|
60
|
234
|
2xc0A |
Factor xa in complex with a pyrrolidine-3,4-dicarboxylic acid inhibitor |
|
140
|
467
|
2xndD |
Crystal structure of bovine f1-c8 sub-complex of atp synthase |
|
146
|
470
|
2xokD |
Refined structure of yeast f1c10 atpase complex to 3 a resolution |
|
60
|
233
|
2xc4A |
Factor xa in complex with a pyrrolidine-3,4-dicarboxylic acid inhibitor |
|
63
|
234
|
2xbxA |
Factor xa in complex with a pyrrolidine-3,4-dicarboxylic acid inhibitor |
|
43
|
180
|
2xcnA |
Crystal structure of hcv ns3 protease with a boronate inhibitor |
|
42
|
180
|
2xcfA |
Crystal structure of hcv ns3 protease with a boronate inhibitor |
|
67
|
234
|
2xbvA |
Factor xa in complex with a pyrrolidine-3,4-dicarboxylic acid inhibitor |
|
64
|
234
|
2xc5A |
Factor xa in complex with a pyrrolidine-3,4-dicarboxylic acid inhibitor |
|
153
|
600
|
2wzqA |
Insertion mutant e173gp174 of the ns3 protease-helicase from dengue virus |
|
63
|
234
|
2xbwA |
Factor xa in complex with a pyrrolidine-3,4-dicarboxylic acid inhibitor |
|
60
|
234
|
2wygA |
Structure and property based design of factor xa inhibitors: pyrrolidin-2-ones with monoaryl p4 motifs |
|
142
|
672
|
2wv9A |
Crystal structure of the ns3 protease-helicase from murray valley encephalitis virus |
|
54
|
235
|
2wpjS |
Factor ixa superactive triple mutant, nacl-soaked |
|
45
|
239
|
2wubA |
Crystal structure of hgfa in complex with the allosteric non- inhibitory antibody fab40.deltatrp |
|
51
|
235
|
2wpmS |
Factor ixa superactive mutant, egr-cmk inhibited |
|
43
|
200
|
2wv5A |
Crystal structure of foot-and-mouth disease virus 3c protease in complex with a decameric peptide corresponding to the vp1-2a cleavage junction with a gln to glu substitution at p1 |
|
53
|
235
|
2wpiS |
Factor ixa superactive double mutant |
|
51
|
235
|
2wpkS |
Factor ixa superactive triple mutant, ethylene glycol-soaked |
|
55
|
233
|
2wyjA |
Structure and property based design of factor xa inhibitors: pyrrolidin-2-ones with monoaryl p4 motifs |
|
53
|
239
|
2wucA |
Crystal structure of hgfa in complex with the allosteric non- inhibitory antibody fab40.deltatrp and ac-kqlr-chloromethylketone |
|
126
|
470
|
2wpdD |
The mg.adp inhibited state of the yeast f1c10 atp synthase |
|
53
|
235
|
2wphS |
Factor ixa superactive triple mutant |
|
135
|
467
|
2wssD |
The structure of the membrane extrinsic region of bovine atp synthase |
|
55
|
235
|
2wplS |
Factor ixa superactive triple mutant, edta-soaked |
|
44
|
201
|
2wv4A |
Crystal structure of foot-and-mouth disease virus 3c protease in complex with a decameric peptide corresponding to the vp1-2a cleavage junction |
|
156
|
598
|
2whxA |
A second conformation of the ns3 protease-helicase from dengue virus |
|
51
|
200
|
2w7uA |
Spla serine protease of staphylococcus aureus (2.4a) |
|
111
|
507
|
2winI |
C3 convertase (c3bbb) stabilized by scin |
|
156
|
467
|
2w6jD |
Low resolution structures of bovine mitochondrial f1-atpase during controlled dehydration: hydration state 5. |
|
34
|
162
|
2w5eA |
Structural and biochemical analysis of human pathogenic astrovirus serine protease at 2.0 angstrom resolution |
|
59
|
234
|
2w3iA |
Crystal structure of fxa in complex with 4,4-disubstituted pyrrolidine-1,2-dicarboxamide inhibitor 2 |
|
149
|
467
|
2w6iD |
Low resolution structures of bovine mitochondrial f1-atpase during controlled dehydration: hydration state 4b. |
|
56
|
234
|
2w3kA |
Crystal structure of fxa in complex with 4,4-disubstituted pyrrolidine-1,2-dicarboxamide inhibitor 1 |
|
65
|
233
|
2vvuA |
Aminopyrrolidine factor xa inhibitor |
|
65
|
234
|
2vwlA |
Aminopyrrolidine factor xa inhibitor |
|
64
|
233
|
2vvcA |
Aminopyrrolidine factor xa inhibitor |
|
61
|
233
|
2w26A |
Factor xa in complex with bay59-7939 |
|
55
|
224
|
2vu8E |
Crystal structure of an insect inhibitor with a fungal trypsin |
|
61
|
233
|
2vvvA |
Aminopyrrolidine-related triazole factor xa inhibitor |
|
64
|
234
|
2vwoA |
Aminopyrrolidine factor xa inhibitor |
|
62
|
233
|
2vwmA |
Aminopyrrolidine factor xa inhibitor |
|
65
|
234
|
2vwnA |
Aminopyrrolidine factor xa inhibitor |
|
58
|
247
|
2viqA |
Fragment-based discovery of mexiletine derivatives as orally bioavailable inhibitors of urokinase-type plasminogen activator |
|
15
|
131
|
2vgcB |
Gamma-chymotrypsin d-para-chloro-1-acetamido boronic acid inhibitor complex |
|
54
|
262
|
2vntA |
Urokinase-type plasminogen activator inhibitor complex with a 1-(7- sulphoamidoisoquinolinyl)guanidine |
|
35
|
183
|
2vb0A |
Crystal structure of coxsackievirus b3 proteinase 3c |
|
57
|
247
|
2viwA |
Fragment-based discovery of mexiletine derivatives as orally bioavailable inhibitors of urokinase-type plasminogen activator |
|
147
|
600
|
2vbcA |
Crystal structure of the ns3 protease-helicase from dengue virus |
|
82
|
300
|
2vj1A |
A structural view of the inactivation of the sars-coronavirus main proteinase by benzotriazole esters |
