urally unique molecule, influences a subset of cancer-related pathways involving heat shock protein 90 (Hsp90). We show that San A-amide specifically binds to the N-middle domain of Hsp90 and allosterically disrupts the binding of proteins thought to interactwith theHsp90 C-terminal domain,while having no effect on an N-terminal domain client protein. This unique mechanism suggests that San A-amide is a potential tool for studying C-terminal binding proteins of Hsp90 as well as a promising lead in the development of new cancer therapeutics
The last decade has seen the molecular chaperone heat shock protein 90 (HSP90) emerge as an exciting...
ABSTRACT: Human Hsp90 isoforms are molecular chaper-ones that are often up-regulated in malignances ...
Hsp90 is an established anti-apoptotic target in cancer therapy.1 Most of the known small-molecule i...
Herein we show that San A-amide, a structurally unique molecule, influences a subset of cancer-relat...
Includes bibliographical references (p. 54-57).Heat Shock Protein 90 (Hsp90) is a molecular chaperon...
Described are the syntheses of 3 Sansalvamide A derivatives that contain biotinylated tags at indivi...
Heat shock protein 90 (Hsp90) is a conserved, abundant, multi-domain protein that functions as a mol...
Abstract: Utilizing the structure-activity relationship we have developed during the synthesis of th...
Heat shock protein 90 (Hsp90) is an ATP dependent molecular chaperone deeply involved in the complex...
This thesis describes the biological evaluation and synthetic development of derivatives of the natu...
Heat shock protein 90 (HSP90) is a molecular chaperone of numerous oncoproteins. Therefore, cancer c...
Classical Hsp90 inhibitors target the N-terminal ATP binding site. While these inhibitors have had s...
Heat shock protein (HSP90), a highly conserved molecular chaperon, is indispensable for the maturati...
BackgroundHeat shock protein 90 (HSP90) has a key role in the maintenance of the cellular proteostas...
AbstractHeat shock protein 90 (Hsp90) is a highly conserved molecular chaperone that plays a vital r...
The last decade has seen the molecular chaperone heat shock protein 90 (HSP90) emerge as an exciting...
ABSTRACT: Human Hsp90 isoforms are molecular chaper-ones that are often up-regulated in malignances ...
Hsp90 is an established anti-apoptotic target in cancer therapy.1 Most of the known small-molecule i...
Herein we show that San A-amide, a structurally unique molecule, influences a subset of cancer-relat...
Includes bibliographical references (p. 54-57).Heat Shock Protein 90 (Hsp90) is a molecular chaperon...
Described are the syntheses of 3 Sansalvamide A derivatives that contain biotinylated tags at indivi...
Heat shock protein 90 (Hsp90) is a conserved, abundant, multi-domain protein that functions as a mol...
Abstract: Utilizing the structure-activity relationship we have developed during the synthesis of th...
Heat shock protein 90 (Hsp90) is an ATP dependent molecular chaperone deeply involved in the complex...
This thesis describes the biological evaluation and synthetic development of derivatives of the natu...
Heat shock protein 90 (HSP90) is a molecular chaperone of numerous oncoproteins. Therefore, cancer c...
Classical Hsp90 inhibitors target the N-terminal ATP binding site. While these inhibitors have had s...
Heat shock protein (HSP90), a highly conserved molecular chaperon, is indispensable for the maturati...
BackgroundHeat shock protein 90 (HSP90) has a key role in the maintenance of the cellular proteostas...
AbstractHeat shock protein 90 (Hsp90) is a highly conserved molecular chaperone that plays a vital r...
The last decade has seen the molecular chaperone heat shock protein 90 (HSP90) emerge as an exciting...
ABSTRACT: Human Hsp90 isoforms are molecular chaper-ones that are often up-regulated in malignances ...
Hsp90 is an established anti-apoptotic target in cancer therapy.1 Most of the known small-molecule i...