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J Comput Aided Mol Des. 2009 Jun;23(6):355-74. doi: 10.1007/s10822-009-9266-3. Epub 2009 Apr 2.

Effects of protein conformation in docking: improved pose prediction through protein pocket adaptation.

Author information

  • Department of Bioengineering and Therapeutic Sciences, University of California, San Francisco, CA 94158-9001, USA. ajain@jainlab.org

Abstract

Computational methods for docking ligands have been shown to be remarkably dependent on precise protein conformation, where acceptable results in pose prediction have been generally possible only in the artificial case of re-docking a ligand into a protein binding site whose conformation was determined in the presence of the same ligand (the "cognate" docking problem). In such cases, on well curated protein/ligand complexes, accurate dockings can be returned as top-scoring over 75% of the time using tools such as Surflex-Dock. A critical application of docking in modeling for lead optimization requires accurate pose prediction for novel ligands, ranging from simple synthetic analogs to very different molecular scaffolds. Typical results for widely used programs in the "cross-docking case" (making use of a single fixed protein conformation) have rates closer to 20% success. By making use of protein conformations from multiple complexes, Surflex-Dock yields an average success rate of 61% across eight pharmaceutically relevant targets. Following docking, protein pocket adaptation and rescoring identifies single pose families that are correct an average of 67% of the time. Consideration of the best of two pose families (from alternate scoring regimes) yields a 75% mean success rate.

PMID:
19340588
[PubMed - indexed for MEDLINE]
PMCID:
PMC2693357
Free PMC Article

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