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RNA structure alignment by a unit-vector approach.

机译:通过单位载体方法进行RNA结构比对。

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MOTIVATION: The recent discovery of tiny RNA molecules such as microRNAs and small interfering RNA are transforming the view of RNA as a simple information transfer molecule. Similar to proteins, the native three-dimensional structure of RNA determines its biological activity. Therefore, classifying the current structural space is paramount for functionally annotating RNA molecules. The increasing numbers of RNA structures deposited in the PDB requires more accurate, automatic and benchmarked methods for RNA structure comparison. In this article, we introduce a new algorithm for RNA structure alignment based on a unit-vector approach. The algorithm has been implemented in the SARA program, which results in RNA structure pairwise alignments and their statistical significance. RESULTS: The SARA program has been implemented to be of general applicability even when no secondary structure can be calculated from the RNA structures. A benchmark against the ARTS program using a set of 1275 non-redundant pairwise structure alignments results in inverted approximately 6% extra alignments with at least 50% structurally superposed nucleotides and base pairs. A first attempt to perform RNA automatic functional annotation based on structure alignments indicates that SARA can correctly assign the deepest SCOR classification to 60% of the query structures. AVAILABILITY: The SARA program is freely available through a World Wide Web server http://sgu.bioinfo.cipf.es/services/SARA/. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
机译:动机:最近发现的微小RNA分子(例如microRNA和小的干扰RNA)正在将RNA的观点转变为简单的信息转移分子。类似于蛋白质,RNA的天然三维结构决定了其生物学活性。因此,对当前结构空间进行分类对于功能上注释RNA分子至关重要。越来越多的RNA结构沉积在PDB中,需要更准确,自动和基准化的RNA结构比较方法。在本文中,我们介绍了一种基于单位载体方法的RNA结构比对新算法。该算法已在SARA程序中实现,这导致RNA结构成对比对及其统计意义。结果:即使无法从RNA结构计算出二级结构,SARA程序也已被普遍应用。使用一组1275个非冗余成对结构比对的ARTS程序基准会导致至少约50%的结构重叠核苷酸和碱基对的反向约6%额外比对。基于结构比对执行RNA自动功能注释的首次尝试表明,SARA可以将最深的SCOR分类正确地分配给查询结构的60%以上。可用性:可通过万维网服务器http://sgu.bioinfo.cipf.es/services/SARA/免费获得SARA程序。补充信息:补充数据可从Bioinformatics在线获得。

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