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{ <http://www.tkuhn.ch/bel2nanopub/RAXXg1wPQjfUNu2QY9g0eo9TG05f0aQcxL3l_-JQLYT3E#_5> ?p ?o ?g. }
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Analysis of the phosphorylation site mutants, S659A, S660A, and S659A,S660A disclosed that mutagenesis of both Ser-659 and Ser-660 was necessary to abolish the activation of HSL toward a triolein substrate after phosphorylation with PKA.
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