GL1X · GenesisL1 explorer

Research workbench

Botulinum neurotoxin A5 cell binding domain in complex with GM1B oligosaccharide

Analyse Botulinum neurotoxin A5 cell binding domain in complex with GM1B oligosaccharide in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7QPU
Type
protein
Length
738 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Botulinum neurotoxin sub-type A5
EC
3.4.24.69
UniProt
C1IPK2
Ligands
GAL, SIA, SO4
Pockets
7 · best druggability 0.81

Structure

x-ray diffraction · 2 distinct chains · 5% helix, 45% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ABotulinum neurotoxin sub-type A5 (EC 3.4.24.69)protein3875% helix, 45% strandC1IPK2
BBotulinum neurotoxin sub-type A5 (EC 3.4.24.69)protein3515% helix, 45% strandC1IPK2

Ligands and binding sites

  • GAL · beta-D-galactopyranose · sugar · chains A
  • SIA · N-acetyl-alpha-neuraminic acid · sugar · chains A
  • SO4 · Sulfate ion · ion · chains B
  • PEG · Di(hydroxyethyl)ether · additive · chains B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17960.810.8465empty
22690.550.7727empty
32830.540.7628empty
4760.520.8520empty
5730.450.8220empty

Interfaces

1 interface between chains.

  • A–B · 746 Ų buried · 8 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 covalent (additive adduct).

Compared structures

  • 7QPU · Botulinum neurotoxin A5 cell binding domain in complex with GM1b oligosaccharide · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.