Cryo-EM structure of Saccharomyces cerevisiae target of rapamycin complex 2

被引:46
作者
Karuppasamy, Manikandan [1 ]
Kusmider, Beata [2 ]
Oliveira, Taiana M. [1 ]
Gaubitz, Christl [2 ]
Prouteau, Manoel [2 ]
Loewith, Robbie [2 ,3 ]
Schaffitzel, Christiane [1 ,4 ]
机构
[1] European Mol Biol Lab, Grenoble Outstat, 71 Ave Martyrs, F-38042 Grenoble, France
[2] Univ Geneva, Inst Genet & Genom Geneva iGE3, Dept Mol Biol, 30 Quai Ernest Ansermet, CH-1211 Geneva, Switzerland
[3] Univ Geneva, Swiss Natl Ctr Competence Res NCCR Chem Biol, 30 Quai Ernest Ansermet, CH-1211 Geneva, Switzerland
[4] Univ Bristol, Sch Biochem, Bristol BS8 1TD, Avon, England
基金
欧洲研究理事会; 英国生物技术与生命科学研究理事会; 瑞士国家科学基金会;
关键词
MAMMALIAN PROTEIN; BINDING PARTNER; TOR; MTOR; RAPTOR; GROWTH; YEAST; RESOLUTION; PATHWAY; PREDICTION;
D O I
10.1038/s41467-017-01862-0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The target of rapamycin (TOR) kinase assembles into two distinct multiprotein complexes, conserved across eukaryote evolution. In contrast to TOR complex 1 (TORC1), TORC2 kinase activity is not inhibited by the macrolide rapamycin. Here, we present the structure of Saccharomyces cerevisiae TORC2 determined by electron cryo-microscopy. TORC2 contains six subunits assembling into a 1.4 MDa rhombohedron. Tor2 and Lst8 form the common core of both TOR complexes. Avo3/Rictor is unique to TORC2, but interacts with the same HEAT repeats of Tor2 that are engaged by Kog1/Raptor in mammalian TORC1, explaining the mutual exclusivity of these two proteins. Density, which we conclude is Avo3, occludes the FKBP12-rapamycin-binding site of Tor2's FRB domain rendering TORC2 rapamycin insensitive and recessing the kinase active site. Although mobile, Avo1/hSin1 further restricts access to the active site as its conserved-region-in-the-middle (CRIM) domain is positioned along an edge of the TORC2 active-site-cleft, consistent with a role for CRIM in substrate recruitment.
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页数:10
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