对接(动物)
计算机科学
虚拟筛选
构象集合
蛋白质-配体对接
计算生物学
药物发现
装订袋
化学
数据挖掘
结合位点
分子动力学
计算化学
生物化学
生物
护理部
医学
作者
Erich Hellemann,Jacob D. Durrant
标识
DOI:10.1021/acs.jctc.3c00478
摘要
Structure-based virtual screening (VS) is an effective method for identifying potential small-molecule ligands, but traditional VS approaches consider only a single binding-pocket conformation. Consequently, they struggle to identify ligands that bind to alternate conformations. Ensemble docking helps address this issue by incorporating multiple conformations into the docking process, but it depends on methods that can thoroughly explore pocket flexibility. We here introduce Sub-Pocket EXplorer (SubPEx), an approach that uses weighted ensemble (WE) path sampling to accelerate binding-pocket sampling. As proof of principle, we apply SubPEx to three proteins relevant to drug discovery: heat shock protein 90, influenza neuraminidase, and yeast hexokinase 2. SubPEx is available free of charge without registration under the terms of the open-source MIT license: http://durrantlab.com/subpex/.
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