The Hsp70 molecular chaperones are ATPases that play critical roles in the pathogenesis of many human diseases, including breast cancer. Hsp70 ATP hydrolysis is relatively weak but is stimulated by J domain-containing proteins. We identified pyrimidinone-peptoid hybrid molecules that inhibit cell proliferation with greater potency than previously described Hsp70 modulators. In many cases, anti-proliferative activity correlated with inhibition of J domain stimulation of Hsp70.\ud \u
Protein-protein interactions (PPIs) are an important category of putative drug targets. Improvements...
Heat shock protein 70 (Hsp70) is a highly conserved molecular chaperone that plays multiple roles in...
The HSP70 family of heat shock proteins consists of molecular chaperones of approximately 70kDa in s...
Chaperone proteins and their cochaperones are perhaps one of the most intriguing systems for investi...
The molecular chaperones of the Hsp70 family have been recognized as targets for anti-cancer therapy...
<div><p>The molecular chaperones of the Hsp70 family have been recognized as targets for anti-cancer...
Hsp70 molecular chaperones play critical roles in the pathogenesis of many human diseases, including...
SummaryHsp70s are important cancer chaperones that act upstream of Hsp90 and exhibit independent ant...
The molecular chaperone and cytoprotective activities of the Hsp70 and Hsp40 chaperones represent th...
The highly conserved heat shock 70 proteins (HSP70) play an integral role in the chaperone network w...
The family of 70-kDa proteins are molecular chaperones responsible for the noncovalent folding of ma...
The cytosol of the mammalian cell is a highly crowded environment, where all of the molecular proces...
The heat shock protein 70 (Hsp70) family of molecular chaperones are highly expressed in tumors. Inh...
The Hsp70 family of molecular chaperones is essential for protein folding, re-folding misfolded clie...
Members of the HSP70 family form a central hub of the molecular chaperone network, controlling prote...
Protein-protein interactions (PPIs) are an important category of putative drug targets. Improvements...
Heat shock protein 70 (Hsp70) is a highly conserved molecular chaperone that plays multiple roles in...
The HSP70 family of heat shock proteins consists of molecular chaperones of approximately 70kDa in s...
Chaperone proteins and their cochaperones are perhaps one of the most intriguing systems for investi...
The molecular chaperones of the Hsp70 family have been recognized as targets for anti-cancer therapy...
<div><p>The molecular chaperones of the Hsp70 family have been recognized as targets for anti-cancer...
Hsp70 molecular chaperones play critical roles in the pathogenesis of many human diseases, including...
SummaryHsp70s are important cancer chaperones that act upstream of Hsp90 and exhibit independent ant...
The molecular chaperone and cytoprotective activities of the Hsp70 and Hsp40 chaperones represent th...
The highly conserved heat shock 70 proteins (HSP70) play an integral role in the chaperone network w...
The family of 70-kDa proteins are molecular chaperones responsible for the noncovalent folding of ma...
The cytosol of the mammalian cell is a highly crowded environment, where all of the molecular proces...
The heat shock protein 70 (Hsp70) family of molecular chaperones are highly expressed in tumors. Inh...
The Hsp70 family of molecular chaperones is essential for protein folding, re-folding misfolded clie...
Members of the HSP70 family form a central hub of the molecular chaperone network, controlling prote...
Protein-protein interactions (PPIs) are an important category of putative drug targets. Improvements...
Heat shock protein 70 (Hsp70) is a highly conserved molecular chaperone that plays multiple roles in...
The HSP70 family of heat shock proteins consists of molecular chaperones of approximately 70kDa in s...