7MFF

Dimeric (BRAF)2:(14-3-3)2 complex bound to SB590885 Inhibitor

Summary for 7MFF

• Entry DOI: 10.2210/pdb7mff/pdb
• EMDB information: 23815
• Descriptor: 14-3-3 protein zeta/delta, Serine/threonine-protein kinase B-raf, (1Z)-5-(2-{4-[2-(DIMETHYLAMINO)ETHOXY]PHENYL}-5-PYRIDIN-4-YL-1H-IMIDAZOL-4-YL)INDAN-1-ONE OXIME (3 entities in total)
• Functional Keywords: b-raf, 14-3-3, b-raf complex, b-raf dimer, active b-raf, sb590885, signaling protein, serine/threonine-protein kinase b-raf
• Biological source: Homo sapiens (Human); More
• Total number of polymer chains: 4
• Total formula weight: 225856.65

Authors

Martinez Fiesco, J.A.,Ping, Z.,Durrant, D.E.,Morrison, D.K. (deposition date: 2021-04-09, release date: 2022-01-26, Last modification date: 2024-11-20)

Primary citation

Martinez Fiesco, J.A.,Durrant, D.E.,Morrison, D.K.,Zhang, P.
Structural insights into the BRAF monomer-to-dimer transition mediated by RAS binding.
Nat Commun, 13:486-486, 2022

PubMed Abstract: RAF kinases are essential effectors of RAS, but how RAS binding initiates the conformational changes needed for autoinhibited RAF monomers to form active dimers has remained unclear. Here, we present cryo-electron microscopy structures of full-length BRAF complexes derived from mammalian cells: autoinhibited, monomeric BRAF:14-3-3:MEK and BRAF:14-3-3 complexes, and an inhibitor-bound, dimeric BRAF:14-3-3 complex, at 3.7, 4.1, and 3.9 Å resolution, respectively. In both autoinhibited, monomeric structures, the RAS binding domain (RBD) of BRAF is resolved, revealing that the RBD forms an extensive contact interface with the 14-3-3 protomer bound to the BRAF C-terminal site and that key basic residues required for RBD-RAS binding are exposed. Moreover, through structure-guided mutational studies, our findings indicate that RAS-RAF binding is a dynamic process and that RBD residues at the center of the RBD:14-3-3 interface have a dual function, first contributing to RAF autoinhibition and then to the full spectrum of RAS-RBD interactions.

PubMed: 35078985
DOI: 10.1038/s41467-022-28084-3

Experimental method

ELECTRON MICROSCOPY (3.89 Å)