|
57
|
178
|
5fb1A |
Crystal structure of a phd finger bound to histone h3 k9me3 peptide |
|
59
|
183
|
5fb0A |
Crystal structure of a phd finger bound to histone h3 t3ph peptide |
|
12
|
55
|
4z0oA |
Cw-type zinc finger of zcwpw2 with f78d mutation |
|
10
|
57
|
4z0rA |
Crystal structure of the cw domain of zcwpw2 mutant f78r in complex with histone h3 peptide |
|
21
|
76
|
5eyaF |
Trim25 ring domain in complex with ubc13-ub conjugate |
|
25
|
120
|
5dinA |
Structural basis for the indispensable role of a unique zinc finger motif in lnx2 ubiquitination |
|
49
|
183
|
4zqlA |
Crystal structure of trim24 with 3,4-dimethoxy-n-(6-(4-methoxyphenoxy)-1,3-dimethyl-2-oxo-2,3-dihydro-1h-benzo[d]imidazol-5-yl)benzenesulfonamide inhibitor |
|
29
|
96
|
5dkaA |
A c2hc zinc finger is essential for the activity of the ring ubiquitin ligase rnf125 |
|
54
|
184
|
4yaxA |
Crystal structure of trim24 phd-bromodomain complexed with n-[6-(4-methoxyphenoxy)-1,3-dimethyl-2-oxo-2,3-dihydro-1h-1,3-benzodiazol-5-yl]benzenesulfonamide (5g) |
|
28
|
127
|
5d1kB |
Crystal structure of ubch5b in complex with the ring-u5br fragment of ao7 |
|
54
|
183
|
4yadA |
Crystal structure of trim24 phd-bromodomain complexed with 2,4-dimethoxy-n-(1-methyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-yl)benzene-1-sulfonamide (3b) |
|
26
|
127
|
5d1mB |
Crystal structure of ubch5b in complex with the ring-u5br fragment of ao7 (p199a) |
|
28
|
129
|
5aiuA |
A complex of rnf4-ring domain, ubc13-ub (isopeptide crosslink) |
|
21
|
129
|
5aitA |
A complex of of rnf4-ring domain, ubev2, ubc13-ub (isopeptide crosslink) |
|
28
|
127
|
5d1lB |
Crystal structure of ubch5b in complex with the ring-u5br fragment of ao7 (y165a) |
|
50
|
183
|
4yatA |
Crystal structure of trim24 phd-bromodomain complexed with n-(1,3-dimethyl-2-oxo-2,3-dihydro-1h-1,3-benzodiazol-5-yl)-4-methoxybenzene-1-sulfonamide (5b) |
|
54
|
183
|
4ybtA |
Crystal structure of trim24 phd-bromodomain complexed with n-{1,3-dimethyl-2-oxo-6-[3-(oxolan-3-ylmethoxy)phenoxy]-2,3-dihydro-1h-1,3-benzodiazol-5-yl}-1-methyl-1h-imidazole-4-sulfonamide (7l) |
|
53
|
184
|
4yc9A |
Crystal structure of trim24 phd-bromodomain complexed with n-(6-{3-[4-(dimethylamino)butoxy]-5-propoxyphenoxy}-1,3-dimethyl-2-oxo-2,3-dihydro-1h-1,3-benzodiazol-5-yl)-3,4-dimethoxybenzene-1-sulfonamide (8i) |
|
18
|
76
|
4xi1A |
Crystal structure of u-box 2 of lubx / legu2 / lpp2887 from legionella pneumophila str. paris, wild-type |
|
36
|
109
|
4wz0A |
Crystal structure of u-box 1 of lubx / legu2 / lpp2887 from legionella pneumophila str. paris |
|
54
|
183
|
4wz3B |
Crystal structure of the complex between lubx/legu2/lpp2887 u-box 1 and homo sapiens ube2d2 |
|
141
|
471
|
4wa6A |
Structure of yeast saga dubm with sgf73 n59d mutant at 2.36 angstroms resolution |
|
18
|
75
|
4wz2A |
Crystal structure of u-box 2 of lubx / legu2 / lpp2887 from legionella pneumophila str. paris, ile175met mutant |
|
36
|
192
|
4x3gA |
Crystal structure of siah1 sina domain in complex with a usp19 peptide |
|
135
|
471
|
4w4uA |
Structure of yeast saga dubm with sgf73 y57a mutant at 2.8 angstroms resolution |
|
27
|
98
|
4up0A |
Ternary crystal structure of the pygo2 phd finger in complex with the b9l hd1 domain and a h3k4me2 peptide |
|
14
|
75
|
4v3kC |
Rnf38-ubch5b-ub complex |
|
15
|
69
|
4v3lC |
Rnf38-ub-ubch5b-ub complex |
|
25
|
96
|
4s3oC |
Pcgf5-ring1b-ubch5c complex |
|
26
|
107
|
4s3oB |
Pcgf5-ring1b-ubch5c complex |
|
11
|
84
|
4ui9B |
Atomic structure of the human anaphase-promoting complex |
|
11
|
64
|
4r2yA |
Crystal structure of apc11 ring domain |
|
8
|
48
|
4qq4A |
Cw-type zinc finger of morc3 in complex with the amino terminus of histone h3 |
|
20
|
69
|
4r7eA |
Structure of bre1 ring domain |
|
9
|
57
|
4qf3A |
Crystal structure of human baz2b phd zinc finger in the free form |
|
9
|
66
|
4ppeA |
Human rnf4 ring domain |
|
294
|
1092
|
4ogeA |
Crystal structure of the type ii-c cas9 enzyme from actinomyces naeslundii |
|
245
|
1094
|
4ogcA |
Crystal structure of the type ii-c cas9 enzyme from actinomyces naeslundii |
|
59
|
178
|
4ptbA |
Crystal structure of human sp100 phd-bromodomain in the free state |
|
8
|
53
|
4qf2A |
Crystal structure of human baz2a phd zinc finger in the free form |
|
9
|
56
|
4q6fA |
Crystal structure of human baz2a phd zinc finger in complex with unmodified h3k4 histone peptide |
|
9
|
82
|
4p5oB |
Structure of an rbx1-ubc12~nedd8-cul1-dcn1 complex: a ring-e3-e2~ubiquitin-like protein-substrate intermediate trapped in action |
|
37
|
124
|
4nn2A |
Protein crystal structure of human borjeson-forssman-lehmann syndrome associated protein phf6 |
|
55
|
232
|
4n4fA |
Crystal structure of the bromodomain-phd finger module of human transcriptional co-activator cbp in complex with di-acetylated histone 4 peptide (h412ack16ac). |
|
55
|
231
|
4n3wA |
Crystal structure of the bromodomain-phd finger module of human transcriptional co-activator cbp in complex with acetylated histone 4 peptide (h4k20ac). |
|
10
|
56
|
4o62A |
Cw-type zinc finger of zcwpw2 in complex with the amino terminus of histone h3 |
|
20
|
116
|
4o64A |
Zinc fingers of kdm2b |
|
116
|
420
|
4msxA |
Crystal structure of an essential yeast splicing factor |
|
29
|
123
|
4llbA |
Crystal structure of moz double phd finger histone h3k14ac complex |
|
28
|
126
|
4lkaA |
Crystal structure of moz double phd finger histone h3k9ac complex |
