1.8.1.B1: thioredoxin glutathione reductase
This is an abbreviated version!
For detailed information about thioredoxin glutathione reductase, go to the full flat file.
Word Map on EC 1.8.1.B1
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1.8.1.B1
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schistosoma
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schistosomiasis
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worm
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mansoni
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praziquantel
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glutaredoxin
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selenocysteine
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antischistosomal
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gssg
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auranofin
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platyhelminth
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flatworm
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dtnb
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fluke
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sjtgr
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fasciola
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oxadiazole
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cysticerci
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hysteretic
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medicine
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taenia
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trematode
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echinococcus
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granulosus
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schistosomicidal
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crassiceps
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gigantica
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selenocysteine-containing
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furoxans
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analysis
- 1.8.1.B1
- schistosoma
- schistosomiasis
- worm
- mansoni
- praziquantel
- glutaredoxin
- selenocysteine
-
antischistosomal
- gssg
- auranofin
-
platyhelminth
- flatworm
- dtnb
- fluke
-
sjtgr
- fasciola
-
oxadiazole
- cysticerci
-
hysteretic
- medicine
-
taenia
-
trematode
-
echinococcus
- granulosus
-
schistosomicidal
- crassiceps
- gigantica
-
selenocysteine-containing
- furoxans
- analysis
Reaction
Synonyms
cTGR, DmTrxR, EgTGR, mTGR, SmTGR, TGR, TGRsec, thioredoxin glutathione reductase, thioredoxin-glutathione reductase, thioredoxin/glutathione reductase
ECTree
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General Information
General Information on EC 1.8.1.B1 - thioredoxin glutathione reductase
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drug target
physiological function
promising drug target for the treatment of schistosomiasis
drug target
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the enzyme is a promising drug target, as this enzyme is parasite-specific and absent in their host. A study identifies compounds with extremely potent antischistosome activity. Certain compounds are active against all major schistosomes across different life cycle stages
drug target
-
the enzyme is a promising drug target, as this enzyme is parasite-specific and absent in their host. A study identifies compounds with extremely potent antischistosome activity. Certain compounds are active against all major schistosomes across different life cycle stages
drug target
-
the enzyme is a promising drug target, as this enzyme is parasite-specific and absent in their host. A study identifies compounds with extremely potent antischistosome activity. Certain compounds are active against all major schistosomes across different life cycle stages
drug target
the enzyme maybe a potential target for the development of novel agents against opisthorschiasis
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the enzyme is able to protect glutamine synthetase from oxidative inactivation, suggesting that the enzyme is competent to contend with oxidative stress
physiological function
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the enzyme is essential for maintaining the thiol-disulfide redox homeostasis of Schistosoma japonicum
physiological function
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the enzyme plays a crucial role in maintaining redox homeostasis
physiological function
the enzyme is crucial for Opisthorchis viverrini survival
physiological function
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the enzyme of the parasite is essential for the survival of schistosomes in the mammalian host
physiological function
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the enzyme plays a principal role in redox homeostasis maintenance
physiological function
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the enzyme plays an essential role in maintaining the redox homeostasis and antioxidant defenses in the parasite Fasciola gigantica. Parasitic flukes have a limited set of antioxidant proteins in contrast to their mammalian hosts. In platyhelminthic parasites, the two systems (glutathione/glutaredoxin system and thioredoxin system) are replaced by a single system of a multifunctional flavin containing chimeric selenoenzyme known as thioredoxin glutathione reductase, which donates electrons to both thioredoxin disulfide and glutathione disulfide in these parasites
physiological function
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the enzyme plays an indispensible role in the redox biochemistry of parasitic flukes
physiological function
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under redox pressure, schistosomes survive in mammalian hosts with the help of thioredoxin glutathione reductase
physiological function
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under redox pressure, schistosomes survive in mammalian hosts with the help of thioredoxin glutathione reductase
physiological function
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under redox pressure, schistosomes survive in mammalian hosts with the help of thioredoxin glutathione reductase