Prediction of the three-dimensional structure of the enzymatic domain of t-PA |
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Authors: | A. Heckel K. M. Hasselbach |
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Affiliation: | (1) Department of Chemical Research, Dr. Karl Thomae GmbH, Birkendorfer Strasse 65, D-7950 Biberach 1, Germany |
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Abstract: | Summary Tissue plasminogen activator (t-PA), an enzyme of the fibrinolytic system, is responsible for lysis of fibrin via activation of plasminogen, and therefore for degradation of blood clots. There are currently no X-ray crystal structure data of the t-PA molecule available either in whole or in part. We therefore predicted the three-dimensional structure of the protease domain by means of computer-graphical methods.The model obtained forms a basis for understanding the binding of plasminogen to the active site of t-PA. In addition, the interactions of various inhibitors with t-PA were studied by modeling them into the active site. The model also yields an explanation for the observed amidolytic activity of t-PA in the single chain form. |
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Keywords: | Modeling Serine protease Computer graphics Fibrinolysis |
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