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Fluorine in PDB, part 87 (files: 3441-3480), PDB 4ymq-4zg9

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: 3441-3480 (PDB 4ymq-4zg9).
  1. 4ymq (F: 6) - X-Ray Co-Structure of Nuclear Receptor Ror-Gammat + SRC2 Peptide with A Benzothiadiazole Dioxide Inverse Agonist
    Other atoms: Na (1);
  2. 4yn4 (F: 1) - Structure of Human Dna Polymerase Beta Complexed with N7BG in the Template Opposite to Incoming Non-Hydrolyzable Dttp with Manganese in the Active Site
    Other atoms: Mn (2); Na (2);
  3. 4yne (F: 1) - (R)-2-Phenylpyrrolidine Substitute Imidazopyridazines: A New Class of Potent and Selective Pan-Trk Inhibitors
  4. 4yp8 (F: 4) - IRAK4-Inhibitor Co-Structure
  5. 4ypq (F: 3) - Crystal Structure of the Ror(Gamma)T Ligand Binding Domain in Complex with 4-(1-(2-Chloro-6-(Trifluoromethyl)Benzoyl)-1H-Indazol-3-Yl) Benzoic Acid
    Other atoms: Mg (1); Cl (1);
  6. 4yps (F: 1) - (R)-2-Phenylpyrrolidine Substitute Imidazopyridazines: A New Class of Potent and Selective Pan-Trk Inhibitors
  7. 4ys1 (F: 1) - Human Aldose Reductase Complexed with A Ligand with An Idd Structure (2) at 1.07 A.
  8. 4ysx (F: 6) - Crystal Structure of Mitochondrial Rhodoquinol-Fumarate Reductase From Ascaris Suum with the Specific Inhibitor NN23
    Other atoms: Fe (20);
  9. 4ysy (F: 6) - Crystal Structure of Mitochondrial Rhodoquinol-Fumarate Reductase From Ascaris Suum with N-[(2,4-Dichlorophenyl)Methyl]-2-(Trifluoromethyl) Benzamide
    Other atoms: Fe (20); Cl (4);
  10. 4yt6 (F: 1) - Factor Viia in Complex with the Inhibitor 4-{[(R)-[5-Ethoxy-2-Fluoro- 3-(Propan-2-Yloxy)Phenyl](4-Phenyl-1H-Imidazol-2-Yl) Methyl]Amino}Benzenecarboximidamide
    Other atoms: Ca (1);
  11. 4yt7 (F: 1) - Factor Viia in Complex with the Inhibitor 2-(2-{(R)-[(4- Carbamimidoylphenyl)Amino][5-Ethoxy-2-Fluoro-3-(Propan-2-Yloxy) Phenyl]Methyl}-1H-Imidazol-4-Yl)Benzamide
    Other atoms: Ca (1);
  12. 4ytf (F: 4) - Discovery of Vx-509 (Decernotinib): A Potent and Selective Janus Kinase (Jak) 3 Inhibitor For the Treatment of Autoimmune Diseases
    Other atoms: Cl (1);
  13. 4yth (F: 4) - Discovery of Vx-509 (Decernotinib): A Potent and Selective Janus Kinase (Jak) 3 Inhibitor For the Treatment of Autoimmune Diseases
    Other atoms: Cl (1);
  14. 4yti (F: 3) - Discovery of Vx-509 (Decernotinib): A Potent and Selective Janus Kinase (Jak) 3 Inhibitor For the Treatment of Autoimmune Disease
  15. 4ytm (F: 6) - Crystal Structure of Mitochondrial Rhodoquinol-Fumarate Reductase From Ascaris Suum with N-Biphenyl-3-Yl-2-(Trifluoromethyl)Benzamide
    Other atoms: Fe (20);
  16. 4ytn (F: 16) - Crystal Structure of Mitochondrial Rhodoquinol-Fumarate Reductase From Ascaris Suum with N-[3-(Pentafluorophenoxy)Phenyl]-2- (Trifluoromethyl)Benzamide
    Other atoms: Fe (20);
  17. 4ytp (F: 3) - Crystal Structure of Porcine Heart Mitochondrial Complex II Bound with N-[(4-Tert-Butylphenyl)Methyl]-2-(Trifluoromethyl)Benzamide
    Other atoms: Fe (10);
  18. 4yur (F: 2) - Crystal Structure of PLK4 Kinase Domain Bound to Centrinone
  19. 4yvc (F: 2) - Rock 1 Bound to Thiazole Inhibitor
  20. 4yxd (F: 3) - Crystal Structure of Porcine Heart Mitochondrial Complex II Bound with Flutolanil
    Other atoms: Fe (10);
  21. 4yyl (F: 3) - Phenolic Acid Derivative Bound to Influenza Strain H1N1 Polymerase Subunit Pa Endonuclease
    Other atoms: Mn (2);
  22. 4yzn (F: 4) - Humanized ROCO4 Bound to Compound 19
  23. 4z2c (F: 2) - Quinolone(Moxifloxacin)-Dna Cleavage Complex of Gyrase From S. Pneumoniae
    Other atoms: Mg (2);
  24. 4z2d (F: 2) - Quinolone(Levofloxacin)-Dna Cleavage Complex of Gyrase From S. Pneumoniae
    Other atoms: Mg (2);
  25. 4z2e (F: 6) - Quinolone(Trovafloxacin)-Dna Cleavage Complex of Gyrase From S. Pneumoniae
    Other atoms: Mg (2);
  26. 4z3o (F: 2) - Quinolone(Moxifloxacin)-Dna Cleavage Complex of Topoisomerase IV From S. Pneumoniae
    Other atoms: Mg (4);
  27. 4z4q (F: 2) - Quinazolinedione(Pd 0305970)-Dna Cleavage Complex of Topoisomerase IV From S. Pneumoniae
    Other atoms: Mg (4);
  28. 4z53 (F: 6) - Quinolone(Trovafloxacin)-Dna Cleavage Complex of Topoisomerase IV From S. Pneumoniae
    Other atoms: Mg (4);
  29. 4z7m (F: 4) - Novel Inhibitors of Bacterial Methionine Aminopeptidase with Broad- Spectrum Biochemical Activity
    Other atoms: Mn (2);
  30. 4z90 (F: 20) - Elic Bound with the Anesthetic Isoflurane in the Resting State
    Other atoms: Cl (4);
  31. 4z91 (F: 20) - Elic Cocrystallized with Isofluorane in A Desensitized State
    Other atoms: Br (20); Cl (4);
  32. 4za8 (F: 5) - Crystal Structure of A Niger FDC1 in Complex with Penta-Fluorocinnamic Acid
    Other atoms: K (2); Mn (1);
  33. 4zab (F: 1) - Structure of A. Niger FDC1 in Complex with Alpha-Fluoro Cinnamic Acid
    Other atoms: K (2); Mn (1);
  34. 4zdz (F: 2) - Saccharomyces Cerevisiae CYP51 (Lanosterol 14-Alpha Demethylase) Y140F Mutant Complexed with Fluconazole
    Other atoms: Fe (1);
  35. 4ze0 (F: 3) - Saccharomyces Cerevisiae CYP51 (Lanosterol 14-Alpha Demethylase) Y140F Mutant Complexed with Voriconazole
    Other atoms: Fe (1);
  36. 4ze1 (F: 2) - Saccharomyces Cerevisiae CYP51 Y140F Mutant Complexed with Posaconazole in the Active Site
    Other atoms: Fe (1);
  37. 4ze3 (F: 2) - Saccharomyces Cerevisiae CYP51 (Lanosterol 14-Alpha Demethylase) Y140H Mutant Complexed with Fluconazole
    Other atoms: Fe (1);
  38. 4zg6 (F: 2) - Structural Basis For Inhibition of Human Autotaxin By Four Novel Compounds
    Other atoms: Zn (4); Ca (2); Cl (2); Na (4);
  39. 4zg7 (F: 2) - Structural Basis For Inhibition of Human Autotaxin By Four Novel Compounds
    Other atoms: Zn (2); Ca (1); Cl (2); Na (2);
  40. 4zg9 (F: 4) - Structural Basis For Inhibition of Human Autotaxin By Four Novel Compounds
    Other atoms: Zn (4); Ca (2); Na (4);
Page generated: Fri May 13 23:05:15 2022

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