|
27
|
230
|
5ku23 |
Expanded poliovirus in complex with vhh 7a |
|
9
|
75
|
5iz7D |
Cryo-em structure of thermally stable zika virus strain h/pf/2013 |
|
40
|
259
|
5ku22 |
Expanded poliovirus in complex with vhh 7a |
|
14
|
101
|
5b1cA |
Crystal structure of den4 ed3 mutant with l387i |
|
11
|
75
|
5ireB |
The cryo-em structure of zika virus |
|
0
|
13
|
5hhgC |
Mouse importin alpha: dengue 2 ns5 c-terminal nls peptide complex |
|
121
|
476
|
5gvuA |
Crystal structure of bvdv ns3 helicase domain |
|
42
|
180
|
5fx6A |
Novel inhibitors of human rhinovirus 3c protease |
|
1
|
12
|
4z0xC |
Structure of hepatitis c virus envelope glycoprotein e2 antigenic region 434-446 bound to the broadly neutralizing antibody hc26am |
|
31
|
210
|
5gxjA |
Zika virus ns2b-ns3 protease |
|
0
|
38
|
5gpiA |
Crystal structures of unlinked ns2b-ns3 protease from zika virus and its complex with a reverse peptide inhibitor |
|
87
|
262
|
5gozA |
Crystal structure of zikv ns5 methyltransferase in complex with gtp and sah |
|
68
|
262
|
5gp1A |
Crystal structure of zikv ns5 methyltransferase in complex with gtp and sah |
|
2
|
53
|
5gj4A |
Structure of ns2b-ns3 protease from zika virus caught after self-cleavage |
|
77
|
504
|
5h37A |
Cryo-em structure of zika virus complexed with fab c10 at ph 8.0 |
|
43
|
180
|
5fx5A |
Novel inhibitors of human rhinovirus 3c protease |
|
23
|
154
|
5gpiB |
Crystal structures of unlinked ns2b-ns3 protease from zika virus and its complex with a reverse peptide inhibitor |
|
28
|
153
|
5gj4B |
Structure of ns2b-ns3 protease from zika virus caught after self-cleavage |
|
202
|
645
|
5fpyA |
Structure of hepatitis c virus (hcv) full-length ns3 complex with small-molecule ligand 5-bromo-1-methyl-1h-indole-2-carboxylic acid (at21457) in an alternate binding site. |
|
2
|
23
|
5fw5C |
Crystal structure of human g3bp1 in complex with semliki forest virus nsp3-25 comprising two fgdf motives |
|
105
|
437
|
5ffmA |
Yellow fever virus helicase |
|
228
|
612
|
5f41A |
Dengue serotype 3 rna-dependent rna polymerase bound to fd-83-ki26 |
|
202
|
645
|
5fpsA |
Structure of hepatitis c virus (hcv) full-length ns3 complex with small-molecule ligand 3-aminobenzene-1,2-dicarboxylic acid (at1246) in an alternate binding site. |
|
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. |
|
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 |
|
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 |
|
40
|
175
|
5e0gA |
1.20 a resolution structure of norovirus 3cl protease in complex with a triazole-based macrocyclic (17-mer) inhibitor |
|
36
|
174
|
5e0jA |
1.20 a resolution structure of norovirus 3cl protease in complex with a triazole-based macrocyclic (21-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 |
|
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) |
|
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 |
