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enzyme (lysozyme)

 
Enzymes
  Enzyme classes:
  EC 1: Oxidoreductases
    EC 1.1
      EC 1.1.1
        EC 1.1.1.1
        EC 1.1.1.2
        EC 1.1.1.3
        EC 1.1.1.4
        EC 1.1.1.5
        EC 1.1.1.6
        EC 1.1.1.7
        EC 1.1.1.8
        EC 1.1.1.9
        EC 1.1.1.10
        EC 1.1.1.11
        EC 1.1.1.12
        EC 1.1.1.13
        EC 1.1.1.14
        EC 1.1.1.15
        EC 1.1.1.16
        EC 1.1.1.17
        EC 1.1.1.18
        EC 1.1.1.19
        EC 1.1.1.20
        EC 1.1.1.21
        EC 1.1.1.22
        EC 1.1.1.23
        EC 1.1.1.24
        EC 1.1.1.25
        EC 1.1.1.26
        EC 1.1.1.27
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        EC 1.1.1.97
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        EC 1.1.1.99
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        EC 1.1.1.101
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        EC 1.1.1.111
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        EC 1.1.1.184
        EC 1.1.1.185
        EC 1.1.1.186
        EC 1.1.1.187
        EC 1.1.1.188
        EC 1.1.1.189
        EC 1.1.1.190
        EC 1.1.1.191
        EC 1.1.1.192
        EC 1.1.1.193
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        EC 1.1.1.196
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        EC 1.1.1.198
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        EC 1.1.1.213
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        EC 1.1.1.215
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        EC 1.1.1.218
        EC 1.1.1.219
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        EC 1.1.1.286
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        EC 1.1.1.288
        EC 1.1.1.289
        EC 1.1.1.290
        EC 1.1.1.291
        EC 1.1.1.292
        EC 1.1.1.293
        EC 1.1.1.294
        EC 1.1.1.295
        EC 1.1.1.296
        EC 1.1.1.297
      EC 1.1.2
      EC 1.1.3
      EC 1.1.4
      EC 1.1.5
      EC 1.1.99
    EC 1.2
    EC 1.3
    EC 1.4
    EC 1.5
    EC 1.6
    EC 1.7
    EC 1.8
    EC 1.9
    EC 1.10
    EC 1.11
    EC 1.12
    EC 1.13
    EC 1.14
    EC 1.15
    EC 1.16
    EC 1.17
    EC 1.18
    EC 1.19
    EC 1.20
    EC 1.21
    EC 1.97
    EC 1.98
    EC 1.99
  EC 2: Transferases
  EC 3: Hydrolases
  EC 4: Lyases
  EC 5: Isomerases
  EC 6: Ligases
  General information:
  Catalytic mechanism
  Enzyme kinetics
  Inhibitors
  Enzymes in industry

EC 1.1.1.188 - (5 Z ,13 E ) - (15 S ) - 9α,11α,15- trihydroxyprosta- 5,13- dienoate:NADP + 11- oxidoreductase (prostaglandin- F synthase)



3D structures of EC 1.1.1.188 - prostaglandin-F synthase in Protein Data Bank

updated: 6 January 2022, 2:15

In total: 41 PDB structures of EC 1.1.1.188 - prostaglandin-F synthase:
  1. 1ry0: Structure of Prostaglandin F Synthase with Prostaglandin D2
  2. 1ry8: Prostaglandin F Synthase Complexed with Nadph and Rutin
  3. 1vbj: The Crystal Structure of Prostaglandin F Synthase from Trypanosoma Brucei
  4. 1xf0: Crystal Structure of Human 17beta-hydroxysteroid Dehydrogenase Type 5 (AKR1C3) Complexed with Delta4- Androstene-3,17-dione and Nadp
  5. 1zq5: Crystal Structure of Human Androgenic 17beta-hydroxysteroid Dehydrogenase Type 5 in Complexed with a Potent Inhibitor Em1404
  6. 6a7b: AKR1C3 Complexed with New Inhibitor with Novel Scaffold
  7. 2f38: Crystal Structure of Prostaglandin F Synathase Containing Bimatoprost
  8. 2fgb: Crystal Structure of Human 17bet A-hydroxysteroid Dehydrogenase Type 5 in Complexes with Peg and Nadp
  9. 3r43: AKR1C3 Complexed with Mefenamic Acid
  10. 3r58: AKR1C3 Complex with Naproxen
  11. 4dbs: Crystal Structure of Human 17beta-hydroxysteroid Dehydrogenase Type 5 (AKR1C3) in Complex with Nadp+ and 3-[4 -(nitronaphthalen-1-amino)) Benzoic Acid
  12. 4dbu: Crystal Structure of Human 17beta-hydroxysteroid Dehydrogenase Type 5 (AKR1C3) in Complex with Nadp+ and 3-((4 -(trifluoromethyl)phenyl) Amino)benzoic Acid
  13. 3uwe: AKR1C3 Complexed with 3-phenoxybenzoic Acid
  14. 3r6i: AKR1C3 Complex with Meclofenamic Acid
  15. 3r7m: AKR1C3 Complex with Sulindac
  16. 3r8g: AKR1C3 Complex with Ibuprofen
  17. 3r8h: AKR1C3 Complex with Zomepirac
  18. 3r94: AKR1C3 Complex with Flurbiprofen
  19. 4f40: X-ray Crystal Structure of Apo Prostaglandin F Synthase from Leishmania Major Friedlin
  20. 4fzi: Crystal Structure of Prostaglandin F Synthase from Trypanosoma Cruzi
  21. 3ufy: AKR1C3 Complex with R-naproxen
  22. 3ug8: AKR1C3 Complex with Indomethacin at Ph 7.5
  23. 3ugr: AKR1C3 Complex with Indomethacin at Ph 6.8
  24. 4g5d: X-ray Crystal Structure of Prostaglandin F Synthase from Leishmania Major Friedlin Bound to Nadph
  25. 4gie: Crystal Structure of Prostaglandin F Synthase from Trypanosoma Cruzi Bound to Nadp
  26. 4fa3: Crystal Structure of Human 17beta-hydroxysteroid Dehydrogenase Type 5 in Complex with (r)-1-(naphthalen-2-ylsulfonyl)piperidine-3- Carboxylic Acid (86)
  27. 4fal: Crystal Structure of Human 17beta-hydroxysteroid Dehydrogenase Type 5 in Complex with 3-((3,4-dihydroisoquinolin-2(1h)-yl)sulfonyl)-n- Methylbenzamide (80)
  28. 4fam: Crystal Structure of Human 17beta-hydroxysteroid Dehydrogenase Type 5 in Complex with 3-((3,4-dihydroisoquinolin-2(1h)-yl)sulfonyl)benzoic Acid (17)
  29. 4dbw: Crystal Structure of Human 17beta-hydroxysteroid Dehydrogenase Type 5 (AKR1C3) in Complex with Nadp+ and 2'-desmethyl-indomethacin
  30. 4dz5: W227F Active Site Mutant of AKR1C3
  31. 6gxk: Crystal Structure of Aldo-keto Reductase 1c3 (AKR1C3) Complexed with Inhibitor.
  32. 4h7c: Crystal Structure of Human 17beta-hydroxysteroid Dehydrogenase Type 5 in Complex with 1-{4-[(2-methyl-1-piperidinyl)sulfonyl]phenyl}-2- Pyrrolidinone
  33. 6f78: Potent and Selective Aldo-keto Reductase 1c3 (AKR1C3) Inhibitors Based on The Benzoisoxazole Moiety: Application of a Bioisosteric Scaffold Hopping Approach to Flufenamic Acid
  34. 6f2u: Potent and Selective Aldo-keto Reductase 1c3 (AKR1C3) Inhibitors Based on The Benzoisoxazole Moiety: Application of a Bioisosteric Scaffold Hopping Approach to Flufenamic Acid
  35. 4hmn: Crystal Structure of Human 17beta-hydroxysteroid Dehydrogenase Type 5 in Complex with (4-(4-chlorophenyl)piperazin-1-yl)(morpholino) Methanone (24)
  36. 4wrh: AKR1C3 Complexed with Breakdown Product of N-(tert-butyl)-2-(2-chloro- 4-(((3-mercapto-5-methyl-4h-1,2,4-triazol-4-yl)amino)methyl)-6- Methoxyphenoxy)acetamide
  37. 5hnu: Crystal Structure of AKR1C3 Complexed with Octyl Gallate
  38. 5hnt: Crystal Structure of AKR1C3 Complexed with Cape
  39. 4zfc: Crystal Structure of AKR1C3 Complexed with Glicazide
  40. 4yvx: Crystal Structure of AKR1C3 Complexed with Glimepiride
  41. 4yvv: Crystal Structure of AKR1C3 Complexed with Glibenclamide
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