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UniProt O14684

Prostaglandin E synthase (O14684)

Prostaglandin E synthase (UniProt O14684), EC 1.11.1.-, 2.5.1.18: 28 experimental structures on GenesisL1, 8 ligands bound. Binding sites, pockets, druggability and 3D structures in GL1X.

UniProt
O14684
Protein
Prostaglandin E synthase
EC
1.11.1.-, 2.5.1.18, 5.3.99.3
Experimental structures
28
Predicted models
0
Ligands
8

Structures

28 records of O14684 in the MolNFT archive: 28 experimental, 0 predicted.

EntryTitleMethodChainsLigandsPockets
3DWWElectron crystallographic structure of human microsomal prostaglandin E synthase 1electron crystallographyA, B, C——
3DWWElectron crystallographic structure of human microsomal prostaglandin E synthase 1electron crystallographyA, B, C——
4AL0Crystal structure of Human PS-1x-ray diffractionA——
4AL0Crystal structure of human ps-1x-ray diffractionA——
4AL1Crystal structure of Human PS-1 GSH-analog complexx-ray diffractionA——
4AL1Crystal structure of human ps-1 gsh-analog complexx-ray diffractionA——
4BPMCrystal structure of a human integral membrane enzymex-ray diffractionA——
4BPMCrystal structure of a human integral membrane enzymex-ray diffractionA——
4WABCrystal structure of mPGES1 solved by native-SAD phasingx-ray diffractionA——
4WABCrystal structure of MPGES1 solved by native-sad phasingx-ray diffractionA——
4YK5Crystal Structures of mPGES-1 Inhibitor Complexesx-ray diffractionA——
4YK5Crystal structures of mpges-1 inhibitor complexesx-ray diffractionA——
4YL0Crystal Structures of mPGES-1 Inhibitor Complexesx-ray diffractionA——
4YL0Crystal structures of mpges-1 inhibitor complexesx-ray diffractionA——
4YL1Crystal Structures of mPGES-1 Inhibitor Complexesx-ray diffractionA——
4YL1Crystal structures of mpges-1 inhibitor complexesx-ray diffractionA——
4YL3Crystal Structures of mPGES-1 Inhibitor Complexesx-ray diffractionA——
4YL3Crystal structures of mpges-1 inhibitor complexesx-ray diffractionA——
5BQGCrystal structure of mpges-1 bound to an inhibitorx-ray diffractionA——
5BQHDiscovery of a potent and selective mpges-1 inhibitor for the treatment of painx-ray diffractionA——
5BQIDiscovery of a potent and selective mpges-1 inhibitor for the treatment of painx-ray diffractionA——
5K0IMPGES1 bound to an inhibitorx-ray diffractionA——
5T36Crystal structure of mpges-1 bound to inhibitorx-ray diffractionA755, GSH—
5T37Crystal structure of mpges-1 bound to inhibitorx-ray diffractionA758, GSH—
5TL9Crystal structure of mpges-1 bound to inhibitorx-ray diffractionA7DN, GSH, JZR—
6VL4Crystal structure of mpges-1 bound to dg-031x-ray diffractionAQY1—
8PYVStructure of Human PS-1 GSH-analog complex, solved at wavelength 2.755 Ax-ray diffractionAPLM, 48T—
O14684AlphaFold monomer V2.0 prediction for prostaglandin E synthase (O14684)———

Ligands

  • GSH · Glutathione · in 3 records
  • 48T · L-gamma-glutamyl-S-(2-biphenyl-4-yl-2-oxoethyl)-L-cysteinylglycine · in 1 record
  • 755 · 4-chloro-2-[({(1S,2S)-2-[(2,2-dimethylpropanoyl) amino]cyclopentyl}methyl)amino]benzoic acid · in 1 record
  • 758 · 2-chloro-5-{[(2,2-dimethylpropanoyl)amino]methyl}-N-(1H-imidazol-2-yl)benzamide · in 1 record
  • 7DN · 2-{2-[(1S,2S)-2-{[1-(8-methylquinolin-2-yl)piperidine-4-carbonyl]amino}cyclopentyl]ethyl}benzoic acid · in 1 record
  • JZR · Hexyl beta-D-glucopyranoside · in 1 record
  • PLM · Palmitic acid · in 1 record
  • QY1 · (2R)-cyclopentyl{4-[(quinolin-2-yl) methoxy]phenyl}acetic acid · in 1 record

Elsewhere

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