Atomistry » Fluorine » PDB 5msb-5njh
Atomistry »
  Fluorine »
    PDB 5msb-5njh »
      5msb »
      5mt0 »
      5mtx »
      5mty »
      5mu6 »
      5mut »
      5mvc »
      5mvd »
      5mwp »
      5mxv »
      5mxx »
      5my8 »
      5myl »
      5myr »
      5mys »
      5myv »
      5mz3 »
      5n1k »
      5n2f »
      5n33 »
      5n3d »
      5n63 »
      5n69 »
      5n7o »
      5n9s »
      5n9t »
      5nad »
      5nai »
      5nat »
      5nar »
      5naw »
      5nb6 »
      5nba »
      5ncq »
      5nd4 »
      5ndd »
      5nft »
      5n2n »

Fluorine in PDB, part 107 (files: 4241-4280), PDB 5msb-5njh

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: 4241-4280 (PDB 5msb-5njh).
  1. 5msb (F: 20) - Crystal Structure of Human Carbonic Anhydrase Isozyme XII with 2,3,5, 6-Tetrafluoro-4[(2-Hydroxyethyl)Sulfonyl]Benzenesulfonamide
    Other atoms: Zn (4);
  2. 5mt0 (F: 1) - Complement Factor D in Complex with A Reversible Indole Carboxylic Acid Based Inhibitor
  3. 5mtx (F: 1) - Dibenzooxepinone Inhibitor 12B in Complex with P38 Mapk
  4. 5mty (F: 2) - Dibenzosuberone Inhibitor 8E in Complex with P38 Mapk
  5. 5mu6 (F: 4) - Human N-Myristoyltransferase (NMT1) with Myristoyl-Coa and Imp-1088 Inhibitor Bound
    Other atoms: Mg (2);
  6. 5mut (F: 4) - Crystal Structure of Potent Human Dihydroorotate Dehydrogenase Inhibitors Based on Hydroxylated Azole Scaffolds
    Other atoms: Cl (3);
  7. 5mvc (F: 4) - Crystal Structure of Potent Human Dihydroorotate Dehydrogenase Inhibitors Based on Hydroxylated Azole Scaffolds
    Other atoms: Cl (5);
  8. 5mvd (F: 4) - Crystal Structure of Potent Human Dihydroorotate Dehydrogenase Inhibitors Based on Hydroxylated Azole Scaffolds
    Other atoms: Cl (3);
  9. 5mwp (F: 1) - The Structure of Mr in Complex with AZD9977.
  10. 5mxv (F: 1) - Structure of Transcriptional Regulatory Repressor Protein - Ethr From Mycobacterium Tuberculosis in Complex with Compound GSK1107112A at 1.63A Resolution
    Other atoms: Cl (1);
  11. 5mxx (F: 3) - Crystal Structure of Human Sr Protein Kinase 1 (SRPK1) in Complex with Compound 1
    Other atoms: Ca (4);
  12. 5my8 (F: 3) - Crystal Structure of SRPK1 in Complex with SPHINX31
  13. 5myl (F: 1) - Structure of Transcriptional Regulatory Repressor Protein - Ethr From Mycobacterium Tuberculosis in Complex with Compound GSK1570606A at 1.72A Resolution
  14. 5myr (F: 1) - Structure of Transcriptional Regulatory Repressor Protein - Ethr From Mycobacterium Tuberculosis in Complex with Compound GSK735816A at 1.83A Resolution
  15. 5mys (F: 1) - Structure of Transcriptional Regulatory Repressor Protein - Ethr From Mycobacterium Tuberculosis in Complex with Compound GSK920684A at 1.59A Resolution
  16. 5myv (F: 12) - Crystal Structure of SRPK2 in Complex with Compound 1
  17. 5mz3 (F: 3) - P38 Alpha Mutant C162S in Complex with CMPD2 [N-(4-Methyl-3-(4,4,5,5- Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenyl)-3-(Trifluoromethyl) Benzamide]
  18. 5n1k (F: 3) - Camp-Dependent Protein Kinase A From Cricetulus Griseus in Complex with Fragment Like Molecule 2-Amino-1-(4-Fluorophenyl)Ethanol
  19. 5n2f (F: 2) - Structure of Pd-L1/Small-Molecule Inhibitor Complex
  20. 5n2n (F: 3) - Crystal Structure of the Receiver Domain of the Histidine Kinase CKI1 From Arabidopsis Thaliana Complexed with MG2+ and BEF3-
    Other atoms: Mg (1);
  21. 5n33 (F: 3) - Camp-Dependent Protein Kinase A From Cricetulus Griseus in Complex with Fragment Like Molecule 3-Amino-5-(Trifluoromethyl)-1H-Pyridin-2- One
  22. 5n3d (F: 3) - Camp-Dependent Protein Kinase A From Cricetulus Griseus in Complex with Fragment Like Molecule 4-(Trifluoromethyl)Benzenecarboximidamide
  23. 5n63 (F: 1) - Crystal Structure of P38ALPHA in Complex with Lipid Pocket Ligand 9C
  24. 5n69 (F: 2) - Cardiac Muscle Myosin S1 Fragment in the Pre-Powerstroke State Co- Crystallized with the Activator Omecamtiv Mecarbil
    Other atoms: Mg (2); V (2);
  25. 5n7o (F: 6) - ETHR2 in Complex with Smart-420 Compound
  26. 5n9s (F: 1) - Ttk Kinase Domain in Complex with Bay 1161909
  27. 5n9t (F: 6) - Crystal Structure of USP7 in Complex with A Potent, Selective and Reversible Small-Molecule Inhibitor
  28. 5nad (F: 5) - Ttk Kinase Domain in Complex with Bay 1217389
  29. 5nai (F: 2) - Mono-Zinc Vim-5 Metallo-Beta-Lactamase in Complex with (1-Chloro-4- Hydroxyisoquinoline-3-Carbonyl)-D-Tryptophan (Compound 1)
    Other atoms: Cl (1); Zn (3);
  30. 5nar (F: 3) - Complement Factor D in Complex with the Inhibitor (S)-Pyrrolidine-1,2- Dicarboxylic Acid 1-[(1-Carbamoyl-1H-Indol-3-Yl)-Amide] 2-[(3- Trifluoromethoxy-Phenyl)-Amide]
  31. 5nat (F: 3) - Complement Factor D in Complex with the Inhibitor (S)-Pyrrolidine-1,2- Dicarboxylic Acid 1-[(1-Methyl-1H-Indol-3-Yl)-Amide] 2-[(3- Trifluoromethoxy-Phenyl)-Amide]
  32. 5naw (F: 3) - Complement Factor D in Complex with the Inhibitor (1R,3S,5R)-2-Aza- Bicyclo[3.1.0]Hexane-2,3-Dicarboxylic Acid 2-[(1-Carbamoyl-1H-Indol- 3-Yl)-Amide] 3-[(3-Trifluoromethoxy-Phenyl)-Amide]
  33. 5nb6 (F: 3) - Complement Factor D in Complex with the Inhibitor (2S,4S)-4-Amino- Pyrrolidine-1,2-Dicarboxylic Acid 1-[(1-Carbamoyl-1H-Indol-3-Yl)- Amide] 2-[(3-Trifluoromethoxy-Phenyl)-Amide]
  34. 5nba (F: 4) - Complement Factor D in Complex with the Inhibitor (2S,4R)-4-Fluoro- Pyrrolidine-1,2-Dicarboxylic Acid 1-[(1-Carbamoyl-1H-Indol-3-Yl)- Amide] 2-[(3-Trifluoromethoxy-Phenyl)-Amide]
  35. 5ncq (F: 3) - Structure of the (Sr) CA2+-Atpase Bound to A Tetrahydrocarbazole and Tnp-Atp
    Other atoms: K (1); Br (2);
  36. 5nd4 (F: 4) - Microtubule-Bound MKLP2 Motor Domain in the Presence of Adp.Alfx
    Other atoms: Mg (2); Al (1);
  37. 5ndd (F: 1) - Crystal Structure of A Thermostabilised Human Protease-Activated Receptor-2 (PAR2) in Complex with AZ8838 at 2.8 Angstrom Resolution
    Other atoms: Na (1);
  38. 5nft (F: 4) - Glucocorticoid Receptor in Complex with AZD5423
  39. 5nge (F: 8) - Crystal Structure of USP7 in Complex with the Non-Covalent Inhibitor, FT671
  40. 5njh (F: 3) - Triazolopyrimidines Stabilize Microtubules By Binding to the Vinca Inhibitor Site of Tubulin
    Other atoms: Mg (5); Cl (1);
Page generated: Thu Dec 28 04:06:40 2023

Last articles

Zn in 8WB0
Zn in 8WAX
Zn in 8WAU
Zn in 8WAZ
Zn in 8WAY
Zn in 8WAV
Zn in 8WAW
Zn in 8WAT
Zn in 8W7M
Zn in 8WD3
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy