Reaction Details |
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Target | Purine nucleoside phosphorylase |
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Ligand | BDBM50042365 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_153331 |
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Ki | 1.1±n/a nM |
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Citation | Kelley, JL; Linn, JA; McLean, EW; Tuttle, JV 9-[(Phosphonoalkyl)benzyl]guanines. Multisubstrate analogue inhibitors of human erythrocyte purine nucleoside phosphorylase. J Med Chem36:3455-63 (1993) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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Purine nucleoside phosphorylase |
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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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BDBM50042365 |
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n/a |
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Name | BDBM50042365 |
Synonyms: | CHEMBL117417 | [3-(2-Amino-6-oxo-1,6-dihydro-purin-9-ylmethyl)-benzylsulfanylmethyl]-phosphonic acid |
Type | Small organic molecule |
Emp. Form. | C14H16N5O4PS |
Mol. Mass. | 381.347 |
SMILES | Nc1nc2n(Cc3cccc(CSCP(O)(O)=O)c3)cnc2c(=O)[nH]1 |
Structure |
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