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SLK09828.1 | Putative S4 domain protein. (68 aa) | ||||
addB | Putative ATP-dependent helicase/deoxyribonuclease subunit B; ATP-dependent DNA helicase; Belongs to the helicase family. AddB/RexB type 1 subfamily. (1145 aa) | ||||
addA | Putative Recombination helicase AddA; ATP-dependent DNA helicase. (1248 aa) | ||||
SLK10199.1 | Putative Polynucleotide adenylyltransferase/metal dependent phosphohydrolase. (452 aa) | ||||
SLK10258.1 | Putative HAD-superfamily hydrolase, subfamily IIB. (261 aa) | ||||
SLK10679.1 | Putative Xaa-pro aminopeptidase. (418 aa) | ||||
SLK10694.1 | Putative Xaa-Pro aminopeptidase 1. (588 aa) | ||||
SLK10718.1 | Putative Hydrolase, TatD family. (261 aa) | ||||
SLK10843.1 | Putative Metallopeptidase, family M24. (358 aa) | ||||
SLK10925.1 | Putative Transcriptional regulatory protein. (230 aa) | ||||
SLK11026.1 | Putative DNA-binding protein HU; Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions. (91 aa) | ||||
SLK11102.1 | Putative RNA binding S1 domain protein. (138 aa) | ||||
fhs | Putative Formate--tetrahydrofolate ligase; Belongs to the formate--tetrahydrofolate ligase family. (556 aa) | ||||
SLK11195.1 | Putative tRNA-dihydrouridine synthase; 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; Belongs to the dus family. (323 aa) | ||||
greA | Putative Transcription elongation factor GreA; Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides. (160 aa) | ||||
tRNA-Pro-1_2 | Putative Thymidylate kinase; Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis; Belongs to the thymidylate kinase family. (209 aa) | ||||
SLK11515.1 | Hypothetical protein. (132 aa) | ||||
ispD | Putative=2-C-methyl-D-erythritol 4-phosphate cytidylyltransferase; Catalyzes the formation of 4-diphosphocytidyl-2-C-methyl-D- erythritol from CTP and 2-C-methyl-D-erythritol 4-phosphate (MEP). (224 aa) | ||||
nusG | Putative Transcription antitermination protein nusG; Participates in transcription elongation, termination and antitermination. (173 aa) | ||||
SLK12017.1 | Putative Two component transcriptional regulator,winged helix family. (231 aa) | ||||
SLK12042.1 | Putative arsenate reductase; Belongs to the ArsC family. (116 aa) | ||||
SLK12047.1 | Putative Ribonucleoside-diphosphate reductase; Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides. (743 aa) | ||||
SLK12057.1 | Putative Ribonucleoside-diphosphate reductase subunit beta; Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides; Belongs to the ribonucleoside diphosphate reductase small chain family. (344 aa) | ||||
glmM | Putative Phosphoglucosamine mutase; Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate; Belongs to the phosphohexose mutase family. (447 aa) | ||||
add | Putative Adenosine deaminase; Belongs to the metallo-dependent hydrolases superfamily. Adenosine and AMP deaminases family. Adenosine deaminase subfamily. (330 aa) | ||||
SLK12358.1 | Putative Cof-like hydrolase, HAD-superfamily,subfamily IIB. (275 aa) | ||||
glpK | Putative Glycerol kinase; Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate. (498 aa) | ||||
SLK12567.1 | Putative M18 family aminopeptidase. (431 aa) | ||||
SLK12852.1 | Putative Beta-glucosidase/6-phospho-beta-glucosid ase/beta-galactosidase; Belongs to the glycosyl hydrolase 1 family. (464 aa) | ||||
SLK12881.1 | Putative Phosphomannose isomerase. (312 aa) | ||||
SLK12912.1 | Putative HAD hydrolase, IIB family. (267 aa) | ||||
SLK12991.1 | Putative L-ribulose 5-phosphate 4-epimerase SgaE. (230 aa) | ||||
SLK12997.1 | Putative hexulose-6-phosphate isomerase. (283 aa) | ||||
SLK13125.1 | Hypothetical protein. (277 aa) | ||||
SLK13241.1 | Putative Acetyltransferase. (186 aa) | ||||
SLK13267.1 | Putative Chloramphenicol acetyltransferase. (221 aa) | ||||
SLK13298.1 | Putative UDP-glucose 4-epimerase; Belongs to the NAD(P)-dependent epimerase/dehydratase family. (336 aa) | ||||
SLK13528.1 | Putative Replicative DNA helicase. (443 aa) | ||||
SLK13578.1 | Putative UvrD/REP helicase. (613 aa) | ||||
SLK13686.1 | Putative Two component transcriptional regulator,winged helix family. (224 aa) | ||||
SLK13945.1 | Hypothetical protein. (387 aa) | ||||
SLK14028.1 | Putative UDP-glucose 4-epimerase; Belongs to the NAD(P)-dependent epimerase/dehydratase family. (345 aa) | ||||
SLK14053.1 | Hypothetical protein. (211 aa) | ||||
SLK14060.1 | Hypothetical protein. (332 aa) | ||||
SLK14128.1 | Putative NAD-dependent epimerase/dehydratase. (369 aa) | ||||
SLK14262.1 | Putative Histidinol-phosphatase (HolPase); Belongs to the PHP hydrolase family. HisK subfamily. (264 aa) | ||||
SLK14273.1 | Putative Two component transcriptional regulator,winged helix family. (232 aa) | ||||
nanE | Putative N-acetylmannosamine-6-phosphate 2-epimerase; Converts N-acetylmannosamine-6-phosphate (ManNAc-6-P) to N- acetylglucosamine-6-phosphate (GlcNAc-6-P). (214 aa) | ||||
nanE-2 | Putative N-acetylmannosamine-6-phosphate 2-epimerase; Converts N-acetylmannosamine-6-phosphate (ManNAc-6-P) to N- acetylglucosamine-6-phosphate (GlcNAc-6-P). (223 aa) | ||||
SLK14348.1 | Putative YhcH/YjgK/YiaL family protein. (150 aa) | ||||
SLK14366.1 | Hypothetical protein. (119 aa) | ||||
aroC | Chorismate synthase; 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. (359 aa) | ||||
aroE | Putative Shikimate 5-dehydrogenase; Involved in the biosynthesis of the chorismate, which leads to the biosynthesis of aromatic amino acids. Catalyzes the reversible NADPH linked reduction of 3-dehydroshikimate (DHSA) to yield shikimate (SA). (268 aa) | ||||
aroQ | Putative=3-dehydroquinate dehydratase; Catalyzes a trans-dehydration via an enolate intermediate. Belongs to the type-II 3-dehydroquinase family. (141 aa) | ||||
SLK14481.1 | Putative Response regulator receiver domain protein. (45 aa) | ||||
SLK14491.1 | Putative Pseudouridine synthase; Belongs to the pseudouridine synthase RsuA family. (227 aa) | ||||
dbpA | Putative ATP-dependent RNA helicase; DEAD-box RNA helicase involved in the assembly of the 50S ribosomal subunit. Has an RNA-dependent ATPase activity, which is specific for 23S rRNA, and a 3' to 5' RNA helicase activity that uses the energy of ATP hydrolysis to destabilize and unwind short rRNA duplexes. (481 aa) | ||||
SLK14674.1 | Hypothetical protein. (89 aa) | ||||
SLK14675.1 | Putative HAD-superfamily hydrolase, subfamily IIB. (267 aa) | ||||
SLK14784.1 | Putative undecaprenyl diphosphate synthase. (213 aa) | ||||
SLK14825.1 | Putative Delta-aminolevulinic acid dehydratase; Belongs to the ALAD family. (321 aa) | ||||
SLK14842.1 | Putative Branched-chain-amino-acid aminotransferase. (340 aa) | ||||
SLK14848.1 | Putative Ketoacid-binding protein. (126 aa) | ||||
pcp | Putative Pyrrolidone-carboxylate peptidase; Removes 5-oxoproline from various penultimate amino acid residues except L-proline; Belongs to the peptidase C15 family. (213 aa) | ||||
SLK15009.1 | Putative Cof-like hydrolase. (218 aa) | ||||
SLK15223.1 | Putative Glutamate dehydrogenase; Belongs to the Glu/Leu/Phe/Val dehydrogenases family. (448 aa) | ||||
SLK15275.1 | Putative Flavodoxin. (141 aa) | ||||
SLK15312.1 | Putative Aminotransferase class IV. (271 aa) | ||||
SLK15321.1 | Putative Chemotaxis protein. (151 aa) | ||||
SLK15351.1 | Putative Methylase of chemotaxis methyl-accepting protein. (255 aa) | ||||
SLK15365.1 | Putative Chemotaxis signal transduction protein CheW. (131 aa) | ||||
SLK15412.1 | Putative Flagellar protein FliS. (127 aa) | ||||
SLK15462.1 | Putative Flagellar biosynthesis/type III secretory pathway protein. (251 aa) | ||||
SLK15469.1 | Putative Flagellar hook assembly protein FlgD; Required for flagellar hook formation. May act as a scaffolding protein. (237 aa) | ||||
SLK15521.1 | Putative Site-determining protein. (287 aa) | ||||
dnaK | Putative Chaperone protein DnaK; Acts as a chaperone; Belongs to the heat shock protein 70 family. (617 aa) | ||||
SLK15842.1 | Putative Cytidine deaminase; This enzyme scavenges exogenous and endogenous cytidine and 2'-deoxycytidine for UMP synthesis; Belongs to the cytidine and deoxycytidylate deaminase family. (133 aa) | ||||
SLK15965.1 | Putative Glycerate dehydrogenase; Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family. (319 aa) | ||||
SLK15968.1 | Putative HAD hydrolase, IIB family. (266 aa) | ||||
SLK16044.1 | Putative Exonuclease, RNase T and DNA polymerase III. (210 aa) | ||||
SLK16155.1 | Putative Transcriptional regulator, AsnC family. (155 aa) | ||||
SLK16165.1 | Putative PHP family phosphohydrolase, histidinol phosphatase. (347 aa) | ||||
SLK16224.1 | Putative Thioredoxin; Belongs to the thioredoxin family. (104 aa) | ||||
purC | Putative Phosphoribosylaminoimidazole-succinocarb oxamide synthase; Belongs to the SAICAR synthetase family. (234 aa) | ||||
purN | Putative Phosphoribosylglycinamide formyltransferase; 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. (203 aa) | ||||
purH | Putative Bifunctional purine biosynthesis protein PurH. (500 aa) | ||||
purD | Putative Phosphoribosylamine--glycine ligase; Belongs to the GARS family. (415 aa) | ||||
SLK16398.1 | Putative Two component transcriptional regulator,winged helix family. (220 aa) | ||||
SLK16442.1 | Hypothetical protein. (722 aa) | ||||
SLK16446.1 | Hypothetical protein. (110 aa) | ||||
gshAB | Putative Glutathione biosynthesis bifunctional protein GshAB; Synthesizes glutathione from L-glutamate and L-cysteine via gamma-L-glutamyl-L-cysteine; In the N-terminal section; belongs to the glutamate--cysteine ligase type 1 family. Type 2 subfamily. (773 aa) | ||||
SLK16809.1 | Putative Transferase, hexapeptide repeat family. (186 aa) | ||||
SLK16864.1 | Putative enoyl-(Acyl-carrier-protein) reductase II. (312 aa) | ||||
SLK16871.1 | Putative Malonyl CoA-acyl carrier protein transacylase. (309 aa) | ||||
SLK16882.1 | Putative=3-oxoacyl-[acyl-carrier-protein] synthase 2; Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. (411 aa) | ||||
SLK16918.1 | Putative Rrf2 family protein. (150 aa) | ||||
nrdR | Putative Transcriptional repressor NrdR; Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes; Belongs to the NrdR family. (151 aa) | ||||
SLK17060.1 | Two-component system, OmpR family, alkaline phosphatase synthesis response regulator PhoP; Putative Response regulator (CheY-like receiver and winged helix DNA-binding domain containing protein). (232 aa) | ||||
SLK17114.1 | Hypothetical protein. (293 aa) | ||||
def | Putative Peptide deformylase; Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions. (147 aa) | ||||
fmt | Putative Methionyl-tRNA formyltransferase; 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; Belongs to the Fmt family. (308 aa) | ||||
SLK17185.1 | Putative Ribulose-phosphate 3-epimerase; Belongs to the ribulose-phosphate 3-epimerase family. (215 aa) | ||||
SLK17189.1 | Putative Thiamine pyrophosphokinase. (211 aa) | ||||
SLK17244.1 | Putative metal-binding protein. (170 aa) | ||||
SLK17360.1 | Putative Isoprenyl transferase; Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids. (253 aa) | ||||
SLK17471.1 | Putative Aspartokinase; Belongs to the aspartokinase family. (400 aa) | ||||
SLK17546.1 | Putative Adenylosuccinate lyase; Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily. (476 aa) | ||||
SLK17811.1 | Putative transcriptional regulator. (160 aa) | ||||
SLK17861.1 | Putative Class II aldolase/adducin family protein. (264 aa) | ||||
SLK17983.1 | Putative Amidase from nicotinamidase family protein. (213 aa) | ||||
SLK17987.1 | Putative Nicotinate phosphoribosyltransferase; Catalyzes the first step in the biosynthesis of NAD from nicotinic acid, the ATP-dependent synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate. Belongs to the NAPRTase family. (490 aa) | ||||
hfq | Putative Protein hfq; RNA chaperone that binds small regulatory RNA (sRNAs) and mRNAs to facilitate mRNA translational regulation in response to envelope stress, environmental stress and changes in metabolite concentrations. Also binds with high specificity to tRNAs. Belongs to the Hfq family. (76 aa) | ||||
mutS | Putative DNA mismatch repair protein MutS; This protein is involved in the repair of mismatches in DNA. It is possible that it carries out the mismatch recognition step. This protein has a weak ATPase activity. (884 aa) | ||||
ispH | Putative (E)-4-hydroxy-3-methyl-but-2-enyl pyrophosphate reductase; 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. Belongs to the IspH family. (635 aa) | ||||
SLK18108.1 | Putative Pseudouridine synthase; Belongs to the pseudouridine synthase RsuA family. (240 aa) | ||||
SLK18235.1 | Hypothetical protein. (148 aa) | ||||
SLK18243.1 | Putative molybdenum cofactor biosynthesis protein; Catalyzes the insertion of molybdate into adenylated molybdopterin with the concomitant release of AMP. Belongs to the MoeA family. (338 aa) | ||||
SLK18263.1 | Putative molybdopterin biosynthesis mog protein. (163 aa) | ||||
SLK18276.1 | Putative Molybdenum cofactor biosynthesis protein MoeA; Catalyzes the insertion of molybdate into adenylated molybdopterin with the concomitant release of AMP. Belongs to the MoeA family. (399 aa) | ||||
SLK18333.1 | Putative Phosphomethylpyrimidine kinase type-1; Belongs to the pyridoxine kinase family. (278 aa) | ||||
DeoA | Putative Pyrimidine-nucleoside phosphorylase. (434 aa) | ||||
SLK18434.1 | Putative NUDIX family hydrolase. (172 aa) | ||||
dxs | Putative=1-deoxy-D-xylulose-5-phosphate synthase; 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); Belongs to the transketolase family. DXPS subfamily. (617 aa) | ||||
folD | Putative Bifunctional protein FolD protein; Catalyzes the oxidation of 5,10-methylenetetrahydrofolate to 5,10-methenyltetrahydrofolate and then the hydrolysis of 5,10- methenyltetrahydrofolate to 10-formyltetrahydrofolate. (282 aa) | ||||
nusB | Hypothetical protein; 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. (134 aa) | ||||
SLK18621.1 | Putative Pseudouridine synthase; Responsible for synthesis of pseudouridine from uracil. Belongs to the pseudouridine synthase RluA family. (303 aa) | ||||
SLK18637.1 | Putative Pyridoxal phosphate enzyme, YggS family; Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis; Belongs to the pyridoxal phosphate-binding protein YggS/PROSC family. (218 aa) | ||||
SLK18726.1 | Putative acyl-CoA hydrolase. (156 aa) | ||||
SLK18852.1 | Putative Nucleoside hydrolase, IUNH family. (323 aa) | ||||
SLK18873.1 | Putative Phosphomannomutase. (575 aa) | ||||
SLK19156.1 | Putative DEAD/DEAH box helicase domain protein. (380 aa) | ||||
deoD | Putative Purine nucleoside phosphorylase DeoD-type. (235 aa) | ||||
SLK19224.1 | Putative Two component transcriptional regulator,winged helix family. (225 aa) | ||||
SLK19364.1 | Putative Endo-beta-N-acetylglucosaminidase. (1228 aa) | ||||
SLK19372.1 | Putative NADH dependent butanol dehydrogenase A. (388 aa) | ||||
SLK19379.1 | Putative hydrolase. (244 aa) | ||||
tgt | Putative Queuine tRNA-ribosyltransferase; Catalyzes the base-exchange of a guanine (G) residue with the queuine precursor 7-aminomethyl-7-deazaguanine (PreQ1) at position 34 (anticodon wobble position) in tRNAs with GU(N) anticodons (tRNA-Asp, - Asn, -His and -Tyr). Catalysis occurs through a double-displacement mechanism. The nucleophile active site attacks the C1' of nucleotide 34 to detach the guanine base from the RNA, forming a covalent enzyme-RNA intermediate. The proton acceptor active site deprotonates the incoming PreQ1, allowing a nucleophilic attack on the C1' of the ribose [...] (380 aa) | ||||
ruvB | Putative Holliday junction ATP-dependent DNA helicase RuvB; The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing. (342 aa) | ||||
ribBA | Putative Riboflavin biosynthesis protein RibA; Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate; In the C-terminal section; belongs to the GTP cyclohydrolase II family. (411 aa) | ||||
SLK19484.1 | Putative Riboflavin synthase, alpha subunit. (216 aa) | ||||
SLK19486.1 | Putative Riboflavin biosynthesis protein RibD; Converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'- phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)-pyrimidinedione 5'- phosphate; In the C-terminal section; belongs to the HTP reductase family. (364 aa) | ||||
pyrF | Putative Orotidine 5''-phosphate decarboxylase,subfamily 2; Belongs to the OMP decarboxylase family. Type 2 subfamily. (291 aa) | ||||
SLK19550.1 | Putative Aspartate carbamoyltransferase; Belongs to the aspartate/ornithine carbamoyltransferase superfamily. (268 aa) | ||||
SLK19718.1 | Putative Replicative DNA helicase; Participates in initiation and elongation during chromosome replication; it exhibits DNA-dependent ATPase activity. Belongs to the helicase family. DnaB subfamily. (434 aa) | ||||
SLK20034.1 | Putative Pyruvate kinase; Belongs to the pyruvate kinase family. (338 aa) | ||||
SLK20048.1 | Putative Dihydropteroate synthase; 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. (269 aa) | ||||
SLK20065.1 | Putative Aminotransferase class IV. (251 aa) | ||||
SLK20080.1 | Putative M18 family aminopeptidase. (463 aa) | ||||
hprK | Putative HPr kinase/phosphorylase; Catalyzes the ATP- as well as the pyrophosphate-dependent phosphorylation of a specific serine residue in HPr, a phosphocarrier protein of the phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS). HprK/P also catalyzes the pyrophosphate-producing, inorganic phosphate-dependent dephosphorylation (phosphorolysis) of seryl-phosphorylated HPr (P-Ser-HPr). The two antagonistic activities of HprK/P are regulated by several intracellular metabolites, which change their concentration in response to the absence or presence of rapidly metabolisab [...] (302 aa) | ||||
SLK20168.1 | Putative helicase. (758 aa) | ||||
SLK20211.1 | Putative UPF0237 protein CcarbDRAFT_0923; Belongs to the UPF0237 family. (89 aa) | ||||
mgsA | Putative Methylglyoxal synthase; Catalyzes the formation of methylglyoxal from dihydroxyacetone phosphate. (122 aa) | ||||
cobQ | Putative Cobyric acid synthase; Catalyzes amidations at positions B, D, E, and G on adenosylcobyrinic A,C-diamide. NH(2) groups are provided by glutamine, and one molecule of ATP is hydrogenolyzed for each amidation. Belongs to the CobB/CobQ family. CobQ subfamily. (494 aa) | ||||
SLK20368.1 | Putative transcriptional regulator; Catalyzes an amino-pyrimidine hydrolysis reaction at the C5' of the pyrimidine moiety of thiamine compounds, a reaction that is part of a thiamine salvage pathway; Belongs to the TenA family. (219 aa) | ||||
thiM | Putative Hydroxyethylthiazole kinase; Catalyzes the phosphorylation of the hydroxyl group of 4- methyl-5-beta-hydroxyethylthiazole (THZ); Belongs to the Thz kinase family. (259 aa) | ||||
SLK20383.1 | Putative Phosphomethylpyrimidine kinase. (266 aa) | ||||
SLK20396.1 | Putative HAD hydrolase, IIB family. (261 aa) | ||||
SLK20512.1 | Putative Alanine racemase; Catalyzes the interconversion of L-alanine and D-alanine. May also act on other amino acids; Belongs to the alanine racemase family. (385 aa) | ||||
SLK20605.1 | Putative Endo-beta-N-acetylglucosaminidase. (928 aa) | ||||
greA-2 | Putative GreA/GreB family elongation factor; Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides. (154 aa) | ||||
SLK20755.1 | Hypothetical protein. (215 aa) | ||||
SLK20769.1 | Putative hydrolase. (238 aa) | ||||
SLK20795.1 | Putative=5-methyltetrahydrofolate--homocysteine methyltransferase. (790 aa) | ||||
SLK20796.1 | Putative Vitamin B12 dependent methionine synthase activation region. (228 aa) | ||||
SLK20797.1 | Putative Methylenetetrahydrofolate reductase; Belongs to the methylenetetrahydrofolate reductase family. (302 aa) | ||||
SLK20866.1 | Putative Pseudouridine synthase; Responsible for synthesis of pseudouridine from uracil. Belongs to the pseudouridine synthase RluA family. (322 aa) | ||||
SLK20879.1 | Putative UvrD/REP helicase. (226 aa) | ||||
SLK20883.1 | Putative Helicase, UvrD/REP family. (435 aa) | ||||
engB | Putative GTP-binding protein EngB; Necessary for normal cell division and for the maintenance of normal septation; Belongs to the TRAFAC class TrmE-Era-EngA-EngB-Septin-like GTPase superfamily. EngB GTPase family. (204 aa) | ||||
clpX | Putative ATP-dependent Clp protease ATP-binding subunit ClpX; ATP-dependent specificity component of the Clp protease. It directs the protease to specific substrates. Can perform chaperone functions in the absence of ClpP. (431 aa) | ||||
SLK21163.1 | Putative Fructose-1,6-bisphosphate aldolase,class II. (287 aa) | ||||
eno | Putative Enolase; Catalyzes the reversible conversion of 2-phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis; Belongs to the enolase family. (430 aa) | ||||
SLK21257.1 | Putative tRNA-dihydrouridine synthase; 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; Belongs to the dus family. (321 aa) | ||||
SLK21271.1 | Putative ATP-dependent RNA helicase. (368 aa) | ||||
SLK21540.1 | Putative HTH-type transcriptional repressor NsrR. (131 aa) | ||||
eno-2 | Putative Enolase; Catalyzes the reversible conversion of 2-phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis; Belongs to the enolase family. (431 aa) | ||||
SLK21682.1 | Putative Cof-like hydrolase. (279 aa) | ||||
SLK21698.1 | Putative Regulatory protein VanR. (238 aa) | ||||
SLK21785.1 | Putative Cytosine deaminase. (420 aa) | ||||
SLK21794.1 | Putative Helicase protein. (1114 aa) | ||||
SLK21807.1 | Putative=23S rRNA (Uracil-5-)-methyltransferase RumA; Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family. (451 aa) | ||||
SLK21833.1 | Putative Pseudouridine synthase, RluA family; Responsible for synthesis of pseudouridine from uracil. Belongs to the pseudouridine synthase RluA family. (294 aa) | ||||
SLK21906.1 | Putative Site-determining protein. (265 aa) | ||||
minC | Putative septum site-determining protein MinC; Cell division inhibitor that blocks the formation of polar Z ring septums. Rapidly oscillates between the poles of the cell to destabilize FtsZ filaments that have formed before they mature into polar Z rings. Prevents FtsZ polymerization; Belongs to the MinC family. (213 aa) | ||||
SLK21996.1 | Putative Pyruvate kinase; Belongs to the pyruvate kinase family. (472 aa) | ||||
SLK22007.1 | Hypothetical protein; Belongs to the UPF0246 family. (255 aa) | ||||
SLK22084.1 | Putative Oxidoreductase, 2-nitropropane dioxygenase family. (355 aa) | ||||
SLK22097.1 | Putative Peptidase M22, glycoprotease. (238 aa) | ||||
SLK22111.1 | Putative Tex-like protein. (723 aa) | ||||
upp | Putative Uracil phosphoribosyltransferase; Catalyzes the conversion of uracil and 5-phospho-alpha-D- ribose 1-diphosphate (PRPP) to UMP and diphosphate. (209 aa) | ||||
rho | Hypothetical protein; Facilitates transcription termination by a mechanism that involves Rho binding to the nascent RNA, activation of Rho's RNA- dependent ATPase activity, and release of the mRNA from the DNA template. (464 aa) | ||||
pyrG | Putative CTP synthase; Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen. Regulates intracellular CTP levels through interactions with the four ribonucleotide triphosphates. (535 aa) | ||||
SLK22259.1 | Putative Cyanophycin synthetase; Belongs to the MurCDEF family. (874 aa) | ||||
SLK22349.1 | Putative Alkaline phosphatase synthesis transcriptional regulatory protein PhoP. (226 aa) | ||||
SLK22393.1 | Putative Non-canonical purine NTP pyrophosphatase; Pyrophosphatase that catalyzes the hydrolysis of nucleoside triphosphates to their monophosphate derivatives, with a high preference for the non-canonical purine nucleotides XTP (xanthosine triphosphate), dITP (deoxyinosine triphosphate) and ITP. Seems to function as a house-cleaning enzyme that removes non-canonical purine nucleotides from the nucleotide pool, thus preventing their incorporation into DNA/RNA and avoiding chromosomal lesions. Belongs to the HAM1 NTPase family. (203 aa) | ||||
ligA | Putative DNA ligase; 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. (663 aa) | ||||
SLK22412.1 | Putative Pseudouridine synthase; Belongs to the pseudouridine synthase RsuA family. (238 aa) | ||||
guaA | Putative GMP synthase [glutamine-hydrolyzing]; Catalyzes the synthesis of GMP from XMP. (510 aa) | ||||
SLK22439.1 | Putative Class II aldolase, tagatose bisphosphate family. (285 aa) | ||||
SLK22533.1 | Putative Pseudouridine synthase; Belongs to the pseudouridine synthase RsuA family. (257 aa) | ||||
SLK22541.1 | Helicase, putative. (701 aa) | ||||
azoR | Putative FMN-dependent NADH-azoreductase; Catalyzes the reductive cleavage of azo bond in aromatic azo compounds to the corresponding amines. Requires NADH, but not NADPH, as an electron donor for its activity; Belongs to the azoreductase type 1 family. (216 aa) | ||||
speH | Putative S-adenosylmethionine decarboxylase proenzyme; Catalyzes the decarboxylation of S-adenosylmethionine to S- adenosylmethioninamine (dcAdoMet), the propylamine donor required for the synthesis of the polyamines spermine and spermidine from the diamine putrescine; Belongs to the prokaryotic AdoMetDC family. Type 1 subfamily. (139 aa) | ||||
SLK22614.1 | Putative DNA-binding response regulator. (225 aa) | ||||
SLK22637.1 | Putative Guanine deaminase GuaD. (162 aa) | ||||
SLK22655.1 | Putative=23S rRNA (Uracil-5-)-methyltransferase RumA; Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family. (458 aa) | ||||
SLK22658.1 | Putative Pyruvate kinase; Belongs to the pyruvate kinase family. (472 aa) | ||||
SLK22721.1 | Putative dTDP-4-dehydrorhamnose 3,5-epimerase. (181 aa) | ||||
SLK22825.1 | Putative UDP-glucose 4-epimerase; Belongs to the NAD(P)-dependent epimerase/dehydratase family. (328 aa) | ||||
glgA | Putative Glycogen synthase; Synthesizes alpha-1,4-glucan chains using ADP-glucose. (478 aa) | ||||
glgB | Putative=1,4-alpha-glucan branching enzyme GlgB; Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position; Belongs to the glycosyl hydrolase 13 family. GlgB subfamily. (678 aa) | ||||
tRNA-Pro-1_6 | Putative pyruvate, phosphate dikinase regulatory protein; Bifunctional serine/threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation/dephosphorylation. (268 aa) | ||||
tRNA-Arg-1_3 | Putative Glycogen synthase; Synthesizes alpha-1,4-glucan chains using ADP-glucose. (477 aa) | ||||
tRNA-Gly-1_8 | Putative MTA/SAH nucleosidase; Catalyzes the irreversible cleavage of the glycosidic bond in both 5'-methylthioadenosine (MTA) and S-adenosylhomocysteine (SAH/AdoHcy) to adenine and the corresponding thioribose, 5'- methylthioribose and S-ribosylhomocysteine, respectively. Belongs to the PNP/UDP phosphorylase family. MtnN subfamily. (231 aa) | ||||
SLK22969.1 | Putative Dihydrofolate reductase; Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis. (162 aa) | ||||
SLK22979.1 | Putative ATP-dependent RNA helicase; Belongs to the DEAD box helicase family. (525 aa) | ||||
SLK22982.1 | Rrf2 family protein, putative transcriptional regulator. (69 aa) | ||||
SLK22983.1 | Rrf2 family protein, putative transcriptional regulator. (59 aa) | ||||
SLK22987.1 | Putative Alkylphosphonate utilization operon protein PhnA. (113 aa) | ||||
SLK23038.1 | Putative Replicative DNA helicase; Participates in initiation and elongation during chromosome replication; it exhibits DNA-dependent ATPase activity. Belongs to the helicase family. DnaB subfamily. (445 aa) |