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Acetylcholinesterase in complex with C7653

Analyse Acetylcholinesterase in complex with C7653 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5FOQ
Type
protein
Length
1,068 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Acetylcholinesterase
EC
3.1.1.7
Ligands
GC8, P15, NAG
Pockets
14 · best druggability 0.77

Structure

x-ray diffraction · 2 distinct chains · 38% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AAcetylcholinesterase (EC 3.1.1.7)protein53538% helix, 18% strand—
BAcetylcholinesterase (EC 3.1.1.7)protein53339% helix, 19% strand—

Ligands and binding sites

  • GC8 · 2-(2,4-dichlorophenoxy)-N-[4-(1-piperidinylmethyl)phenyl]acetamide · ligand · 2 copies · chains A, B
  • P15 · 2,5,8,11,14,17-hexaoxanonadecan-19-ol · ligand · chains A, B
  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 3 copies · chains A, B
  • PG0 · 2-(2-methoxyethoxy)ethanol · additive · 4 copies · chains A, B

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

Pockets

14 pockets found on a 1 Å grid, 8 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12820.770.8934GC8
22830.770.8937GC8
31400.690.8918P15
44150.650.7839empty
53710.620.7834empty

Interfaces

1 interface between chains.

  • A–B · 979 Ų buried · 9 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 disulfide, 3 glycan (disulfide, N-glycosylation).

Compared structures

  • 5FOQ · Acetylcholinesterase in complex with C7653 · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

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