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Your request to link to MMDB for Urokinase-type plasminogen activator/surface receptor


MMDB Description
17489Structural Basis for Selectivity of a Small Molecule, S1- Binding, Sub-micromolar Inhibitor of Urokinase Type Plasminogen Activator
17490Structural Basis for Selectivity of a Small Molecule, S1- Binding, Sub-micromolar Inhibitor of Urokinase Type Plasminogen Activator
17491Structural 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
13454Urokinase Plasminogen Activator B-chain Inhibitor Complex
16693Urokinase Plasminogen Activator B-chain-benzamidine Complex
16694Urokinase Plasminogen Activator B-chain-amiloride Complex
17023Urokinase Plasminogen Activator B Chain-uki-1d Complex
14861Crystal Structure of Human Microurokinase in Complex With 2- Amino-5-hydroxy-benzimidazole
18534a Novel Serine Protease Inhibition Motif Involving a Multi-centered Short Hydrogen Bonding Network at the Active Site
18535a Novel Serine Protease Inhibition Motif Involving a Multi- Centered Short Hydrogen Bonding Network at the Active Site
18536a Novel Serine Protease Inhibition Motif Involving a Multi-centered Short Hydrogen Bonding Network at the Active Site
19157Engineering Inhibitors Highly Selective for the S1 Sites of Ser190 Trypsin-like Serine Protease Drug Targets
72139Engineering Inhibitors Highly Selective for the S1 Sites of Ser190 Trypsin-like Serine Protease Drug Targets
19159Engineering Inhibitors Highly Selective for the S1 Sites of Ser190 Trypsin-like Serine Protease Drug Targets
19160Engineering Inhibitors Highly Selective for the S1 Sites of Ser190 Trypsin-like Serine Protease Drug Targets
19161Engineering Inhibitors Highly Selective for the S1 Sites of Ser190 Trypsin-like Serine Protease Drug Targets
19162Engineering Inhibitors Highly Selective for the S1 Sites of Ser190 Trypsin-like Serine Protease Drug Targets
19386Engineering Inhibitors Highly Selective for the S1 Sites of Ser190 Trypsin-like Serine Protease Drug Targets
56549Sequential 1H NMR Assignments and Secondary Structure of the Kringle Domain From Urokinase
50134LMW U-pa Structure Complexed With Egrcmk (Glu-gly-arg Chloromethyl Ketone)
23914Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-directed Serine Protease Inhibitors
29254Dissecting and Designing Inhibitor Selectivity Determinants at the S1 Site Using an Artificial Ala190 Protease (Ala190 Upa)
29255Dissecting and Designing Inhibitor Selectivity Determinants at the S1 Site Using an Artificial Ala190 Protease (Ala190 Upa)
29256Dissecting and Designing Inhibitor Selectivity Determinants at the S1 Site Using an Artificial Ala190 Protease (Ala190 Upa)
24716Substituted 2-naphthamidine Inhibitors of Urokinase
24717Substituted 2-naphthamidine Inhibitors of Urokinase
24718Substituted 2-naphthamidine Inhibitors of Urokinase
24719Substituted 2-naphthamidine Inhibitors of Urokinase
24720Substituted 2-naphthamidine Inhibitors of Urokinase
24721Substituted 2-naphthamidine Inhibitors of Urokinase
28236Urokinase Plasminogen Activator B-chain-j435 Complex
27438Substituted 2-naphthamidine Inhibitors of Urokinase
27439Substituted 2-naphthamidine Inhibitors of Urokinase
27440Substituted 2-naphthamidine Inhibitors of Urokinase
30010Substituted 2-naphthamadine Inhibitors of Urokinase
57580Solution Structure of the Amino Terminal Fragment of Urokinase-type Plasminogen Activator
28438Urokinase Plasminogen Activator B-chain-jt464 Complex
28439Urokinase Plasminogen Activator B-chain-jt463 Complex
64469Urokinase Type Plasminogen Activator
64470Urokinase Type Plasminogen Activator
64471Urokinase Type Plasminogen Activator
64472Urokinase Type Plasminogen Activator
64473Urokinase Type Plasminogen Activator
64474Urokinase Type Plasminogen Activator
37726Structure of Human Urokinase Plasminogen Activator in Complex With Urokinase Receptor and an Anti-upar Antibody at 1.9 a
42920Crystal Structure of the Free Aminoterminal Fragment of Urokinase Type Plasminogen Activator (Atf)
43398Crystal Structure of Atf-urokinase Receptor Complex
59154NEW Pharmacophore for Serine Protease Inhibition Revealed by Crystal Structure of Human Urokinase-type Plasminogen Activator Complexed With a Cyclic Peptidyl Inhibitor, Upain-1
61484Crystal Structure and Binding Epitopes of Urokinase-type Plasminogen Activator (C122an145q) in Complex With Inhibitors
61485Crystal Structure and Binding Epitopes of Urokinase-type Plasminogen Activator (C122an145qs195a) in Complex With Inhibitors
61486Crystal Structure and Binding Epitopes of Urokinase-type Plasminogen Activator (C122an145qs195a) in Complex With Inhibitors
60287Urokinase Plasminogen Activator B-chain-gppe Complex
62018Fragment-based Discovery of Mexiletine Derivatives as Orally Bioavailable Inhibitors of Urokinase-type Plasminogen Activator
62019Fragment-based Discovery of Mexiletine Derivatives as Orally Bioavailable Inhibitors of Urokinase-type Plasminogen Activator
62020Fragment-based Discovery of Mexiletine Derivatives as Orally Bioavailable Inhibitors of Urokinase-type Plasminogen Activator
62021Fragment-based Discovery of Mexiletine Derivatives as Orally Bioavailable Inhibitors of Urokinase-type Plasminogen Activator
62022Fragment-based Discovery of Mexiletine Derivatives as Orally Bioavailable Inhibitors of Urokinase-type Plasminogen Activator
62023Fragment-based Discovery of Mexiletine Derivatives as Orally Bioavailable Inhibitors of Urokinase-type Plasminogen Activator
62542Urokinase-type Plasminogen Activator Inhibitor Complex With a 1-(7-sulphoamidoisoquinolinyl)guanidine
63295Structure of Urokinase Receptor, Urokinase and Vitronectin Complex
63296Structure of Urokinase Receptor, Urokinase and Vitronectin Complex
77351LOW Molecular Weigth Human Urokinase Type Plasminogen Activator 2-[6- (3'-aminomethyl-biphenyl-3-yloxy)-4-(3-dimethylamino-pyrrolidin-1- Yl)-3,5-difluoro-pyridin-2-yloxy]-4-dimethylamino-benzoic Acid Complex
78465Crystal Structures of Urokinase-type Plasminogen Activator in Complex With 4-(aminomethyl) Benzoic Acid and 4- (Aminomethyl-phenyl)-methanol
78468Crystal Structures of Urokinase-type Plasminogen Activator in Complex With 4-(aminomethyl) Benzoic Acid and 4- (Aminomethyl-phenyl)-methanol
78469The Crystal Structures of 2-aminobenzothiazole-based Inhibitors in Complexes With Urokinase-type Plasminogen Activator
81295Crystal Structure of Complex of Urokinase and a Upain-1 Variant(w3a) in Ph4.6 Condition
81621The Complex Crystal Structure of Urokianse and 2- Aminobenzothiazole
90937The Complex Crystal Structure of Urokianse and 5-nitro-1h-indole-2- Amidine
87648Crystal Structure of a Michaelis Complex Between Plasminogen Activator Inhibitor-1 and Urokinase-type Plasminogen Activator