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MolNFT v1 · #53143 · protein

Crystal structure of mus musculus acetylcholinesterase in complex with AMTS13

2WLS: “Crystal structure of mus musculus acetylcholinesterase in complex with AMTS13”. X-ray diffraction, 2 ligands (X13, NAG), 14 pockets (best druggability 0.76). MolNFT v1 #53143 on GenesisL1: 3D structure, binding sites and pockets in…

PDB
2WLS
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
UniProt
P21836
Ligands
X13, NAG
Pockets
14 · best druggability 0.76

Structure

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

ChainMoleculeTypeResiduesSecondary structureUniProt
AAcetylcholinesterase (EC 3.1.1.7)protein53538% helix, 18% strandP21836
BAcetylcholinesterase (EC 3.1.1.7)protein53338% helix, 18% strandP21836

Ligands and binding sites

  • X13 · N,N,N-trimethyl-13-[(methylsulfonyl)sulfanyl]tridecan-1-aminium · ligand · 2 copies · chains A, B
  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 2 copies · chains A
  • PEG · Di(hydroxyethyl)ether · additive · chains B
  • P6G · Hexaethylene glycol · additive · 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, 7 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12610.760.8934X13
22770.750.8738X13
31500.680.8817P6G
43290.590.7734empty
51940.590.8119empty

Interfaces

1 interface between chains.

  • A–B · 945 Ų buried · 8 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 disulfide, 2 glycan (disulfide, N-glycosylation).

Compared structures

  • 2WLS · Crystal structure of Mus musculus Acetylcholinesterase in complex with AMTS13 · the same entry in another collection · chain A against A, TM-score 1.00
  • P21836 · AlphaFold monomer V2.0 prediction for acetylcholinesterase (P21836) · a predicted model of the same protein · chain B against A, TM-score 1.00

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