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MVP algorithm based prediction method for virulent proteins in bacterial pathogens

机译:基于MVP算法的细菌病原菌有毒蛋白预测方法。

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Identifying whether the uncharacterized protein belongs to a virulent protein or not is important. If it is virulent protein, it is very useful for studying its virulence mechanisms in pathogens as well as designing antiviral drugs. Particularly, with a large number of virulent protein sequences discovered in recent years, it is urgent to develop an automated method to predict the bacterial virulent proteins. In this work, a sequence encoding scheme based on combing DC (Dipeptide Composition) and PseAA (Pseudo Amino Acid) is introduced to represent protein samples. However, this sequence encoding scheme would correspond to a very high dimensional feature vector. A DR (Dimensionality Reduction) algorithm, the so-called MVP (Maximum variance projection) is introduced to extract the key features from the high-dimensional space and reduce the original high-dimensional vector to a lowerdimensional one. Finally, our jackknife test results thus obtained are quite encouraging, which indicate that the above method is used effectively to deal with this complicated problem of predicting virulent proteins in bacterial pathogens.
机译:鉴定未表征的蛋白质是否属于毒性蛋白质很重要。如果它是有毒的蛋白质,则对于研究其在病原体中的毒力机制以及设计抗病毒药物非常有用。特别地,随着近年来发现的大量有毒蛋白质序列,迫切需要开发一种自动方法来预测细菌有毒蛋白质。在这项工作中,引入了基于梳理DC(二肽组成)和PseAA(伪氨基酸)的序列编码方案来代表蛋白质样品。然而,该序列编码方案将对应于非常高维的特征向量。引入了DR(降维)算法,即所谓的MVP(最大方差投影),以从高维空间提取关键特征并将原始高维向量缩减为低维向量。最后,由此获得的折刀测试结果令人鼓舞,这表明上述方法可有效地解决预测细菌病原体中有毒蛋白质这一复杂问题。

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