|
61
|
234
|
5k0hA |
Human factor xa in complex with synthetic inhibitor benzylsulfonyl-dser(benzyl)-gly-4-amidinobenzylamide |
|
49
|
235
|
5kedA |
Structure of the 2.65 angstrom p2(1) crystal of k. pneumonia mrkh |
|
56
|
259
|
5jduB |
Crystal structure for human thrombin mutant d189a |
|
51
|
235
|
5jb9S |
Crystal structure of factor ixa k98t variant in complex with ppack |
|
54
|
235
|
5jbaS |
Crystal structure of factor ixa variant v16i k98t y177t i212v in complex with ppack |
|
51
|
235
|
5jb8S |
Crystal structure of factor ixa variant k98t in complex with egr-chloromethylketone |
|
59
|
224
|
5jbtA |
Mesotrypsin in complex with cleaved amyloid precursor like protein 2 inhibitor (aplp2) |
|
50
|
235
|
5jbcS |
Crystal structure of factor ixa variant v16i k98t y177t i213v in complex with ppack |
|
49
|
245
|
5j4qA |
Alpha-chymotrypsin from bovine pancreas in complex with bowman-birk inhibitor from soybean |
|
149
|
461
|
5ik2D |
Caldalaklibacillus thermarum f1-atpase (epsilon mutant) |
|
51
|
245
|
5j4sA |
Alpha-chymotrypsin from bovine pancreas in complex with a modified bowman-birk inhibitor from soybean |
|
40
|
224
|
5idkA |
Crystal structure of west nile virus ns2b-ns3 protease in complex with a capped dipeptide boronate inhibitor |
|
60
|
254
|
5i46H |
Factor viia in complex with the inhibitor (2r,15r)-2-[(1-aminoisoquinolin-6-yl)amino]-8-fluoro-7-hydroxy-4,15,17-trimethyl-13-oxa-4,11-diazatricyclo[14.2.2.1~6,10~]henicosa-1(18),6(21),7,9,16,19-hexaene-3,12-dione |
|
144
|
605
|
5i25A |
Human recombinant coagulation fxi in complex with a peptide derived from human high molecular weight kininogen (hkp) |
|
83
|
301
|
5hyoA |
X-ray structure of unbound porcine epidemic diarrhea virus 3clpro |
|
43
|
182
|
5hxfA |
Crystal structure of 3c protease from a mild human enterovirus 71 in complex with rupintrivir |
|
156
|
461
|
5hkkD |
Caldalaklibacillus thermarum f1-atpase (wild type) |
|
39
|
189
|
5hm9A |
Crystal structure of mamo protease domain from magnetospirillum magneticum (apo form) |
|
82
|
299
|
5gwzA |
The structure of porcine epidemic diarrhea virus main protease in complex with an inhibitor |
|
56
|
223
|
5gxpA |
Cationic trypsin with gol/pge as dimer at ph 4.6 |
|
61
|
229
|
5fckA |
Complement factor d in complex with compound 5 |
|
223
|
728
|
5ej1A |
Pre-translocation state of bacterial cellulose synthase |
|
246
|
728
|
5eiyA |
Bacterial cellulose synthase bound to a substrate analogue |
|
145
|
466
|
5cdfE |
Structure at 2.3 a of the alpha/beta monomer of the f-atpase from paracoccus denitrificans |
|
21
|
97
|
4chaC |
Structure of alpha-*chymotrypsin refined at 1.68 angstroms resolution |
|
52
|
198
|
9lprA |
Structural basis for broad specificity in alpha-lytic protease mutants |
|
20
|
96
|
8gchG |
Gamma-chymotrypsin is a complex of alpha-chymotrypsin with its own autolysis products |
|
55
|
240
|
7estE |
Interaction of the peptide cf3-leu-ala-nh-c6h4-cf3(tfla) with porcine pancreatic elastase. x-ray studies at 1.8 angstroms |
|
59
|
240
|
9estA |
Structural study of porcine pancreatic elastase complexed with 7-amino-3-(2-bromoethoxy)-4-chloroisocoumarin as a nonreactivatable doubly covalent enzyme-inhibitor complex |
|
63
|
240
|
8estE |
Reaction of porcine pancreatic elastase with 7-substituted 3-alkoxy-4-chloroisocoumarins: design of potent inhibitors using the crystal structure of the complex formed with 4-chloro-3-ethoxy-7-guanidino-isocoumarin |
|
16
|
131
|
8gchF |
Gamma-chymotrypsin is a complex of alpha-chymotrypsin with its own autolysis products |
|
53
|
198
|
8lprA |
Structural basis for broad specificity in alpha-lytic protease mutants |
|
55
|
257
|
8kme2 |
Crystal structure of human alpha-thrombin inhibited with sel2770. |
|
18
|
95
|
7gchG |
Structure of chymotrypsin-*trifluoromethyl ketone inhibitor complexes. comparison of slowly and rapidly equilibrating inhibitors |
|
53
|
198
|
7lprA |
Structural basis for broad specificity in alpha-lytic protease mutants |
|
14
|
131
|
7gchF |
Structure of chymotrypsin-*trifluoromethyl ketone inhibitor complexes. comparison of slowly and rapidly equilibrating inhibitors |
|
52
|
259
|
7kmeH |
Crystal structure of human alpha-thrombin inhibited with sel2711. |
|
53
|
198
|
6lprA |
Structural basis for broad specificity in alpha-lytic protease mutants |
|
18
|
95
|
6gchG |
Structure of chymotrypsin-*trifluoromethyl ketone inhibitor complexes. comparison of slowly and rapidly equilibrating inhibitors |
|
13
|
131
|
6gchF |
Structure of chymotrypsin-*trifluoromethyl ketone inhibitor complexes. comparison of slowly and rapidly equilibrating inhibitors |
|
57
|
240
|
6estA |
Interaction of the peptide cf3-leu-ala-nh-c6h4-cf3(tfla) with porcine pancreatic elastase. x-ray studies at 1.8 angstroms |
|
12
|
131
|
6chaB |
Structure of a tetrahedral transition state complex of alpha-*chymotrypsin at 1.8-*angstroms resolution |
|
19
|
97
|
6chaC |
Structure of a tetrahedral transition state complex of alpha-*chymotrypsin at 1.8-*angstroms resolution |
|
40
|
181
|
5dp9A |
Crystal structure of ev71 3c proteinase in complex with compound 9 |
|
93
|
369
|
5ce1A |
Crystal structure of serine protease hepsin in complex with inhibitor |
|
62
|
223
|
5f6mA |
Isotropic trypsin model for comparison of diffuse scattering |
|
50
|
224
|
5fahA |
Kallikrein-7 in complex with compound1 |
|
22
|
116
|
5c94A |
Infectious bronchitis virus nsp9 |
|
144
|
470
|
5dn6D |
Atp synthase from paracoccus denitrificans |
|
63
|
208
|
5c0uA |
Crystal structure of the copper-bound form of merb mutant d99s |
