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Structure paper

TitleDevelopment of a potent and selective chemical probe for the pleiotropic kinase CK2.
Journal, issue, pagesCell Chem Biol, Vol. 28, Page 546-558.e10, Year 2021
Publish dateJun 2, 2020 (structure data deposition date)
AuthorsWells, C.I. / Drewry, D.H. / Pickett, J.E. / Tjaden, A. / Kramer, A. / Muller, S. / Gyenis, L. / Menyhart, D. / Litchfield, D.W. / Knapp, S. / Axtman, A.D.
External linksCell Chem Biol / PubMed:33484635
MethodsX-ray diffraction
Resolution2.171 - 2.5 Å
Structure data

PDB-6z83:
CK2 alpha bound to chemical probe SGC-CK2-1
Method: X-RAY DIFFRACTION / Resolution: 2.171 Å

PDB-6z84:
CK2 alpha bound to chemical probe SGC-CK2-1 derivative
Method: X-RAY DIFFRACTION / Resolution: 2.5 Å

Chemicals

ChemComp-SO4:
SULFATE ION

ChemComp-QBE:
~{N}-[5-[[3-cyano-7-(cyclopropylamino)-3~{H}-pyrazolo[1,5-a]pyrimidin-5-yl]amino]-2-methyl-phenyl]propanamide

ChemComp-PEG:
DI(HYDROXYETHYL)ETHER

ChemComp-HOH:
WATER

ChemComp-QB8:
~{N}-[1-[3-cyano-7-(cyclopropylamino)pyrazolo[1,5-a]pyrimidin-5-yl]indol-6-yl]ethanamide

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / Kinase / Chemical Probe / Inhibitor / Structural Genomics / Structural Genomics Consortium / SGC

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