Literature DB >> 24737740

Unraveling the specificities of the different human methionine sulfoxide reductases.

Elien Vandermarliere1, Bart Ghesquière, Veronique Jonckheere, Kris Gevaert, Lennart Martens.   

Abstract

The oxidation of free and protein-bound methionine into methionine sulfoxide is a frequently occurring modification caused by ROS. Most organisms express methionine sulfoxide reductases (MSR enzymes) to repair this potentially damaging modification. Humans express three different MSRB enzymes which reside in different cellular compartments. In this study, we have explored the specificity of the human MSRB enzymes both by in silico modeling and by experiments on oxidized peptides. We found that MSRB1 is the least specific MSRB enzyme, which is in agreement with the observation that MSRB1 is the only MSRB enzyme found in the cytosol and the nucleus, and therefore requires a broad specificity to reduce all possible substrates. MSRB2 and MSRB3, which are both found in mitochondria, are more specific but because of their co-occurrence they can likely repair all possible substrates.
© 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  In silico analysis; Methionine sulfoxide reductase; Oxidized methionine; Specificity; Technology

Mesh:

Substances:

Year:  2014        PMID: 24737740     DOI: 10.1002/pmic.201300357

Source DB:  PubMed          Journal:  Proteomics        ISSN: 1615-9853            Impact factor:   3.984


  4 in total

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Journal:  PLoS Genet       Date:  2015-04-02       Impact factor: 5.917

3.  A conserved R type Methionine Sulfoxide Reductase reverses oxidized GrpEL1/Mge1 to regulate Hsp70 chaperone cycle.

Authors:  Praveen Kumar Allu; Yerranna Boggula; Srinivasu Karri; Adinarayana Marada; Thanuja Krishnamoorthy; Naresh Babu V Sepuri
Journal:  Sci Rep       Date:  2018-02-09       Impact factor: 4.379

4.  Sulphur Atoms from Methionines Interacting with Aromatic Residues Are Less Prone to Oxidation.

Authors:  Juan C Aledo; Francisco R Cantón; Francisco J Veredas
Journal:  Sci Rep       Date:  2015-11-24       Impact factor: 4.379

  4 in total

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