Fluorine in PDB, part 140 (files: 5561-5600),
PDB 6e69-6elo
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: 5561-5600 (PDB 6e69-6elo).
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6e69 (F: 4) - Ortho-Substituted Phenyl Sulfonyl Fluoride and Fluorosulfate As Potent Elastase Inhibitory Fragments
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6e6j (F: 6) - BRD2_BROMODOMAIN2 Complex with Inhibitor 744
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6e70 (F: 4) - Structure of Wild Type Human Transthyretin in Complex with Diflunisal
Other atoms:
Ca (2);
-
6e73 (F: 4) - Structure of Human Transthyretin VAL30MET Mutant in Complex with Diflunisal
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6e78 (F: 4) - Structure of Human Transthyretin ASP38ALA Mutant in Complex with Diflunisal
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6e8q (F: 2) - S. Cerevisiae CYP51 Complexed with Posaconazole
Other atoms:
Fe (1);
-
6e9p (F: 12) - Crystal Structure of Tryptophan Synthase From M. Tuberculosis - Open Form with BRD0059 Bound
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6ea1 (F: 7) - X-Ray Crystal Structure of Pf-M1 in Complex with Inhibitor (6DA) and Catalytic Zinc Ion
Other atoms:
Mg (4);
Zn (1);
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6ea2 (F: 3) - X-Ray Crystal Structure of Pf-M1 in Complex with Inhibitor (6H) and Catalytic Zinc Ion
Other atoms:
Mg (4);
Zn (1);
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6ea4 (F: 6) - ERAP2 Bound to Aryl Sulfonamide Uncompetitive Inhibitor
Other atoms:
Zn (2);
-
6eaa (F: 3) - X-Ray Crystal Structure of Pf-M1 in Complex with Inhibitor (6I) and Catalytic Zinc Ion
Other atoms:
Mg (3);
Zn (1);
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6eab (F: 3) - X-Ray Crystal Structure of Pf-M1 in Complex with Inhibitor (6J) and Catalytic Zinc Ion
Other atoms:
Mg (4);
Zn (1);
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6eb7 (F: 3) - Yycf Homologue (SP1227) Receiver Domain Activated By BEF3
Other atoms:
Mn (1);
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6ebe (F: 3) - 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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6ebr (F: 3) - Activation of RR02 Bound to BEF3
Other atoms:
Mn (1);
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6ebw (F: 1) - Halk in Complex with Compound 9 (6-(((1S)-1-(5-Fluoropyridin-2-Yl) Ethyl)Amino)-1-(3-Methyl-1H-Pyrazol-5-Yl)-1H-Pyrrolo[2,3-B]Pyridin-3- Yl)(Morpholin-4-Yl)Methanone
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6ecz (F: 5) - 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);
-
6eda (F: 3) - 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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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);
-
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);
-
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);
-
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);
-
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);
-
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);
-
6eee (F: 36) - X-Ray Crystal Structure of Pf-M17 in Complex with Inhibitor (6K) and Regulatory Zinc Ion
Other atoms:
Zn (12);
-
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);
-
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);
-
6eg9 (F: 6) - IRAK4 in Complex with Ponatinib
Other atoms:
Co (4);
-
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);
-
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);
-
6el5 (F: 1) - Estimation of Relative Drug-Target Residence Times By Random Acceleration Molecular Dynamics Simulation
Other atoms:
Cl (1);
-
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);
-
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
Page generated: Wed Nov 13 08:09:45 2024
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