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-Structure paper
Title | Discovery of 5-{4-fluoro-1-[(6-methyl-2-pyridinyl)acetyl]-2,3-dihydro-1H-indol-5-yl}-7-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine (GSK2656157), a Potent and Selective PERK Inhibitor Selected for Preclinical Development |
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Journal, issue, pages | To be Published |
Publish date | Aug 12, 2013 (structure data deposition date) |
Authors | Axten, J.M. / Romeril, S.P. / Shu, A. / Ralph, J. / Medina, J.R. / Feng, Y. / Li, W.H.H. / Grant, S.W. / Heerding, D.A. / Minthorn, E. ...Axten, J.M. / Romeril, S.P. / Shu, A. / Ralph, J. / Medina, J.R. / Feng, Y. / Li, W.H.H. / Grant, S.W. / Heerding, D.A. / Minthorn, E. / Mencken, T. / Gaul, N. / Goetz, A. / Stanley, T. / Hassell, A.M. / Gampe, R.T. / Atkins, C. / Kumar, R. |
External links | Search PubMed |
Methods | X-ray diffraction |
Resolution | 2.34 Å |
Structure data | PDB-4m7i: |
Chemicals | ChemComp-27D: ChemComp-HOH: |
Source |
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Keywords | TRANSFERASE/TRANSFERASE INHIBITOR / deletion mutant / catalytic domain / TRANSFERASE-TRANSFERASE INHIBITOR complex |