Literature DB >> 12714747

Peroxiredoxin evolution and the regulation of hydrogen peroxide signaling.

Zachary A Wood1, Leslie B Poole, P Andrew Karplus.   

Abstract

Eukaryotic 2-Cys peroxiredoxins (2-Cys Prxs) not only act as antioxidants, but also appear to regulate hydrogen peroxide-mediated signal transduction. We show that bacterial 2-Cys Prxs are much less sensitive to oxidative inactivation than are eukaryotic 2-Cys Prxs. By identifying two sequence motifs unique to the sensitive 2-Cys Prxs and comparing the crystal structure of a bacterial 2-Cys Prx at 2.2 angstrom resolution with other Prx structures, we define the structural origins of sensitivity. We suggest this adaptation allows 2-Cys Prxs to act as floodgates, keeping resting levels of hydrogen peroxide low, while permitting higher levels during signal transduction.

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Year:  2003        PMID: 12714747     DOI: 10.1126/science.1080405

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  456 in total

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3.  Structural and electrostatic asymmetry at the active site in typical and atypical peroxiredoxin dimers.

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Review 6.  APE1/Ref-1 role in redox signaling: translational applications of targeting the redox function of the DNA repair/redox protein APE1/Ref-1.

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Review 7.  Peroxiredoxins in parasites.

Authors:  Michael C Gretes; Leslie B Poole; P Andrew Karplus
Journal:  Antioxid Redox Signal       Date:  2012-01-25       Impact factor: 8.401

Review 8.  Peroxiredoxin functions as a peroxidase and a regulator and sensor of local peroxides.

Authors:  Sue Goo Rhee; Hyun Ae Woo; In Sup Kil; Soo Han Bae
Journal:  J Biol Chem       Date:  2011-12-06       Impact factor: 5.157

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10.  Distinct characteristics of two 2-Cys peroxiredoxins of Vibrio vulnificus suggesting differential roles in detoxifying oxidative stress.

Authors:  Ye-Ji Bang; Man Hwan Oh; Sang Ho Choi
Journal:  J Biol Chem       Date:  2012-10-24       Impact factor: 5.157

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