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AntiDMPpred: a web service for identifying anti-diabetic peptides
被引:17
作者:
Chen, Xue
[1
]
Huang, Jian
[2
]
He, Bifang
[1
]
机构:
[1] Guizhou Univ, Med Coll, Guiyang, Peoples R China
[2] Univ Elect Sci & Technol China, Sch Life Sci & Technol, Chengdu, Peoples R China
来源:
基金:
中国国家自然科学基金;
关键词:
Anti-diabetic peptides;
Peptide descriptors;
Machine learning;
Computational model;
BIOINFORMATICS;
SEMAGLUTIDE;
DATABASE;
IV;
D O I:
10.7717/peerj.13581
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Diabetes mellitus (DM) is a chronic metabolic disease that has been a major threat to human health globally, causing great economic and social adversities. The oral administration of anti-diabetic peptide drugs has become a novel route for diabetes therapy. Numerous bioactive peptides have demonstrated potential anti-diabetic properties and are promising as alternative treatment measures to prevent and manage diabetes. The computational prediction of anti-diabetic peptides can help promote peptide-based drug discovery in the process of searching newly effective therapeutic peptide agents for diabetes treatment. Here, we resorted to random forest to develop a computational model, named AntiDMPpred, for predicting anti-diabetic peptides. A benchmark dataset with 236 anti-diabetic and 236 non-antidiabetic peptides was first constructed. Four types of sequence-derived descriptors were used to represent the peptide sequences. We then combined four machine learning methods and six feature scoring methods to select the non-redundant features, which were fed into diverse machine learning classifiers to train the models. Experimental results show that AntiDMPpred reached an accuracy of 77.12% and area under the receiver operating curve (AUCROC) of 0.8193 in the nested five-fold cross-validation, yielding a satisfactory performance and surpassing other classifiers implemented in the study. The web service is freely accessible at http://i.uestc.edu.cn/AntiDMPpred/cgi-bin/AntiDMPpred.pl. We hope AntiDMPpred could improve the discovery of anti-diabetic bioactive peptides.
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页数:18
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