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Ligand · 5H0

5H0 · (2R,3R)-5-[2-(dimethylamino)ethyl]-2-(4-methoxyphenyl)-4-oxo-2,3,4,5-tetrahydro-1,5-benzothiazepin-3-yl acetate

5H0, (2R,3R)-5-[2-(dimethylamino)ethyl]-2-(4-methoxyphenyl)-4-oxo-2,3,4,5-tetrahydro-1,5-benzothiazepin-3-yl acetate (C22 H26 N2 O4 S, 414.5 g/mol), in the MolNFT structures on GenesisL1: bound in 4 records (2 PDB entries). Every binding…

Component
5H0
Formula
C22 H26 N2 O4 S
Class
ligand
Structures
4
PDB entries
2

Binding sites

5H0 in 4 structures; the first of them:

  • 7RHJ · Cryo-EM structure of human rod CNGA1/B1 channel in L-cis-Diltiazem-blocked open state · 5H0 D801 · binds LEU360, THR361, THR362, GLY385, PHE389, ALA390, VAL393, THR845 and 15 more
  • 7RHK · Cryo-EM structure of human rod CNGA1/B1 channel in L-cis-Diltiazem-trapped closed state · 5H0 A1102 · binds THR361, ILE363, VAL386, PHE389, LEU843, ILE844, PHE872, ILE876 and 17 more
  • 7RHJ · Cryo-EM structure of human rod CNGA1/B1 channel in L-cis-diltiazem- blocked open state · 5H0 D801 · binds LEU360, THR361, THR362, GLY385, PHE389, ALA390, VAL393, THR845 and 15 more
  • 7RHK · Cryo-EM structure of human rod CNGA1/B1 channel in L-cis-diltiazem- trapped closed state · 5H0 A1102 · binds ILE363, PHE389, LEU843, ILE844, PHE872, ILE876, LEU360, THR361 and 13 more

Residues it binds most

THR 4, PHE 4, VAL 4, ILE 4, LEU 4, GLY 4, ALA 3 (residue and the binding sites it lines).

Found with

  • PCG · Cyclic guanosine monophosphate

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