|
36
|
283
|
2hwf1 |
A comparison of the anti-rhinoviral drug binding pocket in hrv14 and hrv1a |
|
41
|
273
|
2hwc1 |
A comparison of the anti-rhinoviral drug binding pocket in hrv14 and hrv1a |
|
52
|
212
|
2halA |
An episulfide cation (thiiranium ring) trapped in the active site of hav 3c proteinase inactivated by peptide-based ketone inhibitors |
|
33
|
238
|
2hwe3 |
A comparison of the anti-rhinoviral drug binding pocket in hrv14 and hrv1a |
|
175
|
570
|
2hcsA |
Crystal structure of rna dependant rna polymerase domain of west nile virus |
|
43
|
253
|
2hwf2 |
A comparison of the anti-rhinoviral drug binding pocket in hrv14 and hrv1a |
|
43
|
253
|
2hwe2 |
A comparison of the anti-rhinoviral drug binding pocket in hrv14 and hrv1a |
|
47
|
255
|
2hwb2 |
A comparison of the anti-rhinoviral drug binding pocket in hrv14 and hrv1a |
|
35
|
283
|
2hwd1 |
A comparison of the anti-rhinoviral drug binding pocket in hrv14 and hrv1a |
|
2
|
40
|
2hwb4 |
A comparison of the anti-rhinoviral drug binding pocket in hrv14 and hrv1a |
|
38
|
236
|
2hwb3 |
A comparison of the anti-rhinoviral drug binding pocket in hrv14 and hrv1a |
|
43
|
253
|
2hwd2 |
A comparison of the anti-rhinoviral drug binding pocket in hrv14 and hrv1a |
|
29
|
127
|
2hd0A |
Structure of the catalytic domain of hepatitis c virus ns2 |
|
174
|
571
|
2hcnA |
Crystal structure of rna dependent rna polymerase domain from west nile virus |
|
87
|
347
|
2h85A |
Crystal structure of nsp 15 from sars |
|
42
|
183
|
2gvfA |
Hcv ns3-4a protease domain complexed with a macrocyclic ketoamide inhibitor, sch419021 |
|
207
|
562
|
2girA |
Hepatitis c virus rna-dependent rna polymerase ns5b with nni-1 inhibitor |
|
201
|
562
|
2haiA |
Crystal structure of hcv ns5b rna polymerase in complex with novel class of dihydropyrone-containing inhibitor. |
|
54
|
212
|
2h9hA |
An episulfide cation (thiiranium ring) trapped in the active site of hav 3c proteinase inactivated by peptide-based ketone inhibitors |
|
84
|
306
|
2gx4A |
Crystal structure of sars coronavirus 3cl protease inhibitor complex |
|
88
|
306
|
2h2zA |
Crystal structure of sars-cov main protease with authentic n and c-termini |
|
209
|
562
|
2giqA |
Hepatitis c virus rna-dependent rna polymerase ns5b with nni-2 inhibitor |
|
30
|
169
|
2ggvB |
Crystal structure of the west nile virus ns2b-ns3 protease, his51ala mutant |
|
29
|
112
|
2h0pA |
Nmr structure of the dengue-4 virus envelope protein domain iii |
|
53
|
212
|
2h6mA |
An episulfide cation (thiiranium ring) trapped in the active site of hav 3c proteinase inactivated by peptide-based ketone inhibitors |
|
9
|
112
|
2griA |
Nmr structure of the sars-cov non-structural protein nsp3a |
|
4
|
44
|
2ggvA |
Crystal structure of the west nile virus ns2b-ns3 protease, his51ala mutant |
|
195
|
562
|
2gc8A |
Structure of a proline sulfonamide inhibitor bound to hcv ns5b polymerase |
|
14
|
93
|
2gg1A |
Nmr solution structure of domain iii of the e-protein of tick-borne langat flavivirus (includes rdc restraints) |
|
39
|
181
|
2fyqA |
Crystal structure of the norwalk virus protease |
|
17
|
116
|
2gdtA |
Nmr structure of the nonstructural protein 1 (nsp1) from the sars coronavirus |
|
41
|
181
|
2fyrA |
Crystal structure of norwalk virus protease grown in the presence of aebsf |
|
29
|
152
|
2fp7B |
West nile virus ns2b/ns3protease in complex with bz-nle-lys-arg-arg-h |
|
0
|
40
|
2fp7A |
West nile virus ns2b/ns3protease in complex with bz-nle-lys-arg-arg-h |
|
119
|
474
|
2f8eX |
Foot and mouth disease virus rna-dependent rna polymerase in complex with uridylylated vpg protein |
|
43
|
183
|
2f9vA |
Hcv ns3 protease domain with ns4a peptide and a ketoamide inhibitor with p1 and p2 cyclopropylalannines |
|
180
|
544
|
2dxsA |
Crystal structure of hcv ns5b rna polymerase complexed with a tetracyclic inhibitor |
|
203
|
563
|
2d41A |
X-ray crystal structure of hepatitis c virus rna-dependent rna polymerase in complex with non-nucleoside inhibitor |
|
203
|
563
|
2d3uA |
X-ray crystal structure of hepatitis c virus rna dependent rna polymerase in complex with non-nucleoside analogue inhibitor |
|
79
|
301
|
2d2dA |
Crystal structure of sars-cov mpro in complex with an inhibitor i2 |
|
205
|
563
|
2d3zA |
X-ray crystal structure of hepatitis c virus rna-dependent rna polymerase in complex with non-nucleoside analogue inhibitor |
|
0
|
15
|
2d7sB |
Foot and mouth disease virus rna-dependent rna polymerase in complex with vpg protein |
|
114
|
474
|
2d7sA |
Foot and mouth disease virus rna-dependent rna polymerase in complex with vpg protein |
|
53
|
212
|
2cxvA |
Dual modes of modification of hepatitis a virus 3c protease by a serine-derived betalactone: selective crystallization and high-resolution structure of the his-102 adduct |
|
167
|
496
|
2ckwA |
The 2.3 a resolution structure of the sapporo virus rna dependant rna polymerase. |
|
183
|
582
|
2cjqA |
Bovine viral diarrhea virus cp7-r12 rna-dependent rna polymerase |
|
84
|
301
|
2c3sA |
Structure of sars cov main proteinase at 1.9 a (ph6.5) |
|
191
|
531
|
2brlA |
Crystal structure of hepatitis c virus polymerase in complex with an allosteric inhibitor (compound 2) |
|
192
|
531
|
2brkA |
Crystal structure of hepatitis c virus polymerase in complex with an allosteric inhibitor (compound 1) |
|
72
|
298
|
2bx4A |
Crystal structure of sars coronavirus main proteinase (p21212) |
