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
      2vew
      2vex
      2vey
      2vfz
      2vh0
      2vh6
      2vj7
      2vk7
      2vkq
      2vnm
      2vnn
      2vp6
      2vpp
      2vqj
      2vqo
      2vqq
      2vr1
      2vs2
      2vtd
      2vtn
      2vto
      2vtp
      2vtq
      2vtt
      2vui
      2vvc
      2vvt
      2vvu
      2vvv
      2vwl
      2vwm
      2vwn
      2vwo
      2vz2
      2w0w
      2w17
      2w1c
      2w3i
      2w3k
      2w4o
      2w5u
      2wap
      2wb4
      2wbk
      2weg
      2weo
      2wf0
      2wf5
      2wf6
      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
    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 20 (951-1000), PDB files 2vew - 2wf7






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 951-1000 (2vew - 2wf7):
  1. 2vew - Crystal Strucutre of Protein Tyrosine Phosphatase 1B in Complex With An Isothiazolidinone-Containing Inhibitor
  2. 2vex - Crystal Strucutre of Protein Tyrosine Phosphatase 1B in Complex With An Isothiazolidinone-Containing Inhibitor
  3. 2vey - Crystal Strucutre of Protein Tyrosine Phosphatase 1B in Complex With An Isothiazolidinone-Containing Inhibitor
  4. 2vfz - Crystal Structure of Alpha-1,3 Galactosyltransferase (R365K) in Complex With Udp-2F-Galactose
  5. 2vh0 - Structure and Property Based Design of Factor Xa Inhibitors: Biaryl Pyrrolidin-2-Ones Incorporating Basic Heterocyclic Motifs
  6. 2vh6 - Structure and Property Based Design of Factor Xa Inhibitors: Pyrrolidin-2-Ones With Biaryl P4 Motifs
  7. 2vj7 - Human Bace-1 in Complex With 3-(Ethylamino)-N-((1S,2R)-2- Hydroxy-1-(Phenylmethyl)-3-(((3-(Trifluoromethyl)Phenyl) Methyl)Amino)Propyl)-5-(2-Oxo-1-Pyrrolidinyl)Benzamide
  8. 2vk7 - The Structure of Clostridium Perfringens Nani Sialidase and Its Catalytic Intermediates
  9. 2vkq - Crystal Structure of Human Cytosolic 5'-Nucleotidase III ( Cn-III, NT5C3) in Complex With Beryllium Trifluoride
  10. 2vnm - Human Bace-1 in Complex With 3-(1,1-Dioxidotetrahydro-2H-1, 2-Thiazin-2-Yl)-5-(Ethylamino)-N-((1S,2R)-2-Hydroxy-1-( Phenylmethyl)-3-(((3-(Trifluoromethyl)Phenyl)Methyl)Amino) Propyl)Benzamide
  11. 2vnn - Human Bace-1 in Complex With 7-Ethyl-N-((1S,2R)-2-Hydroxy-1- (Phenylmethyl)-3-(((3-(Trifluoromethyl)Phenyl)Methyl)Amino) Propyl)-1-Methyl-3,4-Dihydro-1H-(1,2,5)Thiadiazepino(3,4,5- Hi)Indole-9-Carboxamide 2,2-Dioxide
  12. 2vp6 - Structural Studies of Nucleoside Analog and Feedback Inhibitor Binding to Drosophila Melanogaster Multisubstrate Deoxyribonucleoside Kinase
  13. 2vpp - Drosophila Melanogaster Deoxyribonucleoside Kinase Successfully Activates Gemcitabine in Transduced Cancer Cell Lines
  14. 2vqj - Structure of HDAC4 Catalytic Domain Bound to A Trifluoromethylketone Inhbitor
  15. 2vqo - Structure Of HDAC4 Catalytic Domain With A Gain-of-Function Muation Bound to A Trifluoromethylketone Inhbitor
  16. 2vqq - Structure of HDAC4 Catalytic Domain (A Double Cysteine-To- Alanine Mutant) Bound to A Trifluoromethylketone Inhbitor
  17. 2vr1 - Crystal Structure of Biotin Carboxylase From E. Coli in Complex With Atp Analog, ADPCF2P.
  18. 2vs2 - Neutron Diffraction Structure of Endothiapepsin in Complex With A Gem- Diol Inhibitor.
  19. 2vtd - Crystal Structure of Murd Ligase in Complex With D-Glu Containing Sulfonamide Inhibitor
  20. 2vtn - Identification of N-(4-Piperidinyl)-4-(2,6- Dichlorobenzoylamino)-1H-Pyrazole-3-Carboxamide (AT7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment- Based X-Ray Crystallography and Structure Based Drug Design.
  21. 2vto - Identification of N-(4-Piperidinyl)-4-(2,6- Dichlorobenzoylamino)-1H-Pyrazole-3-Carboxamide (AT7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment- Based X-Ray Crystallography and Structure Based Drug Design.
  22. 2vtp - Identification of N-(4-Piperidinyl)-4-(2,6- Dichlorobenzoylamino)-1H-Pyrazole-3-Carboxamide (AT7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment- Based X-Ray Crystallography and Structure Based Drug Design.
  23. 2vtq - Identification of N-(4-Piperidinyl)-4-(2,6- Dichlorobenzoylamino)-1H-Pyrazole-3-Carboxamide (AT7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment- Based X-Ray Crystallography and Structure Based Drug Design.
  24. 2vtt - Identification of N-(4-Piperidinyl)-4-(2,6- Dichlorobenzoylamino)-1H-Pyrazole-3-Carboxamide (AT7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment- Based X-Ray Crystallography and Structure Based Drug Design.
  25. 2vui - Crystal Structure of the Hupr Receiver Domain in Inhibitory Phospho-State
  26. 2vvc - Aminopyrrolidine Factor Xa Inhibitor
  27. 2vvt - Glutamate Racemase (Muri) From E. Faecalis in Complex With A 9-Benzyl Purine Inhibitor
  28. 2vvu - Aminopyrrolidine Factor Xa Inhibitor
  29. 2vvv - Aminopyrrolidine-Related Triazole Factor Xa Inhibitor
  30. 2vwl - Aminopyrrolidine Factor Xa Inhibitor
  31. 2vwm - Aminopyrrolidine Factor Xa Inhibitor
  32. 2vwn - Aminopyrrolidine Factor Xa Inhibitor
  33. 2vwo - Aminopyrrolidine Factor Xa Inhibitor
  34. 2vz2 - Human Mao B in Complex With Mofegiline
  35. 2w0w - Crystal Structure of Glmu From Haemophilus Influenzae in Complex With Quinazoline Inhibitor 2
  36. 2w17 - CDK2 in Complex With the Imidazole Pyrimidine Amide, Compound (S)-8B
  37. 2w1c - Structure Determination of Aurora Kinase in Complex With Inhibitor
  38. 2w3i - Crystal Structure of Fxa in Complex With 4,4-Disubstituted Pyrrolidine-1,2-Dicarboxamide Inhibitor 2
  39. 2w3k - Crystal Structure of Fxa in Complex With 4,4-Disubstituted Pyrrolidine-1,2-Dicarboxamide Inhibitor 1
  40. 2w4o - Crystal Structure of Human CAMK4 in Complex With 4-Amino( Sulfamoyl-Phenylamino)-Triazole-Carbothioic Acid (2,6- Difluoro-Phenyl)-Amide)
  41. 2w5u - Flavodoxin From Helicobacter Pylori in Complex With the C3 Inhibitor
  42. 2wap - 3D-Crystal Structure of Humanized-Rat Fatty Acid Amide Hydrolase (Faah) Conjugated With the Drug-Like Urea Inhibitor Pf-3845
  43. 2wb4 - Activated Diguanylate Cyclase Pled in Complex With C-Di-Gmp
  44. 2wbk - Structure Of The Michaelis Complex Of Beta-Mannosidase, MAN2A, Provides Insight Into the Conformational Itinerary of Mannoside Hydrolysis
  45. 2weg - Thermodynamic Optimisation of Carbonic Anhydrase Fragment Inhibitors
  46. 2weo - Thermodynamic Optimisation of Carbonic Anhydrase Fragment Inhibitors
  47. 2wf0 - Human Bace-1 in Complex With 4-Ethyl-N-((1S,2R)-2-Hydroxy-1- (Phenylmethyl)-3-(((3-(Trifluoromethyl)Phenyl)Methyl)Amino) Propyl)-8-(2-Oxo-1-Pyrrolidinyl)-6-Quinolinecarboxamide
  48. 2wf5 - Structure of Beta-Phosphoglucomutase Inhibited With Glucose- 6-Phospahte and Trifluoromagnesate
  49. 2wf6 - Structure of Beta-Phosphoglucomutase Inhibited With Glucose- 6-Phospahte and Aluminium Tetrafluoride
  50. 2wf7 - Structure of Beta-Phosphoglucomutase Inhibited With Glucose- 6-Phosphonate and Aluminium Tetrafluoride


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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