Pettit F K, Bowie J U
Department of Chemistry and Biochemistry, and UCLA-DOE Laboratory of Structural Biology and Molecular Medicine, Los Angeles, CA, 90095, USA.
J Mol Biol. 1999 Jan 29;285(4):1377-82. doi: 10.1006/jmbi.1998.2411.
Pharmaceutical design is usually directed at developing small molecules that can specifically bind and alter the activity of a target protein. Here, we show that high-affinity binding of small molecules requires a rough patch on a protein surface. Drug design strategies should therefore be targeted to rough areas on a protein. Our results indicate that the roughness of small functional sites may reflect the complex local shapes needed to fit specific interactions into small areas.