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Structure paper

TitleThe discovery of carboline analogs as potent MAPKAP-K2 inhibitors
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 17, Page 4664-4669, Year 2007
Publish dateMay 18, 2007 (structure data deposition date)
AuthorsWu, J.-P. / Wang, J. / Abeywardane, A. / Andersen, D. / Emmanuel, M. / Gautschi, E. / Goldberg, D.R. / Kashem, M.A. / Lukas, S. / Mao, W. ...Wu, J.-P. / Wang, J. / Abeywardane, A. / Andersen, D. / Emmanuel, M. / Gautschi, E. / Goldberg, D.R. / Kashem, M.A. / Lukas, S. / Mao, W. / Martin, L. / Morwick, T. / Moss, N. / Pargellis, C. / Patel, U.R. / Patnaude, L. / Peet, G.W. / Skow, D. / Snow, R.J. / Ward, Y. / Werneburg, B. / White, A.
External linksBioorg. Med. Chem. Lett. / PubMed:17576063
MethodsX-ray diffraction
Resolution2.9 Å
Structure data

PDB-2pzy:
Structure of MK2 Complexed with Compound 76
Method: X-RAY DIFFRACTION / Resolution: 2.9 Å

Chemicals

ChemComp-B18:
(4R)-N-[4-({[2-(DIMETHYLAMINO)ETHYL]AMINO}CARBONYL)-1,3-THIAZOL-2-YL]-4-METHYL-1-OXO-2,3,4,9-TETRAHYDRO-1H-BETA-CARBOLINE-6-CARBOXAMIDE

ChemComp-STU:
STAUROSPORINE / anticancer, antifungal, antibiotic, alkaloid*YM

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / MK2 / Protein Kinase

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