Structural basis for the docking of mTORC1 on the lysosomal surface

التفاصيل البيبلوغرافية
العنوان: Structural basis for the docking of mTORC1 on the lysosomal surface
المؤلفون: Ange-Célia Priso Fils, Xin Gu, Daan Overwijn, Anna Niehaus, Monther Abu-Remaileh, Jibril Fetu Kedir, Sherry X. Zhou, David M. Sabatini, Edward J. Brignole, Kacper B. Rogala, Laura F. Bianchi, Alexia M. S. Bottino, Daniel Leary, Nouf N. Laqtom, Rikke Dueholm
المصدر: Prof. Sabatini via Courtney Crummett
بيانات النشر: American Association for the Advancement of Science (AAAS), 2019.
سنة النشر: 2019
مصطلحات موضوعية: Multidisciplinary, biology, Chemistry, Protein subunit, Guanosine, mTORC1, GTPase, Cell biology, chemistry.chemical_compound, Protein structure, medicine.anatomical_structure, Lysosome, biology.protein, medicine, Signal transduction, biological phenomena, cell phenomena, and immunity, RHEB
الوصف: Complex regulation The protein kinase mTORC1 controls cellular growth in response to external signals. In the presence of nutrients, it localizes on the surface of the lysosome, where it is activated. The Raptor domain of mTORC1 binds to a complex comprising the protein Ragulator and a heterodimer of the Rag guanosine triphosphatase, which can adopt four different nucleotide conformations depending on nutrient availability. Rogala et al. determined the structure of the Raptor-Rag-Ragulator complex at 3.2-angstrom resolution by cryo–electron microscopy. The structure shows why Raptor binds only to a specific nucleotide conformation of the Rag heterodimer and suggests a model for how mTORC1 would dock onto the lysosomal surface, which is a key step in its activation. Science , this issue p. 468
وصف الملف: application/pdf
اللغة: English
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::170b43405b6612595a410c4063e1d3df
https://hdl.handle.net/1721.1/136463
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....170b43405b6612595a410c4063e1d3df
قاعدة البيانات: OpenAIRE