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Structure of G9A set-domain with histone H3K9NORLEUCINE mutant peptide and bound S-adenosylmethionine
Analyse Structure of G9A set-domain with histone H3K9NORLEUCINE mutant peptide and… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 5JIY
- Type
- protein
- Length
- 557 residues
- Chains
- 4
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Histone-lysine N-methyltransferase EHMT2; Histone H3.1 mutant peptide with H3K9NOR-leucine
- EC
- 2.1.1.-, 2.1.1.43
- UniProt
- Q96KQ7
- Ligands
- SAM, ZN
- Pockets
- 10 · best druggability 0.80
Structure
x-ray diffraction · 4 distinct chains · 12% helix, 25% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Histone-lysine N-methyltransferase EHMT2 (EC 2.1.1.-, 2.1.1.43) | protein | 273 | 12% helix, 25% strand | Q96KQ7 |
| F | Histone H3.1 mutant peptide with H3K9NOR-leucine | protein | 8 | 0% helix, 13% strand | — |
| B | Histone-lysine N-methyltransferase EHMT2 (EC 2.1.1.-, 2.1.1.43) | protein | 267 | 12% helix, 25% strand | Q96KQ7 |
| G | Histone H3.1 mutant peptide with H3K9NOR-leucine | protein | 9 | 0% helix, 11% strand | — |
Ligands and binding sites
- SAM · S-adenosylmethionine · ligand · 2 copies · chains A, F, B, G
- ZN · Zinc ion · metal · 8 copies · chains A, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
10 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1052 | 0.80 | 0.82 | 73 | empty |
| 2 | 207 | 0.55 | 0.78 | 23 | SAM |
| 3 | 214 | 0.54 | 0.78 | 27 | SAM |
| 4 | 71 | 0.42 | 0.80 | 20 | empty |
| 5 | 83 | 0.37 | 0.76 | 13 | empty |
Interfaces
3 interfaces between chains.
- A–B · 1237 Ų buried · 20 hydrogen bonds · protein-protein
- B–G · 748 Ų buried · 14 hydrogen bonds · protein-protein
- A–F · 747 Ų buried · 21 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 2 modified (nonstandard).
Compared structures
- 5JIY · Structure of G9a SET-domain with Histone H3K9norLeucine mutant peptide and bound… · the same entry in another collection · chain A against A, TM-score 1.00
- Q96KQ7 · AlphaFold monomer V2.0 prediction for histone-lysine N-methyltransferase EHMT2 (Q96KQ7) · a predicted model of the same protein · chain B against A, TM-score 0.99
Analyse
- Open in the research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides and crosslinks on the 3D structure
- Every structure of UniProt Q96KQ7
- Elsewhere: RCSB PDB 5JIY · PDBe 5JIY · UniProt Q96KQ7
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