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6VHP

Wild type EGFR in complex with LN2899

Summary for 6VHP
Entry DOI10.2210/pdb6vhp/pdb
DescriptorEpidermal growth factor receptor, N-{3-[(4-{4-(4-fluorophenyl)-2-[(2-methoxyethyl)sulfanyl]-1H-imidazol-5-yl}pyridin-2-yl)amino]-4-methoxyphenyl}propanamide (2 entities in total)
Functional Keywordsegfr, inhibitor, transferase-transferase inhibitor complex, transferase/transferase inhibitor
Biological sourceHomo sapiens (Human)
Total number of polymer chains1
Total formula weight37825.74
Authors
Heppner, D.E.,Eck, M.J. (deposition date: 2020-01-10, 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 (3.6 Å)
Structure validation

217705

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