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Comparative Analysis of Protein Structure Alignments

BACKGROUND: Several methods are currently available for the comparison of protein structures. These methods have been analysed regarding the performance in the identification of structurally/evolutionary related proteins, but so far there has been less focus on the objective comparison between the a...

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Autores principales: Mayr, Gabriele, Domingues, Francisco S, Lackner, Peter
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1959231/
https://www.ncbi.nlm.nih.gov/pubmed/17672887
http://dx.doi.org/10.1186/1472-6807-7-50
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author Mayr, Gabriele
Domingues, Francisco S
Lackner, Peter
author_facet Mayr, Gabriele
Domingues, Francisco S
Lackner, Peter
author_sort Mayr, Gabriele
collection PubMed
description BACKGROUND: Several methods are currently available for the comparison of protein structures. These methods have been analysed regarding the performance in the identification of structurally/evolutionary related proteins, but so far there has been less focus on the objective comparison between the alignments produced by different methods. RESULTS: We analysed and compared the structural alignments obtained by different methods using three sets of pairs of structurally related proteins. The first set corresponds to 355 pairs of remote homologous proteins according to the SCOP database (ASTRAL40 set). The second set was derived from the SISYPHUS database and includes 69 protein pairs (SISY set). The third set consists of 40 pairs that are challenging to align (RIPC set). The alignment of pairs of this set requires indels of considerable number and size and some of the proteins are related by circular permutations, show extensive conformational variability or include repetitions. Two standard methods (CE and DALI) were applied to align the proteins in the ASTRAL40 set. The extent of structural similarity identified by both methods is highly correlated and the alignments from the two methods agree on average in more than half of the aligned positions. CE, DALI, as well as four additional methods (FATCAT, MATRAS, C(α)-match and SHEBA) were then compared using the SISY and RIPC sets. The accuracy of the alignments was assessed by comparison to reference alignments. The alignments generated by the different methods on average match more than half of the reference alignments in the SISY set. The alignments obtained in the more challenging RIPC set tend to differ considerably and match reference alignments less successfully than the SISY set alignments. CONCLUSION: The alignments produced by different methods tend to agree to a considerable extent, but the agreement is lower for the more challenging pairs. The results for the comparison to reference alignments are encouraging, but also indicate that there is still room for improvement.
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spelling pubmed-19592312007-08-30 Comparative Analysis of Protein Structure Alignments Mayr, Gabriele Domingues, Francisco S Lackner, Peter BMC Struct Biol Research Article BACKGROUND: Several methods are currently available for the comparison of protein structures. These methods have been analysed regarding the performance in the identification of structurally/evolutionary related proteins, but so far there has been less focus on the objective comparison between the alignments produced by different methods. RESULTS: We analysed and compared the structural alignments obtained by different methods using three sets of pairs of structurally related proteins. The first set corresponds to 355 pairs of remote homologous proteins according to the SCOP database (ASTRAL40 set). The second set was derived from the SISYPHUS database and includes 69 protein pairs (SISY set). The third set consists of 40 pairs that are challenging to align (RIPC set). The alignment of pairs of this set requires indels of considerable number and size and some of the proteins are related by circular permutations, show extensive conformational variability or include repetitions. Two standard methods (CE and DALI) were applied to align the proteins in the ASTRAL40 set. The extent of structural similarity identified by both methods is highly correlated and the alignments from the two methods agree on average in more than half of the aligned positions. CE, DALI, as well as four additional methods (FATCAT, MATRAS, C(α)-match and SHEBA) were then compared using the SISY and RIPC sets. The accuracy of the alignments was assessed by comparison to reference alignments. The alignments generated by the different methods on average match more than half of the reference alignments in the SISY set. The alignments obtained in the more challenging RIPC set tend to differ considerably and match reference alignments less successfully than the SISY set alignments. CONCLUSION: The alignments produced by different methods tend to agree to a considerable extent, but the agreement is lower for the more challenging pairs. The results for the comparison to reference alignments are encouraging, but also indicate that there is still room for improvement. BioMed Central 2007-07-26 /pmc/articles/PMC1959231/ /pubmed/17672887 http://dx.doi.org/10.1186/1472-6807-7-50 Text en Copyright © 2007 Mayr 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.
spellingShingle Research Article
Mayr, Gabriele
Domingues, Francisco S
Lackner, Peter
Comparative Analysis of Protein Structure Alignments
title Comparative Analysis of Protein Structure Alignments
title_full Comparative Analysis of Protein Structure Alignments
title_fullStr Comparative Analysis of Protein Structure Alignments
title_full_unstemmed Comparative Analysis of Protein Structure Alignments
title_short Comparative Analysis of Protein Structure Alignments
title_sort comparative analysis of protein structure alignments
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1959231/
https://www.ncbi.nlm.nih.gov/pubmed/17672887
http://dx.doi.org/10.1186/1472-6807-7-50
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