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Molecular surface comparison: Application to drug design

✍ Scribed by Frank Blaney; P. Finn; Rob Phippen; Mike Wyatt


Publisher
Elsevier Science
Year
1993
Tongue
English
Weight
786 KB
Volume
11
Category
Article
ISSN
0263-7855

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## Abstract Here, we describe a family of methods based on residue–residue connectivity for characterizing binding sites and apply variants of the method to various types of protein–ligand complexes including proteases, allosteric‐binding sites, correctly and incorrectly docked poses, and inhibitor