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Query3d: a new method for high-throughput analysis of functional residues in protein structures
BACKGROUND: The identification of local similarities between two protein structures can provide clues of a common function. Many different methods exist for searching for similar subsets of residues in proteins of known structure. However, the lack of functional and structural information on single...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1866380/ https://www.ncbi.nlm.nih.gov/pubmed/16351754 http://dx.doi.org/10.1186/1471-2105-6-S4-S5 |
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author | Ausiello, Gabriele Via, Allegra Helmer-Citterich, Manuela |
author_facet | Ausiello, Gabriele Via, Allegra Helmer-Citterich, Manuela |
author_sort | Ausiello, Gabriele |
collection | PubMed |
description | BACKGROUND: The identification of local similarities between two protein structures can provide clues of a common function. Many different methods exist for searching for similar subsets of residues in proteins of known structure. However, the lack of functional and structural information on single residues, together with the low level of integration of this information in comparison methods, is a limitation that prevents these methods from being fully exploited in high-throughput analyses. RESULTS: Here we describe Query3d, a program that is both a structural DBMS (Database Management System) and a local comparison method. The method conserves a copy of all the residues of the Protein Data Bank annotated with a variety of functional and structural information. New annotations can be easily added from a variety of methods and known databases. The algorithm makes it possible to create complex queries based on the residues' function and then to compare only subsets of the selected residues. Functional information is also essential to speed up the comparison and the analysis of the results. CONCLUSION: With Query3d, users can easily obtain statistics on how many and which residues share certain properties in all proteins of known structure. At the same time, the method also finds their structural neighbours in the whole PDB. Programs and data can be accessed through the PdbFun web interface. |
format | Text |
id | pubmed-1866380 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-18663802007-05-11 Query3d: a new method for high-throughput analysis of functional residues in protein structures Ausiello, Gabriele Via, Allegra Helmer-Citterich, Manuela BMC Bioinformatics Research Article BACKGROUND: The identification of local similarities between two protein structures can provide clues of a common function. Many different methods exist for searching for similar subsets of residues in proteins of known structure. However, the lack of functional and structural information on single residues, together with the low level of integration of this information in comparison methods, is a limitation that prevents these methods from being fully exploited in high-throughput analyses. RESULTS: Here we describe Query3d, a program that is both a structural DBMS (Database Management System) and a local comparison method. The method conserves a copy of all the residues of the Protein Data Bank annotated with a variety of functional and structural information. New annotations can be easily added from a variety of methods and known databases. The algorithm makes it possible to create complex queries based on the residues' function and then to compare only subsets of the selected residues. Functional information is also essential to speed up the comparison and the analysis of the results. CONCLUSION: With Query3d, users can easily obtain statistics on how many and which residues share certain properties in all proteins of known structure. At the same time, the method also finds their structural neighbours in the whole PDB. Programs and data can be accessed through the PdbFun web interface. BioMed Central 2005-12-01 /pmc/articles/PMC1866380/ /pubmed/16351754 http://dx.doi.org/10.1186/1471-2105-6-S4-S5 Text en Copyright © 2005 Ausiello 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 Ausiello, Gabriele Via, Allegra Helmer-Citterich, Manuela Query3d: a new method for high-throughput analysis of functional residues in protein structures |
title | Query3d: a new method for high-throughput analysis of functional residues in protein structures |
title_full | Query3d: a new method for high-throughput analysis of functional residues in protein structures |
title_fullStr | Query3d: a new method for high-throughput analysis of functional residues in protein structures |
title_full_unstemmed | Query3d: a new method for high-throughput analysis of functional residues in protein structures |
title_short | Query3d: a new method for high-throughput analysis of functional residues in protein structures |
title_sort | query3d: a new method for high-throughput analysis of functional residues in protein structures |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1866380/ https://www.ncbi.nlm.nih.gov/pubmed/16351754 http://dx.doi.org/10.1186/1471-2105-6-S4-S5 |
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