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Crystal structure of the complex of buffalo lactoperoxidase with salicylhydroxamic acid at 2.48 a resolution

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

PDB
3FNL
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
Ligands
HEM, SHA, NAG, MAN, CA, IOD, SCN
Pockets
6 · best druggability 0.81

Structure

x-ray diffraction · 1 distinct chain · 38% helix, 10% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ALactoperoxidase (EC 1.11.1.7)protein59538% helix, 10% strand—

Ligands and binding sites

  • HEM · Protoporphyrin IX containing Fe · ligand · chains A
  • SHA · Salicylhydroxamic acid · 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
  • IOD · Iodide ion · ion · 8 copies · chains A
  • SCN · Thiocyanate ion · ion · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18520.810.8380HEM, SHA
23520.600.7751empty
3980.500.8223empty
4530.350.7812empty
5850.330.7420empty

Modifications

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

Compared structures

  • 3FNL · Crystal Structure of the Complex of Buffalo Lactoperoxidase with Salicylhydroxamic Acid… · the same entry in another collection · chain A against A, TM-score 1.00

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