|
225
|
612
|
5f3tA |
Dengue serotype 3 rna-dependent rna polymerase bound to jf-31-mg46 |
|
0
|
9
|
5fgcA |
Three dimensional structure of broadly neutralizing human anti - hepatitis c virus (hcv) glycoprotein e2 fab fragment hc33.8 |
|
199
|
645
|
5fptA |
Structure of hepatitis c virus (hcv) full-length ns3 complex with small-molecule ligand 2-(1-methyl-1h-indol-3-yl)acetic acid (at3437) in an alternate binding site. |
|
228
|
612
|
5f41A |
Dengue serotype 3 rna-dependent rna polymerase bound to fd-83-ki26 |
|
96
|
256
|
5eiwA |
Dengue 3 ns5 methyltransferase bound to s-adenosyl methionine and fragment nb3c2 |
|
98
|
256
|
5e9qA |
Dengue 3 ns5 methyltransferase bound to s-adenosyl methionine and molecule bf174 |
|
0
|
13
|
5eocP |
Crystal structure of fab c2 in complex with a cyclic variant of hepatitis c virus e2 epitope i |
|
99
|
256
|
5ehiA |
Dengue 3 ns5 methyltransferase bound to s-adenosyl methionine and molecule bf287 |
|
106
|
320
|
5ezsA |
Venezuelan equine encephalitis virus (veev) nonstructural protein 2 (nsp2) cysteine protease inhibited by e64d |
|
98
|
256
|
5eifA |
Dengue 3 ns5 methyltransferase bound to s-adenosyl methionine and fragment nb2c3 |
|
150
|
437
|
5e4fA |
The spring alpha-helix coordinates multiple modes of hcv ns3 helicase action |
|
96
|
256
|
5ekxA |
Dengue 3 ns5 methyltransferase bound to s-adenosylmethionine and fragment nb2e11 |
|
96
|
256
|
5ec8A |
Dengue 3 ns5 methyltransferase bound to s-adenosyl methionine and compound bf175 |
|
110
|
320
|
5ezqA |
Venezuelan equine encephalitis virus (veev) nonstructural protein 2 (nsp2) cysteine protease |
|
99
|
256
|
5ehgA |
Dengue 3 ns5 methyltransferase bound to s-adenosyl methionine and molecule bf341 |
|
39
|
174
|
5e0hA |
1.95 a resolution structure of norovirus 3cl protease in complex with a triazole-based macrocyclic (18-mer) inhibitor |
|
36
|
174
|
5e0jA |
1.20 a resolution structure of norovirus 3cl protease in complex with a triazole-based macrocyclic (21-mer) inhibitor |
|
40
|
175
|
5e0gA |
1.20 a resolution structure of norovirus 3cl protease in complex with a triazole-based macrocyclic (17-mer) inhibitor |
|
41
|
175
|
5dgjA |
1.0a resolution structure of norovirus 3cl protease in complex an oxadiazole-based, cell permeable macrocyclic (20-mer) inhibitor |
|
34
|
174
|
5dg6A |
2.35a resolution structure of norovirus 3cl protease in complex an oxadiazole-based, cell permeable macrocyclic (21-mer) inhibitor |
|
207
|
563
|
5czbA |
Hcv ns5b in complex with ligand idx17119-5 |
|
1
|
13
|
4xvjA |
Structure of the hepatitis c virus envelope glycoprotein e2 antigenic 2 region 412-423 bound to the broadly neutralizing antibody hc33.1 |
|
144
|
453
|
4xgcD |
Crystal structure of the eukaryotic origin recognition complex |
|
40
|
183
|
4xbcA |
1.60 a resolution structure of norovirus 3cl protease complex with a covalently bound dipeptidyl inhibitor (1r,2s)-2-({n-[(benzyloxy)carbonyl]-3-cyclohexyl-l-alanyl}amino)-1-hydroxy-3-[(3s)-2-oxopyrrolidin-3-yl]propane-1-sulfonic acid (hexagonal form) |
|
309
|
878
|
4v0rA |
Dengue virus full length ns5 complexed with gtp and sah |
|
39
|
175
|
4xbbA |
1.85a resolution structure of norovirus 3cl protease complex with a covalently bound dipeptidyl inhibitor diethyl [(1r,2s)-2-[(n-{[(3-chlorobenzyl)oxy]carbonyl}-3-cyclohexyl-l-alanyl)amino]-1-hydroxy-3-(2-oxo-2h-pyrrol-3-yl)propyl]phosphonate |
|
316
|
878
|
4v0qA |
Dengue virus full length ns5 complexed with sah |
|
141
|
466
|
4y2aA |
Crystal structure of coxsackie virus b3 3d polymerase in complex with gpc-n114 inhibitor |
|
40
|
175
|
4xbdA |
1.45a resolution structure of norovirus 3cl protease complex with a covalently bound dipeptidyl inhibitor (1r,2s)-2-({n-[(benzyloxy)carbonyl]-3-cyclohexyl-l-alanyl}amino)-1-hydroxy-3-[(3s)-2-oxopyrrolidin-3-yl]propane-1-sulfonic acid (orthorhombic p form) |
|
152
|
479
|
4wywA |
Mutant k20e of 3d polymerase from foot-and-mouth disease virus |
|
12
|
99
|
4x42A |
Crystal structure of den4 ed3 mutant with epitope two residues substituted from den3 ed3 |
|
31
|
138
|
4wznA |
Crystal structure of the 2b protein soluble domain from hepatitis a virus |
|
141
|
462
|
4wfxA |
Coxsackievirus b3 polymerase - f232l mutant - nacl crystal form |
|
146
|
462
|
4wfyA |
Coxsackievirus b3 polymerase - f232l mutant - amso4 crystal form |
|
203
|
544
|
4wt9A |
Apo crystal structure of hcv ns5b genotype 2a jfh-1 isolate with e86q e87q s15g c223h v321i and delta8 mutations |
|
146
|
462
|
4wfzA |
Coxsackievirus b3 3dpol rna dependent rna polymerase - nacl crystal form |
|
151
|
445
|
4wxpA |
X-ray crystal structure of ns3 helicase from hcv with a bound fragment inhibitor at 2.08 a resolution |
|
153
|
478
|
4wylA |
Mutant k18e of 3d polymerase from foot-and-moth disease virus |
|
208
|
566
|
4tn2A |
Ns5b in complex with lactam-thiophene carboxylic acids |
|
196
|
565
|
4ry7A |
C-terminal mutant (d559e) of hcv/j4 rna polymerase |
|
186
|
566
|
4ry4A |
C-terminal mutant (y448f) of hcv/j4 rna polymerase |
|
200
|
565
|
4ry5A |
C-terminal mutant (w550n) of hcv/j4 rna polymerase |
|
197
|
565
|
4ry6A |
C-terminal mutant (w550a) of hcv/j4 rna polymerase |
|
37
|
182
|
4u01A |
Hcv ns3/4a serine protease in complex with 6570 |
|
48
|
246
|
4qpiC |
Crystal structure of hepatitis a virus |
|
40
|
236
|
4rhv3 |
The use of molecular-replacement phases for the refinement of the human rhinovirus 14 structure |
|
32
|
217
|
4qpiB |
Crystal structure of hepatitis a virus |
|
49
|
255
|
4rhv2 |
The use of molecular-replacement phases for the refinement of the human rhinovirus 14 structure |
|
46
|
246
|
4qpgC |
Crystal structure of empty hepatitis a virus |
|
1
|
21
|
4r8tA |
Structure of jev protease |
