EC: 3.6.1.6

nucleoside diphosphate phosphatase (nucleoside-diphosphate phosphohydrolase)

enzyme lambda metabolic reaction experiment
uniprot:Q8K4Y7 [Ca2+]

UDP + H2O -> Phosphate + UMP
(( (Vmax * S) ) / (Km + S)) buffer: 50 mM HEPES
PH: 7
Temperature: 36

Pathways

pathway id name
BioCyc:HUMAN_PWY-7185 UTP and CTP dephosphorylation I
Reactome:R-HSA-9660826 Purinergic signaling in leishmaniasis infection
Reactome:R-HSA-9664424 Cell recruitment (pro-inflammatory response)
Reactome:R-HSA-9658195 Leishmania infection
Reactome:R-HSA-9824443 Parasitic Infection Pathways
Reactome:R-HSA-1643685 Disease
Reactome:R-MMU-1430728 Metabolism
Reactome:R-CEL-15869 Nucleotide metabolism
Reactome:R-CEL-8956319 Nucleotide catabolism
Reactome:R-CEL-8850843 Phosphate bond hydrolysis by NTPDase proteins
Reactome:R-RNO-1430728 Metabolism
Reactome:R-CEL-1430728 Metabolism
Reactome:R-HSA-1430728 Metabolism
Reactome:R-HSA-15869 Nucleotide metabolism
Reactome:R-HSA-8956319 Nucleotide catabolism
Reactome:R-HSA-8850843 Phosphate bond hydrolysis by NTPDase proteins
Reactome:R-HSA-5663205 Infectious disease
Reactome:R-MMU-15869 Nucleotide metabolism
Reactome:R-MMU-8956319 Nucleotide catabolism
Reactome:R-MMU-8850843 Phosphate bond hydrolysis by NTPDase proteins
Reactome:R-RNO-15869 Nucleotide metabolism
Reactome:R-RNO-8956319 Nucleotide catabolism
Reactome:R-RNO-8850843 Phosphate bond hydrolysis by NTPDase proteins
PathBank:SMP0120670 Adenylosuccinate Lyase Deficiency
PathBank:SMP0000444 Lactose Synthesis
PathBank:SMP0000167 Adenylosuccinate Lyase Deficiency
PathBank:SMP0000220 Xanthine Dehydrogenase Deficiency (Xanthinuria)
PathBank:SMP0000178 Dihydropyrimidinase Deficiency
PathBank:SMP0000512 Xanthinuria Type I
PathBank:SMP0000536 Mitochondrial DNA Depletion Syndrome-3
PathBank:SMP0000580 GLUT-1 Deficiency Syndrome
PathBank:SMP0063634 Lactose Synthesis
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:SMP0120507 UMP Synthase Deficiency (Orotic Aciduria)
PathBank:SMP0120644 GLUT-1 Deficiency Syndrome
PathBank:SMP0000046 Pyrimidine Metabolism
PathBank:SMP0000050 Purine Metabolism
PathBank:SMP0000144 Adenosine Deaminase Deficiency
PathBank:SMP0000203 Molybdenum Cofactor Deficiency
PathBank:SMP0000219 UMP Synthase Deficiency (Orotic Aciduria)
PathBank:SMP0000428 Mercaptopurine Action Pathway
PathBank:SMP0000535 Adenine Phosphoribosyltransferase Deficiency (APRT)
PathBank:SMP0000579 Congenital Disorder of Glycosylation CDG-IId
PathBank:SMP0087473 Pyrimidine Metabolism
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:SMP0120473 Dihydropyrimidinase Deficiency
PathBank:SMP0000365 Gout or Kelley-Seegmiller Syndrome
PathBank:SMP0000210 Purine Nucleoside Phosphorylase Deficiency
PathBank:SMP0000202 MNGIE (Mitochondrial Neurogastrointestinal Encephalopathy)
PathBank:SMP0000430 Thioguanine Action Pathway
PathBank:SMP0000513 Xanthinuria Type II
PathBank:SMP0000537 Myoadenylate Deaminase Deficiency
PathBank:SMP0087332 Purine Metabolism
PathBank:SMP0087448 Lactose Synthesis
PathBank:SMP0063658 Pyrimidine Metabolism
PathBank:SMP0120819 Adenine Phosphoribosyltransferase Deficiency (APRT)
PathBank:SMP0120458 beta-Ureidopropionase Deficiency
PathBank:SMP0120530 MNGIE (Mitochondrial Neurogastrointestinal Encephalopathy)
PathBank:SMP0120643 Congenital Disorder of Glycosylation CDG-IId
PathBank:SMP0000364 Lesch-Nyhan Syndrome (LNS)
PathBank:SMP0000168 AICA-Ribosiduria
PathBank:SMP0000172 beta-Ureidopropionase Deficiency
PathBank:SMP0000427 Azathioprine Action Pathway
PathBank:SMP0087239 Purine Metabolism