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Architecture of a Diels-Alderase ribozyme with a preformed catalytic pocket

机译:具有预先形成的催化口袋的Diels-Alderase核酶的体系结构

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Artificial ribozymes catalyze a variety of chemical reactions. Their structures and reaction mechanisms are largely unknown. We have analyzed a ribozyme catalyzing Diels-Alder cycloaddition reactions by comprehensive mutation analysis and a variety of probing techniques. New tertiary interactions involving base pairs between nucleotides of the 5' terminus and a large internal loop forming a pseudoknot fold were identified. The probing data indicate a preformed tertiary structure that shows no major changes on substrate or product binding. Based on these observations, a molecular architecture featuring a Y-shaped arrangement is proposed. The tertiary structure is formed in a rather unusual way; that is, the opposite sides of the asymmetric internal loop are clamped by the four 5'-terminal nucleotides, forming two adjacent two base-pair helices. It is proposed that the catalytic pocket is formed by a wedge within one of these helices.
机译:人工核酶催化多种化学反应。它们的结构和反应机理在很大程度上是未知的。我们已经通过全面的突变分析和各种探测技术分析了催化Diels-Alder环加成反应的核酶。确定了新的三级相互作用,涉及5'末端核苷酸与形成假结折叠的大内部环之间的碱基对。探测数据表明预制的三级结构对底物或产物的结合无明显变化。基于这些观察,提出了具有Y形排列的分子结构。三级结构以一种非常不寻常的方式形成。也就是说,不对称内部环的相对侧被四个5'末端核苷酸夹住,形成两个相邻的两个碱基对螺旋。提出催化口袋由这些螺旋之一中的楔形物形成。

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