Fluorine in PDB, part 3 (files: 81-120),
PDB 1dvz-1fk9
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: 81-120 (PDB 1dvz-1fk9).
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1dvz (F: 6) - Crystal Structure of Human Transthyretin in Complex with O- Trifluoromethylphenyl Anthranilic Acid
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1dxw (F: 40) - Structure of Hetero Complex of Non Structural Protein (Ns) of Hepatitis C Virus (Hcv) and Synthetic Peptidic Compound
Other atoms:
Zn (20);
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1dy8 (F: 4) - Inhibition of the Hepatitis C Virus NS3/4A Protease. the Crystal Structures of Two Protease-Inhibitor Complexes (Inhibitor II)
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1dy9 (F: 4) - Inhibition of the Hepatitis C Virus NS3/4A Protease. the Crystal Structures of Two Protease-Inhibitor Complexes (Inhibitor I)
Other atoms:
Zn (1);
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1e0v (F: 1) - Xylanase 10A From Sreptomyces Lividans. Cellobiosyl-Enzyme Intermediate at 1.7 A
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1e0x (F: 2) - Xylanase 10A From Sreptomyces Lividans. Xylobiosyl-Enzyme Intermediate at 1.65 A
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1e0y (F: 3) - Structure of the D170S/T457E Double Mutant of Vanillyl-Alcohol Oxidase
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1e1r (F: 3) - Bovine Mitochondrial F1-Atpase Inhibited By MG2+Adp and Aluminium Fluoride
Other atoms:
Mg (5);
Al (1);
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1e2e (F: 3) - Human Thymidylate Kinase Complexed with Thymidine Monophosphate, Adenosine Diphosphate,A Magnesium-Ion and ALF3
Other atoms:
Mg (2);
Al (1);
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1e4i (F: 2) - 2-Deoxy-2-Fluoro-Beta-D-Glucosyl/Enzyme Intermediate Complex of the Beta-Glucosidase From Bacillus Polymyxa
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1e6a (F: 2) - Fluoride-Inhibited Substrate Complex of Saccharomyces Cerevisiae Inorganic Pyrophosphatase
Other atoms:
Mn (8);
Na (1);
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1e70 (F: 1) - 2-F-Glucosylated Myrosinase From Sinapis Alba
Other atoms:
Zn (1);
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1e73 (F: 1) - 2-F-Glucosylated Myrosinase From Sinapis Alba with Bound L-Ascorbate
Other atoms:
Zn (1);
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1e7b (F: 18) - Crystal Structure of Human Serum Albumin Complexed with the General Anesthetic Halothane
Other atoms:
Br (6);
Cl (6);
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1e7c (F: 24) - Human Serum Albumin Complexed with Myristic Acid and the General Anesthetic Halothane
Other atoms:
Br (8);
Cl (8);
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1e8g (F: 6) - Structure of the H61T Double Mutant of Vanillyl-Alcohol Oxidase in Complex with Fluoro-Cresol
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1ea1 (F: 2) - Cytochrome P450 14 Alpha-Sterol Demethylase (CYP51) From Mycobacterium Tuberculosis in Complex with Fluconazole
Other atoms:
Fe (1);
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1eas (F: 3) - Nonpeptidic Inhibitors of Human Leukocyte Elastase. 3. Design, Synthesis, X-Ray Crystallographic Analysis, and Structure-Activity Relationships For A Series of Orally Active 3-Amino-6-Phenylpyridin-2-One Trifluoromethyl Ketones
Other atoms:
Na (1);
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1eat (F: 3) - Nonpeptidic Inhibitors of Human Leukocyte Elastase. 5. Design, Synthesis, and X-Ray Crystallography of A Series of Orally Active 5-Amino-Pyrimidin-6-One-Containing Trifluoromethylketones
Other atoms:
Na (1);
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1eau (F: 2) - Nonpeptidic Inhibitors of Human Leukocyte Elastase. 6. Design of A Potent, Intratracheally Active, Pyridone-Based Trifluoromethyl Ketone
Other atoms:
Na (1);
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1ec0 (F: 2) - Hiv-1 Protease in Complex with the Inhibitor BEA403
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1eek (F: 2) - Solution Structure of A Nonpolar, Non Hydrogen Bonded Base Pair Surrogate in Dna.
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1eet (F: 1) - Hiv-1 Reverse Transcriptase in Complex with the Inhibitor MSC204
Other atoms:
Br (1);
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1ef3 (F: 2) - Fidarestat Bound to Human Aldose Reductase
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1ela (F: 3) - Analogous Inhibitors of Elastase Do Not Always Bind Analogously
Other atoms:
Ca (1);
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1elb (F: 3) - Analogous Inhibitors of Elastase Do Not Always Bind Analogously
Other atoms:
Ca (1);
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1elc (F: 3) - Analogous Inhibitors of Elastase Do Not Always Bind Analogously
Other atoms:
Ca (1);
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1eld (F: 6) - Structural Analysis of the Active Site of Porcine Pancreatic Elastase Based on the X-Ray Crystal Structures of Complexes with Trifluoroacetyl-Dipeptide-Anilide Inhibitors
Other atoms:
Ca (1);
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1ele (F: 6) - Structural Analysis of the Active Site of Porcine Pancreatic Elastase Based on the X-Ray Crystal Structures of Complexes with Trifluoroacetyl-Dipeptide-Anilide Inhibitors
Other atoms:
Ca (1);
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1epo (F: 2) - Direct Observation By X-Ray Analysis of the Tetrahedral "Intermediate" of Aspartic Proteinases
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1epr (F: 2) - A Structural Comparison of 21 Inhibitor Complexes of the Aspartic Proteinase From Endothia Parasitica
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1eqh (F: 2) - The 2.7 Angstrom Model of Ovine Cox-1 Complexed with Flurbiprofen
Other atoms:
Fe (2);
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1exa (F: 1) - Enantiomer Discrimination Illustrated By Crystal Structures of the Human Retinoic Acid Receptor Hrargamma Ligand Binding Domain: the Complex with the Active R-Enantiomer BMS270394.
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1exp (F: 1) - Beta-1,4-Glycanase Cex-Cd
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1exx (F: 2) - Enantiomer Discrimination Illustrated By Crystal Structures of the Human Retinoic Acid Receptor Hrargamma Ligand Binding Domain: the Complex with the Inactive S-Enantiomer BMS270395.
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1f4v (F: 9) - Crystal Structure of Activated Chey Bound to the N-Terminus of Flim
Other atoms:
Mg (3);
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1fc8 (F: 20) - uc(Nmr) Solution Structure of A Chimeric Oligonucleotide Hairpin R(Ggac)D(Ttcg)2'F-A(Gtcc)
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1fdk (F: 3) - Carboxylic Ester Hydrolase (PLA2-MJ33 Inhibitor Complex)
Other atoms:
Ca (1);
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1fjs (F: 2) - Crystal Structure of the Inhibitor Zk-807834 (Ci-1031) Complexed with Factor Xa
Other atoms:
Cl (1);
Ca (1);
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1fk9 (F: 3) - Crystal Structure of Hiv-1 Reverse Transcriptase in Complex with Dmp-266(Efavirenz)
Other atoms:
Cl (1);
Page generated: Wed Nov 13 08:04:41 2024
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