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Protein structure prediction using diversity controlled self-adaptive differential evolution with local search

机译:使用局部控制的多样性控制自适应差异进化预测蛋白质结构

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In this paper, Protein Structure Prediction problem is solved using Diversity Controlled Self-Adaptive Differential Evolution with Local search (DCSaDE-LS). DCSaDE-LS, an improved version of Self-Adaptive Differential Evolution (SaDE), use simple fuzzy system to control the diversity of individuals and local search to maintain a balance between exploration and exploitation. DCSaDE-LS with four different local search replacement strategies are used. SaDE is also implemented for comparison purposes. Algorithms are tested on a peptide Met-enkephalin for force fields ECEPP/2, ECEPP/3 and CHARMM22. Results show that both DCSaDE-LS and SaDE produce the best energy for both force fields. Among the four replacement strategies, DCSaDE-LS1 strategy reports better results than other strategies and SaDE in terms of number of function evaluations, mean energy and success rate. Best conformations obtained using DCSaDE-LS is compared with native structure 1PLW and GEM structure Scheraga. Nonparametric statistical tests for multiple comparisons () with control method are implemented for CHARMM22 observations. A set of unique 100 best conformations obtained from DCSaDE-LS are clustered into 3 independent clusters suggesting the robustness of this methodology and the ability to explore the conformational space available and to populate the near native conformations.
机译:在本文中,使用具有局部搜索的多样性控制的自适应差异进化(DCSaDE-LS)解决了蛋白质结构预测问题。 DCSaDE-LS是自适应差分进化(SaDE)的改进版本,它使用简单的模糊系统来控制个人和本地搜索的多样性,以保持勘探与开发之间的平衡。使用具有四种不同本地搜索替换策略的DCSaDE-LS。 SaDE还出于比较目的而实现。在肽Met-脑啡肽上针对力场ECEPP / 2,ECEPP / 3和CHARMM22测试了算法。结果表明,DCSaDE-LS和SaDE都能为两个力场产生最佳能量。在四种替代策略中,DCSaDE-LS1策略在功能评估的数量,平均精力和成功率方面均比其他策略和SaDE更好。使用DCSaDE-LS获得的最佳构象与本机结构1PLW和GEM结构Scheraga进行比较。针对CHARMM22观测值,采用控制方法对多个比较()进行了非参数统计检验。从DCSaDE-LS获得的一组独特的100个最佳构象被聚集成3个独立的簇,这表明该方法的鲁棒性以及探索可用构象空间并填充近乎天然构象的能力。

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