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6SFR

SOS1 in Complex with Inhibitor BI-68BS

Summary for 6SFR
Entry DOI10.2210/pdb6sfr/pdb
Related6SCM
DescriptorSon of sevenless homolog 1, IMIDAZOLE, 6,7-dimethoxy-~{N}-[(1~{R})-1-phenylethyl]quinazolin-4-amine, ... (4 entities in total)
Functional Keywordsoncology, exchange factor, protein-ligand complex, oncoprotein
Biological sourceHomo sapiens (Human)
Total number of polymer chains2
Total formula weight115101.63
Authors
Kessler, D.,Fischer, G.,Ramharter, J. (deposition date: 2019-08-02, release date: 2020-08-26, Last modification date: 2021-06-02)
Primary citationHofmann, M.H.,Gmachl, M.,Ramharter, J.,Savarese, F.,Gerlach, D.,Marszalek, J.R.,Sanderson, M.P.,Kessler, D.,Trapani, F.,Arnhof, H.,Rumpel, K.,Botesteanu, D.A.,Ettmayer, P.,Gerstberger, T.,Kofink, C.,Wunberg, T.,Zoephel, A.,Fu, S.C.,Teh, J.L.,Bottcher, J.,Pototschnig, N.,Schachinger, F.,Schipany, K.,Lieb, S.,Vellano, C.P.,O'Connell, J.C.,Mendes, R.L.,Moll, J.,Petronczki, M.,Heffernan, T.P.,Pearson, M.,McConnell, D.B.,Kraut, N.
BI-3406, a Potent and Selective SOS1-KRAS Interaction Inhibitor, Is Effective in KRAS-Driven Cancers through Combined MEK Inhibition.
Cancer Discov, 11:142-157, 2021
Cited by
PubMed: 32816843
DOI: 10.1158/2159-8290.CD-20-0142
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.917 Å)
Structure validation

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