核受体的共价连接体
Sreekanth Rajan1, Ho Sup Yoon2
1School of Biological Sciences, Nanyang Technological University, 60 Nanyang Drive, 637551, Singapore.
European journal of medicinal chemistry
|October 19, 2023
概括
这项研究确定了16个人类核受体 (NRs),这些受体与配体共同结合. 在NR联体结合域 (LBD) 中保存的囊蛋白是这些相互作用的关键位置,有助于药物发现.
科学领域:
- 分子生物学分子生物学
- 生物化学 生物化学
- 药理学 药理学是指药理学的学科.
背景情况:
- 核受体 (NR) 是调节生理过程的关键转录因子.
- 与NRs结合的连接物调节基因表达,作为激动剂或抗剂.
- 对NR联体结合域 (LBDs) 的共价联体结合是已知的,但没有全面记录.
研究的目的:
- 编制人类NR-LBDs的综合资料,这些NR-LBDs与连接体形成共价附着.
- 为了识别NR-LBDs中的共价联结体相互作用中涉及的保存残留物.
- 为NR向药物发现提供结构性见解.
主要方法:
- 对人类NR-LBDs与连接体共存相互作用的系统审查和治疗.
- 在NR-LBD结构中对保存的氨酸残留物的分析.
- 对共价联体-NR-LBD相互作用的结构分析.
主要成果:
- 在48个人类NR中,16个被确定为共价联体的标.
- 主要在NR-LBD螺旋3和11中保存的囊蛋白是共价附着的热点.
- 这些反应性半氨酸存在于其他NR中,表明可能出现新的共价联结体发展.
结论:
- 这项工作巩固了对共价NR-连接体相互作用的知识.
- 已识别的保存氨酸为新型共价药物设计提供了标.
- 结构洞察力促进了针对NR相关疾病的向治疗方法的开发.
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