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ET-GRU: using multi-layer gated recurrent units to identify electron transport proteins

BACKGROUND: Electron transport chain is a series of protein complexes embedded in the process of cellular respiration, which is an important process to transfer electrons and other macromolecules throughout the cell. It is also the major process to extract energy via redox reactions in the case of o...

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Autores principales: Le, Nguyen Quoc Khanh, Yapp, Edward Kien Yee, Yeh, Hui-Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6612191/
https://www.ncbi.nlm.nih.gov/pubmed/31277574
http://dx.doi.org/10.1186/s12859-019-2972-5
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author Le, Nguyen Quoc Khanh
Yapp, Edward Kien Yee
Yeh, Hui-Yuan
author_facet Le, Nguyen Quoc Khanh
Yapp, Edward Kien Yee
Yeh, Hui-Yuan
author_sort Le, Nguyen Quoc Khanh
collection PubMed
description BACKGROUND: Electron transport chain is a series of protein complexes embedded in the process of cellular respiration, which is an important process to transfer electrons and other macromolecules throughout the cell. It is also the major process to extract energy via redox reactions in the case of oxidation of sugars. Many studies have determined that the electron transport protein has been implicated in a variety of human diseases, i.e. diabetes, Parkinson, Alzheimer’s disease and so on. Few bioinformatics studies have been conducted to identify the electron transport proteins with high accuracy, however, their performance results require a lot of improvements. Here, we present a novel deep neural network architecture to address this problem. RESULTS: Most of the previous studies could not use the original position specific scoring matrix (PSSM) profiles to feed into neural networks, leading to a lack of information and the neural networks consequently could not achieve the best results. In this paper, we present a novel approach by using deep gated recurrent units (GRU) on full PSSMs to resolve this problem. Our approach can precisely predict the electron transporters with the cross-validation and independent test accuracy of 93.5 and 92.3%, respectively. Our approach demonstrates superior performance to all of the state-of-the-art predictors on electron transport proteins. CONCLUSIONS: Through the proposed study, we provide ET-GRU, a web server for discriminating electron transport proteins in particular and other protein functions in general. Also, our achievement could promote the use of GRU in computational biology, especially in protein function prediction.
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spelling pubmed-66121912019-07-16 ET-GRU: using multi-layer gated recurrent units to identify electron transport proteins Le, Nguyen Quoc Khanh Yapp, Edward Kien Yee Yeh, Hui-Yuan BMC Bioinformatics Research Article BACKGROUND: Electron transport chain is a series of protein complexes embedded in the process of cellular respiration, which is an important process to transfer electrons and other macromolecules throughout the cell. It is also the major process to extract energy via redox reactions in the case of oxidation of sugars. Many studies have determined that the electron transport protein has been implicated in a variety of human diseases, i.e. diabetes, Parkinson, Alzheimer’s disease and so on. Few bioinformatics studies have been conducted to identify the electron transport proteins with high accuracy, however, their performance results require a lot of improvements. Here, we present a novel deep neural network architecture to address this problem. RESULTS: Most of the previous studies could not use the original position specific scoring matrix (PSSM) profiles to feed into neural networks, leading to a lack of information and the neural networks consequently could not achieve the best results. In this paper, we present a novel approach by using deep gated recurrent units (GRU) on full PSSMs to resolve this problem. Our approach can precisely predict the electron transporters with the cross-validation and independent test accuracy of 93.5 and 92.3%, respectively. Our approach demonstrates superior performance to all of the state-of-the-art predictors on electron transport proteins. CONCLUSIONS: Through the proposed study, we provide ET-GRU, a web server for discriminating electron transport proteins in particular and other protein functions in general. Also, our achievement could promote the use of GRU in computational biology, especially in protein function prediction. BioMed Central 2019-07-06 /pmc/articles/PMC6612191/ /pubmed/31277574 http://dx.doi.org/10.1186/s12859-019-2972-5 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Le, Nguyen Quoc Khanh
Yapp, Edward Kien Yee
Yeh, Hui-Yuan
ET-GRU: using multi-layer gated recurrent units to identify electron transport proteins
title ET-GRU: using multi-layer gated recurrent units to identify electron transport proteins
title_full ET-GRU: using multi-layer gated recurrent units to identify electron transport proteins
title_fullStr ET-GRU: using multi-layer gated recurrent units to identify electron transport proteins
title_full_unstemmed ET-GRU: using multi-layer gated recurrent units to identify electron transport proteins
title_short ET-GRU: using multi-layer gated recurrent units to identify electron transport proteins
title_sort et-gru: using multi-layer gated recurrent units to identify electron transport proteins
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6612191/
https://www.ncbi.nlm.nih.gov/pubmed/31277574
http://dx.doi.org/10.1186/s12859-019-2972-5
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