Eukaryotes contain a highly conserved multienzyme system which covalently links a small protein, ubiquitin, to a variety of intracellular proteins that bear degradation signals recognized by this system. The resulting ubiquitin-protein conjugates are degraded by the 26S proteasome, an ATP-dependent protease. Pathways that involve ubiquitin play major roles in a huge variety of processes, including cell differentiation, cell cycle, and responses to stress. In this article we briefly review the design of the ubiquitin system, and describe two recent advances, the finding that ubiquitin ligases interact with specific components of the 26S proteasome, and the demonstration that peptides accelerate their uptake into cells by activating the N-end...
Eukaryotes have evolved the ubiquitin (Ub)/proteasome system to degrade polypeptides. The Ub/proteas...
The N-end rule pathway is a highly conserved process that operates in many different organisms. It r...
The N-end rule relates the in vivo half-life of a protein to the identity of its N-terminal residue....
Eukaryotes contain a highly conserved multienzyme system which covalently links a small protein, ubi...
Eukaryotes contain a highly conserved multienzyme system which covalently links a small protein, ubi...
International audienceThe mechanisms of proteolysis remain to be fully defined. This review focuses ...
One of the proteolytic pathways existing in a cell is ubiquitin- proteasome system (UPS). This highl...
The 2004 Nobel Prize in chemistry for the discovery of protein ubiquitination has led to the recogni...
AbstractIntracellular proteolysis is a tightly regulated process responsible for the targeted remova...
The activity and abundance of proteins within a cell are controlled precisely to ensure the regulat...
The ability of ubiquitin to form up to eight different polyubiquitin chain linkages generates comple...
The proteasome, the primary protease for ubiquitin-dependent proteolysis in eukaryotes, is usually f...
The N-end rule relates the amino terminus to the rate of degradation through the ubiquitin/26 S prot...
Protein degradation by the ubiquitin system controls the intracellular concentrations of many regula...
Substrates of the N-end rule pathway are recognized by the Ubr1 E3 ubiquitin ligase through their de...
Eukaryotes have evolved the ubiquitin (Ub)/proteasome system to degrade polypeptides. The Ub/proteas...
The N-end rule pathway is a highly conserved process that operates in many different organisms. It r...
The N-end rule relates the in vivo half-life of a protein to the identity of its N-terminal residue....
Eukaryotes contain a highly conserved multienzyme system which covalently links a small protein, ubi...
Eukaryotes contain a highly conserved multienzyme system which covalently links a small protein, ubi...
International audienceThe mechanisms of proteolysis remain to be fully defined. This review focuses ...
One of the proteolytic pathways existing in a cell is ubiquitin- proteasome system (UPS). This highl...
The 2004 Nobel Prize in chemistry for the discovery of protein ubiquitination has led to the recogni...
AbstractIntracellular proteolysis is a tightly regulated process responsible for the targeted remova...
The activity and abundance of proteins within a cell are controlled precisely to ensure the regulat...
The ability of ubiquitin to form up to eight different polyubiquitin chain linkages generates comple...
The proteasome, the primary protease for ubiquitin-dependent proteolysis in eukaryotes, is usually f...
The N-end rule relates the amino terminus to the rate of degradation through the ubiquitin/26 S prot...
Protein degradation by the ubiquitin system controls the intracellular concentrations of many regula...
Substrates of the N-end rule pathway are recognized by the Ubr1 E3 ubiquitin ligase through their de...
Eukaryotes have evolved the ubiquitin (Ub)/proteasome system to degrade polypeptides. The Ub/proteas...
The N-end rule pathway is a highly conserved process that operates in many different organisms. It r...
The N-end rule relates the in vivo half-life of a protein to the identity of its N-terminal residue....