locus-tag	class	description
D9V69_00005	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)
D9V69_00010	ENOG4105EE4	it plays a direct role in the translocation of protons across the membrane (By similarity)
D9V69_00020	ENOG4107Z6K	F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation (By similarity)
D9V69_00050	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)
D9V69_00055	ENOG4105CZ8	DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity. The beta chain is required for initiation of replication once it is clamped onto DNA, it slides freely (bidirectional and ATP- independent) along duplex DNA (By similarity)
D9V69_00060	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)
D9V69_00070	ENOG4105NVJ	RNaseP catalyzes the removal of the 5'-leader sequence from pre-tRNA to produce the mature 5'-terminus. It can also cleave other RNA substrates such as 4.5S RNA. The protein component plays an auxiliary but essential role in vivo by binding to the 5'-leader sequence and broadening the substrate specificity of the ribozyme (By similarity)
D9V69_00105	ENOG4106CVF	DNA replication protein
D9V69_00115	ENOG4106H78	methyltransferase
D9V69_00120	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)
D9V69_00125	ENOG4105DEK	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
D9V69_00130	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
D9V69_00140	ENOG4105DQF	Hydrolase
D9V69_00145	ENOG4105DZ2	Transcriptional regulator
D9V69_00150	ENOG4105DSS	Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation (By similarity)
D9V69_00160	ENOG4105K70	DNA-binding protein
D9V69_00165	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
D9V69_00185	ENOG4105C64	Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release (By similarity)
D9V69_00195	ENOG4105E5V	Participates in transcription elongation, termination and antitermination (By similarity)
D9V69_00200	ENOG4105PM1	preprotein translocase subunit SecE
D9V69_00225	ENOG4105D4A	Cell wall formation (By similarity)
D9V69_00230	ENOG4105SYT	Methylenetetrahydrofolate reductase
D9V69_00240	ENOG4105CH7	arginosuccinase
D9V69_00245	ENOG4107YZP	Rhodanese domain protein
D9V69_00255	ENOG4105D7W	serine acetyltransferase
D9V69_00260	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
D9V69_00265	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)
D9V69_00285	ENOG4105DW0	Catalyzes the ADP transfer to D-glycero-D-manno-heptose 1-phosphate, yielding ADP-D,D-heptose (By similarity)
D9V69_00300	ENOG4105C5Y	PTS System
D9V69_00305	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)
D9V69_00310	ENOG4105KZ7	phosphocarrier protein hpr
D9V69_00315	ENOG4105C6T	cysteine synthase
D9V69_00335	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)
D9V69_00345	ENOG41081BH	flagellar hook-basal body complex protein fliE
D9V69_00350	ENOG4105C1F	The M ring may be actively involved in energy transduction (By similarity)
D9V69_00355	ENOG4105CS3	FliG is one of three proteins (FliG, FliN, FliM) that forms the rotor-mounted switch complex (C ring), located at the base of the basal body. This complex interacts with the CheY and CheZ chemotaxis proteins, in addition to contacting components of the motor that determine the direction of flagellar rotation (By similarity)
D9V69_00360	ENOG4108CG0	Flagellar assembly protein
D9V69_00365	ENOG4108JIR	Flagellum-specific ATP synthase
D9V69_00375	ENOG4105WF4	Flagellar hook-length control protein
D9V69_00385	ENOG4105DD5	Flagellar motor switch protein
D9V69_00390	ENOG4105CN7	Flagellar biosynthetic protein FliP
D9V69_00395	ENOG4105VS8	Flagellar biosynthetic protein fliq
D9V69_00400	ENOG4105D19	Role in flagellar biosynthesis (By similarity)
D9V69_00405	ENOG4105W0E	50S ribosomal protein L33
D9V69_00420	ENOG4105F0N	pyrophosphate phospho-hydrolase
D9V69_00425	ENOG4105CMS	peptidase U62, modulator of DNA gyrase
D9V69_00435	ENOG4105CU0	Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA (By similarity)
D9V69_00440	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
D9V69_00450	ENOG4105CV1	Transketolase (EC 2.2.1.1)
D9V69_00465	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
D9V69_00485	ENOG4105CEK	Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine (By similarity)
D9V69_00500	ENOG4108UJE	IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisH subunit provides the glutamine amidotransferase activity that produces the ammonia necessary to HisF for the synthesis of IGP and AICAR (By similarity)
D9V69_00510	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)
D9V69_00515	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
D9V69_00520	ENOG4105C7Q	Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH (By similarity)
D9V69_00525	ENOG4105DHP	deoxycytidine triphosphate deaminase
D9V69_00535	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)
D9V69_00545	ENOG4108R6K	riboflavin synthase, subunit alpha
D9V69_00560	ENOG4107QTR	Required for nitrogen fixation. May be part of a membrane complex functioning as an intermediate in the electron transport to nitrogenase (By similarity)
D9V69_00570	ENOG4108UQQ	Electron transport complex
D9V69_00580	ENOG4105CSM	endonuclease III
D9V69_00595	ENOG4108Z4V	iron-sulfur cluster assembly
D9V69_00600	ENOG4105IPI	Membrane
D9V69_00605	ENOG4105E99	Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) (By similarity)
D9V69_00615	ENOG4108UUX	IF-3 binds to the 30S ribosomal subunit and shifts the equilibrum between 70S ribosomes and their 50S and 30S subunits in favor of the free subunits, thus enhancing the availability of 30S subunits on which protein synthesis initiation begins (By similarity)
D9V69_00625	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)
D9V69_00630	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
D9V69_00635	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
D9V69_00640	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)
D9V69_00645	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)
D9V69_00655	ENOG4105VIE	preprotein translocase, subunit YajC
D9V69_00670	ENOG4105EUJ	GTP cyclohydrolase i
D9V69_00685	ENOG4108KF1	Membrane
D9V69_00690	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)
D9V69_00695	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)
D9V69_00700	ENOG4105DDT	Hydrolyzes diadenosine 5',5'''-P1,P4-tetraphosphate to yield ADP (By similarity)
D9V69_00705	ENOG4108YYV	Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis (By similarity)
D9V69_00710	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
D9V69_00715	ENOG4105C1M	carbamoyl-phosphate synthetase glutamine chain
D9V69_00720	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
D9V69_00735	ENOG4105C07	amino acids such as valine, to avoid such errors it has two additional distinct tRNA(Ile)-dependent editing activities. One activity is designated as 'pretransfer' editing and involves the hydrolysis of activated Val-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Val-tRNA(Ile) (By similarity)
D9V69_00740	ENOG4105DTN	riboflavin biosynthesis protein ribF
D9V69_00760	ENOG4105KWU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
D9V69_00770	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)
D9V69_00775	ENOG4105GKE	subunit e
D9V69_00780	ENOG4107QIZ	NADH dehydrogenase
D9V69_00785	ENOG4107R0R	NADH dehydrogenase subunit g
D9V69_00795	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)
D9V69_00800	ENOG4107UFS	subunit j
D9V69_00810	ENOG4105D65	subunit l
D9V69_00815	ENOG4105C8S	subunit m
D9V69_00820	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)
D9V69_00825	ENOG4105DPM	folylpolyglutamate synthase Dihydrofolate synthase
D9V69_00835	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
D9V69_00840	ENOG4105CTR	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
D9V69_00850	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)
D9V69_00855	ENOG41063JG	Transcriptional regulator
D9V69_00865	ENOG4105C6H	Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction (By similarity)
D9V69_00870	ENOG4105C6K	Malic enzyme
D9V69_00875	ENOG4105XPH	Ferredoxin
D9V69_00880	ENOG4105E05	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
D9V69_00885	ENOG4105BZH	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
D9V69_00890	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)
D9V69_00895	ENOG4105G4C	Periplasmic ligand-binding sensor protein
D9V69_00900	ENOG4105D3R	alkyl hydroperoxide reductase
D9V69_00905	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)
D9V69_00910	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
D9V69_00930	ENOG4105M2J	Glutaredoxin
D9V69_00935	ENOG4105DH5	Responsible for the end-turnover of tRNA specifically removes the terminal AMP residue from uncharged tRNA (tRNA-C-C-A). Also appears to be involved in tRNA biosynthesis (By similarity)
D9V69_00940	ENOG4105CK4	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
D9V69_00950	ENOG4105C3G	gtp-binding protein
D9V69_00955	ENOG4105D98	threonine synthase
D9V69_00960	ENOG4105D5I	Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate (By similarity)
D9V69_00965	ENOG4105CFH	Aspartokinase
D9V69_00970	ENOG4108UGV	hypoxanthine phosphoribosyltransferase
D9V69_00980	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
D9V69_00985	ENOG4108V7X	Transcription factor that acts by binding directly to the RNA polymerase (RNAP). Required for negative regulation of rRNA expression and positive regulation of several amino acid biosynthesis promoters
D9V69_00995	ENOG4105BZ4	penicillin-binding protein
D9V69_01000	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
D9V69_01005	ENOG4108ZQD	Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A (By similarity)
D9V69_01015	ENOG4105DAQ	Component of the pyruvate dehydrogenase (PDH) complex, that catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2) (By similarity)
D9V69_01020	ENOG4107QSN	dihydrolipoamide acetyltransferase
D9V69_01025	ENOG4107QN2	dihydrolipoyl dehydrogenase
D9V69_01045	ENOG4108YX9	iron--sulfur cluster insertion protein erpA
D9V69_01050	ENOG4105CDK	Essential cell division protein that forms a contractile ring structure (Z ring) at the future cell division site. The regulation of the ring assembly controls the timing and the location of cell division. One of the functions of the FtsZ ring is to recruit other cell division proteins to the septum to produce a new cell wall between the dividing cells. Binds GTP and shows GTPase activity (By similarity)
D9V69_01055	ENOG4105CIT	This protein may be involved in anomalous filament growth. May be a component of the septum (By similarity)
D9V69_01060	ENOG4105CPF	Cell wall formation (By similarity)
D9V69_01070	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)
D9V69_01075	ENOG4105CNI	cell division protein FtsW
D9V69_01095	ENOG4107EEN	Catalyzes the addition of meso-diaminopimelic acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan (By similarity)
D9V69_01100	ENOG4105CJN	penicillin-binding protein
D9V69_01115	ENOG4108ZP8	Acetolactate synthase small subunit
D9V69_01120	ENOG4105C7K	acetolactate synthase
D9V69_01130	ENOG4105C0H	protease
D9V69_01135	ENOG4105DMJ	Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate (By similarity)
D9V69_01140	ENOG4105CA1	Removes the N-terminal methionine from nascent proteins (By similarity)
D9V69_01155	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
D9V69_01165	ENOG4105CEA	Catalyzes the NADP-dependent rearrangement and reduction of 1-deoxy-D-xylulose-5-phosphate (DXP) to 2-C-methyl-D-erythritol 4-phosphate (MEP) (By similarity)
D9V69_01170	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
D9V69_01175	ENOG4105E1Z	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane
D9V69_01185	ENOG4105C0B	DNA polymerase III (alpha subunit)
D9V69_01195	ENOG4105D00	flagellar biosynthetic protein flhB
D9V69_01200	ENOG4105D7B	Flagellar biosynthesis protein flha
D9V69_01225	ENOG4108RW0	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
D9V69_01230	ENOG4108UMW	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
D9V69_01235	ENOG4107RZZ	dna polymerase iii epsilon subunit
D9V69_01250	ENOG4105DYA	Acts on guanine, xanthine and to a lesser extent hypoxanthine (By similarity)
D9V69_01255	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
D9V69_01260	ENOG4105VDB	UPF0125 protein
D9V69_01270	ENOG4108Z6B	deaminase
D9V69_01290	ENOG4105C3F	Signal peptidase i
D9V69_01300	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
D9V69_01305	ENOG4107QTF	adenylosuccinate lyase
D9V69_01315	ENOG4105CSJ	Enoyl- acyl-carrier-protein reductase NADH
D9V69_01325	ENOG4105EZI	multiple antibiotic resistance (MarC)-related protein
D9V69_01330	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)
D9V69_01340	ENOG4106EG9	Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) (By similarity)
D9V69_01345	ENOG4107T1C	Catalyzes the conversion of GTP to 2,5-diamino-6- ribosylamino-4(3H)-pyrimidinone 5'-phosphate (DARP), formate and pyrophosphate (By similarity)
D9V69_01355	ENOG4105NAU	thioesterase Superfamily protein
D9V69_01365	ENOG4108S3I	UPF0259 membrane protein
D9V69_01390	ENOG4105DWP	Membrane
D9V69_01395	ENOG4105FE9	pseudouridine synthase
D9V69_01400	ENOG4105ERU	peptidase
D9V69_01405	ENOG4105C73	Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone (By similarity)
D9V69_01410	ENOG4105ECY	inositol monophosphatase
D9V69_01415	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
D9V69_01420	ENOG4105C4E	Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate (By similarity)
D9V69_01425	ENOG4105CUT	histidyl-tRNA synthetase
D9V69_01445	ENOG4108F0W	Catalyzes the transfer of the alpha-amino group from S- adenosyl-L-methionine (SAM) to 7-keto-8-aminopelargonic acid (KAPA) to form 7,8-diaminopelargonic acid (DAPA). It is the only animotransferase known to utilize SAM as an amino donor (By similarity)
D9V69_01450	ENOG4105HHQ	6-phosphogluconolactonase (EC 3.1.1.31)
D9V69_01455	ENOG4108JA2	transcriptioN-repair coupling factor
D9V69_01460	ENOG4105D60	lipoprotein releasing system transmembrane protein
D9V69_01465	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)
D9V69_01475	ENOG4105C17	glyceraldehyde-3-phosphate dehydrogenase
D9V69_01480	ENOG4107R1K	Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1) (By similarity)
D9V69_01485	ENOG4105MHQ	Low-potential electron donor to a number of redox enzymes (By similarity)
D9V69_01490	ENOG4105CVP	deoxyribo-dipyrimidine photolyase
D9V69_01495	ENOG4107QNR	UPF0135 protein
D9V69_01500	ENOG4105C7P	2-oxoglutarate dehydrogenase, E1
D9V69_01505	ENOG4105C7S	Dehydrogenase
D9V69_01515	ENOG4105CTQ	phosphohexokinase
D9V69_01520	ENOG4105D8C	Channel that permits osmotically driven movement of water in both directions. It is involved in the osmoregulation and in the maintenance of cell turgor during volume expansion in rapidly growing cells. It mediates rapid entry or exit of water in response to abrupt changes in osmolarity (By similarity)
D9V69_01525	ENOG4105CP7	Triose-phosphate isomerase
D9V69_01535	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)
D9V69_01560	ENOG4105C3M	thioredoxin reductase
D9V69_01565	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)
D9V69_01575	ENOG4105FAV	ABC, transporter
D9V69_01580	ENOG4105FDK	ABC transporter
D9V69_01585	ENOG4105NXV	High-affinity zinc uptake system protein
D9V69_01590	ENOG4105NXV	High-affinity zinc uptake system protein
D9V69_01595	ENOG4105DR5	peptidase
D9V69_01600	ENOG4105CA9	Pyruvate kinase
D9V69_01605	ENOG4105D8W	glucose-6-phosphate 1-dehydrogenase
D9V69_01615	ENOG4105EE5	Membrane protein terC
D9V69_01620	ENOG41072GX	Peptidase M22 Glycoprotease
D9V69_01625	ENOG4105VJP	Prevents the cell division inhibition by proteins MinC and MinD at internal division sites while permitting inhibition at polar sites. This ensures cell division at the proper site by restricting the formation of a division septum at the midpoint of the long axis of the cell (By similarity)
D9V69_01630	ENOG4107QMS	site-determining protein
D9V69_01640	ENOG4105D8J	Specifically methylates the guanine in position 1207 of 16S rRNA in the 30S particle (By similarity)
D9V69_01655	ENOG4105UYK	outer membrane protein a
D9V69_01660	ENOG4105CJR	Integral membrane protein (MviN
D9V69_01675	ENOG4105CKS	Flagella basal body P-ring formation protein flgA
D9V69_01680	ENOG4105K88	Structural component of flagellum, the bacterial motility apparatus. Part of the rod structure of flagellar basal body (By similarity)
D9V69_01685	ENOG4108ZC9	flagellar basal-body rod protein flgc
D9V69_01690	ENOG4105W00	Flagellar hook capping protein
D9V69_01695	ENOG4105BZE	flagellar hook protein, FlgE
D9V69_01700	ENOG4108KPB	Flagellar basal-body rod protein FlgF
D9V69_01705	ENOG4105CGA	flagellar basal-body rod protein FlgG
D9V69_01715	ENOG4105D92	Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation (By similarity)
D9V69_01725	ENOG4105E1Q	flagellar hook-associated protein
D9V69_01730	ENOG4107QQB	Ribonuclease E
D9V69_01735	ENOG4105EI2	Pseudouridine synthase
D9V69_01755	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
D9V69_01760	ENOG4107QRG	dna polymerase iii
D9V69_01765	ENOG4105F8V	Hydrolase, tatD family
D9V69_01770	ENOG4105CI1	PTS System
D9V69_01775	ENOG4105K59	histidine triad (HIT) protein
D9V69_01785	ENOG4108742	Forms pores that allow passive diffusion of small molecules across the membrane (By similarity)
D9V69_01790	ENOG4105C5S	asparaginyl-tRNA synthetase
D9V69_01805	ENOG4105C4H	Specifically methylates the guanine in position 2445 (m2G2445) and the guanine in position 2069 (m7G2069) of 23S rRNA (By similarity)
D9V69_01810	ENOG4105C5H	ABC transporter
D9V69_01815	ENOG4105C72	UPF0176 protein
D9V69_01820	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)
D9V69_01825	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)
D9V69_01830	ENOG4105DBV	ornithine carbamoyltransferase
D9V69_01835	ENOG4105CXT	aspartate transcarbamylase
D9V69_01845	ENOG4105KME	endoribonuclease L-psp
D9V69_01850	ENOG4105C1J	atp-dependent rna helicase
D9V69_01855	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
D9V69_01865	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
D9V69_01880	ENOG4105CHV	Transcription elongation factor NusA
D9V69_01900	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)
D9V69_01905	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)
D9V69_01910	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)
D9V69_01915	ENOG4105VFK	BolA family
D9V69_01945	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)
D9V69_01950	ENOG4105CQC	Prephenate dehydratase
D9V69_01955	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
D9V69_01965	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)
D9V69_01970	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
D9V69_01980	ENOG4105D1U	peptidase U62 modulator of DNA gyrase
D9V69_01995	ENOG4105C34	Pseudouridine synthase
D9V69_02000	ENOG4106SNF	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane
D9V69_02005	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)
D9V69_02010	ENOG4105VM8	Could accelerate the degradation of some genes transcripts potentially through selective RNA binding (By similarity)
D9V69_02030	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
D9V69_02035	ENOG4105RWS	endonuclease I
D9V69_02040	ENOG4105QF0	Specifically methylates the N3 position of the uracil ring of uridine 1498 (m3U1498) in 16S rRNA. Acts on the fully assembled 30S ribosomal subunit (By similarity)
D9V69_02045	ENOG4105MK2	5-formyltetrahydrofolate cyclo-ligase
D9V69_02070	ENOG4105CX6	glutaminyL-tRNA synthetase
D9V69_02080	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
D9V69_02085	ENOG4105EIZ	Catalyzes the conversion of 6-carboxy-5,6,7,8- tetrahydropterin (CPH4) to 7-carboxy-7-deazaguanine (CDG) (By similarity)
D9V69_02090	ENOG4107ZIF	6-carboxy-5,6,7,8-tetrahydropterin synthase
D9V69_02095	ENOG4108K5P	(LipO)protein
D9V69_02105	ENOG4105CE5	Catalyzes the formation of 4-diphosphocytidyl-2-C- methyl-D-erythritol from CTP and 2-C-methyl-D-erythritol 4- phosphate (MEP) (By similarity)
D9V69_02110	ENOG4108I67	Catalyzes the synthesis of activated sulfate (By similarity)
D9V69_02125	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)
D9V69_02140	ENOG4107EER	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. The flavoprotein component catalyzes the electron flow from NADPH - FAD - FMN to the hemoprotein component (By similarity)
D9V69_02150	ENOG4105C2M	dna polymerase I
D9V69_02160	ENOG4105CI3	gtp-binding protein typa
D9V69_02165	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
D9V69_02170	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)
D9V69_02175	ENOG4105CG1	Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA (By similarity)
D9V69_02180	ENOG4105CRK	lysyL-tRNA synthetase
D9V69_02185	ENOG4105CU5	Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine (By similarity)
D9V69_02195	ENOG4105C0V	Provides the sole de novo source of dTMP for DNA biosynthesis (By similarity)
D9V69_02200	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)
D9V69_02205	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)
D9V69_02210	ENOG4108JU5	Magnesium and cobalt efflux protein
D9V69_02215	ENOG4105C8T	Leucyl-tRNA synthetase
D9V69_02225	ENOG4108Z1W	Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) (By similarity)
D9V69_02235	ENOG4105CM3	Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate (By similarity)
D9V69_02240	ENOG41076UM	multiple antibiotic resistance (MarC)-related protein
D9V69_02250	ENOG4105D2N	Aldolase
D9V69_02255	ENOG4105D64	Mechanosensitive ion channel
D9V69_02260	ENOG4105DSY	exodeoxyribonuclease V, gamma
D9V69_02265	ENOG4107QKA	exodeoxyribonuclease V beta
D9V69_02270	ENOG4107QYX	exodeoxyribonuclease v alpha
D9V69_02280	ENOG4105CA3	membrane-bound lytic murein transglycosylase
D9V69_02290	ENOG4105CG2	Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 (By similarity)
D9V69_02295	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)
D9V69_02300	ENOG4108DQE	riboflavin reductase
D9V69_02315	ENOG4105CTB	Polyprenyl synthetase
D9V69_02325	ENOG4108Z0T	Part of a sulfur-relay system (By similarity)
D9V69_02340	ENOG4107R3R	Cytochrome o ubiquinol oxidase subunit III
D9V69_02345	ENOG4105BZ9	Cytochrome C oxidase, subunit I
D9V69_02350	ENOG4105E2S	oxidase) subunit II
D9V69_02355	ENOG4105M85	Bola protein
D9V69_02365	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)
D9V69_02375	ENOG4105C6P	ATP-dependent serine protease that mediates the selective degradation of mutant and abnormal proteins as well as certain short-lived regulatory proteins. Required for cellular homeostasis and for survival from DNA damage and developmental changes induced by stress. Degrades polypeptides processively to yield small peptide fragments that are 5 to 10 amino acids long. Binds to DNA in a double-stranded, site-specific manner (By similarity)
D9V69_02380	ENOG4105EIN	peptidylprolyl cis-trans isomerase
D9V69_02385	ENOG4105FD2	Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) (By similarity)
D9V69_02390	ENOG4105BZ1	(ABC) transporter
D9V69_02395	ENOG4105BZ1	(ABC) transporter
D9V69_02405	ENOG4107QMP	dna polymerase iii subunits gamma and tau
D9V69_02410	ENOG4105KDX	Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection (By similarity)
D9V69_02415	ENOG4105CJX	Molecular chaperone. Has ATPase activity (By similarity)
D9V69_02430	ENOG4105CN0	Catalyzes the oxidation of 5,10- methylenetetrahydrofolate to 5,10-methenyltetrahydrofolate and then the hydrolysis of 5,10-methenyltetrahydrofolate to 10- formyltetrahydrofolate (By similarity)
D9V69_02445	ENOG4105VEQ	Cold shock protein
D9V69_02470	ENOG4105EK0	Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine (By similarity)
D9V69_02495	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
D9V69_02505	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)
D9V69_02515	ENOG41087H9	50S ribosomal protein L36
D9V69_02520	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)
D9V69_02535	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)
D9V69_02545	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)
D9V69_02550	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)
D9V69_02555	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)
D9V69_02560	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
D9V69_02565	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
D9V69_02580	ENOG41083MP	50s ribosomal protein l29
D9V69_02590	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
D9V69_02605	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
D9V69_02655	ENOG4108ZKU	Part of a sulfur-relay system required for 2-thiolation of 5-methylaminomethyl-2-thiouridine (mnm(5)s(2)U) at tRNA wobble positions (By similarity)
D9V69_02665	ENOG4108V1T	peptidylprolyl cis-trans isomerase
D9V69_02675	ENOG4105C31	Tryptophanyl-tRNA synthetase
D9V69_02680	ENOG4105DJV	ribulose-phosphate 3-epimerase
D9V69_02685	ENOG4105D49	3-dehydroquinate synthase
D9V69_02690	ENOG4105KHV	Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate (By similarity)
D9V69_02715	ENOG4107RUK	Involved in iron-sulfur cluster biogenesis. Binds a 4Fe- 4S cluster, can transfer this cluster to apoproteins, and thereby intervenes in the maturation of Fe S proteins. Could also act as a scaffold chaperone for damaged Fe S proteins (By similarity)
D9V69_02720	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)
D9V69_02725	ENOG4108UUM	single-stranded DNA-binding protein
D9V69_02730	ENOG4105CDU	Replicative dna helicase
D9V69_02735	ENOG4105D7Z	glutathione synthase
D9V69_02745	ENOG4105DFA	alanine racemase domain protein
D9V69_02750	ENOG4105CSA	Coproporphyrinogen iii oxidase
D9V69_02760	ENOG4105CEN	a g-specific adenine glycosylase
D9V69_02765	ENOG4105KMG	Could be a mediator in iron transactions between iron acquisition and iron-requiring processes, such as synthesis and or repair of Fe-S clusters in biosynthetic enzymes (By similarity)
D9V69_02775	ENOG4105CJB	Exodeoxyribonuclease I
D9V69_02805	ENOG4108RNI	3'(2')5'-bisphosphate nucleotidase
D9V69_02810	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
D9V69_02820	ENOG4108ZDX	Binds together with S18 to 16S ribosomal RNA (By similarity)
D9V69_02825	ENOG4105C40	3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs (By similarity)
D9V69_02835	ENOG4105EPW	hflc protein
D9V69_02840	ENOG4107QJR	hflk protein
D9V69_02845	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)
D9V69_02855	ENOG4105CTS	PTS system mannitol-specific
D9V69_02860	ENOG4107QP8	phosphohexose isomerase
D9V69_02865	ENOG4108RBP	3'-to-5' exoribonuclease specific for small oligoribonucleotides (By similarity)
D9V69_02875	ENOG4105C5C	n-acetylmuramoyl-l-alanine amidase
D9V69_02885	ENOG4108R5P	Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery (By similarity)
D9V69_02890	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)
D9V69_02895	ENOG4108ZNX	Heat shock protein
D9V69_02900	ENOG4105DP0	ferredoxin-NADP reductase
D9V69_02905	ENOG4105CAP	With EpmB is involved in the beta-lysylation step of the post-translational modification of translation elongation factor P (EF-P). Catalyzes the ATP-dependent activation of (R)-beta-lysine produced by EpmB, forming a lysyl-adenylate, from which the beta- lysyl moiety is then transferred to the epsilon-amino group of a conserved specific lysine residue in EF-P (By similarity)
D9V69_02930	ENOG4105CJ3	phosphate transporter
D9V69_02935	ENOG4105D94	Major Facilitator Superfamily
D9V69_02945	ENOG4105XQ6	frataxin-like protein
D9V69_02975	ENOG4105C4P	Facilitates transcription termination by a mechanism that involves Rho binding to the nascent RNA, activation of Rho's RNA-dependent ATPase activity, and release of the mRNA from the DNA template (By similarity)
D9V69_02980	ENOG4105K63	Thioredoxin
D9V69_02985	ENOG4105C4R	Atp-dependent dna helicase
D9V69_03010	ENOG4107XTC	May be involved in the formation or repair of Fe-S clusters present in iron-sulfur proteins
D9V69_03015	ENOG4108SWN	Co-chaperone involved in the maturation of iron-sulfur cluster-containing proteins. Seems to help targeting proteins to be folded toward HscA (By similarity)
D9V69_03025	ENOG4108ZIT	Ferredoxin, 2FE-2S