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Science 308 (5726): 1266-1267

Copyright © 2005 by the American Association for the Advancement of Science

CELL BIOLOGY:
Lessons in Rational Drug Design for Protein Kinases

Natalie G. Ahn and Katheryn A. Resing


A Holy Grail of marrying bioinformatics with structural biology is the design of drugs that precisely affect specific cellular targets. Ahn and Resing discuss in their Perspective how combining sequence and structural analysis of the catalytic site of protein kinases allowed one group to rationally design molecules that selectively block p90 ribosomal S6 kinase enzymatic activity in cells.
The authors are in the Department of Chemistry and Biochemistry, University of Colorado, Boulder, CO 80309, USA. E-mail: natalie.ahn{at}colorado.edu


THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
Protein protein interaction inhibition (2P2I) combining high throughput and virtual screening: Application to the HIV-1 Nef protein.
S. Betzi, A. Restouin, S. Opi, S. T. Arold, I. Parrot, F. Guerlesquin, X. Morelli, and Y. Collette (2007)
PNAS 104, 19256-19261
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