Novel inhibitors of Plasmodium Falciparum dUTPase provide a platform for anti-malarial drug design
收藏Protein Data Bank Japan2023-12-13 更新2026-03-21 收录
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https://pdbj.org/mine/summary/1vyq
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Novel inhibitors of Plasmodium Falciparum dUTPase provide a platform for anti-malarial drug design Descriptor: 2,3-DEOXY-3-FLUORO-5-O-TRITYLURIDINE, DEOXYURIDINE 5'-TRIPHOSPHATE NUCLEOTIDOHYDROLASE Authors: Whittingham, J.L, Leal, I, Kasinathan, G, Nguyen, C, Bell, E, Jones, A.F, Berry, C, Benito, A, Turkenburg, J.P, Dodson, E.J, Ruiz Perez, L.M, Wilkinson, A.J, Johansson, N.G, Brun, R, Gilbert, I.H, Gonzalez Pacanowska, D, Wilson, K.S. Deposit date: 2004-05-05 Release date: 2005-05-26 Last modified: 2023-12-13 Method: X-RAY DIFFRACTION (2.4 Å) Cite: Dutpase as a Platform for Antimalarial Drug Design: Structural Basis for the Selectivity of a Class of Nucleoside Inhibitors. Structure, 13, 2005
创建时间：
2004-05-05
