Chlorine in PDB, part 403 (files: 16081-16120),
PDB 6g5l-6gak
Experimental structures of coordination spheres of Chlorine (Cl) in bioorganic
molecules from X-Ray and NMR experiments. Coordination spheres were calculated with 5.0 Angstroms radius
around Chlorine atoms. PDB files: 16081-16120 (PDB 6g5l-6gak).
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6g5l (Cl: 6) - Crystal Structure of Human Carbonic Anhydrase Isozyme XII with 4- Chloro-2-(Cyclohexylamino)-N-(2-Hydroxyethyl)-5-Sulfamoyl-Benzamide
Other atoms:
Zn (4);
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6g5n (Cl: 1) - Crystal Structure of Human SP100 in Complex with Bromodomain-Focused Fragment XS039818E 1-(3-Phenyl-1,2,4-Oxadiazol-5-Yl)Methanamine
Other atoms:
Zn (4);
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6g5p (Cl: 1) - Crystal Structure of Human SP100 in Complex with Bromodomain-Focused Fragment FM009493B 2,3-Dimethoxy-2,3-Dimethyl-2,3-Dihydro-1,4- Benzodioxin-6-Amine
Other atoms:
Zn (4);
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6g5u (Cl: 4) - Crystal Structure of Human Carbonic Anhydrase Isozyme XIII with N- Butyl-2,4-Dichloro-5-Sulfamoyl-Benzamide
Other atoms:
Zn (2);
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6g5v (Cl: 1) - The X-Ray Structure of the Adduct Formed in the Reaction Between Lysozyme and A Platinum(II) Terpyridine Compound (pH 7.0)
Other atoms:
Pt (6);
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6g6k (Cl: 2) - The Crystal Structures of Human Myc:Max Bhlhzip Complex
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6g6t (Cl: 2) - Crystal Structure of Human Carbonic Anhydrase Isozyme II with N-Butyl- 2,4-Dichloro-5-Sulfamoyl-Benzamide
Other atoms:
Zn (1);
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6g6x (Cl: 4) - 14-3-3SIGMA in Complex with A P129BETA3P Mutated Yap PS127 Phosphopeptide
Other atoms:
Na (2);
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6g7a (Cl: 5) - Crystal Structure of Human Carbonic Anhydrase Isozyme XII 2- (Benzylamino)-4-Chloro-N-(2-Hydroxyethyl)-5-Sulfamoyl-Benzamide
Other atoms:
Zn (4);
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6g7d (Cl: 1) - Structure of MET1 From Mycobacterium Hassiacum in Complex with Sam and Glycerol.
Other atoms:
Mg (2);
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6g7f (Cl: 2) - Yeast 20S Proteasome in Complex with Cystargolide B
Other atoms:
Mg (8);
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6g7p (Cl: 2) - Trichodesmium TERY_3377 (Idia) (Futa) with Iron and Water Ligands.
Other atoms:
Fe (2);
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6g7q (Cl: 2) - Trichodesmium TERY_3377 (Idia) (Futa) in Complex with Iron and Citrate Ligands.
Other atoms:
Fe (1);
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6g7r (Cl: 4) - Structure of Fully Reduced Variant E28Q of E. Coli Hydrogenase-1 at pH 8
Other atoms:
Ni (2);
Mg (2);
Fe (24);
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6g8a (Cl: 17) - Lysozyme Solved By Native Sad From A Dataset Collected in 5 Seconds at 1 A Wavelength with Jungfrau Detector
Other atoms:
Na (1);
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6g8f (Cl: 1) - Crystal Structure of Utx Complexed with Gsk-J1
Other atoms:
Mn (1);
Zn (1);
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6g8i (Cl: 1) - 14-3-3SIGMA in Complex with A R124BETA3R Mutated Yap PS127 Phosphopeptide
Other atoms:
Mg (1);
Na (2);
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6g8j (Cl: 1) - 14-3-3SIGMA in Complex with A A130BETA3A Mutated Yap PS127 Phosphopeptide
Other atoms:
Mg (1);
Na (1);
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6g8k (Cl: 2) - 14-3-3SIGMA in Complex with A S131BETA3S Mutated Yap PS127 Phosphopeptide
Other atoms:
Mg (1);
Na (1);
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6g8l (Cl: 1) - 14-3-3SIGMA in Complex with A L132BETA3L Mutated Yap PS127 Phosphopeptide
Other atoms:
Mg (1);
Na (1);
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6g8m (Cl: 2) - Yeast 20S Proteasome in Complex with Cystargolide B Derivative 1
Other atoms:
Mg (8);
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6g8n (Cl: 2) - Yeast 20S Proteasome in Complex with Cystargolide B Derivative 2
Other atoms:
Mg (8);
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6g8p (Cl: 1) - 14-3-3SIGMA in Complex with A P129BETA3P and L132BETA3L Mutated Yap PS127 Phosphopeptide
Other atoms:
Ca (2);
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6g8q (Cl: 2) - 14-3-3SIGMA in Complex with A A130BETA3A and Q133BETA3Q Mutated Yap PS127 Phosphopeptide
Other atoms:
Ca (1);
Na (3);
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6g8x (Cl: 2) - Fragment-Based Discovery of A Highly Potent, Orally Bioavailable Inhibitor Which Modulates the Phosphorylation and Catalytic Activity of ERK1/2
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6g8y (Cl: 1) - Crystal Structures of the Single Pdz Domains From GRASP65 and Their Interaction with the Golgin GM130
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6g91 (Cl: 1) - Fragment-Based Discovery of A Highly Potent, Orally Bioavailable Inhibitor Which Modulates the Phosphorylation and Catalytic Activity of ERK1/2
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6g93 (Cl: 1) - Fragment-Based Discovery of A Highly Potent, Orally Bioavailable Inhibitor Which Modulates the Phosphorylation and Catalytic Activity of ERK1/2
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6g94 (Cl: 4) - Structure of E. Coli Hydrogenase-1 C19G Variant in Complex with Cytochrome B
Other atoms:
Ni (4);
Mg (4);
Fe (50);
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6g97 (Cl: 1) - Fragment-Based Discovery of A Highly Potent, Orally Bioavailable Inhibitor Which Modulates the Phosphorylation and Catalytic Activity of ERK1/2
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6g9a (Cl: 1) - Fragment-Based Discovery of A Highly Potent, Orally Bioavailable Inhibitor Which Modulates the Phosphorylation and Catalytic Activity of ERK1/2
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6g9d (Cl: 1) - Fragment-Based Discovery of A Highly Potent, Orally Bioavailable Inhibitor Which Modulates the Phosphorylation and Catalytic Activity of ERK1/2
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6g9h (Cl: 1) - Fragment-Based Discovery of A Highly Potent, Orally Bioavailable Inhibitor Which Modulates the Phosphorylation and Catalytic Activity of ERK1/2
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6g9i (Cl: 1) - Crystal Structure of Ebolavirus Glycoprotein in Complex with Clomipramine
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6g9j (Cl: 1) - Fragment-Based Discovery of A Highly Potent, Orally Bioavailable Inhibitor Which Modulates the Phosphorylation and Catalytic Activity of ERK1/2
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6g9k (Cl: 1) - Fragment-Based Discovery of A Highly Potent, Orally Bioavailable Inhibitor Which Modulates the Phosphorylation and Catalytic Activity of ERK1/2
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6g9m (Cl: 1) - Fragment-Based Discovery of A Highly Potent, Orally Bioavailable Inhibitor Which Modulates the Phosphorylation and Catalytic Activity of ERK1/2
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6g9n (Cl: 1) - Fragment-Based Discovery of A Highly Potent, Orally Bioavailable Inhibitor Which Modulates the Phosphorylation and Catalytic Activity of ERK1/2
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6gaj (Cl: 4) - Crystal Structure of the T1L Reovirus SIGMA1 Coiled Coil Tail (Iodide)
Other atoms:
I (3);
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6gak (Cl: 2) - Crystal Structure of the T1L Reovirus SIGMA1 Coiled Coil Tail (Chloride)
Page generated: Wed Nov 4 04:04:26 2020
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