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It inhibits protein kinase C by forming hydrogen bonds with specific residues in the C1B subdomain and fits well within the binding pocket of glycogen synthase kinase-3β through interactions with key amino acids (232)

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doi: 10.1371/journal.ppat.1003861 [DOI] [PMC free article] [PubMed] [Google Scholar] [195].Snyder DT, Hedges JF, Jutila MA