亲缘关系
化学
范德瓦尔斯力
结合能
高分子
共价键
Atom(片上系统)
结晶学
结合位点
立体化学
分子
计算化学
生物化学
物理
有机化学
计算机科学
核物理学
嵌入式系统
作者
Irwin D. Kuntz,K. Chen,Kim A. Sharp,Peter A. Kollman
标识
DOI:10.1073/pnas.96.18.9997
摘要
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 ≈−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.
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