Chemical elements
  Fluorine
    Isotopes
    Energy
    Production
    Application
    PDB 16pk-1c8m
    PDB 1c9d-1eau
    PDB 1ec0-1grn
    PDB 1gs4-1j97
    PDB 1jdj-1mu8
    PDB 1mue-1oyt
    PDB 1oz1-1rby
    PDB 1rbz-1tu6
    PDB 1tuy-1w9i
    PDB 1w9j-1yw2
    PDB 1yw9-2ax8
    PDB 2ax9-2dqt
    PDB 2dqu-2ftk
    PDB 2fvd-2hhn
    PDB 2hiw-2izs
    PDB 2j51-2onh
    PDB 2oo8-2pow
    PDB 2pq9-2qzl
    PDB 2qzo-2vev
    PDB 2vew-2wf7
    PDB 2wf8-2xhd
    PDB 2xkk-3ar9
    PDB 3az8-3cej
    PDB 3cem-3dh3
    PDB 3dhf-3el7
    PDB 3el8-3fln
    PDB 3flq-3gc7
    PDB 3gc8-3h7w
    PDB 3h82-3i81
    PDB 3i8d-3jx1
    PDB 3jx2-3ktk
    PDB 3ktu-3lj6
      3ktu
      3kuw
      3kv8
      3kvi
      3kvr
      3kvv
      3kvx
      3kvz
      3kw1
      3kw9
      3kwb
      3kwf
      3kwj
      3kwn
      3kwz
      3kxo
      3l08
      3l0e
      3l1b
      3l2u
      3l2v
      3l2w
      3l3m
      3l4d
      3l58
      3l70
      3l79
      3l7a
      3l7b
      3l7c
      3l7d
      3l8s
      3l8v
      3l9h
      3l9l
      3la3
      3lak
      3lb4
      3lbl
      3lbo
      3ld5
      3len
      3lep
      3lfq
      3lgp
      3lhg
      3lhj
      3lj1
      3lj2
      3lj6
    PDB 3lk9-3mqf
    PDB 3ms4-3nz7
    PDB 3o1g-3p4a
    PDB 3p4b-3ti1
    PDB 3tik-4acx
    PDB 4afe-4fk3
    PDB 4fod-7gch

Fluorine in PDB, part 32 (1551-1600), PDB files 3ktu - 3lj6






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 1551-1600 (3ktu - 3lj6):
  1. 3ktu - Structure of Human 8-Oxoguanine Glycosylase 1 Bound to Fluorninated Oxog-Containing Dna
  2. 3kuw - Structural Basis Of The Activity Ans Substrate Specificity of the Fluoroacetyl-Coa Thioesterase Flk - T42S Mutant in Complex With Fluoro-Acetate
  3. 3kv8 - Structural Basis Of The Activity and Substrate Specificity of the Fluoroacetyl-Coa Thioesterase Flk - Wild Type Flk in Complex With Fluoro-Acetate
  4. 3kvi - Structural Basis Of The Activity and Substrate Specificity of the Fluoroacetyl-Coa Thioesterase Flk - T42A Mutant in Complex With Fluoro-Acetate
  5. 3kvr - Trapping of An Oxocarbenium Ion Intermediate in Up Crystals
  6. 3kvv - Trapping of An Oxocarbenium Ion Intermediate in Up Crystals
  7. 3kvx - JNK3 Bound to Aminopyrimidine Inhibitor, Sr-3562
  8. 3kvz - Structural Basis Of The Activity and Substrate Specificity of the Fluoroacetyl-Coa Thiesterase Flk - Wild Type Flk in Complex With Faccpan
  9. 3kw1 - Structural Basis Of The Activity and Substrate Specificity of the Fluoroacetyl-Coa Flk - Wild Type Flk in Complex With Facopan
  10. 3kw9 - X-Ray Structure of Cathepsin K Covalently Bound to A Triazine Ligand
  11. 3kwb - Structure of Catk Covalently Bound to A Dioxo-Triazine Inhibitor
  12. 3kwf - Human Dpp-IV With Carmegliptin (S)-1-((2S,3S,11BS)-2-Amino- 9,10-Dimethoxy-1,3,4,6,7,11B-Hexahydro-2H-Pyrido[2,1- A]Isoquinolin-3-Yl)-4-Fluoromethyl-Pyrrolidin-2-One
  13. 3kwj - Strucutre of Human Dpp-IV With (2S,3S,11BS)-3-(3-Fluoromethyl-Phenyl)- 9,10-Dimethoxy-1,3,4,6,7,11B-Hexahydro-2H-Pyrido[2,1-A]Isoquinolin-2- Ylamine
  14. 3kwn - Cathepsin S in Complex With Thioether Acetamide P3 Inhibitor
  15. 3kwz - Cathepsin K in Complex With A Non-Selective 2-Cyano- Pyrimidine Inhibitor
  16. 3kxo - An Orally Active Inhibitor Bound At the Active Site of Hpgds
  17. 3l08 - Structure of PI3K Gamma With A Potent Inhibitor: GSK2126458
  18. 3l0e - X-Ray Crystal Structure of A Potent Liver X Receptor Modulator
  19. 3l1b - Complex Structure of Fxr Ligand-Binding Domain With A Tetrahydroazepinoindole Compound
  20. 3l2u - Crystal Structure of the Prototype Foamy Virus (Pfv) Intasome in Complex With Magnesium and GS9137 (Elvitegravir)
  21. 3l2v - Crystal Structure of the Prototype Foamy Virus (Pfv) Intasome in Complex With Manganese and MK0518 (Raltegravir)
  22. 3l2w - Crystal Structure of the Prototype Foamy Virus (Pfv) Intasome in Complex With Manganese and GS9137 (Elvitegravir)
  23. 3l3m - Parp Complexed With A927929
  24. 3l4d - Crystal Structure of Sterol 14-Alpha Demethylase (CYP51) From Leishmania Infantum in Complex With Fluconazole
  25. 3l58 - Structure of Bace Bound to SCH589432
  26. 3l70 - Cytochrome BC1 Complex From Chicken With Trifloxystrobin Bound
  27. 3l79 - Crystal Structure of Glycogen Phosphorylase DK1 Complex
  28. 3l7a - Crystal Structure of Glycogen Phosphorylase DK2 Complex
  29. 3l7b - Crystal Structure of Glycogen Phosphorylase DK3 Complex
  30. 3l7c - Crystal Structure of Glycogen Phosphorylase DK4 Complex
  31. 3l7d - Crystal Structure of Glycogen Phosphorylase DK5 Complex
  32. 3l8s - Human P38 Map Kinase in Complex With Cp-547632
  33. 3l8v - Crystal Structure Of The Tyrosine Kinase Domain of the Hepatocyte Growth Factor Receptor C-Met in Complex With A Biarylamine Based Inhibitor
  34. 3l9h - X-Ray Structure of Mitotic Kinesin-5 (Ksp, KIF11, EG5)in Complex With the Hexahydro-2H-Pyrano[3,2-C]Quinoline Emd 534085
  35. 3l9l - Crystal Structure of Pka With Compound 36
  36. 3la3 - Crystal Structure of Ntca in Complex With 2,2-Difluoropentanedioic Acid
  37. 3lak - Crystal Structure of Hiv-1 Reverse Transcriptase in Complex With N1-Heterocycle Pyrimidinedione Non-Nucleoside Inhibitor
  38. 3lb4 - Two-Site Competitive Inhibition in Dehaloperoxidase-Hemoglobin
  39. 3lbl - Structure of Human MDM2 Protein in Complex With Mi-63-Analog
  40. 3lbo - Human Aldose Reductase Mutant T113C Complexed With IDD594
  41. 3ld5 - Human Aldose Reductase Mutant T113S Complexed With IDD594
  42. 3len - Human Aldose Reductase Mutant T113S Complexed With Zopolrestat
  43. 3lep - Human Aldose Reductase Mutant T113C in Complex With IDD388
  44. 3lfq - Crystal Structure of CDK2 With SAR60, An Aminoindazole Type Inhibitor
  45. 3lgp - Crystal Structure Of Catalytic Domain of Tace With Benzimidazolyl- Thienyl-Tartrate Based Inhibitor
  46. 3lhg - BACE1 in Complex With the Aminohydantoin Compound 4G
  47. 3lhj - Crystal Structure of P38A Mitogen-Activated Protein Kinase in Complex With A Pyrazolopyridinone Inhibitor.
  48. 3lj1 - IRE1 Complexed With CDK1/2 Inhibitor III
  49. 3lj2 - IRE1 Complexed With Jak Inhibitor I
  50. 3lj6 - 3D-Crystal Structure of Humanized-Rat Fatty Acid Amide Hydrolase (Faah) Conjugated With the Drug-Like Urea Inhibitor Pf-3845 At 2.42A Resolution


Acknowledgement

We would like to acknowledge that these pictures of PDB structures of Fluorine coordination spheres were produced with valuable advice from our colleagues from http://3dpdb.com.
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