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分子大小在配体效率中的作用。

The role of molecular size in ligand efficiency.

作者信息

Reynolds Charles H, Bembenek Scott D, Tounge Brett A

机构信息

Johnson & Johnson Pharmaceutical Research and Development, L.L.C., Welsh and McKean Roads, PO Box 776, Spring House, PA 19477, USA.

出版信息

Bioorg Med Chem Lett. 2007 Aug 1;17(15):4258-61. doi: 10.1016/j.bmcl.2007.05.038. Epub 2007 May 17.

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.

摘要

配体效率是一种简单的衡量指标,用于评估配体的效力是源于与蛋白质靶点的最佳契合,还是仅仅由于形成了许多相互作用。对8000多种配体与28种蛋白质靶点的蛋白质-配体结合亲和力进行比较,结果明确表明,平均配体结合亲和力与分子大小并非呈线性关系。因此,按配体大小对配体效率进行缩放很重要,尤其是在涉及小配体(如片段)的情况下。我们提出了一种简单的“契合质量”衡量指标,以消除这种依赖性。

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