Zinc in PDB, part 127 (files: 5041-5080),
PDB 3d7v-3dgm
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: 5041-5080 (PDB 3d7v-3dgm).
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3d7v (Zn: 4) - Crystal Structure of Mcl-1 in Complex with An Mcl-1 Selective BH3 Ligand
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3d81 (Zn: 1) - SIR2-S-Alkylamidate Complex Crystal Structure
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3d8c (Zn: 1) - Factor Inhibiting Hif-1 Alpha D201G Mutant in Complex with Zn(II), Alpha-Ketoglutarate and Hif-1 Alpha 19MER
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3d8w (Zn: 1) - Use of A Carbonic Anhydrase II, IX Active-Site Mimic, For the Purpose of Screening Inhibitors For Possible Anti- Cancer Properties
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3d92 (Zn: 1) - Human Carbonic Anhydrase II Bound with Substrate Carbon Dioxide
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3d9t (Zn: 2) - CIAP1-BIR3 in Complex with N-Terminal Peptide From Caspase- 9 (Atpfqe)
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3d9u (Zn: 1) - The BIR3 Domain of CIAP1 in Complex with the N Terminal Peptide From Smac/Diablo (Avpiaq).
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3d9z (Zn: 1) - Use of Carbonic Anhydrase II, IX Active-Site Mimic, For the Purpose of Screening Inhibitors For Possible Anti-Cancer Properties
Other atoms:
Cl (1);
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3da2 (Zn: 2) - X-Ray Structure of Human Carbonic Anhydrase 13 in Complex with Inhibitor
Other atoms:
Cl (4);
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3daz (Zn: 1) - Use of Carbonic Anhydrase II, IX Active-Site Mimic, For the Purpose of Screening Inhibitors For Possible Anti-Cancer Properties
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3dbh (Zn: 4) - Structural Dissection of A Gating Mechanism Preventing Misactivation of Ubiquitin By NEDD8'S E1 (APPBP1- UBA3ARG190ALA-NEDD8ALA72ARG)
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3dbk (Zn: 1) - Pseudomonas Aeruginosa Elastase with Phosphoramidon
Other atoms:
Ca (1);
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3dbl (Zn: 4) - Structural Dissection of A Gating Mechanism Preventing Misactivation of Ubiquitin By NEDD8'S E1 (APPBP1- UBA3ARG190WT-NEDD8ALA72GLN)
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3dbr (Zn: 4) - Structural Dissection of A Gating Mechanism Preventing Misactivation of Ubiquitin By NEDD8'S E1 (APPBP1- UBA3ARG190GLN-NEDD8ALA72ARG)
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3dbu (Zn: 1) - Use of Carbonic Anhydrase II, IX Active-Site Mimic, For the Purpose of Screening Inhibitors For Possible Anti-Cancer Properties
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3dc3 (Zn: 1) - Use of Carbonic Anhydrase II, IX Active-Site Mimic, For the Purpose of Screening Inhibitors For Possible Anti-Cancer Properties
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3dc8 (Zn: 4) - Crystal Structure of Dihydropyrimidinase From Sinorhizobium Meliloti
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3dc9 (Zn: 1) - Use of Carbonic Anhydrase II, IX Active-Site Mimic, For the Purpose of Screening Inhibitors For Possible Anti-Cancer Properties
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3dcc (Zn: 1) - Use of Carbonic Anhydrase II, IX Active-Site Mimic, For the Purpose of Screening Inhibitors For Possible Anti-Cancer Properties
Other atoms:
Cl (1);
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3dci (Zn: 1) - The Structure of A Putative Arylesterase From Agrobacterium Tumefaciens Str. C58
Other atoms:
Cl (22);
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3dco (Zn: 1) - Drosophila Nod (3DC4) and Bovine Tubulin (1JFF) Docked Into the 11-Angstrom Cryo-Em Map of Nucleotide-Free Nod Complexed to the Microtubule
Other atoms:
Mg (2);
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3dcp (Zn: 3) - Crystal Structure of the Putative Histidinol Phosphatase Hisk From Listeria Monocytogenes. Northeast Structural Genomics Consortium Target LMR141.
Other atoms:
Fe (6);
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3dcs (Zn: 1) - Use of Carbonic Anhydrase II, IX Active-Site Mimic, For the Purpose of Screening Inhibitors For Possible Anti-Cancer Properties
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3dcw (Zn: 1) - Use of Carbonic Anhydrase II, IX Active-Site Mimic, For the Purpose of Screening Inhibitors For Possible Anti-Cancer Properties
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3dd0 (Zn: 1) - Use of Carbonic Anhydrase II, IX Active-Site Mimic, For the Purpose of Screening Inhibitors For Possible Anti-Cancer Properties
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3dd8 (Zn: 1) - Carbonic Anhydrase Inhibitors. Interaction of the Antitumor Sulfamate Emd-486019 with Twelve Mammalian Isoforms: Kinetic and X-Ray Crystallographic Studies
Other atoms:
Hg (1);
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3dda (Zn: 1) - Crystal Structure of the Catalytic Domain of Botulinum Neurotoxin Serotype A with A Snap-25 Peptide
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3ddb (Zn: 1) - Crystal Structure of the Catalytic Domain of Botulinum Neurotoxin Serotype A with A Substrate Analog Peptide
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3ddf (Zn: 1) - Golgi Mannosidase II Complex with (3R,4R,5R)-3,4-Dihydroxy- 5-({[(1R)-2-Hydroxy-1 Phenylethyl]Amino}Methyl) Pyrrolidin- 2-One
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3ddg (Zn: 1) - Golgi Mannosidase II Complex with (3R,4R,5R)-3,4-Dihydroxy- 5-({[(1R)-2-Hydroxy-1 Phenylethyl]Amino}Methyl) Methylpyrrolidin-2-One
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3ddt (Zn: 6) - Crystal Structure of the B2 Box From MURF1 in Dimeric State
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3dff (Zn: 1) - The Crystal Structure of Teicoplanin Pseudoaglycone Deacetylase ORF2
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3dfi (Zn: 1) - The Crystal Structure of Antimicrobial Reagent A40926 Pseudoaglycone Deacetylase DBV21
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3dfk (Zn: 1) - The Crystal Structure of Teicoplanin Pseudoaglycone Deacetylase ORF2* Bound to One of Its Products Decanoic Acid
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3dfm (Zn: 5) - The Crystal Structure of the Zinc Inhibited Form of Teicoplanin Deacetylase ORF2
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3dfv (Zn: 2) - Adjacent Gata Dna Binding
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3dfx (Zn: 2) - Opposite Gata Dna Binding
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3dgd (Zn: 15) - Crystal Structure of the F87M/L110M Mutant of Human Transthyretin at pH 4.6
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3dgl (Zn: 1) - 1.8 A Crystal Structure of A Non-Biological Protein with Bound Atp in A Novel Bent Conformation
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3dgm (Zn: 1) - 2.4 A Structure of A Non-Biological Atp Binding Protein with Adp Bound
Page generated: Sat Feb 15 18:12:55 2025
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