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Crystal structure of SESTD2 in complex with H3.3S31PHK36M peptide

Analyse Crystal structure of SESTD2 in complex with H3.3S31PHK36M peptide in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6J9J
Type
protein
Length
261 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Histone-lysine N-methyltransferase SETD2; H3.3S31PHK36M(29-42)
EC
2.1.1.43, 2.1.1.-
UniProt
Q9BYW2
Ligands
SAH, ZN, SCN
Pockets
2 · best druggability 0.65

Structure

x-ray diffraction · 2 distinct chains · 18% helix, 26% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHistone-lysine N-methyltransferase SETD2 (EC 2.1.1.43, 2.1.1.-)protein24719% helix, 27% strandQ9BYW2
BH3.3S31PHK36M(29-42)protein140% helix, 21% strand—

Ligands and binding sites

  • SAH · S-adenosyl-L-homocysteine · ligand · chains A
  • ZN · Zinc ion · metal · 3 copies · chains A
  • SCN · Thiocyanate ion · ion · 4 copies · chains A, B

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

2 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12140.650.8432SAH
2780.550.8617empty

Interfaces

1 interface between chains.

  • A–B · 1124 Ų buried · 20 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 modified (phosphorylation).

Compared structures

  • 6J9J · crystal structure of SESTD2 in complex with H3.3S31phK36M peptide · the same entry in another collection · chain A against A, 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

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