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Zinc in PDB, part 357 (files: 14241-14280), PDB 6dxs-6ee6

Experimental structures of coordination spheres of Zinc (Zn) in bioorganic molecules from X-Ray and NMR experiments. Coordination spheres were calculated with 5.0 Angstroms radius around Zinc atoms. PDB files: 14241-14280 (PDB 6dxs-6ee6).
  1. 6dxs (Zn: 4) - Crystal Structure of the Ligj Hydratase E284Q Mutant Substrate Complex with (3Z)-2-Keto-4-Carboxy-3-Hexenedioate
  2. 6dxt (Zn: 2) - Structure of USP5 Zinc-Finger Ubiquitin Binding Domain Co-Crystallized with 3-(5-Phenyl-1,3,4-Oxadiazol-2-Yl)Propanoate
  3. 6dy5 (Zn: 3) - Crystal Structure of Double-Stranded Dna Agggatccct in Complex with ZN2+
  4. 6dy9 (Zn: 2) - Crystal Structure of Double-Stranded Dna Gggatccc; Crystals Grown in ZN2+
  5. 6dz8 (Zn: 4) - Crystal Structure of S. Aureus Penicillin Binding Protein 4 (PBP4) Mutant (S75C)
  6. 6dzd (Zn: 2) - Crystal Structure of Bacillus Licheniformis Hypothetical Protein Yfih
    Other atoms: K (1); Cl (1); Na (1);
  7. 6e0a (Zn: 9) - Crystal Structure of Helicobacter Pylori Tlpa Chemoreceptor Ligand Binding Domain
    Other atoms: Cl (1); Ca (1);
  8. 6e0s (Zn: 2) - Crystal Structure of Mem-A1, A Subclass B3 Metallo-Beta-Lactamase Isolated From A Soil Metagenome Library
  9. 6e13 (Zn: 2) - Pseudomonas Putida Pqqb with A Non-Physiological Zinc at the Active Site Binds the Substrate Mimic, 5-Cysteinyl-3,4- Dihydroxyphenylalanine (5-Cys-Dopa), Non-Specifically But Supports the Proposed Function of the Enzyme in Pyrroloquinoline Quinone Biosynthesis.
    Other atoms: Cl (1);
  10. 6e1h (Zn: 1) - Structure of 2:1 Human PTCH1-Shh-N Complex
    Other atoms: Ca (2);
  11. 6e25 (Zn: 20) - uc(Nmr) Solution Structure of the CARD9 Card Bound to Zinc
  12. 6e27 (Zn: 1) - The CARD9 Card Domain-Swapped Dimer with A Zinc Ion Bound to One of the Two Zinc Binding Sites
  13. 6e33 (Zn: 2) - Crystal Structure of PHO7-Dna Complex
  14. 6e4y (Zn: 4) - Anti-PCSK9 Fab 6E2 Bound to the N-Terminal Peptide From PCSK9, Unmodified
    Other atoms: Cl (1);
  15. 6e4z (Zn: 5) - Anti-PCSK9 Fab 6E2 Bound to the Modified N-Terminal Peptide From PCSK9
  16. 6e54 (Zn: 1) - Crystal Structure of Lpxc From Pseudomonas Aeruginosa in Complex with Ligand PT802
    Other atoms: F (2); Ca (2); Cl (2);
  17. 6e6i (Zn: 9) - Crystal Structure of 4-Methyl Hopda Bound to Ligy From Sphingobium Sp. Strain Syk-6
  18. 6e83 (Zn: 40) - Solution Structure of ZZZ3 Zz Domain in Complex with Histone H3 Tail
  19. 6e86 (Zn: 40) - Solution Structure of ZZZ3 Zz Domain in Complex with Histone H3K4AC Peptide
  20. 6e8p (Zn: 1) - Ca IX Mimic Complexed with Steroidal Sulfamate Compound Stx 49
  21. 6e8x (Zn: 1) - Ca IX Mimic Complexed with Steroidal Sulfamate Compound Stx 140
  22. 6e91 (Zn: 1) - Ca IX Mimic Complexed with Steroidal Sulfamate Compound Stx 2484
  23. 6e92 (Zn: 1) - Ca IX Mimic Complexed with Steroidal Sulfamate Compound Stx 2845
  24. 6e93 (Zn: 4) - Crystal Structure of ZBTB38 C-Terminal Zinc Fingers 6-9 in Complex with Methylated Dna
  25. 6e94 (Zn: 4) - Crystal Structure of ZBTB38 C-Terminal Zinc Fingers 6-9 K1055R in Complex with Methylated Dna
  26. 6ea1 (Zn: 1) - X-Ray Crystal Structure of Pf-M1 in Complex with Inhibitor (6DA) and Catalytic Zinc Ion
    Other atoms: F (7); Mg (4);
  27. 6ea2 (Zn: 1) - X-Ray Crystal Structure of Pf-M1 in Complex with Inhibitor (6H) and Catalytic Zinc Ion
    Other atoms: F (3); Mg (4);
  28. 6ea4 (Zn: 2) - ERAP2 Bound to Aryl Sulfonamide Uncompetitive Inhibitor
    Other atoms: F (6);
  29. 6eaa (Zn: 1) - X-Ray Crystal Structure of Pf-M1 in Complex with Inhibitor (6I) and Catalytic Zinc Ion
    Other atoms: F (3); Mg (3);
  30. 6eab (Zn: 1) - X-Ray Crystal Structure of Pf-M1 in Complex with Inhibitor (6J) and Catalytic Zinc Ion
    Other atoms: F (3); Mg (4);
  31. 6ebe (Zn: 1) - Bioreductive 4-Hydroxy-3-Nitro-5-Ureido-Benzenesulfonamides Selectively Target the Tumor-Associated Carbonic Anhydrase Isoforms IX and XII and Show Hypoxia-Enhanced Cytotoxicity Against Human Cancer Cell Lines.
    Other atoms: F (3);
  32. 6ecz (Zn: 1) - Bioreductive 4-Hydroxy-3-Nitro-5-Ureido-Benzenesulfonamides Selectively Target the Tumor-Associated Carbonic Anhydrase Isoforms IX and XII and Show Hypoxia-Enhanced Cytotoxicity Against Human Cancer Cell Lines.
    Other atoms: F (5);
  33. 6eda (Zn: 1) - Bioreductive 4-Hydroxy-3-Nitro-5-Ureido-Benzenesulfonamides Selectively Target the Tumor-Associated Carbonic Anhydrase Isoforms IX and XII and Show Hypoxia-Enhanced Cytotoxicity Against Human Cancer Cell Lines.
    Other atoms: F (3);
  34. 6edb (Zn: 1) - Crystal Structure of Sry.Hcgas-21BP Dsdna Complex
  35. 6edc (Zn: 1) - Hcgas-16BP Dsdna Complex
  36. 6edt (Zn: 2) - Mycobacterium Tuberculosis Rnap Open Promoter Complex with Rbpa/Card and AP3 Promoter
    Other atoms: Mg (1);
  37. 6ee2 (Zn: 12) - X-Ray Crystal Structure of Pf-M17 in Complex with Inhibitor 6I and Regulatory Zinc Ion
    Other atoms: F (36);
  38. 6ee3 (Zn: 1) - X-Ray Crystal Structure of Pf-M1 in Complex with Inhibitor (6K) and Catalytic Zinc Ion
    Other atoms: F (3); Mg (4);
  39. 6ee4 (Zn: 1) - X-Ray Crystal Structure of Pf-M1 in Complex with Inhibitor (6M) and Catalytic Zinc Ion
    Other atoms: F (3); Mg (5);
  40. 6ee6 (Zn: 1) - X-Ray Crystal Structure of Pf-M1 in Complex with Inhibitor (6O) and Catalytic Zinc Ion
    Other atoms: F (3); Mg (3);
Page generated: Sun Dec 15 12:06:55 2024

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