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[30] The extensivity of the -catenin interacting proteins complicates our understanding: -catenin may be directly phosphorylated at Ser552 by Akt, which causes its disassociation from cell-cell contacts and accumulation in cytosol, thereafter 14-3-3 interacts with -catenin (pSer552) and enhances its nuclear translocation

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To determine whether this mutation affected the intracellular ATP content, the ATP pool was quantified and compared to MG1655 cultured in M9 medium (Fig

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