Structure of human G9a SET-domain (EHMT2) in complex with inhibitor 17: N~2~-cyclopentyl-6,7-dimethoxy-N~2~-methyl-N~4~-(1-methylpiperidin-4-yl)quinazoline-2,4-diamine. Determined by X-ray diffraction at 1.6 Å resolution. Released 19 Jul 2017.
Explore 5VSE in 3D Show helices and sheets RCSB PDB PDBe
5VSE contains 25 α-helices and 42 β-strands across 2 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 | 921-923 | 3 | 1 |
| β-strand | 937-938 | 2 | 1 |
| α-helix | 944-947 | 4 | |
| β-strand | 951-952 | 2 | 2 |
| β-strand | 957-958 | 2 | 2 |
| β-strand | 967 | 1 | 3 |
| α-helix | 968-970 | 3 | |
| α-helix | 986-990 | 5 | |
| β-strand | 996 | 1 | 4 |
| β-strand | 1002 | 1 | 4 |
| α-helix | 1011-1013 | 3 | |
| β-strand | 1014-1015 | 2 | 5 |
| α-helix | 1032-1034 | 3 | |
| β-strand | 1040-1044 | 5 | 1 |
| β-strand | 1050-1054 | 5 | 1 |
| β-strand | 1058 | 1 | 6 |
| β-strand | 1063-1067 | 5 | 5 |
| β-strand | 1069-1073 | 5 | 2 |
| α-helix | 1074-1077 | 4 | |
| β-strand | 1086-1088 | 3 | 2 |
| β-strand | 1097-1105 | 9 | 2 |
| α-helix | 1107-1110 | 4 | |
| α-helix | 1111 | 1 | |
| β-strand | 1112-1113 | 2 | 7 |
| β-strand | 1119-1125 | 7 | 5 |
| β-strand | 1135-1140 | 6 | 5 |
| β-strand | 1144 | 1 | 6 |
| α-helix | 1148 | 1 | |
| β-strand | 1149 | 1 | 1 |
| α-helix | 1150 | 1 | |
| β-strand | 1151-1152 | 2 | 7 |
| α-helix | 1156-1162 | 7 | |
| α-helix | 1179-1188 | 10 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 917-919 | 3 | |
| β-strand | 920-923 | 4 | 8 |
| β-strand | 937-939 | 3 | 8 |
| α-helix | 944-947 | 4 | |
| β-strand | 951-952 | 2 | 3 |
| β-strand | 957-958 | 2 | 3 |
| β-strand | 967 | 1 | 2 |
| α-helix | 968-970 | 3 | |
| α-helix | 986-990 | 5 | |
| β-strand | 996 | 1 | 9 |
| β-strand | 1002 | 1 | 9 |
| α-helix | 1011-1013 | 3 | |
| β-strand | 1014-1015 | 2 | 10 |
| α-helix | 1032-1034 | 3 | |
| β-strand | 1040-1044 | 5 | 8 |
| β-strand | 1050-1054 | 5 | 8 |
| β-strand | 1058 | 1 | 11 |
| β-strand | 1063-1067 | 5 | 10 |
| β-strand | 1069-1073 | 5 | 3 |
| α-helix | 1074-1077 | 4 | |
| β-strand | 1086-1089 | 4 | 3 |
| β-strand | 1097-1105 | 9 | 3 |
| α-helix | 1107-1110 | 4 | |
| α-helix | 1111 | 1 | |
| β-strand | 1112-1113 | 2 | 12 |
| β-strand | 1119-1125 | 7 | 10 |
| β-strand | 1135-1140 | 6 | 10 |
| β-strand | 1144 | 1 | 11 |
| α-helix | 1148 | 1 | |
| β-strand | 1149 | 1 | 8 |
| α-helix | 1150 | 1 | |
| β-strand | 1151-1152 | 2 | 12 |
| α-helix | 1156-1162 | 7 | |
| α-helix | 1179-1189 | 11 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Histone-lysine N-methyltransferase EHMT2 | A, B | protein | 275 | Homo sapiens | Q96KQ7 (AlphaFold model) |
>5VSE_1 Histone-lysine N-methyltransferase EHMT2 (chains A, B) TRTEKIICRDVARGYENVPIPCVNGVDGEPCPEDYKYISENCETSTMNIDRNITHLQHCT CVDDCSSSNCLCGQLSIRCWYDKDGRLLQEFNKIEPPLIFECNQACSCWRNCKNRVVQSG IKVRLQLYRTAKMGWGVRALQTIPQGTFICEYVGELISDAEADVREDDSYLFDLDNKDGE VYCIDARYYGNISRFINHLCDPNIIPVRVFMLHQDLRFPRIAFFSSRDIRTGEELGFDYG DRFWDIKSKYFTCQCGSEKCKHSAEAIALEQSRLA
| ID | Name | Formula | Copies |
|---|---|---|---|
| 9HG | N~2~-cyclopentyl-6,7-dimethoxy-N~2~-methyl-N~4~-(1-methylpiperidin-4-yl)quinazo… | C22 H33 N5 O2 | 2 |
| SAM | S-adenosylmethionine | C15 H22 N6 O5 S | 2 |
| ZN | Zinc ion | Zn | 8 |
Structure-activity relationship studies of G9a-like protein (GLP) inhibitors. Xiong, Y., Li, F., Babault, N. et al. Bioorg Med Chem (2017) 25:4414-4423. DOI 10.1016/j.bmc.2017.06.021 · PubMed
Other PDB entries of the same protein (UniProt Q96KQ7 (AlphaFold model), which also has an AlphaFold model), best resolution first:
MolViewer shows 5VSE directly in your browser with nothing to install. Switch between cartoon, ball-and-stick, spacefill and surface views, color by chain, secondary structure or B-factor, measure distances, angles and dihedrals, and share or embed the view.