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Structure paper

TitleThe crystal structure of BRAF in complex with an organoruthenium inhibitor reveals a mechanism for inhibition of an active form of BRAF kinase.
Journal, issue, pagesBiochemistry, Vol. 48, Page 5187-5198, Year 2009
Publish dateDec 23, 2010 (structure data deposition date)
AuthorsXie, P. / Streu, C. / Qin, J. / Bregman, H. / Pagano, N. / Meggers, E. / Marmorstein, R.
External linksBiochemistry / PubMed:19371126
MethodsX-ray diffraction
Resolution3.2 Å
Structure data

PDB-3q4c:
Crystal Structure of Wild Type BRAF kinase domain in complex with organometallic inhibitor CNS292
Method: X-RAY DIFFRACTION / Resolution: 3.2 Å

Chemicals

ChemComp-RSW:
[(1,2,3,4,5,6-eta)-(1S,2R,3R,4R,5S,6S)-1-carboxycyclohexane-1,2,3,4,5,6-hexayl](chloro)(3-methyl-5,7-dioxo-6,7-dihydro-5H-pyrido[2,3-a]pyrrolo[3,4-c]carbazol-12-ide-kappa~2~N~1~,N~12~)ruthenium(1+)

Source
  • homo sapiens (human)
KeywordsTRANSFERASE/TRANSFERASE INHIBITOR / kinase / inhibitor / oncoprotein / melanoma / kinase-kinase inhibitor complex / TRANSFERASE-TRANSFERASE INHIBITOR complex

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