1. Gene
  2. MSRB1 - methionine sulfoxide reductase B1 Gene

MSRB1 - methionine sulfoxide reductase B1 Gene

Homo sapiens

Also known as SELR; SELX; SepR; SEPX1; HSPC270; SELENOR; SELENOX

Gene ID: 51734 | Gene type: protein coding

About MSRB1

Cytogenetic location: 16p13.3 Genomic coordinates (GRCh38): 16:1,938,229-1,943,199 (from NCBI)

This gene has 5 transcripts (splice variants), 282 orthologues and 3 paralogues. Ubiquitous expression in kidney (RPKM 37.2), liver (RPKM 35.6) and 25 other tissues.

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]

MSRB1 Products(3)

mRNA Protein Name
NM_001382264.1 NP_001369193.1 methionine-R-sulfoxide reductase B1 isoform 2
NM_001382265.1 NP_001369194.1 methionine-R-sulfoxide reductase B1 isoform 3
NM_016332.4 NP_057416.1 methionine-R-sulfoxide reductase B1 isoform 1
Gene Ontology
  • Molecular Function
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
23805218 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

MSRB1 Protein Structure

SelR

SelR: SelR domain (11 - 105)

  • 0
  • 100
  • 116 a.a.
Protein Preferred Names Protein Names

methionine-R-sulfoxide reductase B1

selenoprotein R

MSRB1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
MSRB1 Q9NZV6 CLU Homo sapiens P10909-5 23805218
Intra
MSRB1 Q9NZV6 CLU Homo sapiens P10909-5 23805218
Intra
MSRB1 Q9NZV6 CLU Homo sapiens P10909-5 23805218
Intra
MSRB1 Q9NZV6 CLU Homo sapiens P10909-5
Y2H
23805218
Intra
MSRB1 Q9NZV6 CLU Homo sapiens P10909-5 23805218
Intra
MSRB1 Q9NZV6 CLU Homo sapiens P10909-5 23805218
Intra
MSRB1 Q9NZV6 IFT88 Homo sapiens Q13099 32296183
Intra
MSRB1 Q9NZV6 IFT88 Homo sapiens Q13099 32296183
Intra
MSRB1 Q9NZV6 CYSRT1 Homo sapiens A8MQ03 32296183
Intra
MSRB1 Q9NZV6 CYSRT1 Homo sapiens A8MQ03 32296183
Intra
MSRB1 Q9NZV6 INCA1 Homo sapiens Q0VD86 32296183
Intra
MSRB1 Q9NZV6 INCA1 Homo sapiens Q0VD86 32296183
Intra
MSRB1 Q9NZV6 TRIM27 Homo sapiens P14373 32296183
Intra
MSRB1 Q9NZV6 TRIM27 Homo sapiens P14373 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Staphyloenterotoxemia

Staphylococcal Food Poisoning

Staphylococcal Toxaemia Due To Food

Staphyloenterotoxicosis

Keshan Disease

Caused By Deficiency Of Selenium In The Diet

Enlarged Heart And Poor Heart Function

Progressive Myoclonus Epilepsy 1a

Epm1a

Commensal Bacterial Infectious Disease
Cataract

Cataracts

Cat - [Cataract]

Cataract Form

Lens Opacity

Lens Opacities

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Macaca mulatta MSRB1 VGNC VGNC:99524
Mus musculus MSRB1 MGD MGI:1351642
Rattus norvegicus MSRB1 RGD RGD:1583243
Felis catus MSRB1 VGNC VGNC:80602