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dc.contributor.authorTamarit Sumalla, Jordi
dc.contributor.authorBellí i Martínez, Gemma
dc.contributor.authorCabiscol Català, Elisa
dc.contributor.authorHerrero Perpiñán, Enrique
dc.contributor.authorRos Salvador, Joaquim
dc.date.accessioned2015-07-02T09:26:36Z
dc.date.issued2003
dc.identifier.issn0021-9258
dc.identifier.urihttp://hdl.handle.net/10459.1/48398
dc.description.abstractGrx5 is a yeast mitochondrial protein involved in iron- sulfur biogenesis that belongs to a recently described family of monothiolic glutaredoxin-like proteins. No member of this family has been biochemically charac- terized previously. Grx5 contains a conserved cysteine residue (Cys-60) and a non-conserved one (Cys-117). In this work, we have purified wild type and mutant C60S and C117S proteins and characterized their biochemical properties. A redox potential of ؊175 mV was calculated for wild type Grx5. The pKa values obtained by titration of mutant proteins with iodoacetamide at different pHs were 5.0 for Cys-60 and 8.2 for Cys-117. When Grx5 was incubated with glutathione disulfide, a transient mixed disulfide was formed between glutathione and the cys- tein 60 of the protein because of its low pKa. Binding of glutathione to Cys-60 promoted a decrease in the Cys- 117 pKa value that triggered the formation of a disulfide bond between both cysteine residues of the protein, in- dicating that Cys-117 plays an essential role in the cat- alytic mechanism of Grx5. The disulfide bond in Grx5 could be reduced by GSH but at a rate at least 20 times slower than that observed for the reduction of glutare- doxin 1 from E. coli, a dithiolic glutaredoxin. This slow reduction rate could suggest that GSH may not be the physiologic reducing agent of Grx5. The fact that wild type Grx5 efficiently reduced a glutathiolated protein used as a substrate indicated that Grx5 may act as a thiol reductase inside the mitochondria.ca_ES
dc.language.isoengca_ES
dc.publisherThe American Society for Biochemistry and Molecular Biologyca_ES
dc.relation.isformatofReproducció del document publicat a https://doi.org/10.1074/jbc.M303477200ca_ES
dc.relation.ispartofThe Journal of Biological Chemistry, 2003, vol. 278, núm 28, p. 25745-25751ca_ES
dc.rights(c) The American Society for Biochemistry and Molecular Biology, 2003ca_ES
dc.titleBiochemical characterization of yeast mitochondrial Grx5 monothiol glutaredoxinca_ES
dc.typearticleca_ES
dc.identifier.idgrec000005
dc.type.versionpublishedVersionca_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccessca_ES
dc.identifier.doihttps://doi.org/10.1074/jbc.M303477200


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