MSRB1 methionine sulfoxide reductase B1 [ Homo sapiens (human) ]
Source: NCBI Gene (ID 51734)
Source: NCBI Gene (ID 51734)
Symbol: MSRB1
Full name: methionine sulfoxide reductase B1
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Also known as: HSPC270; SELENOR; SELENOX; SELR; SELX; SEPX1; SepR
Summary: The protein encoded by this gene belongs to the methionine-R-sulfoxide reductase B (MsrB) family. Members of this family function as repair enzymes that protect proteins from oxidative stress by catalyzing the reduction of methionine-R-sulfoxides to methionines. This protein is highly expressed in liver and kidney, and is localized to the nucleus and cytosol. It is the only member of the MsrB family that is a selenoprotein, containing a selenocysteine (Sec) residue at its active site. It also has the highest methionine-R-sulfoxide reductase activity compared to other members containing cysteine in place of Sec. Sec is encoded by the UGA codon, which normally signals translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, designated the Sec insertion sequence (SECIS) element, that is necessary for the recognition of UGA as a Sec codon, rather than as a stop signal. A pseudogene of this locus has been identified on chromosome 19. [provided by RefSeq, Aug 2017]
Expression: Ubiquitous expression in kidney (RPKM 37.2), liver (RPKM 35.6) and 25 other tissues
Orthologs: mouse
Gene size: 4971bp
Exon count: 4