TMEM120A is a coenzyme A-binding membrane protein with structural similarities to ELOVL fatty acid elongase

被引:22
|
作者
Xue, Jing [1 ,2 ,3 ]
Han, Yan [1 ,2 ,3 ]
Baniasadi, Hamid [4 ]
Zeng, Weizhong [1 ,2 ,3 ]
Pei, Jimin [2 ,3 ,4 ]
Grishin, Nick, V [2 ,3 ,4 ]
Wang, Junmei [5 ]
Tu, Benjamin P. [4 ]
Jiang, Youxing [1 ,2 ,3 ]
机构
[1] Univ Texas Southwestern Med Ctr Dallas, Dept Physiol, Dallas, TX 75390 USA
[2] Univ Texas Southwestern Med Ctr Dallas, Dept Biophys, Dallas, TX 75390 USA
[3] Univ Texas Southwestern Med Ctr Dallas, Howard Hughes Med Inst, Dallas, TX 75390 USA
[4] Univ Texas Southwestern Med Ctr Dallas, Dept Biochem, Dallas, TX USA
[5] Univ Pittsburgh, Sch Pharm, Dept Pharmaceut Sci, Pittsburgh, PA 15261 USA
来源
ELIFE | 2021年 / 10卷
基金
美国国家科学基金会;
关键词
SERVER; VALIDATION;
D O I
10.7554/eLife.71220
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
TMEM120A, also named as TACAN, is a novel membrane protein highly conserved in vertebrates and was recently proposed to be a mechanosensitive channel involved in sensing mechanical pain. Here we present the single-particle cryogenic electron microscopy (cryo-EM) structure of human TMEM120A, which forms a tightly packed dimer with extensive interactions mediated by the N-terminal coiled coil domain (CCD), the C-terminal transmembrane domain (TMD), and the re-entrant loop between the two domains. The TMD of each TMEM120A subunit contains six transmembrane helices (TMs) and has no clear structural feature of a channel protein. Instead, the six TMs form an a-barrel with a deep pocket where a coenzyme A (CoA) molecule is bound. Intriguingly, some structural features of TMEM120A resemble those of elongase for very long-chain fatty acids (ELOVL) despite the low sequence homology between them, pointing to the possibility that TMEM120A may function as an enzyme for fatty acid metabolism, rather than a mechanosensitive channel.
引用
收藏
页数:16
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