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Crystal structure of human acetylcholinesterase

Analyse Crystal structure of human acetylcholinesterase in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4PQE
Type
protein
Length
528 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Acetylcholinesterase
EC
3.1.1.7
UniProt
P22303
Pockets
6 · best druggability 0.77

Structure

x-ray diffraction · 1 distinct chain · 37% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AAcetylcholinesterase (EC 3.1.1.7)protein52837% helix, 16% strandP22303

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12440.770.9036empty
23530.580.7637empty
31040.440.7818empty
4720.420.8016empty
51080.380.7515empty

Modifications

Observed in the structure: 3 disulfide (disulfide).

Compared structures

  • 4PQE · Crystal Structure of Human Acetylcholinesterase · the same entry in another collection · chain A against A, TM-score 1.00
  • P22303 · AlphaFold monomer V2.0 prediction for acetylcholinesterase (P22303) · a predicted model of the same protein · chain A against A, TM-score 1.00

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