Dror Oranit, Nussinov Ruth, Wolfson Haim J
School of Computer Science, Raymond and Beverly Sackler Faculty of Exact Sciences, Tel Aviv University, Tel Aviv 69978, Israel.
Nucleic Acids Res. 2006 Jul 1;34(Web Server issue):W412-5. doi: 10.1093/nar/gkl312.
RNA molecules with common structural features may share similar functional properties. Structural comparison of RNAs and detection of common substructures is, thus, a highly important task. Nevertheless, the current available tools in the RNA community provide only a partial solution, since they either work at the 2D level or are suitable for detecting predefined or local contiguous tertiary motifs only. Here, we describe a web server built around ARTS, a method for aligning tertiary structures of nucleic acids (both RNA and DNA). ARTS receives a pair of 3D nucleic acid structures and searches for a priori unknown common substructures. The search is truly 3D and irrespective of the order of the nucleotides on the chain. The identified common substructures can be large global folds with hundreds and even thousands of nucleotides as well as small local motifs with at least two successive base pairs. The method is highly efficient and has been used to conduct an all-against-all comparison of all the RNA structures in the Protein Data Bank. The web server together with a software package for download are freely accessible at http://bioinfo3d.cs.tau.ac.il/ARTS.
具有共同结构特征的RNA分子可能具有相似的功能特性。因此,RNA的结构比较和共同子结构的检测是一项极其重要的任务。然而,RNA领域目前可用的工具仅提供了部分解决方案,因为它们要么在二维层面上工作,要么仅适用于检测预定义的或局部连续的三级基序。在此,我们描述了一个围绕ARTS构建的网络服务器,ARTS是一种用于比对核酸(包括RNA和DNA)三级结构的方法。ARTS接收一对三维核酸结构,并搜索先验未知的共同子结构。该搜索是真正的三维搜索,且与链上核苷酸的顺序无关。所识别出的共同子结构可以是具有数百甚至数千个核苷酸的大型全局折叠,也可以是具有至少两个连续碱基对的小型局部基序。该方法效率极高,已用于对蛋白质数据库中所有RNA结构进行全对全比较。该网络服务器以及一个可供下载的软件包可在http://bioinfo3d.cs.tau.ac.il/ARTS上免费获取。