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7AEI

Studies Towards a Reversible EGFR C797S Triple Mutant Inhibitor Series

Summary for 7AEI
Entry DOI10.2210/pdb7aei/pdb
DescriptorEpidermal growth factor receptor, 5-chloranyl-~{N}2-[4-[4-(dimethylamino)piperidin-1-yl]-2-methoxy-5-(1-methylpyrazol-4-yl)phenyl]-~{N}4-(2-dimethylphosphorylphenyl)pyrimidine-2,4-diamine (3 entities in total)
Functional Keywordsegfr, cell cycle
Biological sourceHomo sapiens (Human)
Total number of polymer chains1
Total formula weight38057.36
Authors
Hargreaves, D. (deposition date: 2020-09-17, release date: 2021-06-02, Last modification date: 2024-05-01)
Primary citationFloch, N.,Finlay, M.R.V.,Bianco, A.,Bickerton, S.,Colclough, N.,Cross, D.A.,Cuomo, E.M.,Guerot, C.M.,Hargreaves, D.,Martin, M.J.,McKerrecher, D.,O'Neill, D.J.,Orme, J.P.,Rahi, A.,Smith, P.D.,Ward, R.A.
Abstract 4451: Evaluation of the therapeutic potential of phosphine oxide pyrazole inhibitors in tumors harboring EGFR C797S mutation
Cancer Res., 79:4451-, 2019
Cited by
DOI: 10.1158/1538-7445.AM2019-4451
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.65 Å)
Structure validation

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