Author:
Li Haozheng,Pang Yihe,Liu Bin,Yu Liang
Abstract
Intrinsically disordered regions (IDRs) without stable structure are important for protein structures and functions. Some IDRs can be combined with molecular fragments to make itself completed the transition from disordered to ordered, which are called molecular recognition features (MoRFs). There are five main functions of MoRFs: molecular recognition assembler (MoR_assembler), molecular recognition chaperone (MoR_chaperone), molecular recognition display sites (MoR_display_sites), molecular recognition effector (MoR_effector), and molecular recognition scavenger (MoR_scavenger). Researches on functions of molecular recognition features are important for pharmaceutical and disease pathogenesis. However, the existing computational methods can only predict the MoRFs in proteins, failing to distinguish their different functions. In this paper, we treat MoRF function prediction as a multi-label learning task and solve it with the Binary Relevance (BR) strategy. Finally, we use Support Vector Machine (SVM), Logistic Regression (LR), Decision Tree (DT), and Random Forest (RF) as basic models to construct MoRF-FUNCpred through ensemble learning. Experimental results show that MoRF-FUNCpred performs well for MoRF function prediction. To the best knowledge of ours, MoRF-FUNCpred is the first predictor for predicting the functions of MoRFs. Availability and Implementation: The stand alone package of MoRF-FUNCpred can be accessed from https://github.com/LiangYu-Xidian/MoRF-FUNCpred.
Funder
National Natural Science Foundation of China
Subject
Pharmacology (medical),Pharmacology
Cited by
5 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献