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NES-REBS: A novel nuclear export signal prediction method using regular expressions and biochemical properties

机译:NES-REBS:使用正则表达式和生化特性的新型核出口信号预测方法

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摘要

A nuclear export signal (NES) is a protein localization signal, which is involved in binding of cargo proteins to nuclear export receptor, thus contributes to regulate localization of cellular proteins. Consensus sequences of NES have been used to detect NES from protein sequences, but suffer from poor predictive power. Some recent peering works were proposed to use biochemical properties of experimental verified NES to refine NES candidates. Those methods can achieve high prediction rates, but their execution time will become unacceptable for large-scale NES searching if too much properties are involved. In this work, we developed a novel computational approach, named NES-REBS, to search NES from protein sequences, where biochemical properties of experimental verified NES, including secondary structure and surface accessibility, are utilized to refine NES candidates obtained by matching popular consensus sequences. We test our method by searching 262 experimental verified NES from 221 NES-containing protein sequences. It is obtained that NES-REBS runs in 2-3 mins and performs well by achieving precision rate 47.2% and sensitivity 54.6%.
机译:核输出信号(NES)是一种蛋白质定位信号,参与货物蛋白与核输出受体的结合,因此有助于调节细胞蛋白的定位。 NES的共有序列已用于检测蛋白质序列中的NES,但预测能力差。提出了一些最近的对等工作,以利用经过实验验证的NES的生化特性来精制NES候选物。这些方法可以实现较高的预测率,但是如果涉及太多的属性,则对于大规模NES搜索而言,它们的执行时间将变得不可接受。在这项工作中,我们开发了一种新的计算方法,称为NES-REBS,以从蛋白质序列中搜索NES,在此方法中,经过实验验证的NES的生化特性(包括二级结构和表面可及性)被用来完善通过匹配流行的共有序列而获得的NES候选物。我们通过从221个含NES的蛋白质序列中搜索262个实验验证的NES来测试我们的方法。获得的NES-REBS可以在2-3分钟内运行并通过达到47.2%的准确率和54.6%的灵敏度而表现良好。

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