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6V6K

EGFR(T790M/V948R) in complex with LN2057

Summary for 6V6K
Entry DOI10.2210/pdb6v6k/pdb
DescriptorEpidermal growth factor receptor, CHLORIDE ION, N-[3-({4-[4-(4-fluorophenyl)-2-(methylsulfanyl)-1H-imidazol-5-yl]pyridin-2-yl}amino)-4-methoxyphenyl]propanamide, ... (4 entities in total)
Functional Keywordsegfr, inhibitor, transferase-transferase inhibitor complex, transferase/transferase inhibitor
Biological sourceHomo sapiens (Human)
Total number of polymer chains8
Total formula weight303242.34
Authors
Heppner, D.E.,Eck, M.J. (deposition date: 2019-12-05, release date: 2020-04-22, Last modification date: 2023-10-11)
Primary citationHeppner, D.E.,Gunther, M.,Wittlinger, F.,Laufer, S.A.,Eck, M.J.
Structural Basis for EGFR Mutant Inhibition by Trisubstituted Imidazole Inhibitors.
J.Med.Chem., 63:4293-4305, 2020
Cited by
PubMed: 32243152
DOI: 10.1021/acs.jmedchem.0c00200
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.2 Å)
Structure validation

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