Figure 5.
Figure 5. Self-generated cofactor-assisted substrate interactions of thrombin. Once thrombin has cleaved FPA from fibrinogen, fibrin monomer is formed, to which the thrombin remains attached via exosite I interactions at the N-terminal E domain (A). Factor XIII (FXIII) is also loosely bound to fibrin, but at the C-terminal D domain (B). The fibrin monomers will spontaneously polymerize. It has been proposed that this approximates the thrombin and factor XIII (C), resulting in efficient cleavage of the activation peptide (AP).47 Fibrin(ogen) polypeptide chains are colored as in figure 3A.

Self-generated cofactor-assisted substrate interactions of thrombin. Once thrombin has cleaved FPA from fibrinogen, fibrin monomer is formed, to which the thrombin remains attached via exosite I interactions at the N-terminal E domain (A). Factor XIII (FXIII) is also loosely bound to fibrin, but at the C-terminal D domain (B). The fibrin monomers will spontaneously polymerize. It has been proposed that this approximates the thrombin and factor XIII (C), resulting in efficient cleavage of the activation peptide (AP).47  Fibrin(ogen) polypeptide chains are colored as in figure 3A.

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