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Fluorine in PDB, part 235 (files: 9361-9400), PDB 8gky-8hej

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: 9361-9400 (PDB 8gky-8hej).
  1. 8gky (F: 2) - Human Mitochondrial Serine Hydroxymethyltransferase (SHMT2) Y105F in Complex with Plp, Glycine and AGF359 Inhibitor
  2. 8gkz (F: 1) - Human Mitochondrial Serine Hydroxymethyltransferase (SHMT2) Y105F in Complex with Plp, Glycine and AGF362 Inhibitor
  3. 8gls (F: 1) - Complex of Human Cystic Fibrosis Transmembrane Conductance Regulator (Cftr) and Z1834339853
    Other atoms: Mg (2);
  4. 8gml (F: 1) - Crystal Structure of Human Dna Polymerase Eta Incorporating 5F-Dutp Across Dg
    Other atoms: Ca (1);
  5. 8god (F: 1) - Co-Crystal Structure of Human Protein-Arginine Deiminase Type-4 (PAD4) with Small Molecule Inhibitor Jbi-589
  6. 8gsq (F: 1) - Structure Based Studies Reveal An Atypical Antipsychotic Drug Candidate - Paliperidone As A Potent HSOD1 Modulator with Implications in Als Treatment.
    Other atoms: Zn (9);
  7. 8gtm (F: 6) - Corticotropin-Releasing Hormone Receptor 1(CRF1R) Bound with Bmk-C203 By Xfel
    Other atoms: Br (1);
  8. 8gtw (F: 6) - Sars-Cov-2 3CL Protease (3CLPRO) in Complex with Compound Jzd-26
    Other atoms: Cl (4);
  9. 8gu1 (F: 4) - Crystal Structure of Putative Amino Acid Binding Periplasmic Abc Transporter Protein From Candidatus Liberibacter Asiaticus in Complex with Pimozide
  10. 8gua (F: 3) - Cryo-Em Structure of Cancer-Specific PI3KALPHA Mutant E542K in Complex with Byl-719
  11. 8gub (F: 3) - Cryo-Em Structure of Cancer-Specific PI3KALPHA Mutant H1047R in Complex with Byl-719
  12. 8gud (F: 3) - Cryo-Em Structure of Cancer-Specific PI3KALPHA Mutant E545K in Complex with Byl-719
  13. 8gut (F: 1) - Cryo-Em Structure of Lei-CB2-Gi Complex
  14. 8gvj (F: 3) - Crystal Structure of Cmet Kinase Domain Bound By D6808
  15. 8gvz (F: 1) - Crystal Structure of the Human Dihydroorotase Domain in Complex with the Anticancer Drug 5-Fluorouracil
    Other atoms: Zn (2);
  16. 8gw8 (F: 3) - The Human PTH1 Receptor Bound to An Intracellular Biased Agonist
  17. 8gwm (F: 1) - Sars-Cov-2 E-Rtc Bound with Mmp-NSP9 and Gmppnp
    Other atoms: Zn (8);
  18. 8gxg (F: 1) - The Crystal Structure of Sars-Cov-2 Main Protease in Complex with 14A
  19. 8gzc (F: 2) - Crystal Structure of EP300 Hat Domain in Complex with Compound 10
    Other atoms: Zn (6);
  20. 8h3g (F: 6) - Crystal Structure of Sars-Cov-2 Main Protease (Mpro) E166V Mutant in Complex with Inhibitor Enstrelvir
    Other atoms: Cl (2);
  21. 8h3k (F: 6) - Crystal Structure of Sars-Cov-2 Main Protease (Mpro) Double Mutant (L50F and E166V) in Complex with Inhibitor Enstrelvir
    Other atoms: Cl (2);
  22. 8h3l (F: 12) - Crystal Structure of Sars-Cov-2 Main Protease (Mpro) Double Mutant (T21I and E166V) in Complex with Inhibitor Enstrelvir
    Other atoms: Cl (4);
  23. 8h4y (F: 3) - Crystal Structure of Sars-Cov-2 Main Protease (Mpro) F140L Mutant in Complex with Inhibitor Nirmatrelvir
  24. 8h51 (F: 3) - Crystal Structure of Sars-Cov-2 Main Protease (Mpro) Double Mutant (T21I and E166V) in Complex with Inhibitor Nirmatrelvir
  25. 8h57 (F: 3) - Crystal Structure of Sars-Cov-2 Main Protease (Mpro) A193P Mutant in Complex with Inhibitor Nirmatrelvir
  26. 8h59 (F: 3) - A Fungal Map Kinase in Complex with An Inhibitor
  27. 8h5f (F: 3) - Crystal Structure of Sars-Cov-2 Main Protease (Mpro) L167F Mutant in Complex with Inhibitor Nirmatrelvir
  28. 8h5p (F: 3) - Crystal Structure of Sars-Cov-2 Main Protease (Mpro) Double Mutant (L50F and E166V) in Complex with Inhibitor Nirmatrelvir
  29. 8h6n (F: 3) - Crystal Structure of Sars-Cov-2 Main Protease (Mpro) Mutant (T21I) in Complex with Protease Inhibitor Nirmatrelvir
  30. 8h77 (F: 6) - HSP90-Ahr-P23-XAP2 Complex
  31. 8h7w (F: 3) - Crystal Structure of Sars-Cov-2 Main Protease (Mpro) Mutant (S144A) in Complex with Protease Inhibitor Nirmatrelvir
  32. 8h82 (F: 3) - Crystal Structure of Sars-Cov-2 Main Protease (Mpro) Mutant (E166V) in Complex with Protease Inhibitor Nirmatrelvir
  33. 8hb0 (F: 1) - Structure of Human SGLT2-MAP17 Complex with TA1887
    Other atoms: Na (1);
  34. 8hbf (F: 1) - Structure of Human Soluble Guanylate Cyclase in the No+Rio State at 3.1 Angstrom
    Other atoms: Mg (2); Fe (1);
  35. 8hbk (F: 3) - The Crystal Structure of Sars-Cov-2 3CL Protease in Complex with Ensitrelvir
    Other atoms: Cl (1);
  36. 8hdh (F: 1) - Structure of Human SGLT2-MAP17 Complex with Canagliflozin
    Other atoms: Na (1);
  37. 8he7 (F: 2) - Adp-Ribosyltransferase 1 (PARP1) Catalytic Domain Bound to A Quinazoline-2,4(1H,3H)-Dione Inhibitor
  38. 8he8 (F: 3) - Human Adp-Ribosyltransferase 2 (PARP2) Catalytic Domain Bound to A Quinazoline-2,4(1H,3H)-Dione Inhibitor
  39. 8hef (F: 6) - The Crystal Structure of Deuterated S-217622 (Ensitrelvir) Bound to the Main Protease (3CLPRO/Mpro) of Sars-Cov-2
    Other atoms: Cl (2);
  40. 8hej (F: 6) - Crystal Structure of Transthyretin in Complex with A Covalent Inhibitor Trans-Styrylpyrazole
    Other atoms: Br (4);
Page generated: Wed Jul 16 05:06:38 2025

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