Protein structural similarity search by Ramachandran codes

<p>Abstract</p> <p>Background</p> <p>Protein structural data has increased exponentially, such that fast and accurate tools are necessary to access structure similarity search. To improve the search speed, several methods have been designed to reduce three-dimensional p...

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Main Authors: Chang Chih-Hung, Huang Po-Jung, Lo Wei-Cheng, Lyu Ping-Chiang
Format: Article
Language:English
Published: BMC 2007-08-01
Series:BMC Bioinformatics
Online Access:http://www.biomedcentral.com/1471-2105/8/307
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spelling doaj-1a9e3203bb6a40d1aa758674187c37852020-11-25T00:37:40ZengBMCBMC Bioinformatics1471-21052007-08-018130710.1186/1471-2105-8-307Protein structural similarity search by Ramachandran codesChang Chih-HungHuang Po-JungLo Wei-ChengLyu Ping-Chiang<p>Abstract</p> <p>Background</p> <p>Protein structural data has increased exponentially, such that fast and accurate tools are necessary to access structure similarity search. To improve the search speed, several methods have been designed to reduce three-dimensional protein structures to one-dimensional text strings that are then analyzed by traditional sequence alignment methods; however, the accuracy is usually sacrificed and the speed is still unable to match sequence similarity search tools. Here, we aimed to improve the linear encoding methodology and develop efficient search tools that can rapidly retrieve structural homologs from large protein databases.</p> <p>Results</p> <p>We propose a new linear encoding method, SARST (Structural similarity search Aided by Ramachandran Sequential Transformation). SARST transforms protein structures into text strings through a Ramachandran map organized by nearest-neighbor clustering and uses a regenerative approach to produce substitution matrices. Then, classical sequence similarity search methods can be applied to the structural similarity search. Its accuracy is similar to Combinatorial Extension (CE) and works over 243,000 times faster, searching 34,000 proteins in 0.34 sec with a 3.2-GHz CPU. SARST provides statistically meaningful expectation values to assess the retrieved information. It has been implemented into a web service and a stand-alone Java program that is able to run on many different platforms.</p> <p>Conclusion</p> <p>As a database search method, SARST can rapidly distinguish high from low similarities and efficiently retrieve homologous structures. It demonstrates that the easily accessible linear encoding methodology has the potential to serve as a foundation for efficient protein structural similarity search tools. These search tools are supposed applicable to automated and high-throughput functional annotations or predictions for the ever increasing number of published protein structures in this post-genomic era.</p> http://www.biomedcentral.com/1471-2105/8/307
collection DOAJ
language English
format Article
sources DOAJ
author Chang Chih-Hung
Huang Po-Jung
Lo Wei-Cheng
Lyu Ping-Chiang
spellingShingle Chang Chih-Hung
Huang Po-Jung
Lo Wei-Cheng
Lyu Ping-Chiang
Protein structural similarity search by Ramachandran codes
BMC Bioinformatics
author_facet Chang Chih-Hung
Huang Po-Jung
Lo Wei-Cheng
Lyu Ping-Chiang
author_sort Chang Chih-Hung
title Protein structural similarity search by Ramachandran codes
title_short Protein structural similarity search by Ramachandran codes
title_full Protein structural similarity search by Ramachandran codes
title_fullStr Protein structural similarity search by Ramachandran codes
title_full_unstemmed Protein structural similarity search by Ramachandran codes
title_sort protein structural similarity search by ramachandran codes
publisher BMC
series BMC Bioinformatics
issn 1471-2105
publishDate 2007-08-01
description <p>Abstract</p> <p>Background</p> <p>Protein structural data has increased exponentially, such that fast and accurate tools are necessary to access structure similarity search. To improve the search speed, several methods have been designed to reduce three-dimensional protein structures to one-dimensional text strings that are then analyzed by traditional sequence alignment methods; however, the accuracy is usually sacrificed and the speed is still unable to match sequence similarity search tools. Here, we aimed to improve the linear encoding methodology and develop efficient search tools that can rapidly retrieve structural homologs from large protein databases.</p> <p>Results</p> <p>We propose a new linear encoding method, SARST (Structural similarity search Aided by Ramachandran Sequential Transformation). SARST transforms protein structures into text strings through a Ramachandran map organized by nearest-neighbor clustering and uses a regenerative approach to produce substitution matrices. Then, classical sequence similarity search methods can be applied to the structural similarity search. Its accuracy is similar to Combinatorial Extension (CE) and works over 243,000 times faster, searching 34,000 proteins in 0.34 sec with a 3.2-GHz CPU. SARST provides statistically meaningful expectation values to assess the retrieved information. It has been implemented into a web service and a stand-alone Java program that is able to run on many different platforms.</p> <p>Conclusion</p> <p>As a database search method, SARST can rapidly distinguish high from low similarities and efficiently retrieve homologous structures. It demonstrates that the easily accessible linear encoding methodology has the potential to serve as a foundation for efficient protein structural similarity search tools. These search tools are supposed applicable to automated and high-throughput functional annotations or predictions for the ever increasing number of published protein structures in this post-genomic era.</p>
url http://www.biomedcentral.com/1471-2105/8/307
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