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moaC | Molybdopterin biosynthesis, protein C; Catalyzes the conversion of (8S)-3',8-cyclo-7,8- dihydroguanosine 5'-triphosphate to cyclic pyranopterin monophosphate (cPMP); Belongs to the MoaC family. (161 aa) | ||||
yabI | Orf, hypothetical protein; Residues 1 to 254 of 254 are 98.81 pct identical to residues 1 to 254 of 254 from Escherichia coli K-12 Strain MG1655: B0065. (254 aa) | ||||
Z0377 | Putative dehydrogenase; Residues 11 to 291 of 294 are 46.61 pct identical to residues 8 to 285 of 286 from GenPept 118 : gi|4981536|gb|AAD36074.1|AE001762_1 (AE001762) oxidoreductase, aldo/keto reductase family [Thermotoga maritima]. (294 aa) | ||||
ybbL | Putative ATP-binding component of a transport system; Residues 1 to 225 of 225 are 99.55 pct identical to residues 1 to 225 of 225 from Escherichia coli K-12 Strain MG1655: B0490. (225 aa) | ||||
ybbM | Putative metal resistance protein; Residues 1 to 268 of 268 are 100.00 pct identical to residues 1 to 268 of 268 from Escherichia coli K-12 Strain MG1655: B0491. (268 aa) | ||||
speF | Ornithine decarboxylase isozyme, inducible; Residues 1 to 732 of 732 are 96.44 pct identical to residues 1 to 732 of 732 from Escherichia coli K-12 Strain MG1655: B0693. (732 aa) | ||||
modB | Molybdate transport permease protein; Part of the binding-protein-dependent transport system for molybdenum; probably responsible for the translocation of the substrate across the membrane; Belongs to the binding-protein-dependent transport system permease family. CysTW subfamily. (229 aa) | ||||
moaA | Molybdopterin biosynthesis, protein A; Catalyzes the cyclization of GTP to (8S)-3',8-cyclo-7,8- dihydroguanosine 5'-triphosphate. (329 aa) | ||||
moaB | Molybdopterin biosynthesis, protein B; May be involved in the biosynthesis of molybdopterin. Can bind GTP and has low GTPase activity. Can bind MPT, but has no MPT adenylyl transferase activity; Belongs to the MoaB/Mog family. (170 aa) | ||||
moaE | Molybdopterin converting factor, subunit 2; Residues 1 to 150 of 150 are 98.00 pct identical to residues 1 to 150 of 150 from Escherichia coli K-12 Strain MG1655: B0785. (150 aa) | ||||
plsX | Glycerolphosphate auxotrophy in plsB background; Catalyzes the reversible formation of acyl-phosphate (acyl- PO(4)) from acyl-[acyl-carrier-protein] (acyl-ACP). This enzyme utilizes acyl-ACP as fatty acyl donor, but not acyl-CoA. (346 aa) | ||||
ycfR | Orf, hypothetical protein; Reduces the permeability of the outer membrane to copper. May be involved in the regulation of biofilm formation (By similarity). Belongs to the BhsA/McbA family. (85 aa) | ||||
dosC | Orf, hypothetical protein; Globin-coupled heme-based oxygen sensor protein displaying diguanylate cyclase (DGC) activity in response to oxygen availability. Thus, catalyzes the synthesis of cyclic diguanylate (c-di-GMP) via the condensation of 2 GTP molecules. Cyclic-di-GMP is a second messenger which controls cell surface-associated traits in bacteria (By similarity). (460 aa) | ||||
ompC-2 | Putative outer membrane porin protein; Residues 6 to 366 of 366 are 66.66 pct identical to residues 8 to 365 of 365 from GenPept 118 : gi|215369|gb|AAA32301.1| (J02580) outer membrane porin protein [Bacteriophage PA-2]; Belongs to the Gram-negative porin family. (366 aa) | ||||
ydcT | Putative ATP-binding component of a transport system; Residues 1 to 337 of 337 are 99.40 pct identical to residues 1 to 337 of 337 from Escherichia coli K-12 Strain MG1655: B1441; Belongs to the ABC transporter superfamily. (337 aa) | ||||
ymjC | Hypothetical protein; Residues 5 to 193 of 216 are 25.25 pct identical to residues 1 to 195 of 216 from GenPept 118 : gi|1407795|gb|AAC64864.1| (U60647) unknown [Yersinia pestis]. (216 aa) | ||||
yciF | Putative structural proteins; Residues 1 to 166 of 166 are 99.39 pct identical to residues 1 to 166 of 166 from Escherichia coli K-12 Strain MG1655: B1258. (166 aa) | ||||
katE | Catalase; Serves to protect cells from the toxic effects of hydrogen peroxide. (753 aa) | ||||
ydjX | Orf, hypothetical protein; Residues 1 to 252 of 252 are 97.22 pct identical to residues 1 to 252 of 252 from Escherichia coli K-12 Strain MG1655: B1750. (252 aa) | ||||
ydjZ | Orf, hypothetical protein; Residues 1 to 235 of 235 are 98.72 pct identical to residues 1 to 235 of 235 from Escherichia coli K-12 Strain MG1655: B1752. (235 aa) | ||||
selD | Selenophosphate synthase, H(2)Se added to acrylyl-tRNA; Synthesizes selenophosphate from selenide and ATP. (347 aa) | ||||
prc | Carboxy-terminal protease for penicillin-binding protein 3; Residues 1 to 682 of 682 are 99.85 pct identical to residues 1 to 682 of 682 from Escherichia coli K-12 Strain MG1655: B1830; Belongs to the peptidase S41A family. (682 aa) | ||||
gnd | Gluconate-6-phosphate dehydrogenase, decarboxylating; Catalyzes the oxidative decarboxylation of 6-phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH. (468 aa) | ||||
mrp | Putative ATPase; Binds and transfers iron-sulfur (Fe-S) clusters to target apoproteins. Can hydrolyze ATP; Belongs to the Mrp/NBP35 ATP-binding proteins family. (379 aa) | ||||
yohD | Orf, hypothetical protein; Residues 1 to 204 of 204 are 99.01 pct identical to residues 1 to 204 of 204 from Escherichia coli K-12 Strain MG1655: B2136. (204 aa) | ||||
spr | Putative lipoprotein; A murein DD-endopeptidase with specificity for D-Ala-meso- diaminopimelic acid (mDAP) cross-links. Its role is probably to cleave D-Ala-mDAP cross-links to allow insertion of new glycans and thus cell wall expansion. Functionally redundant with MepM and MepH. Also has weak LD-carboxypeptidase activity on L-mDAP-D-Ala peptide bonds (By similarity). (188 aa) | ||||
yejG | Orf, hypothetical protein; Residues 1 to 114 of 114 are 99.12 pct identical to residues 1 to 114 of 114 from Escherichia coli K-12 Strain MG1655: B2181. (114 aa) | ||||
ompC | Outer membrane protein 1b (Ib;c); Forms pores that allow passive diffusion of small molecules across the outer membrane. (367 aa) | ||||
ppk | Polyphosphate kinase; Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP); Belongs to the polyphosphate kinase 1 (PPK1) family. (688 aa) | ||||
yqaA | Orf, hypothetical protein; Residues 1 to 142 of 142 are 99.29 pct identical to residues 1 to 142 of 142 from Escherichia coli K-12 Strain MG1655: B2689. (142 aa) | ||||
rpoS | RNA polymerase, sigma S (sigma38) factor; Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released. This sigma factor is the master transcriptional regulator of the stationary phase and the general stress response. (330 aa) | ||||
speC | Ornithine decarboxylase isozyme; Residues 1 to 731 of 731 are 98.76 pct identical to residues 1 to 731 of 731 from Escherichia coli K-12 Strain MG1655: B2965. (731 aa) | ||||
yghB | Orf, hypothetical protein; Residues 1 to 219 of 219 are 100.00 pct identical to residues 1 to 219 of 219 from Escherichia coli K-12 Strain MG1655: B3009. (219 aa) | ||||
qseC | Quorum sensing Escherichia coli regulator C; Member of a two-component regulatory system QseB/QseC. Activates the flagella regulon by activating transcription of FlhDC. May activate QseB by phosphorylation. (449 aa) | ||||
yqjA | Orf, hypothetical protein; Residues 1 to 220 of 220 are 100.00 pct identical to residues 1 to 220 of 220 from Escherichia coli K-12 Strain MG1655: B3095. (220 aa) | ||||
rpoN | RNA polymerase, sigma(54 or 60) factor; Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released. (477 aa) | ||||
envZ | Protein histidine kinase/phosphatase sensor for OmpR, modulates expression of ompF and ompC; Residues 1 to 450 of 450 are 99.77 pct identical to residues 1 to 450 of 450 from Escherichia coli K-12 Strain MG1655: B3404. (450 aa) | ||||
ompR | DNA-binding dual transcriptional regulator OmpR; Member of the two-component regulatory system EnvZ/OmpR involved in osmoregulation (particularly of genes ompF and ompC) as well as other genes. Plays a central role in both acid and osmotic stress responses. Binds to the promoter of both ompC and ompF; at low osmolarity it activates ompF transcription, while at high osmolarity it represses ompF and activates ompC transcription. (239 aa) | ||||
gntR | Regulator of gluconate (gnt) operon; Residues 1 to 294 of 321 are 99.31 pct identical to residues 11 to 304 of 313 from Escherichia coli K-12 Strain MG1655: B3438. (321 aa) | ||||
selB | selenocysteinyl-tRNA-specific translation factor; Residues 1 to 614 of 614 are 98.37 pct identical to residues 1 to 614 of 614 from Escherichia coli K-12 Strain MG1655: B3590. (614 aa) | ||||
selA | Selenocysteine synthase: L-seryl-tRNA (Ser) selenium transferase; Converts seryl-tRNA(Sec) to selenocysteinyl-tRNA(Sec) required for selenoprotein biosynthesis; Belongs to the SelA family. (463 aa) | ||||
tnaA | Tryptophanase; Residues 1 to 476 of 476 are 99.78 pct identical to residues 1 to 476 of 476 from Escherichia coli K-12 Strain MG1655: B3708; Belongs to the beta-eliminating lyase family. (476 aa) | ||||
atpD | Membrane-bound ATP synthase, F1 sector, beta-subunit; Produces ATP from ADP in the presence of a proton gradient across the membrane. The catalytic sites are hosted primarily by the beta subunits; Belongs to the ATPase alpha/beta chains family. (460 aa) | ||||
atpG | Membrane-bound ATP synthase, F1 sector, gamma-subunit; Produces ATP from ADP in the presence of a proton gradient across the membrane. The gamma chain is believed to be important in regulating ATPase activity and the flow of protons through the CF(0) complex (By similarity). (287 aa) | ||||
atpA | Membrane-bound ATP synthase, F1 sector, alpha-subunit; Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit. Belongs to the ATPase alpha/beta chains family. (513 aa) | ||||
rfe | UDP-GlcNAc:undecaprenylphosphate GlcNAc-1-phosphate transferase; Catalyzes the transfer of the GlcNAc-1-phosphate moiety from UDP-GlcNAc onto the carrier lipid undecaprenyl phosphate (C55-P), yielding GlcNAc-pyrophosphoryl-undecaprenyl (GlcNAc-PP-C55). (367 aa) | ||||
wecB | UDP-N-acetyl glucosamine -2-epimerase; Catalyzes the reversible epimerization at C-2 of UDP-N- acetylglucosamine (UDP-GlcNAc) and thereby provides bacteria with UDP- N-acetylmannosamine (UDP-ManNAc), the activated donor of ManNAc residues. (390 aa) | ||||
wecC | UDP-N-acetyl-D-mannosaminuronic acid dehydrogenase; Catalyzes the four-electron oxidation of UDP-N-acetyl-D- mannosamine (UDP-ManNAc), reducing NAD(+) and releasing UDP-N- acetylmannosaminuronic acid (UDP-ManNAcA); Belongs to the UDP-glucose/GDP-mannose dehydrogenase family. WecC subfamily. (420 aa) | ||||
wecG | Probable UDP-N-acetyl-D-mannosaminuronic acid transferase; Catalyzes the synthesis of Und-PP-GlcNAc-ManNAcA (Lipid II), the second lipid-linked intermediate involved in enterobacterial common antigen (ECA) synthesis. (246 aa) | ||||
glnG | Response regulator for gln (sensor glnL) (nitrogen regulator I, NRI); Member of the two-component regulatory system NtrB/NtrC, which controls expression of the nitrogen-regulated (ntr) genes in response to nitrogen limitation. Phosphorylated NtrC binds directly to DNA and stimulates the formation of open promoter-sigma54-RNA polymerase complexes. (469 aa) | ||||
glnL | Histidine protein kinase sensor for GlnG regulator (nitrogen regulator II, NRII); Member of the two-component regulatory system NtrB/NtrC, which controls expression of the nitrogen-regulated (ntr) genes in response to nitrogen limitation. Under conditions of nitrogen limitation, NtrB autophosphorylates and transfers the phosphoryl group to NtrC. In the presence of nitrogen, acts as a phosphatase that dephosphorylates and inactivates NtrC. (349 aa) | ||||
fdhE | Affects formate dehydrogenase-N; Residues 1 to 309 of 309 are 99.02 pct identical to residues 1 to 309 of 309 from Escherichia coli K-12 Strain MG1655: B3891. (309 aa) | ||||
fdoI | Formate dehydrogenase, cytochrome B556 (FDO) subunit; Allows to use formate as major electron donor during aerobic respiration. Subunit gamma is probably the cytochrome b556(FDO) component of the formate dehydrogenase (By similarity). (211 aa) | ||||
fdoH | Formate dehydrogenase-O, iron-sulfur subunit; The beta chain is an electron transfer unit containing 4 cysteine clusters involved in the formation of iron-sulfur centers. (300 aa) | ||||
fdoG | Formate dehydrogenase-O, major subunit; Residues 1 to 1016 of 1016 are 99.51 pct identical to residues 1 to 1016 of 1016 from Escherichia coli K-12 Strain MG1655: B3894. (1016 aa) | ||||
fdhD | Affects formate dehydrogenase-N; Required for formate dehydrogenase (FDH) activity. Acts as a sulfur carrier protein that transfers sulfur from IscS to the molybdenum cofactor prior to its insertion into FDH. Belongs to the FdhD family. (277 aa) | ||||
katG | Catalase; Bifunctional enzyme with both catalase and broad-spectrum peroxidase activity; Belongs to the peroxidase family. Peroxidase/catalase subfamily. (726 aa) | ||||
oxyR | Activator, hydrogen peroxide-inducible genes; Hydrogen peroxide sensor. Activates the expression of a regulon of hydrogen peroxide-inducible genes such as katG, gor, ahpC, ahpF, oxyS (a regulatory RNA), dps, fur and grxA. OxyR expression is negatively autoregulated by binding to a 43 bp region upstream of its own coding sequence. OxyR is inactivated by reduction of its essential disulfide bond by the product of GrxA, itself positively regulated by OxyR. Has also a positive regulatory effect on the production of surface proteins that control the colony morphology and auto- aggregation a [...] (305 aa) |