MAS1

MAS proto-oncogene, or MAS1 proto-oncogene, G protein-coupled receptor (MRGA, MAS, MGRA""), is a protein that in humans is encoded by the MAS1 gene.[5] The structure of the MAS1 product indicates that it belongs to the class of receptors that are coupled to GTP-binding proteins and share a conserved structural motif, which is described as a '7-transmembrane segment' following the prediction that these hydrophobic segments form membrane-spanning alpha-helices. The MAS1 protein may be a receptor that, when activated, modulates a critical component in a growth-regulating pathway to bring about oncogenic effects.[5]

MAS1
Identifiers
AliasesMAS1, MAS1 proto-oncogene, G protein-coupled receptor, MAS, MGRA
External IDsOMIM: 165180 MGI: 96918 HomoloGene: 1782 GeneCards: MAS1
Orthologs
SpeciesHumanMouse
Entrez

4142

17171

Ensembl

ENSG00000130368

ENSMUSG00000068037

UniProt

P04201

P30554

RefSeq (mRNA)

NM_002377
NM_001366704

NM_008552

RefSeq (protein)

NP_002368
NP_001353633

NP_032578

Location (UCSC)Chr 6: 159.89 – 159.92 MbChr 17: 13.06 – 13.09 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Agonists of the receptor include angiotensin-(1-7). Antagonist include A-779 (angiotensin-1-7 with c-terminal proline substituted for D-Ala), or D-Pro (angiotensin-1-7 with c-terminal proline submitted for D-proline).

Mas1 proto-oncogene (MAS1, MGRA) is not to be confused with the MAS-related G-protein coupled receptor, a recently believed to be activated by the ligand alamandine (generated by catalysis of Ang A via ACE2 or directly from Ang-(1-7)).

See also

References

  1. GRCh38: Ensembl release 89: ENSG00000130368 - Ensembl, May 2017
  2. GRCm38: Ensembl release 89: ENSMUSG00000068037 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. "Entrez Gene: MAS1 MAS1 oncogene".

Further reading

This article incorporates text from the United States National Library of Medicine, which is in the public domain.

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