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TitleDutpase as a Platform for Antimalarial Drug Design: Structural Basis for the Selectivity of a Class of Nucleoside Inhibitors.
Journal, issue, pagesStructure, Vol. 13, Page 329-, Year 2005
Publish dateMay 5, 2004 (structure data deposition date)
AuthorsWhittingham, J.L. / Leal, I. / Nguyen, C. / Kasinathan, G. / Bell, E. / Jones, A.F. / Berry, C. / Benito, A. / Turkenburg, J.P. / Dodson, E.J. ...Whittingham, J.L. / Leal, I. / Nguyen, C. / Kasinathan, G. / 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.
External linksStructure / PubMed:15698576
MethodsX-ray diffraction
Resolution2.4 Å
Structure data

PDB-1vyq:
Novel inhibitors of Plasmodium Falciparum dUTPase provide a platform for anti-malarial drug design
Method: X-RAY DIFFRACTION / Resolution: 2.4 Å

Chemicals

ChemComp-DUX:
2,3-DEOXY-3-FLUORO-5-O-TRITYLURIDINE

ChemComp-HOH:
WATER

Source
  • plasmodium falciparum (malaria parasite P. falciparum)
KeywordsHYDROLASE / DRUG DESIGN / PLASMODIUM FALCIPARUM / DUTPASE / DEOXYURIDINE NUCLEOTIDOHYDROLASE / MALARIA

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