SISSA, CNR-INFM Democritos and Italian Institute of Technology, I-34151 Trieste, Italy.
Bioinformatics. 2009 Aug 1;25(15):1876-83. doi: 10.1093/bioinformatics/btp339. Epub 2009 May 31.
We have previously demonstrated that proteins may be aligned not only by sequence or structural homology, but also using their dynamical properties. Dynamics-based alignments are sensitive and powerful tools to compare even structurally dissimilar protein families. Here, we propose to use this method to predict protein regions involved in the binding of nucleic acids. We have used the OB-fold, a motif known to promote protein-nucleic acid interactions, to validate our approach.
We have tested the method using this well-characterized nucleic acid binding family. Protein regions consensually involved in statistically significant dynamics-based alignments were found to correlate with nucleic acid binding regions. The validated scheme was next used as a tool to predict which regions of the AXH-domain representatives (a sub-family of the OB-fold for which no DNA/RNA complex is yet available) are putatively involved in binding nucleic acids. The method, therefore, is a promising general approach for predicting functional regions in protein families on the basis of comparative large-scale dynamics.
The software is available upon request from the authors, free of charge for academic users.
Supplementary data are available at Bioinformatics online.
我们之前已经证明,蛋白质不仅可以通过序列或结构同源性进行对齐,还可以通过它们的动力学特性进行对齐。基于动力学的比对是一种敏感而强大的工具,可以比较即使结构上不相似的蛋白质家族。在这里,我们建议使用这种方法来预测参与结合核酸的蛋白质区域。我们使用了 OB 折叠结构域,这是一种已知促进蛋白质-核酸相互作用的基序,来验证我们的方法。
我们使用这个特征良好的核酸结合家族测试了该方法。发现一致性地参与基于统计学显著动力学比对的蛋白质区域与核酸结合区域相关。随后,将经过验证的方案用作工具,预测 AXH 结构域代表(OB 折叠结构域的一个亚家族,目前尚无 DNA/RNA 复合物)的哪些区域可能参与结合核酸。因此,该方法是一种很有前途的通用方法,可以基于比较大规模的动力学来预测蛋白质家族中的功能区域。
可根据作者的要求提供软件,学术用户可免费使用。
补充数据可在 Bioinformatics 在线获取。