32
|
159
|
1z3jA |
Solution structure of mmp12 in the presence of n-isobutyl-n-4-methoxyphenylsulfonyl]glycyl hydroxamic acid (nngh) |
270
|
696
|
1y8jA |
Crystal structure of human nep complexed with an imidazo[4,5-c]pyridine inhibitor |
49
|
168
|
1youA |
Crystal structure of the catalytic domain of mmp-13 complexed with a potent pyrimidinetrione inhibitor |
39
|
158
|
1y93A |
Crystal structure of the catalytic domain of human mmp12 complexed with acetohydroxamic acid at atomic resolution |
158
|
735
|
1y0vA |
Crystal structure of anthrax edema factor (ef) in complex with calmodulin and pyrophosphate |
69
|
199
|
1yp1A |
Crystal structure of a non-hemorrhagic fibrin(ogen)olytic metalloproteinase from venom of agkistrodon acutus |
29
|
159
|
1ycmA |
Solution structure of matrix metalloproteinase 12 (mmp12) in the presence of n-isobutyl-n-[4-methoxyphenylsulfonyl]glycyl hydroxamic acid (nngh) |
47
|
169
|
1xudA |
Matrix metalloproteinase-13 complexed with non-zinc binding inhibitor |
192
|
735
|
1xfzA |
Crystal structure of anthrax edema factor (ef) in complex with calmodulin in the presence of 1 millimolar exogenously added calcium chloride |
178
|
735
|
1xfvA |
Crystal structure of anthrax edema factor (ef) in complex with calmodulin and 3' deoxy-atp |
181
|
735
|
1xfuA |
Crystal structure of anthrax edema factor (ef) truncation mutant, ef-delta 64 in complex with calmodulin |
174
|
735
|
1xfyA |
Crystal structure of anthrax edema factor (ef) in complex with calmodulin |
196
|
735
|
1xfxA |
Crystal structure of anthrax edema factor (ef) in complex with calmodulin in the presence of 10 millimolar exogenously added calcium chloride |
53
|
152
|
1xm5A |
Crystal structure of metal-dependent hydrolase ybey from e. coli, pfam upf0054 |
48
|
169
|
1xucA |
Matrix metalloproteinase-13 complexed with non-zinc binding inhibitor |
47
|
169
|
1xurA |
Matrix metalloproteinase-13 complexed with non-zinc binding inhibitor |
177
|
735
|
1xfwA |
Crystal structure of anthrax edema factor (ef) in complex with calmodulin and 3'5' cyclic amp (camp) |
71
|
198
|
1wniA |
Crystal structure of h2-proteinase |
30
|
144
|
1xaxA |
Nmr structure of hi0004, a putative essential gene product from haemophilus influenzae |
46
|
159
|
1utzA |
Crystal structure of mmp-12 complexed to (2r)-3-({[4-[(pyridin-4-yl)phenyl]-thien-2-yl}carboxamido)(phenyl)propanoic acid |
25
|
166
|
1umtA |
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 |
44
|
159
|
1uttA |
Crystal structure of mmp-12 complexed to 2-(1,3-dioxo-1,3-dihydro-2h-isoindol-2-yl)ethyl-4-(4-ethoxy[1,1-biphenyl]-4-yl)-4-oxobutanoic acid |
31
|
166
|
1umsA |
Stromelysin-1 catalytic domain with hydrophobic inhibitor bound, ph 7.0, 32oc, 20 mm cacl2, 15% acetonitrile; nmr ensemble of 20 structures |
45
|
165
|
1usnA |
Crystal structure of the catalytic domain of human fibroblast stromelysin-1 inhibited with thiadiazole inhibitor pnu-142372 |
43
|
168
|
1ueaA |
Mmp-3/timp-1 complex |
27
|
150
|
1tviA |
Solution structure of tm1509 from thermotoga maritima: vt1, a nesgc target protein |
68
|
235
|
1slmA |
Crystal structure of fibroblast stromelysin-1: the c-truncated human proenzyme |
142
|
468
|
1srpA |
Structural analysis of serratia protease |
111
|
435
|
1su3A |
X-ray structure of human prommp-1: new insights into collagenase action |
259
|
654
|
1s4bP |
Crystal structure of human thimet oligopeptidase. |
160
|
468
|
1smpA |
Crystal structure of a complex between serratia marcescens metallo-protease and an inhibitor from erwinia chrysanthemi |
47
|
168
|
1slnA |
Crystal structure of the catalytic domain of human fibroblast stromelysin-1 inhibited with the n-carboxy-alkyl inhibitor l-702,842 |
163
|
468
|
1satA |
Crystal structure of the 50 kda metallo protease from s. marcescens |
66
|
206
|
1r54A |
Crystal structure of the catalytic domain of human adam33 |
47
|
169
|
1rm8A |
Crystal structure of the catalytic domain of mmp-16/mt3-mmp: characterization of mt-mmp specific features |
43
|
159
|
1rosA |
Crystal structure of mmp-12 complexed to 2-(1,3-dioxo-1,3-dihydro-2h-isoindol-2-yl)ethyl-4-(4-ethoxy[1,1-biphenyl]-4-yl)-4-oxobutanoic acid |
67
|
203
|
1r55A |
Crystal structure of the catalytic domain of human adam 33 |
233
|
696
|
1r1iA |
Structural analysis of neprilysin with various specific and potent inhibitors |
270
|
696
|
1r1jA |
Structural analysis of neprilysin with various specific and potent inhibitors |
272
|
696
|
1r1hA |
Structural analysis of neprilysin with various specific and potent inhibitors |
46
|
159
|
1rmzA |
Crystal structure of the catalytic domain of human mmp12 complexed with the inhibitor nngh at 1.3 a resolution |
61
|
200
|
1qjjA |
Structure of astacin with a hydroxamic acid inhibitor |
251
|
750
|
1pwvA |
Crystal structure of anthrax lethal factor wild-type protein complexed with an optimised peptide substrate. |
251
|
748
|
1pwwA |
Crystal structure of anthrax lethal factor active site mutant protein complexed with an optimised peptide substrate in the presence of zinc. |
245
|
747
|
1pwpA |
Crystal structure of the anthrax lethal factor complexed with small molecule inhibitor nsc 12155 |
47
|
162
|
1qiaA |
Crystal structure of stromelysin catalytic domain |
59
|
200
|
1qjiA |
Structure of astacin with a transition-state analogue inhibitor |
41
|
161
|
1qicA |
Crystal structure of stromelysin catalytic domain |
68
|
197
|
1quaA |
Crystal structure of acutolysin-c, a hemorrhagic toxin from the snake venom of agkistrodon acutus, at 2.2 a resolution |
199
|
750
|
1pwqA |
Crystal structure of anthrax lethal factor complexed with thioacetyl-tyr-pro-met-amide, a metal-chelating peptidyl small molecule inhibitor |