locus-tag	class	description
VEIT17_00010	COG0593	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
VEIT17_00050	COG1195	it is required for DNA replication and normal SOS inducibility. RecF binds preferentially to single-stranded, linear DNA. It also seems to bind ATP
VEIT17_00080	COG0187	DNA topoisomerase II activity
VEIT17_00090	COG0833	amino acid
VEIT17_00110	COG1733	regulation of RNA biosynthetic process
VEIT17_00150	COG0845	Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family
VEIT17_00160	COG1253	flavin adenine dinucleotide binding
VEIT17_00220	COG0438	transferase activity, transferring glycosyl groups
VEIT17_00260	COG3594	Acyltransferase
VEIT17_00270	COG0562	UDP-galactopyranose mutase
VEIT17_00300	COG0438	transferase activity, transferring glycosyl groups
VEIT17_00320	COG2244	polysaccharide biosynthetic process
VEIT17_00450	COG4797	methyltransferase
VEIT17_00450	COG2230	cyclopropane-fatty-acyl-phospholipid synthase
VEIT17_00530	COG0501	Belongs to the peptidase M48B family
VEIT17_00540	COG0811	peptide transport
VEIT17_00550	COG0848	biopolymer transport protein
VEIT17_00590	COG0614	abc-type fe3 -hydroxamate transport system, periplasmic component
VEIT17_00600	COG0609	Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily
VEIT17_00610	COG1120	ATPase activity
VEIT17_00660	COG4771	TonB-dependent receptor
VEIT17_00670	COG0436	Aminotransferase
VEIT17_00680	COG0640	Transcriptional regulator
VEIT17_00700	COG2440	electron transfer flavoprotein-ubiquinone oxidoreductase
VEIT17_00730	COG4221	oxidoreductase activity
VEIT17_00770	COG1173	ABC-type dipeptide oligopeptide nickel transport systems, permease components
VEIT17_00780	COG0747	negative chemotaxis
VEIT17_00790	COG0444	Belongs to the ABC transporter superfamily
VEIT17_00800	COG4608	Belongs to the ABC transporter superfamily
VEIT17_00910	COG0119	Catalyzes the condensation of the acetyl group of acetyl-CoA with 3-methyl-2-oxobutanoate (2-oxoisovalerate) to form 3-carboxy-3-hydroxy-4-methylpentanoate (2-isopropylmalate)
VEIT17_00920	COG0065	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate
VEIT17_00930	COG0066	3-isopropylmalate dehydratase activity
VEIT17_00940	COG0473	3-isopropylmalate dehydrogenase activity
VEIT17_00990	COG2801	Transposase and inactivated derivatives
VEIT17_01000	COG1196	nuclear chromosome segregation
VEIT17_01050	COG0497	DNA recombination
VEIT17_01070	COG1879	ABC-type sugar transport system periplasmic component
VEIT17_01080	COG1172	Belongs to the binding-protein-dependent transport system permease family
VEIT17_01090	COG1129	ABC transporter
VEIT17_01100	COG1869	D-ribose catabolic process
VEIT17_01110	COG0524	Catalyzes the phosphorylation of ribose at O-5 in a reaction requiring ATP and magnesium. The resulting D-ribose-5- phosphate can then be used either for sythesis of nucleotides, histidine, and tryptophan, or as a component of the pentose phosphate pathway
VEIT17_01160	COG0610	Subunit R is required for both nuclease and ATPase activities, but not for modification
VEIT17_01190	COG1122	ATPase activity
VEIT17_01200	COG1122	ATPase activity
VEIT17_01230	COG1387	Histidinol phosphatase and related hydrolases of the PHP family
VEIT17_01240	COG0107	imidazoleglycerol-phosphate synthase activity
VEIT17_01250	COG1966	Carbon starvation protein
VEIT17_01350	COG0780	Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1)
VEIT17_01380	COG0031	Belongs to the cysteine synthase cystathionine beta- synthase family
VEIT17_01390	COG1045	serine acetyltransferase
VEIT17_01410	COG1914	H( )-stimulated, divalent metal cation uptake system
VEIT17_01430	COG3022	response to hydroperoxide
VEIT17_01440	COG0502	Catalyzes the conversion of dethiobiotin (DTB) to biotin by the insertion of a sulfur atom into dethiobiotin via a radical- based mechanism
VEIT17_01460	COG0480	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
VEIT17_01470	COG2731	YhcH YjgK YiaL family protein
VEIT17_01480	COG0697	spore germination
VEIT17_01530	COG3069	C4-dicarboxylate transmembrane transporter activity
VEIT17_01570	COG0512	Glutamine amidotransferase of anthranilate synthase
VEIT17_01570	COG0547	Catalyzes the transfer of the phosphoribosyl group of 5- phosphorylribose-1-pyrophosphate (PRPP) to anthranilate to yield N-(5'-phosphoribosyl)-anthranilate (PRA)
VEIT17_01580	COG0547	Catalyzes the transfer of the phosphoribosyl group of 5- phosphorylribose-1-pyrophosphate (PRPP) to anthranilate to yield N-(5'-phosphoribosyl)-anthranilate (PRA)
VEIT17_01590	COG0134	indole-3-glycerol-phosphate synthase activity
VEIT17_01600	COG0133	tryptophan synthase activity
VEIT17_01610	COG0159	tryptophan synthase activity
VEIT17_01670	COG0060	amino acids such as valine, to avoid such errors it has two additional distinct tRNA(Ile)-dependent editing activities. One activity is designated as 'pretransfer' editing and involves the hydrolysis of activated Val-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Val-tRNA(Ile)
VEIT17_01720	COG0834	ABC-type amino acid transport signal transduction systems periplasmic component domain
VEIT17_01750	COG0561	phosphatase activity
VEIT17_01770	COG0519	Catalyzes the synthesis of GMP from XMP
VEIT17_01770	COG0518	GMP synthase (glutamine-hydrolyzing) activity
VEIT17_01890	COG0456	acetyltransferase
VEIT17_01900	COG1108	ABC-type Mn2 Zn2 transport systems permease components
VEIT17_01910	COG1108	ABC-type Mn2 Zn2 transport systems permease components
VEIT17_01920	COG1121	(ABC) transporter
VEIT17_01930	COG0803	Belongs to the bacterial solute-binding protein 9 family
VEIT17_01980	COG0583	DNA-binding transcription factor activity
VEIT17_01990	COG1151	hydroxylamine reductase activity
VEIT17_02000	COG2220	Zn-dependent hydrolases of the beta-lactamase fold
VEIT17_02030	COG0502	Catalyzes the conversion of dethiobiotin (DTB) to biotin by the insertion of a sulfur atom into dethiobiotin via a radical- based mechanism
VEIT17_02040	COG0420	3'-5' exonuclease activity
VEIT17_02050	COG4717	serine-type aminopeptidase activity
VEIT17_02060	COG0407	Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III
VEIT17_02070	COG0276	Catalyzes the ferrous insertion into protoporphyrin IX
VEIT17_02080	COG1232	Catalyzes the 6-electron oxidation of protoporphyrinogen-IX to form protoporphyrin-IX
VEIT17_02090	COG3253	May function as heme-dependent peroxidase
VEIT17_02100	COG2223	nitrite transmembrane transporter activity
VEIT17_02110	COG0664	- Catabolite gene activator and regulatory subunit of cAMP-dependent protein
VEIT17_02120	COG5013	Belongs to the prokaryotic molybdopterin-containing oxidoreductase family
VEIT17_02130	COG1140	nitrate reductase beta subunit
VEIT17_02140	COG2180	nitrate reductase molybdenum cofactor assembly chaperone
VEIT17_02150	COG2181	nitrate reductase activity
VEIT17_02170	COG3206	protein involved in exopolysaccharide biosynthesis
VEIT17_02190	COG2814	Major facilitator Superfamily
VEIT17_02200	COG0583	DNA-binding transcription factor activity
VEIT17_02220	COG2855	membrane
VEIT17_02230	COG0288	reversible hydration of carbon dioxide
VEIT17_02240	COG0132	Catalyzes a mechanistically unusual reaction, the ATP- dependent insertion of CO2 between the N7 and N8 nitrogen atoms of 7,8-diaminopelargonic acid (DAPA) to form an ureido ring
VEIT17_02250	COG0161	adenosylmethionine-8-amino-7-oxononanoate transaminase activity
VEIT17_02260	COG2704	Responsible for the transport of C4-dicarboxylates from the periplasm across the inner membrane
VEIT17_02280	COG1108	ABC-type Mn2 Zn2 transport systems permease components
VEIT17_02290	COG1121	(ABC) transporter
VEIT17_02300	COG0803	Belongs to the bacterial solute-binding protein 9 family
VEIT17_02310	COG2184	nucleotidyltransferase activity
VEIT17_02420	COG0787	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids
VEIT17_02430	COG1052	Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family
VEIT17_02440	COG1180	Activation of pyruvate formate-lyase under anaerobic conditions by generation of an organic free radical, using S- adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine
VEIT17_02450	COG1882	Formate acetyltransferase
VEIT17_02490	COG2011	ABC-type metal ion transport system permease component
VEIT17_02510	COG1132	(ABC) transporter
VEIT17_02530	COG0471	metal ion transport
VEIT17_02560	COG0626	cystathionine gamma-synthase activity
VEIT17_02570	COG1168	Bifunctional PLP-dependent enzyme with beta-cystaTHIonase and maltose regulon repressor activities
VEIT17_02580	COG1897	L-methionine biosynthetic process from homoserine via O-succinyl-L-homoserine and cystathionine
VEIT17_02590	COG2873	o-acetylhomoserine
VEIT17_02640	COG0701	Predicted permease
VEIT17_02650	COG0523	cobalamin synthesis protein
VEIT17_02660	COG2195	Cleaves the N-terminal amino acid of tripeptides
VEIT17_02670	COG1488	Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP
VEIT17_02690	COG0252	asparaginase activity
VEIT17_02710	COG0668	transmembrane transport
VEIT17_02720	COG1686	Belongs to the peptidase S11 family
VEIT17_02740	COG1600	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)
VEIT17_02760	COG2080	2 iron, 2 sulfur cluster binding
VEIT17_02770	COG2080	2 iron, 2 sulfur cluster binding
VEIT17_02770	COG1529	Aldehyde oxidase and xanthine dehydrogenase
VEIT17_02810	COG1975	Xanthine and CO dehydrogenases maturation factor, XdhC CoxF family
VEIT17_02810	COG3608	succinylglutamate desuccinylase aspartoacylase
VEIT17_02830	COG1624	Catalyzes the condensation of 2 ATP molecules into cyclic di-AMP (c-di-AMP), a second messenger used to regulate differing processes in different bacteria
VEIT17_02840	COG4856	YbbR-like protein
VEIT17_02850	COG2509	5-formyltetrahydrofolate cyclo-ligase activity
VEIT17_02860	COG1109	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate
VEIT17_02900	COG2801	Transposase and inactivated derivatives
VEIT17_02910	COG4735	regulation of single-species biofilm formation
VEIT17_02920	COG2020	methyltransferase activity
VEIT17_02940	COG0449	glutamine-fructose-6-phosphate transaminase (isomerizing) activity
VEIT17_02950	COG0180	Tryptophanyl-tRNA synthetase
VEIT17_02970	COG0834	ABC-type amino acid transport signal transduction systems periplasmic component domain
VEIT17_02980	COG0765	amino acid transport
VEIT17_02990	COG1126	abc transporter atp-binding protein
VEIT17_03010	COG0589	response to stress
VEIT17_03020	COG0640	Transcriptional regulator
VEIT17_03050	COG0725	ABC transporter, periplasmic molybdate-binding protein
VEIT17_03060	COG4149	molybdate abc transporter
VEIT17_03070	COG4148	Part of the ABC transporter complex ModABC involved in molybdenum import. Responsible for energy coupling to the transport system
VEIT17_03120	COG1592	Rubrerythrin
VEIT17_03140	COG0709	Synthesizes selenophosphate from selenide and ATP
VEIT17_03170	COG0778	Nitroreductase
VEIT17_03180	COG2261	transglycosylase associated protein
VEIT17_03200	COG0012	GTP binding
VEIT17_03220	COG0436	Aminotransferase
VEIT17_03260	COG2814	Major facilitator Superfamily
VEIT17_03270	COG0360	Binds together with S18 to 16S ribosomal RNA
VEIT17_03280	COG0629	single-stranded DNA binding
VEIT17_03290	COG0238	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
VEIT17_03320	COG1433	Dinitrogenase iron-molybdenum cofactor
VEIT17_03320	COG0535	radical SAM domain protein
VEIT17_03330	COG0520	Catalyzes the removal of elemental sulfur and selenium atoms from L-cysteine, L-cystine, L-selenocysteine, and L- selenocystine to produce L-alanine
VEIT17_03370	COG0789	Transcriptional regulator
VEIT17_03380	COG1154	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)
VEIT17_03390	COG1154	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)
VEIT17_03410	COG0220	tRNA (guanine-N7-)-methyltransferase activity
VEIT17_03420	COG0772	Belongs to the SEDS family
VEIT17_03510	COG2195	Cleaves the N-terminal amino acid of tripeptides
VEIT17_03540	COG2040	homocysteine
VEIT17_03550	COG0426	domain, Protein
VEIT17_03550	COG1853	conserved protein domain typically associated with flavoprotein oxygenases, DIM6 NTAB family
VEIT17_03560	COG0046	Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL
VEIT17_03570	COG0583	DNA-binding transcription factor activity
VEIT17_03580	COG0503	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis
VEIT17_03610	COG0041	Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR)
VEIT17_03620	COG0152	phosphoribosylaminoimidazolesuccinocarboxamide synthase activity
VEIT17_03630	COG0034	Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine
VEIT17_03640	COG0150	phosphoribosylformylglycinamidine cyclo-ligase activity
VEIT17_03650	COG0299	Catalyzes the transfer of a formyl group from 10- formyltetrahydrofolate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR) and tetrahydrofolate
VEIT17_03670	COG0151	Belongs to the GarS family
VEIT17_03680	COG1169	isochorismate synthase
VEIT17_03690	COG1165	Catalyzes the thiamine diphosphate-dependent decarboxylation of 2-oxoglutarate and the subsequent addition of the resulting succinic semialdehyde-thiamine pyrophosphate anion to isochorismate to yield 2-succinyl-5-enolpyruvyl-6-hydroxy-3- cyclohexene-1-carboxylate (SEPHCHC)
VEIT17_03700	COG0596	Alpha beta hydrolase
VEIT17_03710	COG0447	Converts o-succinylbenzoyl-CoA (OSB-CoA) to 1,4- dihydroxy-2-naphthoyl-CoA (DHNA-CoA)
VEIT17_03720	COG0318	PFAM AMP-dependent synthetase and ligase
VEIT17_03850	COG1649	PFAM Uncharacterised BCR, COG1649
VEIT17_03850	COG0726	polysaccharide deacetylase
VEIT17_03860	COG4632	Exopolysaccharide biosynthesis protein
VEIT17_03860	COG5434	Belongs to the glycosyl hydrolase 28 family
VEIT17_03880	COG0859	PFAM glycosyl transferase family 9
VEIT17_03930	COG0265	Trypsin-like serine proteases, typically periplasmic, contain C-terminal PDZ domain
VEIT17_03980	COG0461	Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP)
VEIT17_03990	COG0284	orotidine-5'-phosphate decarboxylase activity
VEIT17_04040	COG1464	Belongs to the NlpA lipoprotein family
VEIT17_04050	COG1575	Belongs to the MenA family. Type 1 subfamily
VEIT17_04080	COG0251	oxidation-reduction process
VEIT17_04090	COG3681	Belongs to the UPF0597 family
VEIT17_04100	COG2223	nitrite transmembrane transporter activity
VEIT17_04110	COG0590	tRNA wobble adenosine to inosine editing
VEIT17_04160	COG1135	Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system
VEIT17_04170	COG2011	ABC-type metal ion transport system permease component
VEIT17_04180	COG4496	protein, YerC YecD
VEIT17_04190	COG0730	response to heat
VEIT17_04200	COG1028	Short-chain dehydrogenase reductase Sdr
VEIT17_04220	COG3339	Conserved Protein
VEIT17_04230	COG0824	Thioesterase
VEIT17_04240	COG0796	Provides the (R)-glutamate required for cell wall biosynthesis
VEIT17_04270	COG0145	ligase activity
VEIT17_04290	COG0689	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
VEIT17_04330	COG0281	malic enzyme
VEIT17_04380	COG1540	5-oxoprolinase (ATP-hydrolyzing) activity
VEIT17_04390	COG1914	H( )-stimulated, divalent metal cation uptake system
VEIT17_04400	COG2049	5-oxoprolinase (ATP-hydrolyzing) activity
VEIT17_04410	COG1984	allophanate hydrolase subunit 2
VEIT17_04440	COG0534	Mate efflux family protein
VEIT17_04450	COG2885	chlorophyll binding
VEIT17_04460	COG0628	permease
VEIT17_04490	COG1249	Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family
VEIT17_04500	COG3633	Involved in the import of serine and threonine into the cell, with the concomitant import of sodium (symport system)
VEIT17_04510	COG2226	methyltransferase
VEIT17_04550	COG1197	Couples transcription and DNA repair by recognizing RNA polymerase (RNAP) stalled at DNA lesions. Mediates ATP-dependent release of RNAP and its truncated transcript from the DNA, and recruitment of nucleotide excision repair machinery to the damaged site
VEIT17_04560	COG2244	polysaccharide biosynthetic process
VEIT17_04570	COG3956	TIGRFAM MazG family protein
VEIT17_04580	COG0776	regulation of translation
VEIT17_04590	COG0707	Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II)
VEIT17_04610	COG0488	(ABC) transporter
VEIT17_04640	COG0306	phosphate transporter
VEIT17_04670	COG1120	ATPase activity
VEIT17_04730	COG2207	Transcriptional regulator
VEIT17_04730	COG0662	Cupin 2, conserved barrel domain protein
VEIT17_04740	COG4771	TonB-dependent receptor
VEIT17_04750	COG0811	peptide transport
VEIT17_04760	COG0848	biopolymer transport protein
VEIT17_04800	COG0524	Catalyzes the phosphorylation of ribose at O-5 in a reaction requiring ATP and magnesium. The resulting D-ribose-5- phosphate can then be used either for sythesis of nucleotides, histidine, and tryptophan, or as a component of the pentose phosphate pathway
VEIT17_04810	COG0168	Low-affinity potassium transport system. Interacts with trk system potassium uptake protein TrkA
VEIT17_04820	COG0569	domain protein
VEIT17_04860	COG2220	Zn-dependent hydrolases of the beta-lactamase fold
VEIT17_04870	COG0315	cyclic pyranopterin monophosphate synthase activity
VEIT17_04880	COG0219	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
VEIT17_04890	COG3679	Belongs to the UPF0342 family
VEIT17_04910	COG1600	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)
VEIT17_04920	COG1217	gtp-binding protein TYPA
VEIT17_05010	COG0028	Belongs to the TPP enzyme family
VEIT17_05020	COG0440	acetolactate synthase activity
VEIT17_05030	COG0288	reversible hydration of carbon dioxide
VEIT17_05060	COG1473	amidohydrolase
VEIT17_05080	COG0002	Catalyzes the NADPH-dependent reduction of N-acetyl-5- glutamyl phosphate to yield N-acetyl-L-glutamate 5-semialdehyde
VEIT17_05090	COG0548	Belongs to the acetylglutamate kinase family. ArgB subfamily
VEIT17_05100	COG4992	N2-acetyl-L-ornithine:2-oxoglutarate 5-aminotransferase activity
VEIT17_05120	COG1473	amidohydrolase
VEIT17_05130	COG3069	C4-dicarboxylate transmembrane transporter activity
VEIT17_05150	COG2223	nitrite transmembrane transporter activity
VEIT17_05170	COG3859	Proton-coupled thiamine transporter YuaJ
VEIT17_05210	COG0542	response to heat
VEIT17_05220	COG2207	Transcriptional regulator
VEIT17_05240	COG2207	Transcriptional regulator
VEIT17_05240	COG1917	Cupin 2, conserved barrel domain protein
VEIT17_05250	COG1951	Catalyzes the reversible hydration of fumarate to (S)- malate
VEIT17_05260	COG1838	Catalyzes the reversible hydration of fumarate to (S)- malate
VEIT17_05270	COG0471	metal ion transport
VEIT17_05300	COG2233	PERMEase
VEIT17_05320	COG2896	Catalyzes the cyclization of GTP to (8S)-3',8-cyclo-7,8- dihydroguanosine 5'-triphosphate
VEIT17_05350	COG2837	iron assimilation
VEIT17_05360	COG0498	Catalyzes the gamma-elimination of phosphate from L- phosphohomoserine and the beta-addition of water to produce L- threonine
VEIT17_05380	COG3593	DNA synthesis involved in DNA repair
VEIT17_05390	COG1970	mechanosensitive ion channel activity
VEIT17_05470	COG0624	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
VEIT17_05480	COG0078	Reversibly catalyzes the transfer of the carbamoyl group from carbamoyl phosphate (CP) to the N(epsilon) atom of ornithine (ORN) to produce L-citrulline
VEIT17_05490	COG0549	Belongs to the carbamate kinase family
VEIT17_05500	COG0402	S-adenosylhomocysteine deaminase activity
VEIT17_05510	COG1145	4fe-4S ferredoxin, iron-sulfur binding domain protein
VEIT17_05510	COG0493	'glutamate synthase
VEIT17_05540	COG2233	PERMEase
VEIT17_05550	COG1850	ribulose-bisphosphate carboxylase activity
VEIT17_05560	COG1235	May be involved in the transport of PQQ or its precursor to the periplasm
VEIT17_05570	COG1576	Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA
VEIT17_05580	COG0516	GMP reductase activity
VEIT17_05580	COG0517	IMP dehydrogenase activity
VEIT17_05590	COG0544	peptidyl-prolyl cis-trans isomerase activity
VEIT17_05600	COG0740	serine-type endopeptidase activity
VEIT17_05610	COG1219	ATP-dependent specificity component of the Clp protease. It directs the protease to specific substrates. Can perform chaperone functions in the absence of ClpP
VEIT17_05620	COG0466	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
VEIT17_05630	COG0218	Necessary for normal cell division and for the maintenance of normal septation
VEIT17_05650	COG0805	protein transport
VEIT17_05660	COG0525	valine-tRNA ligase activity
VEIT17_05670	COG0285	dihydrofolate synthase activity
VEIT17_05700	COG0427	acetyl-CoA hydrolase
VEIT17_05710	COG1884	Catalyzes the reversible interconversion of isobutyryl- CoA and n-butyryl-CoA, using radical chemistry. Also exhibits GTPase activity, associated with its G-protein domain (MeaI) that functions as a chaperone that assists cofactor delivery and proper holo-enzyme assembly
VEIT17_05710	COG2185	Catalyzes the reversible interconversion of isobutyryl- CoA and n-butyryl-CoA, using radical chemistry. Also exhibits GTPase activity, associated with its G-protein domain (MeaI) that functions as a chaperone that assists cofactor delivery and proper holo-enzyme assembly
VEIT17_05720	COG2185	Catalyzes the reversible interconversion of isobutyryl- CoA and n-butyryl-CoA, using radical chemistry. Also exhibits GTPase activity, associated with its G-protein domain (MeaI) that functions as a chaperone that assists cofactor delivery and proper holo-enzyme assembly
VEIT17_05720	COG1884	Catalyzes the reversible interconversion of isobutyryl- CoA and n-butyryl-CoA, using radical chemistry. Also exhibits GTPase activity, associated with its G-protein domain (MeaI) that functions as a chaperone that assists cofactor delivery and proper holo-enzyme assembly
VEIT17_05740	COG0346	lactoylglutathione lyase activity
VEIT17_05750	COG4799	Acetyl-CoA carboxylase, carboxyltransferase component subunits alpha and beta
VEIT17_05780	COG0511	ligase activity, forming carbon-carbon bonds
VEIT17_05790	COG1883	Na -transporting methylmalonyl-CoA oxaloacetate decarboxylase, beta subunit
VEIT17_05810	COG0490	domain, Protein
VEIT17_05810	COG0471	metal ion transport
VEIT17_05830	COG0471	metal ion transport
VEIT17_05830	COG0490	domain, Protein
VEIT17_05860	COG0597	This protein specifically catalyzes the removal of signal peptides from prolipoproteins
VEIT17_05870	COG0564	pseudouridine synthase activity
VEIT17_05880	COG2065	Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant
VEIT17_05890	COG1323	Belongs to the UPF0348 family
VEIT17_05930	COG0424	maF-like protein
VEIT17_05940	COG2003	Belongs to the UPF0758 family
VEIT17_05950	COG1077	Cell shape determining protein MreB Mrl
VEIT17_05980	COG0768	penicillin binding
VEIT17_05990	COG2894	cell division
VEIT17_06000	COG0772	Belongs to the SEDS family
VEIT17_06030	COG1530	ribonuclease E activity
VEIT17_06040	COG1971	Probably functions as a manganese efflux pump
VEIT17_06050	COG0261	This protein binds to 23S rRNA in the presence of protein L20
VEIT17_06070	COG0211	Belongs to the bacterial ribosomal protein bL27 family
VEIT17_06080	COG4619	ABC transporter
VEIT17_06090	COG0390	transport system, permease component
VEIT17_06100	COG0502	Catalyzes the conversion of dethiobiotin (DTB) to biotin by the insertion of a sulfur atom into dethiobiotin via a radical- based mechanism
VEIT17_06110	COG0608	single-stranded DNA 5'-3' exodeoxyribonuclease activity
VEIT17_06110	COG4199	Single-strand DNA-specific exonuclease, C terminal domain
VEIT17_06120	COG0317	In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance
VEIT17_06130	COG0491	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid
VEIT17_06140	COG0735	belongs to the Fur family
VEIT17_06150	COG0635	Involved in the biosynthesis of porphyrin-containing compound
VEIT17_06170	COG0173	Aspartyl-tRNA synthetase with relaxed tRNA specificity since it is able to aspartylate not only its cognate tRNA(Asp) but also tRNA(Asn). Reaction proceeds in two steps L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp Asn)
VEIT17_06240	COG1546	Belongs to the CinA family
VEIT17_06240	COG1058	Belongs to the CinA family
VEIT17_06250	COG0468	Can catalyze the hydrolysis of ATP in the presence of single-stranded DNA, the ATP-dependent uptake of single-stranded DNA by duplex DNA, and the ATP-dependent hybridization of homologous single-stranded DNAs. It interacts with LexA causing its activation and leading to its autocatalytic cleavage
VEIT17_06260	COG2137	regulation of response to DNA damage stimulus
VEIT17_06270	COG1418	mRNA catabolic process
VEIT17_06280	COG0358	DNA primase activity
VEIT17_06290	COG0568	sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released
VEIT17_06310	COG0602	queuosine metabolic process
VEIT17_06340	COG0327	Belongs to the GTP cyclohydrolase I type 2 NIF3 family
VEIT17_06350	COG3118	belongs to the thioredoxin family
VEIT17_06390	COG0680	Initiates the rapid degradation of small, acid-soluble proteins during spore germination
VEIT17_06410	COG0463	Glycosyl transferase, family 2
VEIT17_06420	COG0791	NLP P60 protein
VEIT17_06420	COG1388	LysM domain
VEIT17_06430	COG0013	Catalyzes the attachment of alanine to tRNA(Ala) in a two-step reaction alanine is first activated by ATP to form Ala- AMP and then transferred to the acceptor end of tRNA(Ala). Also edits incorrectly charged Ser-tRNA(Ala) and Gly-tRNA(Ala) via its editing domain
VEIT17_06440	COG4472	Bacterial protein of unknown function (DUF965)
VEIT17_06450	COG0816	Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA
VEIT17_06460	COG3906	Belongs to the UPF0473 family
VEIT17_06490	COG4122	O-methyltransferase activity
VEIT17_06500	COG0826	peptidase U32
VEIT17_06530	COG0441	Catalyzes the attachment of threonine to tRNA(Thr) in a two-step reaction L-threonine is first activated by ATP to form Thr-AMP and then transferred to the acceptor end of tRNA(Thr)
VEIT17_06540	COG2814	Major facilitator Superfamily
VEIT17_06550	COG0471	metal ion transport
VEIT17_06560	COG0290	IF-3 binds to the 30S ribosomal subunit and shifts the equilibrum between 70S ribosomes and their 50S and 30S subunits in favor of the free subunits, thus enhancing the availability of 30S subunits on which protein synthesis initiation begins
VEIT17_06570	COG0291	Belongs to the bacterial ribosomal protein bL35 family
VEIT17_06580	COG0292	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
VEIT17_06650	COG5290	Psort location Cytoplasmic, score
VEIT17_06680	COG1401	restriction endodeoxyribonuclease activity
VEIT17_06760	COG0546	phosphoglycolate phosphatase activity
VEIT17_06790	COG2071	gamma-glutamyl-gamma-aminobutyrate hydrolase activity
VEIT17_06820	COG2244	polysaccharide biosynthetic process
VEIT17_06830	COG0191	fructose-bisphosphate aldolase activity
VEIT17_06840	COG0564	pseudouridine synthase activity
VEIT17_06870	COG1666	GTP binding
VEIT17_06880	COG1903	Catalyzes the methylation of C-1 in cobalt-precorrin-5B to form cobalt-precorrin-6A
VEIT17_06960	COG0609	Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily
VEIT17_06970	COG1120	ATPase activity
VEIT17_07010	COG4822	anaerobic cobalamin biosynthetic process
VEIT17_07050	COG2033	superoxide reductase activity
VEIT17_07090	COG0008	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)
VEIT17_07110	COG3118	belongs to the thioredoxin family
VEIT17_07130	COG2001	Belongs to the MraZ family
VEIT17_07140	COG0275	rRNA processing
VEIT17_07160	COG0769	Catalyzes the addition of meso-diaminopimelic acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan
VEIT17_07170	COG0770	UDP-N-acetylmuramoyl-tripeptide-D-alanyl-D-alanine ligase activity
VEIT17_07180	COG0472	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan
VEIT17_07200	COG0707	Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II)
VEIT17_07210	COG0773	UDP-N-acetylmuramate-L-alanine ligase activity
VEIT17_07220	COG1181	Belongs to the D-alanine--D-alanine ligase family
VEIT17_07250	COG3856	small basic protein
VEIT17_07260	COG0206	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
VEIT17_07300	COG0177	DNA repair enzyme that has both DNA N-glycosylase activity and AP-lyase activity. The DNA N-glycosylase activity releases various damaged pyrimidines from DNA by cleaving the N- glycosidic bond, leaving an AP (apurinic apyrimidinic) site. The AP-lyase activity cleaves the phosphodiester bond 3' to the AP site by a beta-elimination, leaving a 3'-terminal unsaturated sugar and a product with a terminal 5'-phosphate
VEIT17_07330	COG0254	rRNA binding
VEIT17_07340	COG3872	metal-dependent enzyme
VEIT17_07360	COG2890	protein-(glutamine-N5) methyltransferase activity
VEIT17_07370	COG0009	L-threonylcarbamoyladenylate synthase
VEIT17_07380	COG0394	Belongs to the low molecular weight phosphotyrosine protein phosphatase family
VEIT17_07390	COG0698	ribose 5-phosphate isomerase
VEIT17_07400	COG0112	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
VEIT17_07440	COG0126	phosphoglycerate kinase activity
VEIT17_07450	COG0149	triose-phosphate isomerase activity
VEIT17_07460	COG0696	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate
VEIT17_07470	COG0148	phosphopyruvate hydratase activity
VEIT17_07480	COG2804	Type II secretory pathway, ATPase PulE Tfp pilus assembly pathway, ATPase PilB
VEIT17_07500	COG1459	type II secretion system
VEIT17_07510	COG2165	general secretion pathway protein
VEIT17_07600	COG0703	Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate
VEIT17_07610	COG0205	6-phosphofructokinase activity
VEIT17_07620	COG0845	Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family
VEIT17_07630	COG1136	(ABC) transporter
VEIT17_07640	COG0577	efflux transmembrane transporter activity
VEIT17_07640	COG1136	(ABC) transporter
VEIT17_07660	COG0016	Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily
VEIT17_07670	COG0072	phenylalanine-tRNA ligase activity
VEIT17_07670	COG0073	Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation
VEIT17_07680	COG0826	peptidase U32
VEIT17_07690	COG1193	negative regulation of DNA recombination
VEIT17_07700	COG5009	serine-type D-Ala-D-Ala carboxypeptidase activity
VEIT17_07710	COG0162	Catalyzes the attachment of tyrosine to tRNA(Tyr) in a two-step reaction tyrosine is first activated by ATP to form Tyr- AMP and then transferred to the acceptor end of tRNA(Tyr)
VEIT17_07730	COG1080	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)
VEIT17_07730	COG0574	Belongs to the PEP-utilizing enzyme family
VEIT17_07740	COG0517	IMP dehydrogenase activity
VEIT17_07750	COG1806	Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the
VEIT17_07760	COG0232	Belongs to the dGTPase family. Type 2 subfamily
VEIT17_07770	COG0227	Belongs to the bacterial ribosomal protein bL28 family
VEIT17_07780	COG1200	Critical role in recombination and DNA repair. Helps process Holliday junction intermediates to mature products by catalyzing branch migration. Has a DNA unwinding activity characteristic of a DNA helicase with a 3'- to 5'- polarity. Unwinds branched duplex DNA (Y-DNA)
VEIT17_07790	COG1942	4-Oxalocrotonate Tautomerase
VEIT17_07800	COG0516	GMP reductase activity
VEIT17_07800	COG0517	IMP dehydrogenase activity
VEIT17_07810	COG1922	lipopolysaccharide N-acetylmannosaminouronosyltransferase activity
VEIT17_07820	COG0688	phosphatidylethanolamine metabolic process
VEIT17_07840	COG1215	transferase activity, transferring glycosyl groups
VEIT17_07870	COG0736	holo-[acyl-carrier-protein] synthase activity
VEIT17_07880	COG0062	Bifunctional enzyme that catalyzes the epimerization of the S- and R-forms of NAD(P)HX and the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. This allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration
VEIT17_07880	COG0063	ADP-dependent NAD(P)H-hydrate dehydratase activity
VEIT17_07890	COG0658	competence protein
VEIT17_07890	COG2333	competence protein COMEC
VEIT17_07900	COG0860	N-Acetylmuramoyl-L-alanine amidase
VEIT17_07920	COG0611	Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1
VEIT17_07930	COG0802	atpase or kinase
VEIT17_07940	COG1214	PFAM Peptidase M22, glycoprotease
VEIT17_07990	COG0234	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter
VEIT17_08000	COG0459	protein refolding
VEIT17_08030	COG0396	ATPase activity
VEIT17_08060	COG0520	Catalyzes the removal of elemental sulfur and selenium atoms from L-cysteine, L-cystine, L-selenocysteine, and L- selenocystine to produce L-alanine
VEIT17_08070	COG0822	iron-sulfur transferase activity
VEIT17_08110	COG3880	PFAM UvrB UvrC protein
VEIT17_08120	COG3869	Catalyzes the specific phosphorylation of arginine residues in
VEIT17_08130	COG0542	response to heat
VEIT17_08140	COG1066	DNA-dependent ATPase involved in processing of recombination intermediates, plays a role in repairing DNA breaks. Stimulates the branch migration of RecA-mediated strand transfer reactions, allowing the 3' invading strand to extend heteroduplex DNA faster. Binds ssDNA in the presence of ADP but not other nucleotides, has ATPase activity that is stimulated by ssDNA and various branched DNA structures, but inhibited by SSB. Does not have RecA's homology-searching function
VEIT17_08150	COG4956	integral membrane protein (PIN domain superfamily)
VEIT17_08160	COG0245	2-C-methyl-D-erythritol 2,4-cyclodiphosphate synthase activity
VEIT17_08160	COG1211	2-C-methyl-D-erythritol 4-phosphate cytidylyltransferase activity
VEIT17_08170	COG0008	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)
VEIT17_08180	COG0385	Bile acid
VEIT17_08190	COG0215	cysteine-tRNA ligase activity
VEIT17_08200	COG1939	Involved in correct processing of both the 5' and 3' ends of 23S rRNA precursor. Processes 30S rRNA precursor transcript even in absence of ribonuclease 3 (Rnc)
VEIT17_08210	COG0566	Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family
VEIT17_08240	COG1314	P-P-bond-hydrolysis-driven protein transmembrane transporter activity
VEIT17_08250	COG0557	exoribonuclease II activity
VEIT17_08260	COG0691	Required for rescue of stalled ribosomes mediated by trans-translation. Binds to transfer-messenger RNA (tmRNA), required for stable association of tmRNA with ribosomes. tmRNA and SmpB together mimic tRNA shape, replacing the anticodon stem-loop with SmpB. tmRNA is encoded by the ssrA gene
VEIT17_08280	COG1424	Catalyzes the transformation of pimelate into pimeloyl- CoA with concomitant hydrolysis of ATP to AMP
VEIT17_08320	COG1227	inorganic diphosphatase activity
VEIT17_08330	COG0210	DNA helicase
VEIT17_08340	COG0272	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
VEIT17_08380	COG0154	amidase activity
VEIT17_08390	COG0064	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)
VEIT17_08420	COG1242	4 iron, 4 sulfur cluster binding
VEIT17_08430	COG1702	phosphate starvation-inducible protein PhoH
VEIT17_08450	COG1159	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
VEIT17_08460	COG1253	flavin adenine dinucleotide binding
VEIT17_08570	COG0752	glycyl-tRNA synthetase alpha subunit
VEIT17_08580	COG0751	glycine-tRNA ligase activity
VEIT17_08600	COG0335	large ribosomal subunit rRNA binding
VEIT17_08620	COG0164	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids
VEIT17_08630	COG0792	nuclease activity
VEIT17_08650	COG0758	DNA mediated transformation
VEIT17_08660	COG0550	Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone
VEIT17_08670	COG1206	Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs
VEIT17_08680	COG0682	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins
VEIT17_08690	COG3858	chitin binding
VEIT17_08690	COG1388	LysM domain
VEIT17_08700	COG0495	leucyl-tRNA aminoacylation
VEIT17_08730	COG1555	photosystem II stabilization
VEIT17_08790	COG0028	Belongs to the TPP enzyme family
VEIT17_08800	COG0117	Converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)- pyrimidinedione 5'-phosphate
VEIT17_08800	COG1985	Converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)- pyrimidinedione 5'-phosphate
VEIT17_08820	COG0807	Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate
VEIT17_08820	COG0108	Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate
VEIT17_08840	COG1281	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
VEIT17_08850	COG0005	The purine nucleoside phosphorylases catalyze the phosphorolytic breakdown of the N-glycosidic bond in the beta- (deoxy)ribonucleoside molecules, with the formation of the corresponding free purine bases and pentose-1-phosphate
VEIT17_08860	COG0182	Catalyzes the interconversion of methylthioribose-1- phosphate (MTR-1-P) into methylthioribulose-1-phosphate (MTRu-1- P)
VEIT17_08870	COG0499	May play a key role in the regulation of the intracellular concentration of adenosylhomocysteine
VEIT17_08880	COG0402	S-adenosylhomocysteine deaminase activity
VEIT17_08900	COG2226	methyltransferase
VEIT17_08950	COG0671	phosphoesterase, PA-phosphatase related
VEIT17_08960	COG2720	vancomycin resistance protein
VEIT17_08990	COG1974	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
VEIT17_09000	COG0329	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA)
VEIT17_09010	COG0136	Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate
VEIT17_09020	COG0289	4-hydroxy-tetrahydrodipicolinate reductase
VEIT17_09030	COG1438	arginine binding
VEIT17_09050	COG0061	Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP
VEIT17_09060	COG1189	Ribosomal RNA methyltransferase RrmJ FtsJ
VEIT17_09090	COG1722	exodeoxyribonuclease VII activity
VEIT17_09110	COG0533	Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction
VEIT17_09120	COG0781	Involved in transcription antitermination. Required for transcription of ribosomal RNA (rRNA) genes. Binds specifically to the boxA antiterminator sequence of the ribosomal RNA (rrn) operons
VEIT17_09150	COG0231	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
VEIT17_09160	COG0006	proline dipeptidase activity
VEIT17_09170	COG1187	pseudouridine synthase activity
VEIT17_09180	COG0406	alpha-ribazole phosphatase activity
VEIT17_09210	COG0368	Joins adenosylcobinamide-GDP and alpha-ribazole to generate adenosylcobalamin (Ado-cobalamin). Also synthesizes adenosylcobalamin 5'-phosphate from adenosylcobinamide-GDP and alpha-ribazole 5'-phosphate
VEIT17_09230	COG1492	cobalamin metabolic process
VEIT17_09270	COG0105	UTP biosynthetic process
VEIT17_09290	COG0083	homoserine kinase activity
VEIT17_09300	COG0460	homoserine dehydrogenase
VEIT17_09310	COG4492	Belongs to the UPF0735 family
VEIT17_09330	COG3394	polysaccharide catabolic process
VEIT17_09340	COG0566	Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family
VEIT17_09350	COG1132	(ABC) transporter
VEIT17_09360	COG1132	(ABC) transporter
VEIT17_09370	COG2077	Thiol-specific peroxidase that catalyzes the reduction of hydrogen peroxide and organic hydroperoxides to water and alcohols, respectively. Plays a role in cell protection against oxidative stress by detoxifying peroxides
VEIT17_09380	COG0174	glutamine synthetase
VEIT17_09390	COG1610	YqeY-like protein
VEIT17_09400	COG0828	Belongs to the bacterial ribosomal protein bS21 family
VEIT17_09410	COG0537	adenosine 5'-monophosphoramidase activity
VEIT17_09420	COG0621	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
VEIT17_09430	COG1385	rRNA (uridine-N3-)-methyltransferase activity
VEIT17_09440	COG2264	protein methyltransferase activity
VEIT17_09450	COG0484	heat shock protein binding
VEIT17_09460	COG0443	Heat shock 70 kDa protein
VEIT17_09470	COG0576	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
VEIT17_09480	COG1420	regulation of RNA biosynthetic process
VEIT17_09500	COG0635	Involved in the biosynthesis of porphyrin-containing compound
VEIT17_09510	COG0481	GTPase activity
VEIT17_09520	COG0482	sulfurtransferase activity
VEIT17_09530	COG4100	CystaTHIonine beta-lyase family protein involved in aluminum resistance
VEIT17_09540	COG0324	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)
VEIT17_09550	COG2521	methyltransferase
VEIT17_09550	COG2136	Putative SAM-dependent methyltransferase
VEIT17_09560	COG0323	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
VEIT17_09570	COG0249	that it carries out the mismatch recognition step. This protein has a weak ATPase activity
VEIT17_09580	COG0621	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
VEIT17_09610	COG0442	prolyl-tRNA aminoacylation
VEIT17_09620	COG0821	Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate
VEIT17_09630	COG0750	zinc metalloprotease
VEIT17_09640	COG0743	1-deoxy-D-xylulose-5-phosphate reductoisomerase activity
VEIT17_09650	COG4589	Belongs to the CDS family
VEIT17_09680	COG0233	cytoplasmic translational termination
VEIT17_09690	COG0528	UMP kinase activity
VEIT17_09700	COG0264	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
VEIT17_09710	COG0052	Belongs to the universal ribosomal protein uS2 family
VEIT17_09720	COG0036	Belongs to the ribulose-phosphate 3-epimerase family
VEIT17_09730	COG1162	GTPase activity
VEIT17_09740	COG2815	serine threonine protein kinase
VEIT17_09740	COG0515	serine threonine protein kinase
VEIT17_09750	COG0631	protein serine/threonine phosphatase activity
VEIT17_09760	COG0820	rRNA (adenine-C2-)-methyltransferase activity
VEIT17_09770	COG0781	Involved in transcription antitermination. Required for transcription of ribosomal RNA (rRNA) genes. Binds specifically to the boxA antiterminator sequence of the ribosomal RNA (rrn) operons
VEIT17_09770	COG0144	Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA
VEIT17_09800	COG0223	Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus
VEIT17_09810	COG0242	peptide deformylase activity
VEIT17_09820	COG1198	Involved in the restart of stalled replication forks. Recognizes and binds the arrested nascent DNA chain at stalled replication forks. It can open the DNA duplex, via its helicase activity, and promote assembly of the primosome and loading of the major replicative helicase DnaB onto DNA
VEIT17_09830	COG0192	Catalyzes the formation of S-adenosylmethionine (AdoMet) from methionine and ATP. The overall synthetic reaction is composed of two sequential steps, AdoMet formation and the subsequent tripolyphosphate hydrolysis which occurs prior to release of AdoMet from the enzyme
VEIT17_09840	COG0452	Catalyzes two steps in the biosynthesis of coenzyme A. In the first step cysteine is conjugated to 4'-phosphopantothenate to form 4-phosphopantothenoylcysteine, in the latter compound is decarboxylated to form 4'-phosphopantotheine
VEIT17_09850	COG1758	RNA polymerase activity
VEIT17_09860	COG0194	GDP metabolic process
VEIT17_09890	COG1561	YicC-like family, N-terminal region
VEIT17_09900	COG1293	RNA-binding protein homologous to eukaryotic snRNP
VEIT17_09920	COG0669	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate
VEIT17_09930	COG0742	ribosomal rna small subunit methyltransferase
VEIT17_09940	COG0240	glycerol-3-phosphate dehydrogenase [NAD(P)+] activity
VEIT17_09950	COG0344	acyl-phosphate glycerol-3-phosphate acyltransferase activity
VEIT17_09960	COG1160	GTP binding
VEIT17_09970	COG0761	Catalyzes the conversion of 1-hydroxy-2-methyl-2-(E)- butenyl 4-diphosphate (HMBPP) into a mixture of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP). Acts in the terminal step of the DOXP MEP pathway for isoprenoid precursor biosynthesis
VEIT17_09970	COG0539	negative regulation of cytoplasmic translation
VEIT17_09990	COG0283	belongs to the cytidylate kinase family. Type 1 subfamily
VEIT17_10000	COG2081	HI0933 family
VEIT17_10010	COG1187	pseudouridine synthase activity
VEIT17_10020	COG1386	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
VEIT17_10030	COG1354	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
VEIT17_10050	COG1683	Conserved Protein
VEIT17_10060	COG0491	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid
VEIT17_10070	COG0168	Low-affinity potassium transport system. Interacts with trk system potassium uptake protein TrkA
VEIT17_10080	COG0569	domain protein
VEIT17_10090	COG2996	Protein conserved in bacteria
VEIT17_10100	COG0799	negative regulation of ribosome biogenesis
VEIT17_10110	COG1316	TRANSCRIPTIONal
VEIT17_10120	COG1713	HD superfamily hydrolase involved in NAD metabolism
VEIT17_10130	COG1057	Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD)
VEIT17_10140	COG0014	Catalyzes the NADPH-dependent reduction of L-glutamate 5-phosphate into L-glutamate 5-semialdehyde and phosphate. The product spontaneously undergoes cyclization to form 1-pyrroline-5- carboxylate
VEIT17_10150	COG0263	Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate
VEIT17_10170	COG0536	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. Plays a role in control of the cell cycle, stress response, ribosome biogenesis and in those bacteria that undergo differentiation, in morphogenesis control
VEIT17_10180	COG0793	Belongs to the peptidase S41A family
VEIT17_10190	COG0739	heme binding
VEIT17_10200	COG2177	Part of the ABC transporter FtsEX involved in
VEIT17_10210	COG2884	Cell division ATP-binding protein ftsE
VEIT17_10220	COG1154	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)
VEIT17_10230	COG3959	Transketolase, thiamine diphosphate binding domain
VEIT17_10270	COG1186	Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA
VEIT17_10280	COG0653	protein targeting
VEIT17_10300	COG1278	Cold shock
VEIT17_10320	COG0765	amino acid transport
VEIT17_10330	COG0834	ABC-type amino acid transport signal transduction systems periplasmic component domain
VEIT17_10350	COG1040	competence protein
VEIT17_10360	COG0507	A helicase nuclease that prepares dsDNA breaks (DSB) for recombinational DNA repair. Binds to DSBs and unwinds DNA via a highly rapid and processive ATP-dependent bidirectional helicase activity. Unwinds dsDNA until it encounters a Chi (crossover hotspot instigator) sequence from the 3' direction. Cuts ssDNA a few nucleotides 3' to the Chi site. The properties and activities of the enzyme are changed at Chi. The Chi-altered holoenzyme produces a long 3'-ssDNA overhang and facilitates RecA-binding to the ssDNA for homologous DNA recombination and repair. Holoenzyme degrades any linearized DNA that is unable to undergo homologous recombination. In the holoenzyme this subunit has ssDNA-dependent ATPase and 5'-3' helicase activity. When added to pre-assembled RecBC greatly stimulates nuclease activity and augments holoenzyme processivity. Negatively regulates the RecA-loading ability of RecBCD
VEIT17_10380	COG0196	riboflavin kinase activity
VEIT17_10410	COG0858	One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Associates with free 30S ribosomal subunits (but not with 30S subunits that are part of 70S ribosomes or polysomes). Required for efficient processing of 16S rRNA. May interact with the 5'-terminal helix region of 16S rRNA
VEIT17_10420	COG3064	Membrane
VEIT17_10420	COG0532	One of the essential components for the initiation of protein synthesis. Protects formylmethionyl-tRNA from spontaneous hydrolysis and promotes its binding to the 30S ribosomal subunits. Also involved in the hydrolysis of GTP during the formation of the 70S ribosomal complex
VEIT17_10420	COG0532	One of the essential components for the initiation of protein synthesis. Protects formylmethionyl-tRNA from spontaneous hydrolysis and promotes its binding to the 30S ribosomal subunits. Also involved in the hydrolysis of GTP during the formation of the 70S ribosomal complex
VEIT17_10420	COG3064	Membrane
VEIT17_10430	COG1358	cellular component organization or biogenesis
VEIT17_10450	COG0195	Participates in both transcription termination and antitermination
VEIT17_10460	COG0779	Required for maturation of 30S ribosomal subunits
VEIT17_10480	COG0741	lytic transglycosylase activity
VEIT17_10490	COG0237	dephospho-CoA kinase activity
VEIT17_10500	COG0749	In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity
VEIT17_10500	COG0258	In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity
VEIT17_10510	COG0268	Binds directly to 16S ribosomal RNA
VEIT17_10540	COG1015	Phosphotransfer between the C1 and C5 carbon atoms of pentose
VEIT17_10580	COG0756	dUTP diphosphatase activity
VEIT17_10590	COG1185	polyribonucleotide nucleotidyltransferase activity
VEIT17_10610	COG3638	Part of the ABC transporter complex PhnCDE involved in phosphonates import. Responsible for energy coupling to the transport system
VEIT17_10620	COG4120	Belongs to the binding-protein-dependent transport system permease family
VEIT17_10660	COG1362	aminopeptidase activity
VEIT17_10670	COG2176	DNA-directed DNA polymerase activity
VEIT17_10690	COG0859	PFAM glycosyl transferase family 9
VEIT17_10700	COG0241	D,D-heptose 1,7-bisphosphate phosphatase
VEIT17_10710	COG0451	ADP-glyceromanno-heptose 6-epimerase activity
VEIT17_10720	COG0615	ADP-L-glycero-beta-D-manno-heptose biosynthetic process
VEIT17_10720	COG2870	Catalyzes the ADP transfer from ATP to D-glycero-beta-D- manno-heptose 1-phosphate, yielding ADP-D-glycero-beta-D-manno- heptose
VEIT17_10730	COG0279	D-glycero-D-manno-heptose 7-phosphate biosynthetic process
VEIT17_10750	COG1327	Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes
VEIT17_10770	COG1038	Catalyzes a 2-step reaction, involving the ATP-dependent carboxylation of the covalently attached biotin in the first step and the transfer of the carboxyl group to pyruvate in the second
VEIT17_10780	COG1362	aminopeptidase activity
VEIT17_10790	COG0471	metal ion transport
VEIT17_10810	COG1167	Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain MocR family and their eukaryotic orthologs
VEIT17_10840	COG0115	Belongs to the class-IV pyridoxal-phosphate-dependent aminotransferase family
VEIT17_10860	COG0179	Fumarylacetoacetate (FAA) hydrolase
VEIT17_10930	COG2801	Transposase and inactivated derivatives
VEIT17_11030	COG2265	Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family
VEIT17_11040	COG0861	Integral membrane protein TerC family
VEIT17_11050	COG0861	Integral membrane protein TerC family
VEIT17_11060	COG0534	Mate efflux family protein
VEIT17_11080	COG0322	excinuclease ABC activity
VEIT17_11090	COG0178	The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrA is an ATPase and a DNA-binding protein. A damage recognition complex composed of 2 uvrA and 2 uvrB subunits scans DNA for abnormalities. When the presence of a lesion has been verified by uvrB, the uvrA molecules dissociate
VEIT17_11100	COG0556	nucleotide-excision repair
VEIT17_11120	COG0552	protein localization to endoplasmic reticulum
VEIT17_11130	COG1196	nuclear chromosome segregation
VEIT17_11140	COG0621	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
VEIT17_11150	COG0571	ribonuclease III activity
VEIT17_11160	COG0304	beta-ketoacyl-acyl-carrier-protein synthase II activity
VEIT17_11170	COG2070	2-Nitropropane dioxygenase
VEIT17_11180	COG0236	Carrier of the growing fatty acid chain in fatty acid biosynthesis
VEIT17_11190	COG1028	Short-chain dehydrogenase reductase Sdr
VEIT17_11200	COG0331	[acyl-carrier-protein] S-malonyltransferase activity
VEIT17_11220	COG0332	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
VEIT17_11230	COG0416	fatty acid biosynthetic process
VEIT17_11250	COG0333	Belongs to the bacterial ribosomal protein bL32 family
VEIT17_11270	COG1773	rubredoxin
VEIT17_11310	COG0602	queuosine metabolic process
VEIT17_11440	COG3475	LICD family
VEIT17_11450	COG2148	undecaprenyl-phosphate glucose phosphotransferase activity
VEIT17_11460	COG0399	UDP-4-amino-4-deoxy-L-arabinose aminotransferase
VEIT17_11470	COG3206	protein involved in exopolysaccharide biosynthesis
VEIT17_11470	COG0489	protein tyrosine kinase activity
VEIT17_11560	COG0488	(ABC) transporter
VEIT17_11600	COG1087	Belongs to the NAD(P)-dependent epimerase dehydratase family
VEIT17_11610	COG0166	Belongs to the GPI family
VEIT17_11630	COG0451	ADP-glyceromanno-heptose 6-epimerase activity
VEIT17_11650	COG2606	Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily
VEIT17_11670	COG0365	Catalyzes the conversion of acetate into acetyl-CoA (AcCoA), an essential intermediate at the junction of anabolic and catabolic pathways. AcsA undergoes a two-step reaction. In the first half reaction, AcsA combines acetate with ATP to form acetyl-adenylate (AcAMP) intermediate. In the second half reaction, it can then transfer the acetyl group from AcAMP to the sulfhydryl group of CoA, forming the product AcCoA
VEIT17_11680	COG0183	Belongs to the thiolase family
VEIT17_11690	COG1268	BioY protein
VEIT17_11760	COG0409	Hydrogenase expression formation protein
VEIT17_11770	COG0298	carbon dioxide binding
VEIT17_11780	COG0068	Along with HypE, it catalyzes the synthesis of the CN ligands of the active site iron of NiFe -hydrogenases using carbamoylphosphate as a substrate. It functions as a carbamoyl transferase using carbamoylphosphate as a substrate and transferring the carboxamido moiety in an ATP-dependent reaction to the thiolate of the C-terminal cysteine of HypE yielding a protein-S-carboxamide
VEIT17_11790	COG0820	rRNA (adenine-C2-)-methyltransferase activity
VEIT17_11870	COG1918	ferrous iron import across plasma membrane
VEIT17_11870	COG0370	Transporter of a GTP-driven Fe(2 ) uptake system
VEIT17_11900	COG0550	Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone
VEIT17_11910	COG4108	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
VEIT17_11920	COG0786	glutamate:sodium symporter activity
VEIT17_11930	COG0030	16S rRNA (adenine(1518)-N(6)/adenine(1519)-N(6))-dimethyltransferase activity
VEIT17_11940	COG1658	Required for correct processing of both the 5' and 3' ends of 5S rRNA precursor. Cleaves both sides of a double-stranded region yielding mature 5S rRNA in one step
VEIT17_11950	COG0583	DNA-binding transcription factor activity
VEIT17_11960	COG0620	Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation
VEIT17_11970	COG0229	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
VEIT17_11970	COG0225	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
VEIT17_11980	COG1388	LysM domain
VEIT17_11980	COG3584	3D domain protein
VEIT17_11990	COG0855	Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP)
VEIT17_12020	COG0084	hydrolase, TatD family'
VEIT17_12030	COG0143	Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation
VEIT17_12030	COG0073	Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation
VEIT17_12040	COG0313	Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA
VEIT17_12060	COG1774	PSP1 C-terminal conserved region
VEIT17_12070	COG2812	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
VEIT17_12080	COG0125	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis
VEIT17_12090	COG1982	Orn Lys Arg decarboxylase major
VEIT17_12100	COG0193	aminoacyl-tRNA hydrolase activity
VEIT17_12120	COG1207	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
VEIT17_12130	COG0503	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis
VEIT17_12140	COG1388	LysM domain
VEIT17_12140	COG3584	3D domain protein
VEIT17_12150	COG3004	Na( ) H( ) antiporter that extrudes sodium in exchange for external protons
VEIT17_12160	COG3004	Na( ) H( ) antiporter that extrudes sodium in exchange for external protons
VEIT17_12180	COG3585	molybdate ion transport
VEIT17_12200	COG0341	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
VEIT17_12210	COG0342	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
VEIT17_12230	COG1862	Preprotein translocase
VEIT17_12240	COG0343	queuine tRNA-ribosyltransferase activity
VEIT17_12260	COG2385	sporulation resulting in formation of a cellular spore
VEIT17_12260	COG2247	cell wall binding repeat
VEIT17_12270	COG2255	four-way junction helicase activity
VEIT17_12280	COG0632	four-way junction helicase activity
VEIT17_12290	COG0817	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
VEIT17_12310	COG4752	Belongs to the RNA methyltransferase TrmD family
VEIT17_12360	COG0702	epimerase
VEIT17_12370	COG0336	Belongs to the RNA methyltransferase TrmD family
VEIT17_12380	COG0806	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
VEIT17_12420	COG0541	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
VEIT17_12430	COG2739	Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY ffh. May be a regulatory protein
VEIT17_12440	COG1249	Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family
VEIT17_12460	COG2217	Heavy metal translocating P-type atpase
VEIT17_12470	COG1739	Uncharacterized protein family UPF0029
VEIT17_12490	COG0583	DNA-binding transcription factor activity
VEIT17_12500	COG0167	dihydroorotate dehydrogenase activity
VEIT17_12510	COG0543	2 iron, 2 sulfur cluster binding
VEIT17_12540	COG0044	hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in cyclic amides
VEIT17_12550	COG0540	Belongs to the ATCase OTCase family
VEIT17_12570	COG1481	regulation of sporulation
VEIT17_12580	COG0391	Required for morphogenesis under gluconeogenic growth conditions
VEIT17_12590	COG1660	Displays ATPase and GTPase activities
VEIT17_12600	COG0561	phosphatase activity
VEIT17_12610	COG0497	DNA recombination
VEIT17_12620	COG0497	DNA recombination
VEIT17_12640	COG1284	Uncharacterised 5xTM membrane BCR, YitT family COG1284
VEIT17_12660	COG4372	Transposase
VEIT17_12680	COG1137	ATPase activity
VEIT17_12690	COG1452	involved in the assembly of lipopolysaccharide (LPS) at the surface of the outer membrane
VEIT17_12720	COG1778	Involved in the biosynthesis of lipopolysaccharides (LPSs). Catalyzes the hydrolysis of 3-deoxy-D-manno-octulosonate 8-phosphate (KDO 8-P) to 3-deoxy-D-manno-octulosonate (KDO) and inorganic phosphate
VEIT17_12740	COG2877	3-deoxy-8-phosphooctulonate synthase activity
VEIT17_12750	COG1212	Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria
VEIT17_12760	COG1663	tetraacyldisaccharide 4'-kinase activity
VEIT17_12770	COG1519	Transferase
VEIT17_12780	COG1132	(ABC) transporter
VEIT17_12790	COG0763	Condensation of UDP-2,3-diacylglucosamine and 2,3- diacylglucosamine-1-phosphate to form lipid A disaccharide, a precursor of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell
VEIT17_12810	COG1043	involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell
VEIT17_12820	COG0764	3-hydroxyoctanoyl-[acyl-carrier-protein] dehydratase activity
VEIT17_12830	COG0774	UDP-3-O-[3-hydroxymyristoyl] N-acetylglucosamine deacetylase activity
VEIT17_12840	COG1560	Kdo2-lipid A biosynthetic process
VEIT17_12850	COG1044	Catalyzes the N-acylation of UDP-3-O-acylglucosamine using 3-hydroxyacyl-ACP as the acyl donor. Is involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell
VEIT17_12930	COG1127	ABC transporter
VEIT17_12940	COG0767	ABC-type transport system involved in resistance to organic solvents, permease component
VEIT17_12990	COG0766	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine
VEIT17_13000	COG1494	fructose-1,6-bisphosphatase
VEIT17_13010	COG0176	Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway
VEIT17_13040	COG0402	S-adenosylhomocysteine deaminase activity
VEIT17_13050	COG1982	Orn Lys Arg decarboxylase major
VEIT17_13060	COG1190	Belongs to the class-II aminoacyl-tRNA synthetase family
VEIT17_13070	COG0782	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
VEIT17_13080	COG0042	Catalyzes the synthesis of 5,6-dihydrouridine (D), a modified base found in the D-loop of most tRNAs, via the reduction of the C5-C6 double bond in target uridines
VEIT17_13090	COG1521	Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis
VEIT17_13120	COG0465	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
VEIT17_13140	COG0037	tRNA processing
VEIT17_13160	COG1098	S1 RNA binding domain
VEIT17_13180	COG0039	L-malate dehydrogenase activity
VEIT17_13190	COG2261	transglycosylase associated protein
VEIT17_13210	COG0801	2-amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase
VEIT17_13220	COG1539	Catalyzes the conversion of 7,8-dihydroneopterin to 6- hydroxymethyl-7,8-dihydropterin
VEIT17_13230	COG0294	Catalyzes the condensation of para-aminobenzoate (pABA) with 6-hydroxymethyl-7,8-dihydropterin diphosphate (DHPt-PP) to form 7,8-dihydropteroate (H2Pte), the immediate precursor of folate derivatives
VEIT17_13250	COG0488	(ABC) transporter
VEIT17_13270	COG1619	proteins homologs of microcin C7 resistance protein MccF
VEIT17_13280	COG4166	transmembrane transport
VEIT17_13300	COG4608	Belongs to the ABC transporter superfamily
VEIT17_13310	COG0444	Belongs to the ABC transporter superfamily
VEIT17_13320	COG1173	ABC-type dipeptide oligopeptide nickel transport systems, permease components
VEIT17_13330	COG0601	transmembrane transport
VEIT17_13360	COG2801	Transposase and inactivated derivatives
VEIT17_13390	COG4988	ABC transporter
VEIT17_13400	COG1294	oxidase, subunit
VEIT17_13410	COG1271	oxidase subunit
VEIT17_13420	COG1959	2 iron, 2 sulfur cluster binding
VEIT17_13430	COG0521	Mo-molybdopterin cofactor biosynthetic process
VEIT17_13440	COG0726	polysaccharide deacetylase
VEIT17_13450	COG0421	Catalyzes the irreversible transfer of a propylamine group from the amino donor S-adenosylmethioninamine (decarboxy- AdoMet) to putrescine (1,4-diaminobutane) to yield spermidine
VEIT17_13470	COG0652	PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides
VEIT17_13480	COG1179	involved in molybdopterin and THIamine biosynthesis family 1
VEIT17_13500	COG0419	ATPase involved in DNA repair
VEIT17_13510	COG0420	3'-5' exonuclease activity
VEIT17_13520	COG0648	Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin
VEIT17_13530	COG0735	belongs to the Fur family
VEIT17_13540	COG0513	Belongs to the DEAD box helicase family
VEIT17_13600	COG1012	belongs to the aldehyde dehydrogenase family
VEIT17_13610	COG2183	response to ionizing radiation
VEIT17_13620	COG0262	Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis
VEIT17_13630	COG0207	Catalyzes the reductive methylation of 2'-deoxyuridine- 5'-monophosphate (dUMP) to 2'-deoxythymidine-5'-monophosphate (dTMP) while utilizing 5,10-methylenetetrahydrofolate (mTHF) as the methyl donor and reductant in the reaction, yielding dihydrofolate (DHF) as a by-product. This enzymatic reaction provides an intracellular de novo source of dTMP, an essential precursor for DNA biosynthesis
VEIT17_13640	COG0514	ATP-dependent DNA helicase (RecQ)
VEIT17_13650	COG0591	Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family
VEIT17_13670	COG2230	cyclopropane-fatty-acyl-phospholipid synthase
VEIT17_13670	COG4797	methyltransferase
VEIT17_13690	COG0583	DNA-binding transcription factor activity
VEIT17_13760	COG2301	Belongs to the HpcH HpaI aldolase family
VEIT17_13770	COG3052	prosthetic group binding
VEIT17_13780	COG0471	metal ion transport
VEIT17_13790	COG0583	DNA-binding transcription factor activity
VEIT17_13800	COG0670	Belongs to the BI1 family
VEIT17_13900	COG0001	glutamate-1-semialdehyde 2,1-aminomutase activity
VEIT17_13910	COG0113	porphobilinogen synthase activity
VEIT17_13920	COG0007	Multifunctional enzyme that catalyzes the SAM-dependent methylations of uroporphyrinogen III at position C-2 and C-7 to form precorrin-2 via precorrin-1. Then it catalyzes the NAD- dependent ring dehydrogenation of precorrin-2 to yield sirohydrochlorin. Finally, it catalyzes the ferrochelation of sirohydrochlorin to yield siroheme
VEIT17_13920	COG1587	Uroporphyrinogen-III synthase
VEIT17_13940	COG0373	Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA)
VEIT17_13950	COG0007	Multifunctional enzyme that catalyzes the SAM-dependent methylations of uroporphyrinogen III at position C-2 and C-7 to form precorrin-2 via precorrin-1. Then it catalyzes the NAD- dependent ring dehydrogenation of precorrin-2 to yield sirohydrochlorin. Finally, it catalyzes the ferrochelation of sirohydrochlorin to yield siroheme
VEIT17_13950	COG1648	precorrin-2 dehydrogenase activity
VEIT17_13960	COG2302	S4 RNA-binding domain
VEIT17_13970	COG0345	Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline
VEIT17_13980	COG1799	cell septum assembly
VEIT17_14010	COG0621	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
VEIT17_14020	COG2323	membrane
VEIT17_14050	COG0059	Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate
VEIT17_14060	COG1119	ATPase activity
VEIT17_14080	COG0028	Belongs to the TPP enzyme family
VEIT17_14090	COG1171	Catalyzes the anaerobic formation of alpha-ketobutyrate and ammonia from threonine in a two-step reaction. The first step involved a dehydration of threonine and a production of enamine intermediates (aminocrotonate), which tautomerizes to its imine form (iminobutyrate). Both intermediates are unstable and short- lived. The second step is the nonenzymatic hydrolysis of the enamine imine intermediates to form 2-ketobutyrate and free ammonia. In the low water environment of the cell, the second step is accelerated by RidA
VEIT17_14100	COG0129	dihydroxy-acid dehydratase activity
VEIT17_14120	COG0471	metal ion transport
VEIT17_14130	COG0662	Cupin 2, conserved barrel domain protein
VEIT17_14150	COG1826	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
VEIT17_14160	COG0363	glucosamine-6-phosphate deaminase activity
VEIT17_14170	COG1024	Enoyl-CoA hydratase
VEIT17_14180	COG0103	maturation of SSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA)
VEIT17_14190	COG0102	This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly
VEIT17_14200	COG0522	One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the body of the 30S subunit
VEIT17_14210	COG0583	DNA-binding transcription factor activity
VEIT17_14220	COG1742	UPF0060 membrane protein
VEIT17_14250	COG2038	nicotinate-nucleotide-dimethylbenzimidazole phosphoribosyltransferase activity
VEIT17_14260	COG2038	nicotinate-nucleotide-dimethylbenzimidazole phosphoribosyltransferase activity
VEIT17_14270	COG0287	Prephenate dehydrogenase
VEIT17_14280	COG0534	Mate efflux family protein
VEIT17_14310	COG1013	pyruvate-flavodoxin oxidoreductase activity
VEIT17_14320	COG0674	pyruvate-flavodoxin oxidoreductase activity
VEIT17_14320	COG1014	Oxidoreductase required for the transfer of electrons from pyruvate to flavodoxin
VEIT17_14340	COG0619	Transmembrane (T) component of an energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates
VEIT17_14360	COG1122	ATPase activity
VEIT17_14370	COG0203	ribosomal protein L17
VEIT17_14380	COG0202	RNA polymerase activity
VEIT17_14400	COG0099	Located at the top of the head of the 30S subunit, it contacts several helices of the 16S rRNA. In the 70S ribosome it contacts the 23S rRNA (bridge B1a) and protein L5 of the 50S subunit (bridge B1b), connecting the 2 subunits
VEIT17_14440	COG0201	protein transport
VEIT17_14450	COG0200	Binds to the 23S rRNA
VEIT17_14460	COG1841	ribosomal large subunit assembly
VEIT17_14470	COG0098	Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body
VEIT17_14480	COG0256	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
VEIT17_14500	COG0096	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
VEIT17_14520	COG0094	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
VEIT17_14540	COG0093	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome
VEIT17_14560	COG0255	Belongs to the universal ribosomal protein uL29 family
VEIT17_14570	COG0197	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs
VEIT17_14580	COG0092	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation
VEIT17_14590	COG0091	The globular domain of the protein is located near the polypeptide exit tunnel on the outside of the subunit, while an extended beta-hairpin is found that lines the wall of the exit tunnel in the center of the 70S ribosome
VEIT17_14600	COG0185	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA
VEIT17_14610	COG0090	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
VEIT17_14630	COG0088	Forms part of the polypeptide exit tunnel
VEIT17_14640	COG0087	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
VEIT17_14650	COG0051	transcription antitermination factor activity, RNA binding
VEIT17_14660	COG0050	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis
VEIT17_14680	COG0049	tRNA binding
VEIT17_14690	COG0048	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
VEIT17_14710	COG0086	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates
VEIT17_14720	COG0085	RNA polymerase activity
VEIT17_14730	COG1027	Aspartate ammonia-lyase
VEIT17_14740	COG1807	4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family
VEIT17_14760	COG0222	ribosome binding
VEIT17_14780	COG0081	regulation of translation
VEIT17_14790	COG0080	Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors
VEIT17_14800	COG0250	Participates in transcription elongation, termination and antitermination
VEIT17_14810	COG0690	P-P-bond-hydrolysis-driven protein transmembrane transporter activity
VEIT17_14820	COG0267	Belongs to the bacterial ribosomal protein bL33 family
VEIT17_14840	COG0050	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis
VEIT17_14850	COG1968	undecaprenyl-diphosphatase activity
VEIT17_14880	COG0378	Facilitates the functional incorporation of the urease nickel metallocenter. This process requires GTP hydrolysis, probably effectuated by UreG
VEIT17_14900	COG0190	Catalyzes the oxidation of 5,10- methylenetetrahydrofolate to 5,10-methenyltetrahydrofolate and then the hydrolysis of 5,10-methenyltetrahydrofolate to 10- formyltetrahydrofolate
VEIT17_14910	COG0768	penicillin binding
VEIT17_14920	COG0617	tRNA 3'-terminal CCA addition
VEIT17_14930	COG1760	l-serine dehydratase
VEIT17_14940	COG1760	l-serine dehydratase
VEIT17_14950	COG1151	hydroxylamine reductase activity
VEIT17_15030	COG0355	proton-transporting ATP synthase activity, rotational mechanism
VEIT17_15060	COG0056	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit
VEIT17_15070	COG0712	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
VEIT17_15080	COG0711	Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0)
VEIT17_15090	COG0636	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
VEIT17_15100	COG0356	it plays a direct role in the translocation of protons across the membrane
VEIT17_15130	COG0381	UDP-N-acetylglucosamine 2-epimerase activity
VEIT17_15140	COG0472	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan
VEIT17_15150	COG2848	UPF0210 protein
VEIT17_15160	COG3830	Belongs to the UPF0237 family
VEIT17_15170	COG0033	Phosphoglucomutase
VEIT17_15180	COG1284	Uncharacterised 5xTM membrane BCR, YitT family COG1284
VEIT17_15190	COG1947	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol
VEIT17_15200	COG1802	Transcriptional regulator
VEIT17_15210	COG1115	amino acid carrier protein
VEIT17_15230	COG0334	Belongs to the Glu Leu Phe Val dehydrogenases family
VEIT17_15250	COG2801	Transposase and inactivated derivatives
VEIT17_15270	COG0603	Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0))
VEIT17_15280	COG0708	Exodeoxyribonuclease III
VEIT17_15420	COG0741	lytic transglycosylase activity
VEIT17_15420	COG0791	NLP P60 protein
VEIT17_15430	COG0741	lytic transglycosylase activity
VEIT17_15430	COG0791	NLP P60 protein
VEIT17_15490	COG2946	Replication initiation factor
VEIT17_15500	COG1674	ftsk spoiiie
VEIT17_15580	COG0747	negative chemotaxis
VEIT17_15600	COG0444	Belongs to the ABC transporter superfamily
VEIT17_15610	COG0747	negative chemotaxis
VEIT17_15620	COG1173	ABC-type dipeptide oligopeptide nickel transport systems, permease components
VEIT17_15640	COG0531	amino acid
VEIT17_15650	COG0165	Argininosuccinate lyase
VEIT17_15660	COG0137	argininosuccinate synthase activity
VEIT17_15720	COG0253	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
VEIT17_15730	COG1757	Na H antiporter
VEIT17_15740	COG1105	Belongs to the carbohydrate kinase PfkB family
VEIT17_15750	COG1445	protein-N(PI)-phosphohistidine-fructose phosphotransferase system transporter activity
VEIT17_15750	COG1762	phosphoenolpyruvate-dependent sugar phosphotransferase system
VEIT17_15750	COG1299	protein-N(PI)-phosphohistidine-fructose phosphotransferase system transporter activity
VEIT17_15810	COG0450	alkyl hydroperoxide reductase
VEIT17_15830	COG0504	CTP synthase activity
VEIT17_15840	COG0018	arginyl-trna synthetase
VEIT17_15890	COG0561	phosphatase activity
VEIT17_15910	COG0371	Dehydrogenase
VEIT17_15920	COG1114	Component of the transport system for branched-chain amino acids
VEIT17_15930	COG0243	molybdopterin cofactor binding
VEIT17_15940	COG2055	Belongs to the LDH2 MDH2 oxidoreductase family
VEIT17_15950	COG1620	l-lactate permease
VEIT17_15970	COG2814	Major facilitator Superfamily
VEIT17_16010	COG4576	ethanolamine utilization protein EutN carboxysome structural protein Ccml
VEIT17_16030	COG4820	ethanolamine utilization protein (EutJ)
VEIT17_16040	COG4869	propanediol catabolic process
VEIT17_16090	COG2038	nicotinate-nucleotide-dimethylbenzimidazole phosphoribosyltransferase activity
VEIT17_16120	COG0580	Belongs to the MIP aquaporin (TC 1.A.8) family
VEIT17_16230	COG2038	nicotinate-nucleotide-dimethylbenzimidazole phosphoribosyltransferase activity
VEIT17_16270	COG1454	alcohol dehydrogenase
VEIT17_16300	COG0209	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides
VEIT17_16310	COG0208	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides
VEIT17_16360	COG2876	3-deoxy-7-phosphoheptulonate synthase activity
VEIT17_16370	COG0337	Catalyzes the conversion of 3-deoxy-D-arabino- heptulosonate 7-phosphate (DAHP) to dehydroquinate (DHQ)
VEIT17_16380	COG0128	3-phosphoshikimate 1-carboxyvinyltransferase activity
VEIT17_16390	COG0082	Catalyzes the anti-1,4-elimination of the C-3 phosphate and the C-6 proR hydrogen from 5-enolpyruvylshikimate-3-phosphate (EPSP) to yield chorismate, which is the branch point compound that serves as the starting substrate for the three terminal pathways of aromatic amino acid biosynthesis. This reaction introduces a second double bond into the aromatic ring system
VEIT17_16400	COG0077	Prephenate dehydratase
VEIT17_16400	COG1605	Chorismate mutase
VEIT17_16440	COG0710	3-dehydroquinate dehydratase activity
VEIT17_16450	COG2814	Major facilitator Superfamily
VEIT17_16460	COG1959	2 iron, 2 sulfur cluster binding
VEIT17_16470	COG2252	PERMEase
VEIT17_16530	COG1113	amino acid transport
VEIT17_16560	COG0564	pseudouridine synthase activity
VEIT17_16590	COG0353	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
VEIT17_16600	COG0718	Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection
VEIT17_16610	COG2812	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
VEIT17_16620	COG0070	glutamate synthase
VEIT17_16620	COG0069	glutamate synthase activity
VEIT17_16620	COG0067	glutamate synthase
VEIT17_16630	COG0564	pseudouridine synthase activity
VEIT17_16660	COG0845	Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family
VEIT17_16670	COG0656	L-ascorbic acid biosynthetic process
VEIT17_16680	COG1687	branched-chain amino acid
VEIT17_16690	COG1296	Branched-chain amino acid permease (Azaleucine resistance)
VEIT17_16700	COG1979	alcohol dehydrogenase
VEIT17_16720	COG2801	Transposase and inactivated derivatives
VEIT17_16740	COG0778	Nitroreductase
VEIT17_16740	COG1478	Catalyzes the GTP-dependent successive addition of multiple gamma-linked L-glutamates to the L-lactyl phosphodiester of 7,8-didemethyl-8-hydroxy-5-deazariboflavin (F420-0) to form polyglutamated F420 derivatives
VEIT17_16760	COG1251	Belongs to the nitrite and sulfite reductase 4Fe-4S domain family
VEIT17_16760	COG2146	nitrite reductase [NAD(P)H] activity
VEIT17_16780	COG1556	Lactate utilization protein
VEIT17_16790	COG1139	Iron-sulfur cluster binding protein
VEIT17_16800	COG0247	lactate metabolic process
VEIT17_16820	COG2911	Protein conserved in bacteria
VEIT17_16820	COG1361	Conserved repeat domain
VEIT17_16820	COG3266	domain, Protein
VEIT17_16840	COG1297	OPT oligopeptide transporter protein
VEIT17_16890	COG1408	metallophosphoesterase
VEIT17_16960	COG0239	Important for reducing fluoride concentration in the cell, thus reducing its toxicity
VEIT17_16990	COG1597	lipid kinase activity
VEIT17_17000	COG1074	ATP-dependent DNA helicase activity
VEIT17_17010	COG3857	The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination
VEIT17_17190	COG3209	COG3209 Rhs family protein
VEIT17_17450	COG2801	Transposase and inactivated derivatives
VEIT17_17470	COG2217	Heavy metal translocating P-type atpase
VEIT17_17490	COG0389	Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII
VEIT17_17510	COG0305	Participates in initiation and elongation during chromosome replication
VEIT17_17520	COG0359	binds to the 23S rRNA
VEIT17_17530	COG3887	signaling protein consisting of a modified GGDEF domain and a DHH domain
VEIT17_17580	COG0595	An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay
VEIT17_17600	COG1116	anion transmembrane transporter activity
VEIT17_17600	COG0715	COG0715 ABC-type nitrate sulfonate bicarbonate transport systems periplasmic components
VEIT17_17610	COG0600	ABC-type nitrate sulfonate bicarbonate transport system permease component
VEIT17_17620	COG0715	COG0715 ABC-type nitrate sulfonate bicarbonate transport systems periplasmic components
VEIT17_17630	COG1807	4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family
VEIT17_17640	COG0586	Pfam SNARE associated Golgi protein
VEIT17_17670	COG0515	serine threonine protein kinase
VEIT17_17680	COG2048	Heterodisulfide reductase, subunit B
VEIT17_17690	COG0479	Belongs to the succinate dehydrogenase fumarate reductase iron-sulfur protein family
VEIT17_17700	COG1053	succinate dehydrogenase
VEIT17_17710	COG0745	RESPONSE REGULATOR receiver
VEIT17_17720	COG3850	Histidine kinase
VEIT17_17720	COG5002	protein histidine kinase activity
VEIT17_17730	COG2733	membrane
VEIT17_17740	COG2733	membrane
VEIT17_17760	COG1733	regulation of RNA biosynthetic process
VEIT17_17770	COG2910	NAD(P)H-binding
VEIT17_17790	COG0280	phosphate acetyltransferase
VEIT17_17800	COG1373	ATPase (AAA superfamily
VEIT17_17830	COG0493	'glutamate synthase
VEIT17_17840	COG1168	Bifunctional PLP-dependent enzyme with beta-cystaTHIonase and maltose regulon repressor activities
VEIT17_17900	COG1267	Lipid phosphatase which dephosphorylates phosphatidylglycerophosphate (PGP) to phosphatidylglycerol (PG)
VEIT17_17920	COG2824	Alkylphosphonate utilization operon protein PhnA
VEIT17_17930	COG0789	Transcriptional regulator
VEIT17_18110	COG2826	transposase and inactivated derivatives, IS30 family
VEIT17_18140	COG0753	catalase activity
VEIT17_18160	COG0389	Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII
VEIT17_18190	COG0104	Plays an important role in the de novo pathway of purine nucleotide biosynthesis. Catalyzes the first committed step in the biosynthesis of AMP from IMP
VEIT17_18210	COG0015	Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily
VEIT17_18250	COG0848	biopolymer transport protein
VEIT17_18260	COG0811	peptide transport
VEIT17_18300	COG1703	isobutyryl-CoA mutase activity
VEIT17_18310	COG1884	Catalyzes the reversible interconversion of isobutyryl- CoA and n-butyryl-CoA, using radical chemistry. Also exhibits GTPase activity, associated with its G-protein domain (MeaI) that functions as a chaperone that assists cofactor delivery and proper holo-enzyme assembly
VEIT17_18310	COG2185	Catalyzes the reversible interconversion of isobutyryl- CoA and n-butyryl-CoA, using radical chemistry. Also exhibits GTPase activity, associated with its G-protein domain (MeaI) that functions as a chaperone that assists cofactor delivery and proper holo-enzyme assembly
VEIT17_18320	COG1884	Catalyzes the reversible interconversion of isobutyryl- CoA and n-butyryl-CoA, using radical chemistry. Also exhibits GTPase activity, associated with its G-protein domain (MeaI) that functions as a chaperone that assists cofactor delivery and proper holo-enzyme assembly
VEIT17_18320	COG2185	Catalyzes the reversible interconversion of isobutyryl- CoA and n-butyryl-CoA, using radical chemistry. Also exhibits GTPase activity, associated with its G-protein domain (MeaI) that functions as a chaperone that assists cofactor delivery and proper holo-enzyme assembly
VEIT17_18330	COG2962	Rard protein
VEIT17_18390	COG0277	FAD linked oxidase domain protein
VEIT17_18420	COG1454	alcohol dehydrogenase
VEIT17_18490	COG1846	Transcriptional regulator
VEIT17_18520	COG2271	Major facilitator Superfamily
VEIT17_18530	COG2271	Major facilitator Superfamily
VEIT17_18550	COG1393	Belongs to the ArsC family
VEIT17_18570	COG3549	Plasmid maintenance system killer
VEIT17_18590	COG0519	Catalyzes the synthesis of GMP from XMP
VEIT17_18720	COG3069	C4-dicarboxylate transmembrane transporter activity
VEIT17_18730	COG2195	Cleaves the N-terminal amino acid of tripeptides
VEIT17_18830	COG1595	DNA-templated transcription, initiation
VEIT17_18910	COG0188	A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner
VEIT17_18920	COG1373	ATPase (AAA superfamily
VEIT17_18950	COG1489	DNA binding
VEIT17_18980	COG1251	Belongs to the nitrite and sulfite reductase 4Fe-4S domain family
VEIT17_19060	COG2109	Required for both de novo synthesis of the corrin ring for the assimilation of exogenous corrinoids. Participates in the adenosylation of a variety of incomplete and complete corrinoids
VEIT17_19070	COG0741	lytic transglycosylase activity
VEIT17_19070	COG0739	heme binding
VEIT17_19070	COG1196	nuclear chromosome segregation
VEIT17_19090	COG1160	GTP binding
VEIT17_19100	COG1475	DNA binding
VEIT17_19110	COG1192	Involved in chromosome partitioning
VEIT17_19140	COG0646	methionine synthase
VEIT17_19140	COG0685	methylenetetrahydrofolate reductase (NAD(P)H) activity
VEIT17_19160	COG0357	Ribosomal RNA small subunit methyltransferase G
VEIT17_19200	COG0445	tRNA wobble uridine modification
VEIT17_19210	COG0486	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
VEIT17_19220	COG1847	R3H domain protein
VEIT17_19230	COG0706	membrane insertase activity
VEIT17_19240	COG0594	ribonuclease P activity
VEIT17_19250	COG0230	Belongs to the bacterial ribosomal protein bL34 family