Prediction of enzyme function by combining sequence similarity and protein interactions

<p>Abstract</p> <p>Background</p> <p>A number of studies have used protein interaction data alone for protein function prediction. Here, we introduce a computational approach for annotation of enzymes, based on the observation that similar protein sequences are more lik...

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Main Authors: Sali Andrej, Avilés Francesc X, Querol Enrique, Eswar Narayanan, Espadaler Jordi, Marti-Renom Marc A, Oliva Baldomero
Format: Article
Language:English
Published: BMC 2008-05-01
Series:BMC Bioinformatics
Online Access:http://www.biomedcentral.com/1471-2105/9/249
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spelling doaj-6406342311464131a69c1accfae43b052020-11-24T23:57:16ZengBMCBMC Bioinformatics1471-21052008-05-019124910.1186/1471-2105-9-249Prediction of enzyme function by combining sequence similarity and protein interactionsSali AndrejAvilés Francesc XQuerol EnriqueEswar NarayananEspadaler JordiMarti-Renom Marc AOliva Baldomero<p>Abstract</p> <p>Background</p> <p>A number of studies have used protein interaction data alone for protein function prediction. Here, we introduce a computational approach for annotation of enzymes, based on the observation that similar protein sequences are more likely to perform the same function if they share similar interacting partners.</p> <p>Results</p> <p>The method has been tested against the PSI-BLAST program using a set of 3,890 protein sequences from which interaction data was available. For protein sequences that align with at least 40% sequence identity to a known enzyme, the specificity of our method in predicting the first three EC digits increased from 80% to 90% at 80% coverage when compared to PSI-BLAST.</p> <p>Conclusion</p> <p>Our method can also be used in proteins for which homologous sequences with known interacting partners can be detected. Thus, our method could increase 10% the specificity of genome-wide enzyme predictions based on sequence matching by PSI-BLAST alone.</p> http://www.biomedcentral.com/1471-2105/9/249
collection DOAJ
language English
format Article
sources DOAJ
author Sali Andrej
Avilés Francesc X
Querol Enrique
Eswar Narayanan
Espadaler Jordi
Marti-Renom Marc A
Oliva Baldomero
spellingShingle Sali Andrej
Avilés Francesc X
Querol Enrique
Eswar Narayanan
Espadaler Jordi
Marti-Renom Marc A
Oliva Baldomero
Prediction of enzyme function by combining sequence similarity and protein interactions
BMC Bioinformatics
author_facet Sali Andrej
Avilés Francesc X
Querol Enrique
Eswar Narayanan
Espadaler Jordi
Marti-Renom Marc A
Oliva Baldomero
author_sort Sali Andrej
title Prediction of enzyme function by combining sequence similarity and protein interactions
title_short Prediction of enzyme function by combining sequence similarity and protein interactions
title_full Prediction of enzyme function by combining sequence similarity and protein interactions
title_fullStr Prediction of enzyme function by combining sequence similarity and protein interactions
title_full_unstemmed Prediction of enzyme function by combining sequence similarity and protein interactions
title_sort prediction of enzyme function by combining sequence similarity and protein interactions
publisher BMC
series BMC Bioinformatics
issn 1471-2105
publishDate 2008-05-01
description <p>Abstract</p> <p>Background</p> <p>A number of studies have used protein interaction data alone for protein function prediction. Here, we introduce a computational approach for annotation of enzymes, based on the observation that similar protein sequences are more likely to perform the same function if they share similar interacting partners.</p> <p>Results</p> <p>The method has been tested against the PSI-BLAST program using a set of 3,890 protein sequences from which interaction data was available. For protein sequences that align with at least 40% sequence identity to a known enzyme, the specificity of our method in predicting the first three EC digits increased from 80% to 90% at 80% coverage when compared to PSI-BLAST.</p> <p>Conclusion</p> <p>Our method can also be used in proteins for which homologous sequences with known interacting partners can be detected. Thus, our method could increase 10% the specificity of genome-wide enzyme predictions based on sequence matching by PSI-BLAST alone.</p>
url http://www.biomedcentral.com/1471-2105/9/249
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