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TitleHighly Selective PTK2 Proteolysis Targeting Chimeras to Probe Focal Adhesion Kinase Scaffolding Functions.
Journal, issue, pagesJ. Med. Chem., Vol. 62, Page 2508-2520, Year 2019
Publish dateNov 21, 2018 (structure data deposition date)
AuthorsPopow, J. / Arnhof, H. / Bader, G. / Berger, H. / Ciulli, A. / Covini, D. / Dank, C. / Gmaschitz, T. / Greb, P. / Karolyi-Ozguer, J. ...Popow, J. / Arnhof, H. / Bader, G. / Berger, H. / Ciulli, A. / Covini, D. / Dank, C. / Gmaschitz, T. / Greb, P. / Karolyi-Ozguer, J. / Koegl, M. / McConnell, D.B. / Pearson, M. / Rieger, M. / Rinnenthal, J. / Roessler, V. / Schrenk, A. / Spina, M. / Steurer, S. / Trainor, N. / Traxler, E. / Wieshofer, C. / Zoephel, A. / Ettmayer, P.
External linksJ. Med. Chem. / PubMed:30739444
MethodsX-ray diffraction
Resolution1.99 Å
Structure data

PDB-6i8z:
Crystal structure of PTK2 in complex with BI-4464.
Method: X-RAY DIFFRACTION / Resolution: 1.99 Å

Chemicals

ChemComp-H82:
3-methoxy-~{N}-(1-methylpiperidin-1-ium-4-yl)-4-[[4-[(3-oxidanylidene-1,2-dihydroinden-4-yl)oxy]-5-(trifluoromethyl)pyrimidin-2-yl]amino]benzamide

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / Inhibitor / Protein kinase

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