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Using feature optimization-based support vector machine method to recognize the β-hairpin motifs in enzymes

机译:使用基于特征优化的支持向量机方法识别酶中的β-发夹基序

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摘要

β-Hairpins in enzyme, a kind of special protein with catalytic functions, contain many binding sites which are essential for the functions of enzyme. With the increasing number of observed enzyme protein sequences, it is of especial importance to use bioinformatics techniques to quickly and accurately identify the β-hairpin in enzyme protein for further advanced annotation of structure and function of enzyme. In this work, the proposed method was trained and tested on a non-redundant enzyme β-hairpin database containing 2818 β-hairpins and 1098 non-β-hairpins. With 5-fold cross-validation on the training dataset, the overall accuracy of 90.08% and Matthew’s correlation coefficient (Mcc) of 0.74 were obtained, while on the independent test dataset, the overall accuracy of 88.93% and Mcc of 0.76 were achieved. Furthermore, the method was validated on 845 β-hairpins with ligand binding sites. With 5-fold cross-validation on the training dataset and independent test on the test dataset, the overall accuracies were 85.82% (Mcc of 0.71) and 84.78% (Mcc of 0.70), respectively. With an integration of mRMR feature selection and SVM algorithm, a reasonable high accuracy was achieved, indicating the method to be an effective tool for the further studies of β-hairpins in enzymes structure. Additionally, as a novelty for function prediction of enzymes, β-hairpins with ligand binding sites were predicted. Based on this work, a web server was constructed to predict β-hairpin motifs in enzymes ().
机译:酶中的β-发夹蛋白是一种具有催化功能的特殊蛋白质,含有许多对酶的功能至关重要的结合位点。随着观察到的酶蛋白序列数目的增加,使用生物信息学技术快速准确地鉴定酶蛋白中的β-发夹蛋白以进一步高级地注释酶的结构和功能尤为重要。在这项工作中,在包含2818个β-发夹和1098个非β-发夹的非冗余酶β-发夹数据库上对提出的方法进行了训练和测试。通过对训练数据集进行5倍交叉验证,获得了90.08%的总体准确度和Matthew的相关系数(Mcc)为0.74,而在独立的测试数据集上,其总体准确度达到了88.93%,Mcc达到0.76。此外,该方法在具有配体结合位点的845个β-发夹上得到了验证。通过对训练数据集进行5倍交叉验证和对测试数据集进行独立测试,总体准确性分别为85.82%(Mcc为0.71)和84.78%(Mcc为0.70)。结合mRMR特征选择和SVM算法,获得了合理的高精度,表明该方法是进一步研究酶结构中β-发夹结构的有效工具。另外,作为用于酶功能预测的新颖性,预测了具有配体结合位点的β-发夹。基于这项工作,构建了一个Web服务器来预测酶中的β-发夹基序()。

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