管道(软件)
工作流程
计算机科学
人工智能
药物发现
计算生物学
生物信息学
生物
程序设计语言
数据库
作者
Hazem Mslati,Francesco Gentile,Mohit Pandey,Fuqiang Ban,Artem Cherkasov
标识
DOI:10.1021/acs.jcim.3c01878
摘要
Proteolysis-targeting chimeras (PROTACs) that engage two biological targets at once are a promising technology in degrading clinically relevant protein targets. Since factors that influence the biological activities of PROTACs are more complex than those of a small molecule drug, we explored a combination of computational chemistry and deep learning strategies to forecast PROTAC activity and enable automated design. A new method named PROTACable was developed for the de novo design of PROTACs, which includes a robust 3-D modeling workflow to model PROTAC ternary complexes using a library of E3 ligase and linker and an SE(3)-equivariant graph transformer network to predict the activity of newly designed PROTACs. PROTACable is available at https://github.com/giaguaro/PROTACable/.
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