Atomistry » Fluorine » PDB 461d-4azy
Atomistry »
  Fluorine »
    PDB 461d-4azy »
      461d »
      478d »
      4a36 »
      4a3h »
      4a4l »
      4a4o »
      4a4x »
      4a6l »
      4a7c »
      4a7s »
      4a92 »
      4a98 »
      4aaa »
      4a6v »
      4acu »
      4acx »
      4afe »
      4agd »
      4agw »
      4ajm »
      4amw »
      4amx »
      4an2 »
      4an3 »
      4an9 »
      4anj »
      4ans »
      4anq »
      4anb »
      4anw »
      4aoj »
      4ap7 »
      4ark »
      4asd »
      4aw1 »
      4axx »
      4az0 »
      4az3 »
      4at4 »

Fluorine in PDB, part 57 (files: 2241-2280), PDB 461d-4azy

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: 2241-2280 (PDB 461d-4azy).
  1. 461d (F: 2) - A "Hydrat-Ion Spine" in A B-Dna Minor Groove
    Other atoms: Rb (1); Mg (2);
  2. 478d (F: 2) - Crystal Structure of the B-Dna Dodecamer 5'-D(Cgcgaa(Taf) Tcgcg), Where Taf Is 2'-Deoxy-2'-Fluoro-Arabino-Furanosyl Thymine
    Other atoms: Ca (3);
  3. 4a36 (F: 6) - Structure of Duck Rig-I Helicase Domain Bound to 19-Mer Dsrna and Atp Transition State Analogue
    Other atoms: Mg (2); Al (2);
  4. 4a3h (F: 1) - 2',4' Dinitrophenyl-2-Deoxy-2-Fluro-B-D-Cellobioside Complex of the Endoglucanase CEL5A From Bacillus Agaradhaerens at 1.6 A Resolution
  5. 4a4l (F: 3) - Crystal Structure of Polo-Like Kinase 1 in Complex with A 5-(2-Amino-Pyrimidin-4-Yl)-1H-Pyrrole Inhibitor
    Other atoms: Zn (1);
  6. 4a4o (F: 3) - Crystal Structure of Polo-Like Kinase 1 in Complex with A 2- (2-Amino-Pyrimidin-4-Yl)-1,5,6,7-Tetrahydro-Pyrrolopyridin- 4-One Inhibitor
    Other atoms: Zn (1);
  7. 4a4x (F: 3) - NEK2-Ede Bound to CCT248662
  8. 4a6l (F: 4) - Beta-Tryptase Inhibitor
  9. 4a6v (F: 6) - X-Ray Structures of Oxazole Hydroxamate Ecmetap-Mn Complexes
    Other atoms: Mn (4);
  10. 4a7c (F: 3) - Crystal Structure of PIM1 Kinase with ETP46546
  11. 4a7s (F: 2) - Structure of Human I113T SOD1 Mutant Complexed with 5- Fluorouridine in the P21 Space Group
    Other atoms: Cu (4); Zn (2);
  12. 4a92 (F: 4) - Full-Length Hcv NS3-4A Protease-Helicase in Complex with A Macrocyclic Protease Inhibitor.
    Other atoms: Zn (2);
  13. 4a98 (F: 10) - X-Ray Structure of A Pentameric Ligand Gated Ion Channel From Erwinia Chrysanthemi (Elic) in Complex with Bromoflurazepam
    Other atoms: Br (10);
  14. 4aaa (F: 2) - Crystal Structure of the Human CDKL2 Kinase Domain
  15. 4acu (F: 3) - Aminoimidazoles As Bace-1 Inhibitors. X-Ray Crystal Structure of Beta Secretase Complexed with Compound 14
  16. 4acx (F: 4) - Aminoimidazoles As Bace-1 Inhibitors. X-Ray Crystal Structure of Beta Secretase Complexed with Compound 23
  17. 4afe (F: 3) - NEK2 Bound to Hybrid Compound 21
  18. 4agd (F: 1) - Crystal Structure of VEGFR2 (Juxtamembrane and Kinase Domains) in Complex with Sunitinib (SU11248) (N-2- Diethylaminoethyl)-5-((Z)-(5-Fluoro-2-Oxo-1H-Indol-3- Ylidene)Methyl)-2,4-Dimethyl-1H-Pyrrole-3-Carboxamide)
  19. 4agw (F: 6) - Discovery of A Small Molecule Type II Inhibitor of Wild- Type and Gatekeeper Mutants of Bcr-Abl, Pdgfralpha, Kit, and Src Kinases
  20. 4ajm (F: 1) - Development of A Plate-Based Optical Biosensor Methodology to Identify PDE10 Fragment Inhibitors
    Other atoms: Mg (2); Zn (2);
  21. 4amw (F: 4) - Crystal Structure of the Gracilariopsis Lemaneiformis Alpha- 1,4-Glucan Lyase Covalent Intermediate Complex with 5- Fluoro-Idosyl-Fluoride
  22. 4amx (F: 4) - Crystal Structure of the Gracilariopsis Lemaneiformis Alpha-1,4-Glucan Lyase Covalent Intermediate Complex with 5-Fluoro-Glucosyl-Fluoride
  23. 4an2 (F: 3) - Crystal Structures of Human MEK1 with Carboxamide-Based Allosteric Inhibitor XL518 (Gdc-0973), or Related Analogs.
    Other atoms: Mg (1); I (1);
  24. 4an3 (F: 3) - Crystal Structures of Human MEK1 with Carboxamide-Based Allosteric Inhibitor XL518 (Gdc-0973), or Related Analogs.
    Other atoms: Mg (1); I (1);
  25. 4an9 (F: 3) - Crystal Structures of Human MEK1 with Carboxamide-Based Allosteric Inhibitor XL518 (Gdc-0973), or Related Analogs.
    Other atoms: Mg (1); I (1);
  26. 4anb (F: 3) - Crystal Structures of Human MEK1 with Carboxamide-Based Allosteric Inhibitor XL518 (Gdc-0973), or Related Analogs.
    Other atoms: Mg (1); I (1);
  27. 4anj (F: 4) - Myosin VI (MDINSERT2-Gfp Fusion) Pre-Powerstroke State (Mg.Adp.ALF4)
    Other atoms: Mg (1); Al (1); Ca (3);
  28. 4anq (F: 1) - Structure of G1269A Mutant Anaplastic Lymphoma Kinase in Complex with Crizotinib
    Other atoms: Cl (2);
  29. 4ans (F: 1) - Structure of L1196M,G1269A Double Mutant Anaplastic Lymphoma Kinase in Complex with Crizotinib
    Other atoms: Cl (2);
  30. 4anw (F: 4) - Complexes of PI3KGAMMA with Isoform Selective Inhibitors.
    Other atoms: Cl (2);
  31. 4aoj (F: 3) - Human Trka in Complex with the Inhibitor Az-23
    Other atoms: Cl (3); Zn (6);
  32. 4ap7 (F: 1) - Crystal Structure of C-Met Kinase Domain in Complex with 4-( (6-(4- Fluorophenyl)-(1,2,4)Triazolo(4,3-B)(1,2,4)Triazin-3-Yl)Methyl) Phenol
  33. 4ark (F: 2) - Crystal Structure of the Catalytic Domain of Human Map Kinase Kinase 1 (MEK1) in Complex with A Small Molecule Inhibitor and Adp
    Other atoms: Mg (1); I (1);
  34. 4asd (F: 3) - Crystal Structure of VEGFR2 (Juxtamembrane and Kinase Domains) in Complex with Sorafenib (Bay 43-9006)
    Other atoms: Cl (1);
  35. 4at4 (F: 4) - Crystal Structure of Trkb Kinase Domain in Complex with EX429
  36. 4aw1 (F: 3) - Human PDK1 Kinase Domain in Complex with Allosteric Compound PS210 Bound to the Pif-Pocket
    Other atoms: Mn (1); Cl (3); Na (2);
  37. 4axx (F: 3) - The Catalytically Active Fully Closed Conformation of Human Phosphoglycerate Kinase in Complex with Adp 3-Phosphoglycerate and Beryllium Trifluoride
    Other atoms: Mg (1); Cl (1);
  38. 4az0 (F: 1) - Crystal Structure of Cathepsin A, Complexed with 8A.
    Other atoms: Cd (6);
  39. 4az3 (F: 2) - Crystal Structure of Cathepsin A, Complexed with 15A
    Other atoms: Cd (4);
  40. 4azy (F: 5) - Design and Synthesis of BACE1 Inhibitors with in Vivo Brain Reduction of Beta-Amyloid Peptides (Compound 10)
    Other atoms: Na (1);
Page generated: Fri May 13 22:57:07 2022

Last articles

Zn in 7VD8
Zn in 7V1R
Zn in 7V1Q
Zn in 7VPF
Zn in 7T85
Zn in 7T5F
Zn in 7NF9
Zn in 7M4M
Zn in 7M4O
Zn in 7M4N
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy