Multi-Class Protein Subcellular Localization Prediction using Support Vector Machines

Peng Wai Meng, Jagath Rajapakse
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引用次数: 3

Abstract

Prediction of protein subcellular localization from amino acid sequence is an important step towards elucidating the function of a protein. Here, we present an approach for predicting protein subcellular localizations from eukaryotic sequences using Support Vector Machines. Apart from using amino acid compositions, our prediction approach also considers biochemical characteristics of amino acids and their distribution patterns along the primary sequence of the query proteins. Consequently, improved predictive accuracy has been achieved on the Reinhardt and Hubbard’s dataset. For the four subcellular localizations of eukaryotic proteins, the total prediction accuracy obtained using the “ leave-one-out” cross-validation test is 88.88%. To the best of our knowledge, our approach obtained by far the best prediction accuracy for mitochondrial proteins, which are notoriously difficult to predict among eukaryotic proteins. Performance comparison results also showed that our approach outperformed existing protein subcellular localization prediction methods based solely on amino acid composition.
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基于支持向量机的多类蛋白质亚细胞定位预测
从氨基酸序列预测蛋白质亚细胞定位是阐明蛋白质功能的重要一步。在这里,我们提出了一种使用支持向量机从真核序列预测蛋白质亚细胞定位的方法。除了使用氨基酸组成外,我们的预测方法还考虑了氨基酸的生化特征及其沿查询蛋白一级序列的分布模式。因此,在Reinhardt和Hubbard的数据集上实现了提高的预测精度。对于真核蛋白的四种亚细胞定位,使用“留一”交叉验证试验获得的总预测准确率为88.88%。据我们所知,我们的方法获得了迄今为止最好的预测准确性线粒体蛋白,这是出了名的难以预测真核蛋白。性能比较结果还表明,我们的方法优于现有的仅基于氨基酸组成的蛋白质亚细胞定位预测方法。
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