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7KY0

Inactive conformation of EGFR (T790M/V948R) kinase in complex with BI-4020

Summary for 7KY0
Entry DOI10.2210/pdb7ky0/pdb
DescriptorEpidermal growth factor receptor, (20R)-10,15,20-trimethyl-2-[(4-methylpiperazin-1-yl)methyl]-18,19,20,21-tetrahydro-15H,17H-12,8-(metheno)pyrazolo[3',4':2,3][1,5,10,12]oxatriazacycloheptadecino[12,11-a]benzimidazol-7(6H)-one (2 entities in total)
Functional Keywordsegfr, kinase, inhibitor, macrocycle, transferase, transferase-transferase inhibitor complex, transferase/transferase inhibitor
Biological sourceHomo sapiens (Human)
Total number of polymer chains4
Total formula weight153069.09
Authors
Beyett, T.S.,Eck, M.J. (deposition date: 2020-12-06, release date: 2022-01-19, Last modification date: 2024-05-29)
Primary citationBeyett, T.S.,Rana, J.K.,Schaeffner, I.K.,Heppner, D.E.,Eck, M.J.
Structural Analysis of the Macrocyclic Inhibitor BI-4020 Binding to EGFR Kinase.
Chemmedchem, :e202300343-e202300343, 2024
Cited by
PubMed: 38523074
DOI: 10.1002/cmdc.202300343
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (3.1 Å)
Structure validation

220472

數據於2024-05-29公開中

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