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. 1997 Aug 8;272(32):19649-51.
doi: 10.1074/jbc.272.32.19649.

Selective loss of fibrinogen clotting in a loop-less thrombin

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Selective loss of fibrinogen clotting in a loop-less thrombin

Q D Dang et al. J Biol Chem. .

Abstract

The autolysis loop of thrombin comprises nine residues, from Glu146 to Lys149e, five of which (Ala149a-Lys149e) are inserted relative to trypsin and chymotrypsin. Deletion of the insertion Ala149a-Lys149e causes no significant change in the properties of the enzyme, except for a slight enhancement of protein C activation. Deletion of the entire Glu146-Lys149e loop, however, reduces fibrinogen clotting 240-fold, but decreases protein C activation only 2-fold. This loop-less mutant is de facto an exclusive activator of protein C, having lost the primary procoagulant function of thrombin. Because the autolysis loop affects fibrinogen binding, but not protein C activation, it provides a target for new drugs designed to suppress exclusively the procoagulant activity of thrombin.

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