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Title | Dutpase as a Platform for Antimalarial Drug Design: Structural Basis for the Selectivity of a Class of Nucleoside Inhibitors. |
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Journal, issue, pages | Structure, Vol. 13, Page 329-, Year 2005 |
Publish date | May 5, 2004 (structure data deposition date) |
![]() | Whittingham, 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. |
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Methods | X-ray diffraction |
Resolution | 2.4 Å |
Structure data | ![]() PDB-1vyq: |
Chemicals | ![]() ChemComp-DUX: ![]() ChemComp-HOH: |
Source |
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![]() | HYDROLASE / DRUG DESIGN / PLASMODIUM FALCIPARUM / DUTPASE / DEOXYURIDINE NUCLEOTIDOHYDROLASE / MALARIA |