Fluorine in PDB, part 87 (files: 3441-3480),
PDB 4ymq-4zg9
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: 3441-3480 (PDB 4ymq-4zg9).
-
4ymq (F: 6) - X-Ray Co-Structure of Nuclear Receptor Ror-Gammat + SRC2 Peptide with A Benzothiadiazole Dioxide Inverse Agonist
Other atoms:
Na (1);
-
4yn4 (F: 1) - Structure of Human Dna Polymerase Beta Complexed with N7BG in the Template Opposite to Incoming Non-Hydrolyzable Dttp with Manganese in the Active Site
Other atoms:
Mn (2);
Na (2);
-
4yne (F: 1) - (R)-2-Phenylpyrrolidine Substitute Imidazopyridazines: A New Class of Potent and Selective Pan-Trk Inhibitors
-
4yp8 (F: 4) - IRAK4-Inhibitor Co-Structure
-
4ypq (F: 3) - Crystal Structure of the Ror(Gamma)T Ligand Binding Domain in Complex with 4-(1-(2-Chloro-6-(Trifluoromethyl)Benzoyl)-1H-Indazol-3-Yl) Benzoic Acid
Other atoms:
Mg (1);
Cl (1);
-
4yps (F: 1) - (R)-2-Phenylpyrrolidine Substitute Imidazopyridazines: A New Class of Potent and Selective Pan-Trk Inhibitors
-
4ys1 (F: 1) - Human Aldose Reductase Complexed with A Ligand with An Idd Structure (2) at 1.07 A.
-
4ysx (F: 6) - Crystal Structure of Mitochondrial Rhodoquinol-Fumarate Reductase From Ascaris Suum with the Specific Inhibitor NN23
Other atoms:
Fe (20);
-
4ysy (F: 6) - Crystal Structure of Mitochondrial Rhodoquinol-Fumarate Reductase From Ascaris Suum with N-[(2,4-Dichlorophenyl)Methyl]-2-(Trifluoromethyl) Benzamide
Other atoms:
Fe (20);
Cl (4);
-
4yt6 (F: 1) - Factor Viia in Complex with the Inhibitor 4-{[(R)-[5-Ethoxy-2-Fluoro- 3-(Propan-2-Yloxy)Phenyl](4-Phenyl-1H-Imidazol-2-Yl) Methyl]Amino}Benzenecarboximidamide
Other atoms:
Ca (1);
-
4yt7 (F: 1) - Factor Viia in Complex with the Inhibitor 2-(2-{(R)-[(4- Carbamimidoylphenyl)Amino][5-Ethoxy-2-Fluoro-3-(Propan-2-Yloxy) Phenyl]Methyl}-1H-Imidazol-4-Yl)Benzamide
Other atoms:
Ca (1);
-
4ytf (F: 4) - Discovery of Vx-509 (Decernotinib): A Potent and Selective Janus Kinase (Jak) 3 Inhibitor For the Treatment of Autoimmune Diseases
Other atoms:
Cl (1);
-
4yth (F: 4) - Discovery of Vx-509 (Decernotinib): A Potent and Selective Janus Kinase (Jak) 3 Inhibitor For the Treatment of Autoimmune Diseases
Other atoms:
Cl (1);
-
4yti (F: 3) - Discovery of Vx-509 (Decernotinib): A Potent and Selective Janus Kinase (Jak) 3 Inhibitor For the Treatment of Autoimmune Disease
-
4ytm (F: 6) - Crystal Structure of Mitochondrial Rhodoquinol-Fumarate Reductase From Ascaris Suum with N-Biphenyl-3-Yl-2-(Trifluoromethyl)Benzamide
Other atoms:
Fe (20);
-
4ytn (F: 16) - Crystal Structure of Mitochondrial Rhodoquinol-Fumarate Reductase From Ascaris Suum with N-[3-(Pentafluorophenoxy)Phenyl]-2- (Trifluoromethyl)Benzamide
Other atoms:
Fe (20);
-
4ytp (F: 3) - Crystal Structure of Porcine Heart Mitochondrial Complex II Bound with N-[(4-Tert-Butylphenyl)Methyl]-2-(Trifluoromethyl)Benzamide
Other atoms:
Fe (10);
-
4yur (F: 2) - Crystal Structure of PLK4 Kinase Domain Bound to Centrinone
-
4yvc (F: 2) - Rock 1 Bound to Thiazole Inhibitor
-
4yxd (F: 3) - Crystal Structure of Porcine Heart Mitochondrial Complex II Bound with Flutolanil
Other atoms:
Fe (10);
-
4yyl (F: 3) - Phenolic Acid Derivative Bound to Influenza Strain H1N1 Polymerase Subunit Pa Endonuclease
Other atoms:
Mn (2);
-
4yzn (F: 4) - Humanized ROCO4 Bound to Compound 19
-
4z2c (F: 2) - Quinolone(Moxifloxacin)-Dna Cleavage Complex of Gyrase From S. Pneumoniae
Other atoms:
Mg (2);
-
4z2d (F: 2) - Quinolone(Levofloxacin)-Dna Cleavage Complex of Gyrase From S. Pneumoniae
Other atoms:
Mg (2);
-
4z2e (F: 6) - Quinolone(Trovafloxacin)-Dna Cleavage Complex of Gyrase From S. Pneumoniae
Other atoms:
Mg (2);
-
4z3o (F: 2) - Quinolone(Moxifloxacin)-Dna Cleavage Complex of Topoisomerase IV From S. Pneumoniae
Other atoms:
Mg (4);
-
4z4q (F: 2) - Quinazolinedione(Pd 0305970)-Dna Cleavage Complex of Topoisomerase IV From S. Pneumoniae
Other atoms:
Mg (4);
-
4z53 (F: 6) - Quinolone(Trovafloxacin)-Dna Cleavage Complex of Topoisomerase IV From S. Pneumoniae
Other atoms:
Mg (4);
-
4z7m (F: 4) - Novel Inhibitors of Bacterial Methionine Aminopeptidase with Broad- Spectrum Biochemical Activity
Other atoms:
Mn (2);
-
4z90 (F: 20) - Elic Bound with the Anesthetic Isoflurane in the Resting State
Other atoms:
Cl (4);
-
4z91 (F: 20) - Elic Cocrystallized with Isofluorane in A Desensitized State
Other atoms:
Br (20);
Cl (4);
-
4za8 (F: 5) - Crystal Structure of A Niger FDC1 in Complex with Penta-Fluorocinnamic Acid
Other atoms:
K (2);
Mn (1);
-
4zab (F: 1) - Structure of A. Niger FDC1 in Complex with Alpha-Fluoro Cinnamic Acid
Other atoms:
K (2);
Mn (1);
-
4zdz (F: 2) - Saccharomyces Cerevisiae CYP51 (Lanosterol 14-Alpha Demethylase) Y140F Mutant Complexed with Fluconazole
Other atoms:
Fe (1);
-
4ze0 (F: 3) - Saccharomyces Cerevisiae CYP51 (Lanosterol 14-Alpha Demethylase) Y140F Mutant Complexed with Voriconazole
Other atoms:
Fe (1);
-
4ze1 (F: 2) - Saccharomyces Cerevisiae CYP51 Y140F Mutant Complexed with Posaconazole in the Active Site
Other atoms:
Fe (1);
-
4ze3 (F: 2) - Saccharomyces Cerevisiae CYP51 (Lanosterol 14-Alpha Demethylase) Y140H Mutant Complexed with Fluconazole
Other atoms:
Fe (1);
-
4zg6 (F: 2) - Structural Basis For Inhibition of Human Autotaxin By Four Novel Compounds
Other atoms:
Zn (4);
Ca (2);
Cl (2);
Na (4);
-
4zg7 (F: 2) - Structural Basis For Inhibition of Human Autotaxin By Four Novel Compounds
Other atoms:
Zn (2);
Ca (1);
Cl (2);
Na (2);
-
4zg9 (F: 4) - Structural Basis For Inhibition of Human Autotaxin By Four Novel Compounds
Other atoms:
Zn (4);
Ca (2);
Na (4);
Page generated: Sun Dec 15 10:23:50 2024
|
