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Crystal structure of C-lobe of bovine lactoferrin complexed with 1,2, 5-pentanetriol at 1.98 a resolution

Analyse Crystal structure of C-lobe of bovine lactoferrin complexed with 1,2… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3UK4
Type
protein
Length
341 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Lactotransferrin; C-terminal peptide from lactotransferrin
EC
3.4.21.-
UniProt
P24627
Ligands
XXD, NAG, ZN, FE, CO3, SO4
Pockets
5 · best druggability 0.73

Structure

x-ray diffraction · 2 distinct chains · 33% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ALactotransferrin (EC 3.4.21.-)protein33534% helix, 18% strandP24627
BC-terminal peptide from lactotransferrinprotein60% helix, 0% strandP24627

Ligands and binding sites

  • XXD · (2S)-pentane-1,2,5-triol · ligand · chains A
  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 5 copies · chains A
  • ZN · Zinc ion · metal · 2 copies · chains A
  • FE · Fe (III) ion · metal · chains A
  • CO3 · Carbonate ion · ion · chains A
  • SO4 · Sulfate ion · ion · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12360.730.8839empty
2520.360.8018empty
3710.340.7612empty
4780.340.7516empty
5730.300.7420empty

Interfaces

1 interface between chains.

  • A–B · 270 Ų buried · 1 hydrogen bond · protein-protein

Modifications

Observed in the structure: 10 disulfide, 3 glycan (disulfide, N-glycosylation).

Compared structures

  • 3UK4 · Crystal Structure of C-lobe of Bovine lactoferrin Complexed with 1,2,5-Pentanetriol at… · the same entry in another collection · chain A against A, TM-score 1.00

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