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Prediction of heterotrimeric protein complexes by two-phase learning using neighboring kernels

机译:邻近核预测两相学习的异络蛋白复合物

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Background: Protein complexes play important roles in biological systems such as gene regulatory networks and metabolic pathways. Most methods for predicting protein complexes try to find protein complexes with size more than three. It, however, is known that protein complexes with smaller sizes occupy a large part of whole complexes for several species. In our previous work, we developed a method with several feature space mappings and the domain composition kernel for prediction of heterodimeric protein complexes, which outperforms existing methods. Results: We propose methods for prediction of heterotrimeric protein complexes by extending techniques in the previous work on the basis of the idea that most heterotrimeric protein complexes are not likely to share the same protein with each other. We make use of the discriminant function in support vector machines (SVMs), and design novel feature space mappings for the second phase. As the second classifier, we examine SVMs and relevance vector machines (RVMs). We perform 10-fold cross-validation computational experiments. The results suggest that our proposed two-phase methods and SVM with the extended features outperform the existing method NWE, which was reported to outperform other existing methods such as MCL, MCODE, DPClus, CMC, COACH, RRW, and PPSampler for prediction of heterotrimeric protein complexes. Conclusions: We propose two-phase prediction methods with the extended features, the domain composition kernel, SVMs and RVMs. The two-phase method with the extended features and the domain composition kernel using SVM as the second classifier is particularly useful for prediction of heterotrimeric protein complexes.
机译:背景:蛋白质复合物在基因调节网络和代谢途径等生物系统中起重要作用。预测蛋白质复合物的大多数方法尝试发现尺寸超过三个的蛋白质复合物。然而,众所周知,具有较小尺寸的蛋白质复合物占据几种整个复合物的大部分。在我们以前的工作中,我们开发了一种具有若干特征空间映射和域组成核的方法,用于预测异二聚体蛋白质复合物,其优于现有方法。结果:我们提出了通过基于最先前的工作中的技术在最先进的工作中延伸技术来预测异溶解蛋白质复合物的方法,即大多数杂漆蛋白质复合物不太可能彼此共享相同的蛋白质。我们利用支持向量机(SVM)中的判别功能,并为第二阶段设计新颖的特征空间映射。作为第二分类器,我们检查SVM和相关矢量机(RVM)。我们执行10倍的交叉验证计算实验。结果表明,我们提出的两阶段方法和SVM具有扩展特征的优于现有方法NWE,据报道,始终倾销其他现有方法,如MCL,MCODE,DPCLU,CMC,COACH,RRW和PPSAmpler,用于预测异校式蛋白质复合物。结论:我们提出了双相预测方法,具有扩展特征,域组成核,SVM和RVM。使用SVM具有扩展特征和域组成核的两相方法对于第二分类器特别适用于预测异溶解蛋白质复合物。

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