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Bayesian Classifier for Anchored Protein Sorting Discovery

机译:贝叶斯分类器用于锚定蛋白质分类发现

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A typical cell has a size of only 10 µm while it contains about a billion proteins. Transportation of these proteins from their synthesis sites to their target locations within or outside of the cell is precisely controlled by protein sorting signals. However, genome-wide understanding of protein sorting regulatory signals and mechanisms is still very limited. We formulate the protein sorting motif discovery problem as a classification problem and proposed a Bayesian classifier based motif discovery algorithm (BayesMotif) to find a common type of sorting motifs in which a highly conserved anchor is present along with a less conserved motif regions. Experiments showed that our algorithm has the advantage of finding long lowly conserved sorting signals compared to other protein motif discovery algorithms such as MEME. Our algorithm also has the advantage to easily include additional meta-sequence features that overcomes the limitation of PWM (position weight matrix)
机译:一个典型的细胞大小只有10 µm,而其中却包含约10亿种蛋白质。这些蛋白质从它们的合成位点到细胞内外的目标位置的运输是由蛋白质分选信号精确控制的。但是,全基因组对蛋白质分选调控信号和机制的了解仍然非常有限。我们将蛋白质排序基序发现问题公式化为分类问题,并提出了一种基于贝叶斯分类器的基序发现算法(BayesMotif),以找到一种常见的排序基序类型,其中存在高度保守的锚点以及保守性较低的基序区域。实验表明,与其他蛋白质基序发现算法(例如MEME)相比,我们的算法具有发现长的低保守排序信号的优势。我们的算法还具有轻松包含其他元序列特征的优势,从而克服了PWM(位置权重矩阵)的局限性

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