6M08
Crystal structure of Lp-PLA2 in complex with a novel covalent inhibitor.
Summary for 6M08
Entry DOI | 10.2210/pdb6m08/pdb |
Descriptor | Platelet-activating factor acetylhydrolase, (2S)-2-[(Z)-3-[2-(diethylamino)ethyl-[[4-[4-(trifluoromethyl)phenyl]phenyl]methyl]amino]-1-oxidanyl-3-oxidanylidene-prop-1-enyl]pyrrolidine-1-carboxylic acid (3 entities in total) |
Functional Keywords | lp-pla2, covalent inhibitor, complex structure, serine phospholipase., hydrolase |
Biological source | Homo sapiens (Human) |
Total number of polymer chains | 2 |
Total formula weight | 85067.71 |
Authors | |
Primary citation | 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. Identification of Highly Selective Lipoprotein-Associated Phospholipase A2 (Lp-PLA2) Inhibitors by a Covalent Fragment-Based Approach. J.Med.Chem., 63:7052-7065, 2020 Cited by PubMed: 32459096DOI: 10.1021/acs.jmedchem.0c00372 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.19 Å) |
Structure validation
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