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For the Tyk2 pseudokinase-kinase crystal structure, a number of JAK-activating mutations were found to lie directly in the proposed domain interface while a second surface of activating mutations was found peripheral to the proposed dimer interface, which includes the position for the JAK2 V617F mutation commonly identified in myeloproliferative neoplasms (89)

Heres what the research says

Padia SH, Kemp BA, Howell NL, Siragy HM, Fournie-Zaluski MC, Roques BP, Carey RM

Ongoing use provides prophylactic benefit alongside maintenance of achieved improvements

GPX keeps the thiol-disulfide balance in check and also collaborates with peroxiredoxins and glutathione-S-transferases (GSTs) to maintain redox homeostasis