|
49
|
259
|
1haoH |
Complex of human alpha-thrombin with a 15mer oligonucleotide ggttggtgtggttgg (based on nmr model of dna) |
|
46
|
290
|
6qswAAA |
Complement factor b protease domain in complex with the reversible inhibitor n-(2-bromo-4-methylnaphthalen-1-yl)-4,5-dihydro-1h-imidazol-2-amine. |
|
46
|
289
|
6ravAAA |
Complement factor b protease domain in complex with the reversible inhibitor 4-((2s,4s)-4-ethoxy-1-((5-methoxy-7-methyl-1h-indol-4-yl)methyl)piperidin-2-yl)benzoic acid |
|
48
|
289
|
6qsxAAA |
Complement factor b protease domain in complex with the reversible inhibitor ((2s,4s)-1-((5,7-dimethyl-1h-indol-4-yl)methyl)-4-methoxypiperidin-2-yl)methanol. |
|
50
|
228
|
4cboA |
Crystal structure of complement factor d mutant r202a after ensemble refinement |
|
58
|
259
|
3qlpH |
X-ray structure of the complex between human alpha thrombin and a modified thrombin binding aptamer (mtba) |
|
53
|
258
|
4diiH |
X-ray structure of the complex between human alpha thrombin and thrombin binding aptamer in the presence of potassium ions |
|
60
|
257
|
4dihH |
X-ray structure of the complex between human alpha thrombin and thrombin binding aptamer in the presence of sodium ions |
|
156
|
604
|
6i58A |
Allosteric activation of human prekallikrein by apple domain disc rotation |
|
182
|
610
|
6i44A |
Allosteric activation of human prekallikrein by apple domain disc rotation |
|
61
|
258
|
5ew2H |
Human thrombin sandwiched between two dna aptamers: hd22 and hd1-deltat12 |
|
58
|
258
|
5ew1H |
Human thrombin sandwiched between two dna aptamers: hd22 and hd1-deltat3 |
|
65
|
259
|
6eo7H |
X-ray structure of the complex between human alpha-thrombin and modified 15-mer dna aptamer containing 5-(3-(acetamide-n-yl)-1-propen-1-yl)-2'-deoxyuridine residue |
|
60
|
258
|
6gn7H |
X-ray structure of the complex between human alpha thrombin and nu172, a duplex/quadruplex 26-mer dna aptamer, in the presence of sodium ions. |
|
61
|
259
|
6evvH |
X-ray structure of the complex between human alpha thrombin and nu172, a duplex/quadruplex 26-mer dna aptamer, in the presence of potassium ions. |
|
54
|
223
|
6bfpA |
Bovine trypsin bound to potent inhibitor |
|
116
|
477
|
6bqmA |
Secreted serine protease vesc from vibrio cholerae |
|
50
|
222
|
6qhcA |
Crystal structure of human kallikrein 6 in complex with gsk358180b |
|
156
|
609
|
6o1gA |
Full length human plasma kallikrein with inhibitor |
|
56
|
223
|
6o21A |
Crystal structure of human klk4 in complex with cleaved sfti-fcqr(asn14)[1,14] inhibitor |
|
56
|
239
|
6o1sE |
Structure of human plasma kallikrein protease domain with inhibitor |
|
53
|
222
|
6qhaA |
Crystal structure of human kallikrein 6 in complex with gsk3205388b |
|
50
|
222
|
6qh9A |
Crystal structure of human kallikrein 6 in complex with gsk3239861a |
|
52
|
223
|
6qhbA |
Crystal structure of human kallikrein 6 in complex with gsk578724a |
|
53
|
259
|
6nmbA |
Tranexamic acid is an active site inhibitor of urokinase plasminogen activator |
|
54
|
235
|
6mv4H |
Crystal structure of human coagulation factor ixa |
|
58
|
224
|
6harA |
Crystal structure of mesotrypsin in complex with appi-m17c/i18f/f34c |
|
52
|
223
|
6dwuAA |
Crystal structure of complex of bbki and bovine trypsin |
|
59
|
251
|
6fjtH |
4-chloro-benzamidine in complex with thrombin |
|
57
|
223
|
6dwfA |
Crystal structure of complex of bbki mutant, l55r with bovine trypsin |
|
60
|
246
|
6d3zA |
Protease sfti complex |
|
59
|
223
|
6eatA |
Crystallographic structure of the cyclic nonapeptide derived from the btci inhibitor bound to beta-trypsin in space group p 21 21 21. |
|
63
|
246
|
6d3xA |
Highly potent and selective plasmin inhibitors based on the sunflower trypsin inhibitor-1 scaffold attenuate fibrinolysis in plasma |
|
55
|
223
|
6dwhA |
Crystal structure of complex of bbki and bovine trypsin |
|
57
|
248
|
6d40A |
Highly potent and selective plasmin inhibitors based on the sunflower trypsin inhibitor-1 scaffold attenuate fibrinolysis in plasma |
|
57
|
224
|
6ahsA |
Mouse kallikrein 7 in complex with imidazolinylindole derivative |
|
56
|
223
|
6bvhA |
Trypsin complexed with a modified sunflower trypsin inhibitor, sfti-tctr(n12,n14) |
|
57
|
223
|
6e5mA |
Crystallographic structure of the cyclic nonapeptide derived from the btci inhibitor bound to beta-trypsin in space group p 32 2 1 |
|
53
|
247
|
6a8gA |
The crystal structure of mupain-1-ig in complex with mupa-spd at ph8.5 |
|
60
|
247
|
6d3yA |
Highly potent and selective plasmin inhibitors based on the sunflower trypsin inhibitor-1 scaffold attenuate fibrinolysis in plasma |
|
55
|
224
|
6bx8A |
Human mesotrypsin (prss3) complexed with tissue factor pathway inhibitor variant (tfpi1-kd1-k15r-i17c-i34c) |
|
54
|
247
|
6a8nA |
The crystal structure of mupain-1-ig-2 in complex with mupa-spd at ph8.5 |
|
57
|
245
|
5zc5U |
Upa-nu-09f |
|
56
|
246
|
5zaeU |
Upa-6f-hma |
|
55
|
245
|
5zajU |
Upa-31f |
|
50
|
232
|
6r8xA |
Coagulation factor xi catalytic domain in complex with fab-portion of maa868 |
|
58
|
245
|
5za8U |
Upa-bb2-27f |
|
57
|
246
|
5za7U |
Upa-hma |
|
58
|
245
|
5zafU |
Upa-bb2-28f |
|
59
|
245
|
5z1cU |
The crystal structure of upa in complex with 4-iodobenzylamine at ph7.4 |
