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TitlePotent and Selective Inhibitors of CK2 Kinase Identified through Structure-Guided Hybridization.
Journal, issue, pagesACS Med Chem Lett, Vol. 3, Page 278-283, Year 2012
Publish dateOct 10, 2011 (structure data deposition date)
AuthorsDowling, J.E. / Chuaqui, C. / Pontz, T.W. / Lyne, P.D. / Larsen, N.A. / Block, M.H. / Chen, H. / Su, N. / Wu, A. / Russell, D. ...Dowling, J.E. / Chuaqui, C. / Pontz, T.W. / Lyne, P.D. / Larsen, N.A. / Block, M.H. / Chen, H. / Su, N. / Wu, A. / Russell, D. / Pollard, H. / Lee, J.W. / Peng, B. / Thakur, K. / Ye, Q. / Zhang, T. / Brassil, P. / Racicot, V. / Bao, L. / Denz, C.R. / Cooke, E.
External linksACS Med Chem Lett / PubMed:24900464
MethodsX-ray diffraction
Resolution2.2 Å
Structure data

PDB-3u4u:
Casein kinase 2 in complex with AZ-Inhibitor
Method: X-RAY DIFFRACTION / Resolution: 2.2 Å

Chemicals

ChemComp-LNH:
3-{5-(acetylamino)-3-[3-cyano-7-(cyclopropylamino)pyrazolo[1,5-a]pyrimidin-5-yl]-1H-indol-1-yl}propanoic acid

ChemComp-CL:
Unknown entry

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTransferase/Transferase Inhibitor / Kinase / Transferase / Inhibitor binding / Transferase-Transferase Inhibitor complex

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