Thioredoxin reductase

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thioredoxin reductase 1
Identifiers
Symbol TXNRD1
HUGO 12437
Entrez 7296
OMIM 601112
RefSeq NM_003330
UniProt Q16881
Other data
Locus Chr. 12 q23-q24.1
thioredoxin reductase 2
Identifiers
Symbol TXNRD2
HUGO 18155
Entrez 10587
OMIM 606448
RefSeq NM_006440
UniProt Q9NNW7
Other data
Locus Chr. 22 q11.21
thioredoxin reductase 3
Identifiers
Symbol TXNRD3
HUGO 20667
Entrez 114112
OMIM 606235
RefSeq XM_051264
UniProt Q86VQ6
Other data
Locus Chr. 3 p13-q13.33

Thioredoxin Reductase (TR, TrxR) (EC 1.8.1.9) are the only known enzymes to reduce thioredoxin (Trx).[1] All known kingdom of organisms contain thioredoxin reductase. Two types of thioredoxin reductase evolved independently: prokaryotes, archia and most plants have one type; higher eukaryotes and some plants contain a different one that contains selenocysteine. 3 TRs exist in animals: TR1, TR3 and TGR. Both TR1[2] and TR3[3] are essential proteins for mouse embryogenesis.Since the activity of this enzyme is essential for cell growth and survival, it is a good target for anti-tumor therapy. For example, motexafin gadolinium (MGd) is a new chemotherapeutic agent that selectively targets tumor cells, leading to cell death and apoptosis via inhibition of thioredoxin reductase and ribonucleotide reducatse.

[edit] References

  1. ^ Mustacich D, Powis G. "Thioredoxin reductase". Biochem J 346 Pt 1: 1-8. PMID 10657232. 
  2. ^ Jakupoglu C, Przemeck GK, Schneider M, Moreno SG, Mayr N, Hatzopoulos AK, de Angelis MH, Wurst W, Bornkamm GW, Brielmeier M, Conrad M. Cytoplasmic thioredoxin reductase is essential for embryogenesis but dispensable for cardiac development. Mol. Cell. Biol. 2005 Mar;25(5):1980-8.
  3. ^ Conrad M, Jakupoglu C, Moreno SG, Lippl S, Banjac A, Schneider M, Beck H, Hatzopoulos AK, Just U, Sinowatz F, Schmahl W, Chien KR, Wurst W, Bornkamm GW, Brielmeier M. Essential role for mitochondrial thioredoxin reductase in hematopoiesis, heart development, and heart function. Mol. Cell. Biol. 2004 Nov;24(21):9414-23.

Hashemy, S. I., Ungerstedt, J. S., Zahedi Avval, F., and Holmgren, A. (2006). Motexafin gadolinium, a tumor-selective drug targeting thioredoxin reductase and ribonucleotide reductase. J Biol Chem 281, 10691-10697.