dUTPase as a Platform for Antimalarial Drug Design: Structural Basis for the Selectivity of a Class of Nucleoside Inhibitors-Reference-Cited by-同舟云学术

dUTPase as a Platform for Antimalarial Drug Design: Structural Basis for the Selectivity of a Class of Nucleoside Inhibitors

Published:2005-02 Issue:2 Volume:13 Page:329-338
ISSN:0969-2126
Container-title:Structure
language:en
Short-container-title:Structure

Author:

Whittingham Jean L.,Leal Isabel,Nguyen Corinne,Kasinathan Ganasan,Bell Emma,Jones Andrew F.,Berry Colin,Benito Agustin,Turkenburg Johan P.,Dodson Eleanor J.,Perez Luis M. Ruiz,Wilkinson Anthony J.,Johansson Nils Gunnar,Brun Reto,Gilbert Ian H.,Pacanowska Dolores Gonzalez,Wilson Keith S.

Publisher

Elsevier BV

Subject

Molecular Biology,Structural Biology

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5. Crystal structure of dUTPase from equine infectious anaemia virus: active site metal binding in a substrate analogue complex;Dauter;J. Mol. Biol.,1999

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