Zinc in PDB, part 350 (files: 13961-14000),
PDB 6e8p-6ej0
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: 13961-14000 (PDB 6e8p-6ej0).
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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);
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6ee7 (Zn: 3) - Small Tetraheme Cytochrome C From Shewanella Oneidensis
Other atoms:
Fe (4);
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6ee8 (Zn: 2) - Mycobacterium Tuberculosis Rnap Promoter Unwinding Intermediate Complex with Rbpa/Card and AP3 Promoter
Other atoms:
Mg (1);
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6eea (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 (6);
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6eeb (Zn: 1) - Calmodulin in Complex with Malbrancheamide
Other atoms:
Cl (2);
Ca (4);
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6eec (Zn: 2) - Mycobacterium Tuberculosis Rnap Promoter Unwinding Intermediate Complex with Rbpa/Card and AP3 Promoter Captured By Corallopyronin
Other atoms:
Mg (1);
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6eed (Zn: 1) - X-Ray Crystal Structure of Pf-M1 in Complex with Inhibitor (6P) and Catalytic Zinc Ion
Other atoms:
F (3);
Mg (4);
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6eee (Zn: 12) - X-Ray Crystal Structure of Pf-M17 in Complex with Inhibitor (6K) and Regulatory Zinc Ion
Other atoms:
F (36);
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6eeh (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 (15);
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6eeo (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 (1);
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6efj (Zn: 2) - Crystal Structure of Ndm-1 with Compound 9
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6egl (Zn: 1) - Crystal Structure of A De Novo Three-Stranded Coiled Coil Peptide Containing A D-Leu in the Second Coordination Sphere of A Non- Metalated Tris-Thiolate Binding Site
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6egm (Zn: 1) - Crystal Structure of A De Novo Three-Stranded Coiled Coil Peptide Containing D-Leu in A D-Site Position of A Tris-Thiolate Binding Site
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6egn (Zn: 3) - Crystal Structure of A Three-Stranded Coiled Coil Peptide Containing A Trigonal Planar Hg(II)S3 Site Modified By D-Leu in the Second Coordination Sphere
Other atoms:
Hg (1);
Cl (1);
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6ego (Zn: 1) - Crystal Structure of A De Novo Three-Stranded Coiled Coil Peptide Containing An Ala Residue in the Second Coordination Sphere of the Hg(II)S3 Binding Site
Other atoms:
Hg (1);
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6egp (Zn: 1) - Crystal Structure of A Trigonal Pyramidal Pb(II)S3 Complex in A Three- Stranded Coiled Coil Peptide
Other atoms:
Pb (1);
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6ein (Zn: 1) - Crystal Structure of KDM5B in Complex with S49365A.
Other atoms:
Mn (2);
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6eiu (Zn: 2) - Crystal Structure of KDM5B in Complex with KDOPZ29A
Other atoms:
Mn (2);
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6eiy (Zn: 1) - Crystal Structure of KDM5B in Complex with KDOPZ000034A.
Other atoms:
Mn (2);
Cl (1);
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6ej0 (Zn: 1) - Crystal Structure of KDM5B in Complex with KDOPZ000049A.
Other atoms:
Mn (2);
Page generated: Fri Dec 24 10:31:58 2021
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