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MolNFT v1 · #129900 · protein

The structural basis of the histone demethylase KDM6B histone 3 lysine 27 specificity

5OY3 · Lysine-specific demethylase 6B: “The structural basis of the histone demethylase KDM6B histone 3 lysine 27 specificity”. X-ray diffraction, 3 ligands (AKG, FE, ZN), 7 pockets (best druggability 0.76). MolNFT v1 #129900 on GenesisL1…

PDB
5OY3
Type
protein
Length
467 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Lysine-specific demethylase 6B; Histone 3 peptide H3(17-33)A21M
EC
1.14.11.-
UniProt
O15054
Ligands
AKG, FE, ZN
Pockets
7 · best druggability 0.76

Structure

x-ray diffraction · 2 distinct chains · 34% helix, 23% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ALysine-specific demethylase 6B (EC 1.14.11.-)protein45035% helix, 23% strandO15054
BHistone 3 peptide H3(17-33)A21Mprotein170% helix, 24% strand—

Ligands and binding sites

  • AKG · 2-oxoglutaric acid · ligand · chains A
  • FE · Fe (III) ion · metal · chains A
  • ZN · Zinc ion · metal · chains A
  • EDO · 1,2-ethanediol · additive · 8 copies · chains A
  • TBU · Tertiary-butyl alcohol · additive · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13020.760.8837FE, AKG
21340.540.8222empty
31170.420.7619empty
41060.380.7519EDO
5640.380.7917TBU

Interfaces

1 interface between chains.

  • A–B · 1280 Ų buried · 26 hydrogen bonds · protein-protein

Compared structures

  • 5OY3 · The structural basis of the histone demethylase KDM6B histone 3 lysine 27 specificity · the same entry in another collection · chain A against A, TM-score 1.00
  • O15054 · AlphaFold monomer V2.0 prediction for lysine-specific demethylase 6B (O15054) · a predicted model of the same protein · chain A against A, TM-score 0.99

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