|
52
|
223
|
1fniA |
Crystal structure of porcine beta trypsin with 0.01% polydocanol |
|
54
|
223
|
1fy8E |
Crystal structure of the deltaile16val17 rat anionic trypsinogen-bpti complex |
|
52
|
223
|
1fmgA |
Crystal structure of porcine beta trypsin with 0.04% polydocanol |
|
57
|
224
|
1fy5A |
Fusarium oxysporum trypsin at atomic resolution |
|
49
|
228
|
1fxyA |
Coagulation factor xa-trypsin chimera inhibited with d-phe-pro-arg-chloromethylketone |
|
5
|
43
|
1eptA |
Refined 1.8 angstroms resolution crystal structure of porcine epsilon-trypsin |
|
53
|
223
|
1ezsC |
Crystal structure of ecotin mutant m84r, w67a, g68a, y69a, d70a bound to rat anionic trypsin ii |
|
51
|
223
|
1jirA |
Crystal structure of trypsin complex with amylamine in cyclohexane |
|
57
|
223
|
1f5rA |
Rat trypsinogen mutant complexed with bovine pancreatic trypsin inhibitor |
|
55
|
223
|
1f7zA |
Rat trypsinogen k15a complexed with bovine pancreatic trypsin inhibitor |
|
56
|
223
|
1f0uA |
Bovine trypsin complexed with rpr128515 |
|
53
|
223
|
1f2sE |
Crystal structure of the complex formed between bovine beta-trypsin and mcti-a, a trypsin inhibitor of squash family at 1.8 a resolution |
|
27
|
199
|
1ezxC |
Crystal structure of a serpin:protease complex |
|
4
|
82
|
1eptB |
Refined 1.8 angstroms resolution crystal structure of porcine epsilon-trypsin |
|
55
|
223
|
1f0tA |
Bovine trypsin complexed with rpr131247 |
|
16
|
98
|
1eptC |
Refined 1.8 angstroms resolution crystal structure of porcine epsilon-trypsin |
|
52
|
223
|
1ezuC |
Ecotin y69f, d70p bound to d102n trypsin |
|
50
|
223
|
1ejaA |
Structure of porcine trypsin complexed with bdellastasin, an antistasin-type inhibitor |
|
57
|
223
|
1eb2A |
Trypsin inhibitor complex (bpo) |
|
57
|
223
|
1ejmA |
Crystal structure of the bpti ala16leu mutant in complex with bovine trypsin |
|
53
|
223
|
1dpoA |
Structure of rat trypsin |
|
59
|
223
|
1j8aA |
Crystal structure of benzamidine inhibited bovine pancreatic trypsin at 105k to 1.21a resolution from laboratory source with high number of waters modelled |
|
52
|
223
|
1d6rA |
Crystal structure of cancer chemopreventive bowman-birk inhibitor in ternary complex with bovine trypsin at 2.3 a resolution. structural basis of janus-faced serine protease inhibitor specificity |
|
50
|
223
|
1j15A |
Benzamidine in complex with rat trypsin mutant x99/175/190rt |
|
53
|
223
|
1j14A |
Benzamidine in complex with rat trypsin mutant x99rt |
|
52
|
223
|
1j16A |
Benzamidine in complex with rat trypsin mutant x99/175/190rt |
|
60
|
223
|
1co7E |
R117h mutant rat anionic trypsin complexed with bovine pancreatic trypsin inhibitor (bpti) |
|
49
|
223
|
1j17T |
Factor xa specific inhibitor in complex with rat trypsin mutant x99/175/190rt |
|
55
|
223
|
1c5qA |
Structural basis for selectivity of a small molecule, s1-binding, sub-micromolar inhibitor of urokinase type plasminogen activator |
|
55
|
223
|
1c2eA |
Recruiting zinc to mediate potent, specific inhibition of serine proteases |
|
55
|
223
|
1c1nA |
Recruiting zinc to mediate potent, specific inhibition of serine proteases |
|
53
|
223
|
1braA |
Relocating a negative charge in the binding pocket of trypsin |
|
54
|
223
|
1c5tA |
Structural basis for selectivity of a small molecule, s1-binding, sub-micromolar inhibitor of urokinase type plasminogen activator |
|
55
|
223
|
1c2mA |
Recruiting zinc to mediate potent, specific inhibition of serine proteases |
|
54
|
223
|
1c2jA |
Recruiting zinc to mediate potent, specific inhibition of serine proteases |
|
56
|
223
|
1c1sA |
Recruiting zinc to mediate potent, specific inhibition of serine proteases |
|
51
|
223
|
1btpA |
Unique binding of a novel synthetic inhibitor, n-[3-[4-[4-(amidinophenoxy)-carbonyl]phenyl]-2-methyl-2-propenoyl]-n-allylglycine methanesulfonate to bovine trypsin, revealed by the crystal structure of the complex |
|
55
|
223
|
1c5uA |
Structural basis for selectivity of a small molecule, s1-binding, sub-micromolar inhibitor of urokinase type plasminogen activator |
|
51
|
223
|
1c2dA |
Recruiting zinc to mediate potent, specific inhibition of serine proteases |
|
53
|
223
|
1c2lA |
Recruiting zinc to mediate potent, specific inhibition of serine proteases |
|
54
|
223
|
1c1tA |
Recruiting zinc to mediate potent, specific inhibition of serine proteases |
|
56
|
223
|
1c5vA |
Structural basis for selectivity of a small molecule, s1-binding, sub-micromolar inhibitor of urokinase type plasminogen activator |
|
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 |
