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MolNFT v1 · #81865 · protein

Crystal structure of C-lobe of bovine lactoferrin complexed with gamma amino butyric acid at 1.44 a resolution

3V5A · Lactotransferrin: “Crystal structure of C-lobe of bovine lactoferrin complexed with gamma amino butyric acid at 1.44 a resolution”. X-ray diffraction, 5 ligands (ABU, NAG, ZN), 4 pockets (best druggability 0.72). MolNFT v1 #81865 on…

PDB
3V5A
Type
protein
Length
341 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Lactotransferrin; C-terminal peptide of lactotransferrin
EC
3.4.21.-
UniProt
P24627
Ligands
ABU, NAG, ZN, FE, CO3
Pockets
4 · best druggability 0.72

Structure

x-ray diffraction · 2 distinct chains · 35% helix, 19% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ALactotransferrin (EC 3.4.21.-)protein33536% helix, 19% strandP24627
BC-terminal peptide of lactotransferrinprotein60% helix, 0% strandP24627

Ligands and binding sites

  • ABU · Gamma-amino-butanoic acid · 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 · 2 copies · chains A
  • GOL · Glycerol · additive · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12570.720.8640empty
21730.450.7541NAG
31100.430.7720empty
4610.310.7511empty

Interfaces

1 interface between chains.

  • A–B · 291 Ų buried · 2 hydrogen bonds · protein-protein

Modifications

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

Compared structures

  • 3V5A · Crystal Structure of C-lobe of Bovine Lactoferrin Complexed with Gamma Amino Butyric Acid… · the same entry in another collection · chain A against A, TM-score 1.00

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