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Crystal structure plant lectin in complex with ligand

Analyse Crystal structure plant lectin in complex with ligand in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3WOG
Type
protein
Length
481 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Erythroagglutinin
UniProt
V5YN37
Ligands
NAG, MAN, MN, CA
Pockets
1 · best druggability 0.75

Structure

x-ray diffraction · 2 distinct chains · 5% helix, 47% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AErythroagglutininprotein2384% helix, 46% strandV5YN37
BErythroagglutininprotein2436% helix, 47% strandV5YN37

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 4 copies · chains A, B
  • MAN · alpha-D-mannopyranose · sugar · 2 copies · chains A, B
  • MN · Manganese (II) ion · metal · 2 copies · chains A, B
  • CA · Calcium ion · metal · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15260.750.8364empty

Interfaces

1 interface between chains.

  • A–B · 1011 Ų buried · 11 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 glycan (N-glycosylation).

Compared structures

  • 3WOG · Crystal structure plant lectin in complex with ligand · the same entry in another collection · chain A against A, TM-score 1.00

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