Heus Hans A, Hilbers Cornelis W
NSR Center for Molecular Structure, Design and Synthesis, Laboratory of Biophysical Chemistry, University of Nijmegen, Toernooiveld, Nijmegen, The Netherlands.
Nucleosides Nucleotides Nucleic Acids. 2003 May-Aug;22(5-8):559-71. doi: 10.1081/NCN-120021955.
The structures of tandem non-canonical base pairs, a frequently recurring motif in RNA molecules, are reviewed and analysed. The tandem non-canonical base pair motifs can be roughly divided in three groups, containing seven subgroups based on their base pairing patterns and local geometries. Structural details and helical parameters that can be used to numerically distinguish between the subgroups are tabulated. Remarkably, while the individual helical twists of the tandem and adjacent base pair steps can be substantially smaller or larger than the typical A-form value of 32.7 degrees, the average value is close to A-form. This and other striking regularities resulting from compensating geometrical adjustments, important for understanding and predicting the configurations of non-canonical base pairs geometries are discussed.
对串联非经典碱基对的结构进行了综述和分析,串联非经典碱基对是RNA分子中经常出现的一种基序。串联非经典碱基对基序大致可分为三组,根据其碱基配对模式和局部几何形状包含七个亚组。列出了可用于从数值上区分这些亚组的结构细节和螺旋参数。值得注意的是,虽然串联和相邻碱基对步长的单个螺旋扭曲可能比典型的A-form值32.7度小得多或大得多,但平均值接近A-form。讨论了由补偿性几何调整产生的这一规律以及其他显著规律,这对于理解和预测非经典碱基对几何形状的构型很重要。