G9a in complex with RK-133232 (compound 16g). Determined by X-ray diffraction at 1.81 Å resolution. Released 21 May 2025.
Explore 9KLB in 3D Show helices and sheets RCSB PDB PDBe
9KLB 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 | 920-923 | 4 | 1 |
| β-strand | 937-939 | 3 | 1 |
| 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 | 1074-1079 | 6 | |
| 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 | 1156-1160 | 5 | |
| α-helix | 1179-1183 | 5 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 921-923 | 3 | 8 |
| β-strand | 937-938 | 2 | 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 |
| α-helix | 1001 | 1 | |
| β-strand | 1002 | 1 | 9 |
| α-helix | 1003 | 1 | |
| 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 | 1074-1079 | 6 | |
| β-strand | 1086-1088 | 3 | 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 | 1179-1190 | 12 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Histone-lysine N-methyltransferase EHMT2 | A, B | protein | 283 | Homo sapiens | Q96KQ7 (AlphaFold model) |
>9KLB_1 Histone-lysine N-methyltransferase EHMT2 (chains A, B) GSNRAIRTEKIICRDVARGYENVPIPCVNGVDGEPCPEDYKYISENCETSTMNIDRNITH LQHCTCVDDCSSSNCLCGQLSIRCWYDKDGRLLQEFNKIEPPLIFECNQACSCWRNCKNR VVQSGIKVRLQLYRTAKMGWGVRALQTIPQGTFICEYVGELISDAEADVREDDSYLFDLD NKDGEVYCIDARYYGNISRFINHLCDPNIIPVRVFMLHQDLRFPRIAFFSSRDIRTGEEL GFDYGDRFWDIKSKYFTCQCGSEKCKHSAEAIALEQSRLARLD
| ID | Name | Formula | Copies |
|---|---|---|---|
| A1L57 | ~{N}-[(~{E},2~{S})-4-cyclopropyl-1-[(6-ethoxypyridin-3-yl)amino]-1-oxidanyliden… | C26 H27 N5 O3 | 2 |
| SFG | Sinefungin | C15 H23 N7 O5 | 2 |
| ZN | Zinc ion | Zn | 8 |
Discovery of potent substrate-type lysine methyltransferase G9a inhibitors for the treatment of sickle cell disease. Nishigaya, Y., Takase, S., Sumiya, T. et al. Eur J Med Chem (2025) 293:117721-117721. DOI 10.1016/j.ejmech.2025.117721 · PubMed
Other PDB entries of the same protein (UniProt Q96KQ7 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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