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Fluorine in PDB, part 89 (files: 3521-3560), PDB 4zzj-5ah8

Experimental structures of coordination spheres of Fluorine (F) in bioorganic molecules from X-Ray and NMR experiments. Coordination spheres were calculated with 5.0 Angstroms radius around Fluorine atoms. PDB files: 3521-3560 (PDB 4zzj-5ah8).
  1. 4zzj (F: 3) - SIRT1/Activator/Substrate Complex
    Other atoms: Zn (1);
  2. 4zzy (F: 3) - Structure of Human PARP2 Catalytic Domain Bound to An Isoindolinone Inhibitor
  3. 5a00 (F: 3) - Structure of Human PARP1 Catalytic Domain Bound to An Isoindolinone Inhibitor
  4. 5a09 (F: 3) - Crystal Structure of Human Neutrophil Elastase in Complex with A Dihydropyrimidone Inhibitor
  5. 5a0a (F: 3) - Crystal Structure of Human Neutrophil Elastase in Complex with A Dihydropyrimidone Inhibitor
  6. 5a0b (F: 3) - Crystal Structure of Human Neutrophil Elastase in Complex with A Dihydropyrimidone Inhibitor
  7. 5a0c (F: 6) - Crystal Structure of Human Neutrophil Elastase in Complex with A Dihydropyrimidone Inhibitor
  8. 5a14 (F: 6) - Human CDK2 with Type II Inhibitor
  9. 5a2s (F: 4) - Potent, Selective and Cns-Penetrant Tetrasubstituted Cyclopropane Class Iia Histone Deacetylase (Hdac) Inhibitors
    Other atoms: Zn (4); Na (2);
  10. 5a3h (F: 1) - 2-Deoxy-2-Fluro-B-D-Cellobiosyl/Enzyme Intermediate Complex of the Endoglucanase CEL5A From Bacillus Agaradhearans at 1.8 Angstroms Resolution
  11. 5a3r (F: 3) - Crystal Structure of the (Sr) Calcium Atpase E2.BEF3- Complex Bound to Tnp-Amppcp
    Other atoms: Mg (3); K (1);
  12. 5a43 (F: 2) - Crystal Structure of A Dual Topology Fluoride Ion Channel.
    Other atoms: Na (1);
  13. 5a46 (F: 2) - FGFR1 in Complex with Dovitinib
  14. 5a4l (F: 5) - DYRK1A in Complex with Fluoro Benzothiazole Fragment
  15. 5a5i (F: 3) - Cytochrome 2C9 P450 Inhibitor Complex
    Other atoms: Fe (1); Cl (1);
  16. 5a5j (F: 3) - Cytochrome 2C9 P450 Inhibitor Complex
    Other atoms: Fe (1); Cl (1);
  17. 5a86 (F: 6) - Structure of Pregnane X Receptor in Complex with A Sphingosine 1- Phosphate Receptor 1 Antagonist
    Other atoms: Cl (2);
  18. 5a8g (F: 2) - Crystal Structure of the Wild-Type Staphylococcus Aureus N- Acetylneurminic Acid Lyase in Complex with Fluoropyruvate
  19. 5a8x (F: 3) - Crystal Structure of Human Neutrophil Elastase in Complex with A Dihydropyrimidone Inhibitor
  20. 5a8y (F: 3) - Crystal Structure of Human Neutrophil Elastase in Complex with A Dihydropyrimidone Inhibitor
  21. 5a8z (F: 3) - Crystal Structure of Human Neutrophil Elastase in Complex with A Dihydropyrimidone Inhibitor
  22. 5a9u (F: 1) - Structure of C1156Y Mutant Human Anaplastic Lymphoma Kinase in Complex with Pf-06463922 ((10R)-7-Amino-12-Fluoro-2,10,16-Trimethyl- 15-Oxo- 10,15,16,17-Tetrahydro-2H-8,4-(Metheno)Pyrazolo(4,3-H)(2,5,11) Benzoxadiazacyclotetradecine-3-Carbonitrile).
  23. 5aa8 (F: 1) - Structure of C1156Y,L1198F Mutant Human Anaplastic Lymphoma Kinase in Complex with Pf-06463922 ((10R)-7-Amino-12- Fluoro-2,10,16-Trimethyl-15-Oxo-10,15,16,17-Tetrahydro-2H- 8,4-(Metheno)Pyrazolo(4,3-H)(2,5,11) Benzoxadiazacyclotetradecine-3-Carbonitrile).
  24. 5aa9 (F: 1) - Structure of L1198F Mutant Human Anaplastic Lymphoma Kinase in Complex with Pf-06463922 ((10R)-7-Amino-12-Fluoro-2,10,16-Trimethyl- 15-Oxo- 10,15,16,17-Tetrahydro-2H-8,4-(Metheno)Pyrazolo(4,3-H)(2,5,11) Benzoxadiazacyclotetradecine-3-Carbonitrile).
  25. 5aaa (F: 1) - Structure of L1198F Mutant Human Anaplastic Lymphoma Kinase in Complex with Crizotinib
    Other atoms: Cl (2);
  26. 5aab (F: 1) - Structure of C1156Y,L1198F Mutant Human Anaplastic Lymphoma Kinase in Complex with Crizotinib
    Other atoms: Cl (2);
  27. 5aac (F: 1) - Structure of C1156Y Mutant Human Anaplastic Lymphoma Kinase in Complex with Crizotinib
    Other atoms: Cl (2);
  28. 5abg (F: 2) - Structure of GH84 with Ligand
    Other atoms: Ca (1);
  29. 5acc (F: 3) - A Novel Oral Selective Estrogen Receptor Down-Regulator, AZD9496, Drives Tumour Growth Inhibition in Estrogen Receptor Positive and ESR1 Mutant Models
  30. 5acw (F: 12) - Vim-2-1, Discovery of Novel Inhibitor Scaffolds Against the Metallo- Beta-Lactamase Vim-2 By Spr Based Fragment Screening
    Other atoms: Zn (6); Cl (4);
  31. 5acx (F: 2) - Vim-2-2, Discovery of Novel Inhibitor Scaffolds Against the Metallo- Beta-Lactamase Vim-2 By Spr Based Fragment Screening
    Other atoms: Zn (6); Cl (4);
  32. 5adz (F: 4) - Ether Lipid-Generating Enzyme Agps in Complex with Inhibitor 1A
  33. 5ae1 (F: 4) - Ether Lipid-Generating Enzyme Agps in Complex with Inhibitor ZINC69435460
  34. 5ae2 (F: 4) - Ether Lipid-Generating Enzyme Agps in Complex with Inhibitor 1E
  35. 5aeg (F: 1) - A Bacterial Protein Structure in Glycoside Hydrolase Family 31.
    Other atoms: Cl (2); Ca (3);
  36. 5afk (F: 12) - ALPHA7-Achbp in Complex with Lobeline and Fragment 2
  37. 5agi (F: 1) - Crystal Structure of the Leurs Editing Domain of Candida Albicans Mutant K510A in Complex with the Adduct Formed By AN2690-Amp
  38. 5agj (F: 1) - Crystal Structure of the Leurs Editing Domain of Candida Albicans in Complex with the Adduct AN2690-Amp
  39. 5agz (F: 2) - Disubstituted Bis-Thf Moieties As New P2 Ligands in Non- Peptidal Hiv-1 Protease Inhibitors (II)
    Other atoms: Cl (3);
  40. 5ah8 (F: 6) - Disubstituted Bis-Thf Moieties As New P2 Ligands in Non-Peptidal Hiv-1 Protease Inhibitors (II)
    Other atoms: Cl (3);
Page generated: Fri May 13 23:05:48 2022

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