Abstract
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.
Highlights
Protein phosphorylation is one of the most important post-translational modifications (PSMs) in an organism [1]
Protein phosphorylation is a reversible post-translational modification based on the equilibrium of kinases and phosphatases
We propose a new computational approach, KSIMC, to predict kinase–substrate interactions based on matrix completion
Summary
Protein phosphorylation is one of the most important post-translational modifications (PSMs) in an organism [1]. It is catalyzed by protein kinases, which promote the transfer of a phosphate group to corresponding substrates. Protein phosphatases remove the phosphates from substrates. Protein phosphorylation is a reversible post-translational modification based on the equilibrium of kinases and phosphatases. It plays critical roles in many cellular processes, such as cell metabolism, cell proliferation, cell differentiation, cell apoptosis, and cellular signal transduction [2,3]. Identifying interactions between substrates and its specific kinases may facilitate the study of diseases and drug targets [6,7,8]
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