|
341
|
964
|
3h09A |
The structure of haemophilus influenzae iga1 protease |
|
56
|
229
|
3i78A |
35/99/170/186/220-loops of fxa in sgt |
|
63
|
238
|
3hptB |
Crystal structure of human fxa in complex with (s)-2-cyano-1-(2-methylbenzofuran-5-yl)-3-(2-oxo-1-(2-oxo-2-(pyrrolidin-1-yl)ethyl)azepan-3-yl)guanidine |
|
49
|
223
|
3i29A |
Crystal structure of a binary complex between an mutant trypsin inhibitor with bovine trypsin |
|
56
|
230
|
3i77A |
35/99/170-loops of fxa in sgt |
|
54
|
258
|
3hkiB |
Crystal structure of murine thrombin mutant w215a/e217a in complex with the extracellular fragment of human par1 |
|
53
|
259
|
3hatH |
Active site mimetic inhibition of thrombin |
|
59
|
240
|
3hgpA |
Structure of porcine pancreatic elastase complexed with a potent peptidyl inhibitor fr130180 determined by high resolution crystallography |
|
54
|
258
|
3hk3B |
Crystal structure of murine thrombin mutant w215a/e217a (one molecule in the asymmetric unit) |
|
55
|
312
|
3h5cB |
X-ray structure of protein z-protein z inhibitor complex |
|
46
|
258
|
3hk6B |
Crystal structure of murine thrombin mutant w215a/e217a (two molecules in the asymmetric unit) |
|
59
|
235
|
3h7tA |
Crystal structure of scabies mite inactivated protease paralogue s-d1 (smipp-s-d1) |
|
53
|
259
|
3hkjB |
Crystal structure of human thrombin mutant w215a/e217a in complex with the extracellular fragment of human par1 |
|
63
|
240
|
3hgnA |
Structure of porcine pancreatic elastase complexed with a potent peptidyl inhibitor fr130180 determined by neutron crystallography |
|
57
|
228
|
3h7oA |
Crystal structure of scabies mite inactivated protease paralogue s-i1 (smipp-s-i1) |
|
59
|
317
|
3gcoA |
Crystal structure of degs h198p/d320a mutant modified by dfp in complex with dnrdgnvyqf omp peptide |
|
57
|
223
|
3gy8A |
A comparative study on the inhibition of bovine beta-trypsin by bis-benzamidines diminazene and pentamidine by x-ray crystallography and itc |
|
55
|
223
|
3gy7A |
A comparative study on the inhibition of bovine beta-trypsin by bis-benzamidines diminazene and pentamidine by x-ray crystallography and itc |
|
60
|
223
|
3gy3A |
A comparative study on the inhibition of bovine beta-trypsin by bis-benzamidines diminazene and pentamidine by x-ray crystallography and itc |
|
58
|
223
|
3gy2A |
A comparative study on the inhibition of bovine beta-trypsin by bis-benzamidines diminazene and pentamidine by x-ray crystallography and itc |
|
54
|
223
|
3gy4A |
A comparative study on the inhibition of bovine beta-trypsin by bis-benzamidines diminazene and pentamidine by x-ray crystallography and itc |
|
58
|
317
|
3gdsA |
Crystal structure of degs h198p/d320a mutant modified by dfp in complex with dnrdgnvyyf peptide |
|
43
|
241
|
3gymA |
Structure of prostasin in complex with aprotinin |
|
61
|
316
|
3gdvA |
Crystal structure of degs h198p/d320a mutant modified by dfp and in complex with yqf peptide |
|
15
|
131
|
3gctF |
Structure of gamma-*chymotrypsin in the range $p*h 2.0 to $p*h 10.5 suggests that gamma-chymotrypsin is a covalent acyl-enzyme adduct at low $p*h |
|
51
|
247
|
3gylB |
Structure of prostasin at 1.3 angstroms resolution in complex with a calcium ion. |
|
56
|
223
|
3gy5A |
A comparative study on the inhibition of bovine beta-trypsin by bis-benzamidines diminazene and pentamidine by x-ray crystallography and itc |
|
56
|
259
|
3gisB |
Crystal structure of na-free thrombin in complex with thrombomodulin |
|
72
|
337
|
3gs9A |
Crystal structure of prophage tail protein gp18 (np_465809.1) from listeria monocytogenes egd-e at 1.70 a resolution |
|
57
|
316
|
3gduA |
Crystal structure of degs h198p/d320a mutant modified by dfp and in complex with yrf peptide |
|
51
|
248
|
3gicB |
Structure of thrombin mutant delta(146-149e) in the free form |
|
59
|
317
|
3gcnA |
Crystal structure of degs h198p/d320a mutant modified by dfp in complex with omp peptide (yqf) |
|
49
|
251
|
3govB |
Crystal structure of the catalytic region of human masp-1 |
|
58
|
223
|
3gy6A |
A comparative study on the inhibition of bovine beta-trypsin by the bis-benzamidines diminazene and pentamidine |
|
18
|
95
|
3gctG |
Structure of gamma-*chymotrypsin in the range $p*h 2.0 to $p*h 10.5 suggests that gamma-chymotrypsin is a covalent acyl-enzyme adduct at low $p*h |
|
42
|
227
|
3g01A |
Structure of grc mutant e192r/e193g |
|
15
|
95
|
3gchC |
Chemistry of caged enzymes. binding of photoreversible cinnamates to chymotrypsin |
|
106
|
490
|
3foaA |
Crystal structure of the bacteriophage t4 tail sheath protein, deletion mutant gp18m |
|
79
|
299
|
3fzdA |
Mutation of asn28 disrupts the enzymatic activity and dimerization of sars 3clpro |
|
49
|
227
|
3fzzA |
Structure of grc |
|
66
|
274
|
3fo8D |
Crystal structure of the bacteriophage t4 tail sheath protein, protease resistant fragment gp18pr |
|
14
|
131
|
3gchB |
Chemistry of caged enzymes. binding of photoreversible cinnamates to chymotrypsin |
|
51
|
248
|
3fvfB |
The crystal structure of prostasin complexed with camostat at 1.6 angstroms resolution |
|
60
|
223
|
3fp6E |
Anionic trypsin in complex with bovine pancreatic trypsin inhibitor (bpti) determined to the 1.49 a resolution limit |
|
58
|
234
|
3ffgA |
Factor xa in complex with the inhibitor (r)-6-(2'-((3- hydroxypyrrolidin-1-yl)methyl)biphenyl-4-yl)-1-(3-(5-oxo-4,5-dihydro-1h-1,2,4-triazol-3-yl)phenyl)-3-(trifluoromethyl)-5,6-dihydro-1h-pyrazolo[3,4-c]pyridin- 7(4h)-one |
|
77
|
299
|
3f9hA |
Crystal structure of the f140a mutant of sars-coronovirus 3c-like protease at ph 7.6 |
|
82
|
299
|
3f9fA |
Crystal structure of the f140a mutant of sars-coronovirus 3c-like protease at ph 6.0 |
|
39
|
197
|
3faoA |
Crystal structure of s118a mutant 3clsp of prrsv |
|
76
|
300
|
3f9gA |
Crystal structure of the f140a mutant of sars-coronovirus 3c-like protease at ph 6.5 |
|
107
|
469
|
3fksD |
Yeast f1 atpase in the absence of bound nucleotides |
