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Fluorine in PDB, part 208 (files: 8281-8320), PDB 7s76-7ss6

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: 8281-8320 (PDB 7s76-7ss6).
  1. 7s76 (F: 6) - Hbv Capsid Y132A with Compound 10B at 2.5A Resolution
    Other atoms: Cl (6);
  2. 7s7a (F: 3) - Crystal Structure of CDK2 Liganded with Compound EF3019
  3. 7s84 (F: 3) - Crystal Structure of CDK2 Liganded with Compound TW8972
  4. 7s85 (F: 3) - Crystal Structure of CDK2 Liganded with Compound WN316
  5. 7s9x (F: 3) - Crystal Structure of CDK2 Liganded with Compound WN378
  6. 7sa0 (F: 6) - Crystal Structure of CDK2 Liganded with Compound EF4195
  7. 7sdc (F: 3) - Structure of the Sars-Cov-2 Main Protease in Complex with Inhibitor Mi-09
  8. 7se8 (F: 6) - Crystal Structure of Human Fibrillarin in Complex with Fragment 1 From Cocktail Soak
  9. 7se9 (F: 6) - Crystal Structure of Human Fibrillarin in Complex with Compound 1 From Single Soak
  10. 7sea (F: 3) - Crystal Structure of Human Fibrillarin in Complex with Compound 2 From Cocktail Soak
  11. 7seb (F: 3) - Crystal Structure of Human Fibrillarin in Complex with Compound 2 From Single Soak
  12. 7sec (F: 6) - Crystal Structure of Human Fibrillarin in Complex with Compound 1A
  13. 7sed (F: 3) - Crystal Structure of Human Fibrillarin in Complex with Compound 2A
  14. 7sel (F: 2) - E. Coli Msba in Complex with Lps and Inhibitor G7090 (Compound 3)
    Other atoms: Cl (4);
  15. 7sf3 (F: 3) - Sars-Cov-2 Main Protease (Mpro) in Complex with ML1006M
    Other atoms: Cl (1);
  16. 7sff (F: 3) - Human DNMT1(729-1600) Bound to Zebularine-Containing 12MER Dsdna and Inhibitor GSK3852279B
    Other atoms: Zn (2);
  17. 7sfi (F: 3) - Sars-Cov-2 Main Protease (Mpro) in Complex with ML104
    Other atoms: Cl (1); Ca (1);
  18. 7sfq (F: 40) - Emre S64V Mutant Bound to Tetra(4-Fluorophenyl)Phosphonium at pH 8.0
  19. 7sgh (F: 12) - Sars-Cov-2 Main Protease (Mpro) in Complex with ML124N
  20. 7si3 (F: 4) - Consensus Structure of ATP7B
    Other atoms: Mg (1); Al (1);
  21. 7si4 (F: 1) - Crystal Structure of Eed with Mrtx-2219
  22. 7si5 (F: 1) - Crystal Structure of Eed with Mrtx-1919
    Other atoms: Na (2);
  23. 7si6 (F: 4) - Structure of ATP7B in State 1
    Other atoms: Mg (1); Al (1);
  24. 7si7 (F: 4) - Structure of ATP7B in State 2
    Other atoms: Mg (1); Al (1);
  25. 7si9 (F: 3) - Room Temperature X-Ray Structure of Sars-Cov-2 Main Protease (Mpro) in Complex with Pf-07321332
  26. 7sii (F: 8) - Human Sting Bound to Both Cgamp and 1-[(2-Chloro-6-Fluorophenyl) Methyl]-3,3-Dimethyl-2-Oxo-N-[(2,4,6-Trifluorophenyl)Methyl]-2,3- Dihydro-1H-Indole-6-Carboxamide (Compound 53)
    Other atoms: Cl (2);
  27. 7sj3 (F: 2) - Structure of CDK4-Cyclin D3 Bound to Abemaciclib
  28. 7slr (F: 7) - Hiv Reverse Transcriptase with Compound PYR01
  29. 7sls (F: 7) - Hiv Reverse Transcriptase with Compound PYR02
  30. 7snl (F: 5) - Disulfide Stabilized Hiv-1 Ca Hexamer in Complex with Capsid Inhibitor N-(1-(3-(4-Chloro-1-Methyl-3-(Methylsulfonamido)-1H-Indazol-7-Yl)-4- Oxo-3,4-Dihydropyrido[2,3-D]Pyrimidin-2-Yl)-2-(3,5-Difluorophenyl) Ethyl)-2-(3-(Trifluoromethyl)-4,5,6,7-Tetrahydro-1H-Indazol-1-Yl) Acetamide
    Other atoms: I (4); Cl (8);
  31. 7snn (F: 4) - Disulfide Stabilized Hiv-1 Ca Hexamer in Complex with Capsid Inhibitor N-(1-(3-(4-Chloro-1-Methyl-3-(Methylsulfonamido)-1H-Indazol-7-Yl)-4- Oxo-3,4-Dihydropyrido[2,3-D]Pyrimidin-2-Yl)-2-(3,5-Difluorophenyl) Ethyl)-2-(3-(Difluoromethyl)-5,6-Dihydrocyclopenta[C]Pyrazol-1(4H)- Yl)Acetamide
    Other atoms: I (3); Cl (8);
  32. 7so4 (F: 1) - Crystal Structure of Hiv-1 Y181C Mutant Reverse Transcriptase in Complex with 5-(2-(2-(2,4-Dioxo-3,4-Dihydropyrimidin-1(2H)-Yl) Ethoxy)Phenoxy)-7-Fluoro-2-Naphthonitrile (JLJ635), A Non-Nucleoside Inhibitor
  33. 7so6 (F: 1) - Crystal Structure of Hiv-1 K103N, Y181C Mutant Reverse Transcriptase in Complex with 5-(2-(2-(2,4-Dioxo-3,4-Dihydropyrimidin-1(2H)-Yl) Ethoxy)Phenoxy)-7-Fluoro-2-Naphthonitrile (JLJ635), A Non-Nucleoside Inhibitor
    Other atoms: Mg (1);
  34. 7sp3 (F: 1) - E. Coli Rpph Bound to AP4A
    Other atoms: Mg (3); Cl (1);
  35. 7sps (F: 4) - Crystal Structure of Human Glucose Transporter GLUT3 Bound with Exofacial Inhibitor SA47
  36. 7sq2 (F: 4) - Reprocessed and Refined Structure of Phospholipase C-Beta and Gq Signaling Complex
    Other atoms: Al (1); Ca (1); Mg (2);
  37. 7sql (F: 5) - Crystal Structure of Human Uridine-Cytidine Kinase 2 Complexed with A Weak Small Molecule Inhibitor
    Other atoms: Br (5);
  38. 7sqm (F: 2) - Discovery and Preclinical Pharmacology of INE963, A Potent and Fast- Acting Blood-Stage Antimalarial with A High Barrier to Resistance and Potential For Single-Dose Cure in Uncomplicated Malaria
  39. 7ss1 (F: 2) - The Structure of NTMT1 in Complex with Compound GD433
  40. 7ss6 (F: 3) - Structure of Klebsiella Lpxh in Complex with Jh-Lph-45
    Other atoms: Cl (1); Mn (2);
Page generated: Wed Nov 13 08:13:11 2024

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