PRIMA1

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Proline-rich membrane anchor 1, also known as PRiMA, is a protein that in humans is encoded by the PRIMA1 gene.[4][5]

AliasesPRIMA1, PRIMA, proline rich membrane anchor 1
Chr.Chromosome 12 (mouse)[1]
End103,208,409 bp[1]
Quick facts Identifiers, Aliases ...
PRIMA1
Identifiers
AliasesPRIMA1, PRIMA, proline rich membrane anchor 1
External IDsOMIM: 613851; MGI: 1926097; HomoloGene: 15783; GeneCards: PRIMA1; OMA:PRIMA1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_178004
NM_178013

NM_133364
NM_178023

RefSeq (protein)

NP_821092
NP_821092.1

NP_579942

Location (UCSC)n/aChr 12: 103.16 – 103.21 Mb
PubMed search[2][3]
Wikidata
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Function

PRiMA functions to organize acetylcholinesterase (AChE) into tetramers, and to anchor AChE at neural cell membranes.[4] This is accomplished by the proline rich anchor domain (PRAD) of PRIMA1 which anchors the tetramer of AChE into the plasma membrane of neural cells and myocytes.[6] The PRAD interacts with the C-terminal T-peptide of AChE.[7]

PRiMA plays a role in targeting AChE to the cell surface and, in neuroblastoma cells, PRiMA the limiting factor of such targeting.[5] In both mice and humans, PRiMA exists as two alternative splice variants that differ in their cytoplasmic regions.

Clinical significance

The severity of neurogenerative diseases, such as Alzheimer’s, can be related to the degradation of AChE.[8]

References

Further reading

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