Atomistry » Bromine » PDB 6tlp-6vdv
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Bromine in PDB, part 49 (files: 1921-1960), PDB 6tlp-6vdv

Experimental structures of coordination spheres of Bromine (Br) in bioorganic molecules from X-Ray and NMR experiments. Coordination spheres were calculated with 5.0 Angstroms radius around Bromine atoms. PDB files: 1921-1960 (PDB 6tlp-6vdv).
  1. 6tlp (Br: 2) - Human CK2 Kinase Alpha Subunit in Complex with the Atp-Competitive Inhibitor 5,6-Dibromobenzotriazole
  2. 6tlr (Br: 6) - Human CK2 Kinase Alpha Subunit in Complex with the Atp-Competitive Inhibitor 4,7-Dibromobenzotriazole
    Other atoms: Cl (1); Na (1);
  3. 6tls (Br: 6) - Human CK2 Kinase Alpha Subunit in Complex with the Atp-Competitive Inhibitor 4,6-Dibromobenzotriazole
    Other atoms: Cl (6); Na (1);
  4. 6tlv (Br: 3) - Human CK2 Kinase Alpha Subunit in Complex with the Atp-Competitive Inhibitor 5-Bromobenzotriazole
    Other atoms: Cl (3); Na (1);
  5. 6tlw (Br: 1) - Human CK2 Kinase Alpha Subunit in Complex with the Atp-Competitive Inhibitor 4-Bromobenzotriazole
    Other atoms: Cl (2);
  6. 6tos (Br: 2) - Crystal Structure of the Orexin-1 Receptor in Complex with GSK1059865
    Other atoms: F (2); Na (1);
  7. 6tqd (Br: 9) - D00-D0 Domain of Intimin
    Other atoms: Na (2); Cl (6);
  8. 6tqg (Br: 4) - Pseudomonas Aeruginosa Rmla in Complex with Allosteric Inhibitor
    Other atoms: Cl (8);
  9. 6ts9 (Br: 4) - Crystal Structure of Ges-5 Carbapenemase
  10. 6tu4 (Br: 5) - Structure of Plasmodium ACTIN1 Filament
    Other atoms: Mg (5);
  11. 6tvn (Br: 4) - Crystal Structure of 5-Bromoindoline-2,3-Dione Covalently Bound to the pH Domain of Bruton'S Tyrosine Kinase
    Other atoms: Mg (2); Zn (4);
  12. 6tzr (Br: 2) - A Dna G-Quadruplex/I-Motif Hybrid
    Other atoms: Ba (1);
  13. 6tzs (Br: 2) - A Dna I-Motif/Duplex Hybrid
  14. 6u5m (Br: 2) - Discovery and Optimization of Salicyclic Acid-Derived Sulfonamide Inhibitors of the WDR5:Myc Protein-Protein Interaction
    Other atoms: F (10);
  15. 6u5y (Br: 2) - Discovery and Optimization of Salicyclic Acid-Derived Sulfonamide Inhibitors of the WDR5:Myc Protein-Protein Interaction
    Other atoms: Cl (2);
  16. 6u6w (Br: 2) - Discovery and Optimization of Salicyclic Acid-Derived Sulfonamide Inhibitors of the WDR5:Myc Protein-Protein Interaction
    Other atoms: Cl (2);
  17. 6u80 (Br: 2) - Discovery and Optimization of Salicyclic Acid-Derived Sulfonamide Inhibitors of the WDR5:Myc Protein-Protein Interaction
  18. 6u8b (Br: 2) - Discovery and Optimization of Salicyclic Acid-Derived Sulfonamide Inhibitors of the WDR5:Myc Protein-Protein Interaction
    Other atoms: Cl (2);
  19. 6u8l (Br: 2) - Discovery and Optimization of Salicyclic Acid-Derived Sulfonamide Inhibitors of the WDR5:Myc Protein-Protein Interaction
    Other atoms: F (2);
  20. 6u8o (Br: 1) - Discovery and Optimization of Salicyclic Acid-Derived Sulfonamide Inhibitors of the WDR5:Myc Protein-Protein Interaction
  21. 6uif (Br: 2) - Discovery of Fragment-Inspired Heterocyclic Benzenesulfonmides As Inhibitors of the WDR5-Myc Interaction
    Other atoms: Cl (2);
  22. 6uik (Br: 2) - Discovery of Fragment-Inspired Heterocyclic Benzenesulfonmides As Inhibitors of the WDR5-Myc Interaction
    Other atoms: Cl (2);
  23. 6uj4 (Br: 2) - Discovery of Fragment-Inspired Heterocyclic Benzenesulfonmides As Inhibitors of the WDR5-Myc Interaction
    Other atoms: Cl (2);
  24. 6ujn (Br: 5) - P-Glycoprotein Mutant-C952A-with BDE100
  25. 6ujp (Br: 5) - P-Glycoprotein Mutant-F979A and C952A-with BDE100
  26. 6ujr (Br: 5) - P-Glycoprotein Mutant-F724A and C952A-with BDE100
  27. 6ujs (Br: 10) - P-Glycoprotein Mutant-F728A and C952A-with BDE100
  28. 6ujt (Br: 10) - P-Glycoprotein Mutant-Y303A and C952A-with BDE100
  29. 6ujw (Br: 10) - P-Glycoprotein Mutant-Y306A and C952A-with BDE100
  30. 6umz (Br: 1) - Crystal Structure of Photoactive Yellow Protein (Pyp); 3-Br-P-Coumaric Acid Chromophore
  31. 6un0 (Br: 1) - Crystal Structure of Photoactive Yellow Protein (Pyp); F96(4-if) Construct with 3-Br-P-Coumaric Acid Chromophore
    Other atoms: I (1);
  32. 6uox (Br: 1) - Structure of Itraconazole-Bound NPC1
    Other atoms: Cl (2);
  33. 6uoz (Br: 2) - Discovery of Fragment-Inspired Heterocyclic Benzenesulfonmides As Inhibitors of the WDR5-Myc Interaction
    Other atoms: Cl (2);
  34. 6uyh (Br: 2) - Crystal Structure of Prolyl-Trna Synthetase From Naegleria Fowleri in Complex with Halofuginone and Amppnp
    Other atoms: Mg (2); Cl (2);
  35. 6v9d (Br: 2) - Co-Crystal Structure of the Fluorogenic Mango-IV Homodimer Bound to TO1-Biotin
    Other atoms: K (4);
  36. 6vd3 (Br: 2) - Crystal Structure of Dehaloperoxidase B in Complex with Cofactor Iron(III) Mesoporphyrin IX and Substrate 4-Bromophenol
    Other atoms: Fe (2);
  37. 6vd4 (Br: 3) - Crystal Structure of Dehaloperoxidase B in Complex with Cofactor Iron(III) Mesoporphyrin IX and Substrate 4-Bromo-Ortho-Cresol
    Other atoms: Fe (2);
  38. 6vdr (Br: 2) - Crystal Structure of Dehaloperoxidase B in Complex with Cofactor Iron(III) Deuteroporphyrin IX and Substrate 4-Bromophenol
    Other atoms: Fe (2);
  39. 6vds (Br: 2) - Crystal Structure of Dehaloperoxidase B in Complex with Cofactor Iron(III) Deuteroporphyrin IX and Substrate 4-Bromo-Ortho-Cresol
    Other atoms: Fe (3);
  40. 6vdv (Br: 2) - Crystal Structure of Dehaloperoxidase B in Complex with Cofactor Manganese(III)- Porphyrin and Substrate 4-Bromophenol
    Other atoms: Mn (2);
Page generated: Sat Sep 25 12:44:32 2021

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