Fluorine in PDB, part 38 (files: 1481-1520),
PDB 3hky-3ig6
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: 1481-1520 (PDB 3hky-3ig6).
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3hky (F: 2) - Hcv NS5B Polymerase Genotype 1B in Complex with 1,5 Benzodiazepine 6
Other atoms:
Cl (2);
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3hl7 (F: 2) - Crystal Structure of Human P38ALPHA Complexed with Sd-0006
Other atoms:
Cl (1);
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3hll (F: 4) - Crystal Structure of Human P38ALPHA Complexed with pH-797804
Other atoms:
Br (1);
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3hmi (F: 2) - The Crystal Structure of Human ABL2 in Complex with 5-Amino- 3-{[4-(Aminosulfonyl)Phenyl]Amino}-N-(2,6-Difluorophenyl)- 1H-1,2,4-Triazole-1-Carbothioamide
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3hok (F: 3) - X-Ray Crystal Structure of Human Heme Oxygenase-1 with (2R, 4S)-2-[2-(4-Chlorophenyl)Ethyl]-2-[(1H-Imidazol-1-Yl) Methyl]-4[((5-Trifluoromethylpyridin-2-Yl)Thio)Methyl]-1,3- Dioxolane: A Novel, Inducible Binding Mode
Other atoms:
Fe (2);
Cl (1);
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3hp2 (F: 3) - Crystal Structure of Human P38ALPHA Complexed with A Pyridinone Compound
Other atoms:
Br (1);
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3hp5 (F: 6) - Crystal Structure of Human P38ALPHA Complexed with A Pyrimidopyridazinone Compound
Other atoms:
Cl (2);
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3hp9 (F: 3) - Crystal Structure of Ssb/Exonuclease I in Complex with Inhibitor Cfam
Other atoms:
Mg (1);
Cl (1);
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3hq2 (F: 1) - Bsucp Crystal Structure
Other atoms:
Cl (7);
Zn (7);
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3hq5 (F: 6) - Progesterone Receptor Bound to An Alkylpyrrolidine Ligand.
Other atoms:
Cl (2);
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3hrb (F: 2) - P38 Kinase Crystal Structure in Complex with Small Molecule Inhibitor
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3hub (F: 1) - Human P38 Map Kinase in Complex with Scios-469
Other atoms:
Cl (1);
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3hvc (F: 2) - Crystal Structure of Human P38ALPHA Map Kinase
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3hvh (F: 1) - Rat Catechol O-Methyltransferase in Complex with A Bisubstrate Inhibitor
Other atoms:
Mg (1);
Cl (3);
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3hvi (F: 1) - Rat Catechol O-Methyltransferase in Complex with A Bisubstrate Inhibitor
Other atoms:
Mg (1);
Cl (1);
Na (1);
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3hvj (F: 2) - Rat Catechol O-Methyltransferase in Complex with A Bisubstrate Inhibitor
Other atoms:
Mg (2);
Cl (1);
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3hvk (F: 1) - Rat Catechol O-Methyltransferase in Complex with A Bisubstrate Inhibitor
Other atoms:
Mg (1);
Cl (2);
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3hvn (F: 6) - Crystal Structure of Cytotoxin Protein Suilysin From Streptococcus Suis
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3hzh (F: 3) - Crystal Structure of the Chex-Chey-BEF3-Mg+2 Complex From Borrelia Burgdorferi
Other atoms:
Mg (1);
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3i06 (F: 2) - Crystal Structure of Cruzain Covalently Bound to A Purine Nitrile
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3i25 (F: 6) - Potent Beta-Secretase 1 Hydroxyethylene Inhibitor
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3i28 (F: 1) - Crystal Structure of Soluble Epoxide Hydrolase
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3i61 (F: 3) - Structure of MSS116P Bound to Ssrna and Adp-Beryllium Fluoride
Other atoms:
Mg (1);
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3i62 (F: 4) - Structure of MSS116P Bound to Ssrna and Adp-Aluminum Fluoride
Other atoms:
Mg (1);
Al (1);
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3i6c (F: 3) - Structure-Based Design of Novel PIN1 Inhibitors (II)
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3i6d (F: 6) - Crystal Structure of Ppo From Bacillus Subtilis with Af
Other atoms:
Cl (2);
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3i6r (F: 3) - Plasmodium Falciparum Dihydroorotate Dehydrogenase Bound with Triazolopyrimidine-Based Inhibitor DSM74
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3i81 (F: 1) - Crystal Structure of Insulin-Like Growth Factor 1 Receptor (Igf-1R-Wt) Complex with Bms-754807 [1-(4-((5-Cyclopropyl- 1H-Pyrazol-3-Yl)Amino)Pyrrolo[2,1-F][1,2,4]Triazin-2-Yl)-N- (6-Fluoro-3-Pyridinyl)-2-Methyl-L-Prolinamide]
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3i8d (F: 4) - The Pairing Geometry of the Hydrophobic Thymine Analog 2,4- Difluorotoluene in Duplex Dna As Analyzed By X-Ray Crystallography
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3i9j (F: 2) - Crystal Structure of Adp Ribosyl Cyclase Complexed with A Substrate Analog and A Product Nicotinamide
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3i9m (F: 2) - Crystal Structure of Human CD38 Complexed with An Analog Ara-2'F-Adpr
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3i9n (F: 2) - Crystal Structure of Human CD38 Complexed with An Analog Ribo-2'F-Adp Ribose
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3i9o (F: 2) - Crystal Structure of Adp Ribosyl Cyclase Complexed with Ribo-2'F-Adp Ribose
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3iad (F: 5) - Crystal Structure of Human Phosphodiesterase 4D with Bound Allosteric Modulator
Other atoms:
Mg (4);
Zn (4);
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3ice (F: 18) - Rho Transcription Termination Factor Bound to Rna and Adp- BEF3
Other atoms:
Mg (6);
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3icn (F: 1) - Trypanosoma Cruzi Farnesyl Diphosphate Synthase Homodimer in Complex with Isopentenyl Pyrophosphate and 3-Fluoro-1-(2- Hydroxy-2,2-Bis-Phosphono-Ethyl)-Pyridinium
Other atoms:
Mg (3);
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3id0 (F: 1) - Trypanosoma Cruzi Farnesyl Diphosphate Synthase Homodimer in Complex with 3-Fluoro-1-(2-Hydroxy-2,2-Bisphosphono-Ethyl) Pyridinium
Other atoms:
Mg (3);
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3id8 (F: 1) - Ternary Complex of Human Pancreatic Glucokinase Crystallized with Activator, Glucose and Amp-Pnp
Other atoms:
Mg (1);
K (1);
-
3ies (F: 1) - Firefly Luciferase Inhibitor Complex
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3ig6 (F: 4) - Low Molecular Weigth Human Urokinase Type Plasminogen Activator 2-[6-(3'-Aminomethyl-Biphenyl-3-Yloxy)-4-(3- Dimethylamino-Pyrrolidin-1-Yl)-3,5-Difluoro-Pyridin-2- Yloxy]-4-Dimethylamino-Benzoic Acid Complex
Page generated: Wed Nov 13 08:05:59 2024
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