| Structure Region |
Pdb Id |
Title |
Resolution |
Technique |
 |
1SLM
| crystal structure of fibroblast stromelysin-1: the c-truncated human proenzyme |
1.9 |
x-ray |
 |
1UMS
| stromelysin-1 catalytic domain with hydrophobic inhibitor bound, ph 7.0, 32oc, 20 mm cacl2, 15% acetonitrile; nmr ensemble of 20 structures |
|
nmr, |
 |
1UMT
| stromelysin-1 catalytic domain with hydrophobic inhibitor bound, ph 7.0, 32oc, 20 mm cacl2, 15% acetonitrile; nmr average of 20 structures minimized with restraints |
|
nmr, |
 |
2SRT
| catalytic domain of human stromelysin-1 at ph 5.5 and 40oc complexed with inhibitor |
|
nmr, |
 |
1BM6
| solution structure of the catalytic domain of human stromelysin-1 complexed to a potent non-peptidic inhibitor, nmr, 20 structures |
|
nmr, |
 |
1BQO
| discovery of potent, achiral matrix metalloproteinase inhibitors |
2.3 |
x-ray |
 |
1B3D
| stromelysin-1 |
2.3 |
x-ray |
 |
1CQR
| crystal structure of the stromelysin catalytic domain at 2.0 a resolution |
2 |
x-ray |
 |
1BIW
| design and synthesis of conformationally-constrained mmp inhibitors |
2.5 |
x-ray |
 |
1C3I
| human stromelysin-1 catalytic domain complexed with ro-26- 2812 |
1.83 |
x-ray |
 |
1D7X
| crystal structure of mmp3 complexed with a modified proline scaffold based inhibitor. |
2 |
x-ray |
 |
1D8F
| crystal structure of mmp3 complexed with a piperazine based inhibitor. |
2.4 |
x-ray |
 |
1D5J
| crystal structure of mmp3 complexed with a thiazepine based inhibitor. |
2.6 |
x-ray |
 |
1G49
| a carboxylic acid based inhibitor in complex with mmp3 |
1.9 |
x-ray |
 |
1G05
| heterocycle-based mmp inhibitor with p2'substituents |
2.45 |
x-ray |
 |
1D8M
| crystal structure of mmp3 complexed with a heterocycle- based inhibitor |
2.44 |
x-ray |
 |
1HY7
| a carboxylic acid based inhibitor in complex with mmp3 |
1.5 |
x-ray |
 |
1SLN
| crystal structure of the catalytic domain of human fibroblast stromelysin-1 inhibited with the n-carboxy-alkyl inhibitor l-702,842 |
2.27 |
x-ray |
 |
1UEA
| mmp-3/timp-1 complex |
2.8 |
x-ray |
 |
3USN
| structure of the catalytic domain of human fibroblast stromelysin-1 inhibited with the thiadiazole inhibitor ipnu-107859, nmr, 1 structure |
|
2 |
 |
1CAQ
| x-ray structure of human stromelysin catalytic domain complexes with non-peptide inhibitors: implication for inhibitor selectivity |
1.8 |
x-ray |
 |
1CIZ
| x-ray structure of human stromelysin catalytic domain complexes with non-peptide inhibitors: implication for inhibitor selectivity |
1.64 |
x-ray |
 |
1G4K
| x-ray structure of a novel matrix metalloproteinase inhibitor complexed to stromelysin |
2 |
x-ray |
 |
1OO9
| orientation in solution of mmp-3 catalytic domain and n- timp-1 from residual dipolar couplings |
|
nmr |
 |
1B8Y
| x-ray structure of human stromelysin catalytic domain complexed with non-peptide inhibitors: implications for inhibitor selectivity |
2 |
x-ray |
 |
1C8T
| human stromelysin-1 (e202q) catalytic domain complexed with ro-26-2812 |
2.6 |
x-ray |
 |
1USN
| crystal structure of the catalytic domain of human fibroblast stromelysin-1 inhibited with thiadiazole inhibitor pnu-142372 |
1.8 |
x-ray |
 |
2USN
| crystal structure of the catalytic domain of human fibroblast stromelysin-1 inhibited with thiadiazole inhibitor pnu-141803 |
2.2 |
x-ray |
 |
1QIA
| crystal structure of stromelysin catalytic domain |
2 |
x-ray |
 |
1QIC
| crystal structure of stromelysin catalytic domain |
2 |
x-ray |
 |
1HFS
| crystal structure of the catalytic domain of human fibroblast stromelysin-1 inhibited with the n-carboxy-alkyl inhibitor l-764,004 |
1.7 |
x-ray |
