用xylitol抑制剂复合的葡萄糖异构酶的亚原子分辨率结构的数据
Yongbin Xu1,2, Ki Hyun Nam3
1Department of Bioengineering, College of Life Science, Dalian Minzu University, Dalian 116600, China.
Data in brief
|January 18, 2024
概括
了解葡萄糖异构酶 (GI) 抑制是提高工业效率的关键. 这项研究详细介绍了GI-xylitol复合物的亚原子分辨率结构,揭示了抑制剂结合如何改变酶结构.
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:
- 葡萄糖异构酶 (GI) 对于工业应用至关重要,例如生产高果糖玉米糖.
- 了解胃肠道抑制机制可以优化工业酶效率.
- 之前的工作报告的0.99 Å结构的*Streptomyces rubiginosus*GI (SruGI) 与西利托.
研究的目的:
- 提供详细的数据收集和处理程序,用于SruGI的亚原子分辨率结构复杂的xylitol.
- 为了阐明GI抑制的结构基础由西利托.
主要方法:
- 在亚原子分辨率 (0.99 Å) 的X射线晶体学.
- 对SruGI-xylitol复合物的详细结构分析.
- 数据收集和处理用于高分辨率的结构确定.
主要成果:
- 克西利托尔抑制剂部分与SruGI活性位点内的M1位点结合.
- 利醇结合会诱导酶的金属结合部位和基质通道的形状变化.
- 这项研究区分了SruGI.ru的利结合和利自由状态.
结论:
- 亚原子分辨率结构为GI抑制提供了关键的见解.
- 了解西利托的结合机制可以指导开发更高效的工业酶.
- 详细的结构数据有助于进一步研究酶动力学和抑制剂设计.
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