机构:
Univ Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94143 USAUniv Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94143 USA
Kuntz, ID
[1
]
Chen, K
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机构:Univ Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94143 USA
Chen, K
Sharp, KA
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h-index: 0
机构:Univ Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94143 USA
Sharp, KA
Kollman, PA
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机构:Univ Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94143 USA
Kollman, PA
机构:
[1] Univ Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94143 USA
[2] Johnson Res Fdn, Philadelphia, PA 19104 USA
[3] Univ Penn, Dept Biochem & Biophys, Philadelphia, PA 19104 USA
We explore the question of what are the best ligands for macromolecular targets. A survey of experimental data on a large number of the strongest-binding ligands indicates that the free energy of binding increases with the number of nonhydrogen atoms with an initial slope of approximate to-1.5 kcal/mol (1 cal = 4.18 J) per atom. For ligands that contain more than 15 nonhydrogen atoms, the free energy of binding increases very little with relative molecular mass; This nonlinearity is largely ascribed to nonthermodynamic factors. An analysis of the dominant interactions suggests that van der Waals interactions and hydrophobic effects provide a reasonable basis for understanding binding affinities across the entire set of ligands. Interesting outliers that bind unusually strongly on a per atom basis include metal ions, covalently attached ligands, and a few well known complexes such as biotin-avidin.