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PFAAT version 2.0: A tool for editing, annotating, and analyzing multiple sequence alignments

BACKGROUND: By virtue of their shared ancestry, homologous sequences are similar in their structure and function. Consequently, multiple sequence alignments are routinely used to identify trends that relate to function. This type of analysis is particularly productive when it is combined with struct...

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Autores principales: Caffrey, Daniel R, Dana, Paul H, Mathur, Vidhya, Ocano, Marco, Hong, Eun-Jong, Wang, Yaoyu E, Somaroo, Shyamal, Caffrey, Brian E, Potluri, Shobha, Huang, Enoch S
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2092438/
https://www.ncbi.nlm.nih.gov/pubmed/17931421
http://dx.doi.org/10.1186/1471-2105-8-381
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author Caffrey, Daniel R
Dana, Paul H
Mathur, Vidhya
Ocano, Marco
Hong, Eun-Jong
Wang, Yaoyu E
Somaroo, Shyamal
Caffrey, Brian E
Potluri, Shobha
Huang, Enoch S
author_facet Caffrey, Daniel R
Dana, Paul H
Mathur, Vidhya
Ocano, Marco
Hong, Eun-Jong
Wang, Yaoyu E
Somaroo, Shyamal
Caffrey, Brian E
Potluri, Shobha
Huang, Enoch S
author_sort Caffrey, Daniel R
collection PubMed
description BACKGROUND: By virtue of their shared ancestry, homologous sequences are similar in their structure and function. Consequently, multiple sequence alignments are routinely used to identify trends that relate to function. This type of analysis is particularly productive when it is combined with structural and phylogenetic analysis. RESULTS: Here we describe the release of PFAAT version 2.0, a tool for editing, analyzing, and annotating multiple sequence alignments. Support for multiple annotations is a key component of this release as it provides a framework for most of the new functionalities. The sequence annotations are accessible from the alignment and tree, where they are typically used to label sequences or hyperlink them to related databases. Sequence annotations can be created manually or extracted automatically from UniProt entries. Once a multiple sequence alignment is populated with sequence annotations, sequences can be easily selected and sorted through a sophisticated search dialog. The selected sequences can be further analyzed using statistical methods that explicitly model relationships between the sequence annotations and residue properties. Residue annotations are accessible from the alignment viewer and are typically used to designate binding sites or properties for a particular residue. Residue annotations are also searchable, and allow one to quickly select alignment columns for further sequence analysis, e.g. computing percent identities. Other features include: novel algorithms to compute sequence conservation, mapping conservation scores to a 3D structure in Jmol, displaying secondary structure elements, and sorting sequences by residue composition. CONCLUSION: PFAAT provides a framework whereby end-users can specify knowledge for a protein family in the form of annotation. The annotations can be combined with sophisticated analysis to test hypothesis that relate to sequence, structure and function.
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spelling pubmed-20924382007-11-23 PFAAT version 2.0: A tool for editing, annotating, and analyzing multiple sequence alignments Caffrey, Daniel R Dana, Paul H Mathur, Vidhya Ocano, Marco Hong, Eun-Jong Wang, Yaoyu E Somaroo, Shyamal Caffrey, Brian E Potluri, Shobha Huang, Enoch S BMC Bioinformatics Software BACKGROUND: By virtue of their shared ancestry, homologous sequences are similar in their structure and function. Consequently, multiple sequence alignments are routinely used to identify trends that relate to function. This type of analysis is particularly productive when it is combined with structural and phylogenetic analysis. RESULTS: Here we describe the release of PFAAT version 2.0, a tool for editing, analyzing, and annotating multiple sequence alignments. Support for multiple annotations is a key component of this release as it provides a framework for most of the new functionalities. The sequence annotations are accessible from the alignment and tree, where they are typically used to label sequences or hyperlink them to related databases. Sequence annotations can be created manually or extracted automatically from UniProt entries. Once a multiple sequence alignment is populated with sequence annotations, sequences can be easily selected and sorted through a sophisticated search dialog. The selected sequences can be further analyzed using statistical methods that explicitly model relationships between the sequence annotations and residue properties. Residue annotations are accessible from the alignment viewer and are typically used to designate binding sites or properties for a particular residue. Residue annotations are also searchable, and allow one to quickly select alignment columns for further sequence analysis, e.g. computing percent identities. Other features include: novel algorithms to compute sequence conservation, mapping conservation scores to a 3D structure in Jmol, displaying secondary structure elements, and sorting sequences by residue composition. CONCLUSION: PFAAT provides a framework whereby end-users can specify knowledge for a protein family in the form of annotation. The annotations can be combined with sophisticated analysis to test hypothesis that relate to sequence, structure and function. BioMed Central 2007-10-11 /pmc/articles/PMC2092438/ /pubmed/17931421 http://dx.doi.org/10.1186/1471-2105-8-381 Text en Copyright © 2007 Caffrey 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
Caffrey, Daniel R
Dana, Paul H
Mathur, Vidhya
Ocano, Marco
Hong, Eun-Jong
Wang, Yaoyu E
Somaroo, Shyamal
Caffrey, Brian E
Potluri, Shobha
Huang, Enoch S
PFAAT version 2.0: A tool for editing, annotating, and analyzing multiple sequence alignments
title PFAAT version 2.0: A tool for editing, annotating, and analyzing multiple sequence alignments
title_full PFAAT version 2.0: A tool for editing, annotating, and analyzing multiple sequence alignments
title_fullStr PFAAT version 2.0: A tool for editing, annotating, and analyzing multiple sequence alignments
title_full_unstemmed PFAAT version 2.0: A tool for editing, annotating, and analyzing multiple sequence alignments
title_short PFAAT version 2.0: A tool for editing, annotating, and analyzing multiple sequence alignments
title_sort pfaat version 2.0: a tool for editing, annotating, and analyzing multiple sequence alignments
topic Software
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2092438/
https://www.ncbi.nlm.nih.gov/pubmed/17931421
http://dx.doi.org/10.1186/1471-2105-8-381
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