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...
Main Authors: | , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2008-05-01
|
Series: | BMC Bioinformatics |
Online Access: | http://www.biomedcentral.com/1471-2105/9/249 |
id |
doaj-6406342311464131a69c1accfae43b05 |
---|---|
record_format |
Article |
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 |
work_keys_str_mv |
AT saliandrej predictionofenzymefunctionbycombiningsequencesimilarityandproteininteractions AT avilesfrancescx predictionofenzymefunctionbycombiningsequencesimilarityandproteininteractions AT querolenrique predictionofenzymefunctionbycombiningsequencesimilarityandproteininteractions AT eswarnarayanan predictionofenzymefunctionbycombiningsequencesimilarityandproteininteractions AT espadalerjordi predictionofenzymefunctionbycombiningsequencesimilarityandproteininteractions AT martirenommarca predictionofenzymefunctionbycombiningsequencesimilarityandproteininteractions AT olivabaldomero predictionofenzymefunctionbycombiningsequencesimilarityandproteininteractions |
_version_ |
1725454874590576640 |