虚拟筛选
对接(动物)
计算机科学
人工智能
卷积神经网络
工作流程
机器学习
计算生物学
数据挖掘
生物信息学
药物发现
生物
医学
护理部
数据库
作者
Huicong Liang,Aowei Xie,Ning Hou,Fengjiao Wei,Ting Gao,Jiajie Li,Xinru Gao,Chuanqin Shi,Gaokeng Xiao,Ximing Xu
摘要
ABSTRACT Scoring functions (SFs) of molecular docking is a vital component of structure‐based virtual screening (SBVS). Traditional SFs yield their inherent shortage for idealized approximations and simplifications predicting the binding affinity. Complementarily, SFs based on deep learning (DL) have emerged as powerful tools for capturing intricate features within protein‐ligand (PL) interactions. We here present a docking‐score fusion strategy that integrates pose scores derived from GNINA's convolutional neural network (CNN) with traditional docking scores. Extensive validation on diverse datasets has shown that by means of multiplying Watvina docking score by CNNscore demonstrates state‐of‐the‐art screening power. Furthermore, in a reverse practice, our docking‐score fusion technique was incorporated into the virtual screening (VS) workflow aimed at identifying inhibitors of the challenging target TYK2. Two promising hits with IC 50 9.99 μM and 13.76 μM in vitro were identified from nearly 12 billion molecules.
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