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Specifically, FOXO4-DRI peptide has been researched as a decoy that may compete with FOXO4 for p53 binding, so it may disrupt the FOXO4p53 interaction in laboratory systems

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Structural features of active, Cagri-bound, AMY1R, AMY2R and AMY3R complexes Overall, the consensus structures of AMYRs bound to Cagri or CagriBB exhibited highly similar backbone conformations of the peptide and CTR subunit (Fig

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