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TargetPurine nucleoside phosphorylase
LigandBDBM50022505
Substrate/Competitorn/a
Meas. Tech.ChEBML_153332
Ki 30000±n/a nM
Citation Sanghvi, YSHanna, NBLarson, SBFujitaki, JMWillis, RCSmith, RARobins, RKRevankar, GR Synthesis and evaluation of 5-amino-1-beta-D-ribofuranosyl-1,2,4-triazole-3-carboxamidine and certain related nucleosides as inhibitors of purine nucleoside phosphorylase. J Med Chem31:330-5 (1988) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
Purine nucleoside phosphorylase
Name:Purine nucleoside phosphorylase
Synonyms:Inosine phosphorylase | Inosine-guanosine phosphorylase | NP | PNP | PNPH_HUMAN | Purine nucleoside phosphorylase (PNPase)
Type:Enzyme
Mol. Mass.:32119.53
Organism:Homo sapiens (Human)
Description:n/a
Residue:289
Sequence:
MENGYTYEDYKNTAEWLLSHTKHRPQVAIICGSGLGGLTDKLTQAQIFDYGEIPNFPRST
VPGHAGRLVFGFLNGRACVMMQGRFHMYEGYPLWKVTFPVRVFHLLGVDTLVVTNAAGGL
NPKFEVGDIMLIRDHINLPGFSGQNPLRGPNDERFGDRFPAMSDAYDRTMRQRALSTWKQ
MGEQRELQEGTYVMVAGPSFETVAECRVLQKLGADAVGMSTVPEVIVARHCGLRVFGFSL
ITNKVIMDYESLEKANHEEVLAAGKQAAQKLEQFVSILMASIPLPDKAS
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BDBM50022505
n/a
NameBDBM50022505
Synonyms:1-(3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-1H-[1,2,4]triazole-3-carboxamidine; hydrochloride | CHEMBL542931
TypeSmall organic molecule
Emp. Form.C8H13N5O4
Mol. Mass.243.2199
SMILESNC(=N)c1ncn(n1)C1OC(CO)C(O)[C@@H]1O
Structure
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