Research workbench
Crystal structure of human SETD2 set-domain in complex with H3K36M peptide and sah
Analyse Crystal structure of human SETD2 set-domain in complex with H3K36M peptide and… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 5V22
- Type
- protein
- Length
- 260 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Histone-lysine N-methyltransferase SETD2; Histone H3K36M peptide
- EC
- 2.1.1.43
- UniProt
- Q9BYW2
- Ligands
- SAH, ZN
- Pockets
- 2 · best druggability 0.67
Structure
x-ray diffraction · 2 distinct chains · 20% helix, 26% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Histone-lysine N-methyltransferase SETD2 (EC 2.1.1.43) | protein | 245 | 21% helix, 26% strand | Q9BYW2 |
| B | Histone H3K36M peptide | protein | 15 | 0% helix, 20% strand | — |
Ligands and binding sites
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
2 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 208 | 0.67 | 0.85 | 36 | SAH |
| 2 | 84 | 0.48 | 0.82 | 18 | empty |
Interfaces
1 interface between chains.
- A–B · 1083 Ų buried · 20 hydrogen bonds · protein-protein
Compared structures
- 5V22 · Crystal structure of human SETD2 SET-domain in complex with H3K36M peptide and SAH · the same entry in another collection · chain B against B, TM-score 1.00
- Q9BYW2 · AlphaFold monomer V2.0 prediction for histone-lysine N-methyltransferase SETD2 (Q9BYW2) · a predicted model of the same protein · chain A against A, TM-score 1.00
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 Q9BYW2
- Elsewhere: RCSB PDB 5V22 · PDBe 5V22 · UniProt Q9BYW2
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