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MADOKA: an ultra-fast approach for large-scale protein structure similarity searching
BACKGROUND: Protein comparative analysis and similarity searches play essential roles in structural bioinformatics. A couple of algorithms for protein structure alignments have been developed in recent years. However, facing the rapid growth of protein structure data, improving overall comparison pe...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6929402/ https://www.ncbi.nlm.nih.gov/pubmed/31870277 http://dx.doi.org/10.1186/s12859-019-3235-1 |
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author | Deng, Lei Zhong, Guolun Liu, Chenzhe Luo, Judong Liu, Hui |
author_facet | Deng, Lei Zhong, Guolun Liu, Chenzhe Luo, Judong Liu, Hui |
author_sort | Deng, Lei |
collection | PubMed |
description | BACKGROUND: Protein comparative analysis and similarity searches play essential roles in structural bioinformatics. A couple of algorithms for protein structure alignments have been developed in recent years. However, facing the rapid growth of protein structure data, improving overall comparison performance and running efficiency with massive sequences is still challenging. RESULTS: Here, we propose MADOKA, an ultra-fast approach for massive structural neighbor searching using a novel two-phase algorithm. Initially, we apply a fast alignment between pairwise structures. Then, we employ a score to select pairs with more similarity to carry out a more accurate fragment-based residue-level alignment. MADOKA performs about 6–100 times faster than existing methods, including TM-align and SAL, in massive alignments. Moreover, the quality of structural alignment of MADOKA is better than the existing algorithms in terms of TM-score and number of aligned residues. We also develop a web server to search structural neighbors in PDB database (About 360,000 protein chains in total), as well as additional features such as 3D structure alignment visualization. The MADOKA web server is freely available at: http://madoka.denglab.org/ CONCLUSIONS: MADOKA is an efficient approach to search for protein structure similarity. In addition, we provide a parallel implementation of MADOKA which exploits massive power of multi-core CPUs. |
format | Online Article Text |
id | pubmed-6929402 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-69294022019-12-30 MADOKA: an ultra-fast approach for large-scale protein structure similarity searching Deng, Lei Zhong, Guolun Liu, Chenzhe Luo, Judong Liu, Hui BMC Bioinformatics Methodology BACKGROUND: Protein comparative analysis and similarity searches play essential roles in structural bioinformatics. A couple of algorithms for protein structure alignments have been developed in recent years. However, facing the rapid growth of protein structure data, improving overall comparison performance and running efficiency with massive sequences is still challenging. RESULTS: Here, we propose MADOKA, an ultra-fast approach for massive structural neighbor searching using a novel two-phase algorithm. Initially, we apply a fast alignment between pairwise structures. Then, we employ a score to select pairs with more similarity to carry out a more accurate fragment-based residue-level alignment. MADOKA performs about 6–100 times faster than existing methods, including TM-align and SAL, in massive alignments. Moreover, the quality of structural alignment of MADOKA is better than the existing algorithms in terms of TM-score and number of aligned residues. We also develop a web server to search structural neighbors in PDB database (About 360,000 protein chains in total), as well as additional features such as 3D structure alignment visualization. The MADOKA web server is freely available at: http://madoka.denglab.org/ CONCLUSIONS: MADOKA is an efficient approach to search for protein structure similarity. In addition, we provide a parallel implementation of MADOKA which exploits massive power of multi-core CPUs. BioMed Central 2019-12-24 /pmc/articles/PMC6929402/ /pubmed/31870277 http://dx.doi.org/10.1186/s12859-019-3235-1 Text en © The Author(s) 2019 Open Access This 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 | Methodology Deng, Lei Zhong, Guolun Liu, Chenzhe Luo, Judong Liu, Hui MADOKA: an ultra-fast approach for large-scale protein structure similarity searching |
title | MADOKA: an ultra-fast approach for large-scale protein structure similarity searching |
title_full | MADOKA: an ultra-fast approach for large-scale protein structure similarity searching |
title_fullStr | MADOKA: an ultra-fast approach for large-scale protein structure similarity searching |
title_full_unstemmed | MADOKA: an ultra-fast approach for large-scale protein structure similarity searching |
title_short | MADOKA: an ultra-fast approach for large-scale protein structure similarity searching |
title_sort | madoka: an ultra-fast approach for large-scale protein structure similarity searching |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6929402/ https://www.ncbi.nlm.nih.gov/pubmed/31870277 http://dx.doi.org/10.1186/s12859-019-3235-1 |
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