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(110) showed that endogenously generated NO and ROS contribute to HIF-1 accumulation by inhibiting prolyl hydroxylase domain proteins (PHDs) via S-nitrosation of PHD2, thus preventing HIF-1 degradation during hypoxia (110)

One-carbon units are generated in parallel pathways in the mitochondria and cytoplasm (50, 52, 54, 56, 57), and both sets of enzymes were found to be highly induced following T cell activation (50)

[9] The Long R3 design pushes the same principle further: the Arg-for-Glu swap at position 3 removes a residue important for binding-protein contact, and the 13-residue N-terminal extension further perturbs the IGFBP interface

Molecular basis for the distinct functions of redox-active and FeS-transfering glutaredoxins

101 This allelic variant has been suggested to potentially influence the stability of the GSTP1-1/JNK complex and, subsequently, JNK activity, contingent upon the redox status of the cell

& Caprioli, R