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==Ligand Interactions==
==Ligand Interactions==
[[Image: 1I7G.jpg|375px|right|thumb|Figure 1: Ligand binding domain of PPARα in complex with agonist Az242. [[1i7g]] ]]
[[Image: 1I7G.jpg|400px|right|thumb|Figure 1: Ligand binding domain of PPARα in complex with agonist Az242. [[1i7g]] ]]
PPAR alpha ligands can consist of either synthetic drugs (exogenous) or biological molecules (endogenous). Most common biological molecules that serve as ligands for human PPAR alpha are fatty acids, fatty acid derivatives <ref name="PPAR1"/><ref name="PPAR2"/>. Several enzymes such as 8-, 12-, 15-, and 5-lipoxygenases, the cyclooxygenases and cytochrome P450 utilize fatty acids as substrates to produce putative PPAR alpha ligands. Leukotriene B4 is a well-known putative PPAR alpha ligand, as well as 19- and 20- hydroxyeicosatetraeonic acid, generated from cytochrome P450 as a conversion of arachidonic acid. Oleylethanolamide, a naturally occurring lipid, has also been identified as a high affinity PPAR alpha ligand regulating PPAR alpha activity and lipid metabolism <ref name="PPAR6">PMID:20414453</ref>.
PPAR alpha ligands can consist of either synthetic drugs (exogenous) or biological molecules (endogenous). Most common biological molecules that serve as ligands for human PPAR alpha are fatty acids, fatty acid derivatives <ref name="PPAR1"/><ref name="PPAR2"/>. Several enzymes such as 8-, 12-, 15-, and 5-lipoxygenases, the cyclooxygenases and cytochrome P450 utilize fatty acids as substrates to produce putative PPAR alpha ligands. Leukotriene B4 is a well-known putative PPAR alpha ligand, as well as 19- and 20- hydroxyeicosatetraeonic acid, generated from cytochrome P450 as a conversion of arachidonic acid. Oleylethanolamide, a naturally occurring lipid, has also been identified as a high affinity PPAR alpha ligand regulating PPAR alpha activity and lipid metabolism <ref name="PPAR6">PMID:20414453</ref>.