|
53
|
223
|
1c5pA |
Structural basis for selectivity of a small molecule, s1-binding, sub-micromolar inhibitor of urokinase type plasminogen activator |
|
53
|
223
|
1c2iA |
Recruiting zinc to mediate potent, specific inhibition of serine proteases |
|
54
|
223
|
1c1oA |
Recruiting zinc to mediate potent, specific inhibition of serine proteases |
|
55
|
223
|
1btwA |
Episelection: novel ki ~nanomolar inhibitors of serine proteases selected by binding or chemistry on an enzyme surface |
|
52
|
223
|
1brbE |
Crystal structures of rat anionic trypsin complexed with the protein inhibitors appi and bpti |
|
52
|
223
|
1c2hA |
Recruiting zinc to mediate potent, specific inhibition of serine proteases |
|
54
|
223
|
1c1qA |
Recruiting zinc to mediate potent, specific inhibition of serine proteases |
|
52
|
223
|
1c5sA |
Structural basis for selectivity of a small molecule, s1-binding, sub-micromolar inhibitor of urokinase type plasminogen activator |
|
52
|
223
|
1c2fA |
Recruiting zinc to mediate potent, specific inhibition of serine proteases |
|
54
|
223
|
1btxA |
Episelection: novel ki ~nanomolar inhibitors of serine proteases selected by binding or chemistry on an enzyme surface |
|
50
|
223
|
1c9pA |
Complex of bdellastasin with porcine trypsin |
|
53
|
223
|
1c1rA |
Recruiting zinc to mediate potent, specific inhibition of serine proteases |
|
54
|
223
|
1ce5A |
Bovine pancreas beta-trypsin in complex with benzamidine |
|
56
|
223
|
1c1pA |
Recruiting zinc to mediate potent, specific inhibition of serine proteases |
|
53
|
223
|
1btyA |
Crystal structure of beta-trypsin in complex with benzamidine |
|
51
|
223
|
1brcE |
Relocating a negative charge in the binding pocket of trypsin |
|
53
|
223
|
1c2gA |
Recruiting zinc to mediate potent, specific inhibition of serine proteases |
|
53
|
223
|
1c9tA |
Complex of bdellastasin with bovine trypsin |
|
54
|
223
|
1c5rA |
Structural basis for selectivity of a small molecule, s1-binding, sub-micromolar inhibitor of urokinase type plasminogen activator |
|
48
|
223
|
1c2kA |
Recruiting zinc to mediate potent, specific inhibition of serine proteases |
|
54
|
222
|
1bzxE |
The crystal structure of anionic salmon trypsin in complex with bovine pancreatic trypsin inhibitor |
|
53
|
223
|
1btzA |
Episelection: novel ki ~nanomolar inhibitors of serine proteases selected by binding or chemistry on an enzyme surface |
|
53
|
223
|
1avwA |
Complex porcine pancreatic trypsin/soybean trypsin inhibitor, orthorhombic crystal form |
|
57
|
223
|
1aujA |
Bovine trypsin complexed to meta-cyano-benzylic inhibitor |
|
48
|
223
|
1avxA |
Complex porcine pancreatic trypsin/soybean trypsin inhibitor, tetragonal crystal form |
|
55
|
222
|
1bitA |
The crystal structure of anionic salmon trypsin in a second crystal form |
|
55
|
223
|
1bjuA |
Beta-trypsin complexed with acpu |
|
50
|
223
|
1az8A |
Bovine trypsin complexed to bis-phenylamidine inhibitor |
|
53
|
223
|
1bjvA |
Beta-trypsin complexed with appu |
|
49
|
223
|
1aneA |
Anionic trypsin wild type |
|
17
|
125
|
1aksA |
Crystal structure of the first active autolysate form of the porcine alpha trypsin |
|
55
|
223
|
1aq7A |
Trypsin with inhibitor aeruginosin 98-b |
|
49
|
223
|
1anbA |
Anionic trypsin mutant with ser 214 replaced by glu |
|
53
|
223
|
1ancA |
Anionic trypsin mutant with ser 214 replaced by lys |
|
50
|
223
|
1andA |
Anionic trypsin mutant with arg 96 replaced by his |
|
49
|
223
|
1amhA |
Uncomplexed rat trypsin mutant with asp 189 replaced with ser (d189s) |
|
57
|
223
|
1an1E |
Leech-derived tryptase inhibitor/trypsin complex |
|
16
|
98
|
1aksB |
Crystal structure of the first active autolysate form of the porcine alpha trypsin |
|
56
|
223
|
1a0jA |
Crystal structure of a non-psychrophilic trypsin from a cold-adapted fish species. |
