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Proteolytic digestions of M pro revealed Cys300 as a primary target of glutathionylation, and experiments using a C300S M pro mutant revealed that Cys300 is required for inhibition of activity upon M pro glutathionylation
Liver disease High intracellular content of GSH in liver are congruous with the detoxification functions of this organ
Interestingly, in our previous research, the pre-eclampsia-like performances were reversed after intraperitoneally injecting SRT2104 that can elevate SIRT1 protein expression [17]
