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Exploitation of a novel binding pocket in human lipoprotein-associated phospholipase A2 (lp-PLA<SUB>2</SUB>) discovered through X-ray fragment screening

Analyse Exploitation of a novel binding pocket in human lipoprotein-associated… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5JAH
Type
protein
Length
371 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Platelet-activating factor acetylhydrolase
EC
3.1.1.47
UniProt
Q13093
Ligands
6HQ, CL
Pockets
3 · best druggability 0.56

Structure

x-ray diffraction · 1 distinct chain · 36% helix, 21% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APlatelet-activating factor acetylhydrolase (EC 3.1.1.47)protein37136% helix, 21% strandQ13093

Ligands and binding sites

  • 6HQ · 1,5,5-trimethylimidazolidine-2,4-dione · ligand · chains A
  • CL · Chloride ion · ion · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12220.560.78276HQ
2610.340.7722empty
3620.310.7413empty

Compared structures

  • 5JAH · Exploitation of a Novel Binding Pocket in Human Lipoprotein-Associated Phospholipase A2… · the same entry in another collection · chain A against A, TM-score 1.00
  • Q13093 · AlphaFold monomer V2.0 prediction for platelet-activating factor acetylhydrolase (Q13093) · a predicted model of the same protein · chain A against A, TM-score 1.00

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