KSIMC: Predicting Kinase-Substrate Interactions Based on Matrix Completion

被引:3
|
作者
Gan, Jingzhong [1 ]
Qiu, Jie [1 ]
Deng, Canshang [2 ]
Lan, Wei [2 ]
Chen, Qingfeng [2 ,3 ]
Hu, Yanling [4 ]
机构
[1] Yulin Normal Univ, Sch Comp Sci & Engn, Yulin 537000, Peoples R China
[2] Guangxi Univ, Sch Comp Elect & Informat, Nanning 530004, Peoples R China
[3] Guangxi Univ, State Key Lab Conservat & Utilizat Subtrop Agrobi, Nanning 530004, Peoples R China
[4] Guangxi Med Univ, Ctr Genom & Personalized Med, Nanning 530021, Peoples R China
基金
中国国家自然科学基金;
关键词
protein phosphorylation; kinase-substrate interaction; heterogeneous network; matrix completion; PROTEIN-PHOSPHORYLATION; IN-VIVO; DISEASE; SITES;
D O I
10.3390/ijms20020302
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Protein phosphorylation is an important chemical modification catalyzed by kinases. It plays important roles in many cellular processes. Predicting kinase-substrate interactions is vital to understanding the mechanism of many diseases. Many computational methods have been proposed to identify kinase-substrate interactions. However, the prediction accuracy still needs to be improved. Therefore, it is necessary to develop an efficient computational method to predict kinase-substrate interactions. In this paper, we propose a novel computational approach, KSIMC, to identify kinase-substrate interactions based on matrix completion. Firstly, the kinase similarity and substrate similarity are calculated by aligning sequence of kinase-kinase and substrate-substrate, respectively. Then, the original association network is adjusted based on the similarities. Finally, the matrix completion is used to predict potential kinase-substrate interactions. The experiment results show that our method outperforms other state-of-the-art algorithms in performance. Furthermore, the relevant databases and scientific literature verify the effectiveness of our algorithm for new kinase-substrate interaction identification.
引用
收藏
页数:11
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