Kim Ki Hwan
Hope Drug Discovery Research Laboratory, 260 Southgate Drive, Vernon Hills, IL 60061, USA.
J Comput Aided Mol Des. 2007 Jan-Mar;21(1-3):63-86. doi: 10.1007/s10822-007-9106-2. Epub 2007 Mar 3.
A lead optimization is usually carried out by structure-activity relationship (SAR) and/or quantitative structure-activity relationship (QSAR) studies. One of the assumptions in SAR and QSAR studies is that similar analogs bind to the same binding site in a similar binding mode. One often observes that there are outliers, especially in QSAR. However, most QSAR studies are carried out focusing their attention to the development of QSAR and leave the outliers without much attention. We searched a number of ligand-bound X-ray crystal structures from the protein structure database to find evidences that could indicate a possible source of outliers in SAR or QSAR. Our results show that unusual binding mode could be a source of outliers.
先导化合物优化通常通过构效关系(SAR)和/或定量构效关系(QSAR)研究来进行。SAR和QSAR研究中的一个假设是,相似的类似物以相似的结合模式与相同的结合位点结合。人们经常观察到存在异常值,尤其是在QSAR中。然而,大多数QSAR研究都将注意力集中在QSAR的开发上,而对异常值关注不多。我们从蛋白质结构数据库中搜索了许多配体结合的X射线晶体结构,以寻找可能表明SAR或QSAR中异常值潜在来源的证据。我们的结果表明,异常的结合模式可能是异常值的一个来源。