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3F96

Crystal structure of human plasma platelet activating factor acetylhydrolase covalently inhibited by sarin

Summary for 3F96
Entry DOI10.2210/pdb3f96/pdb
Related3D59 3D5E 3F97 3F98 3F9C
DescriptorPlatelet-activating factor acetylhydrolase (2 entities in total)
Functional Keywordsplasma platelet-activating factor acetylhydrolase, secreted protein, alpha/beta-hydrolase-fold, ldl-bound; lipoprotein associated phospholipase a2, lp-pla2, group viia pla2, glycoprotein, hydrolase, lipid degradation, polymorphism, sarin, disease mutation, secreted
Biological sourceHomo sapiens (Human)
Cellular locationSecreted, extracellular space: Q13093
Total number of polymer chains2
Total formula weight87228.91
Authors
Samanta, U.,Bahnson, B.J. (deposition date: 2008-11-13, release date: 2009-06-23, Last modification date: 2023-09-06)
Primary citationSamanta, U.,Kirby, S.D.,Srinivasan, P.,Cerasoli, D.M.,Bahnson, B.J.
Crystal structures of human group-VIIA phospholipase A2 inhibited by organophosphorus nerve agents exhibit non-aged complexes.
Biochem Pharmacol, 78:420-429, 2009
Cited by
PubMed: 19394314
DOI: 10.1016/j.bcp.2009.04.018
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.1 Å)
Structure validation

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