GL1X · GenesisL1 explorer

Research workbench

Crystal structure of yak lactoperoxidase with partially coordinated Na ion in the distal heme cavity

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

PDB
7C75
Type
protein
Length
595 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
2.7
Source
Bos mutus
Molecule
Lactoperoxidase
UniProt
L8ICE9
Ligands
HEM, NAG, CA, K, ZN, NA
Pockets
6 · best druggability 0.82

Structure

x-ray diffraction · resolution 2.7 · 1 distinct chain · 37% helix, 8% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ALactoperoxidaseprotein59537% helix, 8% strandL8ICE9

Ligands and binding sites

  • HEM · Protoporphyrin IX containing Fe · ligand · chains A
  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 4 copies · chains A
  • CA · Calcium ion · metal · chains A
  • K · Potassium ion · metal · chains A
  • ZN · Zinc ion · metal · chains A
  • NA · Sodium ion · metal · 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, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19430.820.8489HEM, NA
22500.510.7529empty
31240.450.7731empty
4930.440.7919empty
5670.310.7515empty

Modifications

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

Compared structures

  • 7C75 · Crystal structure of yak lactoperoxidase with partially coordinated na ion in the distal… · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.