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Reaction Details
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TargetPurine Nucleoside Phosphorylase (PNP)
LigandAzetidine based compound, (+/-) 42
Substrate/CompetitorInosine
Meas. Tech.PNP Inhibition Assay
pH7.7±n/a
Temperature295.15±n/a K
Ki 1.8±0.2 nM
Km34000±n/a nM
Citation Evans, GBFurneaux, RHGreatrex, BMurkin, ASSchramm, VLTyler, PC Azetidine based transition state analogue inhibitors of N-ribosyl hydrolases and phosphorylases.J Med Chem.51:948-56(2008)[PubMed]
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Purine Nucleoside Phosphorylase (PNP)
NamePurine Nucleoside Phosphorylase (PNP)
SynonymsEC 2.4.2.1 | Inosine phosphorylase
TypeEnzyme
Mol. Mass.32037
OrganismBos taurus (bovine)
Descriptionn/a
Residue289
Sequence
MANGYTYEDYQDTAKWLLSHTEQRPQVAVICGSGLGGLVNKLTQAQTFDYSEIPNFPEST
VPGHAGRLVFGILNGRACVMMQGRFHMYEGYPFWKVTFPVRVFRLLGVETLVVTNAAGGL
NPNFEVGDIMLIRDHINLPGFSGENPLRGPNEERFGVRFPAMSDAYDRDMRQKAHSTWKQ
MGEQRELQEGTYVMLGGPNFETVAECRLLRNLGADAVGMSTVPEVIVARHCGLRVFGFSL
ITNKVIMDYESQGKANHEEVLEAGKQAAQKLEQFVSLLMASIPVSGHTG
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Azetidine based compound, (+/-) 42
NameAzetidine based compound, (+/-) 42
Synonyms:7-{[2-(hydroxymethyl)azetidin-1-yl]methyl}-3H,4H,5H-pyrrolo[3,2-d]pyrimidin-4-one
TypeSmall organic molecule
Emp. Form.C11H14N4O2
Mol. Mass.234.2545
SMILESOCC1CCN1Cc1c[nH]c2c1nc[nH]c2=O
Structure
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Inosine
NameInosine
Synonyms:9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-6,9-dihydro-3H-purin-6-one | Atorel | Hypoxanthosine
TypePurine Nucleoside
Emp. Form.C10H12N4O5
Mol. Mass.268.2261
SMILESOC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c1[nH]cnc2=O
Structure
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