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Soluble APT2 is susceptible to proteasomal degradation, whereas its membrane-bound form is immune to proteasomal-mediated degradation, and its stable binding to the cell membrane requires three consecutive steps: electrostatic attraction, insertion of a hydrophobic ring, and S-acylation by the palmitoyltransferases ZDHHC3 or ZDHHC7 (50)

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This approach not only enables the identification of compounds that target the active site but also facilitates the discovery of compounds that bind to allosteric sites (Fig