可药性
概化理论
细胞色素P450
数量结构-活动关系
计算机科学
基质(水族馆)
药物发现
药物代谢
药物开发
计算生物学
鉴定(生物学)
化学
机器学习
生物化学
药品
药理学
酶
生物
心理学
基因
生态学
发展心理学
植物
作者
Jiamin Chang,Xiaoyu Fan,Boxue Tian
标识
DOI:10.1021/acs.jcim.4c00115
摘要
Cytochrome P450 enzymes (CYPs) play a crucial role in Phase I drug metabolism in the human body, and CYP activity toward compounds can significantly affect druggability, making early prediction of CYP activity and substrate identification essential for therapeutic development. Here, we established a deep learning model for assessing potential CYP substrates, DeepP450, by fine-tuning protein and molecule pretrained models through feature integration with cross-attention and self-attention layers. This model exhibited high prediction accuracy (0.92) on the test set, with area under the receiver operating characteristic curve (AUROC) values ranging from 0.89 to 0.98 in substrate/nonsubstrate predictions across the nine major human CYPs, surpassing current benchmarks for CYP activity prediction. Notably, DeepP450 uses only one model to predict substrates/nonsubstrates for any of the nine CYPs and exhibits certain generalizability on novel compounds and different categories of human CYPs, which could greatly facilitate early stage drug design by avoiding CYP-reactive compounds.
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