Cells are unceasingly confronted by oxidative stresses that oxidize proteins on their cysteines. The thioredoxin (Trx) system, which is a ubiquitous system for thiol and protein repair, is composed of a thioredoxin (TrxA) and a thioredoxin reductase (TrxB). TrxAs reduce disulfide bonds of oxidized proteins and are then usually recycled by a single pleiotropic NAD(P)H-dependent TrxB (NTR). In this work, we first analyzed the composition of Trx systems across Bacteria. Most bacteria have only one NTR, but organisms in some Phyla have several TrxBs. In Firmicutes, multiple TrxBs are observed only in Clostridia, with another peculiarity being the existence of ferredoxin-dependent TrxBs. We used Clostridioides difficile, a pathogenic sporulating...
Thioredoxin (Trx) can regulate disulfide bond reduction of target proteins to maintain the reduced i...
Escherichia coli employs two separate pathways, driven by NADPH to reduce protein disulfides: the th...
The thioredoxin system, involved in the preservation of the reduced state of cytoplasmic proteins, i...
Cells are unceasingly confronted by oxidative stresses that oxidize proteins on their cysteines. The...
Cells are unceasingly confronted by oxidative stresses that oxidize proteins on their cysteines. The...
Cells are unceasingly confronted by oxidative stresses that oxidize proteins on their cysteines. The...
Contains fulltext : 36624.pdf ( ) (Open Access)ABSTRACT: BACKGROUND: Thioredoxin (...
Thioredoxins are important thiol-reactive proteins. Most knowledge about this class of proteins is d...
Thioredoxins are important thiol-reactive proteins. Most knowledge about this class of proteins is d...
The Gram-negative Bacteroides fragilis is the most frequently isolated bacterium from anaerobic infe...
Thioredoxins (Trx) are a class of small multifunctional 12-kDa proteins that are characterized by th...
Thioredoxin (Trx) is a ubiquitous oxidoreductase maintaining protein-bound cysteine residues in the ...
In this report we describe the cloning, organization, and promoter analysis of the Staphylococcus au...
Cyanobacteria evolved the ability to perform oxygenic photosynthesis using light energy to reduce CO...
Results of this study showed that the anaerobic, opportunistic pathogen Bacteroides fragilis lacks t...
Thioredoxin (Trx) can regulate disulfide bond reduction of target proteins to maintain the reduced i...
Escherichia coli employs two separate pathways, driven by NADPH to reduce protein disulfides: the th...
The thioredoxin system, involved in the preservation of the reduced state of cytoplasmic proteins, i...
Cells are unceasingly confronted by oxidative stresses that oxidize proteins on their cysteines. The...
Cells are unceasingly confronted by oxidative stresses that oxidize proteins on their cysteines. The...
Cells are unceasingly confronted by oxidative stresses that oxidize proteins on their cysteines. The...
Contains fulltext : 36624.pdf ( ) (Open Access)ABSTRACT: BACKGROUND: Thioredoxin (...
Thioredoxins are important thiol-reactive proteins. Most knowledge about this class of proteins is d...
Thioredoxins are important thiol-reactive proteins. Most knowledge about this class of proteins is d...
The Gram-negative Bacteroides fragilis is the most frequently isolated bacterium from anaerobic infe...
Thioredoxins (Trx) are a class of small multifunctional 12-kDa proteins that are characterized by th...
Thioredoxin (Trx) is a ubiquitous oxidoreductase maintaining protein-bound cysteine residues in the ...
In this report we describe the cloning, organization, and promoter analysis of the Staphylococcus au...
Cyanobacteria evolved the ability to perform oxygenic photosynthesis using light energy to reduce CO...
Results of this study showed that the anaerobic, opportunistic pathogen Bacteroides fragilis lacks t...
Thioredoxin (Trx) can regulate disulfide bond reduction of target proteins to maintain the reduced i...
Escherichia coli employs two separate pathways, driven by NADPH to reduce protein disulfides: the th...
The thioredoxin system, involved in the preservation of the reduced state of cytoplasmic proteins, i...