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MMDB Description
17482Structural Basis for Selectivity of a Small Molecule, S1- Binding, Sub-micromolar Inhibitor of Urokinase Type Plasminogen Activator
17492Structural Basis for Selectivity of a Small Molecule, S1- Binding, Sub-micromolar Inhibitor of Urokinase Type Plasminogen Activator
182541.00 AA Trypsin From Atlantic Salmon
18617Recruiting Zinc to Mediate Potent, Specific Inhibition of Serine Proteases
35632Expression, Crystallization and Three-dimensional Structure of the Catalytic Domain of Human Plasma Kallikrein: Implications for Structure-based Design of Protease Inhibitors
35633Expression, Crystallization and the Three-dimensional Structure of the Catalytic Domain of Human Plasma Kallikrein: Implications for Structure-based Design of Protease Inhibitors
48262Crystal Structure of Beta-trypsin in Complex With Benzamidine
48316Structural Basis for Selectivity of a Small Molecule, S1-binding, Sub- Micromolar Inhibitor of Urokinase Type Plasminogen Activator
51228Complex of Benzamidine With the Catalytic Domain of Human Two Chain Tissue Plasminogen Activator [(tc)-t-pa]