解决在模型酶中介于两步催化机制的构造变化
Jack B Greisman1, Kevin M Dalton1, Dennis E Brookner1
1Department of Molecular & Cellular Biology, Harvard University, Cambridge, MA, United States.
bioRxiv : the preprint server for biology
|July 3, 2023
概括
像二叶酸还原酶 (DHFR) 这样的酶使用形态动力学来加快反应. 这项研究揭示了DHFR是如何发生的.
科学领域:
- 生物化学 生物化学
- 结构生物学 结构生物学
- 酶学 是一种酶学.
背景情况:
- 酶通过精确地组织基质和氨基酸来加速生化反应.
- 了解蛋白质结构动力学在酶催化中的作用受到实验挑战的限制.
- 大肠杆菌二叶酸减少酶 (DHFR) 调节其对质子和化物转移的活性位点的确切机制尚不清楚.
结论:
- DHFR采用动态的自由能景观来指导其两步催化机制.
- 酶的催化效率是响应基质的质子化状态.
- 形态动力学在调节酶活性部位环境和催化过程中起着至关重要的作用.
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