Skip Navigation


Nucleic Acids Research Advance Access originally published online on April 4, 2008
Nucleic Acids Research 2008 36(9):3025-3030; doi:10.1093/nar/gkn159
This Article
Right arrow Full Text Freely available
Right arrow Print PDF (156K) Freely available
Right arrow Screen PDF (130K) Freely available
Right arrow Supplementary Data
Right arrowOA All Versions of this Article:
36/9/3025    most recent
gkn159v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Guo, Y.
Right arrow Articles by Li, M.
PubMed
Right arrow PubMed Citation
Right arrow Articles by Guo, Y.
Right arrow Articles by Li, M.
Related Collections
Right arrow Computational methods
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, 2008, Vol. 36, No. 9 3025-3030
© 2008 The Author(s)
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.


Computational Biology

Using support vector machine combined with auto covariance to predict protein–protein interactions from protein sequences

Yanzhi Guo1,2, Lezheng Yu1,2, Zhining Wen1,2 and Menglong Li1,2,*

1College of Chemistry, Sichuan University, Chengdu 610064 and 2State Key Laboratory of Biotherapy, Sichuan University, Chengdu 610041, P.R. China

*To whom correspondence should be addressed. Tel: +86 28 89005151; Fax: +86 28 85412356; Email: liml{at}scu.edu.cn

Received January 10, 2008. Revised March 3, 2008. Accepted March 20, 2008.

Compared to the available protein sequences of different organisms, the number of revealed protein–protein interactions (PPIs) is still very limited. So many computational methods have been developed to facilitate the identification of novel PPIs. However, the methods only using the information of protein sequences are more universal than those that depend on some additional information or predictions about the proteins. In this article, a sequence-based method is proposed by combining a new feature representation using auto covariance (AC) and support vector machine (SVM). AC accounts for the interactions between residues a certain distance apart in the sequence, so this method adequately takes the neighbouring effect into account. When performed on the PPI data of yeast Saccharomyces cerevisiae, the method achieved a very promising prediction result. An independent data set of 11 474 yeast PPIs was used to evaluate this prediction model and the prediction accuracy is 88.09%. The performance of this method is superior to those of the existing sequence-based methods, so it can be a useful supplementary tool for future proteomics studies. The prediction software and all data sets used in this article are freely available at http://www.scucic.cn/Predict_PPI/index.htm.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.