Prediction of Enzyme Function Based on Three Parallel Deep CNN and Amino Acid Mutation
During the past decade, due to the number of proteins in PDB database being increased gradually, traditional methods cannot better understand the function of newly discovered enzymes in chemical reactions. Computational models and protein feature representation for predicting enzymatic function are...
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doaj-69f92460ff444807b82c43311c9e3ed62020-11-24T21:14:45ZengMDPI AGInternational Journal of Molecular Sciences1422-00672019-06-012011284510.3390/ijms20112845ijms20112845Prediction of Enzyme Function Based on Three Parallel Deep CNN and Amino Acid MutationRuibo Gao0Mengmeng Wang1Jiaoyan Zhou2Yuhang Fu3Meng Liang4Dongliang Guo5Junlan Nie6School of Information Science and Engineering, Yanshan University, Qinhuangdao 066004, Hebei, ChinaSchool of Information Science and Engineering, Yanshan University, Qinhuangdao 066004, Hebei, ChinaSchool of Information Science and Engineering, Yanshan University, Qinhuangdao 066004, Hebei, ChinaSchool of Information Science and Engineering, Yanshan University, Qinhuangdao 066004, Hebei, ChinaSchool of Information Science and Engineering, Yanshan University, Qinhuangdao 066004, Hebei, ChinaSchool of Information Science and Engineering, Yanshan University, Qinhuangdao 066004, Hebei, ChinaSchool of Information Science and Engineering, Yanshan University, Qinhuangdao 066004, Hebei, ChinaDuring the past decade, due to the number of proteins in PDB database being increased gradually, traditional methods cannot better understand the function of newly discovered enzymes in chemical reactions. Computational models and protein feature representation for predicting enzymatic function are more important. Most of existing methods for predicting enzymatic function have used protein geometric structure or protein sequence alone. In this paper, the functions of enzymes are predicted from many-sided biological information including sequence information and structure information. Firstly, we extract the mutation information from amino acids sequence by the position scoring matrix and express structure information with amino acids distance and angle. Then, we use histogram to show the extracted sequence and structural features respectively. Meanwhile, we establish a network model of three parallel Deep Convolutional Neural Networks (DCNN) to learn three features of enzyme for function prediction simultaneously, and the outputs are fused through two different architectures. Finally, The proposed model was investigated on a large dataset of 43,843 enzymes from the PDB and achieved 92.34% correct classification when sequence information is considered, demonstrating an improvement compared with the previous result.https://www.mdpi.com/1422-0067/20/11/2845enzyme function predictionDCNNamino acid sequencemutation information |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ruibo Gao Mengmeng Wang Jiaoyan Zhou Yuhang Fu Meng Liang Dongliang Guo Junlan Nie |
spellingShingle |
Ruibo Gao Mengmeng Wang Jiaoyan Zhou Yuhang Fu Meng Liang Dongliang Guo Junlan Nie Prediction of Enzyme Function Based on Three Parallel Deep CNN and Amino Acid Mutation International Journal of Molecular Sciences enzyme function prediction DCNN amino acid sequence mutation information |
author_facet |
Ruibo Gao Mengmeng Wang Jiaoyan Zhou Yuhang Fu Meng Liang Dongliang Guo Junlan Nie |
author_sort |
Ruibo Gao |
title |
Prediction of Enzyme Function Based on Three Parallel Deep CNN and Amino Acid Mutation |
title_short |
Prediction of Enzyme Function Based on Three Parallel Deep CNN and Amino Acid Mutation |
title_full |
Prediction of Enzyme Function Based on Three Parallel Deep CNN and Amino Acid Mutation |
title_fullStr |
Prediction of Enzyme Function Based on Three Parallel Deep CNN and Amino Acid Mutation |
title_full_unstemmed |
Prediction of Enzyme Function Based on Three Parallel Deep CNN and Amino Acid Mutation |
title_sort |
prediction of enzyme function based on three parallel deep cnn and amino acid mutation |
publisher |
MDPI AG |
series |
International Journal of Molecular Sciences |
issn |
1422-0067 |
publishDate |
2019-06-01 |
description |
During the past decade, due to the number of proteins in PDB database being increased gradually, traditional methods cannot better understand the function of newly discovered enzymes in chemical reactions. Computational models and protein feature representation for predicting enzymatic function are more important. Most of existing methods for predicting enzymatic function have used protein geometric structure or protein sequence alone. In this paper, the functions of enzymes are predicted from many-sided biological information including sequence information and structure information. Firstly, we extract the mutation information from amino acids sequence by the position scoring matrix and express structure information with amino acids distance and angle. Then, we use histogram to show the extracted sequence and structural features respectively. Meanwhile, we establish a network model of three parallel Deep Convolutional Neural Networks (DCNN) to learn three features of enzyme for function prediction simultaneously, and the outputs are fused through two different architectures. Finally, The proposed model was investigated on a large dataset of 43,843 enzymes from the PDB and achieved 92.34% correct classification when sequence information is considered, demonstrating an improvement compared with the previous result. |
topic |
enzyme function prediction DCNN amino acid sequence mutation information |
url |
https://www.mdpi.com/1422-0067/20/11/2845 |
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