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Fluorine in PDB, part 138 (files: 5481-5520), PDB 6ew7-6fo6

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: 5481-5520 (PDB 6ew7-6fo6).
  1. 6ew7 (F: 2) - Crystal Structure of the BCL6 Btb Domain in Complex with Anilinopyrimidine Ligand
    Other atoms: Cl (6);
  2. 6ex8 (F: 6) - Crystal Structure of Rhodesain in Complex with A Macrolactam Inhibitor
    Other atoms: Cl (2);
  3. 6ey7 (F: 4) - Human Cytomegalovirus Terminase Nuclease Domain, Mn Soaked, Inhibitor Bound
    Other atoms: Mn (10); Cl (1);
  4. 6eyj (F: 6) - E-Selectin Lectin, Egf-Like and Two Scr Domains Complexed with Glycomimetic Ligand NV354
    Other atoms: Ca (2);
  5. 6eyk (F: 3) - E-Selectin Lectin, Egf-Like and Two Scr Domains Complexed with Glycomimetic Ligand NV355
    Other atoms: Ca (2);
  6. 6f0e (F: 1) - Structure of Yeast SEC14P with A Picolinamide Compound
    Other atoms: Br (1);
  7. 6f1w (F: 2) - Crystal Structure of Human Casein Kinase I Delta in Complex with Compound 31A
  8. 6f26 (F: 2) - Crystal Structure of Human Casein Kinase I Delta in Complex with Compound 31B
  9. 6f2u (F: 6) - Potent and Selective Aldo-Keto Reductase 1C3 (AKR1C3) Inhibitors Based on the Benzoisoxazole Moiety: Application of A Bioisosteric Scaffold Hopping Approach to Flufenamic Acid
  10. 6f4z (F: 10) - 2'F-Arag Modified Quadruplex with Flipped G-Tract and Central Tetrad
  11. 6f6i (F: 1) - Crystal Structure of Ebolavirus Glycoprotein in Complex with Paroxetine
  12. 6f78 (F: 12) - Potent and Selective Aldo-Keto Reductase 1C3 (AKR1C3) Inhibitors Based on the Benzoisoxazole Moiety: Application of A Bioisosteric Scaffold Hopping Approach to Flufenamic Acid
    Other atoms: Cl (2);
  13. 6f7b (F: 2) - Crystal Structure of the Human BUB1 Kinase Domain in Complex with Bay 1816032
    Other atoms: Mg (1);
  14. 6f8u (F: 6) - Crystal Structure of the PDE4D Catalytic Domain in Complex with Gebr- 20B
    Other atoms: Mg (5); Zn (2);
  15. 6f9l (F: 1) - Crystal Structure of Barley Beta-Amylase Complexed with 3-Deoxy-3- Fluoro-Maltose
    Other atoms: Cl (1);
  16. 6fc8 (F: 2) - CHK1 Kinase in Complex with Compound 13
  17. 6fdc (F: 4) - Crystal Structure of the PDE4D Catalytic Domain in Complex with Gebr- 32A
    Other atoms: Mg (5); Zn (2);
  18. 6fe0 (F: 12) - Three Dimensional Structure of Human Carbonic Anhydrase IX in Complex with Benzenesulfonamide.
    Other atoms: Zn (4);
  19. 6fe1 (F: 12) - Three Dimensional Structure of Human Carbonic Anhydrase IX in Complex with Benzenesulfonamide.
    Other atoms: Zn (4);
  20. 6fe3 (F: 4) - Crystal Structure of T. Brucei Pde-B1 Catalytic Domain with Inhibitor Npd-1439
    Other atoms: Mg (2); Zn (2);
  21. 6fer (F: 60) - Crystal Structure of Human DDR2 Kinase in Complex with 2-[4,5- Difluoro-2-Oxo-1'-(1H-Pyrazolo[3,4-B]Pyridine-5-Carbonyl) Spiro[Indole-3,4'-Piperidine]-1-Yl]-N-(2,2,2-Trifluoroethyl)Acetamide
  22. 6fet (F: 16) - Crystal Structure of Human Phosphodiesterase 4D2 Catalytic Domain with Inhibitor Npd-1439
    Other atoms: Ni (2); Mg (4); Zn (4);
  23. 6fex (F: 3) - DDR1, 2-[4-Bromo-2-Oxo-1'-(1H-Pyrazolo[4,3-B]Pyridine-5-Carbonyl) Spiro[Indole-3,4'-Piperidine]-1-Yl]-N-(2,2,2-Trifluoroethyl) Acetamide, 1.291A, P212121, Rfree=17.4%
    Other atoms: Br (1); I (4); Cl (4);
  24. 6ffb (F: 1) - 17BETA-Hydroxysteroid Dehydrogenase 14 Variant S205 - Mutant Q148A - in Complex with A Nonsteroidal Inhibitor
    Other atoms: Na (1);
  25. 6ffn (F: 1) - Structure-Based Design and Synthesis of Macrocyclic Human Rhinovirus 3C Protease Inhibitors
  26. 6ffs (F: 2) - Structure-Based Design and Synthesis of Macrocyclic Human Rhinovirus 3C Protease Inhibitors
  27. 6fgf (F: 1) - Crystal Structure of BAZ2A Bromodomain in Complex with 1- Methylpyridinone Compound 2
  28. 6fh7 (F: 1) - Crystal Structure of BAZ2B Bromodomain in Complex with 1- Methylpyridinone Compound 2
  29. 6fio (F: 3) - DDR1, 2-[1'-(1H-Indazole-5-Carbonyl)-4-Methyl-2-Oxospiro[Indole-3,4'- Piperidine]-1-Yl]-N-(2,2,2-Trifluoroethyl)Acetamide, 1.990A, P6522, Rfree=27.7%
  30. 6fiq (F: 3) - DDR1, 1-(1H-Indazole-5-Carbonyl)-5'-Methoxy-1'-[2-Oxo-2-[(2S)-2- (Trifluoromethyl)Pyrrolidin-1-Yl]Ethyl]Spiro[Piperidine-4,3'- Pyrrolo[3,2-B]Pyridine]-2'-One, 1.790A, P212121, Rfree=23.8%
    Other atoms: Cl (1);
  31. 6fmd (F: 4) - Targeting Myeloid Differentiation Using Potent Human Dihydroorotate Dehydrogenase (Hdhodh) Inhibitors Based on 2-Hydroxypyrazolo[1,5- A]Pyridine Scaffold
    Other atoms: Cl (2);
  32. 6fmf (F: 3) - Neuropilin-1 B1 Domain in Complex with EG01377; 2.8 Angstrom Structure
  33. 6fn1 (F: 4) - Zosuquidar and UIC2 Fab Complex of Human-Mouse Chimeric ABCB1 (ABCB1HM)
  34. 6fne (F: 3) - Structure of BRAG2
  35. 6fnf (F: 3) - Crystal Structure of Ephrin A2 (EPHA2) Receptor Protein Kinase with Nvp-BHG712
  36. 6fng (F: 3) - Crystal Structure of Ephrin A2 (EPHA2) Receptor Protein Kinase with An Isomer of Nvp-BHG712
  37. 6fni (F: 3) - Crystal Structure of Ephrin B4 (EPHB4) Receptor Protein Kinase with Nvp-BHG712
  38. 6fnj (F: 6) - Crystal Structure of Ephrin B4 (EPHB4) Receptor Protein Kinase with An Isomer of Nvp-BHG712
  39. 6fo0 (F: 6) - Cryoem Structure of Bovine Cytochrome BC1 in Complex with the Anti- Malarial Compound GSK932121
    Other atoms: Fe (6); Cl (2);
  40. 6fo6 (F: 6) - Cryoem Structure of Bovine Cytochrome BC1 in Complex with the Anti- Malarial Inhibitor SCR0911
    Other atoms: Fe (6);
Page generated: Fri May 13 23:19:05 2022

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