articleJournal of Medicinal ChemistryJan 19, 2007Closed access

Diverse, High-Quality Test Set for the Validation of Protein−Ligand Docking Performance

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Abstract

A procedure for analyzing and classifying publicly available crystal structures has been developed. It has been used to identify high-resolution protein-ligand complexes that can be assessed by reconstructing the electron density for the ligand using the deposited structure factors. The complexes have been clustered according to the protein sequences, and clusters have been discarded if they do not represent proteins thought to be of direct interest to the pharmaceutical or agrochemical industry. Rules have been used to exclude complexes containing non-drug-like ligands. One complex from each cluster has been selected where a structure of sufficient quality was available. The final Astex diverse set contains…

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Authors

7

Topics & keywords

Keywords
  • Docking (animal)
  • Protein–ligand docking
  • Chemistry
  • Ligand (biochemistry)
  • Drug discovery
  • Computational biology
  • Data mining
  • Combinatorial chemistry
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