Sandbox Reserved 1091

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== Generalities ==
== Generalities ==
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The ASP protein is a serine protease that will cut peptide bonds after specific amino acids. The kexin-like serine protease belongs to the subtilisin family (subtilases). The structure of ASP is similar to that of Kex2 <ref>PMID:2646633</ref>, a protease of the subtilisin family, but ASP has a unique extra occluding region close to its active site.
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The ASP protein is a serine protease that will cut peptide bonds after specific amino acids. The kexin-like serine protease belongs to the subtilisin family (subtilases). The structure of ASP is similar to that of Kex2 <ref>PMID:2646633</ref>, a protease of the subtilisin family, but ASP has a unique extra occluding region close to its active site. o
The maturation of ASP is achieved by ORF2. This protein plays the role of an external chaperone and is necessary for the construction of the stable ASP. Indeed, ASP doesn’t contain a propeptide (such as Kex2) that is involved in the proper folding of the protein.
The maturation of ASP is achieved by ORF2. This protein plays the role of an external chaperone and is necessary for the construction of the stable ASP. Indeed, ASP doesn’t contain a propeptide (such as Kex2) that is involved in the proper folding of the protein.

Revision as of 17:01, 11 January 2020

This Sandbox is Reserved from 25/11/2019, through 30/9/2020 for use in the course "Structural Biology" taught by Bruno Kieffer at the University of Strasbourg, ESBS. This reservation includes Sandbox Reserved 1091 through Sandbox Reserved 1115.
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The serine protease from Aeromonas sobria

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References

  1. Fuller RS, Brake A, Thorner J. Yeast prohormone processing enzyme (KEX2 gene product) is a Ca2+-dependent serine protease. Proc Natl Acad Sci U S A. 1989 Mar;86(5):1434-8. PMID:2646633
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