Chlorine in PDB, part 396 (files: 15801-15840),
PDB 6dtp-6e23
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: 15801-15840 (PDB 6dtp-6e23).
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6dtp (Cl: 1) - Crystal Structure of Human 17BETA-Hydroxysteroid Dehydrogenase Type 1 Complexed with EM139
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6du9 (Cl: 1) - Crystal Structure of Human Prion Protein 90-231
Other atoms:
Cd (3);
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6duc (Cl: 11) - Crystal Structure of Mutant Beta-K167T Tryptophan Synthase in Complex with Inhibitor N-(4'-Trifluoromethoxybenzenesulfonyl)-2-Amino-1- Ethylphosphate (F9F) at the Alpha-Site, Cesium Ion at the Metal Coordination Site, and 2-Aminophenol Quinonoid (1D0) at the Beta-Site
Other atoms:
F (3);
Cs (4);
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6dui (Cl: 1) - Crystal Structure of Lpxc From Pseudomonas Aeruginosa in Complex with PT801
Other atoms:
Zn (1);
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6dum (Cl: 7) - ALDH1A1 N121S in Complex with 6-{[(3-Fluorophenyl)Methyl]Sulfanyl}-2- (Oxetan-3-Yl)-5-Phenyl-2,5-Dihydro-4H-Pyrazolo[3,4-D]Pyrimidin-4-One (Compound 13G)
Other atoms:
F (1);
Yb (2);
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6duv (Cl: 3) - Crystal Structure of the Second Bromodomain of Human BRD4 in Complex with MS417 Inhibitor
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6dux (Cl: 5) - 2.25 Angstrom Resolution Crystal Structure of 6-Phospho-Alpha- Glucosidase From Klebsiella Pneumoniae in Complex with Nad.
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6dv0 (Cl: 2) - Hiv-1 Wild Type Protease with Grl-02815A, A Thiochroman Heterocycle with (S)-Boc-Amine Functionality As the P2 Ligand
Other atoms:
Na (1);
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6dv4 (Cl: 2) - Hiv-1 Wild Type Protease with Grl-04315A, A Tetrahydronaphthalene Carboxamide with (R)-Boc-Amine and (S)-Hydroxyl Functionalities As the P2 Ligand
Other atoms:
Na (1);
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6dvv (Cl: 2) - 2.25 Angstrom Resolution Crystal Structure of 6-Phospho-Alpha- Glucosidase From Klebsiella Pneumoniae in Complex with Nad and MN2+.
Other atoms:
Mn (2);
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6dwh (Cl: 2) - Crystal Structure of Complex of Bbki and Bovine Trypsin
Other atoms:
Na (8);
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6dwi (Cl: 6) - Structure of the 4462 Antibody Fab Fragment Bound to A Staphylococcus Aureus Wall Techoic Acid Analog
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6dws (Cl: 2) - Crystal Structure of Human GRP78 in Complex with (2R,3R,4S,5R)-2-(6- Amino-8-((2-Chlorobenzyl)Amino)-9H-Purin-9-Yl)-5-(Hydroxymethyl) Tetrahydrofuran-3,4-Diol
Other atoms:
Mg (2);
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6dxw (Cl: 28) - Human N-Acylethanolamine-Hydrolyzing Acid Amidase (Naaa) Precursor (C126A)
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6dxx (Cl: 12) - Human N-Acylethanolamine-Hydrolyzing Acid Amidase (Naaa) in Complex with Non-Covalent Benzothiazole-Piperazine Inhibitor ARN19702, in Presence of Triton X-100
Other atoms:
F (3);
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6dxy (Cl: 11) - Murine N-Acylethanolamine-Hydrolyzing Acid Amidase (Naaa)
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6dy0 (Cl: 12) - Rabbit N-Acylethanolamine-Hydrolyzing Acid Amidase (Naaa) Covalently Bound to Beta-Lactam Inhibitor ARN726, in Presence of Triton X-100
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6dy1 (Cl: 12) - Rabbit N-Acylethanolamine-Hydrolyzing Acid Amidase (Naaa) with Fatty Acid (Myristate), in Presence of Triton X-100
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6dy2 (Cl: 11) - Guinea Pig N-Acylethanolamine-Hydrolyzing Acid Amidase (Naaa) Covalently Bound to Beta-Lactam Inhibitor ARN726
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6dy7 (Cl: 2) - WDR5 in Complex with A Win Site Inhibitor
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6dya (Cl: 2) - WDR5 in Complex with A Win Site Inhibitor
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6dyf (Cl: 1) - Cu(II)-Bound Structure of the Engineered Cyt CB562 Variant, CH3Y
Other atoms:
Fe (2);
Cu (1);
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6dyi (Cl: 1) - Co(II)-Bound Structure of the Engineered Cyt CB562 Variant, H3
Other atoms:
Co (1);
Fe (1);
Ca (6);
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6dyz (Cl: 2) - Crystal Structure of Human 5'-Deoxy-5'-Methylthioadenosine Phosphorylase in Complex with (3R,4S)-1-((4-Amino-5H-Pyrrolo[3,2- D]Pyrimidin-7-Yl)Methyl)-4-((Prop-2-Yn-1-Ylthio)Methyl)Pyrrolidin-3- Ol
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6dz0 (Cl: 1) - Crystal Structure of Human 5'-Deoxy-5'-Methylthioadenosine Phosphorylase in Complex with (3R,4S)-1-((4-Amino-5H-Pyrrolo[3,2- D]Pyrimidin-7-Yl)Methyl)-4-((Pent-4-Yn-1-Ylthio)Methyl)Pyrrolidin-3- Ol
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6dz2 (Cl: 4) - Crystal Structure of Human 5'-Deoxy-5'-Methylthioadenosine Phosphorylase in Complex with (3R,4S)-1-((4-Amino-5H-Pyrrolo[3,2- D]Pyrimidin-7-Yl)Methyl)-4-(((3-(1-Benzyl-1H-1,2,3-Triazol-4-Yl) Propyl)Thio)Methyl)Pyrrolidin-3-Ol
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6dz3 (Cl: 5) - Crystal Structure of Human 5'-Deoxy-5'-Methylthioadenosine Phosphorylase in Complex with (3R,4S)-1-((4-Amino-5H-Pyrrolo[3,2- D]Pyrimidin-7-Yl)Methyl)-4-(((3-(1-Butyl-1H-1,2,3-Triazol-4-Yl) Propyl)Thio)Methyl)Pyrrolidin-3-Ol
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6dz4 (Cl: 8) - Crystal Structure of Salmonella Typhimurium Tryptophan Synthase with Sodium Ion at the Metal Coordination Site and [3-Hydroxy-2-Methyl-5- Phosphonooxymethyl-Pyridin-4-Ylmethyl]-Serine (Pls) at the Beta-Site.
Other atoms:
Na (2);
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6dzd (Cl: 1) - Crystal Structure of Bacillus Licheniformis Hypothetical Protein Yfih
Other atoms:
K (1);
Zn (2);
Na (1);
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6dzn (Cl: 6) - Pan-Ebolavirus Human Antibody Adi-15878 Fab
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6dzo (Cl: 13) - Crystal Structure of Salmonella Typhimurium Tryptophan Synthase Mutant Beta-Q114A with 2-({[4-(Trifluoromethoxy)Phenyl]Sulfonyl}Amino)Ethyl Dihydrogen Phosphate (F9F) at the Alpha-Site, Cesium Ion at the Metal Coordination Site, and [3-Hydroxy-2-Methyl-5-Phosphonooxymethyl- Pyridin-4-Ylmethyl]-Serine (Pls) at the Beta-Site.
Other atoms:
F (3);
Cs (4);
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6e03 (Cl: 1) - Sperm Whale Myoglobin Nitrosoethane Adduct
Other atoms:
Fe (1);
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6e0a (Cl: 1) - Crystal Structure of Helicobacter Pylori Tlpa Chemoreceptor Ligand Binding Domain
Other atoms:
Ca (1);
Zn (9);
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6e0v (Cl: 9) - Apo Crystal Structure of the Colanidase Tailspike Protein GP150 of Phage PHI92
Other atoms:
Sr (24);
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6e12 (Cl: 1) - Crystal Structure of the ALR8543 Protein in Complex with Oleic Acid and Magnesium Ion From Nostoc Sp. Pcc 7120, Northeast Structural Genomics Consortium Target NSR141
Other atoms:
Mg (2);
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6e13 (Cl: 1) - 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:
Zn (2);
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6e1q (Cl: 4) - ATGH3.15 Acyl Acid Amido Synthetase in Complex with 2,4-Db
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6e1r (Cl: 3) - Crystal Structure of the Acinetobacter Phage VB_APIP_P1 Tailspike Protein
Other atoms:
Na (3);
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6e1y (Cl: 2) - Discovery of Potent 2-Aryl-6,7-Dihydro-5HPYRROLO[ 1,2-A]Imidazoles As WDR5 Win-Site Inhibitors Using Fragment-Based Methods and Structure- Based Design
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6e23 (Cl: 4) - Displacement of WDR5 From Chromatin By A Pharmacological Win Site Inhibitor with Picomolar Affinity
Other atoms:
F (2);
Page generated: Fri May 13 21:46:45 2022
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