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LNBase in complex with LNB-NHAcCAS

Analyse LNBase in complex with LNB-NHAcCAS in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5BXS
Type
protein
Length
1,265 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
2.2
Source
Bifidobacterium bifidum JCM 1254
Molecule
Lacto-N-biosidase
EC
3.2.1.140
UniProt
B3TLD6
Ligands
GC2, GAL, SO4
Pockets
13 · best druggability 0.68

Structure

x-ray diffraction · resolution 2.2 · 2 distinct chains · 31% helix, 24% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ALacto-N-biosidase (EC 3.2.1.140)protein63330% helix, 24% strandB3TLD6
BLacto-N-biosidase (EC 3.2.1.140)protein63231% helix, 24% strandB3TLD6

Ligands and binding sites

  • GC2 · 6-acetamido-6-deoxy-castanospermine · ligand · 2 copies · chains A, B
  • GAL · beta-D-galactopyranose · sugar · 2 copies · chains A, B
  • SO4 · Sulfate ion · ion · 2 copies · chains A, B

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

Pockets

13 pockets found on a 1 Å grid, 7 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16150.680.7774empty
21900.650.8529GAL, GC2
32080.640.8434GAL, GC2
44730.640.7756empty
51130.530.8319empty

Interfaces

1 interface between chains.

  • A–B · 1808 Ų buried · 32 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide (disulfide).

Compared structures

  • 5BXS · Lnbase in complex with lnb-nhaccas · the same entry in another collection · chain A against A, TM-score 1.00

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