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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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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. |
format | Online Article Text |
id | pubmed-3908855 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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