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TitleStructural Studies of Fourth-Generation EGFR Inhibitors Reveal Insights into Selective T790M and C797S Targeting.
Journal, issue, pagesAcs Med. Chem. Lett., Year 2026
Publish dateSep 12, 2024 (structure data deposition date)
AuthorsDamghani, T. / Song, S. / Lin, K.S. / Li, J. / Heppner, D.E.
External linksAcs Med. Chem. Lett. / PubMed:41684669
MethodsX-ray diffraction
Resolution2.13 - 2.4 Å
Structure data

PDB-9dm8:
EGFR wildtype in complex with BI-8128
Method: X-RAY DIFFRACTION / Resolution: 2.13 Å

PDB-9ngp:
EGFR wildtype in complex with BI-4732
Method: X-RAY DIFFRACTION / Resolution: 2.4 Å

Chemicals

PDB-1a6k:
AQUOMET-MYOGLOBIN, ATOMIC RESOLUTION

ChemComp-MES:
2-(N-MORPHOLINO)-ETHANESULFONIC ACID / pH buffer*YM

ChemComp-HOH:
WATER

PDB-1bx7:
HIRUSTASIN FROM HIRUDO MEDICINALIS AT 1.2 ANGSTROMS

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / Kinase / drug discovery / cancer / Drug Resistance

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