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Molecular mechanisms of plasminogen activation: bacterial cofactors provide clues.
- Source :
-
Trends in biochemical sciences [Trends Biochem Sci] 2000 Feb; Vol. 25 (2), pp. 53-9. - Publication Year :
- 2000
-
Abstract
- Plasminogen activation is a key event in the fibrinolytic system that results in the dissolution of blood clots, and also promotes cell migration and tissue remodelling. The recent structure determinations of microplasmin in complex with the bacterial plasminogen activators staphylokinase and streptokinase have provided novel insights into the molecular mechanisms of plasminogen activation and cofactor function. These bacterial proteins are cofactor molecules that contribute to exosite formation and enhance the substrate presentation to the enzyme. At the same time, they modulate the specificity of plasmin towards substrates and inhibitors, making a 'specificity switch' possible.
- Subjects :
- Amino Acid Sequence
Fibrinolysin metabolism
Humans
Metalloendopeptidases chemistry
Molecular Sequence Data
Peptide Fragments metabolism
Plasminogen chemistry
Plasminogen Activators chemistry
Streptokinase chemistry
Streptokinase metabolism
Fibrinolysin antagonists & inhibitors
Fibrinolysin chemistry
Metalloendopeptidases metabolism
Peptide Fragments chemistry
Plasminogen metabolism
Plasminogen Activators metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0968-0004
- Volume :
- 25
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Trends in biochemical sciences
- Publication Type :
- Academic Journal
- Accession number :
- 10664583
- Full Text :
- https://doi.org/10.1016/s0968-0004(99)01521-2