TY - JOUR
T1 - MoRF-FUNCpred
T2 - Molecular Recognition Feature Function Prediction Based on Multi-Label Learning and Ensemble Learning
AU - Li, Haozheng
AU - Pang, Yihe
AU - Liu, Bin
AU - Yu, Liang
N1 - Publisher Copyright:
Copyright © 2022 Li, Pang, Liu and Yu.
PY - 2022/3/8
Y1 - 2022/3/8
N2 - 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.
AB - 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.
KW - binary relevance
KW - ensemble learning
KW - intrinsically disordered regions
KW - molecular recognition features
KW - multi-label learning
UR - http://www.scopus.com/inward/record.url?scp=85127333796&partnerID=8YFLogxK
U2 - 10.3389/fphar.2022.856417
DO - 10.3389/fphar.2022.856417
M3 - Article
AN - SCOPUS:85127333796
SN - 1663-9812
VL - 13
JO - Frontiers in Pharmacology
JF - Frontiers in Pharmacology
M1 - 856417
ER -