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The effect of mutations on 14-3-3ζ protein dimer formation and conformation as demonstrated by native-PAGE analysis (A) and limited trypsinolysis (B). For trypsinolysis, mutant and wild-type 14-3-3ζ proteins (as labeled) were incubated with (+) or without (−) trypsin before separation on SDS-PAGE. Proteins were visualized for A and B by Coomassie staining.
