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Crystal structure of human JMJD2A in complex with compound 35

Analyse Crystal structure of human JMJD2A in complex with compound 35 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5A7W
Type
protein
Length
691 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Lysine-specific demethylase 4A
EC
1.14.11.-
UniProt
O75164
Ligands
35M, MN, ZN, SO4
Pockets
9 · best druggability 0.71

Structure

x-ray diffraction · 2 distinct chains · 32% helix, 24% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ALysine-specific demethylase 4A (EC 1.14.11.-)protein34531% helix, 24% strandO75164
BLysine-specific demethylase 4A (EC 1.14.11.-)protein34632% helix, 24% strandO75164

Ligands and binding sites

  • 35M · 2-[5-[(4-hydroxyphenyl)carbonylamino]-2-oxidanyl-phenyl]pyridine-4-carboxylic acid · ligand · 2 copies · chains A, B
  • MN · Manganese (II) ion · metal · 2 copies · chains A, B
  • ZN · Zinc ion · metal · 2 copies · chains A, B
  • SO4 · Sulfate ion · ion · 2 copies · chains A, B
  • EDO · 1,2-ethanediol · additive · 5 copies · chains A, B
  • DMS · Dimethyl sulfoxide · additive · 2 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, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14260.710.823835M, DMS
23990.710.823835M, DMS
35700.640.7566EDO
41120.550.8322EDO
51140.520.8224EDO

Interfaces

1 interface between chains.

  • A–B · 399 Ų buried · 4 hydrogen bonds · protein-protein

Compared structures

  • 5A7W · Crystal structure of human JMJD2A in complex with compound 35 · the same entry in another collection · chain A against A, TM-score 1.00

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