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Energy Profile Bayes and Thompson Optimized Convolutional Neural Network protein structure prediction
In living organisms, proteins are considered as the executants of biological functions. Owing to its pivotal role played in protein folding patterns, comprehension of protein structure is a challenging issue. Moreover, owing to numerous protein sequence exploration in protein data banks and complica...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer London
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9542649/ https://www.ncbi.nlm.nih.gov/pubmed/36245797 http://dx.doi.org/10.1007/s00521-022-07868-0 |
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author | Nallasamy, Varanavasi Seshiah, Malarvizhi |
author_facet | Nallasamy, Varanavasi Seshiah, Malarvizhi |
author_sort | Nallasamy, Varanavasi |
collection | PubMed |
description | In living organisms, proteins are considered as the executants of biological functions. Owing to its pivotal role played in protein folding patterns, comprehension of protein structure is a challenging issue. Moreover, owing to numerous protein sequence exploration in protein data banks and complication of protein structures, experimental methods are found to be inadequate for protein structural class prediction. Hence, it is very much advantageous to design a reliable computational method to predict protein structural classes from protein sequences. In the recent few years there has been an elevated interest in using deep learning to assist protein structure prediction as protein structure prediction models can be utilized to screen a large number of novel sequences. In this regard, we propose a model employing Energy Profile for atom pairs in conjunction with the Legion-Class Bayes function called Energy Profile Legion-Class Bayes Protein Structure Identification model. Followed by this, we use a Thompson Optimized convolutional neural network to extract features between amino acids and then the Thompson Optimized SoftMax function is employed to extract associations between protein sequences for predicting secondary protein structure. The proposed Energy Profile Bayes and Thompson Optimized Convolutional Neural Network (EPB-OCNN) method tested distinct unique protein data and was compared to the state-of-the-art methods, the Template-Based Modeling, Protein Design using Deep Graph Neural Networks, a deep learning-based S-glutathionylation sites prediction tool called a Computational Framework, the Deep Learning and a distance-based protein structure prediction using deep learning. The results obtained when applied with the Biopython tool with respect to protein structure prediction time, protein structure prediction accuracy, specificity, recall, F-measure, and precision, respectively, are measured. The proposed EPB-OCNN method outperformed the state-of-the-art methods, thereby corroborating the objective. |
format | Online Article Text |
id | pubmed-9542649 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer London |
record_format | MEDLINE/PubMed |
spelling | pubmed-95426492022-10-11 Energy Profile Bayes and Thompson Optimized Convolutional Neural Network protein structure prediction Nallasamy, Varanavasi Seshiah, Malarvizhi Neural Comput Appl Original Article In living organisms, proteins are considered as the executants of biological functions. Owing to its pivotal role played in protein folding patterns, comprehension of protein structure is a challenging issue. Moreover, owing to numerous protein sequence exploration in protein data banks and complication of protein structures, experimental methods are found to be inadequate for protein structural class prediction. Hence, it is very much advantageous to design a reliable computational method to predict protein structural classes from protein sequences. In the recent few years there has been an elevated interest in using deep learning to assist protein structure prediction as protein structure prediction models can be utilized to screen a large number of novel sequences. In this regard, we propose a model employing Energy Profile for atom pairs in conjunction with the Legion-Class Bayes function called Energy Profile Legion-Class Bayes Protein Structure Identification model. Followed by this, we use a Thompson Optimized convolutional neural network to extract features between amino acids and then the Thompson Optimized SoftMax function is employed to extract associations between protein sequences for predicting secondary protein structure. The proposed Energy Profile Bayes and Thompson Optimized Convolutional Neural Network (EPB-OCNN) method tested distinct unique protein data and was compared to the state-of-the-art methods, the Template-Based Modeling, Protein Design using Deep Graph Neural Networks, a deep learning-based S-glutathionylation sites prediction tool called a Computational Framework, the Deep Learning and a distance-based protein structure prediction using deep learning. The results obtained when applied with the Biopython tool with respect to protein structure prediction time, protein structure prediction accuracy, specificity, recall, F-measure, and precision, respectively, are measured. The proposed EPB-OCNN method outperformed the state-of-the-art methods, thereby corroborating the objective. Springer London 2022-10-07 2023 /pmc/articles/PMC9542649/ /pubmed/36245797 http://dx.doi.org/10.1007/s00521-022-07868-0 Text en © The Author(s), under exclusive licence to Springer-Verlag London Ltd., part of Springer Nature 2022, Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Original Article Nallasamy, Varanavasi Seshiah, Malarvizhi Energy Profile Bayes and Thompson Optimized Convolutional Neural Network protein structure prediction |
title | Energy Profile Bayes and Thompson Optimized Convolutional Neural Network protein structure prediction |
title_full | Energy Profile Bayes and Thompson Optimized Convolutional Neural Network protein structure prediction |
title_fullStr | Energy Profile Bayes and Thompson Optimized Convolutional Neural Network protein structure prediction |
title_full_unstemmed | Energy Profile Bayes and Thompson Optimized Convolutional Neural Network protein structure prediction |
title_short | Energy Profile Bayes and Thompson Optimized Convolutional Neural Network protein structure prediction |
title_sort | energy profile bayes and thompson optimized convolutional neural network protein structure prediction |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9542649/ https://www.ncbi.nlm.nih.gov/pubmed/36245797 http://dx.doi.org/10.1007/s00521-022-07868-0 |
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