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6U2G

BRAF-MEK complex with AMP-PCP bound to BRAF

Summary for 6U2G
Entry DOI10.2210/pdb6u2g/pdb
DescriptorDual specificity mitogen-activated protein kinase kinase 1, Serine/threonine-protein kinase B-raf, PHOSPHOMETHYLPHOSPHONIC ACID ADENYLATE ESTER, ... (6 entities in total)
Functional Keywordskinase, amp-pcp, dimer, signaling protei, transferase
Biological sourceHomo sapiens (Human)
More
Total number of polymer chains2
Total formula weight79879.59
Authors
Liau, N.P.D.,Wendorff, T.,Hymowitz, S.,Sudhamsu, J. (deposition date: 2019-08-19, release date: 2019-08-28, Last modification date: 2023-10-11)
Primary citationLiau, N.P.D.,Wendorff, T.J.,Quinn, J.G.,Steffek, M.,Phung, W.,Liu, P.,Tang, J.,Irudayanathan, F.J.,Izadi, S.,Shaw, A.S.,Malek, S.,Hymowitz, S.G.,Sudhamsu, J.
Negative regulation of RAF kinase activity by ATP is overcome by 14-3-3-induced dimerization.
Nat.Struct.Mol.Biol., 27:134-141, 2020
Cited by
PubMed Abstract: The RAS-RAF-MEK-ERK signaling axis is frequently activated in human cancers. Physiological concentrations of ATP prevent formation of RAF kinase-domain (RAF) dimers that are critical for activity. Here we present a 2.9-Å-resolution crystal structure of human BRAF in complex with MEK and the ATP analog AMP-PCP, revealing interactions between BRAF and ATP that induce an inactive, monomeric conformation of BRAF. We also determine how 14-3-3 relieves the negative regulatory effect of ATP through a 2.5-Å-resolution crystal structure of the BRAF-14-3-3 complex, in which dimeric 14-3-3 enforces a dimeric BRAF assembly to increase BRAF activity. Our data suggest that most oncogenic BRAF mutations alter interactions with ATP and counteract the negative effects of ATP binding by lowering the threshold for RAF dimerization and pathway activation. Our study establishes a framework for rationalizing oncogenic BRAF mutations and provides new avenues for improved RAF-inhibitor discovery.
PubMed: 31988522
DOI: 10.1038/s41594-019-0365-0
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.886 Å)
Structure validation

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數據於2024-11-06公開中

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