EED in complex with an allosteric PRC2 inhibitor. Determined by X-ray diffraction at 2.49 Å resolution. Released 1 Feb 2017.
Explore 5GSA in 3D Show helices and sheets RCSB PDB PDBe
5GSA contains 12 α-helices and 59 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 | 94-96 | 3 | |
| β-strand | 98-101 | 4 | 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 |
| β-strand | 350-357 | 8 | 6 |
| β-strand | 369-370 | 2 | 7 |
| β-strand | 376-380 | 5 | 7 |
| β-strand | 386-390 | 5 | 7 |
| β-strand | 400-404 | 5 | 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 | 288-291 | 4 | |
| 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 | 400 | 1 | 14 |
| β-strand | 404 | 1 | 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 | 41-62 | 22 | |
| α-helix | 65-67 | 3 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 41-61 | 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 | 29 | Homo sapiens | Q15910 (AlphaFold model) |
>5GSA_1 Polycomb protein EED (chains A, B) GKKCKYSFKCVNSLKEDHNQPLFGVQFNWHSKEGDPLVFATVGSNRVTLYECHSQGEIRL LQSYVDADADENFYTCAWTYDSNTSHPLLAVAGSRGIIRIINPITMQCIKHYVGHGNAIN ELKFHPRDPNLLLSVSKDHALRLWNIQTDTLVAIFGGVEGHRDEVLSADYDLLGEKIMSC GMDHSLKLWRINSKRMMNAIKESYDYNPNKTNRPFISQKIHFPDFSTRDIHRNYVDCVRW LGDLILSKSCENAIVCWKPGKMEDDIDKIKPSESNVTILGRFDYSQCDIWYMRFSMDFWQ KMLALGNQVGKLYVWDLEVEDPHKAKCTTLTHHKCGAAIRQTSFSRDSSILIAVCDDASI WRWDRLR
>5GSA_2 Histone-lysine N-methyltransferase EZH2 (chains C, D) SMFSSNRQKILERTEILNQEWKQRRIQPV
| ID | Name | Formula | Copies |
|---|---|---|---|
| 73K | N-(furan-2-ylmethyl)-8-(4-methylsulfonylphenyl)-[1,2,4]triazolo[4,3-c]pyrimidin… | C17 H15 N5 O3 S | 2 |
An allosteric PRC2 inhibitor targeting the H3K27me3 binding pocket of. Qi, W., Zhao, K., Gu, J. et al. Nat Chem Biol (2017) 13:381-388. DOI 10.1038/nchembio.2304 · 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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