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6JRX

EGFR T790M/C797S in complex with compound 6i

Summary for 6JRX
Entry DOI10.2210/pdb6jrx/pdb
DescriptorEpidermal growth factor receptor, N-{trans-4-[3-(2-chlorophenyl)-7-{[3-methyl-4-(4-methylpiperazin-1-yl)phenyl]amino}-2-oxo-3,4-dihydropyrimido[4,5-d]pyrimidin-1(2H)-yl]cyclohexyl}propanamide (3 entities in total)
Functional Keywordsegfr t790m/c797s, inhibitor, complex, transferase
Biological sourceHomo sapiens (Human)
Total number of polymer chains1
Total formula weight38251.72
Authors
Zhu, S.J.,Yun, C.H. (deposition date: 2019-04-06, release date: 2020-04-15, Last modification date: 2024-03-27)
Primary citationYang, J.,Shibu, M.A.,Kong, L.,Luo, J.,BadrealamKhan, F.,Huang, Y.,Tu, Z.C.,Yun, C.H.,Huang, C.Y.,Ding, K.,Lu, X.
Design, Synthesis, and Structure-Activity Relationships of 1,2,3-Triazole Benzenesulfonamides as New Selective Leucine-Zipper and Sterile-alpha Motif Kinase (ZAK) Inhibitors.
J.Med.Chem., 63:2114-2130, 2020
Cited by
PubMed: 31244114
DOI: 10.1021/acs.jmedchem.9b00664
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.201 Å)
Structure validation

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