Atomistry » Fluorine » PDB 2oh4-2pdk
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Fluorine in PDB, part 21 (files: 801-840), PDB 2oh4-2pdk

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: 801-840 (PDB 2oh4-2pdk).
  1. 2oh4 (F: 4) - Crystal Structure of VEGFR2 with A Benzimidazole-Urea Inhibitor
  2. 2ohn (F: 1) - X-Ray Crystal Structure of Beta Secretase Complexed with 4- (4-Fluorobenzyl)Piperidine
    Other atoms: I (3);
  3. 2oi4 (F: 1) - Crystal Structure of Human PIM1 in Complex with Fluorinated Ruthenium Pyridocarbazole
    Other atoms: Ru (1); Cl (1);
  4. 2ojj (F: 1) - Crystal Structure of ERK2 in Complex with (S)-N-(1-(3- Chloro-4-Fluorophenyl)-2-Hydroxyethyl)-4-(4-(3- Chlorophenyl)-1H-Pyrazol-3-Yl)-1H-Pyrrole-2-Carboxamide
    Other atoms: Cl (2);
  5. 2ole (F: 6) - Crystal Structure of Human Dipeptidyl Peptidase IV (Dppiv) Complex with Cyclic Hydrazine Derivatives
  6. 2ong (F: 2) - Crystal Structure of of Limonene Synthase with 2- Fluorogeranyl Diphosphate (Fgpp).
    Other atoms: Mn (6);
  7. 2onh (F: 2) - Crystal Structure of of Limonene Synthase with 2- Fluorolinalyl Diphosphate(Flpp)
    Other atoms: Mn (6);
  8. 2oo8 (F: 3) - Synthesis, Structural Analysis, and Sar Studies of Triazine Derivatives As Potent, Selective Tie-2 Inhibitors
  9. 2oow (F: 2) - Mif Bound to A Fluorinated Oxim Derivative
  10. 2op3 (F: 6) - The Structure of Cathepsin S with A Novel 2- Arylphenoxyacetaldehyde Inhibitor Derived By the Substrate Activity Screening (Sas) Method
  11. 2opa (F: 1) - Ywhb Binary Complex with 2-Fluoro-P-Hydroxycinnamate
  12. 2opb (F: 2) - Structure of K57A Hpnmt with Inhibitor 3-Fluoromethyl-7- Thiomorpholinosulfonamide-Thiq and Adohcy
  13. 2oph (F: 2) - Human Dipeptidyl Peptidase IV in Complex with An Alpha Amino Acid Inhibitor
    Other atoms: Na (1);
  14. 2opm (F: 1) - Human Farnesyl Diphosphate Synthase Complexed with Bisphosphonate Bph-461
    Other atoms: Mg (3);
  15. 2opp (F: 1) - Crystal Structure of Hiv-1 Reverse Transcriptase in Complex with GW420867X.
    Other atoms: Mg (1);
  16. 2opq (F: 1) - Crystal Structure of L100I Mutant Hiv-1 Reverse Transcriptase in Complex with GW420867X.
  17. 2opr (F: 1) - Crystal Structure of K101E Mutant Hiv-1 Reverse Transcriptase in Complex with GW420867X.
  18. 2ops (F: 1) - Crystal Structure of Y188C Mutant Hiv-1 Reverse Transcriptase in Complex with GW420867X.
  19. 2oqi (F: 3) - Human Dipeptidyl Peptidase IV (DPP4) with Piperidinone- Constrained Phenethylamine
  20. 2oqv (F: 3) - Human Dipeptidyl Peptidase IV (DPP4) with Piperidine- Constrained Phenethylamine
  21. 2osc (F: 3) - Synthesis, Structural Analysis, and Sar Studies of Triazine Derivatives As Potent, Selective Tie-2 Inhibitors
  22. 2ow1 (F: 6) - Mmp-9 Active Site Mutant with Trifluoromethyl Hydroxamate Inhibitor
    Other atoms: Cl (3); Ca (8); Zn (4);
  23. 2ow2 (F: 4) - Mmp-9 Active Site Mutant with Difluoro Butanoic Acid Inhibitor
    Other atoms: Cl (2); Ca (6); Zn (4);
  24. 2p15 (F: 6) - Crystal Structure of the Er Alpha Ligand Binding Domain with the Agonist Ortho-Trifluoromethylphenylvinyl Estradiol
  25. 2p2v (F: 1) - Crystal Structure Analysis of Monofunctional Alpha-2,3- Sialyltransferase Cst-I From Campylobacter Jejuni
    Other atoms: Cl (1);
  26. 2p3g (F: 1) - Crystal Structure of A Pyrrolopyridine Inhibitor Bound to Mapkap Kinase-2
  27. 2p4i (F: 6) - Evolution of A Highly Selective and Potent 2-(Pyridin-2-Yl)- 1,3,5-Triazine Tie-2 Kinase Inhibitor
  28. 2p4y (F: 6) - Crystal Structure of Human Ppar-Gamma-Ligand Binding Domain Complexed with An Indole-Based Modulator
    Other atoms: Cl (2);
  29. 2p54 (F: 3) - A Crystal Structure of Ppar Alpha Bound with SRC1 Peptide and GW735
  30. 2p55 (F: 3) - X-Ray Structure of the Human Mitogen-Activated Protein Kinase Kinase 1 (MEK1) in A Complex with Ligand and Mgatp
    Other atoms: Mg (1);
  31. 2p83 (F: 6) - Potent and Selective Isophthalamide S2 Hydroxyethylamine Inhibitor of BACE1
  32. 2p8h (F: 1) - Crystal Structure of Human Beta Secretase Complexed with Inhibitor
  33. 2p8s (F: 24) - Human Dipeptidyl Peptidase IV/CD26 in Complex with A Cyclohexalamine Inhibitor
    Other atoms: Na (1);
  34. 2pb1 (F: 2) - Exo-B-(1,3)-Glucanase From Candida Albicans in Complex with Unhydrolysed and Covalently Linked 2,4-Dinitrophenyl-2- Deoxy-2-Fluoro-B-D-Glucopyranoside at 1.9 A
  35. 2pd5 (F: 3) - Human Aldose Reductase Mutant V47I Complexed with Zopolrestat
  36. 2pd9 (F: 1) - Human Aldose Reductase Mutant V47I Complexed with Fidarestat.
  37. 2pdb (F: 3) - Human Aldose Reductase Mutant F121P Complexed with Zopolrestat.
  38. 2pdf (F: 3) - Human Aldose Reductase Mutant L300P Complexed with Zopolrestat.
  39. 2pdi (F: 3) - Human Aldose Reductase Mutant L300A Complexed with Zopolrestat at 1.55 A.
  40. 2pdk (F: 1) - Human Aldose Reductase Mutant L301M Complexed with Sorbinil.
Page generated: Wed Nov 4 04:16:27 2020

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