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Entropy-accelerated exact clustering of protein decoys

机译:熵加速蛋白质诱饵的精确聚类

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Motivation: Clustering is commonly used to identify the best decoy among many generated in protein structure prediction when using energy alone is insufficient. Calculation of the pairwise distance matrix for a large decoy set is computationally expensive. Typically, only a reduced set of decoys using energy filtering is subjected to clustering analysis. A fast clustering method for a large decoy set would be beneficial to protein structure prediction and this still poses a challenge.Results: We propose a method using propagation of geometric constraints to accelerate exact clustering, without compromising the distance measure. Our method can be used with any metric distance. Metrics that are expensive to compute and have known cheap lower and upper bounds will benefit most from the method. We compared our method's accuracy against published results from the SPICKER clustering software on 40 large decoy sets from the I-TASSER protein folding engine. We also performed some additional speed comparisons on six targets from the 'semfold' decoy set. In our tests, our method chose a better decoy than the energy criterion in 25 out of 40 cases versus 20 for SPICKER. Our method also was shown to be consistently faster than another fast software performing exact clustering named Calibur. In some cases, our approach can even outperform the speed of an approximate method.
机译:动机:当仅使用能量不足时,通常使用聚类来确定蛋白质结构预测中产生的许多最佳诱饵。大诱饵组的成对距离矩阵的计算在计算上是昂贵的。通常,仅对使用能量过滤的一组减少的诱饵进行聚类分析。针对大型诱饵组的快速聚类方法将有利于蛋白质结构的预测,但这仍然带来了挑战。结果:我们提出了一种利用几何约束的传播来加速精确聚类的方法,而不会影响距离度量。我们的方法可以用于任何公制距离。该方法最有利于计算成本高昂且已知上下限便宜的度量标准。我们将我们方法的准确性与SPICKER聚类软件在I-TASSER蛋白质折叠引擎的40个大型诱饵组上发表的结果进行了比较。我们还对“弯折”诱饵组中的六个目标进行了其他速度比较。在我们的测试中,我们的方法在40个案例中有25个案例选择了比能量准则更好的诱饵,而SPICKER案例则选择了20个案例。我们的方法还被证明比另一种执行精确聚类的快速软件Calibur更快。在某些情况下,我们的方法甚至可以超过近似方法的速度。

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