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Predicting beta-turns in proteins using support vector machines with fractional polynomials

BACKGROUND: β-turns are secondary structure type that have essential role in molecular recognition, protein folding, and stability. They are found to be the most common type of non-repetitive structures since 25% of amino acids in protein structures are situated on them. Their prediction is consider...

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Autores principales: Elbashir, Murtada Khalafallah, Wang, Jianxin, Wu, Fang-Xiang, Wang, Lusheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3908855/
https://www.ncbi.nlm.nih.gov/pubmed/24565438
http://dx.doi.org/10.1186/1477-5956-11-S1-S5
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author Elbashir, Murtada Khalafallah
Wang, Jianxin
Wu, Fang-Xiang
Wang, Lusheng
author_facet Elbashir, Murtada Khalafallah
Wang, Jianxin
Wu, Fang-Xiang
Wang, Lusheng
author_sort Elbashir, Murtada Khalafallah
collection PubMed
description BACKGROUND: β-turns are secondary structure type that have essential role in molecular recognition, protein folding, and stability. They are found to be the most common type of non-repetitive structures since 25% of amino acids in protein structures are situated on them. Their prediction is considered to be one of the crucial problems in bioinformatics and molecular biology, which can provide valuable insights and inputs for the fold recognition and drug design. RESULTS: We propose an approach that combines support vector machines (SVMs) and logistic regression (LR) in a hybrid prediction method, which we call (H-SVM-LR) to predict β-turns in proteins. Fractional polynomials are used for LR modeling. We utilize position specific scoring matrices (PSSMs) and predicted secondary structure (PSS) as features. Our simulation studies show that H-SVM-LR achieves Qtotal of 82.87%, 82.84%, and 82.32% on the BT426, BT547, and BT823 datasets respectively. These values are the highest among other β-turns prediction methods that are based on PSSMs and secondary structure information. H-SVM-LR also achieves favorable performance in predicting β-turns as measured by the Matthew's correlation coefficient (MCC) on these datasets. Furthermore, H-SVM-LR shows good performance when considering shape strings as additional features. CONCLUSIONS: In this paper, we present a comprehensive approach for β-turns prediction. Experiments show that our proposed approach achieves better performance compared to other competing prediction methods.
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spelling pubmed-39088552014-02-13 Predicting beta-turns in proteins using support vector machines with fractional polynomials Elbashir, Murtada Khalafallah Wang, Jianxin Wu, Fang-Xiang Wang, Lusheng Proteome Sci Research BACKGROUND: β-turns are secondary structure type that have essential role in molecular recognition, protein folding, and stability. They are found to be the most common type of non-repetitive structures since 25% of amino acids in protein structures are situated on them. Their prediction is considered to be one of the crucial problems in bioinformatics and molecular biology, which can provide valuable insights and inputs for the fold recognition and drug design. RESULTS: We propose an approach that combines support vector machines (SVMs) and logistic regression (LR) in a hybrid prediction method, which we call (H-SVM-LR) to predict β-turns in proteins. Fractional polynomials are used for LR modeling. We utilize position specific scoring matrices (PSSMs) and predicted secondary structure (PSS) as features. Our simulation studies show that H-SVM-LR achieves Qtotal of 82.87%, 82.84%, and 82.32% on the BT426, BT547, and BT823 datasets respectively. These values are the highest among other β-turns prediction methods that are based on PSSMs and secondary structure information. H-SVM-LR also achieves favorable performance in predicting β-turns as measured by the Matthew's correlation coefficient (MCC) on these datasets. Furthermore, H-SVM-LR shows good performance when considering shape strings as additional features. CONCLUSIONS: In this paper, we present a comprehensive approach for β-turns prediction. Experiments show that our proposed approach achieves better performance compared to other competing prediction methods. BioMed Central 2013-11-07 /pmc/articles/PMC3908855/ /pubmed/24565438 http://dx.doi.org/10.1186/1477-5956-11-S1-S5 Text en Copyright © 2013 Elbashir et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. 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
Elbashir, Murtada Khalafallah
Wang, Jianxin
Wu, Fang-Xiang
Wang, Lusheng
Predicting beta-turns in proteins using support vector machines with fractional polynomials
title Predicting beta-turns in proteins using support vector machines with fractional polynomials
title_full Predicting beta-turns in proteins using support vector machines with fractional polynomials
title_fullStr Predicting beta-turns in proteins using support vector machines with fractional polynomials
title_full_unstemmed Predicting beta-turns in proteins using support vector machines with fractional polynomials
title_short Predicting beta-turns in proteins using support vector machines with fractional polynomials
title_sort predicting beta-turns in proteins using support vector machines with fractional polynomials
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3908855/
https://www.ncbi.nlm.nih.gov/pubmed/24565438
http://dx.doi.org/10.1186/1477-5956-11-S1-S5
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