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ISFOLD:基于非螺旋RNA基序序列比对中的等排性特征预测碱基对结构

ISFOLD: structure prediction of base pairs in non-helical RNA motifs from isostericity signatures in their sequence alignments.

作者信息

Mokdad Ali, Frankel Alan D

机构信息

Department of Biochemistry and Biophysics, University of California at San Francisco, 600 16th Street, San Francisco, CA 94143-2280, USA.

出版信息

J Biomol Struct Dyn. 2008 Apr;25(5):467-72. doi: 10.1080/07391102.2008.10531239.

Abstract

The existence and identity of non-Watson-Crick base pairs (bps) within RNA bulges, internal loops, and hairpin loops cannot reliably be predicted by existing algorithms. We have developed the Isfold (Isosteric Folding) program as a tool to examine patterns of nucleotide substitutions from sequence alignments or mutation experiments and identify plausible bp interactions. We infer these interactions based on the observation that each non-Watson-Crick bp has a signature pattern of isosteric substitutions where mutations can be made that preserve the 3D structure. Isfold produces a dynamic representation of predicted bps within defined motifs in order of their probabilities. The software was developed under Windows XP, and is capable of running on PC and MAC with Matlab 7.1 (SP3) or higher. A PC stand-alone version that does not require Matlab also is available. This software and a user manual are freely available at www.ucsf.edu/frankel/isfold.

摘要

RNA凸起、内环和发夹环中非沃森-克里克碱基对(bps)的存在和身份,无法通过现有算法可靠预测。我们开发了Isfold(等排折叠)程序,作为一种工具来检查序列比对或突变实验中的核苷酸取代模式,并识别可能的碱基对相互作用。我们基于以下观察结果推断这些相互作用:每个非沃森-克里克碱基对都有一个等排取代的特征模式,在这种模式下进行突变可以保留三维结构。Isfold会按概率顺序动态呈现定义基序内预测碱基对的情况。该软件是在Windows XP系统下开发的,能够在安装了Matlab 7.1(SP3)或更高版本的PC和MAC上运行。也有一个不需要Matlab的PC独立版本。该软件和用户手册可在www.ucsf.edu/frankel/isfold上免费获取。

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