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5GMP

Crystal structure of EGFR 696-1022 T790M in complex with XTF-262

Summary for 5GMP
Entry DOI10.2210/pdb5gmp/pdb
DescriptorEpidermal growth factor receptor, N-[3-[2-[[2-methoxy-4-(4-methylpiperazin-1-yl)phenyl]amino]-5-methyl-7-oxidanylidene-pyrido[2,3-d]pyrimidin-8-yl]phenyl]prop-2-enamide (3 entities in total)
Functional Keywordsegfr, t790m, xtf-262, inhibitor, transferase
Biological sourceHomo sapiens (Human)
Cellular locationCell membrane; Single-pass type I membrane protein. Isoform 2: Secreted: P00533
Total number of polymer chains1
Total formula weight38176.20
Authors
Yan, X.E.,Yun, C.H. (deposition date: 2016-07-14, release date: 2017-06-28, Last modification date: 2023-11-08)
Primary citationYu, L.,Huang, M.,Xu, T.,Tong, L.,Yan, X.E.,Zhang, Z.,Xu, Y.,Yun, C.,Xie, H.,Ding, K.,Lu, X.
A structure-guided optimization of pyrido[2,3-d]pyrimidin-7-ones as selective inhibitors of EGFR(L858R/T790M) mutant with improved pharmacokinetic properties.
Eur J Med Chem, 126:1107-1117, 2017
Cited by
PubMed: 28033579
DOI: 10.1016/j.ejmech.2016.12.006
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.797 Å)
Structure validation

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