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Your request to link to MMDB for Urokinase-type plasminogen activator
| MMDB Description | |
|---|---|
| 17489 | Structural Basis for Selectivity of a Small Molecule, S1- Binding, Sub-micromolar Inhibitor of Urokinase Type Plasminogen Activator |
| 17490 | Structural Basis for Selectivity of a Small Molecule, S1- Binding, Sub-micromolar Inhibitor of Urokinase Type Plasminogen Activator |
| 17491 | Structural Basis for Selectivity of a Small Molecule, S1- Binding, Sub-micromolar Inhibitor of Urokinase Type Plasminogen Activator |
| 17492 | Structural Basis for Selectivity of a Small Molecule, S1- Binding, Sub-micromolar Inhibitor of Urokinase Type Plasminogen Activator |
| 13454 | Urokinase Plasminogen Activator B-chain Inhibitor Complex |
| 16693 | Urokinase Plasminogen Activator B-chain-benzamidine Complex |
| 16694 | Urokinase Plasminogen Activator B-chain-amiloride Complex |
| 17023 | Urokinase Plasminogen Activator B Chain-uki-1d Complex |
| 14861 | Crystal Structure of Human Microurokinase in Complex With 2- Amino-5-hydroxy-benzimidazole |
| 18534 | a Novel Serine Protease Inhibition Motif Involving a Multi-centered Short Hydrogen Bonding Network at the Active Site |
| 18535 | a Novel Serine Protease Inhibition Motif Involving a Multi- Centered Short Hydrogen Bonding Network at the Active Site |
| 18536 | a Novel Serine Protease Inhibition Motif Involving a Multi-centered Short Hydrogen Bonding Network at the Active Site |
| 19157 | Engineering Inhibitors Highly Selective for the S1 Sites of Ser190 Trypsin-like Serine Protease Drug Targets |
| 72139 | Engineering Inhibitors Highly Selective for the S1 Sites of Ser190 Trypsin-like Serine Protease Drug Targets |
| 19159 | Engineering Inhibitors Highly Selective for the S1 Sites of Ser190 Trypsin-like Serine Protease Drug Targets |
| 19160 | Engineering Inhibitors Highly Selective for the S1 Sites of Ser190 Trypsin-like Serine Protease Drug Targets |
| 19161 | Engineering Inhibitors Highly Selective for the S1 Sites of Ser190 Trypsin-like Serine Protease Drug Targets |
| 19162 | Engineering Inhibitors Highly Selective for the S1 Sites of Ser190 Trypsin-like Serine Protease Drug Targets |
| 19386 | Engineering Inhibitors Highly Selective for the S1 Sites of Ser190 Trypsin-like Serine Protease Drug Targets |
| 56549 | Sequential 1H NMR Assignments and Secondary Structure of the Kringle Domain From Urokinase |
| 50134 | LMW U-pa Structure Complexed With Egrcmk (Glu-gly-arg Chloromethyl Ketone) |
| 23914 | Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-directed Serine Protease Inhibitors |
| 29254 | Dissecting and Designing Inhibitor Selectivity Determinants at the S1 Site Using an Artificial Ala190 Protease (Ala190 Upa) |
| 29255 | Dissecting and Designing Inhibitor Selectivity Determinants at the S1 Site Using an Artificial Ala190 Protease (Ala190 Upa) |
| 29256 | Dissecting and Designing Inhibitor Selectivity Determinants at the S1 Site Using an Artificial Ala190 Protease (Ala190 Upa) |
| 24716 | Substituted 2-naphthamidine Inhibitors of Urokinase |
| 24717 | Substituted 2-naphthamidine Inhibitors of Urokinase |
| 24718 | Substituted 2-naphthamidine Inhibitors of Urokinase |
| 24719 | Substituted 2-naphthamidine Inhibitors of Urokinase |
| 24720 | Substituted 2-naphthamidine Inhibitors of Urokinase |
| 24721 | Substituted 2-naphthamidine Inhibitors of Urokinase |
| 28236 | Urokinase Plasminogen Activator B-chain-j435 Complex |
| 27438 | Substituted 2-naphthamidine Inhibitors of Urokinase |
| 27439 | Substituted 2-naphthamidine Inhibitors of Urokinase |
| 27440 | Substituted 2-naphthamidine Inhibitors of Urokinase |
| 30010 | Substituted 2-naphthamadine Inhibitors of Urokinase |
| 57580 | Solution Structure of the Amino Terminal Fragment of Urokinase-type Plasminogen Activator |
| 28438 | Urokinase Plasminogen Activator B-chain-jt464 Complex |
| 28439 | Urokinase Plasminogen Activator B-chain-jt463 Complex |
| 64469 | Urokinase Type Plasminogen Activator |
| 64470 | Urokinase Type Plasminogen Activator |
| 64471 | Urokinase Type Plasminogen Activator |
| 64472 | Urokinase Type Plasminogen Activator |
| 64473 | Urokinase Type Plasminogen Activator |
| 64474 | Urokinase Type Plasminogen Activator |
| 37726 | Structure of Human Urokinase Plasminogen Activator in Complex With Urokinase Receptor and an Anti-upar Antibody at 1.9 a |
| 42920 | Crystal Structure of the Free Aminoterminal Fragment of Urokinase Type Plasminogen Activator (Atf) |
| 43398 | Crystal Structure of Atf-urokinase Receptor Complex |
| 59154 | NEW Pharmacophore for Serine Protease Inhibition Revealed by Crystal Structure of Human Urokinase-type Plasminogen Activator Complexed With a Cyclic Peptidyl Inhibitor, Upain-1 |
| 61484 | Crystal Structure and Binding Epitopes of Urokinase-type Plasminogen Activator (C122an145q) in Complex With Inhibitors |
| 61485 | Crystal Structure and Binding Epitopes of Urokinase-type Plasminogen Activator (C122an145qs195a) in Complex With Inhibitors |
| 61486 | Crystal Structure and Binding Epitopes of Urokinase-type Plasminogen Activator (C122an145qs195a) in Complex With Inhibitors |
| 60287 | Urokinase Plasminogen Activator B-chain-gppe Complex |
| 62018 | Fragment-based Discovery of Mexiletine Derivatives as Orally Bioavailable Inhibitors of Urokinase-type Plasminogen Activator |
| 62019 | Fragment-based Discovery of Mexiletine Derivatives as Orally Bioavailable Inhibitors of Urokinase-type Plasminogen Activator |
| 62020 | Fragment-based Discovery of Mexiletine Derivatives as Orally Bioavailable Inhibitors of Urokinase-type Plasminogen Activator |
| 62021 | Fragment-based Discovery of Mexiletine Derivatives as Orally Bioavailable Inhibitors of Urokinase-type Plasminogen Activator |
| 62022 | Fragment-based Discovery of Mexiletine Derivatives as Orally Bioavailable Inhibitors of Urokinase-type Plasminogen Activator |
| 62023 | Fragment-based Discovery of Mexiletine Derivatives as Orally Bioavailable Inhibitors of Urokinase-type Plasminogen Activator |
| 62542 | Urokinase-type Plasminogen Activator Inhibitor Complex With a 1-(7-sulphoamidoisoquinolinyl)guanidine |
| 63295 | Structure of Urokinase Receptor, Urokinase and Vitronectin Complex |
| 63296 | Structure of Urokinase Receptor, Urokinase and Vitronectin Complex |
| 77351 | LOW 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 |
| 78465 | Crystal Structures of Urokinase-type Plasminogen Activator in Complex With 4-(aminomethyl) Benzoic Acid and 4- (Aminomethyl-phenyl)-methanol |
| 78468 | Crystal Structures of Urokinase-type Plasminogen Activator in Complex With 4-(aminomethyl) Benzoic Acid and 4- (Aminomethyl-phenyl)-methanol |
| 78469 | The Crystal Structures of 2-aminobenzothiazole-based Inhibitors in Complexes With Urokinase-type Plasminogen Activator |
| 81295 | Crystal Structure of Complex of Urokinase and a Upain-1 Variant(w3a) in Ph4.6 Condition |
| 81621 | The Complex Crystal Structure of Urokianse and 2- Aminobenzothiazole |
| 90937 | The Complex Crystal Structure of Urokianse and 5-nitro-1h-indole-2- Amidine |
| 87648 | Crystal Structure of a Michaelis Complex Between Plasminogen Activator Inhibitor-1 and Urokinase-type Plasminogen Activator |