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1 Bioinformatics Center, Institute for Chemical Research, Kyoto University, Kyoto 611-0111, Japan
2 Centre de Géostatistique, Ecole des Mines de Paris, 77300 Fontainebleau, France
3 Division of Bioinformatics, Medical Institute of Bioregulation, Kyushu University, Fukuoka 812-8582, Japan
(RECEIVED May 20, 2005; FINAL REVISION August 22, 2005; ACCEPTED August 22, 2005)
As the number of complete genomes rapidly increases, accurate methods to automatically predict the subcellular location of proteins are increasingly useful to help their functional annotation. In order to improve the predictive accuracy of the many prediction methods developed to date, a novel representation of protein sequences is proposed. This representation involves local compositions of amino acids and twin amino acids, and local frequencies of distance between successive (basic, hydrophobic, and other) amino acids. For calculating the local features, each sequence is split into three parts: N-terminal, middle, and C-terminal. The N-terminal part is further divided into four regions to consider ambiguity in the length and position of signal sequences. We tested this representation with support vector machines on two data sets extracted from the SWISS-PROT database. Through fivefold cross-validation tests, overall accuracies of more than 87% and 91% were obtained for eukaryotic and prokaryotic proteins, respectively. It is concluded that considering the respective features in the N-terminal, middle, and C-terminal parts is helpful to predict the subcellular location.
Keywords: subcellular location; signal sequence; amino acid composition; distance frequency; support vector machine; predictive accuracy
Article and publication are at http://www.proteinscience.org/cgi/doi/10.1110/ps.051597405.
Reprint requests to: Setsuro Matsuda, Bioinformatics Center, Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto 611-0011, Japan; e-mail: smatsuda{at}kuicr.kyoto-u.ac.jp; fax: +81-774-38-3022.
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