The mammalian target of rapamycin (mTOR) is a key protein kinase controlling cellular metabolism and growth. It is part of the two structurally and functionally distinct multiprotein complexes mTORC1 and mTORC2. Dysregulation of mTOR occurs in diabetes, cancer and neurological disease. We report the architecture of human mTORC2 at intermediate resolution, revealing a conserved binding site for accessory proteins on mTOR and explaining the structural basis for the rapamycin insensitivity of the complex.
Architecture of the human mTORC2 core complex
E. Stuttfeld,Christopher H. S. Aylett,S. Imseng,D. Boehringer,A. Scaiola,E. Sauer,M. Hall,T. Maier,N. Ban
Published 2018 in eLife
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PUBLICATION RECORD
- Publication year
2018
- Venue
eLife
- Publication date
2018-02-09
- Fields of study
Biology, Medicine, Chemistry
- Identifiers
- External record
- Source metadata
Semantic Scholar, PubMed
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