Fluorine in PDB, part 137 (files: 5441-5480),
PDB 6edl-6evh
Experimental structures of coordination spheres of Fluorine (F) in bioorganic
molecules from X-Ray and NMR experiments. Coordination spheres were calculated with 5.0 Angstroms radius
around Fluorine atoms. PDB files: 5441-5480 (PDB 6edl-6evh).
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6edl (F: 2) - Halk in Complex with Compound 1 (S)-N-(1-(2,4-Difluorophenyl)Ethyl)-3- (3-Methyl-1H-Pyrazol-5-Yl)Imidazo[1,2-B]Pyridazin-6-Amine
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6ee2 (F: 36) - X-Ray Crystal Structure of Pf-M17 in Complex with Inhibitor 6I and Regulatory Zinc Ion
Other atoms:
Zn (12);
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6ee3 (F: 3) - X-Ray Crystal Structure of Pf-M1 in Complex with Inhibitor (6K) and Catalytic Zinc Ion
Other atoms:
Mg (4);
Zn (1);
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6ee4 (F: 3) - X-Ray Crystal Structure of Pf-M1 in Complex with Inhibitor (6M) and Catalytic Zinc Ion
Other atoms:
Mg (5);
Zn (1);
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6ee6 (F: 3) - X-Ray Crystal Structure of Pf-M1 in Complex with Inhibitor (6O) and Catalytic Zinc Ion
Other atoms:
Mg (3);
Zn (1);
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6eea (F: 6) - Bioreductive 4-Hydroxy-3-Nitro-5-Ureido-Benzenesulfonamides Selectively Target the Tumor-Associated Carbonic Anhydrase Isoforms IX and XII and Show Hypoxia-Enhanced Cytotoxicity Against Human Cancer Cell Lines.
Other atoms:
Zn (1);
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6eed (F: 3) - X-Ray Crystal Structure of Pf-M1 in Complex with Inhibitor (6P) and Catalytic Zinc Ion
Other atoms:
Mg (4);
Zn (1);
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6eee (F: 36) - X-Ray Crystal Structure of Pf-M17 in Complex with Inhibitor (6K) and Regulatory Zinc Ion
Other atoms:
Zn (12);
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6eeh (F: 15) - Bioreductive 4-Hydroxy-3-Nitro-5-Ureido-Benzenesulfonamides Selectively Target the Tumor-Associated Carbonic Anhydrase Isoforms IX and XII and Show Hypoxia-Enhanced Cytotoxicity Against Human Cancer Cell Lines.
Other atoms:
Zn (1);
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6eeo (F: 1) - Bioreductive 4-Hydroxy-3-Nitro-5-Ureido-Benzenesulfonamides Selectively Target the Tumor-Associated Carbonic Anhydrase Isoforms IX and XII and Show Hypoxia-Enhanced Cytotoxicity Against Human Cancer Cell Lines.
Other atoms:
Zn (1);
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6eg9 (F: 6) - IRAK4 in Complex with Ponatinib
Other atoms:
Co (4);
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6ega (F: 6) - IRAK4 in Complex with A Type II Inhibitor
Other atoms:
Co (6);
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6ehu (F: 18) - The Crystal Structure of CK2ALPHA in Complex with Compound 32
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6ei4 (F: 2) - Crystal Structure of Tyrosinase From Bacillus Megaterium with B5N Inhibitor in the Active Site
Other atoms:
Cu (4);
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6eim (F: 8) - Human STK10 Bound to GW683134A
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6eis (F: 16) - DYRK1A in Complex with Jwc-055
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6ekh (F: 3) - Crystal Structure of Activated Chey From Methanoccocus Maripaludis
Other atoms:
Mg (1);
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6el5 (F: 1) - Estimation of Relative Drug-Target Residence Times By Random Acceleration Molecular Dynamics Simulation
Other atoms:
Cl (1);
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6el6 (F: 1) - Glucocorticoid Receptor in Complex with Compound 4
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6el7 (F: 2) - Glucocorticoid Receptor in Complex with Compound 31
Other atoms:
Br (1);
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6el9 (F: 2) - Glucocorticoid Receptor in Complex with AZD9567
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6elo (F: 1) - Estimation of Relative Drug-Target Residence Times By Random Acceleration Molecular Dynamics Simulation
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6eog (F: 6) - Human Galectin-3C in Complex with A Galactose Derivative
Other atoms:
Cl (6);
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6eol (F: 3) - Human Galectin-3C in Complex with A Galactose Derivative
Other atoms:
Cl (2);
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6eor (F: 8) - DPP9 - 1G244
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6epr (F: 2) - The ATAD2 Bromodomain in Complex with Compound Uzh-DS15
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6eq4 (F: 2) - MTH1 in Complex with Fragment 8
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6eq7 (F: 2) - MTH1 in Complex with Fragment 11
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6eqm (F: 7) - Crystal Structure of Human Bace-1 in Complex with CNP520
Other atoms:
Cl (1);
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6es0 (F: 4) - Crystal Structure of the Kinase Domain of Human RIPK2 in Complex with the Activation Loop Targeting Inhibitor Cs-R35
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6esn (F: 1) - Ligand Complex of Rorg Lbd
Other atoms:
Na (1);
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6et4 (F: 1) - Human Dihydroorotate Dehydrogenase in Complex with Novel Inhibitor
Other atoms:
Cl (3);
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6etj (F: 1) - Human PFKFB3 in Complex with KAN0438241
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6eum (F: 3) - Crystal Structure of Bcii Metallo-Beta-Lactamase in Complex with Dz- 307
Other atoms:
Zn (2);
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6euv (F: 16) - Structure of the Midlink and Cap-Binding Domains of Influenza A Polymerase PB2 Subunit with A Bound Azaindole Cap-Binding Inhibitor (Vx-787)
Other atoms:
Ni (4);
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6euw (F: 2) - Crystal Structure of the Cap-Binding Domain of the PB2 Subunit of Influenza A/H5N1 Polymerase Bound to An Azaindazole Inhibitor
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6eux (F: 2) - Structure of the Midlink and Cap-Binding Domains of Influenza B Polymerase PB2 Subunit with A Bound Azaindazole Cap-Binding Inhibitor
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6euy (F: 6) - Structure of the Midlink and Cap-Binding Domains of Influenza A Polymerase PB2 Subunit with A Bound Azaindazole Cap-Binding Inhibitor
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6evc (F: 5) - Structure of E282Q A. Niger FDC1 in Complex with Pentafluoro-Cinnamic Acid
Other atoms:
K (2);
Mn (1);
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6evh (F: 1) - Lipoaminopeptide Helioferin A and B From Mycogone Rosea
Other atoms:
Cl (1);
Page generated: Fri May 13 23:18:49 2022
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