Biology:Membrane-bound transcription factor site-1 protease

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Short description: Mammalian protein found in Homo sapiens


A representation of the 3D structure of the protein myoglobin showing turquoise α-helices.
Generic protein structure example

Membrane-bound transcription factor site-1 protease, or site-1 protease (S1P) for short, also known as subtilisin/kexin-isozyme 1 (SKI-1), is an enzyme (EC 3.4.21.112) that in humans is encoded by the MBTPS1 gene.[1] S1P cleaves the endoplasmic reticulum loop of sterol regulatory element-binding protein (SREBP) transcription factors.[2][3]

Function

This gene encodes a member of the subtilisin-like proprotein convertase family, which includes proteases that process protein and peptide precursors trafficking through regulated or constitutive branches of the secretory pathway. The encoded protein undergoes an initial autocatalytic processing event in the endoplasmic reticulum (ER) to generate a heterodimer which exits the ER and sorts to the cis/medial-Golgi where a second autocatalytic event takes place and the catalytic activity is acquired. It encodes a type 1 membrane bound protease which is ubiquitously expressed and regulates cholesterol or lipid homeostasis via cleavage of substrates at non-basic residues.[1]

Clinical significance

Mutations in this gene may be associated with lysosomal dysfunction.[1]

See also

References

  1. 1.0 1.1 1.2 "Entrez Gene: Membrane-bound transcription factor peptidase, site 1". https://www.ncbi.nlm.nih.gov/gene/8720. 
  2. "A proteolytic pathway that controls the cholesterol content of membranes, cells, and blood". Proc. Natl. Acad. Sci. U.S.A. 96 (20): 11041–8. 1999. doi:10.1073/pnas.96.20.11041. PMID 10500120. Bibcode1999PNAS...9611041B. 
  3. "Genomic structure and chromosomal mapping of the human site-1 protease (S1P) gene". J. Hum. Genet. 45 (4): 212–7. 2000. doi:10.1007/s100380070029. PMID 10944850. 

External links

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