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5J9Z

EGFR-T790M in complex with pyrazolopyrimidine inhibitor 1a

Summary for 5J9Z
Entry DOI10.2210/pdb5j9z/pdb
DescriptorEpidermal growth factor receptor, (R)-1-(3-(4-amino-3-(1-methyl-1H-indol-3-yl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)piperidin-1-yl)prop-2-en-1-one (3 entities in total)
Functional Keywordstyrosine kinase, covalent inhibitor, drug resistance, transferase
Biological sourceHomo sapiens (Human)
Total number of polymer chains1
Total formula weight37550.50
Authors
Becker, C.,Engel, J.,Rauh, D. (deposition date: 2016-04-11, release date: 2016-08-17, Last modification date: 2024-01-10)
Primary citationEngel, J.,Becker, C.,Lategahn, J.,Keul, M.,Ketzer, J.,Muhlenberg, T.,Kollipara, L.,Schultz-Fademrecht, C.,Zahedi, R.P.,Bauer, S.,Rauh, D.
Insight into the Inhibition of Drug-Resistant Mutants of the Receptor Tyrosine Kinase EGFR.
Angew.Chem.Int.Ed.Engl., 55:10909-10912, 2016
Cited by
PubMed: 27496389
DOI: 10.1002/anie.201605011
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.5 Å)
Structure validation

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