...
首页> 外文期刊>Biochimica et Biophysica Acta. Gene Regulatory Mechanisms >Kinetics of nucleotide entry into RNA polymerase active site provides mechanism for efficiency and fidelity
【24h】

Kinetics of nucleotide entry into RNA polymerase active site provides mechanism for efficiency and fidelity

机译:核苷酸进入RNA聚合酶活性位点的动力学提供了效率和保真度的机制

获取原文
获取原文并翻译 | 示例
           

摘要

During transcription, RNA polymerase II elongates RNA by adding nucleotide triphosphates (NTPs) complementary to a DNA template. Structural studies have suggested that NTPs enter and exit the active site via the narrow secondary pore but details have remained unclear. A kinetic model is presented that integrates molecular dynamics simulations with experimental data. Previous simulations of trigger loop dynamics and the dynamics of matched and mismatched NTPs in and near the active site were combined with new simulations describing NTP exit from the active site via the secondary pore. Markov state analysis was applied to identify major states and estimate kinetic rates for transitions between those states. The kinetic model predicts elongation and misincorporation rates in close agreement with experiment and provides mechanistic hypotheses for how NTP entry and exit via the secondary pore is feasible and a key feature for achieving high elongation and low misincorporation rates during RNA elongation. (C) 2017 Elsevier B.V. All rights reserved.
机译:在转录期间,RNA聚合酶II通过将核苷酸三磷酸(NTPS)互补地互补的DNA模板来伸长RNA。结构研究表明,NTP通过狭窄的二级孔进入和离开活性位点,但细节仍不清楚。提出了一种动力学模型,其与实验数据集成了分子动力学模拟。先前的触发循环动态和活动站点中和附近匹配和不匹配的NTP的动态的模拟与通过次要孔隙的NTP从活性网站注入NTP退出的新模拟。马尔可夫国家分析旨在确定这些州之间过渡的主要国家和估算动力率。动力学模型与实验密切一致地预测伸长率和MISlincoration率,并提供了通过二次孔的NTP进入和退出的机械假设是可行的,并且在RNA伸长期间实现高伸长率和低的MISlinnoration速率的关键特征。 (c)2017 Elsevier B.v.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号