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Structure of the N terminal domain of BC2L-C lectin (1-131) in complex with globo H (H-type 3) and CAS no 912569-62-1

Analyse Structure of the N terminal domain of BC2L-C lectin (1-131) in complex with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6ZZW
Type
protein
Length
395 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Lectin
UniProt
B4EH86
Ligands
QT5, GAL, GLA, NGA, FUC, NA
Pockets
2 · best druggability 0.68

Structure

x-ray diffraction · 2 distinct chains · 3% helix, 56% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, CLectinprotein1312% helix, 56% strandB4EH86
BLectinprotein1335% helix, 56% strandB4EH86

Ligands and binding sites

  • QT5 · [3-(2-methylimidazol-1-yl)phenyl]methanamine · ligand · 3 copies · chains A, C, B
  • GAL · beta-D-galactopyranose · sugar · 5 copies · chains C, B, A
  • GLA · alpha-D-galactopyranose · sugar · 3 copies · chains A, C, B
  • NGA · 2-acetamido-2-deoxy-beta-D-galactopyranose · sugar · 3 copies · chains A, C, B
  • FUC · alpha-L-fucopyranose · sugar · 3 copies · chains A, C, B
  • NA · Sodium ion · metal · chains A

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

Pockets

2 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11060.680.9119empty
2560.550.8919empty

Interfaces

3 interfaces between chains.

  • A–B · 1028 Ų buried · 18 hydrogen bonds · protein-protein
  • C–B · 1015 Ų buried · 17 hydrogen bonds · protein-protein
  • A–C · 989 Ų buried · 17 hydrogen bonds · protein-protein

Compared structures

  • 6ZZW · Structure of the N terminal domain of Bc2L-C lectin (1-131) in complex with Globo H… · the same entry in another collection · chain A against A, TM-score 1.00

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