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Bioinformatics 2007 23(24):3312-3319; doi:10.1093/bioinformatics/btm515
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© The Author 2007. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Co-evolving residues in membrane proteins

Angelika Fuchs 1, Antonio J. Martin-Galiano 1, Matan Kalman 2, Sarel Fleishman 2, Nir Ben-Tal 2 and Dmitrij Frishman 1,*

1Department of Genome Oriented Bioinformatics, Technische Universität München, Wissenschaftszentrum Weihenstephan, 85350 Freising, Germany and 2Department of Biochemistry, George S. Wise Faculty of Life Sciences, Tel-Aviv University, 69978 Ramat Aviv, Israel

*To whom correspondence should be addressed.


   Abstract

Motivation: The analysis of co-evolving residues has been exhaustively evaluated for the prediction of intramolecular amino acid contacts in soluble proteins. Although a variety of different methods for the detection of these co-evolving residues have been developed, the fraction of correctly predicted contacts remained insufficient for their reliable application in the construction of structural models. Membrane proteins, which constitute between one-fourth and one-third of all proteins in an organism, were only considered in few individual case studies.

Results: We present the first general study of correlated mutations in {alpha}-helical membrane proteins. Using seven different prediction algorithms, we extracted co-evolving residues for 14 membrane proteins having a solved 3D structure. On average, distances between correlated pairs of residues lying on different transmembrane segments were found to be significantly smaller compared to a random prediction. Covariation of residues was frequently found in direct sequence neighborhood to helix–helix contacts. Based on the results obtained from individual prediction methods, we constructed a consensus prediction for every protein in the dataset that combines obtained correlations from different prediction algorithms and simultaneously removes likely false positives. Using this consensus prediction, 53% of all predicted residue pairs were found within one helix turn of an observed helix–helix contact. Based on the combination of co-evolving residues detected with the four best prediction algorithms, interacting helices could be predicted with a specificity of 83% and sensitivity of 42%.

Availability: http://webclu.bio.wzw.tum.de/helixcorr/

Contact: d.frishman{at}wzw.tum.de

Supplementary information: Supplementary data are available at Bioinformatics online.

Associate Editor: Anna Tramontano


Received on July 25, 2007; revised on September 10, 2007; accepted on October 8, 2007

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