Reaction Details |
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Target | Purine nucleoside phosphorylase |
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Ligand | BDBM50422435 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_162007 (CHEMBL764178) |
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Ki | 0.180000±n/a nM |
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Citation | Evans, GB; Furneaux, RH; Lewandowicz, A; Schramm, VL; Tyler, PC Synthesis of second-generation transition state analogues of human purine nucleoside phosphorylase. J Med Chem46:5271-6 (2003) [PubMed] Article |
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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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BDBM50422435 |
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n/a |
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Name | BDBM50422435 |
Synonyms: | CHEMBL2311112 |
Type | Small organic molecule |
Emp. Form. | C10H13N5O4 |
Mol. Mass. | 267.2413 |
SMILES | OC[C@H]1N[C@H]([C@H](O)[C@@H]1O)c1[nH]nc2c1nc[nH]c2=O |
Structure |
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