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).
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6dxs (Zn: 4) - Crystal Structure of the Ligj Hydratase E284Q Mutant Substrate Complex with (3Z)-2-Keto-4-Carboxy-3-Hexenedioate
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6dxt (Zn: 2) - Structure of USP5 Zinc-Finger Ubiquitin Binding Domain Co-Crystallized with 3-(5-Phenyl-1,3,4-Oxadiazol-2-Yl)Propanoate
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6dy5 (Zn: 3) - Crystal Structure of Double-Stranded Dna Agggatccct in Complex with ZN2+
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6dy9 (Zn: 2) - Crystal Structure of Double-Stranded Dna Gggatccc; Crystals Grown in ZN2+
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6dz8 (Zn: 4) - Crystal Structure of S. Aureus Penicillin Binding Protein 4 (PBP4) Mutant (S75C)
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6dzd (Zn: 2) - Crystal Structure of Bacillus Licheniformis Hypothetical Protein Yfih
Other atoms:
K (1);
Cl (1);
Na (1);
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6e0a (Zn: 9) - Crystal Structure of Helicobacter Pylori Tlpa Chemoreceptor Ligand Binding Domain
Other atoms:
Cl (1);
Ca (1);
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6e0s (Zn: 2) - Crystal Structure of Mem-A1, A Subclass B3 Metallo-Beta-Lactamase Isolated From A Soil Metagenome Library
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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);
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6e1h (Zn: 1) - Structure of 2:1 Human PTCH1-Shh-N Complex
Other atoms:
Ca (2);
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6e25 (Zn: 20) - uc(Nmr) Solution Structure of the CARD9 Card Bound to Zinc
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6e27 (Zn: 1) - The CARD9 Card Domain-Swapped Dimer with A Zinc Ion Bound to One of the Two Zinc Binding Sites
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6e33 (Zn: 2) - Crystal Structure of PHO7-Dna Complex
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6e4y (Zn: 4) - Anti-PCSK9 Fab 6E2 Bound to the N-Terminal Peptide From PCSK9, Unmodified
Other atoms:
Cl (1);
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6e4z (Zn: 5) - Anti-PCSK9 Fab 6E2 Bound to the Modified N-Terminal Peptide From PCSK9
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6e54 (Zn: 1) - Crystal Structure of Lpxc From Pseudomonas Aeruginosa in Complex with Ligand PT802
Other atoms:
F (2);
Ca (2);
Cl (2);
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6e6i (Zn: 9) - Crystal Structure of 4-Methyl Hopda Bound to Ligy From Sphingobium Sp. Strain Syk-6
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6e83 (Zn: 40) - Solution Structure of ZZZ3 Zz Domain in Complex with Histone H3 Tail
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6e86 (Zn: 40) - Solution Structure of ZZZ3 Zz Domain in Complex with Histone H3K4AC Peptide
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6e8p (Zn: 1) - Ca IX Mimic Complexed with Steroidal Sulfamate Compound Stx 49
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6e8x (Zn: 1) - Ca IX Mimic Complexed with Steroidal Sulfamate Compound Stx 140
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6e91 (Zn: 1) - Ca IX Mimic Complexed with Steroidal Sulfamate Compound Stx 2484
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6e92 (Zn: 1) - Ca IX Mimic Complexed with Steroidal Sulfamate Compound Stx 2845
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6e93 (Zn: 4) - Crystal Structure of ZBTB38 C-Terminal Zinc Fingers 6-9 in Complex with Methylated Dna
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6e94 (Zn: 4) - Crystal Structure of ZBTB38 C-Terminal Zinc Fingers 6-9 K1055R in Complex with Methylated Dna
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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);
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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);
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6ea4 (Zn: 2) - ERAP2 Bound to Aryl Sulfonamide Uncompetitive Inhibitor
Other atoms:
F (6);
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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);
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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);
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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);
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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);
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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);
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6edb (Zn: 1) - Crystal Structure of Sry.Hcgas-21BP Dsdna Complex
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6edc (Zn: 1) - Hcgas-16BP Dsdna Complex
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6edt (Zn: 2) - Mycobacterium Tuberculosis Rnap Open Promoter Complex with Rbpa/Card and AP3 Promoter
Other atoms:
Mg (1);
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6ee2 (Zn: 12) - X-Ray Crystal Structure of Pf-M17 in Complex with Inhibitor 6I and Regulatory Zinc Ion
Other atoms:
F (36);
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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);
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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);
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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: Wed Nov 13 13:31:00 2024
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