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3IQV

Crystal Structure of human 14-3-3 sigma in Complex with Raf1 peptide (6mer) and stabilisator Fusicoccin

Summary for 3IQV
Entry DOI10.2210/pdb3iqv/pdb
Related3cu8 3iqj 3iqu
Descriptor14-3-3 protein sigma, 6-mer peptide from RAF proto-oncogene serine/threonine-protein kinase, FUSICOCCIN, ... (6 entities in total)
Functional Keywordssignal transduction, nucleus, phosphoprotein, secreted, protein binding, signaling protein
Biological sourceHomo sapiens (human)
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Cellular locationCytoplasm: P31947 P04049
Total number of polymer chains2
Total formula weight28167.54
Authors
Ottmann, C.,Weyand, M. (deposition date: 2009-08-21, release date: 2010-09-01, Last modification date: 2023-11-22)
Primary citationMolzan, M.,Schumacher, B.,Ottmann, C.,Baljuls, A.,Polzien, L.,Weyand, M.,Thiel, P.,Rose, R.,Rose, M.,Kuhenne, P.,Kaiser, M.,Rapp, U.R.,Kuhlmann, J.,Ottmann, C.
Impaired binding of 14-3-3 to C-RAF in Noonan syndrome suggests new approaches in diseases with increased Ras signaling.
Mol.Cell.Biol., 30:4698-4711, 2010
Cited by
PubMed Abstract: The Ras-RAF-mitogen-activated protein kinase (Ras-RAF-MAPK) pathway is overactive in many cancers and in some developmental disorders. In one of those disorders, namely, Noonan syndrome, nine activating C-RAF mutations cluster around Ser(259), a regulatory site for inhibition by 14-3-3 proteins. We show that these mutations impair binding of 14-3-3 proteins to C-RAF and alter its subcellular localization by promoting Ras-mediated plasma membrane recruitment of C-RAF. By presenting biophysical binding data, the 14-3-3/C-RAFpS(259) crystal structure, and cellular analyses, we indicate a mechanistic link between a well-described human developmental disorder and the impairment of a 14-3-3/target protein interaction. As a broader implication of these findings, modulating the C-RAFSer(259)/14-3-3 protein-protein interaction with a stabilizing small molecule may yield a novel potential approach for treatment of diseases resulting from an overactive Ras-RAF-MAPK pathway.
PubMed: 20679480
DOI: 10.1128/MCB.01636-09
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.2 Å)
Structure validation

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