|
22
|
103
|
4awjA |
Pvhl:elob:eloc complex, in complex with capped hydroxyproline |
|
27
|
103
|
4bksA |
Von hippel lindau protein:elonginb:elonginc complex, in complex with (2s,4r)-1-ethanoyl-n-[[4-(1,3-oxazol-5-yl)phenyl]methyl]-4-oxidanyl-pyrrolidine-2-carboxamide |
|
19
|
76
|
4bbnF |
Nedd4 hect-ub:ub complex |
|
212
|
916
|
4ajwA |
Discovery and optimization of new benzimidazole- and benzoxazole-pyrimidone selective pi3kbeta inhibitors for the treatment of phosphatase and tensin homologue (pten)-deficient cancers |
|
13
|
76
|
4bozB |
Structure of otud2 otu domain in complex with k11-linked di ubiquitin |
|
21
|
86
|
4b6wA |
Architecture of trypanosoma brucei tubulin-binding cofactor b |
|
249
|
945
|
4anuA |
Complexes of pi3kgamma with isoform selective inhibitors. |
|
17
|
76
|
4bbnC |
Nedd4 hect-ub:ub complex |
|
274
|
949
|
3zvvA |
Fragment bound to pi3kinase gamma |
|
21
|
96
|
4b0eA |
Crystal structure of the caf1a usher protein n-terminal domain from yersinia pestis |
|
20
|
76
|
4bosC |
Structure of otud2 otu domain in complex with ubiquitin k11-linked peptide |
|
23
|
102
|
4bksD |
Von hippel lindau protein:elonginb:elonginc complex, in complex with (2s,4r)-1-ethanoyl-n-[[4-(1,3-oxazol-5-yl)phenyl]methyl]-4-oxidanyl-pyrrolidine-2-carboxamide |
|
280
|
940
|
3zimA |
Discovery of a potent and isoform-selective targeted covalent inhibitor of the lipid kinase pi3kalpha |
|
206
|
952
|
4aofA |
Selective small molecule inhibitor discovered by chemoproteomic assay platform reveals regulation of th17 cell differentiation by pi3kgamma |
|
256
|
945
|
4anwA |
Complexes of pi3kgamma with isoform selective inhibitors. |
|
101
|
344
|
4baxA |
Crystal structure of glutamine synthetase from streptomyces coelicolor |
|
249
|
946
|
4anvA |
Complexes of pi3kgamma with isoform selective inhibitors. |
|
282
|
947
|
3zw3A |
Fragment based discovery of a novel and selective pi3 kinase inhibitor |
|
21
|
77
|
4auqC |
Structure of birc7-ubch5b-ub complex. |
|
25
|
104
|
4bktA |
Von hippel lindau protein:elonginb:elonginc complex, in complex with (2s,4r)-n-methyl-1-[2-(3-methyl-1,2-oxazol-5-yl)ethanoyl]-4-oxidanyl-pyrrolidine-2-carboxamide |
|
24
|
104
|
4b9kA |
Pvhl-elob-eloc complex_(2s,4r)-1-(3-amino-2-methylbenzoyl)-4-hydroxy-n-(4-(4-methylthiazol-5-yl)benzyl)pyrrolidine-2-carboxamide bound |
|
21
|
135
|
4b0mA |
Complex of the caf1an usher domain, caf1m chaperone and caf1 subunit from yersinia pestis |
|
22
|
104
|
4b95A |
Pvhl-elob-elob-eloc complex_(2s,4r)-1-(2-chlorophenyl)carbonyl-n-[(4-chlorophenyl)methyl]-4-oxidanyl-pyrrolidine-2-carboxamide bound |
|
23
|
75
|
3znhB |
Crimean congo hemorrhagic fever virus otu domain in complex with ubiquitin-propargyl. |
|
43
|
146
|
3znzB |
Crystal structure of otulin otu domain (c129a) in complex with met1- di ubiquitin |
|
20
|
76
|
4ap4C |
Rnf4 - ubch5a - ubiquitin heterotrimeric complex |
|
19
|
103
|
3ztdA |
Pvhl54-213-elob-eloc complex _ methyl 4-(((2s,4r)-4-hydroxy-1-(2-(3- methylisoxazol-5-yl)acetyl)pyrrolidine-2-carboxamido)methyl)benzoate |
|
29
|
138
|
4a90A |
Crystal structure of mouse sap18 residues 1-143 |
|
21
|
104
|
3ztcA |
Pvhl54-213-elob-eloc complex _ (2s,4r)-n-((1,1'-biphenyl)-4-ylmethyl)- 4-hydroxy-1-(2-(3-methylisoxazol-5-yl)acetyl)pyrrolidine-2- carboxamide |
|
29
|
125
|
4a8xC |
Structure of the core asap complex |
|
19
|
77
|
3zniD |
Structure of phosphotyr363-cbl-b - ubch5b-ub - zap-70 peptide complex |
|
16
|
99
|
3zrcA |
Pvhl54-213-elob-eloc complex (4r)-4-hydroxy-1-[(3-methylisoxazol-5-yl)acetyl]-n-[4-(1,3-oxazol-5-yl)benzyl]-l-prolinamide bound |
|
18
|
80
|
4a20A |
Crystal structure of the ubl domain of mdy2 (get5) at 1.78a |
|
116
|
368
|
4a9aA |
Structure of rbg1 in complex with tma46 dfrp domain |
|
160
|
475
|
3zxrA |
Crystal structure of mycobacterium tuberculosis glutamine synthetase in complex with tri-substituted imidazole inhibitor (3-(2-tert-butyl- 5-(pyridin-4-yl)-1h-imidazol-4-yl)quinoline) and l-methionine-s- sulfoximine phosphate. |
|
162
|
550
|
3zq4A |
Unusual, dual endo- and exo-nuclease activity in the degradosome explained by crystal structure analysis of rnase j1 |
|
192
|
628
|
3zyyX |
Reductive activator for corrinoid,iron-sulfur protein |
|
22
|
103
|
3zrfA |
Pvhl54-213-elob-eloc complex_apo |
|
155
|
475
|
4acfA |
Crystal structure of mycobacterium tuberculosis glutamine synthetase in complex with imidazopyridine inhibitor ((4-(6-bromo-3-(butylamino)imidazo(1,2-a)pyridin-2-yl)phenoxy) acetic acid) and l-methionine-s-sulfoximine phosphate. |
|
59
|
214
|
4a3pA |
Structure of usp15 dusp-ubl deletion mutant |
|
19
|
81
|
3zo5B |
Structure of senp2-loop1 in complex with presumo-2 |
|
18
|
81
|
4aswC |
Structure of the complex between the n-terminal dimerisation domain of sgt2 and the ubl domain of get5 |
|
29
|
143
|
4a6qA |
Crystal structure of mouse sap18 residues 6-143 |
|
160
|
475
|
3zxvA |
Crystal structure of mycobacterium tuberculosis glutamine synthetase in complex with tri-substituted imidazole inhibitor (4-(2-tert-butyl- 4-(6-methoxynaphthalen-2-yl)-1h-imidazol-5-yl)pyridin-2-amine) and l- methionine-s-sulfoximine phosphate |
|
20
|
102
|
3zunA |
Pvhl54-213-elob-eloc complex_(2s,4r)-4-hydroxy-1-(2-(3-methylisoxazol- 5-yl)acetyl)-n-(4-nitrobenzyl)pyrrolidine-2-carboxamide bound |
|
28
|
105
|
4ajyB |
Von hippel-lindau protein-elonginb-elonginc complex, bound to hif1- alpha peptide |
|
64
|
217
|
4a3oA |
Crystal structure of the usp15 dusp-ubl monomer |
|
9
|
104
|
3zkjC |
Crystal structure of ankyrin repeat and socs box-containing protein 9 (asb9) in complex with elonginb and elonginc |
|
35
|
115
|
3walA |
Crystal structure of human lc3a_2-121 |
|
18
|
73
|
3zlzA |
Lys6-linked tri-ubiquitin |
