UniProt P08254
P08254
P08254 (UniProt P08254): 86 experimental structures on GenesisL1, 3 ligands bound. Binding sites, pockets, druggability and 3D structures in GL1X.
- UniProt
- P08254
- Experimental structures
- 86
- Predicted models
- 0
- Ligands
- 3
Structures
86 records of P08254 in the MolNFT archive: 86 experimental, 0 predicted.
| Entry | Title | Method | Chains | Ligands | Pockets |
|---|---|---|---|---|---|
| 1B3D | Stromelysin-1 | x-ray diffraction | A, B | — | — |
| 1B3D | Stromelysin-1 | x-ray diffraction | A, B | — | — |
| 1B8Y | X-ray structure of human stromelysin catalytic domain complexed with non-peptide inhibitors… | x-ray diffraction | A | — | — |
| 1B8Y | X-ray structure of human stromelysin catalytic domain complexed with non-peptide inhibitors… | x-ray diffraction | A | — | — |
| 1BIW | Design and synthesis of conformationally-constrained mmp inhibitors | x-ray diffraction | A, B | — | — |
| 1BIW | Design and synthesis of conformationally-constrained mmp inhibitors | x-ray diffraction | A, B | — | — |
| 1BM6 | Solution structure of the catalytic domain of human stromelysin-1 complexed to a potent… | solution nmr | A | — | — |
| 1BM6 | Solution structure of the catalytic domain of human stromelysin-1 complexed to a potent… | solution nmr | A | — | — |
| 1BQO | Discovery of potent, achiral matrix metalloproteinase inhibitors | x-ray diffraction | A, B | — | — |
| 1BQO | Discovery of potent, achiral matrix metalloproteinase inhibitors | x-ray diffraction | A, B | — | — |
| 1C3I | Human stromelysin-1 catalytic domain complexed with ro-26-2812 | x-ray diffraction | A, B | — | — |
| 1C3I | Human stromelysin-1 catalytic domain complexed with ro-26-2812 | x-ray diffraction | A, B | — | — |
| 1C8T | Human stromelysin-1 (E202Q) catalytic domain complexed with ro-26-2812 | x-ray diffraction | A, B | — | — |
| 1C8T | Human stromelysin-1 (E202Q) catalytic domain complexed with ro-26-2812 | x-ray diffraction | A, B | — | — |
| 1CAQ | X-ray structure of human stromelysin catalytic domain complexes with non-peptide inhibitors… | x-ray diffraction | A | — | — |
| 1CAQ | X-ray structure of human stromelysin catalytic domain complexes with non-peptide inhibitors… | x-ray diffraction | A | — | — |
| 1CIZ | X-ray structure of human stromelysin catalytic domain complexes with non-peptide inhibitors… | x-ray diffraction | A | — | — |
| 1CIZ | X-ray structure of human stromelysin catalytic domain complexes with non-peptide inhibitors… | x-ray diffraction | A | — | — |
| 1CQR | Crystal structure of the stromelysin catalytic domain at 2.0 a resolution | x-ray diffraction | A, B | — | — |
| 1CQR | Crystal structure of the stromelysin catalytic domain at 2.0 a resolution | x-ray diffraction | A, B | — | — |
| 1D5J | Crystal structure of MMP3 complexed with a thiazepine based inhibitor. | x-ray diffraction | A, B | — | — |
| 1D5J | Crystal structure of MMP3 complexed with a thiazepine based inhibitor. | x-ray diffraction | A, B | — | — |
| 1D7X | Crystal structure of MMP3 complexed with a modified proline scaffold based inhibitor. | x-ray diffraction | A, B | — | — |
| 1D7X | Crystal structure of MMP3 complexed with a modified proline scaffold based inhibitor. | x-ray diffraction | A, B | — | — |
| 1D8F | Crystal structure of MMP3 complexed with a piperazine based inhibitor. | x-ray diffraction | A, B | — | — |
| 1D8F | Crystal structure of MMP3 complexed with a piperazine based inhibitor. | x-ray diffraction | A, B | — | — |
| 1D8M | Crystal structure of MMP3 complexed with a heterocycle-based inhibitor | x-ray diffraction | A, B | — | — |
| 1D8M | Crystal structure of MMP3 complexed with a heterocycle- based inhibitor | x-ray diffraction | A, B | — | — |
| 1G05 | Heterocycle-based mmp inhibitor with P2'SUBSTITUENTS | x-ray diffraction | A, B | — | — |
| 1G05 | Heterocycle-based mmp inhibitor with P2'SUBSTITUENTS | x-ray diffraction | A, B | — | — |
| 1G49 | A carboxylic acid based inhibitor in complex with MMP3 | x-ray diffraction | A, B | — | — |
| 1G49 | A carboxylic acid based inhibitor in complex with MMP3 | x-ray diffraction | A, B | — | — |
| 1G4K | X-ray Structure of a Novel Matrix Metalloproteinase Inhibitor Complexed to Stromelysin | x-ray diffraction | A, B, C | — | — |
| 1G4K | X-ray structure of a novel matrix metalloproteinase inhibitor complexed to stromelysin | x-ray diffraction | A, B, C | — | — |
| 1HFS | Crystal structure of the catalytic domain of human fibroblast stromelysin-1 inhibited with the… | x-ray diffraction | A | — | — |
| 1HFS | Crystal structure of the catalytic domain of human fibroblast stromelysin-1 inhibited with the… | x-ray diffraction | A | — | — |
| 1HY7 | A carboxylic acid based inhibitor in complex with MMP3 | x-ray diffraction | A, B | — | — |
| 1HY7 | A carboxylic acid based inhibitor in complex with MMP3 | x-ray diffraction | A, B | — | — |
| 1OO9 | Orientation in Solution of MMP-3 Catalytic Domain and N-TIMP-1 from Residual Dipolar Couplings | solution nmr | A | — | — |
| 1OO9 | Orientation in solution of mmp-3 catalytic domain and N-timp-1 from residual dipolar couplings | solution nmr | A | — | — |
| 1QIA | Crystal structure of stromelysin catalytic domain | x-ray diffraction | A, B, C, D | — | — |
| 1QIA | Crystal structure of stromelysin catalytic domain | x-ray diffraction | A, B, C, D | — | — |
| 1QIC | Crystal structure of stromelysin catalytic domain | x-ray diffraction | A, B, C, D | — | — |
| 1QIC | Crystal structure of stromelysin catalytic domain | x-ray diffraction | A, B, C, D | — | — |
| 1SLM | Crystal structure of fibroblast stromelysin-1: the C-truncated human proenzyme | x-ray diffraction | A | — | — |
| 1SLM | Crystal structure of fibroblast stromelysin-1: the C-truncated human proenzyme | x-ray diffraction | A | — | — |
| 1SLN | Crystal structure of the catalytic domain of human fibroblast stromelysin-1 inhibited with the… | x-ray diffraction | A | — | — |
| 1SLN | Crystal structure of the catalytic domain of human fibroblast stromelysin-1 inhibited with the… | x-ray diffraction | A | — | — |
| 1UEA | Mmp-3/TIMP-1 complex | x-ray diffraction | A, C | — | — |
| 1UEA | Mmp-3/TIMP-1 complex | x-ray diffraction | A, C | — | — |
| 1UMS | Stromelysin-1 catalytic domain with hydrophobic inhibitor bound, pH 7.0, 32OC, 20 mm CACL2, 15%… | solution nmr | A | — | — |
| 1UMS | Stromelysin-1 catalytic domain with hydrophobic inhibitor bound, pH 7.0, 32OC, 20 mm CACL2, 15%… | solution nmr | A | — | — |
| 1UMT | Stromelysin-1 catalytic domain with hydrophobic inhibitor bound, ph 7.0, 32oc, 20 mm cacl2, 15%… | solution nmr | A | — | — |
| 1UMT | Stromelysin-1 catalytic domain with hydrophobic inhibitor bound, pH 7.0, 32OC, 20 mm CACL2, 15%… | solution nmr | A | — | — |
| 1USN | Crystal structure of the catalytic domain of human fibroblast stromelysin-1 inhibited with… | x-ray diffraction | A | — | — |
| 1USN | Crystal structure of the catalytic domain of human fibroblast stromelysin-1 inhibited with… | x-ray diffraction | A | — | — |
| 2D1O | Stromelysin-1 (MMP-3) complexed to a hydroxamic acid inhibitor | x-ray diffraction | A, B | — | — |
| 2D1O | Stromelysin-1 (mmp-3) complexed to a hydroxamic acid inhibitor | x-ray diffraction | A, B | — | — |
| 2JNP | Solution structure of matrix metalloproteinase 3 (MMP-3) in the presence of… | solution nmr | A | — | — |
| 2JNP | Solution structure of matrix metalloproteinase 3 (mmp-3) in the presence of… | solution nmr | A | — | — |
26 records more on the page itself.
Ligands
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