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Crystal structure of jmjc domain of human histone demethylase uty in complex with N05859B

Analyse Crystal structure of jmjc domain of human histone demethylase uty in complex… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5FXV
Type
protein
Length
881 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Histone demethylase uty
UniProt
O14607
Ligands
MN1, ZN, MN
Pockets
9 · best druggability 0.79

Structure

x-ray diffraction · 2 distinct chains · 36% helix, 23% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHistone demethylase utyprotein44236% helix, 24% strandO14607
BHistone demethylase utyprotein43936% helix, 23% strandO14607

Ligands and binding sites

  • MN1 · 4-carboxypiperidine · ligand · 2 copies · chains A, B
  • ZN · Zinc ion · metal · 2 copies · chains A, B
  • MN · Manganese (II) ion · metal · 2 copies · chains A, B
  • EDO · 1,2-ethanediol · additive · 10 copies · chains A, B

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

Pockets

9 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110720.790.80102empty
25310.720.8147MN, MN1
34710.700.8145MN, MN1
42440.590.7925empty
5570.450.8418empty

Interfaces

1 interface between chains.

  • A–B · 1068 Ų buried · 9 hydrogen bonds · protein-protein

Compared structures

  • 5FXV · Crystal structure of JmjC domain of human histone demethylase UTY in complex with N05859b · the same entry in another collection · chain A against A, TM-score 1.00
  • O14607 · AlphaFold monomer V2.0 prediction for histone demethylase uty (O14607) · a predicted model of the same protein · chain B against A, TM-score 0.99

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