SDHA
SDHD公司
SDHB系统
生物
突变
氧化磷酸化
柠檬酸循环
生物化学
计算生物学
蛋白质结构
线粒体
化学
突变
琥珀酸脱氢酶
基因
新陈代谢
种系突变
作者
Zhanqiang Du,Xiaoting Zhou,Yuezheng Lai,Jinxu Xu,Yuying Zhang,Shan Zhou,Ziyan Feng,Long Yu,Yanting Tang,Weiwei Wang,Lu Yu,Changlin Tian,Ting Ran,Hongming Chen,Luke W. Guddat,Fengjiang Liu,Yan Gao,Zihe Rao,Hongri Gong
标识
DOI:10.1073/pnas.2216713120
摘要
Human complex II is a key protein complex that links two essential energy-producing processes: the tricarboxylic acid cycle and oxidative phosphorylation. Deficiencies due to mutagenesis have been shown to cause mitochondrial disease and some types of cancers. However, the structure of this complex is yet to be resolved, hindering a comprehensive understanding of the functional aspects of this molecular machine. Here, we have determined the structure of human complex II in the presence of ubiquinone at 2.86 Å resolution by cryoelectron microscopy, showing it comprises two water-soluble subunits, SDHA and SDHB, and two membrane-spanning subunits, SDHC and SDHD. This structure allows us to propose a route for electron transfer. In addition, clinically relevant mutations are mapped onto the structure. This mapping provides a molecular understanding to explain why these variants have the potential to produce disease.
科研通智能强力驱动
Strongly Powered by AbleSci AI