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passages.text: Our data imply that among the typically used control reagents in phorbol ester experiments on PKC (C1-domain antagonists like calphostin C, inactive 4α phorbol esters, inhibitors of ATP binding like bisindolylmaleimide), only potent and selective inhibitors of ATP binding to PKC would allow one to distinguish phorbol ester-mediated effects on PKC from those on Munc13 proteins (assuming that Munc13s do not bind these ligands with a binding site outside the C1-domain).
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