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Using Multi-scale Glide Zoom Window Feature Extraction Approach to Predict Protein Homo-oligomer Types

机译:使用多尺度滑翔缩放窗口特征提取方法预测蛋白质均聚物类型

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摘要

The concept of multi-scale glide zoom window was proposed and a novel approach of multi-scale glide zoom window feature extraction was used for predicting protein homo-oligomers. Based on the concept of multi-scale glide zoom window, we choose two scale glide zoom window: whole protein sequence glide zoom window and kin amino acid glide zoom window, and for every scale glide zoom window, three feature vectors of amino acids distance sum, amino acids mean distance and amino acids distribution, were extracted. A series of feature sets were constructed by combining these feature vectors with amino acids composition to form pseudo amino acid compositions (PseAAC). The support vector machine (SVM) was used as base classifier. The 75.37% total accuracy is arrived in jackknife test in the weighted factor conditions, which is 10.05% higher than that of conventional amino acid composition method in same condition. The results show that multi-scale glide zoom window method of extracting feature vectors from protein sequence is effective and feasible, and the feature vectors of multi-scale glide zoom window may contain more protein structure information.
机译:提出了多尺度滑行缩放窗口的概念,并提出了一种新的多尺度滑行缩放窗口特征提取的方法来预测蛋白质同源寡聚体。基于多尺度滑行缩放窗口的概念,我们选择两种尺度滑行缩放窗口:全蛋白质序列滑行缩放窗口和亲缘氨基酸滑行缩放窗口,并且对于每个缩放滑行缩放窗口,氨基酸距离和的三个特征向量提取氨基酸平均距离和氨基酸分布。通过将这些特征向量与氨基酸组成组合以形成假氨基酸组成(PseAAC),可以构建一系列特征集。支持向量机(SVM)被用作基础分类器。在加权因子条件下通过折刀测试达到了75.37%的总准确度,比相同条件下常规氨基酸组成法的准确度高10.05%。结果表明,从蛋白质序列中提取特征向量的多尺度滑移缩放窗口方法是有效可行的,并且多尺度滑移缩放窗口的特征向量可能包含更多的蛋白质结构信息。

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