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Third, the structural location of Gid12 would obstruct a Gid4-bound substrate from accessing the ubiquitylation active site of the Ubc8~ubiquitin intermediate bound to the Gid2-Gid9 catalytic module 21,22,25,26,30,31
ZhaWLiangGXiaoJStuderEJHylemonPBPandakWMet al
Among these strategies, small-molecular compounds (e.g., RSL3 and ML162) directly engage GPX4 by covalently binding to selenocysteine, culminating in ferroptosis induction
Tokuda, E
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G.IshimotoA
