Structure of G9a SET-domain with Histone H3K9norLeucine mutant peptide and bound S-adenosylmethionine. Determined by X-ray diffraction at 1.48 Å resolution. Released 14 Sept 2016.
Explore 5JIY in 3D Show helices and sheets RCSB PDB PDBe
5JIY contains 22 α-helices and 44 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 |
|---|---|---|---|
| α-helix | 917-919 | 3 | |
| 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 | 986-989 | 4 | |
| 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 | 1179-1187 | 9 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 921-923 | 3 | 8 |
| β-strand | 937-938 | 2 | 8 |
| β-strand | 951-952 | 2 | 3 |
| β-strand | 957-958 | 2 | 3 |
| β-strand | 967 | 1 | 2 |
| α-helix | 968-970 | 3 | |
| α-helix | 986-989 | 4 | |
| 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 | 1149-1150 | 2 | 8 |
| β-strand | 1151-1152 | 2 | 12 |
| α-helix | 1156-1162 | 7 | |
| α-helix | 1179-1186 | 8 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 9 | 1 | 2 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Histone-lysine N-methyltransferase EHMT2 | A, B | protein | 274 | Homo sapiens | Q96KQ7 (AlphaFold model) |
| Histone H3.1 mutant peptide with H3K9nor-leucine | F, G | protein | 11 | Homo sapiens | P68431 (AlphaFold model) |
>5JIY_1 Histone-lysine N-methyltransferase EHMT2 (chains A, B) IRTEKIICRDVARGYENVPIPCVNGVDGEPCPEDYKYISENCETSTMNIDRNITHLQHCT CVDDCSSSNCLCGQLSIRCWYDKDGRLLQEFNKIEPPLIFECNQACSCWRNCKNRVVQSG IKVRLQLYRTAKMGWGVRALQTIPQGTFICEYVGELISDAEADVREDDSYLFDLDNKDGE VYCIDARYYGNISRFINHLCDPNIIPVRVFMLHQDLRFPRIAFFSSRDIRTGEELGFDYG DRFWDIKSKYFTCQCGSEKCKHSAEAIALEQSRL
>5JIY_2 Histone H3.1 mutant peptide with H3K9nor-leucine (chains F, G) TKQTARLSTGG
S-adenosyl methionine is necessary for inhibition of the methyltransferase G9a by the lysine 9 to methionine mutation on histone H3. Jayaram, H., Hoelper, D., Jain, S.U. et al. Proc Natl Acad Sci U S A (2016) 113:6182-6187. DOI 10.1073/pnas.1605523113 · 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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