N82_00680	ENOG4105BZU	Histidine kinase
G6N82_00690	ENOG4105BZN	citrate synthase
G6N82_00695	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)
G6N82_00700	ENOG4108EQH	DNA internalization-related competence protein ComEC Rec2
G6N82_00710	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
G6N82_00715	ENOG4108YXW	Together with MoaA, is involved in the conversion of 5'- GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
G6N82_00720	ENOG4105DK0	Indole-3-glycerol phosphate synthase
G6N82_00725	ENOG4108I0Q	anthranilate phosphoribosyltransferase
G6N82_00730	ENOG4105DDQ	anthranilate synthase
G6N82_00735	ENOG4108T58	Mg2 transport protein CorA
G6N82_00740	ENOG4105CRQ	synthase (Component I)
G6N82_00755	ENOG4105CP7	Triose-phosphate isomerase
G6N82_00765	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
G6N82_00770	ENOG4108ZNX	Heat shock protein
G6N82_00775	ENOG4105VW4	glutaredoxin 3
G6N82_00795	ENOG4108J2P	Alpha beta hydrolase fold
G6N82_00800	ENOG4105EGS	Mechanosensitive ion channel
G6N82_00850	ENOG4107QXI	Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs (By similarity)
G6N82_00890	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)
G6N82_00895	ENOG4108Z1B	Cyclase dehydrase
G6N82_00900	ENOG4105CEV	competence damage-inducible protein
G6N82_00905	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)
G6N82_00910	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)
G6N82_00920	ENOG4105CUX	Signal transduction histidine kinase
G6N82_00935	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
G6N82_00940	ENOG4105KW8	RNA chaperone that binds small regulatory RNA (sRNAs) and mRNAs to facilitate mRNA translational regulation in response to envelope stress, environmental stress and changes in metabolite concentrations. Also binds with high specificity to tRNAs (By similarity)
G6N82_00945	ENOG4105C1N	GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis (By similarity)
G6N82_00950	ENOG4105DXN	mazG family
G6N82_00960	ENOG4108H5C	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)
G6N82_00965	ENOG4105F8V	Hydrolase, tatD family
G6N82_00975	ENOG4107QRG	dna polymerase iii
G6N82_00980	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
G6N82_00985	ENOG4105DZ1	carboxypeptidase
G6N82_00990	ENOG4105CVE	Lytic murein transglycosylase
G6N82_01000	ENOG4105RX7	peptidase S8 and S53, subtilisin, kexin, sedolisin
G6N82_01005	ENOG4105BZU	Histidine kinase
G6N82_01010	ENOG4105CKD	glutathione-regulated potassium-efflux system protein
G6N82_01030	ENOG4105C40	3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs (By similarity)
G6N82_01035	ENOG4107R1M	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) (By similarity)
G6N82_01045	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
G6N82_01050	ENOG4105CSH	Transporter
G6N82_01080	ENOG4105CFG	Acts as a chaperone (By similarity)
G6N82_01100	ENOG4105KEG	ribosomal-protein-alanine acetyltransferase
G6N82_01115	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
G6N82_01120	ENOG4105CI8	Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons (By similarity)
G6N82_01125	ENOG4105ED0	Phosphorolytic exoribonuclease that removes nucleotide residues following the -CCA terminus of tRNA and adds nucleotides to the ends of RNA molecules by using nucleoside diphosphates as substrates (By similarity)
G6N82_01130	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)
G6N82_01145	ENOG4105CSA	Coproporphyrinogen iii oxidase
G6N82_01150	ENOG4105C13	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
G6N82_01165	ENOG4108ZXC	Two component transcriptional regulator, luxr family
G6N82_01230	ENOG41080XQ	Signal transduction protein with cbs domains
G6N82_01240	ENOG4107RBR	Receptor
G6N82_01295	ENOG4105D6J	arsenicaL-resistance protein
G6N82_01305	ENOG4105CU0	Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA (By similarity)
G6N82_01310	ENOG4105E1C	Regulator of peptidoglycan synthesis that is essential for the function of penicillin-binding protein 1A (PBP1a) (By similarity)
G6N82_01315	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)
G6N82_01325	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)
G6N82_01340	ENOG4108W2P	Methyl-accepting chemotaxis
G6N82_01350	ENOG4105CD3	dihydroorotase
G6N82_01370	ENOG4105EHZ	conserved protein UCP016719
G6N82_01380	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)
G6N82_01415	ENOG4105CSU	acyl-Coa dehydrogenase
G6N82_01425	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
G6N82_01430	ENOG41081UC	Inherit from COG: Competence protein
G6N82_01440	ENOG4108HRN	Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate (By similarity)
G6N82_01450	ENOG4108HMW	glycyl-tRNA synthetase, alpha subunit
G6N82_01475	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)
G6N82_01480	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
G6N82_01495	ENOG4108W6C	Dehydrogenase
G6N82_01500	ENOG4105C3G	gtp-binding protein
G6N82_01510	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)
G6N82_01520	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)
G6N82_01530	ENOG4105N3I	Involved in formation and maintenance of cell shape (By similarity)
G6N82_01545	ENOG4105CNI	cell division protein FtsW
G6N82_01560	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)
G6N82_01565	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
G6N82_01595	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)
G6N82_01620	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)
G6N82_01625	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
G6N82_01635	ENOG4107SKI	cobyrinic Acid a,c-diamide synthase
G6N82_01640	ENOG4108YZG	isomerase
G6N82_01645	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)
G6N82_01655	ENOG4108Z11	Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes (By similarity)
G6N82_01670	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)
G6N82_01680	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)
G6N82_01690	ENOG4105E3A	(ABC) transporter
G6N82_01695	ENOG4105DA5	(ABC) transporter
G6N82_01700	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)
G6N82_01710	ENOG4108ZEF	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate (By similarity)
G6N82_01720	ENOG41083BM	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
G6N82_01735	ENOG4108JIU	phosphoribosylformylglycinamidine synthase ii
G6N82_01780	ENOG4105EAC	phosphoserine phosphatase
G6N82_01785	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)
G6N82_01790	ENOG4105C7K	acetolactate synthase
G6N82_01800	ENOG4105C6M	Alpha-keto-beta-hydroxylacyl reductoisomerase
G6N82_01805	ENOG4108YYC	ycei family
G6N82_01850	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
G6N82_01860	ENOG4105BZU	Histidine kinase
G6N82_01865	ENOG4105C8U	phosphate abc transporter
G6N82_01875	ENOG4105BZY	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
G6N82_01885	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
G6N82_01890	ENOG4105C0B	DNA polymerase III (alpha subunit)
G6N82_01910	ENOG4105CUB	amino acid
G6N82_01915	ENOG4105C8J	)-transporter
G6N82_01920	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
G6N82_01930	ENOG4105DHU	Bile acid
G6N82_01935	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
G6N82_01950	ENOG4107RET	Isocitrate lyase
G6N82_01970	ENOG4105ECY	inositol monophosphatase
G6N82_01975	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)
G6N82_01985	ENOG4106HMZ	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)
G6N82_02000	ENOG4105BZA	Phosphoglycerate kinase
G6N82_02010	ENOG4105CV1	Transketolase (EC 2.2.1.1)
G6N82_02030	ENOG4105MK2	5-formyltetrahydrofolate cyclo-ligase
G6N82_02040	ENOG4107XDQ	Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA (By similarity)
G6N82_02055	ENOG4107QSN	dihydrolipoamide acetyltransferase
G6N82_02060	ENOG4105CPP	Dehydrogenase, E1 component
G6N82_02070	ENOG4105C0V	Provides the sole de novo source of dTMP for DNA biosynthesis (By similarity)
G6N82_02085	ENOG4105CHR	reductase
G6N82_02095	ENOG4105KJF	protein tyrosine phosphatase
G6N82_02100	ENOG4105CB5	ATP-dependent DNA helicase recG
G6N82_02120	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)
G6N82_02135	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
G6N82_02150	ENOG4105ECY	inositol monophosphatase
G6N82_02160	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
G6N82_02170	ENOG4108S0S	Nucleotidyl transferase
G6N82_02175	ENOG4105EHM	Aminoglycoside phosphotransferase
G6N82_02180	ENOG4105K8N	protein family UPF0079, ATPase
G6N82_02185	ENOG4105I8F	Histidine kinase
G6N82_02190	ENOG4105C3E	May play a key role in the regulation of the intracellular concentration of adenosylhomocysteine (By similarity)
G6N82_02195	ENOG4105EHV	domain protein
G6N82_02225	ENOG4105EUJ	GTP cyclohydrolase i
G6N82_02260	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)
G6N82_02265	ENOG4105C13	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
G6N82_02280	ENOG4105KHV	Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate (By similarity)
G6N82_02285	ENOG4105D49	3-dehydroquinate synthase
G6N82_02290	ENOG4105DUX	Transporter
G6N82_02295	ENOG4107VWA	Catalyzes the hydrolysis of N-formyl-L-kynurenine to L- kynurenine, the second step in the kynurenine pathway of tryptophan degradation (By similarity)
G6N82_02315	ENOG4108UKI	Enoyl-CoA hydratase
G6N82_02325	ENOG4107QX3	carboxylase
G6N82_02330	ENOG4108VHC	Short-chain dehydrogenase reductase Sdr
G6N82_02340	ENOG4105FC8	fad dependent oxidoreductase
G6N82_02350	ENOG4105C1J	atp-dependent rna helicase
G6N82_02355	ENOG4105K3M	)-transporter
G6N82_02360	ENOG4105KAV	tspo and mbr like protein
G6N82_02370	ENOG4107QP8	phosphohexose isomerase
G6N82_02385	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)
G6N82_02390	ENOG4107PU6	Membrane
G6N82_02415	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)
G6N82_02425	ENOG4105F03	Provides the (R)-glutamate required for cell wall biosynthesis (By similarity)
G6N82_02430	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)
G6N82_02480	ENOG4105E3Q	saccharopine dehydrogenase
G6N82_02500	ENOG4105C3M	thioredoxin reductase
G6N82_02510	ENOG4108IUM	Glycogen debranching enzyme
G6N82_02515	ENOG4107QIX	Phosphoglucomutase (EC 5.4.2.2
G6N82_02520	ENOG4105CXW	Synthesizes alpha-1,4-glucan chains using ADP-glucose (By similarity)
G6N82_02525	ENOG4107QQ4	Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans (By similarity)
G6N82_02530	ENOG4105C9C	Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position (By similarity)
G6N82_02535	ENOG4107QQN	Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties (By similarity)
G6N82_02560	ENOG4105WH1	Two component transcriptional regulator luxr family
G6N82_02570	ENOG4105D3Q	Sugar transferase
G6N82_02585	ENOG4105CPK	Glycosyl transferase (Group 1
G6N82_02625	ENOG4105C1B	dTDP-glucose 4-6-dehydratase
G6N82_02630	ENOG4105EJZ	Glucose-1-phosphate cytidylyltransferase
G6N82_02665	ENOG4105C6V	Glycerol-3-phosphate dehydrogenase
G6N82_02695	ENOG4105CMR	udp-glucose 4-epimerase
G6N82_02700	ENOG4108RZ2	Glycoside hydrolase family 16
G6N82_02725	ENOG4105EUZ	Beta-lactamase domain protein
G6N82_02735	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
G6N82_02740	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
G6N82_02750	ENOG4105C9M	aspartyl-trna synthetase
G6N82_02755	ENOG4105ZIE	Exonuclease involved in the 3' processing of various precursor tRNAs. Initiates hydrolysis at the 3'-terminus of an RNA molecule and releases 5'-mononucleotides (By similarity)
G6N82_02760	ENOG4105C5Q	Transcriptional regulator
G6N82_02770	ENOG4105BZQ	cdp-diacylglycerol-glycerol-3-phosphate 3-phosphatidyltransferase
G6N82_02785	ENOG4105C7K	acetolactate synthase
G6N82_02795	ENOG4105BZU	Histidine kinase
G6N82_02800	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)
G6N82_02805	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)
G6N82_02810	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)
G6N82_02815	ENOG4107835	probably involved in intracellular septation (By similarity)
G6N82_02830	ENOG4105DFH	Transport of potassium into the cell (By similarity)
G6N82_02840	ENOG4105KWW	Biogenesis protein
G6N82_02850	ENOG4105DA4	cytochrome c-type biogenesis protein
G6N82_02855	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)
G6N82_02865	ENOG41060IM	Heme exporter protein
G6N82_02890	ENOG41082FS	50S ribosomal protein L31
G6N82_02900	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)
G6N82_02915	ENOG4105DZP	Membrane-associated zinc metalloprotease
G6N82_02925	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
G6N82_02930	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)
G6N82_02935	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
G6N82_02950	ENOG4105FS7	Transcriptional regulator
G6N82_02955	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)
G6N82_02960	ENOG4105CE9	30S ribosomal protein S2
G6N82_02975	ENOG41071I4	Phosphatidylserine decarboxylase proenzyme
G6N82_02990	ENOG4105C2N	RNA methyltransferase TrmH family group 3
G6N82_03000	ENOG4105K70	DNA-binding protein
G6N82_03015	ENOG4105MP9	class II Aldolase
G6N82_03020	ENOG4105KDX	Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection (By similarity)
G6N82_03025	ENOG4107QMP	dna polymerase iii subunits gamma and tau
G6N82_03055	ENOG4105CQ7	ATP-dependent helicase
G6N82_03065	ENOG4105EAH	synthase
G6N82_03070	ENOG4105EHE	chorismate mutase- prephenate dehydrogenase
G6N82_03080	ENOG4105IFJ	Histidine kinase
G6N82_03085	ENOG4105XJC	Two component transcriptional regulator (Winged helix family
G6N82_03100	ENOG4105C5H	ABC transporter
G6N82_03115	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)
G6N82_03120	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)
G6N82_03125	ENOG4105VIE	preprotein translocase, subunit YajC
G6N82_03135	ENOG4105CI0	Citrate lyase
G6N82_03150	ENOG4108Z38	Catalyzes a trans-dehydration via an enolate intermediate (By similarity)
G6N82_03155	ENOG4105KM4	Acetyl-CoA carboxylase, biotin carboxyl carrier protein
G6N82_03160	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
G6N82_03165	ENOG4105F7P	transcriptional regulator AsnC family
G6N82_03245	ENOG4105DK7	lysyl-tRNA synthetase
G6N82_03260	ENOG4108Z4X	TRANSCRIPTIONal
G6N82_03270	ENOG4105CI2	imidazolone-5-propionate hydrolase
G6N82_03295	ENOG4105CNE	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane (By similarity)
G6N82_03320	ENOG4105C26	Dehydrogenase
G6N82_03330	ENOG4105FR1	rard protein
G6N82_03345	ENOG4106XY2	Folate-binding protein involved in regulating the level of ATP-DnaA and in the modification of some tRNAs. It is probably a key factor in regulatory networks that act via tRNA modification, such as initiation of chromosomal replication (By similarity)
G6N82_03365	ENOG4105K46	50S ribosomal protein l27
G6N82_03370	ENOG4105KK9	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
G6N82_03385	ENOG4108ZAF	Molybdopterin
G6N82_03395	ENOG4105CM1	Catalyzes, together with MoaC, the conversion of 5'-GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
G6N82_03420	ENOG4105D98	threonine synthase
G6N82_03430	ENOG4107RFD	Non-specific O-methyltransferase that catalyzes the 2 O- methylation steps in the ubiquinone biosynthetic pathway (By similarity)
G6N82_03440	ENOG4107QS1	Cytochrome C Oxidase, Subunit III
G6N82_03445	ENOG4105FT1	Exerts its effect at some terminal stage of cytochrome c oxidase synthesis, probably by being involved in the insertion of the copper B into subunit I (By similarity)
G6N82_03455	ENOG4105BZ9	Cytochrome C oxidase, subunit I
G6N82_03465	ENOG4107VCP	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)
G6N82_03470	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)
G6N82_03480	ENOG4105KJV	Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein (By similarity)
G6N82_03485	ENOG4105C3F	Signal peptidase i
G6N82_03495	ENOG4107ZJC	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
G6N82_03555	ENOG4105EUB	pirin domain protein
G6N82_03565	ENOG4105D74	hydrolase
G6N82_03575	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)
G6N82_03595	ENOG4105CG2	Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 (By similarity)
G6N82_03600	ENOG4105EAY	pump that utilizes the energy of pyrophosphate hydrolysis as the driving force for
G6N82_03605	ENOG4105C29	acyl-CoA thioesterase
G6N82_03615	ENOG4107R7I	amino acid
G6N82_03630	ENOG4107ZSV	Receptor
G6N82_03670	ENOG4105CEU	Arginine dihydrolase
G6N82_03695	ENOG4105C1J	atp-dependent rna helicase
G6N82_03700	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)
G6N82_03710	ENOG4105CBX	hi0933 family
G6N82_03720	ENOG410626R	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)
G6N82_03725	ENOG4105CHI	Involved in the active translocation of vitamin B12 (cyanocobalamin) across the outer membrane to the periplasmic space. It derives its energy for transport by interacting with the trans-periplasmic membrane protein TonB (By similarity)
G6N82_03730	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)
G6N82_03735	ENOG4108Z03	MAF-like protein
G6N82_03765	ENOG4107RAN	Peptidase, M16
G6N82_03770	ENOG4105VR9	phosphoribosylformylglycinamidine synthase
G6N82_03775	ENOG4105D21	Phosphoribosylformylglycinamidine synthase I
G6N82_03815	ENOG4108EHX	EamA-like transporter family
G6N82_03830	ENOG4105C09	Bile acid
G6N82_03870	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)
G6N82_03875	ENOG4105W8H	transhydrogenase (subunit alpha
G6N82_03880	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)
G6N82_03900	ENOG4105EEI	dihydropteroate synthase
G6N82_03910	ENOG4105CEC	DNA methylase N-4 N-6
G6N82_03925	ENOG4105D8V	Glucose sorbosone dehydrogenase
G6N82_03945	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
G6N82_03955	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)
G6N82_03970	ENOG4105C3J	Cysteine desulfurase
G6N82_03980	ENOG4105DHZ	alpha beta
G6N82_04005	ENOG4105DJ1	Phosphoenolpyruvate Carboxylase
G6N82_04010	ENOG4105E3W	Two component transcriptional regulator (Winged helix family
G6N82_04015	ENOG4105EB3	Histidine kinase
G6N82_04020	ENOG4107UZ6	Catalyzes the ATP- as well as the pyrophosphate- dependent phosphorylation of a specific serine residue in HPr, a phosphocarrier protein of the phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS). HprK P also catalyzes the pyrophosphate-producing, inorganic phosphate-dependent dephosphorylation (phosphorolysis) of seryl-phosphorylated HPr (P- Ser-HPr)
G6N82_04025	ENOG4105C21	Displays ATPase and GTPase activities (By similarity)
G6N82_04030	ENOG4105DAS	pts system
G6N82_04040	ENOG4108RWN	rrna methyltransferase
G6N82_04060	ENOG4108Z02	Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions (By similarity)
G6N82_04065	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)
G6N82_04070	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)
G6N82_04075	ENOG4105DI7	Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs (By similarity)
G6N82_04085	ENOG4105HDK	L-asparaginase
G6N82_04110	ENOG4105CXG	d-lactate dehydrogenase
G6N82_04120	ENOG4105CNM	Receptor
G6N82_04145	ENOG4105E3A	(ABC) transporter
G6N82_04165	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
G6N82_04170	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
G6N82_04175	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
G6N82_04180	ENOG4107RUZ	Sss sodium solute transporter superfamily
G6N82_04190	ENOG4108Z4T	Peptidase M50
G6N82_04200	ENOG4107104	thymidine kinase
G6N82_04205	ENOG4105CFC	Transporter
G6N82_04215	ENOG4107ZGG	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)
G6N82_04240	ENOG4105K7D	Required for maturation of 30S ribosomal subunits (By similarity)
G6N82_04245	ENOG4105E51	psp operon transcriptional activator
G6N82_04255	ENOG41087YS	Phage shock protein A
G6N82_04295	ENOG4105P9C	Participates in cysteine desulfuration mediated by SufS. Cysteine desulfuration mobilizes sulfur from L-cysteine to yield L-alanine and constitutes an essential step in sulfur metabolism for biosynthesis of a variety of sulfur-containing biomolecules. Functions as a sulfur acceptor for SufS, by mediating the direct transfer of the sulfur atom from the S-sulfanylcysteine of SufS, an intermediate product of cysteine desulfuration process (By similarity)
G6N82_04315	ENOG4108TGP	Thioesterase superfamily protein
G6N82_04320	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
G6N82_04330	ENOG4105MQS	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
G6N82_04375	ENOG4105CUU	Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) (By similarity)
G6N82_04380	ENOG4108EHY	type IV secretion system
G6N82_04400	ENOG4105EJX	conjugal transfer ATPase
G6N82_04415	ENOG4105E4C	Lytic transglycosylase catalytic
G6N82_04450	ENOG4105CHR	reductase
G6N82_04460	ENOG4105C1G	acyl-Coa dehydrogenase
G6N82_04480	ENOG4105CG3	alpha amylase, catalytic region
G6N82_04490	ENOG4105QV4	Tryptophan halogenase
G6N82_04495	ENOG4107RNH	Outer membrane receptor FepA
G6N82_04505	ENOG4105QV4	Tryptophan halogenase
G6N82_04555	ENOG4105ETE	Transcriptional regulator (LacI family
G6N82_04560	ENOG4108FN7	Aldo keto reductase
G6N82_04565	ENOG4105D4R	Catalyzes the desulfonation of aliphatic sulfonates (By similarity)
G6N82_04570	ENOG4105C6V	Glycerol-3-phosphate dehydrogenase
G6N82_04575	ENOG4107YFT	Nadph-dependent fmn reductase
G6N82_04580	ENOG4105C66	Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate (By similarity)
G6N82_04590	ENOG4108XM1	transcriptional regulator AsnC family
G6N82_04595	ENOG4105E6M	Sulphatase-modifying factor protein
G6N82_04600	ENOG4107SS6	2-dehydro-3-deoxygluconokinase
G6N82_04620	ENOG4108RTU	Aldolase
G6N82_04630	ENOG4107EJG	GntR family transcriptional regulator
G6N82_04635	ENOG4105FGE	Short-chain dehydrogenase reductase Sdr
G6N82_04640	ENOG4105C01	Dihydroxy-acid dehydratase
G6N82_04645	ENOG4105ENH	Sulfatase
G6N82_04650	ENOG41061MV	Arylsulfatase
G6N82_04655	ENOG4105ENH	Sulfatase
G6N82_04660	ENOG4105CNT	hydrolase family 2
G6N82_04665	ENOG4105CNT	hydrolase family 2
G6N82_04705	ENOG4105E39	Enoyl-CoA hydratase
G6N82_04715	ENOG4105CHR	reductase
G6N82_04725	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)
G6N82_04755	ENOG4105C04	l-carnitine dehydratase bile acid-inducible protein F
G6N82_04760	ENOG4105C1G	acyl-Coa dehydrogenase
G6N82_04805	ENOG4105CQB	FAD linked oxidase domain protein
G6N82_04820	ENOG4105CB2	alcohol dehydrogenase
G6N82_04845	ENOG4105C26	Dehydrogenase
G6N82_04860	ENOG4108UAU	isochorismatase
G6N82_04870	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
G6N82_04875	ENOG4105MQS	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
G6N82_04880	ENOG4105CBH	Hydroxymethylglutaryl-CoA lyase
G6N82_04885	ENOG4105C04	l-carnitine dehydratase bile acid-inducible protein F
G6N82_04910	ENOG4107R6G	Catalyzes the S-adenosylmethionine monomethyl esterification of trans-aconitate (By similarity)
G6N82_04920	ENOG4105CJH	Alcohol dehydrogenase zinc-binding domain protein
G6N82_04925	ENOG4105JQN	Transcriptional regulator
G6N82_04945	ENOG4108EMS	branched-chain alpha-keto acid dehydrogenase subunit E2
G6N82_04955	ENOG4105CHI	Involved in the active translocation of vitamin B12 (cyanocobalamin) across the outer membrane to the periplasmic space. It derives its energy for transport by interacting with the trans-periplasmic membrane protein TonB (By similarity)
G6N82_04965	ENOG4105CQB	FAD linked oxidase domain protein
G6N82_04975	ENOG410626R	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)
G6N82_04995	ENOG4105C26	Dehydrogenase
G6N82_05010	ENOG4105QPS	Monooxygenase
G6N82_05015	ENOG4105CZ6	Can catalyze the oxidation of choline to betaine aldehyde and betaine aldehyde to glycine betaine (By similarity)
G6N82_05060	ENOG4107XKH	Specifically methylates the N7 position of a guanine in 16S rRNA (By similarity)
G6N82_05070	ENOG4108J2P	Alpha beta hydrolase fold
G6N82_05100	ENOG4107R6G	Catalyzes the S-adenosylmethionine monomethyl esterification of trans-aconitate (By similarity)
G6N82_05105	ENOG4105CT4	transporter
G6N82_05120	ENOG4105CIF	Ornithine Cyclodeaminase
G6N82_05130	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)
G6N82_05135	ENOG4105C26	Dehydrogenase
G6N82_05140	ENOG4107RGD	Major Facilitator superfamily
G6N82_05155	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)
G6N82_05170	ENOG4107QPD	alcohol dehydrogenase
G6N82_05185	ENOG4108K2P	TRANSCRIPTIONal
G6N82_05195	ENOG4105DV9	Methylaspartate ammonia-lyase
G6N82_05230	ENOG4107QRH	Arylsulfatase (Ec 3.1.6.1)
G6N82_05235	ENOG4105ETE	Transcriptional regulator (LacI family
G6N82_05250	ENOG4105EDQ	levansucrase EC 2.4.1.10
G6N82_05270	ENOG4105CSX	c4-dicarboxylate anaerobic carrier
G6N82_05280	ENOG4105D44	asparaginase
G6N82_05295	ENOG4105CFF	transcriptional regulator
G6N82_05300	ENOG4105VJY	transcriptional regulator
G6N82_05315	ENOG4105D05	Receptor
G6N82_05325	ENOG4105CEC	DNA methylase N-4 N-6
G6N82_05375	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)
G6N82_05390	ENOG4105C8P	)-transporter
G6N82_05395	ENOG4105C28	cystathionine
G6N82_05420	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)
G6N82_05430	ENOG4105KCK	Peptidoglycan-associated lipoprotein
G6N82_05435	ENOG4107R6Y	Involved in the TonB-independent uptake of proteins (By similarity)
G6N82_05445	ENOG4105M8F	Biopolymer transport protein exbD tolR
G6N82_05450	ENOG4105E02	MotA TolQ exbB proton channel
G6N82_05455	ENOG4107YD3	Thioesterase
G6N82_05460	ENOG4105K59	histidine triad (HIT) protein
G6N82_05465	ENOG4105KPZ	phosphoribosyl-atp pyrophosphatase
G6N82_05470	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)
G6N82_05475	ENOG4105CJV	Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase
G6N82_05485	ENOG4105ECC	imidazole-glycerol-phosphate dehydratase
G6N82_05495	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
G6N82_05500	ENOG4105UYK	outer membrane protein a
G6N82_05505	ENOG4105BZU	Histidine kinase
G6N82_05510	ENOG4105CHR	reductase
G6N82_05515	ENOG4105C1G	acyl-Coa dehydrogenase
G6N82_05520	ENOG4105X7H	acyl-CoA dehydrogenase
G6N82_05530	ENOG4105CC9	acyl-Coa dehydrogenase
G6N82_05535	ENOG4107QPD	alcohol dehydrogenase
G6N82_05550	ENOG4105DMJ	Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate (By similarity)
G6N82_05560	ENOG4108IGT	Dipeptidase
G6N82_05640	ENOG4105KME	endoribonuclease L-psp
G6N82_05645	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)
G6N82_05660	ENOG4105CPQ	Dehydrogenase
G6N82_05680	ENOG4105CD3	dihydroorotase
G6N82_05685	ENOG4105DRY	peptidase s9 prolyl oligopeptidase active site domain protein
G6N82_05695	ENOG4108VRQ	UPF0314 protein
G6N82_05715	ENOG4108URH	decarboxylase
G6N82_05735	ENOG4105CZQ	inner membrane transport protein YdhC
G6N82_05745	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)
G6N82_05750	ENOG4108Q79	6-phosphogluconolactonase (EC 3.1.1.31)
G6N82_05755	ENOG4108RMU	ferritin dps family protein
G6N82_05770	ENOG4105DQ4	alcohol dehydrogenase
G6N82_05800	ENOG4105C26	Dehydrogenase
G6N82_05825	ENOG4105CGU	Enoyl-CoA hydratase
G6N82_05855	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
G6N82_05860	ENOG4107QK8	The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor
G6N82_05865	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)
G6N82_05870	ENOG4105D43	The glycine cleavage system catalyzes the degradation of glycine (By similarity)
G6N82_05890	ENOG4105SYT	Methylenetetrahydrofolate reductase
G6N82_05895	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)
G6N82_06000	ENOG4105BZU	Histidine kinase
G6N82_06010	ENOG4105BZU	Histidine kinase
G6N82_06015	ENOG4105BZU	Histidine kinase
G6N82_06020	ENOG4107QNJ	CoA-transferase subunit B
G6N82_06060	ENOG4105CHR	reductase
G6N82_06065	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
G6N82_06075	ENOG4105CHR	reductase
G6N82_06130	ENOG4107QUT	magnesium and cobalt transport protein CorA
G6N82_06150	ENOG4105CHI	Involved in the active translocation of vitamin B12 (cyanocobalamin) across the outer membrane to the periplasmic space. It derives its energy for transport by interacting with the trans-periplasmic membrane protein TonB (By similarity)
G6N82_06180	ENOG41067CV	Integrase
G6N82_06255	ENOG4105W5Q	DNA repair protein (RadC
G6N82_06275	ENOG4105CHM	Aminotransferase
G6N82_06280	ENOG4105D1N	poly(r)-hydroxyalkanoic acid synthase, class
G6N82_06290	ENOG4105KAE	Involved in the modulation of the specificity of the ClpAP-mediated ATP-dependent protein degradation (By similarity)
G6N82_06335	ENOG4105CK4	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
G6N82_06345	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
G6N82_06350	ENOG4105XDF	Protein of unknown function (DUF1272)
G6N82_06355	ENOG4105DWF	phosphomethylpyrimidine kinase
G6N82_06370	ENOG4105C9X	ppx gppa phosphatase
G6N82_06375	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)
G6N82_06380	ENOG4105G9V	cytochrome C
G6N82_06400	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
G6N82_06425	ENOG4105D44	asparaginase
G6N82_06435	ENOG4105E18	UPF0276 protein
G6N82_06455	ENOG4105NCT	RNA Polymerase
G6N82_06470	ENOG4108UI1	Probably functions as a manganese efflux pump (By similarity)
G6N82_06475	ENOG4105DGU	Histone deacetylase
G6N82_06495	ENOG4105DIT	ErfK YbiS YcfS YnhG family protein
G6N82_06505	ENOG4108I0Z	Aconitate hydratase
G6N82_06510	ENOG41085GJ	domain protein
G6N82_06515	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)
G6N82_06530	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)
G6N82_06535	ENOG4105D10	5-enolpyruvylshikimate-3-phosphate phospholyase
G6N82_06545	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)
G6N82_06555	ENOG4108JU3	Alkyl hydroperoxide reductase
G6N82_06595	ENOG4105IX2	One of the proteins required for the normal export of preproteins out of the cell cytoplasm. It is a molecular chaperone that binds to a subset of precursor proteins, maintaining them in a translocation-competent state. It also specifically binds to its receptor SecA (By similarity)
G6N82_06600	ENOG4105CJR	Integral membrane protein (MviN
G6N82_06605	ENOG4105C31	Tryptophanyl-tRNA synthetase
G6N82_06615	ENOG4108Z1K	This enzyme is involved in nucleotide metabolism it produces dUMP, the immediate precursor of thymidine nucleotides and it decreases the intracellular concentration of dUTP so that uracil cannot be incorporated into DNA (By similarity)
G6N82_06620	ENOG4105CJS	Phosphopantothenoylcysteine decarboxylase
G6N82_06645	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)
G6N82_06655	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)
G6N82_06660	ENOG4105D06	uba thif-type nad fad binding protein
G6N82_06665	ENOG4105NDF	NAD-dependent protein deacetylase which modulates the activities of several enzymes which are inactive in their acetylated form. May also have NAD-dependent lysine demalonylase and desuccinylase activity (By similarity)
G6N82_06685	ENOG4107QJT	sodium dicarboxylate symporter
G6N82_06690	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)
G6N82_06705	ENOG4108TGY	Glutathione S-transferase
G6N82_06730	ENOG4107HP6	Transcriptional regulator
G6N82_06740	ENOG4105CS1	NAD(P)H quinone oxidoreductase
G6N82_06750	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)
G6N82_06855	ENOG4105VG0	50S ribosomal protein l34
G6N82_06860	ENOG41067YR	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)
G6N82_06865	ENOG4105VAS	Could be involved in insertion of integral membrane proteins into the membrane (By similarity)
G6N82_06875	ENOG4105WHM	Necessary for normal cell division and for the maintenance of normal septation (By similarity)
G6N82_06895	ENOG4105YK5	50S ribosomal protein L36
G6N82_06910	ENOG4107T42	This enzyme scavenge exogenous and endogenous cytidine and 2'-deoxycytidine for UMP synthesis (By similarity)
G6N82_06920	ENOG4108ZTZ	UPF0262 protein
G6N82_06930	ENOG4105CQX	Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol (By similarity)
G6N82_06935	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)
G6N82_06955	ENOG4108IG5	Transcriptional regulator
G6N82_06965	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)
G6N82_06975	ENOG4105ENJ	RND efflux system, outer membrane lipoprotein
G6N82_07000	ENOG410846T	CoA-transferase family III
G6N82_07010	ENOG4105E5V	Participates in transcription elongation, termination and antitermination (By similarity)
G6N82_07020	ENOG4105BZG	amino acid carrier protein
G6N82_07030	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)
G6N82_07035	ENOG4106ECF	Uncharacterized protein conserved in bacteria (DUF2155)
G6N82_07065	ENOG4107RCI	amp-dependent synthetase and ligase
G6N82_07095	ENOG4108KPZ	tonB-dependent Receptor
G6N82_07135	ENOG4105K8U	2-Amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase
G6N82_07140	ENOG4105C4K	Nad synthetase
G6N82_07150	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)
G6N82_07160	ENOG4105CYJ	ribosomal RNA small subunit methyltransferase B
G6N82_07180	ENOG4105CE2	Aldehyde oxidase and xanthine dehydrogenase, molybdopterin binding
G6N82_07190	ENOG4107QJR	hflk protein
G6N82_07195	ENOG4105EPW	hflc protein
G6N82_07205	ENOG4105BZ4	penicillin-binding protein
G6N82_07210	ENOG4105E0X	reductase
G6N82_07235	ENOG4105DWV	Homoserine O-trans-acetylase
G6N82_07245	ENOG4105CIH	Imidazole acetol-phosphate transaminase
G6N82_07270	ENOG4105CAK	Cell division ATP-binding protein ftsE
G6N82_07275	ENOG4106D71	domain protein
G6N82_07285	ENOG4105DCF	alanine dehydrogenase
G6N82_07290	ENOG4105C1G	acyl-Coa dehydrogenase
G6N82_07310	ENOG4107RHB	Catalyzes the reversible phosphorylation of S-methyl-5'- thioadenosine (MTA) to adenine and 5-methylthioribose-1-phosphate. Involved in the breakdown of MTA, a major by-product of polyamine biosynthesis. Responsible for the first step in the methionine salvage pathway after MTA has been generated from S- adenosylmethionine. Has broad substrate specificity with 6- aminopurine nucleosides as preferred substrates (By similarity)
G6N82_07315	ENOG4108UAU	isochorismatase
G6N82_07340	ENOG4105DRR	Transcriptional regulator, GntR family
G6N82_07345	ENOG4105C04	l-carnitine dehydratase bile acid-inducible protein F
G6N82_07350	ENOG4105CBH	Hydroxymethylglutaryl-CoA lyase
G6N82_07360	ENOG4107U7N	hydantoinase B oxoprolinase
G6N82_07365	ENOG4105S64	Formate nitrite transporter
G6N82_07370	ENOG4105EE6	Alcohol dehydrogenase zinc-binding domain protein
G6N82_07380	ENOG4105DHP	deoxycytidine triphosphate deaminase
G6N82_07390	ENOG4105EG6	Saccharopine dehydrogenase
G6N82_07445	ENOG4105CAS	nag kinase
G6N82_07470	ENOG4105E05	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
G6N82_07480	ENOG4108HWB	Non-specific O-methyltransferase that catalyzes the 2 O- methylation steps in the ubiquinone biosynthetic pathway (By similarity)
G6N82_07495	ENOG4105BZU	Histidine kinase
G6N82_07515	ENOG4105BZH	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
G6N82_07525	ENOG4108A04	Beta-lactamase
G6N82_07550	ENOG4108IYU	L-aspartate oxidase
G6N82_07560	ENOG4105DA5	(ABC) transporter
G6N82_07585	ENOG4105EA8	2-Nitropropane dioxygenase
G6N82_07610	ENOG4105CEY	Amp-dependent synthetase and ligase
G6N82_07635	ENOG4107T31	5'-nucleotidase
G6N82_07670	ENOG4107QX3	carboxylase
G6N82_07680	ENOG4105C1G	acyl-Coa dehydrogenase
G6N82_07690	ENOG4108IJ8	ABC transporter
G6N82_07705	ENOG4105C3B	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
G6N82_07710	ENOG4105CEY	Amp-dependent synthetase and ligase
G6N82_07715	ENOG4105E1P	Modifies, by uridylylation or deuridylylation the PII (GlnB) regulatory protein (By similarity)
G6N82_07720	ENOG4107ZSV	Receptor
G6N82_07725	ENOG4105DFA	alanine racemase domain protein
G6N82_07735	ENOG4105CNU	cell division protein FtsK
G6N82_07750	ENOG4106MAR	Phosphate-selective porin O and P
G6N82_07755	ENOG4105BZU	Histidine kinase
G6N82_07790	ENOG4105JJR	Histidine kinase
G6N82_07795	ENOG4105D7A	ATP-binding protein
G6N82_07810	ENOG4108YZN	class I peptide chain release factor
G6N82_07815	ENOG4105W0E	50S ribosomal protein L33
G6N82_07835	ENOG4107QJN	gtp cyclohydrolase ii
G6N82_07865	ENOG4105IYB	L-carnitine dehydratase bile acid-inducible protein F
G6N82_07870	ENOG4105CHU	acetyl-coa acetyltransferase
G6N82_07875	ENOG4108M9J	MaoC like domain protein
G6N82_07880	ENOG4105CSR	polyphosphate kinase 2
G6N82_07885	ENOG4105MIR	Phenylalanine 4-monooxygenase
G6N82_07890	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
G6N82_07900	ENOG4105BZ1	(ABC) transporter
G6N82_07915	ENOG4105CHU	acetyl-coa acetyltransferase
G6N82_07940	ENOG4105E39	Enoyl-CoA hydratase
G6N82_07945	ENOG4105D5S	Excises uracil residues from the DNA which can arise as a result of misincorporation of dUMP residues by DNA polymerase or due to deamination of cytosine (By similarity)
G6N82_07990	ENOG4105CHR	reductase
G6N82_08015	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
G6N82_08035	ENOG4105DR5	peptidase
G6N82_08045	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
G6N82_08050	ENOG4105CE6	Adenylation and deadenylation of glutamate--ammonia ligase (By similarity)
G6N82_08060	ENOG4105DWY	Agmatine deiminase
G6N82_08065	ENOG4105C22	threonyL-tRNA synthetase
G6N82_08095	ENOG4105DEN	Luciferase family
G6N82_08100	ENOG4105C7I	Dehydrogenase
G6N82_08110	ENOG4105EH2	Catalyzes the conversion of epoxyqueuosine (oQ) to queuosine (Q), which is a hypermodified base found in the wobble positions of tRNA(Asp), tRNA(Asn), tRNA(His) and tRNA(Tyr) (By similarity)
G6N82_08115	ENOG4108IUX	(ABC) transporter
G6N82_08130	ENOG4105E0X	reductase
G6N82_08145	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)
G6N82_08150	ENOG4105FDP	GntR family transcriptional regulator
G6N82_08155	ENOG4105DUX	Transporter
G6N82_08160	ENOG4105CI2	imidazolone-5-propionate hydrolase
G6N82_08175	ENOG410903C	(LipO)protein
G6N82_08180	ENOG4108UKI	Enoyl-CoA hydratase
G6N82_08190	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)
G6N82_08200	ENOG4107U7B	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)
G6N82_08210	ENOG4105EWK	phytoene
G6N82_08215	ENOG4105DC1	bifunctional purine biosynthesis protein purh
G6N82_08225	ENOG4105DJV	ribulose-phosphate 3-epimerase
G6N82_08245	ENOG4105CH2	amidohydrolase
G6N82_08265	ENOG4105ETE	Transcriptional regulator (LacI family
G6N82_08275	ENOG4105QV4	Tryptophan halogenase
G6N82_08315	ENOG4105D0M	Protease HtpX homolog
G6N82_08320	ENOG4105DRC	Na( ) H( ) antiporter that extrudes sodium in exchange for external protons (By similarity)
G6N82_08335	ENOG4108HRK	Histidine kinase
G6N82_08345	ENOG4105D18	nicotinate-nucleotide pyrophosphorylase
G6N82_08360	ENOG4108Z6B	deaminase
G6N82_08365	ENOG4105KDC	50s ribosomal protein l28
G6N82_08370	ENOG4108K5P	(LipO)protein
G6N82_08380	ENOG4105DVS	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
G6N82_08385	ENOG4105C12	Phosphoribosylglycinamide synthetase
G6N82_08420	ENOG4108Z4V	iron-sulfur cluster assembly
G6N82_08425	ENOG4105VG1	fes assembly suf system protein
G6N82_08435	ENOG4105JRK	feS assembly protein SufD
G6N82_08460	ENOG4108ZF1	Transcriptional regulator, BadM Rrf2 family
G6N82_08475	ENOG4107QYT	Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor (By similarity)
G6N82_08480	ENOG4105CFB	Gamma-glutamyltranspeptidase (EC 2.3.2.2)
G6N82_08485	ENOG4108IQE	Amp-dependent synthetase and ligase
G6N82_08500	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)
G6N82_08510	ENOG4107TQK	Catalyzes the oxidation of the C8 methyl side group on heme O porphyrin ring into a formyl group (By similarity)
G6N82_08525	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)
G6N82_08530	ENOG4108UJD	30S ribosomal protein S9
G6N82_08550	ENOG4108NEV	two component transcriptional regulator, LytTR family
G6N82_08605	ENOG4105F0V	Cell wall hydrolase
G6N82_08620	ENOG4107RM2	PTS IIA-like nitrogen-regulatory protein PtsN
G6N82_08625	ENOG4107TNS	sigma 54 modulation protein ribosomal protein S30ea
G6N82_08635	ENOG4108ZQD	Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A (By similarity)
G6N82_08640	ENOG4105E2X	shikimate dehydrogenase
G6N82_08645	ENOG4108UHJ	MAF-like protein
G6N82_08650	ENOG4105CF9	Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation dephosphorylation (By similarity)
G6N82_08655	ENOG4105CFZ	Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III (By similarity)
G6N82_08670	ENOG4105BZU	Histidine kinase
G6N82_08690	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)
G6N82_08695	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)
G6N82_08700	ENOG4107YTN	Specifically methylates the N7 position of guanine in position 527 of 16S rRNA (By similarity)
G6N82_08730	ENOG4105CSU	acyl-Coa dehydrogenase
G6N82_08750	ENOG4108VJ1	Transcriptional regulator (CarD family
G6N82_08755	ENOG4108Z4U	Ferredoxin
G6N82_08770	ENOG4105E4C	Lytic transglycosylase catalytic
G6N82_08775	ENOG4105D52	delta-aminolevulinic acid dehydratase
G6N82_08780	ENOG4108YYQ	gCN5-related N-acetyltransferase
G6N82_08795	ENOG41084XA	UPF0235 protein
G6N82_08820	ENOG4105DRY	peptidase s9 prolyl oligopeptidase active site domain protein
G6N82_08860	ENOG4105CEY	Amp-dependent synthetase and ligase
G6N82_08870	ENOG4105DR5	peptidase
G6N82_08875	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)
G6N82_08880	ENOG4107WK2	Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) (By similarity)
G6N82_08890	ENOG4108UXA	Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA (By similarity)
G6N82_08900	ENOG4105CN1	protease
G6N82_08950	ENOG4105C1B	dTDP-glucose 4-6-dehydratase
G6N82_08965	ENOG4105E5V	Participates in transcription elongation, termination and antitermination (By similarity)
G6N82_08975	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
G6N82_08985	ENOG4105C1B	dTDP-glucose 4-6-dehydratase
G6N82_08990	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
G6N82_09005	ENOG4105CAQ	asparagine synthetase
G6N82_09020	ENOG4105D7W	serine acetyltransferase
G6N82_09040	ENOG4107QVI	Methyltransferase, type 11
G6N82_09070	ENOG4105CJT	Mannose-1-phosphate guanylyltransferase
G6N82_09085	ENOG4105D75	Capsular exopolysaccharide family
G6N82_09105	ENOG4105CSJ	Enoyl- acyl-carrier-protein reductase NADH
G6N82_09110	ENOG4107U9T	Pfam:Ribonuclease_BN
G6N82_09115	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)
G6N82_09120	ENOG4108S7T	Catalyzes the oxidation of either pyridoxine 5'- phosphate (PNP) or pyridoxamine 5'-phosphate (PMP) into pyridoxal 5'-phosphate (PLP) (By similarity)
G6N82_09125	ENOG41076HS	cation diffusion facilitator family transporter
G6N82_09145	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
G6N82_09165	ENOG4105ENT	Efflux transporter rnd family, mfp subunit
G6N82_09175	ENOG4106BRA	Membrane
G6N82_09190	ENOG4105BZJ	Electron transfer flavoprotein
G6N82_09195	ENOG4105CMV	Succinyl-CoA synthetase subunit beta
G6N82_09200	ENOG4108RNI	3'(2')5'-bisphosphate nucleotidase
G6N82_09205	ENOG4108ZG0	Ompa motb domain protein
G6N82_09220	ENOG4105M02	This protein specifically catalyzes the removal of signal peptides from prolipoproteins (By similarity)
G6N82_09230	ENOG4105DTN	riboflavin biosynthesis protein ribF
G6N82_09240	ENOG4105CY8	phosphoribosylaminoimidazole carboxylase atpase subunit
G6N82_09245	ENOG4108UM6	Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) (By similarity)
G6N82_09250	ENOG4105DKJ	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
G6N82_09270	ENOG4107RUY	(E1 component), alpha subunit
G6N82_09275	ENOG4105CPP	Dehydrogenase, E1 component
G6N82_09310	ENOG4105VJY	transcriptional regulator
G6N82_09320	ENOG41061TZ	Short-chain dehydrogenase reductase Sdr
G6N82_09350	ENOG4105C1G	acyl-Coa dehydrogenase
G6N82_09370	ENOG4105CJH	Alcohol dehydrogenase zinc-binding domain protein
G6N82_09380	ENOG4105CJH	Alcohol dehydrogenase zinc-binding domain protein
G6N82_09400	ENOG4105CHR	reductase
G6N82_09410	ENOG4105DAB	fumarate reductase succinate dehydrogenase flavoprotein domain protein
G6N82_09450	ENOG4105CJH	Alcohol dehydrogenase zinc-binding domain protein
G6N82_09485	ENOG4107RGD	Major Facilitator superfamily
G6N82_09540	ENOG4105CD8	aminopeptidase N
G6N82_09545	ENOG4105DBW	Multi-copper polyphenol oxidoreductase laccase
G6N82_09550	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)
G6N82_09555	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)
G6N82_09560	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)
G6N82_09565	ENOG4109003	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis (By similarity)
G6N82_09570	ENOG4108RM3	Phosphatase with a broad specificity. Its primary physiological function is to dephosphorylate 3'-phosphoadenosine 5'-phosphate (PAP) and 3'-phosphoadenosine 5'-phosphosulfate (PAPS). Thus, plays a role in mycobacterial sulfur metabolism, since it can serve as a key regulator of the sulfate assimilation pathway by controlling the pools of PAP and PAPS in the cell. To a lesser extent, is also able to hydrolyze inositol 1-phosphate (I- 1-P), fructose 1,6-bisphosphate (FBP) (to fructose 6-phosphate (F- 6-P)) and AMP in vitro, but this might has no significance in vivo
G6N82_09580	ENOG4105C11	sulfate adenylyltransferase), subunit 2
G6N82_09590	ENOG4105WH1	Two component transcriptional regulator luxr family
G6N82_09595	ENOG4108IAA	Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate (By similarity)
G6N82_09620	ENOG4107QRT	dEAD DEAH box helicase
G6N82_09630	ENOG4105M8F	Biopolymer transport protein exbD tolR
G6N82_09655	ENOG4105D6E	homoserine dehydrogenase
G6N82_09665	ENOG4105CBT	Fructose-1,6-bisphosphatase
G6N82_09670	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
G6N82_09695	ENOG41082BR	50S ribosomal protein L35
G6N82_09700	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)
G6N82_09710	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
G6N82_09715	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
G6N82_09720	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)
G6N82_09740	ENOG4108YZA	Nitrogen regulatory protein pii
G6N82_09745	ENOG4105BZU	Histidine kinase
G6N82_09770	ENOG4107RT5	aminobenzoyl-glutamate utilization protein B
G6N82_09785	ENOG4105C8Y	Acetylornithine aminotransferase
G6N82_09790	ENOG4105DBV	ornithine carbamoyltransferase
G6N82_09795	ENOG4105F4C	Redox regulated molecular chaperone. Protects both thermally unfolding and oxidatively damaged proteins from irreversible aggregation. Plays an important role in the bacterial defense system toward oxidative stress (By similarity)
G6N82_09805	ENOG4105FD2	Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) (By similarity)
G6N82_09815	ENOG4108Z7T	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
G6N82_09830	ENOG4105IJJ	transcriptional regulator, crp fnr family
G6N82_09840	ENOG4105P0T	Usg family
G6N82_09845	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)
G6N82_09850	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
G6N82_09900	ENOG4105DEF	Extracellular solute-binding protein, family 5
G6N82_09910	ENOG4105HJ8	Catalyzes the oxidative cleavage of the L-tryptophan (L- Trp) pyrrole ring (By similarity)
G6N82_09915	ENOG4107VWA	Catalyzes the hydrolysis of N-formyl-L-kynurenine to L- kynurenine, the second step in the kynurenine pathway of tryptophan degradation (By similarity)
G6N82_09930	ENOG4106F3G	Catalyzes the tRNA-independent activation of glutamate in presence of ATP and the subsequent transfer of glutamate onto a tRNA(Asp). Glutamate is transferred on the 2-amino-5-(4,5- dihydroxy-2-cyclopenten-1-yl) moiety of the queuosine in the wobble position of the QUC anticodon (By similarity)
G6N82_09940	ENOG4108WBT	adenosyltransferase
G6N82_09945	ENOG4105DYT	3-hydroxyacyl-CoA dehydrogenase
G6N82_09960	ENOG4105D86	that it carries out the mismatch recognition step. This protein has a weak ATPase activity (By similarity)
G6N82_09965	ENOG4105C6K	Malic enzyme
G6N82_09970	ENOG4105EAC	phosphoserine phosphatase
G6N82_09975	ENOG4105CZ1	Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA (By similarity)
G6N82_09985	ENOG4105DTW	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
G6N82_09990	ENOG4108IUZ	ABC transporter
G6N82_10000	ENOG4105F0N	pyrophosphate phospho-hydrolase
G6N82_10005	ENOG4105CUT	histidyl-tRNA synthetase
G6N82_10010	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
G6N82_10015	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)
G6N82_10025	ENOG4105CE8	Transfers the fatty acyl group on membrane lipoproteins (By similarity)
G6N82_10030	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
G6N82_10070	ENOG4105C2M	dna polymerase I
G6N82_10095	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
G6N82_10100	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
G6N82_10110	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)
G6N82_10115	ENOG4108VZM	50s ribosomal protein L10
G6N82_10125	ENOG4105VMP	Transcriptional regulator
G6N82_10135	ENOG4108IIJ	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
G6N82_10140	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
G6N82_10160	ENOG4105CA9	Pyruvate kinase
G6N82_10170	ENOG4105Y2X	UPF0335 protein
G6N82_10175	ENOG4105K8R	UPF0145 protein
G6N82_10195	ENOG4105CDY	transcriptional regulatory protein
G6N82_10200	ENOG4105NHU	Nuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves the cruciform structure in supercoiled DNA by nicking to strands with the same polarity at sites symmetrically opposed at the junction in the homologous arms and leaves a 5'-terminal phosphate and a 3'-terminal hydroxyl group (By similarity)
G6N82_10205	ENOG4105KUZ	arsenate reductase
G6N82_10215	ENOG4106MZZ	glycerophosphoryl diester phosphodiesterase
G6N82_10220	ENOG4107RFD	Non-specific O-methyltransferase that catalyzes the 2 O- methylation steps in the ubiquinone biosynthetic pathway (By similarity)
G6N82_10225	ENOG4105CFH	Aspartokinase
G6N82_10240	ENOG4105BZU	Histidine kinase
G6N82_10245	ENOG4108HH9	Catalyzes two reactions the first one is the production of beta-formyl glycinamide ribonucleotide (GAR) from formate, ATP and beta GAR
G6N82_10250	ENOG4105EA8	2-Nitropropane dioxygenase
G6N82_10285	ENOG4107QX8	SPFH domain, Band 7 family protein
G6N82_10355	ENOG4108HFV	
G6N82_10360	ENOG4105C0D	helicase
G6N82_10370	ENOG4107QMH	DNA methylase
G6N82_10425	ENOG4105C26	Dehydrogenase
G6N82_10430	ENOG4105EVH	UPF0753 protein
G6N82_10440	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
G6N82_10460	ENOG4105E3B	Multicopper oxidase
G6N82_10465	ENOG4105VPX	protein, conserved in bacteria
G6N82_10475	ENOG4105CEV	competence damage-inducible protein
G6N82_10480	ENOG4105CT3	Monooxygenase
G6N82_10495	ENOG4105C1G	acyl-Coa dehydrogenase
G6N82_10505	ENOG4105CHU	acetyl-coa acetyltransferase
G6N82_10530	ENOG4105D4P	Coproporphyrinogen iii oxidase
G6N82_10560	ENOG4105D6P	C-type cytochrome. Part of the cbb3-type cytochrome c oxidase complex (By similarity)
G6N82_10580	ENOG4105DS0	Transcriptional regulator, Crp Fnr family
G6N82_10590	ENOG4105DS0	Transcriptional regulator, Crp Fnr family
G6N82_10625	ENOG4105BZU	Histidine kinase
G6N82_10635	ENOG4105BZU	Histidine kinase
G6N82_10690	ENOG4105D3R	alkyl hydroperoxide reductase
G6N82_10715	ENOG4105CF3	3-Hydroxyisobutyrate dehydrogenase
G6N82_10730	ENOG4105JHE	Major Facilitator Superfamily
G6N82_10740	ENOG4105CEY	Amp-dependent synthetase and ligase
G6N82_10785	ENOG4107SCK	Monooxygenase
G6N82_10810	ENOG4105VCQ	rubredoxin
G6N82_10815	ENOG4108IPT	Naphthoate synthase
G6N82_10820	ENOG4105D2B	acyl-CoA dehydrogenase
G6N82_10825	ENOG4105D2B	acyl-CoA dehydrogenase
G6N82_10830	ENOG4105CHR	reductase
G6N82_10835	ENOG4105CEY	Amp-dependent synthetase and ligase
G6N82_10845	ENOG4105CEY	Amp-dependent synthetase and ligase
G6N82_10850	ENOG4105CEY	Amp-dependent synthetase and ligase
G6N82_10860	ENOG4108UKI	Enoyl-CoA hydratase
G6N82_10865	ENOG4105C04	l-carnitine dehydratase bile acid-inducible protein F
G6N82_10870	ENOG4107Z7P	Ferredoxin
G6N82_10880	ENOG4105KME	endoribonuclease L-psp
G6N82_10890	ENOG4105CHU	acetyl-coa acetyltransferase
G6N82_10895	ENOG4105EA8	2-Nitropropane dioxygenase
G6N82_10910	ENOG4105EMU	Dehydrogenase
G6N82_10915	ENOG4108JGH	Tetr family transcriptional regulator
G6N82_10945	ENOG4107QRH	Arylsulfatase (Ec 3.1.6.1)
G6N82_10980	ENOG4105DFP	Integrase
G6N82_11020	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)
G6N82_11035	ENOG4108ZZ3	UPF0260 protein
G6N82_11060	ENOG4105CE1	Ferrous iron transport protein b
G6N82_11065	ENOG4108UUM	single-stranded DNA-binding protein
G6N82_11100	ENOG4105C4N	this subunit has chaperone activity. The binding of ATP and its subsequent hydrolysis by HslU are essential for unfolding of protein substrates subsequently hydrolyzed by HslV. HslU recognizes the N-terminal part of its protein substrates and unfolds these before they are guided to HslV for hydrolysis (By similarity)
G6N82_11115	ENOG4108JJ7	ABC transporter
G6N82_11175	ENOG4105BZU	Histidine kinase
G6N82_11180	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
G6N82_11185	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
G6N82_11195	ENOG4105CBS	Chea signal transduction histidine kinase
G6N82_11205	ENOG4108XHQ	(2Fe-2S)-binding domain protein
G6N82_11210	ENOG4108ESX	Receptor
G6N82_11235	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)
G6N82_11245	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
G6N82_11255	ENOG4105D0I	Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate (By similarity)
G6N82_11300	ENOG4105BZ3	General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) (By similarity)
G6N82_11315	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)
G6N82_11345	ENOG4105ETE	Transcriptional regulator (LacI family
G6N82_11350	ENOG4105CBM	Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 (By similarity)
G6N82_11360	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
G6N82_11365	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)
G6N82_11375	ENOG4108ESX	Receptor
G6N82_11380	ENOG4105PF9	Transcriptional regulator
G6N82_11395	ENOG4107SV1	subunit D
G6N82_11400	ENOG41082A2	Alpha beta hydrolase
G6N82_11420	ENOG4107EPK	O-methyltransferase, family 2
G6N82_11425	ENOG4107XHQ	chlorophyll synthesis pathway, bchC
G6N82_11430	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)
G6N82_11435	ENOG41060GA	Chlorophyllide reductase subunit Y
G6N82_11465	ENOG4105J6N	PhotosynthetiC reaction center cytochrome c subunit
G6N82_11480	ENOG4107QZT	geranylgeranyl reductase
G6N82_11485	ENOG4105SS7	PucC protein
G6N82_11490	ENOG4105DB3	bacteriochlorophyll chlorophyll a synthase
G6N82_11495	ENOG4105D4D	transcriptional regulator
G6N82_11510	ENOG4108VJI	2-vinyl bacteriochlorophyllide hydratase
G6N82_11515	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)
G6N82_11520	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)
G6N82_11525	ENOG4105CTK	cobaltochelatase, cobn subunit
G6N82_11530	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)
G6N82_11535	ENOG4108MIC	Mg-protoporphyrin IX methyl transferase
G6N82_11540	ENOG4105XCI	PucC protein
G6N82_11545	ENOG4108S36	Photosynthetic reaction center
G6N82_11565	ENOG4105FBB	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)
G6N82_11570	ENOG4108TF2	Photosynthetic complex assembly protein 2
G6N82_11575	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)
G6N82_11585	ENOG4108PZW	LysR family Transcriptional regulator
G6N82_11590	ENOG4105C26	Dehydrogenase
G6N82_11615	ENOG4105BZJ	Electron transfer flavoprotein
G6N82_11620	ENOG4105C10	Electron transfer flavoprotein
G6N82_11630	ENOG4107ZSV	Receptor
G6N82_11725	ENOG4105CJH	Alcohol dehydrogenase zinc-binding domain protein
G6N82_11740	ENOG4105KF3	Short-chain dehydrogenase reductase Sdr
G6N82_11745	ENOG4105C1G	acyl-Coa dehydrogenase
G6N82_11775	ENOG4105C1G	acyl-Coa dehydrogenase
G6N82_11790	ENOG4108IPT	Naphthoate synthase
G6N82_11795	ENOG4105CYC	Transferase
G6N82_11800	ENOG4105DE9	3-keto-5-aminohexanoate cleavage enzyme
G6N82_11805	ENOG4105DYT	3-hydroxyacyl-CoA dehydrogenase
G6N82_11810	ENOG4105CV8	reductase
G6N82_11835	ENOG4107ZSV	Receptor
G6N82_11850	ENOG4105J5T	Amp-dependent synthetase and ligase
G6N82_11865	ENOG4105CJH	Alcohol dehydrogenase zinc-binding domain protein
G6N82_11875	ENOG4105C04	l-carnitine dehydratase bile acid-inducible protein F
G6N82_11880	ENOG4105CAH	Chromate
G6N82_11905	ENOG4105CEY	Amp-dependent synthetase and ligase
G6N82_11925	ENOG4108SUT	Major Facilitator Superfamily
G6N82_11935	ENOG4105D07	Signal peptide peptidase, SppA
G6N82_11945	ENOG4105CD3	dihydroorotase
G6N82_11975	ENOG4108UQY	Iron-storage protein
G6N82_11990	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
G6N82_12005	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
G6N82_12010	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)
G6N82_12015	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)
G6N82_12020	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)
G6N82_12030	ENOG4107RDJ	Sulfotransferase
G6N82_12055	ENOG4105PGM	cation diffusion facilitator family transporter
G6N82_12095	ENOG4108VBV	N-Acetylmuramoyl-L-alanine amidase
G6N82_12130	ENOG4105DRC	Na( ) H( ) antiporter that extrudes sodium in exchange for external protons (By similarity)
G6N82_12135	ENOG410802X	bacteriophage n4 adsorption protein b
G6N82_12165	ENOG4105CA4	amino acids such as threonine, to avoid such errors, it has a posttransfer editing activity that hydrolyzes mischarged Thr-tRNA(Val) in a tRNA-dependent manner (By similarity)
G6N82_12200	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)
G6N82_12210	ENOG4105EI2	Pseudouridine synthase
G6N82_12215	ENOG41082CG	Protein CrcB homolog
G6N82_12235	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)
G6N82_12240	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)
G6N82_12250	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)
G6N82_12255	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)
G6N82_12290	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)
G6N82_12300	ENOG4105CHI	Involved in the active translocation of vitamin B12 (cyanocobalamin) across the outer membrane to the periplasmic space. It derives its energy for transport by interacting with the trans-periplasmic membrane protein TonB (By similarity)
G6N82_12305	ENOG4107RDJ	Sulfotransferase
G6N82_12315	ENOG4105CHI	Involved in the active translocation of vitamin B12 (cyanocobalamin) across the outer membrane to the periplasmic space. It derives its energy for transport by interacting with the trans-periplasmic membrane protein TonB (By similarity)
G6N82_12340	ENOG4107RNH	Outer membrane receptor FepA
G6N82_12345	ENOG4105F2C	Acetyl-CoA acetyltransferase
G6N82_12425	ENOG4105FC8	fad dependent oxidoreductase
G6N82_12430	ENOG4106YAV	Domain of unknown function (DUF1508)
G6N82_12435	ENOG4108UMW	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
G6N82_12440	ENOG4105CUV	Homoserine Kinase
G6N82_12445	ENOG4105C48	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
G6N82_12455	ENOG4105C75	arginyL-tRNA synthetase
G6N82_12465	ENOG4107QPA	Cleaves GlcNAc linked beta-1,4 to MurNAc tripeptides (By similarity)
G6N82_12470	ENOG4108KVX	Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpB that pull DNA away from mid-cell into both cell halves (By similarity)
G6N82_12475	ENOG4105K8I	Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpA that pull DNA away from mid-cell into both cell halves (By similarity)
G6N82_12480	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)
G6N82_12485	ENOG41081BE	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)
G6N82_12490	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)
G6N82_12505	ENOG4105CF3	3-Hydroxyisobutyrate dehydrogenase
G6N82_12510	ENOG4105C7B	Threonine dehydratase
G6N82_12515	ENOG4105DWA	May conjugate Arg from its aminoacyl-tRNA to the N- termini of proteins containing an N-terminal aspartate or glutamate
G6N82_12535	ENOG4105VZ8	Transcriptional regulator
G6N82_12550	ENOG4105C5F	glutamine synthetase
G6N82_12555	ENOG4108YZA	Nitrogen regulatory protein pii
G6N82_12580	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)
G6N82_12585	ENOG4105CA1	Removes the N-terminal methionine from nascent proteins (By similarity)
G6N82_12595	ENOG4105CA5	Required for the export of heme to the periplasm for the biogenesis of c-type cytochromes (By similarity)
G6N82_12600	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)
G6N82_12605	ENOG4105KZX	Pterin carbinolamine dehydratase
G6N82_12615	ENOG4105CHR	reductase
G6N82_12635	ENOG4105C6T	cysteine synthase
G6N82_12650	ENOG4107YUR	Cell division protein mraZ
G6N82_12655	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
G6N82_12680	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
G6N82_12685	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
G6N82_12695	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)
G6N82_12700	ENOG4105DFU	Cell wall formation (By similarity)
G6N82_12710	ENOG4105CPF	Cell wall formation (By similarity)
G6N82_12715	ENOG4108UFP	Essential cell division protein (By similarity)
G6N82_12745	ENOG4105II7	pyrroline-5-carboxylate reductase
G6N82_12750	ENOG4105HFZ	Membrane
G6N82_12770	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
G6N82_12775	ENOG4105CGT	Catalyzes the transfer of a phosphate group to glutamate to form glutamate 5-phosphate which rapidly cyclizes to 5- oxoproline (By similarity)
G6N82_12790	ENOG4105ET3	Reduction of activated sulfate into sulfite (By similarity)
G6N82_12800	ENOG4105ET1	Component of the sulfite reductase complex that catalyzes the 6-electron reduction of sulfite to sulfide. This is one of several activities required for the biosynthesis of L- cysteine from sulfate (By similarity)
G6N82_12810	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)
G6N82_12825	ENOG4105KHC	sulfurtransferase
G6N82_12835	ENOG4105CSD	Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1) (By similarity)
G6N82_12855	ENOG4105D1H	recombination factor protein RarA
G6N82_12860	ENOG4105NTW	Transcriptional regulator
G6N82_12870	ENOG4105CPK	Glycosyl transferase (Group 1
G6N82_12875	ENOG4107QM1	Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine (By similarity)
G6N82_12885	ENOG4105C49	Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine (By similarity)
G6N82_12920	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
G6N82_12930	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)
G6N82_12945	ENOG4105CH7	arginosuccinase
G6N82_12950	ENOG4107QX9	Thiol disulfide interChange protein
G6N82_12960	ENOG4107S1E	Beta-lactamase
G6N82_12965	ENOG4105CHI	Involved in the active translocation of vitamin B12 (cyanocobalamin) across the outer membrane to the periplasmic space. It derives its energy for transport by interacting with the trans-periplasmic membrane protein TonB (By similarity)
G6N82_12985	ENOG4107R7I	amino acid
G6N82_12990	ENOG4105DUM	transcriptional regulator, lysR family
G6N82_13000	ENOG4105CHI	Involved in the active translocation of vitamin B12 (cyanocobalamin) across the outer membrane to the periplasmic space. It derives its energy for transport by interacting with the trans-periplasmic membrane protein TonB (By similarity)
G6N82_13010	ENOG4105CK2	sodium dicarboxylate symporter
G6N82_13020	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
G6N82_13025	ENOG4108IQF	Catalyzes the conversion of acetate into acetyl-CoA (AcCoA), an essential intermediate at the junction of anabolic and catabolic pathways. AcsA undergoes a two-step reaction. In the first half reaction, AcsA combines acetate with ATP to form acetyl-adenylate (AcAMP) intermediate. In the second half reaction, it can then transfer the acetyl group from AcAMP to the sulfhydryl group of CoA, forming the product AcCoA (By similarity)
G6N82_13035	ENOG4108XI2	Domain of unknown function (DUF1963)
G6N82_13040	ENOG4107QPD	alcohol dehydrogenase
G6N82_13060	ENOG4108RXX	maleylacetoacetate isomerase
G6N82_13065	ENOG4105C1G	acyl-Coa dehydrogenase
G6N82_13080	ENOG4105KK9	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
G6N82_13090	ENOG4105CSF	NADPH-dependent glycerol-3-phosphate dehydrogenase
G6N82_13095	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)
G6N82_13155	ENOG410626R	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)
G6N82_13175	ENOG4105CFB	Gamma-glutamyltranspeptidase (EC 2.3.2.2)
G6N82_13180	ENOG4105CK7	Sodium proline symporter
G6N82_13185	ENOG4105CI3	gtp-binding protein typa
G6N82_13190	ENOG4105D05	Receptor
G6N82_13200	ENOG41085PJ	rdd domain containing protein
G6N82_13210	ENOG4108I0Y	(ABC) transporter
G6N82_13215	ENOG4108UJV	acyl-CoA thioesterase i
G6N82_13220	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)
G6N82_13250	ENOG4105HA9	of methanol dehydrogenase type
G6N82_13260	ENOG4105M2E	Channel that opens in response to stretch forces in the membrane lipid bilayer. May participate in the regulation of osmotic pressure changes within the cell (By similarity)
G6N82_13275	ENOG4105EY2	Catalyzes the hydrolysis of N(2)-succinylarginine into N(2)-succinylornithine, ammonia and CO(2) (By similarity)
G6N82_13290	ENOG4107QP3	malate synthase g
G6N82_13295	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)
G6N82_13305	ENOG4105DBD	Chaperone involved in the correct folding and assembly of outer membrane proteins. Recognizes specific patterns of aromatic residues and the orientation of their side chains, which are found more frequently in integral outer membrane proteins. May act in both early periplasmic and late outer membrane-associated steps of protein maturation (By similarity)
G6N82_13310	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)
G6N82_13315	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)
G6N82_13330	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)
G6N82_13345	ENOG4108V3E	phosphoribosylglycinamide formyltransferase
G6N82_13350	ENOG4105CXB	phosphoribosylaminoimidazole synthetase
G6N82_13360	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)
G6N82_13365	ENOG4105D7W	serine acetyltransferase
G6N82_13380	ENOG4105KF3	Short-chain dehydrogenase reductase Sdr
G6N82_13390	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)
G6N82_13415	ENOG4107ZDE	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
G6N82_13420	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)
G6N82_13430	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)
G6N82_13435	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
G6N82_13440	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)
G6N82_13445	ENOG4105E2B	Taurine dioxygenase
G6N82_13465	ENOG4108K3A	Glutathione S-transferase
G6N82_13470	ENOG4105EXX	Deoxyribodipyrimidine photolyase-related protein
G6N82_13475	ENOG4105C25	Primosomal protein n'
G6N82_13490	ENOG4105CW3	Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway (By similarity)
G6N82_13505	ENOG4105C8N	cysteinyl-tRNA synthetase
G6N82_13510	ENOG4105C5I	Dehydrogenase
G6N82_13535	ENOG4105C5X	domain protein
G6N82_13545	ENOG41067VY	50S ribosomal protein L32
G6N82_13555	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)
G6N82_13560	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)
G6N82_13565	ENOG4105WJX	transcriptional regulator MERR family
G6N82_13570	ENOG4105CDB	Required for chromosome condensation and partitioning (By similarity)
G6N82_13590	ENOG4105CEN	a g-specific adenine glycosylase
G6N82_13605	ENOG4105E09	nadh pyrophosphatase
G6N82_13610	ENOG4108Z33	Thiol disulfide Interchange Protein
G6N82_13625	ENOG4105CJW	magnesium transporter
G6N82_13640	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)
G6N82_13655	ENOG4108MHR	Repressor involved in choline regulation of the bet genes (By similarity)
G6N82_13660	ENOG4105CPT	Alpha beta hydrolase
G6N82_13665	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)
G6N82_13670	ENOG4107RCQ	(CBS) domain
G6N82_13685	ENOG41090R7	Ferric uptake
G6N82_13690	ENOG4108YXV	Transcriptional regulator
G6N82_13695	ENOG4108RTV	Catalyzes the transfer of acetyl from acetyl-CoA to desacetylmycothiol (Cys-GlcN-Ins) to form mycothiol (By similarity)
G6N82_13700	ENOG41072GX	Peptidase M22 Glycoprotease
G6N82_13705	ENOG4108RDT	NADH dehydrogenase NAD(P)H nitroreductase)
G6N82_13710	ENOG41083MR	nifu domain-containing protein
G6N82_13720	ENOG4105C7V	phospho-2-dehydro-3-deoxyheptonate aldolase
G6N82_13725	ENOG4105E46	N-alpha,N-alpha,N-alpha-trimethyl-L-histidine metabolic process
G6N82_13730	ENOG41067HS	methyltransferase
G6N82_13740	ENOG4105CYX	Short-chain dehydrogenase reductase Sdr
G6N82_13750	ENOG4105CT4	transporter
G6N82_13755	ENOG4105CYM	Glutathione S-transferase
G6N82_13775	ENOG4108V3G	Catalyzes the reductive cleavage of azo bond in aromatic azo compounds to the corresponding amines. Requires NADH, but not NADPH, as an electron donor for its activity (By similarity)
G6N82_13780	ENOG4105C2I	pirin domain protein
G6N82_13785	ENOG4107RSM	transcriptional regulator
G6N82_13815	ENOG4105C72	UPF0176 protein
G6N82_13820	ENOG4105CM2	brancheD-chain amino acid aminotransferase
G6N82_13830	ENOG4105DX0	Hemolysin A
G6N82_13850	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)
G6N82_13855	ENOG4105CKK	Glycosyl transferase, family 2
G6N82_13890	ENOG4105NWN	ApaG protein
G6N82_13895	ENOG4105ETT	transcriptional Regulator, LysR family
G6N82_13925	ENOG4107GWN	repeat protein
G6N82_13995	ENOG4105DFG	type I secretion outer membrane protein
G6N82_14010	ENOG4105C42	Type I secretion membrane fusion protein (HlyD
G6N82_14025	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)
G6N82_14030	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)
G6N82_14035	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)
G6N82_14040	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
G6N82_14045	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
G6N82_14050	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)
G6N82_14055	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)
G6N82_14060	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)
G6N82_14065	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
G6N82_14070	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
G6N82_14075	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)
G6N82_14080	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
G6N82_14085	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
G6N82_14090	ENOG41083MP	50s ribosomal protein l29
G6N82_14095	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
G6N82_14100	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
G6N82_14105	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
G6N82_14110	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
G6N82_14115	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)
G6N82_14120	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)
G6N82_14125	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)
G6N82_14130	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)
G6N82_14135	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)
G6N82_14140	ENOG41084HQ	50S ribosomal protein L30
G6N82_14145	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
G6N82_14150	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)
G6N82_14155	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)
G6N82_14165	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
G6N82_14170	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)
G6N82_14175	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
G6N82_14180	ENOG4108ZT0	50S ribosomal protein l17
G6N82_14205	ENOG4105EN6	Membrane
G6N82_14215	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)
G6N82_14230	ENOG4107QN2	dihydrolipoyl dehydrogenase
G6N82_14235	ENOG4105C7S	Dehydrogenase
G6N82_14240	ENOG4105C7P	2-oxoglutarate dehydrogenase, E1
G6N82_14245	ENOG4105CH8	Succinyl-CoA ligase ADP-forming subunit alpha
G6N82_14250	ENOG4105C80	Catalyzes the reversible oxidation of malate to oxaloacetate (By similarity)
G6N82_14275	ENOG4108IPX	Part of the ABC transporter complex HmuTUV involved in hemin import. Responsible for energy coupling to the transport system (By similarity)
G6N82_14340	ENOG4105CV9	cyclopropane-fatty-acyl-phospholipid synthase
G6N82_14350	ENOG4108IUZ	ABC transporter
G6N82_14355	ENOG4105EQW	The exact function is not known. Can catalyze the reduction of a variety of substrates like dimethyl sulfoxide, trimethylamine N-oxide, phenylmethyl sulfoxide and L-methionine sulfoxide. Cannot reduce cyclic N-oxides. Shows no activity as sulfite oxidase (By similarity)
G6N82_14370	ENOG4105JAB	phenazine biosynthesis protein, phzf family
G6N82_14380	ENOG4108RPX	mosc domain containing protein
G6N82_14385	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
G6N82_14395	ENOG4108RRZ	Transcription elongation factor GreB
G6N82_14400	ENOG4107SC1	transglycosylase
G6N82_14405	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
G6N82_14410	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
G6N82_14440	ENOG4107R6G	Catalyzes the S-adenosylmethionine monomethyl esterification of trans-aconitate (By similarity)
G6N82_14445	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)
G6N82_14450	ENOG4105CKD	glutathione-regulated potassium-efflux system protein
G6N82_14455	ENOG4105DGM	nitrilase cyanide hydratase and apolipoprotein n-acyltransferase
G6N82_14485	ENOG4105CQB	FAD linked oxidase domain protein
G6N82_14500	ENOG4105FQP	Beta-lactamase
G6N82_14505	ENOG4105C4R	Atp-dependent dna helicase
G6N82_14510	ENOG4106H78	methyltransferase
G6N82_14520	ENOG4105DVW	rieske (2Fe-2S)
G6N82_14525	ENOG4105EYM	Major Facilitator superfamily
G6N82_14530	ENOG4105DPM	folylpolyglutamate synthase Dihydrofolate synthase
G6N82_14535	ENOG4108IDZ	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)
G6N82_14540	ENOG4105F6H	The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate (By similarity)
G6N82_14550	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
G6N82_14555	ENOG4108ZGB	N-(5'-phosphoribosyl)anthranilate isomerase
G6N82_14565	ENOG4106EG9	Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) (By similarity)
G6N82_14575	ENOG4105C83	adenylosuccinate lyase
G6N82_14580	ENOG4105W5Q	DNA repair protein (RadC
G6N82_14605	ENOG4105EE4	it plays a direct role in the translocation of protons across the membrane (By similarity)
G6N82_14610	ENOG4107Q7J	ATP synthase subunit C
G6N82_14615	ENOG4108VHN	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)
G6N82_14620	ENOG4108733	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)
G6N82_14635	ENOG4108RW0	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
G6N82_14650	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)
G6N82_14655	ENOG4105CAT	Cytidine monophosphate kinase
G6N82_14665	ENOG4105CMY	5-enolpyruvylshikimate-3-phosphate synthase
G6N82_14680	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
G6N82_14685	ENOG4105K5M	30s ribosomal protein S16
G6N82_14690	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)
G6N82_14700	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
G6N82_14705	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)
G6N82_14720	ENOG4105CM3	Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate (By similarity)
G6N82_14730	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
G6N82_14735	ENOG4105CW7	secretion protein, HlyD family
G6N82_14740	ENOG4107MII	Sugar-specific transcriptional regulator TrmB
G6N82_14775	ENOG4105D9I	Responsible for the addition of glutamate residues to the C-terminus of ribosomal protein S6 (By similarity)
G6N82_14780	ENOG4105D9I	Responsible for the addition of glutamate residues to the C-terminus of ribosomal protein S6 (By similarity)
G6N82_14790	ENOG4105FYV	Amp nucleosidase
G6N82_14800	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
G6N82_14805	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)
G6N82_14810	ENOG4108ZDX	Binds together with S18 to 16S ribosomal RNA (By similarity)
G6N82_14825	ENOG4105CEY	Amp-dependent synthetase and ligase