通过血清素N-乙转移酶对有序基质结合的结构基础:以1.8A分辨率的酶复合物与双基质模拟物结合
A B Hickman1, M A Namboodiri, D C Klein
1Laboratory of Developmental Neurobiology, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892-0560, USA.
Cell
|May 13, 1999
概括
这项研究揭示了血清素N-乙转移酶如何与乙辅酶A结合,导致形成血清素结合部位的形状变化. 结构洞察力还突出了一个水道和Tyr-168的特点.
科学领域:
- 生物化学 生物化学
- 结构生物学 结构生物学
- 时间生物学 时间生物学
背景情况:
- 氨酸N-乙转移酶 (SNAT) 对于氨酸的合成至关重要.
- 黑色素调节昼夜节律.
- SNAT属于GNAT乙转移酶超级家族.
研究的目的:
- 阐明SNAT活动的结构基础.
- 了解乙-CoA结合和血清素结合部位形成的机制.
- 为了研究特定残留物的催化作用.
主要方法:
- 无基质和模拟结合的SNAT的X射线晶体学.
- 不同酶状态的结构比较.
- 位点定向的突变发生.
主要成果:
- 乙辅酶A (AcCoA) 的结合会诱导SNAT中显著的结构变化.
- 这种变化导致了血清素结合部位的形成.
- 一个充满水的通道和Tyr-168参与了催化.
结论:
- SNAT的形状灵活性是其功能的关键.
- 该酶利用特定的结构特征来促进乙转移和质子去除.
- Tyr-168在SNAT的催化机制中起着至关重要的作用.
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