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A critical assessment of hidden markov model sub-optimal sampling strategies applied to the generation of peptide 3D models

机译:隐性马尔可夫模型次优采样策略对肽3D模型生成的关键评估

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Hidden Markov Model derived structural alphabets are a probabilistic framework in which the complete conformational space of a peptidic chain is described in terms of probability distributions that can be sampled to identify conformations of largest probabilities. Here, we assess how three strategies to sample sub-optimal conformationsViterbi k-best, forward backtrack and a taboo sampling approachcan lead to the efficient generation of peptide conformations. We show that the diversity of sampling is essential to compensate biases introduced in the estimates of the probabilities, and we find that only the forward backtrack and a taboo sampling strategies can efficiently generate native or near-native models. Finally, we also find such approaches are as efficient as former protocols, while being one order of magnitude faster, opening the door to the large scale de novo modeling of peptides and mini-proteins. (c) 2016 Wiley Periodicals, Inc.
机译:隐马尔可夫模型派生的结构字母是一个概率框架,其中根据概率分布描述了肽链的完整构象空间,可以对概率分布进行采样以识别最大概率的构象。在这里,我们评估了采样次优构象的三种策略是如何通过Viterbi k-best,正向回溯和禁忌采样方法来有效生成肽构象的。我们表明,采样的多样性对于补偿概率估计中引入的偏差至关重要,并且我们发现,只有正向回溯和禁忌采样策略才能有效地生成本地或接近本地的模型。最后,我们还发现这种方法与以前的协议一样有效,但速度快一个数量级,为肽和微型蛋白的大规模从头建模打开了大门。 (c)2016年威利期刊有限公司

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