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Erythrina crystagalli lectin

Analyse Erythrina crystagalli lectin in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1UZY
Type
protein
Length
476 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Lectin
UniProt
Q6YD91
Ligands
NAG, BGC, GAL, FUC, BMA, XYP, MAN, FUL, CA, MN
Pockets
1 · best druggability 0.35

Structure

x-ray diffraction · 2 distinct chains · 4% helix, 45% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ALectinprotein2384% helix, 44% strandQ6YD91
BLectinprotein2384% helix, 46% strandQ6YD91

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 4 copies · chains A, B
  • BGC · beta-D-glucopyranose · sugar · 2 copies · chains A, B
  • GAL · beta-D-galactopyranose · sugar · 2 copies · chains A, B
  • FUC · alpha-L-fucopyranose · sugar · chains A
  • BMA · beta-D-mannopyranose · sugar
  • XYP · beta-D-xylopyranose · sugar
  • MAN · alpha-D-mannopyranose · sugar
  • FUL · beta-L-fucopyranose · sugar · chains B
  • CA · Calcium ion · metal · 2 copies · chains A, B
  • MN · Manganese (II) ion · metal · 2 copies · chains A, B
  • EPE · 4-(2-hydroxyethyl)-1-piperazine ethanesulfonic acid · additive · 4 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, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1600.350.7815empty

Interfaces

1 interface between chains.

  • A–B · 836 Ų buried · 10 hydrogen bonds · protein-protein

Modifications

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

Compared structures

  • 1UZY · Erythrina crystagalli lectin · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

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