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A Probabilistic Programming Approach to Protein Structure Superposition

机译:蛋白质结构叠加的概率规划方法

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Optimal superposition of protein structures is crucial for understanding their structure, function, dynamics and evolution. We investigate the use of probabilistic programming to superimpose protein structures guided by a Bayesian model. Our model THESEUS-PP is based on the THESEUS model, a probabilistic model of protein superposition based on rotation, translation and perturbation of an underlying, latent mean structure. The model was implemented in the deep probabilistic programming language Pyro. Unlike conventional methods that minimize the sum of the squared distances, THESEUS takes into account correlated atom positions and heteroscedasticity (i.e., atom positions can feature different variances). THESEUS performs maximum likelihood estimation using iterative expectation-maximization. In contrast, THESEUS-PP allows automated maximum a-posteriori (MAP)estimation using suitable priors over rotation, translation, variances and latent mean structure. The results indicate that probabilistic programming is a powerful new paradigm for the formulation of Bayesian probabilistic models concerning biomolecular structure. Specifically, we envision the use of the THESEUS-PP model as a suitable error model or likelihood in Bayesian protein structure prediction using deep probabilistic programming.
机译:蛋白质结构的最佳叠加对于理解其结构,功能,动力学和进化至关重要。我们调查使用概率编程来叠加由贝叶斯模型指导的蛋白质结构。我们的模型THESEUS-PP基于THESEUS模型,THESEUS模型是基于潜在的潜在均值结构的旋转,平移和扰动的蛋白质叠加概率模型。该模型是在深度概率编程语言Pyro中实现的。与最小化平方距离之和的常规方法不同,THESEUS考虑了相关的原子位置和异方差性(即原子位置可能具有不同的方差)。 THESEUS使用迭代期望最大化执行最大似然估计。相比之下,THESEUS-PP可以使用旋转,平移,方差和潜在均值结构上的适当先验值来自动进行最大后验(MAP)估计。结果表明,概率编程是一种有关生物分子结构的贝叶斯概率模型的强大新范式。具体而言,我们设想使用THESEUS-PP模型作为使用深度概率编程进行贝叶斯蛋白质结构预测的合适误差模型或可能性。

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