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8D73

Crystal Structure of EGFR LRTM with compound 7

Summary for 8D73
Entry DOI10.2210/pdb8d73/pdb
DescriptorEpidermal growth factor receptor, GLYCEROL, (3S,4R)-3-fluoro-1-(4-{[4-(methylamino)-1-(propan-2-yl)pyrido[3,4-d]pyridazin-7-yl]amino}pyrimidin-2-yl)piperidin-4-ol, ... (4 entities in total)
Functional Keywordsprotein kinase, inhibitor, kinase domain, mutation, signaling protein
Biological sourceHomo sapiens (human)
Total number of polymer chains2
Total formula weight80604.67
Authors
Kim, J.L. (deposition date: 2022-06-07, release date: 2022-07-27, Last modification date: 2023-10-18)
Primary citationEno, M.S.,Brubaker, J.D.,Campbell, J.E.,De Savi, C.,Guzi, T.J.,Williams, B.D.,Wilson, D.,Wilson, K.,Brooijmans, N.,Kim, J.,Ozen, A.,Perola, E.,Hsieh, J.,Brown, V.,Fetalvero, K.,Garner, A.,Zhang, Z.,Stevison, F.,Woessner, R.,Singh, J.,Timsit, Y.,Kinkema, C.,Medendorp, C.,Lee, C.,Albayya, F.,Zalutskaya, A.,Schalm, S.,Dineen, T.A.
Discovery of BLU-945, a Reversible, Potent, and Wild-Type-Sparing Next-Generation EGFR Mutant Inhibitor for Treatment-Resistant Non-Small-Cell Lung Cancer.
J.Med.Chem., 65:9662-9677, 2022
Cited by
PubMed: 35838760
DOI: 10.1021/acs.jmedchem.2c00704
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.17 Å)
Structure validation

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