|
21
|
97
|
1jm7B |
Solution structure of the brca1/bard1 ring-domain heterodimer |
|
4
|
65
|
1hyjA |
Solution structure of the eea1 fyve domain |
|
7
|
65
|
1hyiA |
Solution structure of the eea1 fyve domain complexed with inositol 1,3-bisphosphate |
|
4
|
55
|
1iymA |
Ring-h2 finger domain of el5 |
|
10
|
51
|
1f62A |
Wstf-phd |
|
9
|
65
|
1g25A |
Solution structure of the n-terminal domain of the human tfiih mat1 subunit |
|
4
|
78
|
1e4uA |
N-terminal ring finger domain of human not-4 |
|
20
|
103
|
1jm7A |
Solution structure of the brca1/bard1 ring-domain heterodimer |
|
13
|
76
|
3kdeC |
Crystal structure of the thap domain from d. melanogaster p-element transposase in complex with its natural dna binding site |
|
48
|
142
|
3ldyA |
An extraordinary mechanism of dna perturbation exhibited by the rare-cutting hnh restriction endonuclease paci |
|
46
|
142
|
3m7kA |
Crystal structure of paci-dna enzyme product complex |
|
23
|
105
|
4r8pK |
Crystal structure of the ring1b/bmi1/ubch5c prc1 ubiquitylation module bound to the nucleosome core particle |
|
129
|
472
|
4zuxU |
Saga dub module ubp8/sgf11/sus1/sgf73 bound to ubiqitinated nucleosome |
|
58
|
205
|
3u5nA |
Crystal structure of the complex of trim33 phd-bromo and h3(1-20)k9me3k14ac histone peptide |
|
56
|
204
|
3u5pA |
Crystal structure of the complex of trim33 phd-bromo and h3(1-28)k9me3k14ack18ack23ac histone peptide |
|
173
|
561
|
5lktA |
Crystal structure of the p300 acetyltransferase catalytic core with butyryl-coenzyme a. |
|
164
|
561
|
5lkzA |
Crystal structure of the p300 acetyltransferase catalytic core with crotonyl-coenzyme a. |
|
166
|
558
|
5lkuA |
Crystal structure of the p300 acetyltransferase catalytic core with coenzyme a. |
|
170
|
560
|
5lkxA |
Crystal structure of the p300 acetyltransferase catalytic core with propionyl-coenzyme a. |
|
30
|
100
|
5kh7A |
Crystal structure of fragment (3-[6-oxo-3-(3-pyridinyl)-1(6h)-pyridazinyl]propanoic acid) bound in the ubiquitin binding pocket of the hdac6 zinc-finger domain |
|
30
|
101
|
5kh3A |
Crystal structure of fragment (3-(5-chloro-1,3-benzothiazol-2-yl)propanoic acid) bound in the ubiquitin binding pocket of the hdac6 zinc-finger domain |
|
14
|
65
|
5jg6A |
Apc11-ubv shows role of noncovalent ring-ubiquitin interactions in processive multiubiquitination and ubiquitin chain elongation by apc/c |
|
24
|
112
|
5i3lA |
Dpf3b in complex with h3k14ac peptide |
|
51
|
180
|
5h1uA |
Complex structure of trim24 phd-bromodomain and inhibitor 2 |
|
50
|
182
|
5h1tA |
Complex structure of trim24 phd-bromodomain and inhibitor 1 |
|
16
|
79
|
5ferA |
Complex of trim25 ring with ubch5-ub |
|
11
|
57
|
5tbnA |
Solution nmr structure of phf20 phd domain in complex with a histone h3k4me2 peptide |
|
8
|
59
|
5c13A |
Crystal structure of taf3 phd finger bound to histone h3c4me3 peptide |
|
9
|
52
|
5c11A |
Crystal structure of jarid1a phd finger bound to histone h3c4me3 peptide |
|
26
|
116
|
5b77A |
Crystal structrue of moz double phd finger in complex with histone h3 propionylation at k14 |
|
29
|
119
|
5b78A |
Crystal structure of moz double phd finger mutant-s210d/n235r in complex with histone h3 crotonylation at k14 |
|
32
|
99
|
5b8dA |
Crystal structure of a low occupancy fragment candidate (n-(4-methyl-1,3-thiazol-2-yl)propanamide) bound adjacent to the ubiquitin binding pocket of the hdac6 zinc-finger domain |
|
26
|
120
|
5b76A |
Crystal structure of moz double phd finger domain in complex with histone h3 crotonylation at k14 |
|
31
|
118
|
5b79A |
Crystal structure of dpf2 double phd finger |
|
25
|
119
|
5b75A |
Crystal structure of moz double phd finger in complex with histone h3 butyrylation at k14 |
|
52
|
183
|
4ybmA |
Crystal structure of trim24 phd-bromodomain complexed with n-{6-[3-(benzyloxy)phenoxy]-1,3-dimethyl-2-oxo-2,3-dihydro-1h-1,3-benzodiazol-5-yl}-3,4-dimethoxybenzene-1-sulfonamide (7b) |
|
57
|
183
|
4ybsA |
Crystal structure of trim24 phd-bromodomain complexed with n-{1,3-dimethyl-6-[3-(2-methylpropoxy)phenoxy]-2-oxo-2,3-dihydro-1h-1,3-benzodiazol-5-yl}-1,2-dimethyl-1h-imidazole-4-sulfonamide (7g) |
|
18
|
78
|
4tkpB |
Complex of ubc13 with the ring domain of the trim5alpha retroviral restriction factor |
|
54
|
184
|
4yabA |
Crystal structure of trim24 phd-bromodomain complexed with 1-methyl-5-(2-methyl-1 3-thiazol-4-yl)-2 3-dihydro-1h-indol-2-one (1) |
|
25
|
98
|
4up5A |
Crystal structure of the pygo2 phd finger in complex with the b9l hd1 domain and a chemical fragment |
|
76
|
291
|
4f1pA |
Crystal structure of mutant s554d for arfgap and ank repeat domain of acap1 |
|
11
|
85
|
4f52B |
Structure of a glomulin-rbx1-cul1 complex |
|
10
|
75
|
4ccgX |
Structure of an e2-e3 complex |
|
43
|
193
|
4c9zA |
Crystal structure of siah1 at 1.95 a resolution |
|
42
|
192
|
4ca1A |
Crystal structure of siah1 at 1.58 a resolution. |
|
48
|
136
|
4aycA |
Rnf8 ring domain structure |
|
72
|
218
|
4avxA |
Hepatocyte growth factor-regulated tyrosine kinase substrate (hgs-hrs) bound to an ip2 compound at 1.68 a resolution |
|
33
|
115
|
4b7yC |
Crystal structure of the msl1-msl2 complex |
|
11
|
57
|
4auqB |
Structure of birc7-ubch5b-ub complex. |
|
30
|
129
|
4ap4A |
Rnf4 - ubch5a - ubiquitin heterotrimeric complex |
