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2000
Volume 16, Issue 25
  • ISSN: 1568-0266
  • E-ISSN: 1873-4294

Abstract

Background. The high sequence and structural homology among the hsp90 paralogs – Hsp90α, Hsp90β, Grp94, and Trap-1 – has made the development of paralog-specific inhibitors a challenging proposition. Objective. This review surveys the state of developments in structural analysis, compound screening, and structure-based design that have been brought to bear on this problem. Results. First generation compounds that selectively bind to Hsp90, Grp94, or Trap-1 have been identified. Conclusion. With the proof of principle firmly established, the prospects for further progress are bright.

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/content/journals/ctmc/10.2174/1568026616666160413141154
2016-10-01
2025-01-10
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/content/journals/ctmc/10.2174/1568026616666160413141154
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  • Article Type:
    Research Article
Keyword(s): Grp94; Hsp90; Paralog-selective inhibitor; Screening; Structure-based design; Trap-1
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