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Fluorine in PDB, part 134 (files: 5321-5360), PDB 6e4w-6el5

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: 5321-5360 (PDB 6e4w-6el5).
  1. 6e4w (F: 2) - Structure of Ampk Bound to Activator
    Other atoms: Cl (3);
  2. 6e54 (F: 2) - Crystal Structure of Lpxc From Pseudomonas Aeruginosa in Complex with Ligand PT802
    Other atoms: Zn (1); Ca (2); Cl (2);
  3. 6e59 (F: 7) - Crystal Structure of the Human NK1 Tachykinin Receptor
  4. 6e5g (F: 6) - Crystal Structure of Human TEAD2-Yap Binding Domain Covalently Bound to An Allosteric Regulator
  5. 6e69 (F: 4) - Ortho-Substituted Phenyl Sulfonyl Fluoride and Fluorosulfate As Potent Elastase Inhibitory Fragments
  6. 6e6j (F: 6) - BRD2_BROMODOMAIN2 Complex with Inhibitor 744
  7. 6e70 (F: 4) - Structure of Wild Type Human Transthyretin in Complex with Diflunisal
    Other atoms: Ca (2);
  8. 6e73 (F: 4) - Structure of Human Transthyretin VAL30MET Mutant in Complex with Diflunisal
  9. 6e78 (F: 4) - Structure of Human Transthyretin ASP38ALA Mutant in Complex with Diflunisal
  10. 6e8q (F: 2) - S. Cerevisiae CYP51 Complexed with Posaconazole
    Other atoms: Fe (1);
  11. 6e9p (F: 12) - Crystal Structure of Tryptophan Synthase From M. Tuberculosis - Open Form with BRD0059 Bound
  12. 6ea1 (F: 7) - X-Ray Crystal Structure of Pf-M1 in Complex with Inhibitor (6DA) and Catalytic Zinc Ion
    Other atoms: Mg (4); Zn (1);
  13. 6ea2 (F: 3) - X-Ray Crystal Structure of Pf-M1 in Complex with Inhibitor (6H) and Catalytic Zinc Ion
    Other atoms: Mg (4); Zn (1);
  14. 6ea4 (F: 6) - ERAP2 Bound to Aryl Sulfonamide Uncompetitive Inhibitor
    Other atoms: Zn (2);
  15. 6eaa (F: 3) - X-Ray Crystal Structure of Pf-M1 in Complex with Inhibitor (6I) and Catalytic Zinc Ion
    Other atoms: Mg (3); Zn (1);
  16. 6eab (F: 3) - X-Ray Crystal Structure of Pf-M1 in Complex with Inhibitor (6J) and Catalytic Zinc Ion
    Other atoms: Mg (4); Zn (1);
  17. 6eb7 (F: 3) - Yycf Homologue (SP1227) Receiver Domain Activated By BEF3
    Other atoms: Mn (1);
  18. 6ebe (F: 3) - Bioreductive 4-Hydroxy-3-Nitro-5-Ureido-Benzenesulfonamides Selectively Target the Tumor-Associated Carbonic Anhydrase Isoforms IX and XII and Show Hypoxia-Enhanced Cytotoxicity Against Human Cancer Cell Lines.
    Other atoms: Zn (1);
  19. 6ebr (F: 3) - Activation of RR02 Bound to BEF3
    Other atoms: Mn (1);
  20. 6ebw (F: 1) - Halk in Complex with Compound 9 (6-(((1S)-1-(5-Fluoropyridin-2-Yl) Ethyl)Amino)-1-(3-Methyl-1H-Pyrazol-5-Yl)-1H-Pyrrolo[2,3-B]Pyridin-3- Yl)(Morpholin-4-Yl)Methanone
  21. 6ecz (F: 5) - Bioreductive 4-Hydroxy-3-Nitro-5-Ureido-Benzenesulfonamides Selectively Target the Tumor-Associated Carbonic Anhydrase Isoforms IX and XII and Show Hypoxia-Enhanced Cytotoxicity Against Human Cancer Cell Lines.
    Other atoms: Zn (1);
  22. 6eda (F: 3) - Bioreductive 4-Hydroxy-3-Nitro-5-Ureido-Benzenesulfonamides Selectively Target the Tumor-Associated Carbonic Anhydrase Isoforms IX and XII and Show Hypoxia-Enhanced Cytotoxicity Against Human Cancer Cell Lines.
    Other atoms: Zn (1);
  23. 6edl (F: 2) - Halk in Complex with Compound 1 (S)-N-(1-(2,4-Difluorophenyl)Ethyl)-3- (3-Methyl-1H-Pyrazol-5-Yl)Imidazo[1,2-B]Pyridazin-6-Amine
  24. 6ee2 (F: 36) - X-Ray Crystal Structure of Pf-M17 in Complex with Inhibitor 6I and Regulatory Zinc Ion
    Other atoms: Zn (12);
  25. 6ee3 (F: 3) - X-Ray Crystal Structure of Pf-M1 in Complex with Inhibitor (6K) and Catalytic Zinc Ion
    Other atoms: Mg (4); Zn (1);
  26. 6ee4 (F: 3) - X-Ray Crystal Structure of Pf-M1 in Complex with Inhibitor (6M) and Catalytic Zinc Ion
    Other atoms: Mg (5); Zn (1);
  27. 6ee6 (F: 3) - X-Ray Crystal Structure of Pf-M1 in Complex with Inhibitor (6O) and Catalytic Zinc Ion
    Other atoms: Mg (3); Zn (1);
  28. 6eea (F: 6) - Bioreductive 4-Hydroxy-3-Nitro-5-Ureido-Benzenesulfonamides Selectively Target the Tumor-Associated Carbonic Anhydrase Isoforms IX and XII and Show Hypoxia-Enhanced Cytotoxicity Against Human Cancer Cell Lines.
    Other atoms: Zn (1);
  29. 6eed (F: 3) - X-Ray Crystal Structure of Pf-M1 in Complex with Inhibitor (6P) and Catalytic Zinc Ion
    Other atoms: Mg (4); Zn (1);
  30. 6eee (F: 36) - X-Ray Crystal Structure of Pf-M17 in Complex with Inhibitor (6K) and Regulatory Zinc Ion
    Other atoms: Zn (12);
  31. 6eeh (F: 15) - Bioreductive 4-Hydroxy-3-Nitro-5-Ureido-Benzenesulfonamides Selectively Target the Tumor-Associated Carbonic Anhydrase Isoforms IX and XII and Show Hypoxia-Enhanced Cytotoxicity Against Human Cancer Cell Lines.
    Other atoms: Zn (1);
  32. 6eeo (F: 1) - Bioreductive 4-Hydroxy-3-Nitro-5-Ureido-Benzenesulfonamides Selectively Target the Tumor-Associated Carbonic Anhydrase Isoforms IX and XII and Show Hypoxia-Enhanced Cytotoxicity Against Human Cancer Cell Lines.
    Other atoms: Zn (1);
  33. 6eg9 (F: 6) - IRAK4 in Complex with Ponatinib
    Other atoms: Co (4);
  34. 6ega (F: 6) - IRAK4 in Complex with A Type II Inhibitor
    Other atoms: Co (6);
  35. 6ehu (F: 18) - The Crystal Structure of CK2ALPHA in Complex with Compound 32
  36. 6ei4 (F: 2) - Crystal Structure of Tyrosinase From Bacillus Megaterium with B5N Inhibitor in the Active Site
    Other atoms: Cu (4);
  37. 6eim (F: 8) - Human STK10 Bound to GW683134A
  38. 6eis (F: 16) - DYRK1A in Complex with Jwc-055
  39. 6ekh (F: 3) - Crystal Structure of Activated Chey From Methanoccocus Maripaludis
    Other atoms: Mg (1);
  40. 6el5 (F: 1) - Estimation of Relative Drug-Target Residence Times By Random Acceleration Molecular Dynamics Simulation
    Other atoms: Cl (1);
Page generated: Tue Dec 1 09:27:12 2020

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