8G4H
KRAS G13C complex with GDP imaged on a cryo-EM imaging scaffold
Summary for 8G4H
Entry DOI | 10.2210/pdb8g4h/pdb |
EMDB information | 29720 |
Descriptor | RCG-33 - Cryo-EM imaging scaffold subunit B fused to DARPin, GTPase KRas, GUANOSINE-5'-DIPHOSPHATE, ... (4 entities in total) |
Functional Keywords | cryoem imaging scaffold, cancer, gtpase, signaling protein |
Biological source | synthetic construct More |
Total number of polymer chains | 2 |
Total formula weight | 55359.81 |
Authors | Castells-Graells, R.,Sawaya, M.R.,Yeates, T.O. (deposition date: 2023-02-09, release date: 2023-08-09, Last modification date: 2023-09-27) |
Primary citation | Castells-Graells, R.,Meador, K.,Arbing, M.A.,Sawaya, M.R.,Gee, M.,Cascio, D.,Gleave, E.,Debreczeni, J.E.,Breed, J.,Leopold, K.,Patel, A.,Jahagirdar, D.,Lyons, B.,Subramaniam, S.,Phillips, C.,Yeates, T.O. Cryo-EM structure determination of small therapeutic protein targets at 3 angstrom -resolution using a rigid imaging scaffold. Proc.Natl.Acad.Sci.USA, 120:e2305494120-e2305494120, 2023 Cited by PubMed Abstract: Cryoelectron microscopy (Cryo-EM) has enabled structural determination of proteins larger than about 50 kDa, including many intractable by any other method, but it has largely failed for smaller proteins. Here, we obtain structures of small proteins by binding them to a rigid molecular scaffold based on a designed protein cage, revealing atomic details at resolutions reaching 2.9 Å. We apply this system to the key cancer signaling protein KRAS (19 kDa in size), obtaining four structures of oncogenic mutational variants by cryo-EM. Importantly, a structure for the key G12C mutant bound to an inhibitor drug (AMG510) reveals significant conformational differences compared to prior data in the crystalline state. The findings highlight the promise of cryo-EM scaffolds for advancing the design of drug molecules against small therapeutic protein targets in cancer and other human diseases. PubMed: 37669364DOI: 10.1073/pnas.2305494120 PDB entries with the same primary citation |
Experimental method | ELECTRON MICROSCOPY (2.87 Å) |
Structure validation
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