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8G4H

KRAS G13C complex with GDP imaged on a cryo-EM imaging scaffold

Summary for 8G4H
Entry DOI10.2210/pdb8g4h/pdb
EMDB information29720
DescriptorRCG-33 - Cryo-EM imaging scaffold subunit B fused to DARPin, GTPase KRas, GUANOSINE-5'-DIPHOSPHATE, ... (4 entities in total)
Functional Keywordscryoem imaging scaffold, cancer, gtpase, signaling protein
Biological sourcesynthetic construct
More
Total number of polymer chains2
Total formula weight55359.81
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 citationCastells-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: 37669364
DOI: 10.1073/pnas.2305494120
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2.87 Å)
Structure validation

226707

數據於2024-10-30公開中

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