Summary for 9O5E
| Entry DOI | 10.2210/pdb9o5e/pdb |
| EMDB information | 70141 |
| Descriptor | GATOR complex protein NPRL3, GATOR complex protein NPRL2, KICSTOR complex protein SZT2, ... (4 entities in total) |
| Functional Keywords | lysosome, gator1, kicstor, cell growth, amino acid sensing, mtor, kptn, itfg2, c12orf66, szt2, nprl2, nprl3, depdc5, cell cycle |
| Biological source | Homo sapiens (human) More |
| Total number of polymer chains | 8 |
| Total formula weight | 1350325.50 |
| Authors | Bayly-Jones, C.,Lupton, C.J.,Chang, Y.G.,Ellisdon, A.M. (deposition date: 2025-04-10, release date: 2026-01-21) |
| Primary citation | Lupton, C.J.,Bayly-Jones, C.,Dong, S.,Lam, T.,Luo, W.,Jones, G.D.,Mastos, C.,Frescher, N.J.,Lim, S.S.,Keen, A.C.,Formosa, L.E.,Venugopal, H.,Chang, Y.G.,Halls, M.L.,Ellisdon, A.M. Structure of the lysosomal KICSTOR-GATOR1-SAMTOR nutrient-sensing supercomplex. Cell, 2026 Cited by PubMed Abstract: The guanosine triphosphate (GTP)-bound state of the heterodimeric Rag GTPases functions as a molecular switch regulating mechanistic target of rapamycin complex 1 (mTORC1) activation at the lysosome downstream of amino acid fluctuations. Under low amino acid conditions, GTPase-activating protein (GAP) activity toward Rags 1 (GATOR1) promotes RagA GTP hydrolysis, preventing mTORC1 activation. KICSTOR recruits and regulates GATOR1 at the lysosome by undefined mechanisms. Here, we resolve the KICSTOR-GATOR1 structure, revealing a striking ∼60-nm crescent-shaped assembly. GATOR1 anchors to KICSTOR via an extensive interface, and mutations that disrupt this interaction impair mTORC1 regulation. The S-adenosylmethionine sensor SAMTOR binds KICSTOR in a manner incompatible with metabolite binding, providing structural insight into methionine sensing via SAMTOR-KICSTOR association. We discover that KICSTOR and GATOR1 form a dimeric supercomplex. This assembly restricts GATOR1 to an orientation that favors the low-affinity active GAP mode of Rag GTPase engagement while sterically restricting access to the high-affinity inhibitory mode, consistent with a model of an active lysosomal GATOR1 docking complex. PubMed: 41512879DOI: 10.1016/j.cell.2025.12.005 PDB entries with the same primary citation |
| Experimental method | ELECTRON MICROSCOPY (5 Å) |
Structure validation
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