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9O5E

The dimeric KICSTOR-GATOR1 supercomplex

This is a non-PDB format compatible entry.
Summary for 9O5E
Entry DOI10.2210/pdb9o5e/pdb
EMDB information70141
DescriptorGATOR complex protein NPRL3, GATOR complex protein NPRL2, KICSTOR complex protein SZT2, ... (4 entities in total)
Functional Keywordslysosome, gator1, kicstor, cell growth, amino acid sensing, mtor, kptn, itfg2, c12orf66, szt2, nprl2, nprl3, depdc5, cell cycle
Biological sourceHomo sapiens (human)
More
Total number of polymer chains8
Total formula weight1350325.50
Authors
Bayly-Jones, C.,Lupton, C.J.,Chang, Y.G.,Ellisdon, A.M. (deposition date: 2025-04-10, release date: 2026-01-21)
Primary citationLupton, 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: 41512879
DOI: 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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PDB entries from 2026-01-14

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