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5LZ9

Fragment-based inhibitors of Lipoprotein associated Phospholipase A2

Summary for 5LZ9
Entry DOI10.2210/pdb5lz9/pdb
DescriptorPlatelet-activating factor acetylhydrolase, CHLORIDE ION, SODIUM ION, ... (5 entities in total)
Functional Keywordslp-pla2 phospholipase, hydrolase, lipid metabolism, inhibitors, lp-pla2#4
Biological sourceHomo sapiens (Human)
Cellular locationSecreted, extracellular space: Q13093
Total number of polymer chains1
Total formula weight44656.03
Authors
Woolford, A.,Day, P. (deposition date: 2016-09-29, release date: 2016-12-21)
Primary citationWoolford, A.J.,Day, P.J.,Beneton, V.,Berdini, V.,Coyle, J.E.,Dudit, Y.,Grondin, P.,Huet, P.,Lee, L.Y.,Manas, E.S.,McMenamin, R.L.,Murray, C.W.,Page, L.W.,Patel, V.K.,Potvain, F.,Rich, S.J.,Sang, Y.,Somers, D.O.,Trottet, L.,Wan, Z.,Zhang, X.
Fragment-Based Approach to the Development of an Orally Bioavailable Lactam Inhibitor of Lipoprotein-Associated Phospholipase A2 (Lp-PLA2).
J. Med. Chem., 59:10738-10749, 2016
Cited by
PubMed: 27933945
DOI: 10.1021/acs.jmedchem.6b01427
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.06 Å)
Structure validation

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