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239 A mass spectrometry-based kinetic profiling method performed with a variety of oxidants, including cysteine persulfide (CSSH), 384 reveals a striking asymmetry of trans -persulfidation within each CstR dimer unit within the tetramer, with one side of the dimer reacting and ultimately closing to a cross-linked product far faster than the opposite side of the dimer

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Notably, this still showed steep declines in output