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Crystal structure of jmjc domain of human histone demethylase uty in complex with N08619B

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
5FY1
Type
protein
Length
888 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Histone demethylase uty
UniProt
O14607
Ligands
0R0, ZN, MN
Pockets
11 · best druggability 0.77

Structure

x-ray diffraction · 2 distinct chains · 37% helix, 23% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHistone demethylase utyprotein44237% helix, 23% strandO14607
BHistone demethylase utyprotein44636% helix, 24% strandO14607

Ligands and binding sites

  • 0R0 · 2-hydroxybenzonitrile · ligand · 2 copies · chains A
  • ZN · Zinc ion · metal · 2 copies · chains A, B
  • MN · Manganese (II) ion · metal · 2 copies · chains A, B
  • EDO · 1,2-ethanediol · additive · 31 copies · chains A, B
  • DMS · Dimethyl sulfoxide · additive · 3 copies · chains A, B

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

Pockets

11 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14020.770.8649EDO
25260.720.8154MN, DMS, EDO
36400.720.7965EDO
45030.710.8144MN, DMS, EDO
52630.600.7925empty

Interfaces

1 interface between chains.

  • A–B · 1255 Ų buried · 17 hydrogen bonds · protein-protein

Compared structures

  • 5FY1 · Crystal structure of JmjC domain of human histone demethylase UTY in complex with N08619b · 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 A against A, TM-score 0.97

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