Proprotein convertase subtilisin/kexin type 1 inhibitor

Mammalian protein found in Homo sapiens From Wikipedia, the free encyclopedia

Proprotein convertase subtilisin/kexin type 1 inhibitor is a protein by the name of proSAAS that in humans is encoded by the PCSK1N gene. [5]

AliasesPCSK1N, PROSAAS, SAAS, SCG8, SgVIII, BigLEN, PEN, proprotein convertase subtilisin/kexin type 1 inhibitor
End48,835,610 bp[1]
Quick facts PCSK1N, Identifiers ...
PCSK1N
Identifiers
AliasesPCSK1N, PROSAAS, SAAS, SCG8, SgVIII, BigLEN, PEN, proprotein convertase subtilisin/kexin type 1 inhibitor
External IDsOMIM: 300399; MGI: 1353431; HomoloGene: 8315; GeneCards: PCSK1N; OMA:PCSK1N - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_013271

NM_013892

RefSeq (protein)

NP_037403

NP_038920

Location (UCSC)Chr X: 48.83 – 48.84 MbChr X: 7.79 – 7.79 Mb
PubMed search[3][4]
Wikidata
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Function

This protein is expressed largely in cells possessing a regulated secretory pathway, such as endocrine/neuroendocrine cells and neurons. The intact proSAAS protein, as well as the carboxyy-terminal peptide containing the inhibitory hexapeptide LLRVKR, functions as an inhibitor of prohormone convertase 1/3, which accomplishes the initial proteolytic cleavage of peptide precursors. ProSAAS is further processed at the N- and C-termini into multiple short peptides, leaving the central segment intact. This central, unprocessed portion of the protein may function as a neural- and endocrine-specific chaperone due to its potent ability to block the aggregation of beta amyloid and alpha synuclein in vitro, and to block oligomer cytotoxicity in cells.[6][7] Recent data show that nigral proSAAS expression blocks the deterioration of the striatonigral pathway in a synuclein rat model of Parkinson's disease.[8] ProSAAS also oligomerizes and undergoes liquid-liquid phase separation.[9] Differential expression of this gene may be associated with obesity.

References

Further reading

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