EC: 3.6.1.58

8-oxo-dGDP phosphatase (8-oxo-dGDP phosphohydrolase)

enzyme lambda metabolic reaction experiment
uniprot:Q6ZVK8 [8-oxo-dGDP phosphatase(Enzyme) wildtype His-tagged]

8_oxo_dGDP + H2O -> Phosphate + 8_oxo_dGMP		 (( (Vmax * S) ) / (Km + S)) buffer: 20 mM Tris-HCl, 80 µg/ml BSA, 8 mM MgCl2, 40 mM NaCl, 5 mM DTT, 2% glycerol
PH: 8
Temperature: 30
uniprot:Q6ZVK8 [8-oxo-dGDP phosphatase(Enzyme) wildtype His-tagged]

H2O + 8_oxo_GDP -> Phosphate + 8_oxo_GMP		 (( (Vmax * S) ) / (Km + S)) buffer: 20 mM Tris-HCl, 80 µg/ml BSA, 8 mM MgCl2, 40 mM NaCl, 5 mM DTT, 2% glycerol
PH: 8
Temperature: 30

Pathways

pathway id name
Reactome:R-DRE-2393930 Phosphate bond hydrolysis by NUDT proteins
Reactome:R-HSA-2393930 Phosphate bond hydrolysis by NUDT proteins
Reactome:R-MMU-1430728 Metabolism
Reactome:R-MMU-2393930 Phosphate bond hydrolysis by NUDT proteins
Reactome:R-RNO-2393930 Phosphate bond hydrolysis by NUDT proteins
Reactome:R-DRE-74259 Purine catabolism
Reactome:R-HSA-74259 Purine catabolism
Reactome:R-MMU-74259 Purine catabolism
Reactome:R-RNO-74259 Purine catabolism
Reactome:R-DRE-1430728 Metabolism
Reactome:R-RNO-1430728 Metabolism
Reactome:R-DRE-15869 Nucleotide metabolism
Reactome:R-DRE-8956319 Nucleotide catabolism
Reactome:R-HSA-1430728 Metabolism
Reactome:R-HSA-15869 Nucleotide metabolism
Reactome:R-HSA-8956319 Nucleotide catabolism
Reactome:R-MMU-15869 Nucleotide metabolism
Reactome:R-MMU-8956319 Nucleotide catabolism
Reactome:R-RNO-15869 Nucleotide metabolism
Reactome:R-RNO-8956319 Nucleotide catabolism
PathBank:SMP0120670 Adenylosuccinate Lyase Deficiency
PathBank:SMP0000167 Adenylosuccinate Lyase Deficiency
PathBank:SMP0000220 Xanthine Dehydrogenase Deficiency (Xanthinuria)
PathBank:SMP0000512 Xanthinuria Type I
PathBank:SMP0000536 Mitochondrial DNA Depletion Syndrome-3
PathBank:SMP0120669 Adenosine Deaminase Deficiency
PathBank:SMP0120673 AICA-Ribosiduria
PathBank:SMP0120709 Gout or Kelley-Seegmiller Syndrome
PathBank:SMP0120717 Xanthine Dehydrogenase Deficiency (Xanthinuria)
PathBank:SMP0120797 Xanthinuria Type II
PathBank:SMP0120821 Myoadenylate Deaminase Deficiency
PathBank:SMP0000050 Purine Metabolism
PathBank:SMP0000144 Adenosine Deaminase Deficiency
PathBank:SMP0000203 Molybdenum Cofactor Deficiency
PathBank:SMP0000428 Mercaptopurine Action Pathway
PathBank:SMP0000535 Adenine Phosphoribosyltransferase Deficiency (APRT)
PathBank:SMP0120728 Lesch-Nyhan Syndrome (LNS)
PathBank:SMP0120752 Molybdenum Cofactor Deficiency
PathBank:SMP0120756 Purine Nucleoside Phosphorylase Deficiency
PathBank:SMP0120796 Xanthinuria Type I
PathBank:SMP0120820 Mitochondrial DNA Depletion Syndrome
PathBank:SMP0000365 Gout or Kelley-Seegmiller Syndrome
PathBank:SMP0000210 Purine Nucleoside Phosphorylase Deficiency
PathBank:SMP0000430 Thioguanine Action Pathway
PathBank:SMP0000513 Xanthinuria Type II
PathBank:SMP0000537 Myoadenylate Deaminase Deficiency
PathBank:SMP0087332 Purine Metabolism
PathBank:SMP0120819 Adenine Phosphoribosyltransferase Deficiency (APRT)
PathBank:SMP0000364 Lesch-Nyhan Syndrome (LNS)
PathBank:SMP0000168 AICA-Ribosiduria
PathBank:SMP0000427 Azathioprine Action Pathway