Leukotriene-C4 synthase

The enzymeleukotriene-C4synthase(EC 4.4.1.20)catalyzesthe reaction

leukotriene-C4synthase
Leukotriene C4synthase dodecamer, Human
Identifiers
EC no.4.4.1.20
CAS no.90698-32-1
Databases
IntEnzIntEnz view
BRENDABRENDA entry
ExPASyNiceZyme view
KEGGKEGG entry
MetaCycmetabolic pathway
PRIAMprofile
PDBstructuresRCSB PDBPDBePDBsum
Gene OntologyAmiGO/QuickGO
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PMCarticles
PubMedarticles
NCBIproteins
leukotriene C4leukotriene A4+ glutathione

This enzyme belongs to the family oflyases,specifically the class of carbon-sulfur lyases. Thesystematic nameof this enzyme class isleukotriene-C4glutathione-lyase (leukotriene-A4-forming).Other names in common use includeleukotriene C4synthetase,LTC4 synthase,LTC4 synthetase,leukotriene A4:glutathioneS-leukotrienyltransferase,(7E,9E,11Z,14Z)-(5S,6R)-5,6-epoxyicosa-7,9,11,14-tetraenoate:glutathione leukotriene-transferase, (epoxide-ring-opening),(7E,9E,11Z,14Z)-(5S,6R)-6-(glutathion-S-yl)-5-hydroxyicosa-7,9,11,14-tetraenoate glutathione-lyase (epoxide-forming).This enzyme participates inarachidonic acid metabolism.

Structural studies

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As of late 2007, 3structureshave been solved for this class of enzymes, withPDBaccession codes2PNO,2UUH,and2UUI.

References

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  • Bach MK, Brashler JR, Morton DR Jr (1984). "Solubilization and characterization of the leukotriene C4synthetase of rat basophil leukemia cells: a novel, particulate glutathioneS-transferase ".Arch. Biochem. Biophys.230(2): 455–65.doi:10.1016/0003-9861(84)90426-0.PMID6324687.
  • Shimizu T (1988). "Enzymes functional in the syntheses of leukotrienes and related compounds".Int. J. Biochem.20(7): 661–6.doi:10.1016/0020-711X(88)90160-7.PMID2846379.
  • Lam BK, Austen KF (2002). "Leukotriene C4synthase: a pivotal enzyme in cellular biosynthesis of the cysteinyl leukotrienes ".Prostaglandins. Other. Lipid. Mediat.68–69: 511–20.doi:10.1016/S0090-6980(02)00052-7.PMID12432940.
  • Christmas P, Weber BM, McKee M, Brown D, Soberman RJ (2002)."Membrane localization and topology of leukotriene C4synthase ".J. Biol. Chem.277(32): 28902–8.doi:10.1074/jbc.M203074200.PMID12023288.