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7T4I

Crystal Structure of wild type EGFR in complex with TAK-788

Summary for 7T4I
Entry DOI10.2210/pdb7t4i/pdb
DescriptorEpidermal growth factor receptor, propan-2-yl 2-[[4-[2-(dimethylamino)ethyl-methyl-amino]-2-methoxy-5-(propanoylamino)phenyl]amino]-4-(1-methylindol-3-yl)pyrimidine-5-carboxylate (3 entities in total)
Functional Keywordskinase, inhibitor, complex, covalent, hydrolase
Biological sourceHomo sapiens (human)
Total number of polymer chains1
Total formula weight37948.90
Authors
Skene, R.J.,Lane, W. (deposition date: 2021-12-10, release date: 2022-12-07, Last modification date: 2023-10-25)
Primary citationHuang, W.S.,Li, F.,Gong, Y.,Zhang, Y.,Youngsaye, W.,Xu, Y.,Zhu, X.,Greenfield, M.T.,Kohlmann, A.,Taslimi, P.M.,Toms, A.,Zech, S.G.,Zhou, T.,Das, B.,Jang, H.G.,Tugnait, M.,Ye, Y.E.,Gonzalvez, F.,Baker, T.E.,Nadworny, S.,Ning, Y.,Wardwell, S.D.,Zhang, S.,Gould, A.E.,Hu, Y.,Lane, W.,Skene, R.J.,Zou, H.,Clackson, T.,Narasimhan, N.I.,Rivera, V.M.,Dalgarno, D.C.,Shakespeare, W.C.
Discovery of mobocertinib, a potent, oral inhibitor of EGFR exon 20 insertion mutations in non-small cell lung cancer.
Bioorg.Med.Chem.Lett., 80:129084-129084, 2022
Cited by
PubMed: 36423823
DOI: 10.1016/j.bmcl.2022.129084
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.61 Å)
Structure validation

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