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Ligand · L0S

L0S · methyl (R)-N-[(1E)-1-(diethylamino)ethylidene]-P-methylphosphonamidate

L0S, methyl (R)-N-[(1E)-1-(diethylamino)ethylidene]-P-methylphosphonamidate (C8 H19 N2 O2 P, 206.2 g/mol), in the MolNFT structures on GenesisL1: bound in 5 records (3 PDB entries). Every binding site with its residues within 4.5 Å, the…

Component
L0S
Formula
C8 H19 N2 O2 P
Class
ligand
Structures
5
PDB entries
3

Binding sites

L0S in 5 structures; the first of them:

  • 6NTH · Crystal Structure of Recombinant Human Acetylcholinesterase Inhibited by (S) Stereoisomer… · L0S A608 · binds TRP86, GLY120, GLY121, GLY122, TYR133, GLU202, SER203, ALA204 and 5 more
  • 6NTK · Crystal Structure of Recombinant Human Acetylcholinesterase Inhibited by A-232 · L0S A606 · binds TRP86, GLY121, GLY122, TYR133, GLU202, SER203, ALA204, TRP236 and 5 more
  • 6NTH · Crystal structure of recombinant human acetylcholinesterase inhibited by (S) stereoisomer… · L0S A608 · binds TRP86, GLY120, GLY121, GLY122, TYR133, GLU202, SER203, ALA204 and 5 more
  • 6NTK · Crystal structure of recombinant human acetylcholinesterase inhibited by a-232 · L0S A606 · binds TRP86, GLY121, GLY122, TYR133, GLU202, SER203, ALA204, TRP236 and 5 more
  • 6NTM · Crystal structure of recombinant human acetylcholinesterase inhibited by a-232 in complex… · L0S A604 · binds TRP86, GLY120, GLY121, GLY122, TYR133, GLU202, SER203, ALA204 and 6 more

Residues it binds most

PHE 10, GLY 10, TYR 10, TRP 10, ALA 10, GLU 10, HIS 10, SER 10 (residue and the binding sites it lines).

Found with

  • FUC · alpha-L-fucopyranose
  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose
  • 7PE · 2-(2-(2-(2-(2-(2-ethoxyethoxy)ethoxy)ethoxy)ethoxy) ethoxy)ethanol
  • HI6 · 4-(aminocarbonyl)-1-[({2-[(E)-(hydroxyimino)methyl]pyridinium-1-yl}methoxy)methyl]pyridinium

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