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Using K-minimum increment of diversity to predict secretory proteins of malaria parasite based on groupings of amino acids

机译:使用K最小多样性增量基于氨基酸分组预测疟原虫的分泌蛋白

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Due to the complexity of Plasmodium falci-parumis genome, predicting secretory proteins of P. falciparum is more difficult than other species. In this study, based on the measure of diversity definition, a new K-nearest neighbor method, K-minimum increment of diversity (K-MID), is introduced to predict secretory proteins. The prediction performance of the K-MID by using amino acids composition as the only input vector achieves 88.89% accuracy with 0.78 Mathew's correlation coefficient (MCC). Further, the several reduced amino acids alphabets are applied to predict secretory proteins and the results show that the prediction results are improved to 90.67% accuracy with 0.83 MCC by using the 169 dipeptide compositions of the reduced amino acids alphabets obtained from Protein Blocks method.
机译:由于恶性疟原虫疟原虫基因组的复杂性,预测恶性疟原虫的分泌蛋白比其他物种困难。在这项研究中,基于多样性定义的度量,引入了一种新的K最近邻方法,即K最小多样性增量(K-MID),以预测分泌蛋白。通过使用氨基酸成分作为唯一输入向量,K-MID的预测性能达到88.89%的准确度,而Mathew相关系数(MCC)为0.78。此外,将几种还原氨基酸字母应用于预测分泌蛋白,结果表明,通过使用从Protein Blocks方法获得的169种还原氨基酸字母的二肽组合物,预测结果以0.83 MCC的精度提高到90.67%。

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