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The kindest cuts of all: crystal structures of Kex2 and furin reveal secrets of precursor processing.
- Source :
-
Trends in biochemical sciences [Trends Biochem Sci] 2004 Feb; Vol. 29 (2), pp. 80-7. - Publication Year :
- 2004
-
Abstract
- Pro-hormone or pro-protein convertases are a conserved family of eukaryotic serine proteases found in the secretory pathway. These endoproteases mature precursors for peptides and proteins that perform a wide range of physiologically important and clinically relevant functions. The first member of this family to be identified was Kex2 in the yeast Saccharomyces cerevisiae. One mammalian member of this family - furin - is responsible for processing substrates that include insulin pro-receptor, human immunodeficiency virus gp160 glycoprotein, Ebola virus glycoprotein, and anthrax protective antigen. Recent determination of the crystal structures for the catalytic core domains of both Kex2 and furin - the first for any members of this family - provide remarkable insights and a new level of understanding of substrate specificity and catalysis by the pro-protein convertases.
- Subjects :
- Animals
Binding Sites
Calcium metabolism
Catalysis
Endopeptidase K chemistry
Forecasting
Furin chemistry
Humans
Models, Molecular
Proprotein Convertases chemistry
Protein Conformation
Protein Structure, Tertiary
Saccharomyces cerevisiae
Saccharomyces cerevisiae Proteins chemistry
Substrate Specificity
Subtilisins chemistry
Terminology as Topic
Crystallography, X-Ray
Furin metabolism
Proprotein Convertases metabolism
Protein Precursors metabolism
Protein Processing, Post-Translational
Saccharomyces cerevisiae Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0968-0004
- Volume :
- 29
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Trends in biochemical sciences
- Publication Type :
- Academic Journal
- Accession number :
- 15102434
- Full Text :
- https://doi.org/10.1016/j.tibs.2003.12.006