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TitleStructural basis for the design of bisubstrate inhibitors of protein kinase CK2 provided by complex structures with the substrate-competitive inhibitor heparin.
Journal, issue, pagesEur. J. Med. Chem., Vol. 214, Page 113223-113223, Year 2021
Publish dateDec 12, 2020 (structure data deposition date)
AuthorsSchnitzler, A. / Niefind, K.
External linksEur. J. Med. Chem. / PubMed:33571828
MethodsX-ray diffraction
Resolution1.34 - 2.55 Å
Structure data

PDB-7b8h:
Monoclinic structure of human protein kinase CK2 catalytic subunit in complex with a heparin oligo saccharide
Method: X-RAY DIFFRACTION / Resolution: 1.34 Å

PDB-7b8i:
Tetragonal structure of human protein kinase CK2 catalytic subunit in complex with a heparin oligo saccharide
Method: X-RAY DIFFRACTION / Resolution: 2.55 Å

Chemicals

ChemComp-GOL:
GLYCEROL

ChemComp-NIO:
NICOTINIC ACID / medication*YM

ChemComp-HOH:
WATER

ChemComp-SO4:
SULFATE ION

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / protein kinase CK2 / casein kinase 2 / catalytic subunit CK2alpha / heparin

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