DegSampler:用于检测E3结合位点的折叠Gibbs采样器

O. Maruyama, Fumiko Matsuzaki
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引用次数: 0

摘要

在本文中,我们解决了在E3泛素连接酶(E3)特异性底物蛋白中寻找序列基序的问题。我们通过设计基于氨基酸索引的似然函数和基于蛋白质序列无序度的先验分布,建立了位点的后验概率分布。这些设计来源于底物蛋白中E3结合位点的已知特征。然后,我们设计了一种称为DegSampler的后验概率分布的折叠吉布斯抽样算法。我们使用36组E3s特异性底物蛋白进行了计算实验,并将DegSampler与流行的motif finder MEME和GLAM2的性能进行了比较。结果表明,DegSampler在寻找E3结合基序方面优于其他方法。因此,DegSampler是在底物蛋白中寻找E3基序的一个很有前途的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Regular Paper] DegSampler: Collapsed Gibbs Sampler for Detecting E3 Binding Sites
In this paper, we address the problem of finding sequence motifs in substrate proteins specific to E3 ubiquitin ligases (E3s). We formulated a posterior probability distribution of sites by designing a likelihood function based on amino acid indexing and a prior distribution based on the disorderness of protein sequences. These designs are derived from known characteristics of E3 binding sites in substrate proteins. Then, we devise a collapsed Gibbs sampling algorithm for the posterior probability distribution called DegSampler. We performed computational experiments using 36 sets of substrate proteins specific to E3s and compared the performance of DegSampler with those of popular motif finders, MEME and GLAM2. The results showed that DegSampler was superior to the others in finding E3 binding motifs. Thus, DegSampler is a promising tool for finding E3 motifs in substrate proteins.
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