An Extensive and Diverse Set of Molecular Overlays for the Validation of Pharmacophore Programs

The pharmacophore hypothesis plays a central role in both the design and optimization of drug-like ligands. Pharmacophore patterns are invoked to explain the binding affinity of ligands and to enable the design of chemically distinct scaffolds that show affinity for a protein target of interest. The importance of pharmacophores in rationalizing ligand affinity has led to numerous algorithms that seek to overlay ligands based on their pharmacophoric features. All such algorithms must be validated with respect to known ligand overlays, usually by extracting ligand overlay sets from the Protein Data Bank (PDB). This validation step creates the problem of which of the known overlays to select and from which proteins. The large number of structures and protein families in the PDB makes it difficult to establish a definitive overlay set; as a result, validation studies have rarely employed the same data sets. We have therefore undertaken an exhaustive analysis of the RCSB PDB to identify 121 distinct ligand ove...