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KSIMC: Predicting Kinase–Substrate Interactions Based on Matrix Completion
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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6358935/ https://www.ncbi.nlm.nih.gov/pubmed/30646505 http://dx.doi.org/10.3390/ijms20020302 |
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author | Gan, Jingzhong Qiu, Jie Deng, Canshang Lan, Wei Chen, Qingfeng Hu, Yanling |
author_facet | Gan, Jingzhong Qiu, Jie Deng, Canshang Lan, Wei Chen, Qingfeng Hu, Yanling |
author_sort | Gan, Jingzhong |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-6358935 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-63589352019-02-06 KSIMC: Predicting Kinase–Substrate Interactions Based on Matrix Completion Gan, Jingzhong Qiu, Jie Deng, Canshang Lan, Wei Chen, Qingfeng Hu, Yanling Int J Mol Sci Article 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. MDPI 2019-01-14 /pmc/articles/PMC6358935/ /pubmed/30646505 http://dx.doi.org/10.3390/ijms20020302 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Gan, Jingzhong Qiu, Jie Deng, Canshang Lan, Wei Chen, Qingfeng Hu, Yanling KSIMC: Predicting Kinase–Substrate Interactions Based on Matrix Completion |
title | KSIMC: Predicting Kinase–Substrate Interactions Based on Matrix Completion |
title_full | KSIMC: Predicting Kinase–Substrate Interactions Based on Matrix Completion |
title_fullStr | KSIMC: Predicting Kinase–Substrate Interactions Based on Matrix Completion |
title_full_unstemmed | KSIMC: Predicting Kinase–Substrate Interactions Based on Matrix Completion |
title_short | KSIMC: Predicting Kinase–Substrate Interactions Based on Matrix Completion |
title_sort | ksimc: predicting kinase–substrate interactions based on matrix completion |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6358935/ https://www.ncbi.nlm.nih.gov/pubmed/30646505 http://dx.doi.org/10.3390/ijms20020302 |
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