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Title | Discovery and Characterization of the Potent and Highly Selective 1,7-Naphthyridine-Based Inhibitors BAY-091 and BAY-297 of the Kinase PIP4K2A. |
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Journal, issue, pages | J. Med. Chem., Vol. 64, Page 15883-15911, Year 2021 |
Publish date | Apr 7, 2020 (structure data deposition date) |
Authors | Wortmann, L. / Brauer, N. / Holton, S.J. / Irlbacher, H. / Weiske, J. / Lechner, C. / Meier, R. / Karen, J. / Sioberg, C.B. / Putter, V. ...Wortmann, L. / Brauer, N. / Holton, S.J. / Irlbacher, H. / Weiske, J. / Lechner, C. / Meier, R. / Karen, J. / Sioberg, C.B. / Putter, V. / Christ, C.D. / Ter Laak, A. / Lienau, P. / Lesche, R. / Nicke, B. / Cheung, S.H. / Bauser, M. / Haegebarth, A. / von Nussbaum, F. / Mumberg, D. / Lemos, C. |
External links | J. Med. Chem. / PubMed:34699202 |
Methods | X-ray diffraction |
Resolution | 1.95 - 2.5 Å |
Structure data | PDB-6ym3: PDB-6ym4: PDB-6ym5: |
Chemicals | ChemComp-OYZ: ChemComp-PO4: ChemComp-HOH: ChemComp-P4Z: ChemComp-GOL: ChemComp-OZ5: |
Source |
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Keywords | TRANSFERASE / PIP4K2A |