Article ID Journal Published Year Pages File Type
1366213 Bioorganic & Medicinal Chemistry Letters 2007 4 Pages PDF
Abstract

Ligand efficiency is a simple metric for assessing whether a ligand derives its potency from optimal fit with the protein target or simply by virtue of making many contacts. Comparison of protein–ligand binding affinities for over 8000 ligands with 28 protein targets shows conclusively that the average ligand binding affinities are not linear with molecular size. It is therefore important to scale ligand efficiencies by the size of the ligand, particularly where small ligands (e.g., fragments) are involved. We propose a simple ‘fit quality’ metric that removes this dependence.

Graphical abstractAverage and maximal ligand efficiencies decrease as ligand size increases. We propose a method for scaling ligand efficiencies that removes this dependence on molecular size.Figure optionsDownload full-size imageDownload as PowerPoint slide

Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
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