In silico studies on tryparedoxin peroxidase of Leishmania infantum: Structural aspects

Bishal Kumar Singh, Vikash Kumar Dubey

Research output: Contribution to journalArticlepeer-review

7 Scopus citations

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.

Original languageEnglish (US)
Pages (from-to)626-630
Number of pages5
JournalCurrent Pharmaceutical Biotechnology
Volume10
Issue number6
DOIs
StatePublished - 2009
Externally publishedYes

Keywords

  • Drug design
  • Homology Modelling
  • Peroxidase activity
  • Structure-Function

ASJC Scopus subject areas

  • Biotechnology
  • Pharmaceutical Science

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