Skip Navigation

This Article
Right arrow FREE Full Text (Print PDF) Freely available
Right arrow FREE Full Text (Screen PDF)
Right arrow Comments: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when Comments are posted
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 ISI Web of Science
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 Search for citing articles in:
ISI Web of Science (15)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Cao, J.
Right arrow Articles by Ahmad, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Cao, J.
Right arrow Articles by Ahmad, S.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Bioinformatics Vol. 19 no. 2 2003
Pages 234-240
© 2003 Oxford University Press

A naive Bayes model to predict coupling between seven transmembrane domain receptors and G-proteins

Jack Cao *, Rosemarie Panetta , Shiyi Yue , Alain Steyaert , Michele Young-Bellido and Sultan Ahmad

Department of Molecular Sciences, AstraZeneca R&D Montreal, 7171 Frederick-Banting Street, St-Laurent, Quebec H4S 1Z9, Canada

Received on May 3, 2002 ; revised on July 23, 2002 ; accepted on August 27, 2002

Motivation: An understanding of the coupling between a G-protein coupled receptor (GPCR) and a specific class of heterotrimeric GTP-binding proteins (G-proteins) is vital for further comprehending the function of the receptor within a cell. However, predicting G-protein coupling based on the amino acid sequence of a receptor has been a daunting task. While experimental data for G-protein coupling exist, published models that rely on sequence based prediction are few. In this study, we have developed a Naive Bayes model to successfully predict G-protein coupling specificity by training over 80 GPCRs with known coupling. Each intracellular domain of GPCRs was treated as a discrete random variable, conditionally independent of one another. In order to determine the conditional probability distributions of these variables, ClustalW-generated phylogenetic trees were used as an approximation for the clustering of the intracellular domain sequences. The sampling of an intracellular domain sequence was achieved by identifying the cluster containing the homologue with the highest sequence similarity.

Results: Out of 55 GPCRs validated, the model yielded a correct classification rate of 72%. Our model also predicted multiple G-protein coupling for most of the GPCRs in the validation set. The Bayesian approach in this work offers an alternative to the experimental approach in order to answer the biological problem of GPCR/G-protein coupling selectivity.

Availability: Academic users should send their request for the perl program for calculating likelihood probabilities at jack.cao{at}astrazeneca.com.

Supplementary Information: The materials can be viewed at http://www.astrazeneca-montreal.com/AZRDM_info/supporting_info.pdf.

* To whom correspondence should be addressed.


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


This article has been cited by other articles:


Home page
Protein Eng Des SelHome page
T. Muramatsu and M. Suwa
Statistical analysis and prediction of functional residues effective for GPCR-G-protein coupling selectivity
Protein Eng. Des. Sel., June 1, 2006; 19(6): 277 - 283.
[Abstract] [Full Text] [PDF]


Home page
BioinformaticsHome page
E. Duprat, M.-P. Lefranc, and O. Gascuel
A simple method to predict protein-binding from aligned sequences--application to MHC superfamily and {beta}2-microglobulin
Bioinformatics, February 15, 2006; 22(4): 453 - 459.
[Abstract] [Full Text] [PDF]


Home page
BioinformaticsHome page
N. G. Sgourakis, P. G. Bagos, and S. J. Hamodrakas
Prediction of the coupling specificity of GPCRs to four families of G-proteins using hidden Markov models and artificial neural networks
Bioinformatics, November 15, 2005; 21(22): 4101 - 4106.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
Y. Yabuki, T. Muramatsu, T. Hirokawa, H. Mukai, and M. Suwa
GRIFFIN: a system for predicting GPCR-G-protein coupling selectivity using a support vector machine and a hidden Markov model
Nucleic Acids Res., July 1, 2005; 33(suppl_2): W148 - W153.
[Abstract] [Full Text] [PDF]



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.