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The protein encoded by MSRB3 catalyzes the reduction of methionine sulfoxide to methionine. Additionally we are shipping MSRB3 Antibodies (9) and MSRB3 Kits (3) and many more products for this protein.
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Human MSRB3 Protein expressed in Escherichia coli (E. coli) - ABIN667884
Kwon, Kwon, Bae, Cho, Park: Role of the methionine sulfoxide reductase MsrB3 in cold acclimation in Arabidopsis. in Plant & cell physiology 2007
MsrB3 deficiency activates the cell cycle inhibitors p21 (show CDKN1A Proteins) and p27 (show PAK2 Proteins).
DNA methylation (show HELLS Proteins) shows genome-wide association of NFIX (show MLZE Proteins), RAPGEF2 (show RAPGEF2 Proteins) and MSRB3 with gestational age at birth.
these data provide evidence that the ER-type of MsrB3 plays an important role in protection against ER stress, suggesting that MsrB3 may be involved in the regulation of ER homeostasis.
Taken together, these data provide evidence that the ER type of MsrB (show MSRB2 Proteins), MsrB3A, plays an important role in protection mechanisms against oxidative, cold and heat stresses and, moreover, in the regulation of fruit fly aging.
Results identified an antimicrobial peptide (show cAMP Proteins) from the human methionine sulfoxide reductase B3 protein.
an in vitro assay revealed that p.Cys89Gly completely abolished MSRB3 enzymatic activity and that p.Arg19X is a null allele for MSRB3 mitochondrial isoforms, indicating that DFNB74 deafness might be a mitochondrial disease limited to the inner ear.
data suggest that MsrB3 plays an essential role in maintaining the integrity of hair cells, possibly explaining the pathogenesis of DFNB74 deafness in humans caused by MSRB3 deficiency.
MsrB3 deficiency activates the cell cycle inhibitors p21 and p27 (show CDKN1B Proteins).
data suggest that, in mice, MsrB3 is largely or exclusively an endoplasmic reticulum-resident protein, and that the reduction of methionine-R-sulfoxides in different cellular compartments is provided by individual MsrB (show MSRB2 Proteins) isozymes. [MsrB3]
The protein encoded by this gene catalyzes the reduction of methionine sulfoxide to methionine. This enzyme acts as a monomer and requires zinc as a cofactor. Several transcript variants encoding two different isoforms have been found for this gene. One of the isoforms localizes to mitochondria while the other localizes to endoplasmic reticula.
methionine-R-sulfoxide reductase B3
, methionine-R-sulfoxide reductase B3, mitochondrial
, Methionine-R-sulfoxide reductase B3, mitochondrial