|
60
|
263
|
3s8pA |
Crystal structure of the set domain of human histone-lysine n-methyltransferase suv420h1 in complex with s-adenosyl-l-methionine |
|
151
|
429
|
3s7bA |
Structural basis of substrate methylation and inhibition of smyd2 |
|
152
|
429
|
3s7fA |
Structural basis of substrate methylation and inhibition of smyd2 |
|
150
|
429
|
3s7dA |
Structural basis of substrate methylation and inhibition of smyd2 |
|
51
|
168
|
5v3gA |
Prdm9-allele-c znf8-13 |
|
148
|
425
|
3ru0A |
Cocrystal structure of human smyd3 with inhibitor sinefungin bound |
|
76
|
240
|
3rq4A |
Crystal structure of suppressor of variegation 4-20 homolog 2 |
|
67
|
270
|
3rjwA |
Crystal structure of histone lysine methyltransferase g9a with an inhibitor |
|
139
|
430
|
3ribA |
Human lysine methyltransferase smyd2 in complex with adohcy |
|
139
|
526
|
4qeoA |
Crystal structure of kryptonite in complex with mchh dna, h3(1-15) peptide and sah |
|
118
|
526
|
4qepA |
Crystal structure of kryptonite in complex with mchg dna and sah |
|
33
|
123
|
5ww0A |
Crystal structure of set7, a novel histone methyltransferase in schizossacharomyces pombe |
|
10
|
28
|
5wukB |
Crystal structure of eed [g255d] in complex with ezh2 peptide and eed226 compound |
|
131
|
813
|
5wg6A |
Human polycomb repressive complex 2 in complex with gsk126 inhibitor |
|
48
|
162
|
5w1yA |
Setd8 in complex with a covalent inhibitor |
|
149
|
431
|
5wcgA |
Set and mynd domain containing protein 2 |
|
64
|
262
|
5wbvA |
Crystal structure of the set domain of human suv420h1 in complex with inhibitor |
|
69
|
260
|
5v9jA |
Crystal structure of catalytic domain of glp with ms0105 |
|
64
|
261
|
5vsdA |
Structure of human glp set-domain (ehmt1) in complex with inhibitor 13 |
|
75
|
273
|
5vscA |
Structure of human g9a set-domain (ehmt2) in complex with inhibitor 13 |
|
75
|
216
|
5vbcA |
Crystal structure of atxr5 in complex with histone h3.1 |
|
71
|
270
|
5v9iA |
Crystal structure of catalytic domain of g9a with ms0105 |
|
68
|
215
|
5vacA |
Crystal structure of atxr5 set domain in complex with k36me3 histone h3 peptide |
|
66
|
215
|
5vahA |
Crystal structure of atxr5 set domain in complex with histone h3 di-methylated on r26 |
|
66
|
216
|
5va6A |
Crystal structure of atxr5 in complex with histone h3.1 mono-methylated on r26 |
|
67
|
257
|
5v22A |
Crystal structure of human setd2 set-domain in complex with h3k36m peptide and sah |
|
44
|
162
|
5v2nA |
Crystal structure of apo human setd8 |
|
53
|
217
|
5updA |
Methyltransferase domain of human wolf-hirschhorn syndrome candidate 1-like protein 1 (whsc1l1) |
|
9
|
26
|
5u62C |
Crystal structure of eed in complex with h3k27me3 peptide and 6-(benzo[d][1,3]dioxol-4-ylmethyl)-5,6,7,8-tetrahydroimidazo[1,5-a]pyridin-3-amine |
|
9
|
26
|
5u5tC |
Crystal structure of eed in complex with h3k27me3 peptide and 3-(benzo[d][1,3]dioxol-4-ylmethyl)piperidine-1-carboximidamide |
|
72
|
261
|
5ttgA |
Crystal structure of catalytic domain of glp with ms012 |
|
46
|
160
|
5tegA |
Crystal structure of hsetd8 in complex with histone h4k20 norleucine mutant peptide and s-adenosylmethionine |
|
38
|
143
|
5th7A |
Complex of setd8 with ms453 |
|
73
|
269
|
5ttfA |
Crystal structure of catalytic domain of g9a with ms012 |
|
74
|
267
|
5tuyA |
Structure of human g9a set-domain (ehmt2) in complex with inhibitor ms0124 |
|
67
|
261
|
5tuzA |
Structure of human glp set-domain (ehmt1) in complex with inhibitor ms0124 |
|
19
|
59
|
5tfpA |
Crystal structure of the setdb2 amino terminal domain |
|
34
|
143
|
5t5gA |
Human setd8 in complex with ms2177 |
|
70
|
264
|
5t0mA |
A histone h3k9m mutation traps histone methyltransferase clr4 to prevent heterochromatin spreading |
|
72
|
268
|
5t0kA |
Structure of g9a set-domain with h3k9m mutant peptide and sam |
|
12
|
42
|
5svhB |
Crystal structure of the kix domain of cbp in complex with a mll/c-myb chimera |
|
109
|
328
|
5mw3A |
Crystal structure of dot1l in complex with inhibitor cpd1 [n6-(2,6-dichlorophenyl)-n6-(pent-2-yn-1-yl)quinoline-4,6-diamine] and inhibitor cpd2 [(r)-1-(7h-pyrrolo[2,3-d]pyrimidin-4-yl)piperidin-3-amine] |
|
53
|
246
|
5lsxA |
Structure of the epigenetic oncogene mmset and inhibition by n-alkyl sinefungin derivatives |
|
39
|
161
|
4z4pA |
Structure of the mll4 set domain |
|
141
|
426
|
5hi7A |
Co-crystal structure of human smyd3 with an aza-sah compound |
|
10
|
29
|
5h24C |
Eed in complex with prc2 allosteric inhibitor compound 8 |
|
10
|
29
|
5h25C |
Eed in complex with prc2 allosteric inhibitor compound 11 |
|
11
|
29
|
5h15C |
Eed in complex with prc2 allosteric inhibitor eed709 |
|
66
|
251
|
5ayfA |
Crystal structure of set7/9 in complex with cyproheptadine |
|
10
|
29
|
5gsaC |
Eed in complex with an allosteric prc2 inhibitor |
