Reaction Details |
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Target | Purine nucleoside phosphorylase |
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Ligand | BDBM50293087 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1875753 (CHEMBL4377147) |
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Ki | 0.890000±n/a nM |
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Citation | Cheviet, T; Lefebvre-Tournier, I; Wein, S; Peyrottes, S Plasmodium Purine Metabolism and Its Inhibition by Nucleoside and Nucleotide Analogues. J Med Chem62:8365-8391 (2019) [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: | Purine Nucleoside Phosphorylase (PNP) | pfPNP |
Type: | Enzyme |
Mol. Mass.: | 26857.85 |
Organism: | Plasmodium falciparum |
Description: | n/a |
Residue: | 245 |
Sequence: | MDNLLRHLKISKEQITPVVLVVGDPGRVDKIKVVCDSYVDLAYNREYKSVECHYKGQKFL
CVSHGVGSAGCAVCFEELCQNGAKVIIRAGSCGSLQPDLIKRGDICICNAAVREDRVSHL
LIHGDFPAVGDFDVYDTLNKCAQELNVPVFNGISVSSDMYYPNKIIPSRLEDYSKANAAV
VEMELATLMVIGTLRKVKTGGILIVDGCPFKWDEGDFDNNLVPHQLENMIKIALGACAKL
ATKYA
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BDBM50293087 |
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n/a |
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Name | BDBM50293087 |
Synonyms: | 2-amino-7-(((3R,4R)-3-hydroxy-4-(hydroxymethyl)pyrrolidin-1-yl)methyl)-3H-pyrrolo[3,2-d]pyrimidin-4(5H)-one | CHEMBL475750 |
Type | Small organic molecule |
Emp. Form. | C12H17N5O3 |
Mol. Mass. | 279.2951 |
SMILES | Nc1nc2c(CN3C[C@H](O)[C@@H](CO)C3)c[nH]c2c(=O)[nH]1 |r| |
Structure |
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