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-Structure paper
Title | Identification of Highly Selective Lipoprotein-Associated Phospholipase A2 (Lp-PLA2) Inhibitors by a Covalent Fragment-Based Approach. |
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Journal, issue, pages | J. Med. Chem., Vol. 63, Page 7052-7065, Year 2020 |
Publish date | Feb 20, 2020 (structure data deposition date) |
Authors | Huang, F. / Hu, H. / Wang, K. / Peng, C. / Xu, W. / Zhang, Y. / Gao, J. / Liu, Y. / Zhou, H. / Huang, R. ...Huang, F. / Hu, H. / Wang, K. / Peng, C. / Xu, W. / Zhang, Y. / Gao, J. / Liu, Y. / Zhou, H. / Huang, R. / Li, M. / Shen, J. / Xu, Y. |
External links | J. Med. Chem. / PubMed:32459096 |
Methods | X-ray diffraction |
Resolution | 2.1 - 2.64 Å |
Structure data | PDB-6m06: PDB-6m07: PDB-6m08: |
Chemicals | ChemComp-BWF: ChemComp-HOH: ChemComp-BWO: ChemComp-BWL: |
Source |
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Keywords | HYDROLASE / Lp-PLA2 / Covalent inhibitor / Complex structure / Serine phospholipase / Serine phospholipase. |