HIRUSTASIN FROM HIRUDO MEDICINALIS AT 1.2 ANGSTROMS
The 1.2 A crystal structure of hirustasin reveals the intrinsic flexibility of a family of highly disulphide-bridged inhibitors.
A New Structural Class of Serine Protease Inhibitors Revealed by the Structure of the Hirustasin-Kallikrein Complex
Erratum. A New Structural Class of Serine Protease Inhibitors Revealed by the Structure of the Hirustasin-Kallikrein Complex
Recombinant Hirustasin: Production in Yeast, Crystallization, and Interaction with Serine Proteases
TWO DIFFERENT INDEPENDENT METHODS WERE USED FOR STRUCTURE SOLUTION
ANISOTROPIC REFINEMENT REDUCED FREE R (NO CUTOFF) BY 2%
MOEWS & KRETSINGER, J.MOL.BIOL.91(1973)201-2
ANTI-COAGULANT, PEPTIDIC INHIBITORS, CONFORMATIONAL FLEXIBILITY, SERINE PROTEASE INHIBITOR