Chlorine in PDB, part 297 (files: 11841-11880),
PDB 5eaf-5eic
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: 11841-11880 (PDB 5eaf-5eic).
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5eaf (Cl: 4) - Saccharomyces Cerevisiae CYP51 Complexed with the Plant Pathogen Inhibitor Fluquinconazole
Other atoms:
F (2);
Fe (2);
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5eag (Cl: 3) - Saccharomyces Cerevisiae CYP51 Complexed with the Plant Pathogen Inhibitor Prochloraz
Other atoms:
Fe (1);
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5eah (Cl: 8) - Saccharomyces Cerevisiae CYP51 Complexed with the Plant Pathogen Inhibitor Difenoconazole
Other atoms:
Fe (1);
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5eaj (Cl: 4) - Crystal Structure of Dhfr in 0% Isopropanol
Other atoms:
Ca (1);
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5eal (Cl: 1) - Crystal Structure of Human WDR5 in Complex with Compound 9H
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5eap (Cl: 1) - Crystal Structure of Human WDR5 in Complex with Compound 9E
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5ebd (Cl: 2) - Crystal Structure of ECCB1 of Mycobacterium Tuberculosis in Spacegroup P21 (State IV)
Other atoms:
Ca (1);
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5ebk (Cl: 7) - Trypanothione Reductase in Complex with 6-(Sec-Butoxy)-2-((3- Chlorophenyl)Thio)Pyrimidin-4-Amine
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5ebv (Cl: 2) - Crystal Structure of Acetyltransferase Eis From Mycobacterium Tuberculosis in Complex with Inhibitor 11C and Coa
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5ec4 (Cl: 1) - Crystal Structure of Acetyltransferase Eis From Mycobacterium Tuberculosis in Complex with Inhibitor 13G and Coa
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5ec8 (Cl: 1) - Dengue 3 NS5 Methyltransferase Bound to S-Adenosyl Methionine and Compound BF175
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5ed7 (Cl: 6) - Crystal Structure of Hsv-1 UL21 C-Terminal Domain
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5edb (Cl: 1) - Human Fatty Acid Binding Protein 4 in Complex with 6-Chloro-2-Methyl- 4-Phenyl-Quinoline-3-Carboxylic Acid at 1.18A
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5edc (Cl: 2) - Human FABP4 in Complex with 6-Chloro-4-Phenyl-2-Piperidin-1-Yl- Quinoline-3-Carboxylic Acid at 1.29A
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5ede (Cl: 4) - Human PDE10A in Complex with 1-(4-Chloro-Phenyl)-3-Methyl-1H-Thieno[2, 3-C]Pyrazole-5-Carboxylic Acid (Tetrahydro-Furan-2-Ylmethyl)-Amide at 2.2A
Other atoms:
Mg (4);
Zn (4);
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5edg (Cl: 4) - Human PDE10A in Complex with 3-(2-Chloro-5-Phenyl-3H-Imidazol-4-Yl)-1- (3-Trifluoromethoxy-Phenyl)-1H-Pyridazin-4-One at 2.30A
Other atoms:
F (12);
Mg (4);
Zn (4);
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5edi (Cl: 4) - Human PDE10A, 6-Chloro-5,8-Dimethyl-2-[2-(2-Methyl-5-Pyrrolidin-1-Yl- 2H-[1,2,4]Triazol-3-Yl)-Ethyl]-[1,2,4]Triazolo[1,5-A]Pyridine, 2.20A, H3, Rfree=23.5%
Other atoms:
Mg (4);
Zn (4);
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5edq (Cl: 1) - Egfr Kinase (T790M/L858R) with Inhibitor Compound 15: ~{N}-(7- Chloranyl-1~{H}-Indazol-3-Yl)-7,7-Dimethyl-2-(1~{H}-Pyrazol-4-Yl)- 5~{H}-Furo[3,4-D]Pyrimidin-4-Amine
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5edt (Cl: 1) - Crystal Structure of Mycobacterium Tuberculosis CYP121 in Complex with LIG9
Other atoms:
Fe (1);
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5ee3 (Cl: 6) - Complex Structure of OSYCHF1 with Amp-Pnp
Other atoms:
Mg (2);
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5ee5 (Cl: 7) - Structure of Human ARL1 in Complex with the Dcb Domain of BIG1
Other atoms:
Mg (4);
Na (14);
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5ee7 (Cl: 2) - Crystal Structure of the Human Glucagon Receptor (Gcgr) in Complex with the Antagonist Mk-0893
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5eeh (Cl: 15) - Crystal Structure of Carminomycin-4-O-Methyltransferase Dnrk in Complex with Sah and 2-Chloro-4-Nitrophenol
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5eei (Cl: 5) - Crystal Structure of Danio Rerio Histone Deacetylase 6 Catalytic Domain 2 in Complex with Saha
Other atoms:
Mg (2);
K (4);
Zn (2);
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5eek (Cl: 1) - Crystal Structure of Danio Rerio Histone Deacetylase 6 Catalytic Domain 2 in Complex with Trichostatin A
Other atoms:
K (2);
Zn (1);
I (31);
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5een (Cl: 2) - Crystal Structure of Danio Rerio Histone Deacetylase 6 Catalytic Domain 2 in Complex with Belinostat
Other atoms:
K (4);
Zn (2);
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5efd (Cl: 1) - Crystal Structure of A Surface Pocket Creating Mutant (W6A) of An Alkali Thermostable GH10 Xylanase From Bacillus Sp. Ng-27
Other atoms:
Mg (2);
Na (2);
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5eff (Cl: 1) - Crystal Structure of An Aromatic Mutant (F4A) of An Alkali Thermostable GH10 Xylanase From Bacillus Sp. Ng-27
Other atoms:
Mg (2);
Na (2);
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5egm (Cl: 1) - Development of A Novel Tricyclic Class of Potent and Selective Fixa Inhibitors
Other atoms:
Na (1);
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5egv (Cl: 4) - Crystal Structure of the Er-Alpha Ligand-Binding Domain (Y537S) in Complex the 3,4-Diaryl-Furan Derivative 3-Chloranyl-4-[4-(2- Chloranyl-4-Oxidanyl-Phenyl)Furan-3-Yl]Phenol
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5eh7 (Cl: 2) - Human Carbonic Anhydrase II in Complex with Ligand
Other atoms:
Zn (1);
Na (1);
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5ehc (Cl: 1) - Co-Crystal Structure of EIF4E with Nucleotide Mimetic Inhibitor.
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5ehd (Cl: 4) - Crystal Structure of Human Nucleophosmin-Core in Complex with Cytochrome C
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5ehg (Cl: 1) - Dengue 3 NS5 Methyltransferase Bound to S-Adenosyl Methionine and Molecule BF341
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5ehi (Cl: 1) - Dengue 3 NS5 Methyltransferase Bound to S-Adenosyl Methionine and Molecule BF287
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5ehp (Cl: 4) - Non-Receptor Protein Tyrosine Phosphatase SHP2 in Complex with Allosteric Inhibitor SHP836
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5ehr (Cl: 4) - Non-Receptor Protein Tyrosine Phosphatase SHP2 in Complex with Allosteric Inhibitor SHP099
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5ehw (Cl: 2) - Human Carbonic Anhydrase II in Complex with Ligand
Other atoms:
Zn (1);
Na (1);
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5ei4 (Cl: 1) - First Domain of Human Bromodomain BRD4 in Complex with Inhibitor 8-(5- Amino-1H-[1,2,4]Triazol-3-Ylsulfanylmethyl)-3-(4-Chlorobenzyl)-7- Ethyl-3,7-Dihydropurine-2,6-Dione
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5eic (Cl: 1) - Crystal Structure of the Bromodomain of Human Crebbp in Complex with Ayc
Page generated: Sat Jul 12 01:36:22 2025
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