|
110
|
337
|
5xveA |
Crystal structure of human usp2 c276s mutant in complex with ubiquitin |
|
109
|
347
|
5vs6A |
Structure of dub complex |
|
106
|
345
|
5ngeA |
Crystal structure of usp7 in complex with the non-covalent inhibitor, ft671 |
|
89
|
299
|
5nh0A |
Structure of human coronavirus nl63 main protease in complex with the alpha-ketoamide tert-butyl ((s)-4-(benzylamino)-3,4-dioxo-1-((s)-2-oxopyrrolidin-3-yl)b- utan-2-yl)carbamate (tert-butyl -glnlactam-co-co-nh-benzyl) |
|
87
|
300
|
5nh0B |
Structure of human coronavirus nl63 main protease in complex with the alpha-ketoamide tert-butyl ((s)-4-(benzylamino)-3,4-dioxo-1-((s)-2-oxopyrrolidin-3-yl)b- utan-2-yl)carbamate (tert-butyl -glnlactam-co-co-nh-benzyl) |
|
108
|
346
|
5ngfA |
Crystal structure of usp7 in complex with the covalent inhibitor, ft827 |
|
30
|
132
|
5nfyM |
Sars-cov nsp10/nsp14 dynamic complex |
|
95
|
306
|
5n19A |
Structure of sars coronavirus main protease in complex with the alpha-ketoamide (s)-n-benzyl-3-((s)-2-cinnamamido-3-phenylpropanamido)-2-oxo-4-((s)-2-oxopyrrolidin-3-yl)butanamide |
|
115
|
357
|
5n9tA |
Crystal structure of usp7 in complex with a potent, selective and reversible small-molecule inhibitor |
|
111
|
357
|
5n9rA |
Crystal structure of usp7 in complex with a potent, selective and reversible small-molecule inhibitor |
|
77
|
289
|
5mpbV |
26s proteasome in presence of amp-pnp (s3) |
|
93
|
395
|
5mpc8 |
26s proteasome in presence of befx (s4) |
|
7
|
19
|
5mn9C |
Crystal structure of mindy-1 tmiu in complex with k48-diub |
|
75
|
289
|
5mpcV |
26s proteasome in presence of befx (s4) |
|
77
|
289
|
5mpdV |
26s proteasome in presence of atp (s1) |
|
81
|
289
|
5mpeV |
26s proteasome in presence of atp (s2) |
|
98
|
356
|
5lrxE |
Structure of a20 otu domain bound to ubiquitin |
|
94
|
336
|
5l8hA |
Structure of usp46-ubvme |
|
93
|
336
|
5l8wA |
Structure of usp12-ub-prg/uaf1 |
|
75
|
308
|
5lrvA |
Structure of cezanne/otud7b otu domain bound to lys11-linked diubiquitin |
|
84
|
288
|
5lrwA |
Structure of cezanne/otud7b otu domain bound to ubiquitin |
|
100
|
355
|
5lrxA |
Structure of a20 otu domain bound to ubiquitin |
|
111
|
340
|
5kycB |
Crystal structure of usp7 catalytic domain [v302k] mutant in complex with ubiquitin (malonate bound) |
|
110
|
345
|
5kyeA |
Crystal structure of usp7 catalytic domain [h294e] mutant in complex with ubiquitin |
|
110
|
343
|
5kybA |
Crystal structure of the apo-form of usp7 catalytic domain [v302k] mutant |
|
71
|
257
|
5ko3A |
Structure of a core papain-like protease of mers coronavirus with utility for structure-based drug design |
|
113
|
344
|
5kyfB |
Crystal structure of usp7 catalytic domain [l299a] mutant in complex with ubiquitin |
|
73
|
257
|
5jqsA |
Crystal structure of deubiquitinase mindy-1 in complex with ubiquitin |
|
107
|
370
|
5jtjA |
Usp7cd-ctp in complex with ubiquitin |
|
64
|
334
|
5k1cA |
Crystal structure of the uaf1/wdr20/usp12 complex |
|
30
|
199
|
5jjwB |
Crystal structure of the hat domain of sart3 in complex with usp15 dusp-ubl domain |
|
156
|
671
|
5j7tA |
Molecular understanding of usp7 substrate recognition and c-terminal activation |
|
133
|
577
|
5jtvA |
Usp7cd-ubl45 in complex with ubiquitin |
|
82
|
299
|
5gwzA |
The structure of porcine epidemic diarrhea virus main protease in complex with an inhibitor |
|
176
|
672
|
5fwiC |
Structure of usp7 catalytic domain and three ubl-domains |
|
67
|
386
|
5gjqx |
Structure of the human 26s proteasome bound to usp14-ubal |
|
32
|
79
|
5f22A |
C-terminal domain of sars-cov nsp8 complex with nsp7 |
|
92
|
346
|
6ghaA |
Usp15 catalytic domain structure |
|
96
|
348
|
6gh9A |
Usp15 catalytic domain in complex with small molecule |
|
67
|
289
|
6fvyV |
26s proteasome, s6 state |
|
61
|
289
|
6fvwV |
26s proteasome, s4 state |
|
68
|
289
|
6fvxV |
26s proteasome, s5 state |
|
68
|
289
|
6fvtV |
26s proteasome, s1 state |
|
66
|
289
|
6fvuV |
26s proteasome, s2 state |
|
78
|
289
|
6fvvV |
26s proteasome, s3 state |
|
41
|
152
|
6fnnA |
Caldiarchaeum subterraneum ubiquitin:rpn11-homolog complex |
|
125
|
343
|
6fgeA |
Crystal structure of human zufsp/zup1 in complex with ubiquitin |
|
112
|
357
|
6f5hA |
Crystal structure of usp7 in complex with a 4-hydroxypiperidine based inhibitor |
|
31
|
112
|
6dxtA |
Structure of usp5 zinc-finger ubiquitin binding domain co-crystallized with 3-(5-phenyl-1,3,4-oxadiazol-2-yl)propanoate |
|
118
|
339
|
6ei1A |
Crystal structure of the covalent complex between deubiquitinase zufsp (zup1) and ubiquitin-pa |
