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2000
Volume 10, Issue 6
  • ISSN: 1389-2010
  • E-ISSN: 1873-4316

Abstract

Tryparedoxin peroxidase (TryP) is a key enzyme of the trypanothione-dependent metabolism for removal of oxidative stress in leishmania. These enzymes function as antioxidants through their peroxidase and peroxynitrite reductase activities. Inhibitors of this enzyme are presumed to be antilesihmania drugs and structural studies are prerequisite of rational drug design. We have constructed three dimensional structure of TryP of Leishmania infantum using comparative modeling. Structural analysis reveals several interesting features. Moreover, it shows remarkable structural difference with human host glutathione peroxidase, an enzyme involved in similar function and TryP from Leishmania major.

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/content/journals/cpb/10.2174/138920109789069305
2009-09-01
2025-04-10
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/content/journals/cpb/10.2174/138920109789069305
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  • Article Type:
    Research Article
Keyword(s): Drug design; Homology Modelling; Peroxidase activity; Structure-Function
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