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-Structure paper
Title | Development of thioquinazolinones, allosteric Chk1 kinase inhibitors. |
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Journal, issue, pages | Bioorg. Med. Chem. Lett., Vol. 19, Page 1240-1244, Year 2009 |
Publish date | Nov 14, 2008 (structure data deposition date) |
Authors | Converso, A. / Hartingh, T. / Garbaccio, R.M. / Tasber, E. / Rickert, K. / Fraley, M.E. / Yan, Y. / Kreatsoulas, C. / Stirdivant, S. / Drakas, B. ...Converso, A. / Hartingh, T. / Garbaccio, R.M. / Tasber, E. / Rickert, K. / Fraley, M.E. / Yan, Y. / Kreatsoulas, C. / Stirdivant, S. / Drakas, B. / Walsh, E.S. / Hamilton, K. / Buser, C.A. / Mao, X. / Abrams, M.T. / Beck, S.C. / Tao, W. / Lobell, R. / Sepp-Lorenzino, L. / Zugay-Murphy, J. / Sardana, V. / Munshi, S.K. / Jezequel-Sur, S.M. / Zuck, P.D. / Hartman, G.D. |
External links | Bioorg. Med. Chem. Lett. / PubMed:19155174 |
Methods | X-ray diffraction |
Resolution | 1.9 Å |
Structure data | PDB-3f9n: |
Chemicals | ChemComp-38M: ChemComp-SO4: ChemComp-HOH: |
Source |
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Keywords | TRANSFERASE / chek1 / chk1 / kinase / cell cycle checkpoint / ATP-binding / Cytoplasm / DNA damage / DNA repair / Nucleotide-binding / Nucleus / Phosphoprotein / Polymorphism / Serine/threonine-protein kinase / Ubl conjugation |