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DETECT-a Density Estimation Tool for Enzyme ClassificaTion and its application to Plasmodium falciparum

机译:DETECT-酶分类的密度估计工具及其在恶性疟原虫中的应用

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Motivation: A major challenge in genomics is the accurate annotation of component genes. Enzymes are typically predicted using homology-based search methods, where the membership of a protein to an enzyme family is based on single-sequence comparisons. As such, these methods are often error-prone and lack useful measures of reliability for the prediction.Results: Here, we present DETECT, a probabilistic method for enzyme prediction that accounts for the sequence diversity across enzyme families. By comparing the global alignment scores of an unknown protein to those of all known enzymes, an integrated likelihood score can be readily calculated, ranking the reaction classes relevant for that protein. Comparisons to BLAST reveal significant improvements in enzyme annotation accuracy. Applied to Plasmodium falciparum, we identify potential annotation errors and predict novel enzymes of therapeutic interest.
机译:动机:基因组学的主要挑战是准确地注释成分基因。通常使用基于同源性的搜索方法预测酶,其中蛋白质属于酶家族的成员身份是基于单序列比较。因此,这些方法通常容易出错,并且缺乏用于预测的有用度量。结果:在这里,我们介绍DETECT,一种用于酶预测的概率方法,该方法可解释整个酶家族的序列多样性。通过将未知蛋白质的整体比对得分与所有已知酶的整体比对得分进行比较,可以很容易地计算出综合似然得分,从而对与该蛋白质相关的反应类别进行排名。与BLAST的比较揭示了酶注释准确性的显着提高。应用于恶性疟原虫,我们识别潜在的注释错误,并预测具有治疗意义的新型酶。

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