articleJournal of Medicinal ChemistrySep 23, 2006Closed access

Extra Precision Glide:  Docking and Scoring Incorporating a Model of Hydrophobic Enclosure for Protein−Ligand Complexes

Schrodinger (United States) · Columbia University

PubMed
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Abstract

A novel scoring function to estimate protein-ligand binding affinities has been developed and implemented as the Glide 4.0 XP scoring function and docking protocol. In addition to unique water desolvation energy terms, protein-ligand structural motifs leading to enhanced binding affinity are included: (1) hydrophobic enclosure where groups of lipophilic ligand atoms are enclosed on opposite faces by lipophilic protein atoms, (2) neutral-neutral single or correlated hydrogen bonds in a hydrophobically enclosed environment, and (3) five categories of charged-charged hydrogen bonds. The XP scoring function and docking protocol have been developed to reproduce experimental binding affinities for a set of 198…

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Authors

8

Topics & keywords

Keywords
  • Chemistry
  • Docking (animal)
  • Affinities
  • Hydrogen bond
  • Ligand (biochemistry)
  • Binding affinities
  • Searching the conformational space for docking
  • Hydrophobic effect
UN Sustainable Development Goals
  • Clean water and sanitation
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