Extra Precision Glide: Docking and Scoring Incorporating a Model of Hydrophobic Enclosure for Protein−Ligand Complexes
Schrodinger (United States) · Columbia University
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…
Citation impact
- FWCI
- 47.19
- Percentile
- 100%
- References
- 43
Authors
8- RARichard A. FriesnerCorresponding
Schrodinger (United States), Columbia University
- RBRobert B. Murphy
Columbia University, Schrodinger (United States)
- MPMatthew P. Repasky
Schrodinger (United States), Columbia University
- LLLeah L. Frye
Schrodinger (United States), Columbia University
- JRJeremy R. Greenwood
Schrodinger (United States), Columbia University
Topics & keywords
- Chemistry
- Docking (animal)
- Affinities
- Hydrogen bond
- Ligand (biochemistry)
- Binding affinities
- Searching the conformational space for docking
- Hydrophobic effect
- Clean water and sanitation