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Structure paper

TitleImidazo[4,5-b]pyridine inhibitors of B-Raf kinase.
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 23, Page 5896-5899, Year 2013
Publish dateAug 19, 2013 (structure data deposition date)
AuthorsNewhouse, B.J. / Wenglowsky, S. / Grina, J. / Laird, E.R. / Voegtli, W.C. / Ren, L. / Ahrendt, K. / Buckmelter, A. / Gloor, S.L. / Klopfenstein, N. ...Newhouse, B.J. / Wenglowsky, S. / Grina, J. / Laird, E.R. / Voegtli, W.C. / Ren, L. / Ahrendt, K. / Buckmelter, A. / Gloor, S.L. / Klopfenstein, N. / Rudolph, J. / Wen, Z. / Li, X. / Feng, B.
External linksBioorg. Med. Chem. Lett. / PubMed:24042006
MethodsX-ray diffraction
Resolution3.6 Å
Structure data

PDB-4mbj:
Human B-Raf Kinase Domain in Complex with an Imidazopyridine-based Inhibitor
Method: X-RAY DIFFRACTION / Resolution: 3.6 Å

Chemicals

ChemComp-DFS:
2,6-difluoro-N-(1H-imidazo[4,5-b]pyridin-6-yl)-3-[(propylsulfonyl)amino]benzamide

Source
  • homo sapiens (human)
KeywordsTRANSFERASE/TRANSFERASE INHIBITOR / Kinase / TRANSFERASE-TRANSFERASE INHIBITOR complex

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