Fluorine in PDB, part 141 (files: 5601-5640),
PDB 6eog-6fet
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: 5601-5640 (PDB 6eog-6fet).
-
6eog (F: 6) - Human Galectin-3C in Complex with A Galactose Derivative
Other atoms:
Cl (6);
-
6eol (F: 3) - Human Galectin-3C in Complex with A Galactose Derivative
Other atoms:
Cl (2);
-
6eor (F: 8) - DPP9 - 1G244
-
6epr (F: 2) - The ATAD2 Bromodomain in Complex with Compound Uzh-DS15
-
6eq4 (F: 2) - MTH1 in Complex with Fragment 8
-
6eq7 (F: 2) - MTH1 in Complex with Fragment 11
-
6eqm (F: 7) - Crystal Structure of Human Bace-1 in Complex with CNP520
Other atoms:
Cl (1);
-
6es0 (F: 4) - Crystal Structure of the Kinase Domain of Human RIPK2 in Complex with the Activation Loop Targeting Inhibitor Cs-R35
-
6esn (F: 1) - Ligand Complex of Rorg Lbd
Other atoms:
Na (1);
-
6et4 (F: 1) - Human Dihydroorotate Dehydrogenase in Complex with Novel Inhibitor
Other atoms:
Cl (3);
-
6etj (F: 1) - Human PFKFB3 in Complex with KAN0438241
-
6eum (F: 3) - Crystal Structure of Bcii Metallo-Beta-Lactamase in Complex with Dz- 307
Other atoms:
Zn (2);
-
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);
-
6euw (F: 2) - Crystal Structure of the Cap-Binding Domain of the PB2 Subunit of Influenza A/H5N1 Polymerase Bound to An Azaindazole Inhibitor
-
6eux (F: 2) - Structure of the Midlink and Cap-Binding Domains of Influenza B Polymerase PB2 Subunit with A Bound Azaindazole Cap-Binding Inhibitor
-
6euy (F: 6) - Structure of the Midlink and Cap-Binding Domains of Influenza A Polymerase PB2 Subunit with A Bound Azaindazole Cap-Binding Inhibitor
-
6evc (F: 5) - Structure of E282Q A. Niger FDC1 in Complex with Pentafluoro-Cinnamic Acid
Other atoms:
K (2);
Mn (1);
-
6evh (F: 1) - Lipoaminopeptide Helioferin A and B From Mycogone Rosea
Other atoms:
Cl (1);
-
6ew7 (F: 2) - Crystal Structure of the BCL6 Btb Domain in Complex with Anilinopyrimidine Ligand
Other atoms:
Cl (6);
-
6ex8 (F: 6) - Crystal Structure of Rhodesain in Complex with A Macrolactam Inhibitor
Other atoms:
Cl (2);
-
6ey7 (F: 4) - Human Cytomegalovirus Terminase Nuclease Domain, Mn Soaked, Inhibitor Bound
Other atoms:
Mn (10);
Cl (1);
-
6eyj (F: 6) - E-Selectin Lectin, Egf-Like and Two Scr Domains Complexed with Glycomimetic Ligand NV354
Other atoms:
Ca (2);
-
6eyk (F: 3) - E-Selectin Lectin, Egf-Like and Two Scr Domains Complexed with Glycomimetic Ligand NV355
Other atoms:
Ca (2);
-
6f0e (F: 1) - Structure of Yeast SEC14P with A Picolinamide Compound
Other atoms:
Br (1);
-
6f1w (F: 2) - Crystal Structure of Human Casein Kinase I Delta in Complex with Compound 31A
-
6f26 (F: 2) - Crystal Structure of Human Casein Kinase I Delta in Complex with Compound 31B
-
6f2u (F: 6) - Potent and Selective Aldo-Keto Reductase 1C3 (AKR1C3) Inhibitors Based on the Benzoisoxazole Moiety: Application of A Bioisosteric Scaffold Hopping Approach to Flufenamic Acid
-
6f4z (F: 10) - 2'F-Arag Modified Quadruplex with Flipped G-Tract and Central Tetrad
-
6f6i (F: 1) - Crystal Structure of Ebolavirus Glycoprotein in Complex with Paroxetine
-
6f78 (F: 12) - Potent and Selective Aldo-Keto Reductase 1C3 (AKR1C3) Inhibitors Based on the Benzoisoxazole Moiety: Application of A Bioisosteric Scaffold Hopping Approach to Flufenamic Acid
Other atoms:
Cl (2);
-
6f7b (F: 2) - Crystal Structure of the Human BUB1 Kinase Domain in Complex with Bay 1816032
Other atoms:
Mg (1);
-
6f8u (F: 6) - Crystal Structure of the PDE4D Catalytic Domain in Complex with Gebr- 20B
Other atoms:
Mg (5);
Zn (2);
-
6f9l (F: 1) - Crystal Structure of Barley Beta-Amylase Complexed with 3-Deoxy-3- Fluoro-Maltose
Other atoms:
Cl (1);
-
6fc8 (F: 2) - CHK1 Kinase in Complex with Compound 13
-
6fdc (F: 4) - Crystal Structure of the PDE4D Catalytic Domain in Complex with Gebr- 32A
Other atoms:
Mg (5);
Zn (2);
-
6fe0 (F: 12) - Three Dimensional Structure of Human Carbonic Anhydrase IX in Complex with Benzenesulfonamide.
Other atoms:
Zn (4);
-
6fe1 (F: 12) - Three Dimensional Structure of Human Carbonic Anhydrase IX in Complex with Benzenesulfonamide.
Other atoms:
Zn (4);
-
6fe3 (F: 4) - Crystal Structure of T. Brucei Pde-B1 Catalytic Domain with Inhibitor Npd-1439
Other atoms:
Mg (2);
Zn (2);
-
6fer (F: 60) - Crystal Structure of Human DDR2 Kinase in Complex with 2-[4,5- Difluoro-2-Oxo-1'-(1H-Pyrazolo[3,4-B]Pyridine-5-Carbonyl) Spiro[Indole-3,4'-Piperidine]-1-Yl]-N-(2,2,2-Trifluoroethyl)Acetamide
-
6fet (F: 16) - Crystal Structure of Human Phosphodiesterase 4D2 Catalytic Domain with Inhibitor Npd-1439
Other atoms:
Ni (2);
Mg (4);
Zn (4);
Page generated: Sun Dec 15 10:25:50 2024
|
