64
|
167
|
1ge5A |
Zinc peptidase from grifola frondosa |
65
|
167
|
1ge7A |
Zinc peptidase from grifola frondosa |
40
|
159
|
1gkdA |
Mmp9 active site mutant-inhibitor complex |
63
|
163
|
1ge6A |
Zinc peptidase from grifola frondosa |
158
|
748
|
1jkyA |
Crystal structure of the anthrax lethal factor (lf): wild-type lf complexed with the n-terminal sequence of mapkk2 |
46
|
168
|
1g4kA |
X-ray structure of a novel matrix metalloproteinase inhibitor complexed to stromelysin |
46
|
169
|
1g05A |
Heterocycle-based mmp inhibitor with p2'substituents |
44
|
169
|
1g49A |
A carboxylic acid based inhibitor in complex with mmp3 |
64
|
167
|
1g12A |
Zinc peptidase from grifola frondosa |
48
|
158
|
1jj9A |
Crystal structure of mmp8-barbiturate complex reveals mechanism for collagen substrate recognition |
81
|
367
|
1fblA |
Structure of full-length porcine synovial collagenase (mmp1) reveals a c-terminal domain containing a calcium-linked, four-bladed beta-propeller |
49
|
166
|
1jizA |
Crystal structure analysis of human macrophage elastase mmp-12 |
45
|
158
|
1jh1A |
Crystal structure of mmp-8 complexed with a 6h-1,3,4-thiadiazine derived inhibitor |
31
|
158
|
1flsA |
Solution structure of the catalytic fragment of human collagenase-3 (mmp-13) complexed with a hydroxamic acid inhibitor |
149
|
470
|
1jiwP |
Crystal structure of the apr-aprin complex |
47
|
158
|
1jk3A |
Crystal structure of human mmp-12 (macrophage elastase) at true atomic resolution |
100
|
421
|
1eakA |
Catalytic domain of prommp-2 e404q mutant |
70
|
177
|
1eb6A |
Deuterolysin from aspergillus oryzae |
270
|
696
|
1dmtA |
Structure of human neutral endopeptidase complexed with phosphoramidon |
48
|
157
|
1japA |
Complex of pro-leu-gly-hydroxylamine with the catalytic domain of matrix metallo proteinase-8 (met80 form) |
251
|
747
|
1j7nA |
Anthrax toxin lethal factor |
47
|
164
|
1janA |
Complex of pro-leu-gly-hydroxylamine with the catalytic domain of matrix metallo proteinase-8 (phe79 form) |
62
|
202
|
1dthA |
Metalloprotease |
42
|
158
|
1jaoA |
Complex of 3-mercapto-2-benzylpropanoyl-ala-gly-nh2 with the catalytic domain of matrix metallo proteinase-8 (met80 form) |
43
|
158
|
1jaqA |
Complex of 1-hydroxylamine-2-isobutylmalonyl-ala-gly-nh2 with the catalytic domain of matrix metallo proteinase-8 (met80 form) |
46
|
169
|
1d7xA |
Crystal structure of mmp3 complexed with a modified proline scaffold based inhibitor. |
46
|
169
|
1d5jA |
Crystal structure of mmp3 complexed with a thiazepine based inhibitor. |
46
|
169
|
1d8fA |
Crystal structure of mmp3 complexed with a piperazine based inhibitor. |
44
|
169
|
1d8mA |
Crystal structure of mmp3 complexed with a heterocycle-based inhibitor |
45
|
164
|
1cxvA |
Structure of recombinant mouse collagenase-3 (mmp-13) |
47
|
168
|
1cizA |
X-ray structure of human stromelysin catalytic domain complexes with non-peptide inhibitors: implication for inhibitor selectivity |
45
|
169
|
1cqrA |
Crystal structure of the stromelysin catalytic domain at 2.0 a resolution |
133
|
630
|
1ck7A |
Gelatinase a (full-length) |
43
|
162
|
1cgfA |
Crystal structures of recombinant 19-kda human fibroblast collagenase complexed to itself |
35
|
174
|
1bqqM |
Crystal structure of the mt1-mmp--timp-2 complex |
40
|
168
|
1cglA |
Structure of the catalytic domain of fibroblast collagenase complexed with an inhibitor |
49
|
132
|
1c7kA |
Crystal structure of the zinc protease |
48
|
168
|
1caqA |
X-ray structure of human stromelysin catalytic domain complexes with non-peptide inhibitors: implication for inhibitor selectivity |
41
|
162
|
1cgeA |
Crystal structures of recombinant 19-kda human fibroblast collagenase complexed to itself |
52
|
170
|
1c3iA |
Human stromelysin-1 catalytic domain complexed with ro-26-2812 |
50
|
167
|
1c8tA |
Human stromelysin-1 (e202q) catalytic domain complexed with ro-26-2812 |
73
|
197
|
1budA |
Acutolysin a from snake venom of agkistrodon acutus at ph 5.0 |
50
|
165
|
1bzsA |
Crystal structure of mmp8 complexed with hmr2909 |
78
|
197
|
1bswA |
Acutolysin a from snake venom of agkistrodon acutus at ph 7.5 |
35
|
174
|
1buvM |
Crystal structure of the mt1-mmp-timp-2 complex |
47
|
169
|
1bqoA |
Discovery of potent, achiral matrix metalloproteinase inhibitors |
76
|
200
|
1atlA |
Structural interaction of natural and synthetic inhibitors with the venom metalloproteinase, atrolysin c (form-d) |
84
|
255
|
1bkcA |
Catalytic domain of tnf-alpha converting enzyme (tace) |
44
|
169
|
1b3dA |
Stromelysin-1 |
46
|
169
|
1biwA |
Design and synthesis of conformationally-constrained mmp inhibitors |