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. Determined by X-ray diffraction at 1.9 Å resolution. Released 11 Jan 2017.
Explore 5U62 in 3D Show helices and sheets RCSB PDB PDBe
5U62 contains 13 α-helices and 58 β-strands across 4 chains. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 82-89 | 8 | 1 |
| α-helix | 94-95 | 2 | |
| β-strand | 96-101 | 6 | 2 |
| α-helix | 106 | 1 | |
| α-helix | 110 | 1 | |
| β-strand | 111-117 | 7 | 2 |
| β-strand | 120-126 | 7 | 2 |
| β-strand | 132-139 | 8 | 2 |
| β-strand | 147-154 | 8 | 3 |
| β-strand | 161-167 | 7 | 3 |
| β-strand | 172-176 | 5 | 3 |
| β-strand | 181-186 | 6 | 3 |
| β-strand | 193-198 | 6 | 4 |
| β-strand | 205-210 | 6 | 4 |
| β-strand | 215-219 | 5 | 4 |
| β-strand | 224-229 | 6 | 4 |
| β-strand | 239-244 | 6 | 5 |
| β-strand | 250-255 | 6 | 5 |
| β-strand | 260-264 | 5 | 5 |
| α-helix | 268-279 | 12 | |
| β-strand | 292-294 | 3 | 4 |
| β-strand | 299-301 | 3 | 5 |
| β-strand | 311-315 | 5 | 6 |
| β-strand | 318-322 | 5 | 6 |
| β-strand | 327-333 | 7 | 6 |
| α-helix | 340-342 | 3 | |
| β-strand | 350-357 | 8 | 6 |
| β-strand | 368-370 | 3 | 7 |
| β-strand | 376-380 | 5 | 7 |
| β-strand | 386-390 | 5 | 7 |
| β-strand | 402-404 | 3 | 7 |
| β-strand | 413-418 | 6 | 1 |
| β-strand | 424-429 | 6 | 1 |
| β-strand | 433-439 | 7 | 1 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 82-89 | 8 | 8 |
| α-helix | 94-95 | 2 | |
| β-strand | 96-101 | 6 | 9 |
| α-helix | 106 | 1 | |
| β-strand | 111-117 | 7 | 9 |
| β-strand | 120-126 | 7 | 9 |
| β-strand | 132-139 | 8 | 9 |
| β-strand | 147-154 | 8 | 10 |
| β-strand | 161-167 | 7 | 10 |
| β-strand | 172-176 | 5 | 10 |
| β-strand | 181-186 | 6 | 10 |
| β-strand | 193-198 | 6 | 11 |
| β-strand | 205-210 | 6 | 11 |
| β-strand | 215-219 | 5 | 11 |
| β-strand | 224-229 | 6 | 11 |
| β-strand | 239-244 | 6 | 12 |
| β-strand | 250-255 | 6 | 12 |
| β-strand | 260-264 | 5 | 12 |
| α-helix | 268-279 | 12 | |
| α-helix | 288-289 | 2 | |
| β-strand | 292-294 | 3 | 11 |
| β-strand | 299-301 | 3 | 12 |
| β-strand | 311-315 | 5 | 13 |
| β-strand | 318-322 | 5 | 13 |
| β-strand | 327-333 | 7 | 13 |
| β-strand | 350-357 | 8 | 13 |
| β-strand | 368-370 | 3 | 14 |
| β-strand | 376-380 | 5 | 14 |
| β-strand | 386-390 | 5 | 14 |
| β-strand | 402-404 | 3 | 14 |
| β-strand | 413-418 | 6 | 8 |
| β-strand | 424-429 | 6 | 8 |
| β-strand | 433-439 | 7 | 8 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 44-62 | 19 | |
| α-helix | 65-67 | 3 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 42-62 | 21 | |
| α-helix | 65-67 | 3 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Polycomb protein EED | A, B | protein | 367 | Homo sapiens | O75530 (AlphaFold model) |
| Histone-lysine N-methyltransferase EZH2 | C, D | protein | 30 | Homo sapiens | Q15910 (AlphaFold model) |
>5U62_1 Polycomb protein EED (chains A, B) GKKCKYSFKCVNSLKEDHNQPLFGVQFNWHSKEGDPLVFATVGSNRVTLYECHSQGEIRL LQSYVDADADENFYTCAWTYDSNTSHPLLAVAGSRGIIRIINPITMQCIKHYVGHGNAIN ELKFHPRDPNLLLSVSKDHALRLWNIQTDTLVAIFGGVEGHRDEVLSADYDLLGEKIMSC GMDHSLKLWRINSKRMMNAIKESYDYNPNKTNRPFISQKIHFPDFSTRDIHRNYVDCVRW LGDLILSKSCENAIVCWKPGKMEDDIDKIKPSESNVTILGRFDYSQCDIWYMRFSMDFWQ KMLALGNQVGKLYVWDLEVEDPHKAKCTTLTHHKCGAAIRQTSFSRDSSILIAVCDDASI WRWDRLR
>5U62_2 Histone-lysine N-methyltransferase EZH2 (chains C, D) KSMFSSNRQKILERTEILNQEWKQRRIQPV
| ID | Name | Formula | Copies |
|---|---|---|---|
| 7WD | (6S)-6-[(2H-1,3-benzodioxol-4-yl)methyl]-5,6,7,8-tetrahydroimidazo[1,5-a]pyridi… | C15 H17 N3 O2 | 2 |
| YT3 | Yttrium (III) ion | Y | 2 |
Water and common crystallization additives (GOL) are not listed.
Structure-Guided Design of EED Binders Allosterically Inhibiting the Epigenetic Polycomb Repressive Complex 2 (PRC2) Methyltransferase. Lingel, A., Sendzik, M., Huang, Y. et al. J Med Chem (2017) 60:415-427. DOI 10.1021/acs.jmedchem.6b01473 · PubMed
Other PDB entries of the same protein (UniProt O75530 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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