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Structure paper

TitleIbrutinib targets mutant-EGFR kinase with a distinct binding conformation.
Journal, issue, pagesOncotarget, Vol. 7, Page 69760-69769, Year 2016
Publish dateNov 21, 2017 (structure data deposition date)
AuthorsWang, A. / Yan, X.E. / Wu, H. / Wang, W. / Hu, C. / Chen, C. / Zhao, Z. / Zhao, P. / Li, X. / Wang, L. ...Wang, A. / Yan, X.E. / Wu, H. / Wang, W. / Hu, C. / Chen, C. / Zhao, Z. / Zhao, P. / Li, X. / Wang, L. / Wang, B. / Ye, Z. / Wang, J. / Wang, C. / Zhang, W. / Gray, N.S. / Weisberg, E.L. / Chen, L. / Liu, J. / Yun, C.H. / Liu, Q.
External linksOncotarget / PubMed:27626175
MethodsX-ray diffraction
Resolution1.95 Å
Structure data

PDB-5yu9:
Crystal structure of EGFR 696-1022 T790M in complex with Ibrutinib
Method: X-RAY DIFFRACTION / Resolution: 1.95 Å

Chemicals

ChemComp-1E8:
1-{(3R)-3-[4-amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]piperidin-1-yl}prop-2-en-1-one

ChemComp-CL:
Unknown entry

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsONCOPROTEIN / EGFR / T790M / ibrutinib / inhibitor

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