5X2F
Crystal structure of EGFR 696-1022 T790M/V948R in complex with SKLB(6)
Summary for 5X2F
| Entry DOI | 10.2210/pdb5x2f/pdb |
| Related | 5X26 5X27 5X28 5X2A 5X2C 5X2K |
| Descriptor | Epidermal growth factor receptor, 9-cyclohexyl-N2-[4-(4-methylpiperazin-1-yl)phenyl]-N8-phenyl-purine-2,8-diamine (3 entities in total) |
| Functional Keywords | egfr, t790m, v948r, sklb, transferase |
| Biological source | Homo sapiens (Human) |
| Cellular location | Cell membrane; Single-pass type I membrane protein. Isoform 2: Secreted: P00533 |
| Total number of polymer chains | 4 |
| Total formula weight | 152828.88 |
| Authors | Yun, C.H. (deposition date: 2017-01-31, release date: 2018-02-07, Last modification date: 2024-03-27) |
| Primary citation | Zhu, S.J.,Zhao, P.,Yang, J.,Ma, R.,Yan, X.E.,Yang, S.Y.,Yang, J.W.,Yun, C.H. Structural insights into drug development strategy targeting EGFR T790M/C797S. Oncotarget, 9:13652-13665, 2018 Cited by PubMed Abstract: Treatment of non-small-cell lung cancers (NSCLCs) harboring primary EGFR oncogenic mutations such as L858R and exon 19 deletion delE746_A750 (Del-19) using gefitinib/erlotinib ultimately fails due to the emergence of T790M mutation. Though WZ4002/CO-1686/AZD9291 are effective in overcoming EGFR T790M by targeting Cys797 via covalent bonding, their efficacy is again limited due to the emergence of C797S mutation. New agents effectively inhibiting EGFR T790M without covalent linkage through Cys 797 may solve this problem. We presented here crystal structures of EGFR activating/drug-resistant mutants in complex with a panel of reversible inhibitors along with mutagenesis and enzyme kinetic data. These data revealed a previously un-described hydrophobic clamp structure in the EGFR kinase which may be exploited to facilitate development of next generation drugs targeting EGFR T790M with or without concomitant C797S. Interestingly, mutations in the hydrophobic clamp that hinder drug binding often also weaken ATP binding and/or abolish kinase activity, thus do not readily result in resistance to the drugs. PubMed: 29568384DOI: 10.18632/oncotarget.24113 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (2.2 Å) |
Structure validation
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