27
|
171
|
1eubA |
Solution structure of the catalytic domain of human collagenase-3 (mmp-13) complexed to a potent non-peptidic sulfonamide inhibitor |
25
|
163
|
1hovA |
Solution structure of a catalytic domain of mmp-2 complexed with sc-74020 |
27
|
169
|
1aykA |
Inhibitor-free catalytic fragment of human fibroblast collagenase, nmr, 30 structures |
24
|
173
|
1bm6A |
Solution structure of the catalytic domain of human stromelysin-1 complexed to a potent non-peptidic inhibitor, nmr, 20 structures |
30
|
158
|
1fm1A |
Solution structure of the catalytic fragment of human collagenase-3 (mmp-13) complexed with a hydroxamic acid inhibitor |
50
|
158
|
5l7fA |
Crystal structure of mmp12 mutant k421a in complex with rxp470.1 conjugated with fluorophore cy5,5 in space group p21. |
45
|
159
|
5l79A |
Crystal structure of mmp12 in complex with rxp470.1 conjugated with fluorophore cy5,5 in space group p21212. |
275
|
696
|
5jmyA |
Neprilysin complexed with lbq657 |
46
|
157
|
5i43A |
Crystal structure of the catalytic domain of mmp-12 in complex with a selective sugar-conjugated triazole-linked carboxylate chelator water-soluble inhibitor (dc32). |
50
|
156
|
5i4oA |
Crystal structure of the catalytic domain of mmp-12 in complex with a selective sugar-conjugated triazole-linked carboxylate zinc-chelator water-soluble inhibitor (dc28). |
44
|
157
|
5i12A |
Crystal structure of the catalytic domain of mmp-9 in complex with a selective sugar-conjugated arylsulfonamide carboxylate water-soluble inhibitor (dc27). |
48
|
157
|
5i3mA |
Crystal structure of the catalytic domain of mmp-12 in complex with a selective sugar-conjugated thiourea-linked carboxylate zinc-chelator water-soluble inhibitor (dc31). |
48
|
158
|
5i0lA |
Crystal structure of the catalytic domain of mmp-12 in complex with a selective sugar-conjugated arylsulfonamide carboxylate water-soluble inhibitor (dc27). |
50
|
157
|
5i2zA |
Crystal structure of the catalytic domain of mmp-12 in complex with a selective sugar-conjugated triazole-linked carboxylate chelating water-soluble inhibitor (dc24). |
42
|
157
|
966cA |
Crystal structure of fibroblast collagenase-1 complexed to a diphenyl-ether sulphone based hydroxamic acid |
44
|
168
|
830cA |
Collagenase-3 (mmp-13) complexed to a sulphone-based hydroxamic acid |
46
|
170
|
5b5oA |
Crystal structure of the catalytic domain of mmp-13 complexed with n-phenyl-4-((4h-1,2,4-triazol-3-ylsulfanyl)methyl)-1,3-thiazol-2-amine |
45
|
169
|
5boyA |
X-ray co-structure of mmp-13 with ethyl 5-(1-methyl-1h-imidazol-5-yl)-1h-indole-2-carboxylate |
44
|
169
|
5botA |
X-ray co-structure of mmp-13 with ethyl 5-carbamoyl-1h-indole-2-carboxylate |
48
|
169
|
5bpaA |
X-ray co-structure of mmp-13 with 4-[({5-[2-(ethoxycarbonyl)-1h-indol-5-yl]-1-methyl-1h-pyrazol-3-yl}formamido)methyl]benzoate |
274
|
697
|
4cthA |
Neprilysin variant g399v,g714k in complex with phosphoramidon |
49
|
168
|
4dpeA |
Structure of mmp3 complexed with a platinum-based inhibitor. |
196
|
512
|
4dv8A |
Anthrax lethal factor metalloproteinase in complex with the hydroxamic acid based small molecule pt8421 |
43
|
159
|
4efsA |
Human mmp12 in complex with l-glutamate motif inhibitor |
67
|
205
|
4dd8A |
Adam-8 metalloproteinase domain with bound batimastat |
123
|
406
|
4df9A |
Crystal structure of a putative peptidase (bf3526) from bacteroides fragilis nctc 9343 at 2.17 a resolution |
27
|
169
|
4aykA |
Catalytic fragment of human fibroblast collagenase complexed with cgs-27023a, nmr, 30 structures |
81
|
367
|
4auoA |
Crystal structure of mmp-1(e200a) in complex with a triple-helical collagen peptide |
53
|
163
|
4axqA |
Crystal structure of archaemetzincin (amza) from archaeoglobus fulgidus at 1.4 a resolution |
41
|
169
|
3zxhA |
Mmp-13 complexed with 2-napthylsulfonamide hydroxamic acid inhibitor |
50
|
158
|
4a3wA |
Crystal structure of archaemetzincin (amza) from archaeoglobus fulgidus at 2.16 a resolution complexed with citrate |
43
|
160
|
456cA |
Crystal structure of collagenase-3 (mmp-13) complexed to a diphenyl-ether sulphone based hydroxamic acid |
260
|
660
|
3zukA |
Crystal structure of mycobacterium tuberculosis zinc metalloprotease zmp1 in complex with inhibitor |
73
|
201
|
4aigA |
Adamalysin ii with phosphonate inhibitor |
52
|
158
|
3zvsA |
Crystal structure of archaemetzincin (amza) from archaeoglobus fulgidus at 1.4 a resolution complexed with malonate |
47
|
169
|
4a7bA |
Mmp13 in complex with a novel selective non zinc binding inhibitor cmpd22 |
46
|
170
|
3wv3A |
Crystal structure of the catalytic domain of mmp-13 complexed with n-(3-methoxybenzyl)-4-oxo-3,4-dihydrothieno[2,3-d]pyrimidine-2-carboxamide |
46
|
170
|
3wv1A |
Crystal structure of the catalytic domain of mmp-13 complexed with 4-(2-((6-fluoro-2-((3-methoxybenzyl)carbamoyl)-4-oxo-3,4-dihydroquinazolin-5-yl)oxy)ethyl)benzoic acid |
44
|
169
|
3wv2A |
Crystal structure of the catalytic domain of mmp-13 complexed with n-(3-methoxybenzyl)-4-oxo-3,4-dihydroquinazoline-2-carboxamide |
71
|
200
|
3vtgA |
High choriolytic enzyme 1 (hce-1), a hatching enzyme zinc-protease from oryzias latipes (medaka fish) |
35
|
168
|
3usnA |
Structure of the catalytic domain of human fibroblast stromelysin-1 inhibited with the thiadiazole inhibitor ipnu-107859, nmr, 1 structure |
148
|
470
|
3vi1A |
Crystal structure of pseudomonas aerginosa alkaline protease complexed with substance p(1-6) |
49
|
159
|
3v96B |
Complex of matrix metalloproteinase-10 catalytic domain (mmp-10cd) with tissue inhibitor of metalloproteinases-1 (timp-1) |
49
|
158
|
3uvcA |
Mmp12 in a complex with the dimeric adduct: 5-(5-phenylhydantoin)-5-phenylhydantoin |
156
|
461
|
3u1rA |
Structure analysis of a new psychrophilic marine protease |
48
|
169
|
3tvcA |
Human mmp13 in complex with l-glutamate motif inhibitor |
47
|
159
|
3tskA |
Human mmp12 in complex with l-glutamate motif inhibitor |
52
|
159
|
3tt4A |
Human mmp8 in complex with l-glutamate motif inhibitor |
46
|
159
|
3ts4A |
Human mmp12 in complex with l-glutamate motif inhibitor |
47
|
156
|
3shiA |
Crystal structure of human mmp1 catalytic domain at 2.2 a resolution |