虚拟筛选
可转让性
诱饵
力场(虚构)
计算机科学
范德瓦尔斯力
蛋白质配体
溶剂化
功能(生物学)
对接(动物)
机器学习
药物发现
数据挖掘
人工智能
化学
生物信息学
医学
生物
分子
生物化学
受体
护理部
有机化学
罗伊特
进化生物学
作者
Shuangye Yin,Lada Biedermannová,Jiřı́ Vondrášek,Nikolay V. Dokholyan
摘要
Virtual screening is becoming an important tool for drug discovery. However, the application of virtual screening has been limited by the lack of accurate scoring functions. Here, we present a novel scoring function, MedusaScore, for evaluating protein−ligand binding. MedusaScore is based on models of physical interactions that include van der Waals, solvation, and hydrogen bonding energies. To ensure the best transferability of the scoring function, we do not use any protein−ligand experimental data for parameter training. We then test the MedusaScore for docking decoy recognition and binding affinity prediction and find superior performance compared to other widely used scoring functions. Statistical analysis indicates that one source of inaccuracy of MedusaScore may arise from the unaccounted entropic loss upon ligand binding, which suggests avenues of approach for further MedusaScore improvement.
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