locus-tag	class	description
GVO57_RS00065	ENOG4105BZU	Histidine kinase
GVO57_RS00090	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)
GVO57_RS00095	ENOG4105BZU	Histidine kinase
GVO57_RS00100	ENOG4105EIX	cytochrome c1
GVO57_RS00110	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)
GVO57_RS00115	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)
GVO57_RS00125	ENOG4105E39	Enoyl-CoA hydratase
GVO57_RS00130	ENOG4105CC9	acyl-Coa dehydrogenase
GVO57_RS00135	ENOG4105C1G	acyl-Coa dehydrogenase
GVO57_RS00155	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)
GVO57_RS00160	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
GVO57_RS00165	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)
GVO57_RS00175	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)
GVO57_RS00180	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)
GVO57_RS00185	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
GVO57_RS00190	ENOG41084HQ	50S ribosomal protein L30
GVO57_RS00195	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)
GVO57_RS00200	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)
GVO57_RS00205	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)
GVO57_RS00210	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)
GVO57_RS00215	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)
GVO57_RS00220	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
GVO57_RS00225	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
GVO57_RS00230	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
GVO57_RS00235	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
GVO57_RS00240	ENOG41083MP	50s ribosomal protein l29
GVO57_RS00245	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
GVO57_RS00250	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
GVO57_RS00260	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
GVO57_RS00265	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
GVO57_RS00270	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)
GVO57_RS00275	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)
GVO57_RS00280	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)
GVO57_RS00285	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
GVO57_RS00290	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
GVO57_RS00295	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)
GVO57_RS00300	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)
GVO57_RS00305	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)
GVO57_RS00310	ENOG4107YXA	Transcriptional regulator, BadM Rrf2 family
GVO57_RS00340	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
GVO57_RS00355	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)
GVO57_RS00360	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
GVO57_RS00365	ENOG4105CBM	Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 (By similarity)
GVO57_RS00405	ENOG4105HHA	aminodeoxychorismate lyase
GVO57_RS00410	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
GVO57_RS00415	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
GVO57_RS00435	ENOG4107QVN	Key enzyme in the regulation of glycerol uptake and metabolism (By similarity)
GVO57_RS00445	ENOG4105C0B	DNA polymerase III (alpha subunit)
GVO57_RS00460	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)
GVO57_RS00475	ENOG4105KME	endoribonuclease L-psp
GVO57_RS00480	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)
GVO57_RS00485	ENOG4105D60	lipoprotein releasing system transmembrane protein
GVO57_RS00490	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)
GVO57_RS00495	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)
GVO57_RS00500	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)
GVO57_RS00505	ENOG4107QPA	Cleaves GlcNAc linked beta-1,4 to MurNAc tripeptides (By similarity)
GVO57_RS00515	ENOG4105C75	arginyL-tRNA synthetase
GVO57_RS00530	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)
GVO57_RS00535	ENOG4105CIT	This protein may be involved in anomalous filament growth. May be a component of the septum (By similarity)
GVO57_RS00545	ENOG4105CPF	Cell wall formation (By similarity)
GVO57_RS00550	ENOG4105D4A	Cell wall formation (By similarity)
GVO57_RS00575	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
GVO57_RS00600	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
GVO57_RS00615	ENOG4105C6T	cysteine synthase
GVO57_RS00630	ENOG4108YX9	iron--sulfur cluster insertion protein erpA
GVO57_RS00635	ENOG4105DR5	peptidase
GVO57_RS00640	ENOG4105ED9	Protein of unknown function (DUF455)
GVO57_RS00645	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
GVO57_RS00650	ENOG4105CE6	Adenylation and deadenylation of glutamate--ammonia ligase (By similarity)
GVO57_RS00660	ENOG41074H6	response regulator
GVO57_RS00675	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)
GVO57_RS00685	ENOG4108ZNX	Heat shock protein
GVO57_RS00705	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
GVO57_RS00710	ENOG4105CI8	Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons (By similarity)
GVO57_RS00715	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)
GVO57_RS00720	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)
GVO57_RS00730	ENOG4105DYT	3-hydroxyacyl-CoA dehydrogenase
GVO57_RS00760	ENOG41067HS	methyltransferase
GVO57_RS00765	ENOG4105E46	N-alpha,N-alpha,N-alpha-trimethyl-L-histidine metabolic process
GVO57_RS00780	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)
GVO57_RS00790	ENOG4105CCA	Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle (By similarity)
GVO57_RS00810	ENOG4108QDE	fad dependent oxidoreductase
GVO57_RS00815	ENOG4105K6V	RNA polymerase
GVO57_RS00830	ENOG4106MZZ	glycerophosphoryl diester phosphodiesterase
GVO57_RS00840	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)
GVO57_RS00860	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)
GVO57_RS00875	ENOG4107WTJ	Methyl-accepting chemotaxis sensory transducer
GVO57_RS00885	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
GVO57_RS00895	ENOG4105BZU	Histidine kinase
GVO57_RS00900	ENOG41065U4	response regulator
GVO57_RS00905	ENOG4105CBS	Chea signal transduction histidine kinase
GVO57_RS00915	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
GVO57_RS01015	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)
GVO57_RS01020	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)
GVO57_RS01035	ENOG4107R33	ppx gppa phosphatase
GVO57_RS01040	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)
GVO57_RS01055	ENOG4105C03	ribonuclease
GVO57_RS01060	ENOG4105C5C	n-acetylmuramoyl-l-alanine amidase
GVO57_RS01065	ENOG4108JQC	penicillin-binding protein 1A
GVO57_RS01070	ENOG4105CG1	Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA (By similarity)
GVO57_RS01080	ENOG4105W5Q	DNA repair protein (RadC
GVO57_RS01090	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)
GVO57_RS01095	ENOG4107WK2	Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) (By similarity)
GVO57_RS01105	ENOG4108UXA	Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA (By similarity)
GVO57_RS01115	ENOG4105CN1	protease
GVO57_RS01145	ENOG4105DA5	(ABC) transporter
GVO57_RS01155	ENOG4105D1U	peptidase U62 modulator of DNA gyrase
GVO57_RS01175	ENOG4105BZU	Histidine kinase
GVO57_RS01180	ENOG4108YZA	Nitrogen regulatory protein pii
GVO57_RS01195	ENOG4105M02	This protein specifically catalyzes the removal of signal peptides from prolipoproteins (By similarity)
GVO57_RS01205	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)
GVO57_RS01210	ENOG4105CQX	Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol (By similarity)
GVO57_RS01235	ENOG4108IAA	Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate (By similarity)
GVO57_RS01240	ENOG4107QJE	Chromosome Partitioning Protein
GVO57_RS01270	ENOG4107QRT	dEAD DEAH box helicase
GVO57_RS01290	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)
GVO57_RS01300	ENOG4105CHM	Aminotransferase
GVO57_RS01305	ENOG4105CRQ	synthase (Component I)
GVO57_RS01340	ENOG4105C9U	ATP-dependent DNA helicase RecQ
GVO57_RS01345	ENOG4105DRC	Na( ) H( ) antiporter that extrudes sodium in exchange for external protons (By similarity)
GVO57_RS01350	ENOG4105ECY	inositol monophosphatase
GVO57_RS01355	ENOG4105CMS	peptidase U62, modulator of DNA gyrase
GVO57_RS01360	ENOG4105C4G	Synthesis of 3-octaprenyl-4-hydroxybenzoate (By similarity)
GVO57_RS01365	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)
GVO57_RS01375	ENOG4105ECM	Sensor protein basS pmrB
GVO57_RS01380	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
GVO57_RS01400	ENOG4105BZU	Histidine kinase
GVO57_RS01410	ENOG4105BZU	Histidine kinase
GVO57_RS01415	ENOG4108ZXC	Two component transcriptional regulator, luxr family
GVO57_RS01445	ENOG4108JIR	Flagellum-specific ATP synthase
GVO57_RS01450	ENOG4105KHD	Has a post-transcriptional repressor function in flagellum biogenesis. Associates with the 5'-UTR of fljK mRNA and promotes its degradation (By similarity)
GVO57_RS01470	ENOG4105CPI	Metal Dependent Phosphohydrolase
GVO57_RS01510	ENOG4105CGA	flagellar basal-body rod protein FlgG
GVO57_RS01515	ENOG4105CGA	flagellar basal-body rod protein FlgG
GVO57_RS01525	ENOG4107W7W	Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation (By similarity)
GVO57_RS01540	ENOG410822I	Flagellar hook capping protein
GVO57_RS01550	ENOG4105D7B	Flagellar biosynthesis protein flha
GVO57_RS01555	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
GVO57_RS01560	ENOG4105DD5	Flagellar motor switch protein
GVO57_RS01565	ENOG4105C1F	The M ring may be actively involved in energy transduction (By similarity)
GVO57_RS01575	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)
GVO57_RS01585	ENOG4105K88	Structural component of flagellum, the bacterial motility apparatus. Part of the rod structure of flagellar basal body (By similarity)
GVO57_RS01600	ENOG4105D92	Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation (By similarity)
GVO57_RS01605	ENOG4106909	Flagellar assembly regulator FliX
GVO57_RS01610	ENOG4105D00	flagellar biosynthetic protein flhB
GVO57_RS01615	ENOG4105D19	Role in flagellar biosynthesis (By similarity)
GVO57_RS01625	ENOG4105UVF	flagellar hook-basal body complex protein fliE
GVO57_RS01630	ENOG4108ZC9	flagellar basal-body rod protein flgc
GVO57_RS01645	ENOG4105CN7	Flagellar biosynthetic protein FliP
GVO57_RS01660	ENOG4105ER2	Ompa motb domain protein
GVO57_RS01675	ENOG4108VYJ	response regulator receiver protein
GVO57_RS01680	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
GVO57_RS01690	ENOG4108V3W	Chemotaxis protein, CheW
GVO57_RS01695	ENOG4105CBS	Chea signal transduction histidine kinase
GVO57_RS01700	ENOG4108VYJ	response regulator receiver protein
GVO57_RS01710	ENOG4107RD7	Flagellar Motor Protein, MotA
GVO57_RS01715	ENOG41060XD	Flagellar protein FlaF
GVO57_RS01725	ENOG4105BZU	Histidine kinase
GVO57_RS01735	ENOG4105BZU	Histidine kinase
GVO57_RS01775	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
GVO57_RS01785	ENOG4105C1B	dTDP-glucose 4-6-dehydratase
GVO57_RS01795	ENOG4108I19	Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis (By similarity)
GVO57_RS01800	ENOG4108MX3	Polysaccharide Biosynthesis Protein
GVO57_RS01810	ENOG4105DRR	Transcriptional regulator, GntR family
GVO57_RS01815	ENOG4105CBH	Hydroxymethylglutaryl-CoA lyase
GVO57_RS01830	ENOG4105C04	l-carnitine dehydratase bile acid-inducible protein F
GVO57_RS01835	ENOG4108UAU	isochorismatase
GVO57_RS01845	ENOG4108RXX	maleylacetoacetate isomerase
GVO57_RS01870	ENOG4105CUB	amino acid
GVO57_RS01875	ENOG4108UKI	Enoyl-CoA hydratase
GVO57_RS01880	ENOG4105CSH	Transporter
GVO57_RS01885	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)
GVO57_RS01890	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)
GVO57_RS01920	ENOG4107R5M	Catalyzes the transfer of a N-acetyl-glucosamine moiety to 1D-myo-inositol 3-phosphate to produce 1D-myo-inositol 2- acetamido-2-deoxy-glucopyranoside 3-phosphate in the mycothiol biosynthesis pathway (By similarity)
GVO57_RS01925	ENOG4105DTN	riboflavin biosynthesis protein ribF
GVO57_RS01945	ENOG4105C28	cystathionine
GVO57_RS01955	ENOG4105EXX	Deoxyribodipyrimidine photolyase-related protein
GVO57_RS01970	ENOG4108M3P	Membrane
GVO57_RS01975	ENOG4105D0M	Protease HtpX homolog
GVO57_RS01985	ENOG4108YIQ	Alpha beta hydrolase
GVO57_RS02000	ENOG4108RW0	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
GVO57_RS02020	ENOG4107QYT	Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor (By similarity)
GVO57_RS02025	ENOG4105C6K	Malic enzyme
GVO57_RS02045	ENOG4105D74	hydrolase
GVO57_RS02060	ENOG4105CYC	Transferase
GVO57_RS02075	ENOG4108ZXC	Two component transcriptional regulator, luxr family
GVO57_RS02100	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)
GVO57_RS02110	ENOG4105CUT	histidyl-tRNA synthetase
GVO57_RS02120	ENOG4105F0N	pyrophosphate phospho-hydrolase
GVO57_RS02130	ENOG4105F2C	Acetyl-CoA acetyltransferase
GVO57_RS02135	ENOG4108TKH	Nitroreductase
GVO57_RS02195	ENOG4105NAU	thioesterase Superfamily protein
GVO57_RS02205	ENOG41082R8	50S ribosomal protein l32
GVO57_RS02210	ENOG4105C6B	Catalyzes the reversible formation of acyl-phosphate (acyl-PO(4)) from acyl- acyl-carrier-protein (acyl-ACP). This enzyme utilizes acyl-ACP as fatty acyl donor, but not acyl-CoA (By similarity)
GVO57_RS02215	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)
GVO57_RS02220	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)
GVO57_RS02225	ENOG4105WJX	transcriptional regulator MERR family
GVO57_RS02240	ENOG4105E6K	4-Hydroxyphenylpyruvate dioxygenase
GVO57_RS02245	ENOG4105F1J	Homogentisate 1,2-dioxygenase
GVO57_RS02260	ENOG410846T	CoA-transferase family III
GVO57_RS02330	ENOG4105C2C	drug resistance transporter, Bcr CflA
GVO57_RS02385	ENOG4105E6M	Sulphatase-modifying factor protein
GVO57_RS02405	ENOG4108Z03	MAF-like protein
GVO57_RS02410	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)
GVO57_RS02430	ENOG4105EAY	pump that utilizes the energy of pyrophosphate hydrolysis as the driving force for
GVO57_RS02435	ENOG4105CG2	Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 (By similarity)
GVO57_RS02440	ENOG4107XZX	Involved in the transcription termination process (By similarity)
GVO57_RS02450	ENOG4107VBH	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)
GVO57_RS02455	ENOG4105D74	hydrolase
GVO57_RS02460	ENOG4105EUB	pirin domain protein
GVO57_RS02495	ENOG4108JJ7	ABC transporter
GVO57_RS02505	ENOG4105C10	Electron transfer flavoprotein
GVO57_RS02510	ENOG4105BZJ	Electron transfer flavoprotein
GVO57_RS02515	ENOG4105CMV	Succinyl-CoA synthetase subunit beta
GVO57_RS02570	ENOG4105Z4Q	MltA-interacting MipA family protein
GVO57_RS02575	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)
GVO57_RS02605	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
GVO57_RS02615	ENOG4105KZX	Pterin carbinolamine dehydratase
GVO57_RS02630	ENOG4105CA5	Required for the export of heme to the periplasm for the biogenesis of c-type cytochromes (By similarity)
GVO57_RS02635	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
GVO57_RS02640	ENOG4105D98	threonine synthase
GVO57_RS02670	ENOG4105BZ9	Cytochrome C oxidase, subunit I
GVO57_RS02675	ENOG4105CV4	Subunits I and II form the functional core of the enzyme complex. Electrons originating in cytochrome c are transferred via heme a and Cu(A) to the binuclear center formed by heme a3 and Cu(B) (By similarity)
GVO57_RS02680	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)
GVO57_RS02685	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)
GVO57_RS02690	ENOG4105KJV	Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein (By similarity)
GVO57_RS02695	ENOG4105C3F	Signal peptidase i
GVO57_RS02700	ENOG4108V1T	peptidylprolyl cis-trans isomerase
GVO57_RS02720	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
GVO57_RS02730	ENOG4105JAB	phenazine biosynthesis protein, phzf family
GVO57_RS02735	ENOG41076HS	cation diffusion facilitator family transporter
GVO57_RS02740	ENOG4108S7T	Catalyzes the oxidation of either pyridoxine 5'- phosphate (PNP) or pyridoxamine 5'-phosphate (PMP) into pyridoxal 5'-phosphate (PLP) (By similarity)
GVO57_RS02745	ENOG4105CQC	Prephenate dehydratase
GVO57_RS02750	ENOG4105G9V	cytochrome C
GVO57_RS02755	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
GVO57_RS02765	ENOG4105C49	Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine (By similarity)
GVO57_RS02790	ENOG4105D10	5-enolpyruvylshikimate-3-phosphate phospholyase
GVO57_RS02795	ENOG4105CSJ	Enoyl- acyl-carrier-protein reductase NADH
GVO57_RS02805	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)
GVO57_RS02820	ENOG4105CEN	a g-specific adenine glycosylase
GVO57_RS02875	ENOG4108IUZ	ABC transporter
GVO57_RS02880	ENOG4105DTW	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
GVO57_RS02895	ENOG4108YXU	transcriptional regulator AsnC family
GVO57_RS02910	ENOG4105DP0	ferredoxin-NADP reductase
GVO57_RS02915	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)
GVO57_RS02940	ENOG4108UXN	response regulator
GVO57_RS02945	ENOG4105W0E	50S ribosomal protein L33
GVO57_RS02960	ENOG41082BR	50S ribosomal protein L35
GVO57_RS02965	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)
GVO57_RS02980	ENOG4105MP9	class II Aldolase
GVO57_RS03010	ENOG4106BRA	Membrane
GVO57_RS03030	ENOG4105D1N	poly(r)-hydroxyalkanoic acid synthase, class
GVO57_RS03040	ENOG4105CHM	Aminotransferase
GVO57_RS03115	ENOG4105K59	histidine triad (HIT) protein
GVO57_RS03120	ENOG4105CUB	amino acid
GVO57_RS03135	ENOG4105CA9	Pyruvate kinase
GVO57_RS03150	ENOG4105Y2X	UPF0335 protein
GVO57_RS03155	ENOG4105CDY	transcriptional regulatory protein
GVO57_RS03160	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)
GVO57_RS03165	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)
GVO57_RS03170	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)
GVO57_RS03175	ENOG4107YD3	Thioesterase
GVO57_RS03180	ENOG4105E02	MotA TolQ exbB proton channel
GVO57_RS03185	ENOG4108ZZF	transport protein (ExbD)
GVO57_RS03200	ENOG4105KCK	Peptidoglycan-associated lipoprotein
GVO57_RS03220	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)
GVO57_RS03225	ENOG4107QR8	Thioredoxin
GVO57_RS03235	ENOG4105KPY	Small multidrug resistance protein
GVO57_RS03290	ENOG4105CGK	Exodeoxyribonuclease III
GVO57_RS03295	ENOG4107QJN	gtp cyclohydrolase ii
GVO57_RS03300	ENOG4107UB3	HAD-superfamily hydrolase subfamily IA variant 3
GVO57_RS03305	ENOG4105DFA	alanine racemase domain protein
GVO57_RS03320	ENOG4105TXM	Domain of unknown function (DUF3576)
GVO57_RS03325	ENOG4105C8T	Leucyl-tRNA synthetase
GVO57_RS03340	ENOG4105FA0	parb-like partition protein
GVO57_RS03345	ENOG4107QJE	Chromosome Partitioning Protein
GVO57_RS03350	ENOG4107YTN	Specifically methylates the N7 position of guanine in position 527 of 16S rRNA (By similarity)
GVO57_RS03355	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)
GVO57_RS03360	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)
GVO57_RS03375	ENOG4108ZCF	integral membrane protein
GVO57_RS03380	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)
GVO57_RS03385	ENOG4108YXA	Membrane
GVO57_RS03390	ENOG4105CFZ	Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III (By similarity)
GVO57_RS03395	ENOG4105CF9	Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation dephosphorylation (By similarity)
GVO57_RS03400	ENOG4108UHJ	MAF-like protein
GVO57_RS03405	ENOG4105E2X	shikimate dehydrogenase
GVO57_RS03410	ENOG4108ZQD	Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A (By similarity)
GVO57_RS03415	ENOG4107RZZ	dna polymerase iii epsilon subunit
GVO57_RS03420	ENOG4107TNS	sigma 54 modulation protein ribosomal protein S30ea
GVO57_RS03425	ENOG4107RM2	PTS IIA-like nitrogen-regulatory protein PtsN
GVO57_RS03460	ENOG4108ZZ3	UPF0260 protein
GVO57_RS03470	ENOG4108JQC	penicillin-binding protein 1A
GVO57_RS03475	ENOG4105E0X	reductase
GVO57_RS03495	ENOG4105D86	that it carries out the mismatch recognition step. This protein has a weak ATPase activity (By similarity)
GVO57_RS03500	ENOG4105E1P	Modifies, by uridylylation or deuridylylation the PII (GlnB) regulatory protein (By similarity)
GVO57_RS03505	ENOG4107ZSV	Receptor
GVO57_RS03530	ENOG4105D7A	ATP-binding protein
GVO57_RS03535	ENOG4105C0H	protease
GVO57_RS03545	ENOG4107QJR	hflk protein
GVO57_RS03560	ENOG4105BZH	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
GVO57_RS03580	ENOG4105E05	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
GVO57_RS03600	ENOG4105FR1	rard protein
GVO57_RS03615	ENOG4105DR5	peptidase
GVO57_RS03630	ENOG4108Z4U	Ferredoxin
GVO57_RS03635	ENOG4108VJ1	Transcriptional regulator (CarD family
GVO57_RS03650	ENOG4105CJW	magnesium transporter
GVO57_RS03655	ENOG4108R5K	PPIases accelerate the folding of proteins (By similarity)
GVO57_RS03660	ENOG41082CG	Protein CrcB homolog
GVO57_RS03670	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)
GVO57_RS03690	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
GVO57_RS03700	ENOG4105KPZ	phosphoribosyl-atp pyrophosphatase
GVO57_RS03710	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)
GVO57_RS03715	ENOG4105CJV	Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase
GVO57_RS03725	ENOG4105ECC	imidazole-glycerol-phosphate dehydratase
GVO57_RS03735	ENOG4105C9Q	fumarate hydratase class II
GVO57_RS03775	ENOG4105EQK	-acetyltransferase
GVO57_RS03780	ENOG4107R6G	Catalyzes the S-adenosylmethionine monomethyl esterification of trans-aconitate (By similarity)
GVO57_RS03865	ENOG4105D3Q	Sugar transferase
GVO57_RS03885	ENOG4107T0X	DNA ligase
GVO57_RS03890	ENOG4107TK4	histidinol-phosphate phosphatase
GVO57_RS03895	ENOG4105FAT	Acyl-transferase
GVO57_RS03900	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)
GVO57_RS03905	ENOG4108IYU	L-aspartate oxidase
GVO57_RS03915	ENOG4108TWJ	NADH dehydrogenase subunit 5
GVO57_RS03920	ENOG4105EVH	UPF0753 protein
GVO57_RS03945	ENOG4105CC9	acyl-Coa dehydrogenase
GVO57_RS03950	ENOG4105C1G	acyl-Coa dehydrogenase
GVO57_RS03955	ENOG4105C29	acyl-CoA thioesterase
GVO57_RS03965	ENOG4105C1G	acyl-Coa dehydrogenase
GVO57_RS03975	ENOG4105KDC	50s ribosomal protein l28
GVO57_RS03985	ENOG4105ER2	Ompa motb domain protein
GVO57_RS03990	ENOG4107RD7	Flagellar Motor Protein, MotA
GVO57_RS04020	ENOG4105D92	Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation (By similarity)
GVO57_RS04030	ENOG4105CGA	flagellar basal-body rod protein FlgG
GVO57_RS04045	ENOG4105W00	Flagellar hook capping protein
GVO57_RS04050	ENOG4108ZC9	flagellar basal-body rod protein flgc
GVO57_RS04095	ENOG4105DN4	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
GVO57_RS04105	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
GVO57_RS04110	ENOG4105X6K	flagellar hook-basal body complex protein fliE
GVO57_RS04115	ENOG4105C1F	The M ring may be actively involved in energy transduction (By similarity)
GVO57_RS04120	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)
GVO57_RS04130	ENOG4108JIR	Flagellum-specific ATP synthase
GVO57_RS04155	ENOG4105DD5	Flagellar motor switch protein
GVO57_RS04165	ENOG4105CN7	Flagellar biosynthetic protein FliP
GVO57_RS04170	ENOG4105VS8	Flagellar biosynthetic protein fliq
GVO57_RS04200	ENOG4105C4K	Nad synthetase
GVO57_RS04205	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)
GVO57_RS04210	ENOG4107104	thymidine kinase
GVO57_RS04220	ENOG4105BZU	Histidine kinase
GVO57_RS04225	ENOG4105C2M	dna polymerase I
GVO57_RS04230	ENOG4108M8H	domain protein
GVO57_RS04250	ENOG4105DC1	bifunctional purine biosynthesis protein purh
GVO57_RS04255	ENOG4105DYT	3-hydroxyacyl-CoA dehydrogenase
GVO57_RS04260	ENOG4105CHR	reductase
GVO57_RS04265	ENOG4105CHR	reductase
GVO57_RS04280	ENOG4105C1G	acyl-Coa dehydrogenase
GVO57_RS04295	ENOG4105DNH	Major Facilitator
GVO57_RS04300	ENOG4105C1G	acyl-Coa dehydrogenase
GVO57_RS04305	ENOG4105CHR	reductase
GVO57_RS04330	ENOG4105EIZ	Catalyzes the conversion of 6-carboxy-5,6,7,8- tetrahydropterin (CPH4) to 7-carboxy-7-deazaguanine (CDG) (By similarity)
GVO57_RS04345	ENOG4105D6W	Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps (By similarity)
GVO57_RS04355	ENOG4105CSF	NADPH-dependent glycerol-3-phosphate dehydrogenase
GVO57_RS04375	ENOG4105DWV	Homoserine O-trans-acetylase
GVO57_RS04395	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
GVO57_RS04400	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
GVO57_RS04410	ENOG4105DK7	lysyl-tRNA synthetase
GVO57_RS04430	ENOG4108ZI0	d,d-heptose 1,7-bisphosphate phosphatase
GVO57_RS04435	ENOG4107Z67	Catalyzes the ADP transfer to D-glycero-D-manno-heptose 1-phosphate, yielding ADP-D,D-heptose (By similarity)
GVO57_RS04440	ENOG4105F55	Catalyzes the isomerization of sedoheptulose 7-phosphate in D-glycero-D-manno-heptose 7-phosphate (By similarity)
GVO57_RS04485	ENOG4105DDI	hemolysin-type calcium-binding region
GVO57_RS04500	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
GVO57_RS04515	ENOG4105FAW	cDP-glucose 4,6-dehydratase
GVO57_RS04520	ENOG4105EJZ	Glucose-1-phosphate cytidylyltransferase
GVO57_RS04535	ENOG4108F2G	Chain length determinant protein
GVO57_RS04565	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
GVO57_RS04570	ENOG4105CBT	Fructose-1,6-bisphosphatase
GVO57_RS04580	ENOG4105D6E	homoserine dehydrogenase
GVO57_RS04605	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
GVO57_RS04610	ENOG4108NWD	Cytochrome
GVO57_RS04615	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)
GVO57_RS04620	ENOG4105CV9	cyclopropane-fatty-acyl-phospholipid synthase
GVO57_RS04625	ENOG4105CDH	Citrulline--aspartate ligase
GVO57_RS04650	ENOG4105CKK	Glycosyl transferase, family 2
GVO57_RS04670	ENOG4105EZI	multiple antibiotic resistance (MarC)-related protein
GVO57_RS04675	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)
GVO57_RS04685	ENOG4105CAS	nag kinase
GVO57_RS04725	ENOG4106SNF	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane
GVO57_RS04735	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)
GVO57_RS04755	ENOG4105C77	DNA ligase that catalyzes the formation of phosphodiester linkages between 5'-phosphoryl and 3'-hydroxyl groups in double-stranded DNA using NAD as a coenzyme and as the energy source for the reaction. It is essential for DNA replication and repair of damaged DNA (By similarity)
GVO57_RS04765	ENOG4105MIR	Phenylalanine 4-monooxygenase
GVO57_RS04770	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
GVO57_RS04775	ENOG4105CHR	reductase
GVO57_RS04780	ENOG4108W2P	Methyl-accepting chemotaxis
GVO57_RS04795	ENOG4105C00	Succinate dehydrogenase (Flavoprotein subunit)
GVO57_RS04810	ENOG4105EMN	RNA polymerase sigma factor
GVO57_RS04820	ENOG4105HFZ	Membrane
GVO57_RS04825	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)
GVO57_RS04830	ENOG4108R5K	PPIases accelerate the folding of proteins (By similarity)
GVO57_RS04835	ENOG4108ZEF	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate (By similarity)
GVO57_RS04840	ENOG4105CTB	Polyprenyl synthetase
GVO57_RS04855	ENOG4108ZTZ	UPF0262 protein
GVO57_RS04860	ENOG4105KG3	cytidine deaminase
GVO57_RS04865	ENOG4105DHP	deoxycytidine triphosphate deaminase
GVO57_RS04870	ENOG4105EHE	chorismate mutase- prephenate dehydrogenase
GVO57_RS04875	ENOG4105EAH	synthase
GVO57_RS04880	ENOG4105CSV	Glutaminase
GVO57_RS04885	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
GVO57_RS04895	ENOG4105BZY	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
GVO57_RS04920	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)
GVO57_RS04925	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)
GVO57_RS04940	ENOG4108NVM	synthesis repressor PhaR
GVO57_RS04955	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)
GVO57_RS04960	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
GVO57_RS04965	ENOG4105CSH	Transporter
GVO57_RS04995	ENOG4107ZDE	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
GVO57_RS05005	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)
GVO57_RS05015	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)
GVO57_RS05020	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
GVO57_RS05025	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)
GVO57_RS05035	ENOG4105K85	Involved in the cellular defense against the biological effects of O6-methylguanine (O6-MeG) in DNA. Repairs alkylated guanine in DNA by stoichiometrically transferring the alkyl group at the O-6 position to a cysteine residue in the enzyme. This is a suicide reaction the enzyme is irreversibly inactivated (By similarity)
GVO57_RS05040	ENOG4105C0H	protease
GVO57_RS05045	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)
GVO57_RS05050	ENOG4105C25	Primosomal protein n'
GVO57_RS05055	ENOG4108ZHJ	Organic hydroperoxide resistance protein
GVO57_RS05070	ENOG4105CW3	Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway (By similarity)
GVO57_RS05080	ENOG4107T5V	SNARE associated Golgi
GVO57_RS05085	ENOG4105D7Z	glutathione synthase
GVO57_RS05095	ENOG4105CU0	Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA (By similarity)
GVO57_RS05105	ENOG4105D9N	nucleoside
GVO57_RS05110	ENOG4108R5P	Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery (By similarity)
GVO57_RS05115	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)
GVO57_RS05120	ENOG4108IIJ	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
GVO57_RS05125	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
GVO57_RS05145	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)
GVO57_RS05160	ENOG4105CH7	arginosuccinase
GVO57_RS05165	ENOG4107ZT5	Thiol disulfide interchange protein
GVO57_RS05170	ENOG4105DMJ	Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate (By similarity)
GVO57_RS05185	ENOG4108Z4V	iron-sulfur cluster assembly
GVO57_RS05190	ENOG4105VG1	fes assembly suf system protein
GVO57_RS05200	ENOG4105JRK	feS assembly protein SufD
GVO57_RS05230	ENOG4105C7B	Threonine dehydratase
GVO57_RS05235	ENOG4105DWA	May conjugate Arg from its aminoacyl-tRNA to the N- termini of proteins containing an N-terminal aspartate or glutamate
GVO57_RS05240	ENOG4105EFQ	Two component transcriptional regulator (Winged helix family
GVO57_RS05250	ENOG4105CJH	Alcohol dehydrogenase zinc-binding domain protein
GVO57_RS05255	ENOG4105CGZ	zinc metallopeptidase
GVO57_RS05275	ENOG4105CH2	amidohydrolase
GVO57_RS05285	ENOG410903D	sensor protein
GVO57_RS05330	ENOG4105HJ8	Catalyzes the oxidative cleavage of the L-tryptophan (L- Trp) pyrrole ring (By similarity)
GVO57_RS05335	ENOG4105C9B	Cysteine desulfurase
GVO57_RS05350	ENOG4105KK9	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
GVO57_RS05360	ENOG4105C12	Phosphoribosylglycinamide synthetase
GVO57_RS05385	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)
GVO57_RS05400	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
GVO57_RS05420	ENOG4105CY8	phosphoribosylaminoimidazole carboxylase atpase subunit
GVO57_RS05425	ENOG4108UM6	Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) (By similarity)
GVO57_RS05430	ENOG4105DKJ	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
GVO57_RS05445	ENOG4105YK5	50S ribosomal protein L36
GVO57_RS05450	ENOG4105EJU	HAD-superfamily hydrolase subfamily IA variant 3
GVO57_RS05455	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)
GVO57_RS05460	ENOG4107RNH	Outer membrane receptor FepA
GVO57_RS05470	ENOG4108HRK	Histidine kinase
GVO57_RS05475	ENOG4105DY9	regulatoR
GVO57_RS05500	ENOG4106MAR	Phosphate-selective porin O and P
GVO57_RS05540	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)
GVO57_RS05555	ENOG4105CGT	Catalyzes the transfer of a phosphate group to glutamate to form glutamate 5-phosphate which rapidly cyclizes to 5- oxoproline (By similarity)
GVO57_RS05560	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
GVO57_RS05590	ENOG4108HMW	glycyl-tRNA synthetase, alpha subunit
GVO57_RS05595	ENOG4105C38	Glycyl-tRNA synthetase beta subunit
GVO57_RS05600	ENOG4108HRN	Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate (By similarity)
GVO57_RS05645	ENOG4105CWG	Catalyzes the last two steps in the biosynthesis of 5- methylaminomethyl-2-thiouridine (mnm(5)s(2)U) at the wobble position (U34) in tRNA. Catalyzes the FAD-dependent demodification of cmnm(5)s(2)U34 to nm(5)s(2)U34, followed by the transfer of a methyl group from S-adenosyl-L-methionine to nm(5)s(2)U34, to form mnm(5)s(2)U34 (By similarity)
GVO57_RS05650	ENOG4107ZJC	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
GVO57_RS05665	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)
GVO57_RS05670	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)
GVO57_RS05675	ENOG41089I4	Inherit from COG: Glycosyl transferase, family 2
GVO57_RS05690	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)
GVO57_RS05710	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)
GVO57_RS05720	ENOG4105DJ0	Poly(A) Polymerase
GVO57_RS05725	ENOG4105P8F	nudix hydrolase
GVO57_RS05740	ENOG4105CYM	Glutathione S-transferase
GVO57_RS05745	ENOG4105H9W	Short-chain dehydrogenase reductase Sdr
GVO57_RS05750	ENOG4105XUA	cytochrome c
GVO57_RS05810	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)
GVO57_RS05820	ENOG4105E5V	Participates in transcription elongation, termination and antitermination (By similarity)
GVO57_RS05830	ENOG4107SDU	Methyl-accepting chemotaxis
GVO57_RS05855	ENOG4105VEQ	Cold shock protein
GVO57_RS05875	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)
GVO57_RS05880	ENOG4107QJE	Chromosome Partitioning Protein
GVO57_RS05920	ENOG4105BZU	Histidine kinase
GVO57_RS05925	ENOG4105BZU	Histidine kinase
GVO57_RS06000	ENOG4107ZSV	Receptor
GVO57_RS06060	ENOG4108ZXC	Two component transcriptional regulator, luxr family
GVO57_RS06065	ENOG4105BZU	Histidine kinase
GVO57_RS06075	ENOG41080XP	Cbs domain
GVO57_RS06090	ENOG4108JJ6	Type I secretion system ATPase
GVO57_RS06140	ENOG4105EEX	Two component transcriptional regulator (Winged helix family
GVO57_RS06150	ENOG4108R80	One of the components of the high-affinity ATP-driven potassium transport (or KDP) system, which catalyzes the hydrolysis of ATP coupled with the exchange of hydrogen and potassium ions. The C subunit may be involved in assembly of the KDP complex (By similarity)
GVO57_RS06155	ENOG4105C8X	One of the components of the high-affinity ATP-driven potassium transport (or KDP) system, which catalyzes the hydrolysis of ATP coupled with the exchange of hydrogen and potassium ions (By similarity)
GVO57_RS06160	ENOG4105D9K	One of the components of the high-affinity ATP-driven potassium transport (or KDP) system, which catalyzes the hydrolysis of ATP coupled with the exchange of hydrogen and potassium ions (By similarity)
GVO57_RS06195	ENOG4108S01	response regulator
GVO57_RS06200	ENOG4108ZGX	Histidine kinase
GVO57_RS06205	ENOG4105KCT	ABC transporter
GVO57_RS06210	ENOG4108M15	ABC transporter
GVO57_RS06230	ENOG4105CKI	cobalamin synthesis protein
GVO57_RS06245	ENOG4108UDW	Transcriptional regulator, luxr family
GVO57_RS06315	ENOG4105CN1	protease
GVO57_RS06375	ENOG4105E0X	reductase
GVO57_RS06405	ENOG4105C5H	ABC transporter
GVO57_RS06415	ENOG4105XJC	Two component transcriptional regulator (Winged helix family
GVO57_RS06420	ENOG4105IFJ	Histidine kinase
GVO57_RS06425	ENOG4105C9K	Endothelin-converting enzyme 1
GVO57_RS06435	ENOG4105CDZ	Carboxymethylenebutenolidase (EC 3.1.1.45)
GVO57_RS06440	ENOG4105DRY	peptidase s9 prolyl oligopeptidase active site domain protein
GVO57_RS06445	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)
GVO57_RS06465	ENOG4105K7D	Required for maturation of 30S ribosomal subunits (By similarity)
GVO57_RS06495	ENOG4105D1H	recombination factor protein RarA
GVO57_RS06515	ENOG4105E3B	Multicopper oxidase
GVO57_RS06555	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
GVO57_RS06585	ENOG4107RCQ	(CBS) domain
GVO57_RS06590	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)
GVO57_RS06595	ENOG4105C9A	Phoh family
GVO57_RS06600	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)
GVO57_RS06610	ENOG41090R7	Ferric uptake
GVO57_RS06615	ENOG4108YXV	Transcriptional regulator
GVO57_RS06625	ENOG41072GX	Peptidase M22 Glycoprotease
GVO57_RS06630	ENOG4108RDT	NADH dehydrogenase NAD(P)H nitroreductase)
GVO57_RS06635	ENOG41083MR	nifu domain-containing protein
GVO57_RS06645	ENOG4105C1J	atp-dependent rna helicase
GVO57_RS06655	ENOG4105C48	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
GVO57_RS06665	ENOG4105D43	The glycine cleavage system catalyzes the degradation of glycine (By similarity)
GVO57_RS06670	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)
GVO57_RS06675	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
GVO57_RS06680	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
GVO57_RS06695	ENOG4105C8Q	Methyl-accepting chemotaxis
GVO57_RS06700	ENOG4105C1G	acyl-Coa dehydrogenase
GVO57_RS06710	ENOG4107R0V	Pyruvate dehydrogenase
GVO57_RS06715	ENOG4105CPP	Dehydrogenase, E1 component
GVO57_RS06720	ENOG4107QSN	dihydrolipoamide acetyltransferase
GVO57_RS06735	ENOG4108UN4	phage SPO1 DNA polymerase-related protein
GVO57_RS06770	ENOG4105CAK	Cell division ATP-binding protein ftsE
GVO57_RS06805	ENOG4105CIH	Imidazole acetol-phosphate transaminase
GVO57_RS06810	ENOG4105DJV	ribulose-phosphate 3-epimerase
GVO57_RS06820	ENOG4105C1X	Bifunctional enzyme with both catalase and broad- spectrum peroxidase activity (By similarity)
GVO57_RS06830	ENOG4105C0V	Provides the sole de novo source of dTMP for DNA biosynthesis (By similarity)
GVO57_RS06845	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)
GVO57_RS06860	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)
GVO57_RS06870	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
GVO57_RS06890	ENOG4105CE1	Ferrous iron transport protein b
GVO57_RS06895	ENOG4108UUM	single-stranded DNA-binding protein
GVO57_RS06910	ENOG4107ZSV	Receptor
GVO57_RS06915	ENOG4105EUJ	GTP cyclohydrolase i
GVO57_RS06920	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
GVO57_RS06925	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)
GVO57_RS06955	ENOG4105CV1	Transketolase (EC 2.2.1.1)
GVO57_RS06970	ENOG4105BZA	Phosphoglycerate kinase
GVO57_RS06980	ENOG4106I2R	Coenzyme F420 hydrogenase dehydrogenase, beta
GVO57_RS06985	ENOG4105EIE	fructose-bisphosphate aldolase
GVO57_RS06990	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)
GVO57_RS06995	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)
GVO57_RS07000	ENOG4105ECY	inositol monophosphatase
GVO57_RS07015	ENOG4105KWU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
GVO57_RS07020	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)
GVO57_RS07025	ENOG4105CYU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
GVO57_RS07030	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)
GVO57_RS07040	ENOG4107QIZ	NADH dehydrogenase
GVO57_RS07050	ENOG4108IEH	NADH dehydrogenase subunit g
GVO57_RS07055	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)
GVO57_RS07060	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)
GVO57_RS07065	ENOG4105DF2	NADH dehydrogenase subunit j
GVO57_RS07070	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)
GVO57_RS07075	ENOG4105D65	subunit l
GVO57_RS07080	ENOG4105C8S	subunit m
GVO57_RS07085	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)
GVO57_RS07090	ENOG4105HJX	Biotin- acetyl-CoA-carboxylase ligase
GVO57_RS07095	ENOG4107QNB	Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis (By similarity)
GVO57_RS07125	ENOG4105CHU	acetyl-coa acetyltransferase
GVO57_RS07140	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
GVO57_RS07145	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)
GVO57_RS07150	ENOG4105CEY	Amp-dependent synthetase and ligase
GVO57_RS07155	ENOG4105DXM	phenylacetic acid degradation protein
GVO57_RS07165	ENOG4105C3G	gtp-binding protein
GVO57_RS07175	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
GVO57_RS07180	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)
GVO57_RS07305	ENOG4105CF2	Mu-like prophage FluMu protein GP28
GVO57_RS07340	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)
GVO57_RS07375	ENOG4105HVQ	Regulatory factor of maltose metabolism
GVO57_RS07380	ENOG4105DS7	Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair (By similarity)
GVO57_RS07515	ENOG4105Y2X	UPF0335 protein
GVO57_RS07535	ENOG4108Z7T	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
GVO57_RS07545	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)
GVO57_RS07605	ENOG4105CMY	5-enolpyruvylshikimate-3-phosphate synthase
GVO57_RS07615	ENOG4105CAT	Cytidine monophosphate kinase
GVO57_RS07625	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)
GVO57_RS07630	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)
GVO57_RS07640	ENOG4108UMW	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
GVO57_RS07660	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)
GVO57_RS07665	ENOG4108VZM	50s ribosomal protein L10
GVO57_RS07670	ENOG4105FC8	fad dependent oxidoreductase
GVO57_RS07690	ENOG4105CK2	sodium dicarboxylate symporter
GVO57_RS07700	ENOG4108VAC	response regulator
GVO57_RS07705	ENOG4108KHS	signal transduction Histidine kinase
GVO57_RS07735	ENOG4105CY0	Metallo-Beta-Lactamase
GVO57_RS07740	ENOG4105C5F	glutamine synthetase
GVO57_RS07745	ENOG4108YZA	Nitrogen regulatory protein pii
GVO57_RS07755	ENOG4105CA1	Removes the N-terminal methionine from nascent proteins (By similarity)
GVO57_RS07780	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
GVO57_RS07810	ENOG4105CI2	imidazolone-5-propionate hydrolase
GVO57_RS07815	ENOG4105CF3	3-Hydroxyisobutyrate dehydrogenase
GVO57_RS07825	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)
GVO57_RS07860	ENOG4105CPF	Cell wall formation (By similarity)
GVO57_RS07880	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)
GVO57_RS07885	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)
GVO57_RS07895	ENOG4105D6Z	AFG1 family ATPase
GVO57_RS07900	ENOG4105C80	Catalyzes the reversible oxidation of malate to oxaloacetate (By similarity)
GVO57_RS07910	ENOG4105C7P	2-oxoglutarate dehydrogenase, E1
GVO57_RS07915	ENOG4105C7S	Dehydrogenase
GVO57_RS07920	ENOG4107QN2	dihydrolipoyl dehydrogenase
GVO57_RS07930	ENOG4105EN6	Membrane
GVO57_RS07935	ENOG4107Y3V	-acetyltransferase
GVO57_RS07940	ENOG4105D07	Signal peptide peptidase, SppA
GVO57_RS07945	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
GVO57_RS07950	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
GVO57_RS07960	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
GVO57_RS07985	ENOG4105QV4	Tryptophan halogenase
GVO57_RS07995	ENOG4105CG3	alpha amylase, catalytic region
GVO57_RS08035	ENOG41090KH	cytochrome o ubiquinol oxidase (subunit iv)
GVO57_RS08040	ENOG4105CCU	oxidase (Subunit III)
GVO57_RS08045	ENOG4105BZ9	Cytochrome C oxidase, subunit I
GVO57_RS08050	ENOG4105E2S	oxidase) subunit II
GVO57_RS08075	ENOG4105DH2	Converts cobyric acid to cobinamide by the addition of aminopropanol on the F carboxylic group (By similarity)
GVO57_RS08080	ENOG4105CAA	catalyzes amidations at positions B, D, E, and G on adenosylcobyrinic A,C-diamide. NH(2) groups are provided by glutamine, and one molecule of ATP is hydrogenolyzed for each amidation (By similarity)
GVO57_RS08090	ENOG4105EHG	Permease protein
GVO57_RS08100	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)
GVO57_RS08105	ENOG41068B1	Cob-I-yrinic acid a,c-diamide adenosyltransferase
GVO57_RS08125	ENOG4105CEY	Amp-dependent synthetase and ligase
GVO57_RS08135	ENOG4108RIR	Molybdenum cofactor biosynthesis protein
GVO57_RS08140	ENOG4105E4C	Lytic transglycosylase catalytic
GVO57_RS08150	ENOG4105DWH	electron transfer flavoprotein-ubiquinone oxidoreductase
GVO57_RS08165	ENOG4105C8Q	Methyl-accepting chemotaxis
GVO57_RS08170	ENOG4105CTR	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
GVO57_RS08185	ENOG4105C01	Dihydroxy-acid dehydratase
GVO57_RS08230	ENOG4105DHZ	alpha beta
GVO57_RS08255	ENOG4107QMP	dna polymerase iii subunits gamma and tau
GVO57_RS08260	ENOG4105KDX	Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection (By similarity)
GVO57_RS08300	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
GVO57_RS08305	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
GVO57_RS08310	ENOG4105BZU	Histidine kinase
GVO57_RS08320	ENOG4108VBV	N-Acetylmuramoyl-L-alanine amidase
GVO57_RS08330	ENOG4105DJ1	Phosphoenolpyruvate Carboxylase
GVO57_RS08345	ENOG4105CM3	Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate (By similarity)
GVO57_RS08355	ENOG4105W5Q	DNA repair protein (RadC
GVO57_RS08370	ENOG410689M	(LipO)protein
GVO57_RS08385	ENOG4105EE4	it plays a direct role in the translocation of protons across the membrane (By similarity)
GVO57_RS08390	ENOG4105VD1	ATP synthase subunit C
GVO57_RS08395	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)
GVO57_RS08400	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)
GVO57_RS08410	ENOG4108VHC	Short-chain dehydrogenase reductase Sdr
GVO57_RS08415	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)
GVO57_RS08420	ENOG4107UIS	Involved in DNA repair and RecF pathway recombination (By similarity)
GVO57_RS08425	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)
GVO57_RS08435	ENOG4105NWN	ApaG protein
GVO57_RS08460	ENOG4105GVR	general secretion pathway protein D
GVO57_RS08465	ENOG4107QHF	type ii secretion system protein e
GVO57_RS08475	ENOG4108VAU	general secretion pathway protein G
GVO57_RS08500	ENOG4105R04	type II secretion system protein K
GVO57_RS08540	ENOG41060IM	Heme exporter protein
GVO57_RS08550	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)
GVO57_RS08555	ENOG4105DA4	cytochrome c-type biogenesis protein
GVO57_RS08560	ENOG4107QX9	Thiol disulfide interChange protein
GVO57_RS08565	ENOG4105KWW	Biogenesis protein
GVO57_RS08570	ENOG4106FI7	cytochrome c-type biogenesis protein
GVO57_RS08580	ENOG4105DCF	alanine dehydrogenase
GVO57_RS08585	ENOG4105EW9	transcriptional regulator AsnC family
GVO57_RS08590	ENOG4105DFH	Transport of potassium into the cell (By similarity)
GVO57_RS08595	ENOG4105CYM	Glutathione S-transferase
GVO57_RS08605	ENOG4108EQM	faD-dependent pyridine nucleotide-disulfide oxidoreductase
GVO57_RS08665	ENOG4105HMI	Membrane
GVO57_RS08670	ENOG4105DJG	MaoC domain protein dehydratase
GVO57_RS08680	ENOG4105C1G	acyl-Coa dehydrogenase
GVO57_RS08685	ENOG4107QX3	carboxylase
GVO57_RS08700	ENOG4107YFT	Nadph-dependent fmn reductase
GVO57_RS08705	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
GVO57_RS08715	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
GVO57_RS08725	ENOG4105K8U	2-Amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase
GVO57_RS08730	ENOG4105E50	uracil-dna glycosylase
GVO57_RS08735	ENOG4105ET3	Reduction of activated sulfate into sulfite (By similarity)
GVO57_RS08760	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)
GVO57_RS08765	ENOG4105C26	Dehydrogenase
GVO57_RS08770	ENOG4105CNG	UPF0061 protein
GVO57_RS08825	ENOG4105C26	Dehydrogenase
GVO57_RS08845	ENOG4105CF3	3-Hydroxyisobutyrate dehydrogenase
GVO57_RS08855	ENOG4105C6V	Glycerol-3-phosphate dehydrogenase
GVO57_RS08860	ENOG4105C40	3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs (By similarity)
GVO57_RS08890	ENOG4105D06	uba thif-type nad fad binding protein
GVO57_RS08930	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)
GVO57_RS08945	ENOG4105E3A	(ABC) transporter
GVO57_RS08960	ENOG4105C8Y	Acetylornithine aminotransferase
GVO57_RS08965	ENOG4105DBV	ornithine carbamoyltransferase
GVO57_RS08970	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)
GVO57_RS08980	ENOG4107ENK	receptor
GVO57_RS08985	ENOG4107RGH	Aldehyde dehydrogenase
GVO57_RS09005	ENOG4105DFU	Cell wall formation (By similarity)
GVO57_RS09015	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)
GVO57_RS09025	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)
GVO57_RS09065	ENOG41087YS	Phage shock protein A
GVO57_RS09070	ENOG4105E51	psp operon transcriptional activator
GVO57_RS09080	ENOG4107835	probably involved in intracellular septation (By similarity)
GVO57_RS09085	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)
GVO57_RS09090	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)
GVO57_RS09095	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)
GVO57_RS09100	ENOG4105BZU	Histidine kinase
GVO57_RS09110	ENOG4105C8N	cysteinyl-tRNA synthetase
GVO57_RS09115	ENOG4105BZU	Histidine kinase
GVO57_RS09120	ENOG4105VG0	50S ribosomal protein l34
GVO57_RS09125	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)
GVO57_RS09130	ENOG4105VAS	Could be involved in insertion of integral membrane proteins into the membrane (By similarity)
GVO57_RS09140	ENOG4105WHM	Necessary for normal cell division and for the maintenance of normal septation (By similarity)
GVO57_RS09145	ENOG4108TGY	Glutathione S-transferase
GVO57_RS09150	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)
GVO57_RS09160	ENOG4105D7W	serine acetyltransferase
GVO57_RS09170	ENOG4105KF3	Short-chain dehydrogenase reductase Sdr
GVO57_RS09190	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
GVO57_RS09195	ENOG4105KM4	Acetyl-CoA carboxylase, biotin carboxyl carrier protein
GVO57_RS09200	ENOG4108Z38	Catalyzes a trans-dehydration via an enolate intermediate (By similarity)
GVO57_RS09215	ENOG4107TQK	Catalyzes the oxidation of the C8 methyl side group on heme O porphyrin ring into a formyl group (By similarity)
GVO57_RS09230	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)
GVO57_RS09260	ENOG4108W2P	Methyl-accepting chemotaxis
GVO57_RS09265	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)
GVO57_RS09275	ENOG4108Z6Z	Transcriptional regulator
GVO57_RS09280	ENOG4105CSU	acyl-Coa dehydrogenase
GVO57_RS09295	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)
GVO57_RS09300	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)
GVO57_RS09400	ENOG4105M6F	mutator MutT protein
GVO57_RS09415	ENOG4105VW4	glutaredoxin 3
GVO57_RS09485	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)
GVO57_RS09495	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
GVO57_RS09515	ENOG4105E2Y	ABC, transporter
GVO57_RS09520	ENOG41061ZR	Transcriptional regulator
GVO57_RS09530	ENOG4105E0K	tonB-dependent siderophore receptor
GVO57_RS09535	ENOG4105CIG	ABC transporter
GVO57_RS09550	ENOG4105BZU	Histidine kinase
GVO57_RS09555	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
GVO57_RS09580	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)
GVO57_RS09615	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
GVO57_RS09660	ENOG4107QXI	Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs (By similarity)
GVO57_RS09675	ENOG4105C7V	phospho-2-dehydro-3-deoxyheptonate aldolase
GVO57_RS09680	ENOG4106FI7	cytochrome c-type biogenesis protein
GVO57_RS09690	ENOG4108RWN	rrna methyltransferase
GVO57_RS09695	ENOG41080Z8	PHOSPHOCARRIER protein
GVO57_RS09700	ENOG4105YHU	PTS system
GVO57_RS09705	ENOG4105C21	Displays ATPase and GTPase activities (By similarity)
GVO57_RS09715	ENOG4105EB3	Histidine kinase
GVO57_RS09720	ENOG4105E3W	Two component transcriptional regulator (Winged helix family
GVO57_RS09730	ENOG4105CYJ	ribosomal RNA small subunit methyltransferase B
GVO57_RS09755	ENOG4105CHF	Glutathione S-transferase
GVO57_RS09760	ENOG4105CK2	sodium dicarboxylate symporter
GVO57_RS09765	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)
GVO57_RS09780	ENOG4105C5H	ABC transporter
GVO57_RS09790	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)
GVO57_RS09795	ENOG4105CM1	Catalyzes, together with MoaC, the conversion of 5'-GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
GVO57_RS09805	ENOG4108JA2	transcriptioN-repair coupling factor
GVO57_RS09815	ENOG4105CB5	ATP-dependent DNA helicase recG
GVO57_RS09825	ENOG4107QP8	phosphohexose isomerase
GVO57_RS09830	ENOG4105C3F	Signal peptidase i
GVO57_RS09840	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)
GVO57_RS09845	ENOG4105DS0	Transcriptional regulator, Crp Fnr family
GVO57_RS09850	ENOG4105D21	Phosphoribosylformylglycinamidine synthase I
GVO57_RS09855	ENOG4105VR9	phosphoribosylformylglycinamidine synthase
GVO57_RS09885	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
GVO57_RS09890	ENOG4105CHR	reductase
GVO57_RS09915	ENOG4105KVH	Transcriptional regulator
GVO57_RS09920	ENOG4105ECR	NmrA family
GVO57_RS09925	ENOG4105KUZ	arsenate reductase
GVO57_RS09930	ENOG4105C3M	thioredoxin reductase
GVO57_RS09960	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
GVO57_RS09970	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)
GVO57_RS09975	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)
GVO57_RS10000	ENOG4105DI7	Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs (By similarity)
GVO57_RS10005	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)
GVO57_RS10010	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)
GVO57_RS10015	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)
GVO57_RS10035	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
GVO57_RS10040	ENOG4105K5M	30s ribosomal protein S16
GVO57_RS10045	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)
GVO57_RS10055	ENOG4107QP3	malate synthase g
GVO57_RS10065	ENOG4105BZ1	(ABC) transporter
GVO57_RS10080	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)
GVO57_RS10085	ENOG4105C3Y	UTP-glucose-1-phosphate uridylyltransferase
GVO57_RS10100	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)
GVO57_RS10105	ENOG4105CSU	acyl-Coa dehydrogenase
GVO57_RS10110	ENOG4105DDT	Hydrolyzes diadenosine 5',5'''-P1,P4-tetraphosphate to yield ADP (By similarity)
GVO57_RS10115	ENOG4105FDP	GntR family transcriptional regulator
GVO57_RS10120	ENOG41069NU	Nitroreductase
GVO57_RS10130	ENOG4105DUX	Transporter
GVO57_RS10135	ENOG4105D6T	Catalyzes the deamination of 5-methylthioadenosine and S-adenosyl-L-homocysteine into 5-methylthioinosine and S-inosyl-L- homocysteine, respectively. Is also able to deaminate adenosine (By similarity)
GVO57_RS10150	ENOG4105CPC	Aldo Keto reductase
GVO57_RS10155	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
GVO57_RS10160	ENOG4105XDF	Protein of unknown function (DUF1272)
GVO57_RS10165	ENOG4105DWF	phosphomethylpyrimidine kinase
GVO57_RS10170	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
GVO57_RS10180	ENOG4105EEI	dihydropteroate synthase
GVO57_RS10195	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)
GVO57_RS10200	ENOG4105W8H	transhydrogenase (subunit alpha
GVO57_RS10205	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)
GVO57_RS10225	ENOG4105D2H	Uronic isomerase
GVO57_RS10235	ENOG4105DEI	Mannitol dehydrogenase
GVO57_RS10245	ENOG4105DPW	Major facilitator superfamily MFS_1
GVO57_RS10275	ENOG4107HP6	Transcriptional regulator
GVO57_RS10295	ENOG4107S9D	Alpha beta hydrolase
GVO57_RS10320	ENOG4105C08	Histidine kinase
GVO57_RS10330	ENOG4105XJC	Two component transcriptional regulator (Winged helix family
GVO57_RS10380	ENOG4105E0K	tonB-dependent siderophore receptor
GVO57_RS10425	ENOG4105DFP	Integrase
GVO57_RS10500	ENOG4105CVE	Lytic murein transglycosylase
GVO57_RS10505	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
GVO57_RS10510	ENOG4107QRG	dna polymerase iii
GVO57_RS10520	ENOG4105F8V	Hydrolase, tatD family
GVO57_RS10525	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)
GVO57_RS10565	ENOG4108C33	Resolvase
GVO57_RS10580	ENOG4105DXN	mazG family
GVO57_RS10585	ENOG4105D4P	Coproporphyrinogen iii oxidase
GVO57_RS10610	ENOG4105D6P	C-type cytochrome. Part of the cbb3-type cytochrome c oxidase complex (By similarity)
GVO57_RS10630	ENOG4105CKU	formyltetrahydrofolate synthetase
GVO57_RS10640	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)
GVO57_RS10645	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
GVO57_RS10650	ENOG4105ES5	Histidine kinase
GVO57_RS10670	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)
GVO57_RS10675	ENOG4107TH8	cina domain protein
GVO57_RS10680	ENOG4108Z1B	Cyclase dehydrase
GVO57_RS10685	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)
GVO57_RS10695	ENOG41082FS	50S ribosomal protein L31
GVO57_RS10710	ENOG4105E1Z	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane
GVO57_RS10715	ENOG4105DZP	Membrane-associated zinc metalloprotease
GVO57_RS10735	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)
GVO57_RS10745	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)
GVO57_RS10750	ENOG4105CE9	30S ribosomal protein S2
GVO57_RS10765	ENOG41071I4	Phosphatidylserine decarboxylase proenzyme
GVO57_RS10785	ENOG4107QM5	aconitate hydratase
GVO57_RS10800	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)
GVO57_RS10805	ENOG4105EKE	dihydroorotase
GVO57_RS10830	ENOG4107F83	nucleotidyltransferase DNA polymerase involved in DNA
GVO57_RS10870	ENOG4105CEY	Amp-dependent synthetase and ligase
GVO57_RS10880	ENOG4105CHU	acetyl-coa acetyltransferase
GVO57_RS10895	ENOG4105CE4	GlcNAc 6-P deacetylase
GVO57_RS10900	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
GVO57_RS10905	ENOG4105FDP	GntR family transcriptional regulator
GVO57_RS10915	ENOG4105E2D	ec 3.2.1.52
GVO57_RS10920	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)
GVO57_RS10935	ENOG4105CMU	LysR family (Transcriptional regulator
GVO57_RS10955	ENOG4105E18	UPF0276 protein
GVO57_RS10970	ENOG4105E18	UPF0276 protein
GVO57_RS11055	ENOG4108NF7	phage-type endonuclease
GVO57_RS11105	ENOG4108IYS	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)
GVO57_RS11120	ENOG4105F7P	transcriptional regulator AsnC family
GVO57_RS11130	ENOG4105D1Q	UPF0246 protein
GVO57_RS11140	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)
GVO57_RS11195	ENOG4105CSM	endonuclease III
GVO57_RS11205	ENOG4105VZ8	Transcriptional regulator
GVO57_RS11230	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)
GVO57_RS11235	ENOG4107ZSV	Receptor
GVO57_RS11245	ENOG4105CPC	Aldo Keto reductase
GVO57_RS11250	ENOG4105D4R	Catalyzes the desulfonation of aliphatic sulfonates (By similarity)
GVO57_RS11260	ENOG4105SYT	Methylenetetrahydrofolate reductase
GVO57_RS11265	ENOG4105C3R	Methionine synthase
GVO57_RS11275	ENOG4105C3R	Methionine synthase
GVO57_RS11285	ENOG4105C83	adenylosuccinate lyase
GVO57_RS11295	ENOG4105CFG	Acts as a chaperone (By similarity)
GVO57_RS11310	ENOG4105CP7	Triose-phosphate isomerase
GVO57_RS11315	ENOG4105EIN	peptidylprolyl cis-trans isomerase
GVO57_RS11320	ENOG4105CRQ	synthase (Component I)
GVO57_RS11325	ENOG4105DWV	Homoserine O-trans-acetylase
GVO57_RS11330	ENOG4105DDQ	anthranilate synthase
GVO57_RS11335	ENOG4108I0Q	anthranilate phosphoribosyltransferase
GVO57_RS11340	ENOG4105DK0	Indole-3-glycerol phosphate synthase
GVO57_RS11345	ENOG4108YXW	Together with MoaA, is involved in the conversion of 5'- GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
GVO57_RS11350	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
GVO57_RS11355	ENOG4105DS7	Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair (By similarity)
GVO57_RS11365	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)
GVO57_RS11370	ENOG4105BZN	citrate synthase
GVO57_RS11380	ENOG4105BZU	Histidine kinase
GVO57_RS11390	ENOG4107RNA	Nickel ABC transporter, periplasmic nickel-binding protein
GVO57_RS11400	ENOG4105D18	nicotinate-nucleotide pyrophosphorylase
GVO57_RS11405	ENOG4105D0I	Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate (By similarity)
GVO57_RS11410	ENOG4108RW0	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
GVO57_RS11420	ENOG4105NA0	Transcriptional regulator
GVO57_RS11445	ENOG4105MQS	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
GVO57_RS11450	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
GVO57_RS11490	ENOG4105KAV	tspo and mbr like protein
GVO57_RS11495	ENOG4107QZT	geranylgeranyl reductase
GVO57_RS11510	ENOG4105D4D	transcriptional regulator
GVO57_RS11520	ENOG4108VJI	2-vinyl bacteriochlorophyllide hydratase
GVO57_RS11525	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)
GVO57_RS11530	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)
GVO57_RS11535	ENOG4105CTK	cobaltochelatase, cobn subunit
GVO57_RS11540	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)
GVO57_RS11545	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)
GVO57_RS11550	ENOG4105XCI	PucC protein
GVO57_RS11575	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)
GVO57_RS11580	ENOG4108TF2	Photosynthetic complex assembly protein 2
GVO57_RS11585	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)
GVO57_RS11595	ENOG4105J6N	PhotosynthetiC reaction center cytochrome c subunit
GVO57_RS11615	ENOG4105ZA6	Antenna complexes are light-harvesting systems, which transfer the excitation energy to the reaction centers (By similarity)
GVO57_RS11625	ENOG41060GA	Chlorophyllide reductase subunit Y
GVO57_RS11630	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)
GVO57_RS11635	ENOG4107XHQ	chlorophyll synthesis pathway, bchC
GVO57_RS11640	ENOG4107EPK	O-methyltransferase, family 2
GVO57_RS11670	ENOG4108ZEY	Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its highly electrophilic allylic isomer, dimethylallyl diphosphate (DMAPP) (By similarity)
GVO57_RS11675	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)
GVO57_RS11680	ENOG4105CK2	sodium dicarboxylate symporter
GVO57_RS11685	ENOG4105C79	DNA protecting protein DprA
GVO57_RS11695	ENOG4105F03	Provides the (R)-glutamate required for cell wall biosynthesis (By similarity)
GVO57_RS11700	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)
GVO57_RS11720	ENOG4108UJU	UPF0301 protein
GVO57_RS11730	ENOG4105FYV	Amp nucleosidase
GVO57_RS11745	ENOG4105EKD	Catalyzes the hydrolytic deamination of adenine to hypoxanthine. Plays an important role in the purine salvage pathway and in nitrogen catabolism (By similarity)
GVO57_RS11750	ENOG4108M9J	MaoC like domain protein
GVO57_RS11765	ENOG410841Q	phosphoesterase PA-phosphatase related protein
GVO57_RS11770	ENOG4105CI2	imidazolone-5-propionate hydrolase
GVO57_RS11800	ENOG4108YZN	class I peptide chain release factor
GVO57_RS11810	ENOG4105CS1	NAD(P)H quinone oxidoreductase
GVO57_RS11815	ENOG4105C2I	pirin domain protein
GVO57_RS11820	ENOG4105EXG	Transcriptional regulator
GVO57_RS11830	ENOG4105ECY	inositol monophosphatase
GVO57_RS11840	ENOG4107W75	Flagellin
GVO57_RS11850	ENOG41080HT	Transcriptional regulator, arsr family
GVO57_RS11855	ENOG4108V62	Rhodanese domain protein
GVO57_RS11860	ENOG4108VCT	Sulfite exporter TauE/SafE
GVO57_RS11870	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
GVO57_RS11885	ENOG4105K63	Thioredoxin
GVO57_RS11900	ENOG4108S0S	Nucleotidyl transferase
GVO57_RS11905	ENOG4105EHM	Aminoglycoside phosphotransferase
GVO57_RS11910	ENOG4108097	ATP-binding protein
GVO57_RS11915	ENOG4105I8F	Histidine kinase
GVO57_RS11930	ENOG4105C3B	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
GVO57_RS11950	ENOG4105DBW	Multi-copper polyphenol oxidoreductase laccase
GVO57_RS11965	ENOG4105DHJ	ABC, transporter
GVO57_RS11980	ENOG4105CD8	aminopeptidase N
GVO57_RS11985	ENOG4105C5Q	Transcriptional regulator
GVO57_RS11990	ENOG4105BZ1	(ABC) transporter
GVO57_RS12005	ENOG4105CHU	acetyl-coa acetyltransferase
GVO57_RS12020	ENOG4105C3E	May play a key role in the regulation of the intracellular concentration of adenosylhomocysteine (By similarity)
GVO57_RS12035	ENOG4108YZG	isomerase
GVO57_RS12040	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)
GVO57_RS12045	ENOG4108Z11	Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes (By similarity)
GVO57_RS12075	ENOG4105DWY	Agmatine deiminase
GVO57_RS12100	ENOG4108Z0R	Transferase
GVO57_RS12110	ENOG4105D52	delta-aminolevulinic acid dehydratase
GVO57_RS12115	ENOG4107TE5	Lipid kinase
GVO57_RS12120	ENOG4107QJQ	Mate efflux family protein
GVO57_RS12125	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)
GVO57_RS12140	ENOG4105E26	Catalyzes the methyl esterification of L-isoaspartyl residues in peptides and proteins that result from spontaneous decomposition of normal L-aspartyl and L-asparaginyl residues. It plays a role in the repair and or degradation of damaged proteins (By similarity)
GVO57_RS12155	ENOG4108UJD	30S ribosomal protein S9
GVO57_RS12180	ENOG4105CZF	Catalyzes the conversion of dethiobiotin (DTB) to biotin by the insertion of a sulfur atom into dethiobiotin via a radical- based mechanism (By similarity)
GVO57_RS12190	ENOG4108UKI	Enoyl-CoA hydratase
GVO57_RS12200	ENOG4107QX3	carboxylase
GVO57_RS12215	ENOG4105DC8	reductase
GVO57_RS12220	ENOG4105KK9	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
GVO57_RS12225	ENOG4105K46	50S ribosomal protein l27
GVO57_RS12240	ENOG4105C4W	S-formylglutathione hydrolase
GVO57_RS12250	ENOG4107QPD	alcohol dehydrogenase
GVO57_RS12300	ENOG4105CM2	brancheD-chain amino acid aminotransferase
GVO57_RS12305	ENOG41090HR	transcriptional regulator
GVO57_RS12310	ENOG4105II7	pyrroline-5-carboxylate reductase
GVO57_RS12320	ENOG4105BZU	Histidine kinase
GVO57_RS12335	ENOG4105KAV	tspo and mbr like protein
GVO57_RS12340	ENOG4105BZS	acriflavin resistance protein
GVO57_RS12360	ENOG4105EHZ	conserved protein UCP016719
GVO57_RS12370	ENOG4105DZ0	fad dependent oxidoreductase
GVO57_RS12395	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)
GVO57_RS12410	ENOG4105EY2	Catalyzes the hydrolysis of N(2)-succinylarginine into N(2)-succinylornithine, ammonia and CO(2) (By similarity)
GVO57_RS12435	ENOG4105CXT	aspartate transcarbamylase
GVO57_RS12455	ENOG4107QJE	Chromosome Partitioning Protein
GVO57_RS12470	ENOG4105EAC	phosphoserine phosphatase
GVO57_RS12475	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)
GVO57_RS12485	ENOG4108ZP8	Acetolactate synthase small subunit
GVO57_RS12490	ENOG4105C6M	Alpha-keto-beta-hydroxylacyl reductoisomerase
GVO57_RS12495	ENOG4108YYC	ycei family
GVO57_RS12500	ENOG4105BZU	Histidine kinase
GVO57_RS12525	ENOG4105KHV	Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate (By similarity)
GVO57_RS12535	ENOG4105M08	Membrane
GVO57_RS12580	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
GVO57_RS12585	ENOG4105F6H	The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate (By similarity)
GVO57_RS12590	ENOG4107QTG	Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl- CoA (By similarity)
GVO57_RS12595	ENOG4105DPM	folylpolyglutamate synthase Dihydrofolate synthase
GVO57_RS12625	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)
GVO57_RS12630	ENOG4105CJR	Integral membrane protein (MviN
GVO57_RS12635	ENOG4105C31	Tryptophanyl-tRNA synthetase
GVO57_RS12645	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)
GVO57_RS12650	ENOG4105KQV	Binds directly to 16S ribosomal RNA (By similarity)
GVO57_RS12655	ENOG4105C1G	acyl-Coa dehydrogenase
GVO57_RS12660	ENOG4105CC9	acyl-Coa dehydrogenase
GVO57_RS12670	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)
GVO57_RS12680	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)
GVO57_RS12700	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)
GVO57_RS12715	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
GVO57_RS12720	ENOG4107SC1	transglycosylase
GVO57_RS12725	ENOG4108RRZ	Transcription elongation factor GreB
GVO57_RS12730	ENOG4105CSR	polyphosphate kinase 2
GVO57_RS12740	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)
GVO57_RS12755	ENOG4105CUU	Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) (By similarity)
GVO57_RS12770	ENOG4105CXB	phosphoribosylaminoimidazole synthetase
GVO57_RS12775	ENOG4108V3E	phosphoribosylglycinamide formyltransferase
GVO57_RS12780	ENOG4105C26	Dehydrogenase
GVO57_RS12790	ENOG4105CHU	acetyl-coa acetyltransferase
GVO57_RS12840	ENOG4105C3T	may be the GTPase, regulating ATP sulfurylase activity (By similarity)
GVO57_RS12890	ENOG4105C0P	Mg chelatase subunit ChlI
GVO57_RS12895	ENOG4108X7C	Antioxidant protein with alkyl hydroperoxidase activity. Required for the reduction of the AhpC active site cysteine residues and for the regeneration of the AhpC enzyme activity (By similarity)
GVO57_RS12900	ENOG4105D3R	alkyl hydroperoxide reductase
GVO57_RS12905	ENOG4105C5Q	Transcriptional regulator
GVO57_RS12910	ENOG4108ZAF	Molybdopterin
GVO57_RS12940	ENOG4105EE6	Alcohol dehydrogenase zinc-binding domain protein
GVO57_RS12945	ENOG4105ETE	Transcriptional regulator (LacI family
GVO57_RS12950	ENOG4105DPW	Major facilitator superfamily MFS_1
GVO57_RS12955	ENOG4107ZSV	Receptor
GVO57_RS12975	ENOG4105CGP	Urocanate hydratase
GVO57_RS12985	ENOG4105C84	Histidine ammonia-lyase
GVO57_RS12990	ENOG4105CI2	imidazolone-5-propionate hydrolase
GVO57_RS13005	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
GVO57_RS13010	ENOG4105CW7	secretion protein, HlyD family
GVO57_RS13040	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
GVO57_RS13045	ENOG4105CBA	glutamine phosphoribosylpyrophosphate amidotransferase
GVO57_RS13050	ENOG4105UBK	short-chain dehydrogenase reductase
GVO57_RS13055	ENOG4105DGU	Histone deacetylase
GVO57_RS13060	ENOG4105CVP	deoxyribo-dipyrimidine photolyase
GVO57_RS13080	ENOG4108UHF	Joins Ado-cobinamide-GDP and alpha-ribazole to generate adenosylcobalamin (Ado-cobalamin) (By similarity)
GVO57_RS13085	ENOG4105CUP	Catalyzes the synthesis of alpha-ribazole-5'-phosphate from nicotinate mononucleotide (NAMN) and 5,6- dimethylbenzimidazole (DMB) (By similarity)
GVO57_RS13095	ENOG4105C2X	Arabinose 5-phosphate isomerase
GVO57_RS13120	ENOG4105FE9	pseudouridine synthase
GVO57_RS13125	ENOG4106H78	methyltransferase
GVO57_RS13130	ENOG4106YAV	Domain of unknown function (DUF1508)
GVO57_RS13145	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)
GVO57_RS13165	ENOG4105CJN	penicillin-binding protein
GVO57_RS13180	ENOG4108IUX	(ABC) transporter
GVO57_RS13205	ENOG4105CJ2	(LipO)protein
GVO57_RS13210	ENOG4107E2E	PKHD-type hydroxylase
GVO57_RS13215	ENOG4105WQ5	TonB family
GVO57_RS13220	ENOG4108ESX	Receptor
GVO57_RS13245	ENOG4105EBR	Carboxylesterase
GVO57_RS13255	ENOG4105CHR	reductase
GVO57_RS13265	ENOG4107KJX	Transcriptional regulator
GVO57_RS13290	ENOG4108UQY	Iron-storage protein
GVO57_RS13300	ENOG4105M2Z	protein tyrosine serine phosphatase
GVO57_RS13315	ENOG4105CKI	cobalamin synthesis protein
GVO57_RS13320	ENOG4106TD9	Diguanylate cyclase
GVO57_RS13365	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
GVO57_RS13380	ENOG4107HP6	Transcriptional regulator
GVO57_RS13420	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
GVO57_RS13425	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
GVO57_RS13435	ENOG4105CDA	abc transporter atp-binding protein
GVO57_RS13440	ENOG4105DRP	amino acid AbC transporter
GVO57_RS13445	ENOG4105E5Q	amino acid AbC transporter
GVO57_RS13460	ENOG4105H9W	Short-chain dehydrogenase reductase Sdr
GVO57_RS13475	ENOG4107QNJ	CoA-transferase subunit B
GVO57_RS13570	ENOG4106CY5	excisionase
GVO57_RS13610	ENOG4105C4Q	deoxyguanosinetriphosphate triphosphohydrolase-like protein
GVO57_RS13635	ENOG4105DFP	Integrase
GVO57_RS13660	ENOG4105WD1	Membrane
GVO57_RS13675	ENOG4105BZU	Histidine kinase
GVO57_RS13680	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
GVO57_RS13705	ENOG4105C7I	Dehydrogenase
GVO57_RS13715	ENOG4108ZT0	50S ribosomal protein l17
GVO57_RS13725	ENOG4105CI2	imidazolone-5-propionate hydrolase
GVO57_RS13740	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)
GVO57_RS13755	ENOG4108UJV	acyl-CoA thioesterase i
GVO57_RS13760	ENOG4108I0Y	(ABC) transporter
GVO57_RS13795	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
GVO57_RS13850	ENOG4106032	Glutathionylspermidine synthase
GVO57_RS13865	ENOG4105CFH	Aspartokinase
GVO57_RS13870	ENOG4105EA8	2-Nitropropane dioxygenase
GVO57_RS13895	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
GVO57_RS13900	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
GVO57_RS13905	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
GVO57_RS13920	ENOG4105CMM	transposase
GVO57_RS13930	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)
GVO57_RS14035	ENOG4105XJC	Two component transcriptional regulator (Winged helix family
GVO57_RS14120	ENOG4108KSB	HipA-like N-terminal domain
GVO57_RS14210	ENOG4107QSV	RmuC domain protein
GVO57_RS14285	ENOG4108YXQ	IS66 Orf2 family protein
GVO57_RS14360	ENOG4105C0D	helicase
GVO57_RS14375	ENOG4107SID	ATP-dependent exodnase (exonuclease v)
GVO57_RS14380	ENOG4107SID	ATP-dependent exodnase (exonuclease v)
GVO57_RS14440	ENOG4105W5Q	DNA repair protein (RadC
GVO57_RS14490	ENOG4105DY0	carbon monoxide dehydrogenase operon C protein
GVO57_RS14500	ENOG4105CUG	Oligopeptidase b