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Probabilistic annotation of protein sequences based on functional classifications

BACKGROUND: One of the most evident achievements of bioinformatics is the development of methods that transfer biological knowledge from characterised proteins to uncharacterised sequences. This mode of protein function assignment is mostly based on the detection of sequence similarity and the premi...

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Detalles Bibliográficos
Autores principales: Levy, Emmanuel D, Ouzounis, Christos A, Gilks, Walter R, Audit, Benjamin
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1361783/
https://www.ncbi.nlm.nih.gov/pubmed/16354297
http://dx.doi.org/10.1186/1471-2105-6-302
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author Levy, Emmanuel D
Ouzounis, Christos A
Gilks, Walter R
Audit, Benjamin
author_facet Levy, Emmanuel D
Ouzounis, Christos A
Gilks, Walter R
Audit, Benjamin
author_sort Levy, Emmanuel D
collection PubMed
description BACKGROUND: One of the most evident achievements of bioinformatics is the development of methods that transfer biological knowledge from characterised proteins to uncharacterised sequences. This mode of protein function assignment is mostly based on the detection of sequence similarity and the premise that functional properties are conserved during evolution. Most automatic approaches developed to date rely on the identification of clusters of homologous proteins and the mapping of new proteins onto these clusters, which are expected to share functional characteristics. RESULTS: Here, we inverse the logic of this process, by considering the mapping of sequences directly to a functional classification instead of mapping functions to a sequence clustering. In this mode, the starting point is a database of labelled proteins according to a functional classification scheme, and the subsequent use of sequence similarity allows defining the membership of new proteins to these functional classes. In this framework, we define the Correspondence Indicators as measures of relationship between sequence and function and further formulate two Bayesian approaches to estimate the probability for a sequence of unknown function to belong to a functional class. This approach allows the parametrisation of different sequence search strategies and provides a direct measure of annotation error rates. We validate this approach with a database of enzymes labelled by their corresponding four-digit EC numbers and analyse specific cases. CONCLUSION: The performance of this method is significantly higher than the simple strategy consisting in transferring the annotation from the highest scoring BLAST match and is expected to find applications in automated functional annotation pipelines.
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spelling pubmed-13617832006-02-10 Probabilistic annotation of protein sequences based on functional classifications Levy, Emmanuel D Ouzounis, Christos A Gilks, Walter R Audit, Benjamin BMC Bioinformatics Research Article BACKGROUND: One of the most evident achievements of bioinformatics is the development of methods that transfer biological knowledge from characterised proteins to uncharacterised sequences. This mode of protein function assignment is mostly based on the detection of sequence similarity and the premise that functional properties are conserved during evolution. Most automatic approaches developed to date rely on the identification of clusters of homologous proteins and the mapping of new proteins onto these clusters, which are expected to share functional characteristics. RESULTS: Here, we inverse the logic of this process, by considering the mapping of sequences directly to a functional classification instead of mapping functions to a sequence clustering. In this mode, the starting point is a database of labelled proteins according to a functional classification scheme, and the subsequent use of sequence similarity allows defining the membership of new proteins to these functional classes. In this framework, we define the Correspondence Indicators as measures of relationship between sequence and function and further formulate two Bayesian approaches to estimate the probability for a sequence of unknown function to belong to a functional class. This approach allows the parametrisation of different sequence search strategies and provides a direct measure of annotation error rates. We validate this approach with a database of enzymes labelled by their corresponding four-digit EC numbers and analyse specific cases. CONCLUSION: The performance of this method is significantly higher than the simple strategy consisting in transferring the annotation from the highest scoring BLAST match and is expected to find applications in automated functional annotation pipelines. BioMed Central 2005-12-14 /pmc/articles/PMC1361783/ /pubmed/16354297 http://dx.doi.org/10.1186/1471-2105-6-302 Text en Copyright ©2005 Levy 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
Levy, Emmanuel D
Ouzounis, Christos A
Gilks, Walter R
Audit, Benjamin
Probabilistic annotation of protein sequences based on functional classifications
title Probabilistic annotation of protein sequences based on functional classifications
title_full Probabilistic annotation of protein sequences based on functional classifications
title_fullStr Probabilistic annotation of protein sequences based on functional classifications
title_full_unstemmed Probabilistic annotation of protein sequences based on functional classifications
title_short Probabilistic annotation of protein sequences based on functional classifications
title_sort probabilistic annotation of protein sequences based on functional classifications
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1361783/
https://www.ncbi.nlm.nih.gov/pubmed/16354297
http://dx.doi.org/10.1186/1471-2105-6-302
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