17
|
99
|
5hiyA |
Crystal structure of pedv nsp9 mutant-c59a |
43
|
219
|
5hc1A |
Structure of eav nsp11 h141a mutant at 3.10a |
0
|
13
|
5hhgC |
Mouse importin alpha: dengue 2 ns5 c-terminal nls peptide complex |
14
|
99
|
5hizA |
The structure of pedv nsp9 |
46
|
219
|
5hbzA |
Structure of eav nsp11 k170a mutant at 3.10a |
11
|
75
|
5ireB |
The cryo-em structure of zika virus |
54
|
167
|
5holA |
The crystal structure of the mers-cov macro domain with adp-ribose |
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 |
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 |
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 |
87
|
262
|
5gozA |
Crystal structure of zikv ns5 methyltransferase in complex with gtp and sah |
0
|
9
|
5h5zC |
Crystal structure of bony fish mhc class i, peptide and b2m ii |
68
|
262
|
5gp1A |
Crystal structure of zikv ns5 methyltransferase in complex with gtp and sah |
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 |
177
|
664
|
5fj6A |
Structure of the p2 polymerase inside in vitro assembled bacteriophage phi6 polymerase complex |
105
|
437
|
5ffmA |
Yellow fever virus helicase |
177
|
664
|
5fj7C |
Structure of the p2 polymerase inside in vitro assembled bacteriophage phi6 polymerase complex, with p1 included |
0
|
8
|
4zuhC |
Complex structure of pedv 3clpro mutant (c144a) with a peptide substrate. |
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 |
225
|
612
|
5f3tA |
Dengue serotype 3 rna-dependent rna polymerase bound to jf-31-mg46 |
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. |
0
|
9
|
5fgcA |
Three dimensional structure of broadly neutralizing human anti - hepatitis c virus (hcv) glycoprotein e2 fab fragment hc33.8 |
0
|
13
|
5eocP |
Crystal structure of fab c2 in complex with a cyclic variant of hepatitis c virus e2 epitope i |
99
|
256
|
5ehgA |
Dengue 3 ns5 methyltransferase bound to s-adenosyl methionine and molecule bf341 |
86
|
317
|
5e6jA |
Structure of sars plpro bound to a lys48-linked di-ubiquitin activity based probe |
110
|
320
|
5ezqA |
Venezuelan equine encephalitis virus (veev) nonstructural protein 2 (nsp2) cysteine protease |
91
|
306
|
4yogA |
Hku4-3clpro bound to non-covalent inhibitor 3b |
85
|
299
|
4zroA |
2.1 a x-ray structure of fipv-3clpro bound to covalent inhibitor |
51
|
223
|
5eyiA |
Structure of prrsv apo-nsp11 at 2.16a |
96
|
256
|
5ekxA |
Dengue 3 ns5 methyltransferase bound to s-adenosylmethionine and fragment nb2e11 |
99
|
256
|
5ehiA |
Dengue 3 ns5 methyltransferase bound to s-adenosyl methionine and molecule bf287 |
150
|
437
|
5e4fA |
The spring alpha-helix coordinates multiple modes of hcv ns3 helicase action |
44
|
219
|
5f17A |
Structure of eav nsp11 k170a mutant at 3.19a |
91
|
306
|
4yoiA |
Structure of hku4 3clpro bound to non-covalent inhibitor 1a |
98
|
256
|
5eifA |
Dengue 3 ns5 methyltransferase bound to s-adenosyl methionine and fragment nb2c3 |
98
|
256
|
5e9qA |
Dengue 3 ns5 methyltransferase bound to s-adenosyl methionine and molecule bf174 |
106
|
320
|
5ezsA |
Venezuelan equine encephalitis virus (veev) nonstructural protein 2 (nsp2) cysteine protease inhibited by e64d |
96
|
256
|
5eiwA |
Dengue 3 ns5 methyltransferase bound to s-adenosyl methionine and fragment nb3c2 |
96
|
256
|
5ec8A |
Dengue 3 ns5 methyltransferase bound to s-adenosyl methionine and compound bf175 |
39
|
174
|
5e0hA |
1.95 a resolution structure of norovirus 3cl protease in complex with a triazole-based macrocyclic (18-mer) inhibitor |
84
|
300
|
5eu8A |
Structure of fipv main protease in complex with dual inhibitors |