Crowder S, Holton J, Alber T
Department of Molecular and Cell Biology, University of California, Berkeley, CA 94720-3206, USA.
J Mol Biol. 2001 Jul 20;310(4):793-800. doi: 10.1006/jmbi.2001.4740.
The RNA recognition motif (RRM) is one of the most common eukaryotic protein motifs. RRM sequences form a conserved globular structure known as the RNA-binding domain (RBD) or the ribonucleoprotein domain. Many proteins that contain RRM sequences bind RNA in a sequence-specific manner. To investigate the basis for the RNA-binding specificity of RRMs, we subjected 330 aligned RRM sequences to covariance analysis. The analysis revealed a single network of covariant amino acid pairs comprising the buried core of the RBD and a surface patch. Structural studies have implicated a subset of these residues in RNA binding. The covariance linkages identify a larger set of amino acid residues, including some not directly in contact with bound RNA, that may influence RNA-binding specificity.
RNA识别基序(RRM)是真核生物中最常见的蛋白质基序之一。RRM序列形成一种保守的球状结构,称为RNA结合结构域(RBD)或核糖核蛋白结构域。许多含有RRM序列的蛋白质以序列特异性方式结合RNA。为了研究RRM的RNA结合特异性的基础,我们对330个比对的RRM序列进行了协方差分析。分析揭示了一个由协变氨基酸对组成的单一网络,该网络构成了RBD的埋藏核心和一个表面区域。结构研究表明这些残基中的一部分与RNA结合有关。协方差联系识别出一组更大的氨基酸残基,包括一些不直接与结合的RNA接触的残基,这些残基可能影响RNA结合特异性。