Protein complex identification based on weighted PPI network with multi-source information

被引:3
|
作者
Yu, Yang [1 ,2 ]
Zheng, Zeyu [1 ,3 ]
机构
[1] Chinese Acad Sci, Shenyang Inst Automat, Beijing, Peoples R China
[2] Shenyang Normal Univ, Software Coll, Shenyang, Liaoning, Peoples R China
[3] Univ Chinese Acad Sci, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
Protein complex identification; Weighted graph; Multi-source information; GENE ONTOLOGY; MODULES; SEQUENCE;
D O I
10.1016/j.jtbi.2019.06.005
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Proteins form complexes to accomplish biological functions such as transcription of DNA, translation of mRNA and cell growth. Detection of protein complexes from protein-protein interaction (PPI) networks is the first step for the analysis of biological processes and pathways. Here, we propose a new framework by incorporating Gene Ontology (GO), amino acid background frequency (AABF) and data from von Mering (von Mering data) to identify protein complexes. Firstly, based on the semantic similarity of GO, we construct a weighted PPI network. Secondly, von Mering data is added to construct six types of weighted graphs. Lastly, by integrating density, diameter and cosine similarity, we define a new condition for clustering proteins in these weighted protein network by selecting specific node as key node. Comparison and analysis results indicate that our proposed method could achieve better performances than some classic existing approaches in regard to f-measure and precision. (C) 2019 Elsevier Ltd. All rights reserved.
引用
收藏
页码:77 / 83
页数:7
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