Fluorine in PDB, part 138 (files: 5481-5520),
PDB 6ew7-6fo6
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: 5481-5520 (PDB 6ew7-6fo6).
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6ew7 (F: 2) - Crystal Structure of the BCL6 Btb Domain in Complex with Anilinopyrimidine Ligand
Other atoms:
Cl (6);
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6ex8 (F: 6) - Crystal Structure of Rhodesain in Complex with A Macrolactam Inhibitor
Other atoms:
Cl (2);
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6ey7 (F: 4) - Human Cytomegalovirus Terminase Nuclease Domain, Mn Soaked, Inhibitor Bound
Other atoms:
Mn (10);
Cl (1);
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6eyj (F: 6) - E-Selectin Lectin, Egf-Like and Two Scr Domains Complexed with Glycomimetic Ligand NV354
Other atoms:
Ca (2);
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6eyk (F: 3) - E-Selectin Lectin, Egf-Like and Two Scr Domains Complexed with Glycomimetic Ligand NV355
Other atoms:
Ca (2);
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6f0e (F: 1) - Structure of Yeast SEC14P with A Picolinamide Compound
Other atoms:
Br (1);
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6f1w (F: 2) - Crystal Structure of Human Casein Kinase I Delta in Complex with Compound 31A
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6f26 (F: 2) - Crystal Structure of Human Casein Kinase I Delta in Complex with Compound 31B
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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
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6f4z (F: 10) - 2'F-Arag Modified Quadruplex with Flipped G-Tract and Central Tetrad
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6f6i (F: 1) - Crystal Structure of Ebolavirus Glycoprotein in Complex with Paroxetine
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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);
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6f7b (F: 2) - Crystal Structure of the Human BUB1 Kinase Domain in Complex with Bay 1816032
Other atoms:
Mg (1);
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6f8u (F: 6) - Crystal Structure of the PDE4D Catalytic Domain in Complex with Gebr- 20B
Other atoms:
Mg (5);
Zn (2);
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6f9l (F: 1) - Crystal Structure of Barley Beta-Amylase Complexed with 3-Deoxy-3- Fluoro-Maltose
Other atoms:
Cl (1);
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6fc8 (F: 2) - CHK1 Kinase in Complex with Compound 13
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6fdc (F: 4) - Crystal Structure of the PDE4D Catalytic Domain in Complex with Gebr- 32A
Other atoms:
Mg (5);
Zn (2);
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6fe0 (F: 12) - Three Dimensional Structure of Human Carbonic Anhydrase IX in Complex with Benzenesulfonamide.
Other atoms:
Zn (4);
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6fe1 (F: 12) - Three Dimensional Structure of Human Carbonic Anhydrase IX in Complex with Benzenesulfonamide.
Other atoms:
Zn (4);
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6fe3 (F: 4) - Crystal Structure of T. Brucei Pde-B1 Catalytic Domain with Inhibitor Npd-1439
Other atoms:
Mg (2);
Zn (2);
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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
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6fet (F: 16) - Crystal Structure of Human Phosphodiesterase 4D2 Catalytic Domain with Inhibitor Npd-1439
Other atoms:
Ni (2);
Mg (4);
Zn (4);
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6fex (F: 3) - DDR1, 2-[4-Bromo-2-Oxo-1'-(1H-Pyrazolo[4,3-B]Pyridine-5-Carbonyl) Spiro[Indole-3,4'-Piperidine]-1-Yl]-N-(2,2,2-Trifluoroethyl) Acetamide, 1.291A, P212121, Rfree=17.4%
Other atoms:
Br (1);
I (4);
Cl (4);
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6ffb (F: 1) - 17BETA-Hydroxysteroid Dehydrogenase 14 Variant S205 - Mutant Q148A - in Complex with A Nonsteroidal Inhibitor
Other atoms:
Na (1);
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6ffn (F: 1) - Structure-Based Design and Synthesis of Macrocyclic Human Rhinovirus 3C Protease Inhibitors
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6ffs (F: 2) - Structure-Based Design and Synthesis of Macrocyclic Human Rhinovirus 3C Protease Inhibitors
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6fgf (F: 1) - Crystal Structure of BAZ2A Bromodomain in Complex with 1- Methylpyridinone Compound 2
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6fh7 (F: 1) - Crystal Structure of BAZ2B Bromodomain in Complex with 1- Methylpyridinone Compound 2
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6fio (F: 3) - DDR1, 2-[1'-(1H-Indazole-5-Carbonyl)-4-Methyl-2-Oxospiro[Indole-3,4'- Piperidine]-1-Yl]-N-(2,2,2-Trifluoroethyl)Acetamide, 1.990A, P6522, Rfree=27.7%
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6fiq (F: 3) - DDR1, 1-(1H-Indazole-5-Carbonyl)-5'-Methoxy-1'-[2-Oxo-2-[(2S)-2- (Trifluoromethyl)Pyrrolidin-1-Yl]Ethyl]Spiro[Piperidine-4,3'- Pyrrolo[3,2-B]Pyridine]-2'-One, 1.790A, P212121, Rfree=23.8%
Other atoms:
Cl (1);
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6fmd (F: 4) - Targeting Myeloid Differentiation Using Potent Human Dihydroorotate Dehydrogenase (Hdhodh) Inhibitors Based on 2-Hydroxypyrazolo[1,5- A]Pyridine Scaffold
Other atoms:
Cl (2);
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6fmf (F: 3) - Neuropilin-1 B1 Domain in Complex with EG01377; 2.8 Angstrom Structure
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6fn1 (F: 4) - Zosuquidar and UIC2 Fab Complex of Human-Mouse Chimeric ABCB1 (ABCB1HM)
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6fne (F: 3) - Structure of BRAG2
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6fnf (F: 3) - Crystal Structure of Ephrin A2 (EPHA2) Receptor Protein Kinase with Nvp-BHG712
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6fng (F: 3) - Crystal Structure of Ephrin A2 (EPHA2) Receptor Protein Kinase with An Isomer of Nvp-BHG712
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6fni (F: 3) - Crystal Structure of Ephrin B4 (EPHB4) Receptor Protein Kinase with Nvp-BHG712
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6fnj (F: 6) - Crystal Structure of Ephrin B4 (EPHB4) Receptor Protein Kinase with An Isomer of Nvp-BHG712
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6fo0 (F: 6) - Cryoem Structure of Bovine Cytochrome BC1 in Complex with the Anti- Malarial Compound GSK932121
Other atoms:
Fe (6);
Cl (2);
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6fo6 (F: 6) - Cryoem Structure of Bovine Cytochrome BC1 in Complex with the Anti- Malarial Inhibitor SCR0911
Other atoms:
Fe (6);
Page generated: Fri May 13 23:19:05 2022
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