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Bayesian Classifier for Anchored Protein Sorting Discovery

机译:锚定蛋白分类发现的贝叶斯分类器

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A typical cell has a size of only 10μm 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:典型的电池的尺寸仅为10μm,而含有约10亿蛋白质。将这些蛋白质从它们的合成位点传送到细胞内或外部的目标位置,精确地由蛋白质分选信号控制。然而,对蛋白质分类调节信号和机制的基因组理解仍然非常有限。我们将蛋白质分选Motif发现问题作为分类问题,提出了一种基于贝叶斯分类器的基于基于主题的基本发现算法(Bayesmotif),以找到一种公共类型的分拣图案,其中高度保守的锚固件与较少保守的图案区域一起存在。实验表明,我们的算法具有与其他MEME等其他蛋白质主题发现算法相比找到长低劣避免的分类信号的优点。我们的算法还具有容易地包括克服PWM(位置权重矩阵)的限制的附加元序列特征的优点。

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