类型IIβ 酸丁酸酶的结构:为界面酸化而平的蛋白质酶折叠
V D Rao1, S Misra, I V Boronenkov
1Laboratory of Molecular Biology, National Institute of Diabetes, Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892-0580, USA.
Cell
|September 30, 1998
概括
对于细胞信号传递至关重要的酸酸激酶进行了结构分析. 类型IIβ 酸丁酸盐激酶揭示了一个共同的蛋白激酶核心,这表明所有这些酶都属于一个超级家族.
科学领域:
- 生物化学 生物化学
- 分子生物学分子生物学
- 结构生物学 结构生物学
背景情况:
- 酸酸酶是细胞信号转导通路中的关键酶.
- 它们的功能是通过在特定位置化酸的化环化.
- 了解它们的结构对于阐明它们的功能和调节至关重要.
研究的目的:
- 为了确定IIbeta类型的酸丁酸酸盐激酶的三维结构.
- 识别与酶功能,基质特异性和细胞局部化相关的结构特征.
- 为了建立一个更大的酶超级家族内的酸酸酶酶的关系.
主要方法:
- 使用X射线晶体学来确定蛋白质结构.
- 使用生物信息分析来比较保存的残留物,并确定功能部位.
- 用分子建模来可视化酶-基质和酶-膜相互作用.
主要成果:
- 结构显示出一个圆盘形的同极体,具有明显的基本平面,表明对等离子体膜的静电吸引力.
- 一个保存的基本残留集群可能形成了酸酸盐特异性位点.
- 基质结合部位是可访问的,支持酸丁酸3-和5-酸盐的双重特异性.
结论:
- 所有的氨基酸酶很可能共享一个共同的蛋白质酶ATP结合核心,属于一个超级家族.
- 已识别的结构特征为膜准和基板识别提供了一种机制.
- 这项研究提供了关于基因在膜接口上的基因因的 in situ 酸化的见解.
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