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Structure paper

TitleSelective RET inhibitor TAS0953/HM06
Journal, issue, pagesTo be published
Publish dateJan 8, 2021 (structure data deposition date)
AuthorsMiyazaki, I. / Ishida, K. / Suzuki, T.
External linksSearch PubMed
MethodsX-ray diffraction
Resolution1.64 - 2.75 Å
Structure data

PDB-7du8:
Crystal structure of human Proto-oncogene tyrosine-protein kinase receptor Ret in complex with Selpercatinib
Method: X-RAY DIFFRACTION / Resolution: 2.75 Å

PDB-7du9:
Crystal structure of human Proto-oncogene tyrosine-protein kinase receptor Ret in complex with Pralsetinib
Method: X-RAY DIFFRACTION / Resolution: 2.31 Å

PDB-7dua:
Crystal structure of human Proto-oncogene tyrosine-protein kinase receptor Ret in complex with 4-amino-7-(1-methylcyclopropyl)-N-(5-methyl-1H-pyrazol-3-yl)pyrrolo[2,3-d]pyrimidine-5-carboxamide
Method: X-RAY DIFFRACTION / Resolution: 1.64 Å

Chemicals

ChemComp-Q6G:
Selpercatinib

ChemComp-HOH:
WATER

ChemComp-Q4J:
Pralsetinib

ChemComp-HJ0:
4-azanyl-7-(1-methylcyclopropyl)-~{N}-(5-methyl-1~{H}-pyrazol-3-yl)pyrrolo[2,3-d]pyrimidine-5-carboxamide

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / TYROSINE-PROTEIN KINASE

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