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Tools for integrated sequence-structure analysis with UCSF Chimera
BACKGROUND: Comparing related structures and viewing the structures in the context of sequence alignments are important tasks in protein structure-function research. While many programs exist for individual aspects of such work, there is a need for interactive visualization tools that: (a) provide a...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1570152/ https://www.ncbi.nlm.nih.gov/pubmed/16836757 http://dx.doi.org/10.1186/1471-2105-7-339 |
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author | Meng, Elaine C Pettersen, Eric F Couch, Gregory S Huang, Conrad C Ferrin, Thomas E |
author_facet | Meng, Elaine C Pettersen, Eric F Couch, Gregory S Huang, Conrad C Ferrin, Thomas E |
author_sort | Meng, Elaine C |
collection | PubMed |
description | BACKGROUND: Comparing related structures and viewing the structures in the context of sequence alignments are important tasks in protein structure-function research. While many programs exist for individual aspects of such work, there is a need for interactive visualization tools that: (a) provide a deep integration of sequence and structure, far beyond mapping where a sequence region falls in the structure and vice versa; (b) facilitate changing data of one type based on the other (for example, using only sequence-conserved residues to match structures, or adjusting a sequence alignment based on spatial fit); (c) can be used with a researcher's own data, including arbitrary sequence alignments and annotations, closely or distantly related sets of proteins, etc.; and (d) interoperate with each other and with a full complement of molecular graphics features. We describe enhancements to UCSF Chimera to achieve these goals. RESULTS: The molecular graphics program UCSF Chimera includes a suite of tools for interactive analyses of sequences and structures. Structures automatically associate with sequences in imported alignments, allowing many kinds of crosstalk. A novel method is provided to superimpose structures in the absence of a pre-existing sequence alignment. The method uses both sequence and secondary structure, and can match even structures with very low sequence identity. Another tool constructs structure-based sequence alignments from superpositions of two or more proteins. Chimera is designed to be extensible, and mechanisms for incorporating user-specific data without Chimera code development are also provided. CONCLUSION: The tools described here apply to many problems involving comparison and analysis of protein structures and their sequences. Chimera includes complete documentation and is intended for use by a wide range of scientists, not just those in the computational disciplines. UCSF Chimera is free for non-commercial use and is available for Microsoft Windows, Apple Mac OS X, Linux, and other platforms from . |
format | Text |
id | pubmed-1570152 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-15701522006-09-19 Tools for integrated sequence-structure analysis with UCSF Chimera Meng, Elaine C Pettersen, Eric F Couch, Gregory S Huang, Conrad C Ferrin, Thomas E BMC Bioinformatics Software BACKGROUND: Comparing related structures and viewing the structures in the context of sequence alignments are important tasks in protein structure-function research. While many programs exist for individual aspects of such work, there is a need for interactive visualization tools that: (a) provide a deep integration of sequence and structure, far beyond mapping where a sequence region falls in the structure and vice versa; (b) facilitate changing data of one type based on the other (for example, using only sequence-conserved residues to match structures, or adjusting a sequence alignment based on spatial fit); (c) can be used with a researcher's own data, including arbitrary sequence alignments and annotations, closely or distantly related sets of proteins, etc.; and (d) interoperate with each other and with a full complement of molecular graphics features. We describe enhancements to UCSF Chimera to achieve these goals. RESULTS: The molecular graphics program UCSF Chimera includes a suite of tools for interactive analyses of sequences and structures. Structures automatically associate with sequences in imported alignments, allowing many kinds of crosstalk. A novel method is provided to superimpose structures in the absence of a pre-existing sequence alignment. The method uses both sequence and secondary structure, and can match even structures with very low sequence identity. Another tool constructs structure-based sequence alignments from superpositions of two or more proteins. Chimera is designed to be extensible, and mechanisms for incorporating user-specific data without Chimera code development are also provided. CONCLUSION: The tools described here apply to many problems involving comparison and analysis of protein structures and their sequences. Chimera includes complete documentation and is intended for use by a wide range of scientists, not just those in the computational disciplines. UCSF Chimera is free for non-commercial use and is available for Microsoft Windows, Apple Mac OS X, Linux, and other platforms from . BioMed Central 2006-07-12 /pmc/articles/PMC1570152/ /pubmed/16836757 http://dx.doi.org/10.1186/1471-2105-7-339 Text en Copyright © 2006 Meng 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 | Software Meng, Elaine C Pettersen, Eric F Couch, Gregory S Huang, Conrad C Ferrin, Thomas E Tools for integrated sequence-structure analysis with UCSF Chimera |
title | Tools for integrated sequence-structure analysis with UCSF Chimera |
title_full | Tools for integrated sequence-structure analysis with UCSF Chimera |
title_fullStr | Tools for integrated sequence-structure analysis with UCSF Chimera |
title_full_unstemmed | Tools for integrated sequence-structure analysis with UCSF Chimera |
title_short | Tools for integrated sequence-structure analysis with UCSF Chimera |
title_sort | tools for integrated sequence-structure analysis with ucsf chimera |
topic | Software |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1570152/ https://www.ncbi.nlm.nih.gov/pubmed/16836757 http://dx.doi.org/10.1186/1471-2105-7-339 |
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