Gohlke H, Klebe G
Department of Pharmaceutical Chemistry, Philipps University of Marburg, Marbacher Weg 6, 35032 Marburg, Germany.
Curr Opin Struct Biol. 2001 Apr;11(2):231-5. doi: 10.1016/s0959-440x(00)00195-0.
In virtual screening, small-molecule ligands are docked into protein binding sites and their binding affinity is predicted. Knowledge-based, regression-based and first-principle-based methods have been developed to rank computer-generated binding modes. As a result of still existing deficiencies, a best compromise might be the combination of several scoring schemes into a consensus scoring approach.
在虚拟筛选中,小分子配体被对接至蛋白质结合位点,并预测其结合亲和力。已开发出基于知识、基于回归和基于第一性原理的方法,对计算机生成的结合模式进行排序。由于仍然存在缺陷,最佳折衷方案可能是将几种评分方案组合成一种共识评分方法。