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Inhibiting the system xC(-)/glutathione axis selectively targets cancers with mutant-p53 accumulation

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The glutathione peptide of one inhibitor, termed productive binding, occupies the G-subsite with multiple interactions similar to those observed for other glutathione S-transferases, while the glutathione backbone of the second inhibitor, termed unproductive binding, exhibits only weak interactions mediated by two polar contacts

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