Chlorine in PDB, part 192 (files: 7641-7680),
PDB 4c0n-4c8d
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: 7641-7680 (PDB 4c0n-4c8d).
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4c0n (Cl: 1) - Crystal Structure of Non Symbiotic Plant Hemoglobin AHB3 (GLB3) From Arabidopsis Thaliana
Other atoms:
Fe (1);
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4c0r (Cl: 6) - Molecular and Structural Basis of Glutathione Import in Gram-Positive Bacteria Via Gsht and the Cystine Abc Importer Tcybc of Streptococcus Mutans.
Other atoms:
Cd (40);
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4c0z (Cl: 14) - The N-Terminal Domain of the Streptococcus Pyogenes Pilus Tip Adhesin Cpa
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4c10 (Cl: 1) - Cryo-Em Reconstruction of Empty Enterovirus 71 in Complex with A Neutralizing Antibody E19
Other atoms:
Na (6);
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4c13 (Cl: 1) - X-Ray Crystal Structure of Staphylococcus Aureus Mure with Udp-Murnac-Ala-Glu-Lys
Other atoms:
Mg (2);
K (1);
-
4c1k (Cl: 2) - Crystal Structure of Pyrococcus Furiosus 3-Deoxy-D-Arabino- Heptulosonate 7-Phosphate Synthase
Other atoms:
Cd (6);
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4c1l (Cl: 4) - Crystal Structure of Pyrococcus Furiosus 3-Deoxy-D-Arabino- Heptulosonate 7-Phosphate Synthase I181D Interface Mutant
Other atoms:
K (2);
Mn (2);
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4c1m (Cl: 2) - Myeloperoxidase in Complex with the Revesible Inhibitor HX1
Other atoms:
F (12);
Fe (2);
Ca (2);
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4c27 (Cl: 1) - Crystal Structure of Trypanosoma Cruzi CYP51 Bound to the Inhibitor (R)-N-(3-(1H-Indol-3-Yl)-1-Oxo-1-(Pyridin-4- 4-Ylamino)Propan-2-Yl)-2-Fluoro-4-(4-(4-(Trifluoromethyl) Phenyl)Piperazin-1-Yl)Benzamide
Other atoms:
F (12);
Fe (2);
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4c28 (Cl: 5) - Crystal Structure of Trypanosoma Cruzi CYP51 Bound to the Inhibitor (R)-N-(3-(1H-Indol-3-Yl)-1-Oxo-1-(Pyridin-4- Ylamino)Propan-2-Yl)-4-(4-(4-Chlorophenyl)Piperazin-1-Yl)- 2-Fluorobenzamide.
Other atoms:
F (4);
Fe (2);
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4c2n (Cl: 2) - Crystal Structure of Human Testis Angiotensin-I Converting Enzyme Mutant E403R
Other atoms:
Zn (1);
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4c2o (Cl: 2) - Crystal Structure of Human Testis Angiotensin-I Converting Enzyme Mutant D465T
Other atoms:
Zn (1);
-
4c2p (Cl: 2) - Crystal Structure of Human Testis Angiotensin-I Converting Enzyme Mutant R522K in Complex with Captopril
Other atoms:
Zn (1);
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4c2q (Cl: 1) - Crystal Structure of Human Testis Angiotensin-I Converting Enzyme Mutant R522K
Other atoms:
Zn (1);
-
4c2r (Cl: 1) - Crystal Structure of Human Testis Angiotensin-I Converting Enzyme Mutant R522Q
Other atoms:
Zn (1);
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4c2z (Cl: 12) - Human N-Myristoyltransferase (NMT1) with Myristoyl-Coa and Inhibitor Bound
Other atoms:
Mg (2);
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4c3l (Cl: 1) - Structure of Wildtype Pii From S. Elongatus at High Resolution
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4c3o (Cl: 6) - Structure and Function of An Oxygen Tolerant Nife Hydrogenase From Salmonella
Other atoms:
Ni (3);
Mg (3);
Fe (36);
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4c3t (Cl: 2) - The Carbonic Anhydrase From Thermovibrio Ammonificans Reveals An Interesting Intermolecular Disulfide Contributing to Increasing Thermal Stability of This Enzyme
Other atoms:
Zn (2);
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4c3u (Cl: 6) - Extensive Counter-Ion Interactions with Subtilisin in Aqueous Medium, Cs Derivative
Other atoms:
Cs (10);
Ca (1);
Na (1);
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4c3w (Cl: 2) - Vanadium(IV)-Picolinate Complexed with Lysozyme
Other atoms:
V (1);
Na (1);
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4c3x (Cl: 8) - Crystal Structure of 3-Ketosteroid DELTA1-Dehydrogenase From Rhodococcus Erythropolis SQ1
Other atoms:
Na (4);
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4c4g (Cl: 1) - Structure-Based Design of Orally Bioavailable Pyrrolopyridine Inhibitors of the Mitotic Kinase MPS1
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4c4h (Cl: 1) - Structure-Based Design of Orally Bioavailable Pyrrolopyridine Inhibitors of the Mitotic Kinase MPS1
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4c4i (Cl: 1) - Structure-Based Design of Orally Bioavailable Pyrrolopyridine Inhibitors of the Mitotic Kinase MPS1
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4c4j (Cl: 1) - Structure-Based Design of Orally Bioavailable Pyrrolopyridine Inhibitors of the Mitotic Kinase MPS1
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4c4n (Cl: 1) - Crystal Structure of the Sonic Hedgehog-Heparin Complex
Other atoms:
Ca (4);
Zn (2);
-
4c4x (Cl: 8) - Crystal Structure of Human Bifunctional Epoxide Hydroxylase 2 Complexed with C9
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4c4y (Cl: 1) - Crystal Structure of Human Bifunctional Epoxide Hydroxylase 2 Complexed with A4
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4c66 (Cl: 1) - Discovery of Epigenetic Regulator I-BET762: Lead Optimization to Afford A Clinical Candidate Inhibitor of the Bet Bromodomains
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4c68 (Cl: 5) - Plasmodium Vivax N-Myristoyltransferase in Complex with A Peptidomimetic Inhibitor
Other atoms:
Mg (3);
-
4c6h (Cl: 1) - Haloalkane Dehalogenase with 1-Hexanol
-
4c6u (Cl: 1) - Crystal Structure of M. Tuberculosis Kasa in Complex with TLM5
Other atoms:
K (1);
-
4c6y (Cl: 1) - Ancestral Pnca (Last Common Ancestors of Gram-Positive and Gram-Negative Bacteria) Beta-Lactamase Class A
Other atoms:
Na (2);
-
4c7r (Cl: 5) - Inward Facing Conformation of the Trimeric Betaine Transporter Betp in Complex with Lipids
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4c7y (Cl: 2) - Aldehyde Oxidoreductase From Desulfovibrio Gigas (Mop), Soaked with Sodium Dithionite and Sodium Sulfide
Other atoms:
Mo (1);
Mg (3);
Fe (4);
-
4c7z (Cl: 2) - Aldehyde Oxidoreductase From Desulfovibrio Gigas (Mop), Activated with Sodium Dithionite and Sodium Sulfide
Other atoms:
Mo (1);
Mg (3);
Fe (4);
-
4c80 (Cl: 3) - Aldehyde Oxidoreductase From Desulfovibrio Gigas (Mop), Soaked with Hydrogen Peroxide
Other atoms:
Mo (1);
Mg (3);
Fe (4);
Na (2);
-
4c81 (Cl: 3) - Ispf (Plasmodium Falciparum) Cdp Complex
Other atoms:
Zn (2);
-
4c8d (Cl: 1) - Crystal Structure of Jmjc Domain of Human Histone 3 Lysine- Specific Demethylase 3B (KDM3B)
Other atoms:
Mn (1);
Page generated: Sat Feb 15 16:34:55 2025
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