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Crystal structure of bovine lactoperoxidase at 2.34 a resolution reveals multiple anion binding sites

Analyse Crystal structure of bovine lactoperoxidase at 2.34 a resolution reveals… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2PT3
Type
protein
Length
595 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Lactoperoxidase
EC
1.11.1.7
UniProt
P80025
Ligands
HEM, NAG, MAN, CA, PO4
Pockets
7 · best druggability 0.81

Structure

x-ray diffraction · 1 distinct chain · 37% helix, 9% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ALactoperoxidase (EC 1.11.1.7)protein59537% helix, 9% strandP80025

Ligands and binding sites

  • HEM · Protoporphyrin IX containing Fe · ligand · chains A
  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 8 copies · chains A
  • MAN · alpha-D-mannopyranose · sugar · 2 copies
  • CA · Calcium ion · metal · chains A
  • PO4 · Phosphate ion · ion · 16 copies · chains A

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
18170.810.8472PO4, HEM
22570.610.8041empty
31170.490.8023empty
4840.440.8022empty
5900.380.7618PO4

Modifications

Observed in the structure: 7 disulfide, 4 glycan, 2 cofactor, 1 modified (disulfide, N-glycosylation, heme attachment, phosphorylation).

Compared structures

  • 2PT3 · Crystal structure of bovine lactoperoxidase at 2.34 A resolution reveals multiple anion… · the same entry in another collection · chain A against A, TM-score 1.00
  • P80025 · AlphaFold monomer V2.0 prediction for lactoperoxidase (P80025) · a predicted model of the same protein · chain A against A, TM-score 0.96

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