Department of Computer Science, National Chiao Tung University, 1001 Tashuei Rd., Hsinchu, Taiwan.
Comput Biol Med. 2012 Jan;42(1):93-105. doi: 10.1016/j.compbiomed.2011.10.013. Epub 2011 Nov 17.
This study proposes a general framework for structural motif discovery. The framework is based on a modular design in which the system components can be modified or replaced independently to increase its applicability to various studies. It is a two-stage approach that first converts protein 3D structures into structural alphabet sequences, and then applies a sequence motif-finding tool to these sequences to detect conserved motifs. We named the structural motif database we built the SA-Motifbase, which provides the structural information conserved at different hierarchical levels in SCOP. For each motif, SA-Motifbase presents its 3D view; alphabet letter preference; alphabet letter frequency distribution; and the significance. SA-Motifbase is available at http://bioinfo.cis.nctu.edu.tw/samotifbase/.
本研究提出了一种用于结构基序发现的通用框架。该框架基于模块化设计,系统组件可以独立修改或替换,以提高其在各种研究中的适用性。它是一种两阶段方法,首先将蛋白质 3D 结构转换为结构字母序列,然后应用序列基序发现工具来检测这些序列中的保守基序。我们将构建的结构基序数据库命名为 SA-Motifbase,它提供了 SCOP 中不同层次结构上保守的结构信息。对于每个基序,SA-Motifbase 都提供其 3D 视图、字母偏好、字母频率分布以及显著性。SA-Motifbase 可在 http://bioinfo.cis.nctu.edu.tw/samotifbase/ 获得。