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It does not disrupt the interaction between dimers in the glutaminase tetramer but binds to the hydrophobic pocket between the monomer-monomer interface of the GAC, located at the junction where the N-terminal and C-terminal of the enzyme meet the catalytic domain, thereby preventing the GAC from activating conformational changes (Wilson et al., 2013

: "Oridonin confers protection against arsenic-induced toxicity through activation of the Nrf2-mediated defensive response." in: Environmental health perspectives , Vol

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