深度学习
人工智能
计算机科学
泛素连接酶
泛素
机器学习
人工神经网络
药物发现
嵌入
内德4
深层神经网络
计算生物学
生物信息学
生物
生物化学
基因
作者
Jia Wang,Gui-Qing Pan,Jianqiang Li,Xuequn Shang,Zhu‐Hong You,Yuan Huang
标识
DOI:10.1109/bibm58861.2023.10385619
摘要
Identifying the substrates of ubiquitin protein ligase (E3) and deubiquitinases (DUB) contributes to the discovery of potential therapeutic targets for diseases. However, experimental identification of E3/DUB-substrate interactions is costly and time-consuming. Current computational methods for predicting E3/DUB-substrate interactions rely heavily on specific domain knowledge and involve complex and diverse biological data processing. To address this challenge, we proposed a deep learning prediction model, named Deep-USIpred, which predicts E3/DUB-substrate interactions using protein sequences. The proposed Deep-USIpred model encodes protein sequences with a pretrained model and utilizes 1DCNN-BNN deep learning algorithm to make a robust prediction model. We evaluated the performance of the proposed model on real datasets, and our experimental results show that it can achieve excellent prediction performance on the tasks of ESI and DSI. Our proposed method provides a promising alternative for the prediction of E3/DUB-substrate interactions, which has the potential to accelerate drug discovery for various diseases. The source code and dataset are available at https://github.com/PGTSING/Deep-USIpred.
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