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In this case, two cysteines must undergo oxidative modification, one to sulfinic acid and another to sulfenic acid (γ-Cys131 and γ-Cys133, respectively, in bacterial thiocyanate hydrolase), in order to create the nonheme iron binding site critical to its enzymatic function [121, 122]
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superantigen [ soo″p r-an′tľ-j n ] molecules that are potent T lymphocyte mitogens that act by simultaneously binding directly to class II MHC molecules and to conserved regions of the T-cell receptor
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