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Crystal structure of potassium induced heme modification in yak lactoperoxidase at 2.20 a resolution

Analyse Crystal structure of potassium induced heme modification in yak lactoperoxidase… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7DMR
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
L8ICE9
Ligands
HEM, NAG, ZN, CA, K, CL
Pockets
7 · best druggability 0.82

Structure

x-ray diffraction · 1 distinct chain · 37% helix, 10% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ALactoperoxidase (EC 1.11.1.7)protein59537% helix, 10% strandL8ICE9

Ligands and binding sites

  • HEM · Protoporphyrin IX containing Fe · ligand · chains A
  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 5 copies · chains A
  • ZN · Zinc ion · metal · 2 copies · chains A
  • CA · Calcium ion · metal · chains A
  • K · Potassium ion · metal · chains A
  • CL · Chloride ion · ion · 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, 1 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19880.820.8384HEM, K
2840.470.8120empty
31100.410.7627empty
4760.390.7816empty
5530.360.7914empty

Modifications

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

Compared structures

  • 7DMR · Crystal structure of potassium induced heme modification in yak lactoperoxidase at 2.20 A… · the same entry in another collection · chain A against A, TM-score 1.00

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