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Enhanced statistics for local alignment of multiple alignments improves prediction of protein function and structure

机译:多个比对的局部比对的增强统计数据改善了蛋白质功能和结构的预测

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Motivation: Improved comparisons of multiple sequence alignments (profiles) with other profiles can identify subtle relationships between protein families and motifs significantly beyond the resolution of sequence-based comparisons.Results: The local alignment of multiple alignments (LAMA) method was modified to estimate alignment score significance by applying a new measure based on Fisher's combining method. To verify the new procedure, we used known protein structures, sequence annotations and cyclical relations consistency analysis (CYRCA) sets of consistently aligned blocks. Using the new significance measure improved the sensitivity of LAMA without altering its selectivity. The program performed better than other profile-to-profile methods (COMPASS and Prof-sim) and a sequence-to-profile method (PSI-BLAST). The testing was large scale and used several parameters, including pseudo-counts profile calculations and local ungapped blocks or more extended gapped profiles. This comparison provides guidelines to the relative advantages of each method for different cases. We demonstrate and discuss the unique advantages of using block multiple alignments of protein motifs.
机译:动机:改进了多个序列比对(图谱)与其他图谱的比较,可以识别蛋白质家族和基序之间的微妙关系,大大超出了基于序列的比较的分辨率。通过采用基于Fisher合并方法的新度量来评估重要性。为了验证新程序,我们使用了已知的蛋白质结构,序列注释和循环比对一致性分析(CYRCA)组一致排列的区块。使用新的显着性测量方法可以提高LAMA的灵敏度,而不会改变其选择性。该程序的性能优于其他配置文件到配置文件方法(COMPASS和Prof-sim)和序列配置文件方法(PSI-BLAST)。该测试是大规模的,并使用了多个参数,包括伪计数轮廓计算和局部未缺口块或更多扩展的缺口轮廓。这种比较为每种方法在不同情况下的相对优势提供了指导。我们演示和讨论使用蛋白质基序的块多重比对的独特优势。

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