GPx1 |
Detoxifies peroxides in aqueous compartment of cellular cytosol |
[58] |
GPx2 |
Expressed in cytosol of liver and tissues of the digestive system |
[59] |
GPx3 |
Synthesized primarily by kidney; secreted into plasma for transport to other tissues |
[60] |
GPx4 |
Prevents and reverses oxidative damage to lipids in brain and other tissues |
[61] |
TRx1 |
Reduces T(SH)2, vitamin C, polyphenols, and other substrates to regulate intercellular redox state |
[62–64] |
TRx2 |
Located in mitochondria and controls and regulates redox state |
[63, 64] |
TRx3 |
Reduces mitochondrial glutathione disulfide, abundant in testes |
[63, 64] |
MsrB1 |
Restores oxidatively damaged methionine (R-sulfoxides) to native configuration |
[64] |
DIO1 |
Converts T4 (thyroxine) prohormone into T3 (active thyroid hormone) |
[65] |
DIO2 |
Regulates thyroid hormone status, activating as well as inactivating T3
|
[65] |
DIO3 |
Activates thyroid hormone in brain, placenta, important in fetal development |
[65] |
SPS2 |
Creates the Se-phosphate precursor required for synthesis of all selenoproteins |
[64] |
SelM |
Notably high expression levels in the brain, possible thiol-disulfide oxidoreductase |
[64, 66] |
SelN |
Interacts with ryanodine receptor, mutations result in congenital muscular dystrophy |
[64] |
SelP |
Transports Se in plasma (10 Sec/molecule) and delivers Se to brain and endocrine tissues |
[64] |
SelW |
Expressed in a variety of tissues and may regulate redox state of 14-3-3 proteins |
[64, 66, 67] |
Sel15 |
Oxidoreductase that may assist in disulfide formation and protein folding |
[64] |