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Updated: Jun 27, 2025

Defining Hsp33's Redox-regulated Chaperone Activity and Mapping Conformational Changes on Hsp33 Using Hydrogen-deuterium Exchange Mass Spectrometry
10:24

Defining Hsp33's Redox-regulated Chaperone Activity and Mapping Conformational Changes on Hsp33 Using Hydrogen-deuterium Exchange Mass Spectrometry

Published on: June 7, 2018

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氧化应激介导的RUNX3错位发生通过Jun激活域结合蛋白1和基因素修饰发生

Kyoung Ah Kang1,2, Mei Jing Piao1,2, Pincha Devage Sameera Madushan Fernando1,2

  • 1Jeju Research Center for Natural Medicine, Jeju National University, Jeju, 63243, Republic of Korea.

Applied biochemistry and biotechnology
|April 29, 2024
PubMed
概括

氧化应激会导致RUNX3从细胞核移动到细胞质,使这种瘤抑制剂失活. 基质子的修改和特定的酶活性变化调解了这个过程.

关键词:
细胞质局部化局部化基因组胺基因的修改关节激活域结合蛋白1 关节激活域结合蛋白1氧化应激是一种氧化应激.运行域转录因子3 运行域转录因子3

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