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J. Lipid Res.
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Originally published In Press as doi:10.1194/jlr.M500530-JLR200 on January 27, 2006

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Journal of Lipid Research, Vol. 47, 824-831, April 2006
Copyright © 2006 by American Society for Biochemistry and Molecular Biology

Prediction of the functional class of lipid binding proteins from sequence-derived properties irrespective of sequence similarity

H. H. Lin*, L. Y. Han*, H. L. Zhang*, C. J. Zheng*, B. Xie* and Y. Z. Chen*,{dagger},1

* Bioinformatics and Drug Design Group, Department of Computational Science, National University of Singapore, Singapore 117543
{dagger} Shanghai Center for Bioinformatics Technology, Shanghai 200235, People's Republic of China

Published, JLR Papers in Press, January 27, 2006.

1 To whom correspondence should be addressed. e-mail: yzchen{at}cz3.nus.edu.sg

Lipid binding proteins play important roles in signaling, regulation, membrane trafficking, immune response, lipid metabolism, and transport. Because of their functional and sequence diversity, it is desirable to explore additional methods for predicting lipid binding proteins irrespective of sequence similarity. This work explores the use of support vector machines (SVMs) as such a method. SVM prediction systems are developed using 14,776 lipid binding and 133,441 nonlipid binding proteins and are evaluated by an independent set of 6,768 lipid binding and 64,761 nonlipid binding proteins. The computed prediction accuracy is 78.9, 79.5, 82.2, 79.5, 84.4, 76.6, 90.6, 79.0, and 89.9% for lipid degradation, lipid metabolism, lipid synthesis, lipid transport, lipid binding, lipopolysaccharide biosynthesis, lipoprotein, lipoyl, and all lipid binding proteins, respectively. The accuracy for the nonmember proteins of each class is 99.9, 99.2, 99.6, 99.8, 99.9, 99.8, 98.5, 99.9, and 97.0%, respectively. Comparable accuracies are obtained when homologous proteins are considered as one, or by using a different SVM kernel function. Our method predicts 86.8% of the 76 lipid binding proteins nonhomologous to any protein in the Swiss-Prot database and 89.0% of the 73 known lipid binding domains as lipid binding. These findings suggest the usefulness of SVMs for facilitating the prediction of lipid binding proteins. Our software can be accessed at the SVMProt server (http://jing.cz3.nus.edu.sg/cgi-bin/svmprot.cgi).

Supplementary key words lipid-protein interactions • lipid-modifying enzymes • lipid metabolism • support vector machine


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Nucleic Acids ResHome page
Z. R. Li, H. H. Lin, L. Y. Han, L. Jiang, X. Chen, and Y. Z. Chen
PROFEAT: a web server for computing structural and physicochemical features of proteins and peptides from amino acid sequence.
Nucleic Acids Res., July 1, 2006; 34(Web Server issue): W32 - W37.
[Abstract] [Full Text] [PDF]




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