Fluorine in PDB, part 59 (files: 2321-2360),
PDB 4bkz-4c62
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: 2321-2360 (PDB 4bkz-4c62).
-
4bkz (F: 1) - Crystal Structure of Unphosphorylated Maternal Embryonic Leucine Zipper Kinase (Melk) in Complex with A Benzodipyrazole Inhibitor
-
4bm8 (F: 8) - Galectin-3C in Complex with Bisamido-Thiogalactoside Derivate 3
-
4bmm (F: 12) - Crystal Structure of Trypanosoma Cruzi CYP51 Bound to the Inhibitor (R)-N-(3-(1H-Indol-3-Yl)-1-Oxo-1-(Pyridin-4- Ylamino)Propan-2-Yl)- 2',3,5'-Trifluoro-(1,1'-Biphenyl)-4-Carboxamide
Other atoms:
Fe (4);
-
4bnk (F: 8) - Crystal Structure of S. Aureus Fabi in Complex with Nadp and 5-Fluoro-2-Phenoxyphenol
Other atoms:
Cl (1);
-
4bnt (F: 12) - Crystal Structure of 3-Oxoacyl-(Acyl-Carrier-Protein) Reductase (Fabg) From Pseudomonas Aeruginosa in Complex with 2-(Trifluoromethyl)-1H-Benzimidazole at 2.3A Resolution
-
4bo3 (F: 6) - Crystal Structure of 3-Oxoacyl-(Acyl-Carrier-Protein) Reductase (Fabg) From Pseudomonas Aeruginosa in Complex with 2-(3-(Trifluoromethyl)Anilino)Pyridine-3-Sulfonamide at 2.5A Resolution
Other atoms:
Ni (1);
-
4bo8 (F: 2) - Crystal Structure of 3-Oxoacyl-(Acyl-Carrier-Protein) Reductase (Fabg) From Pseudomonas Aeruginosa in Complex with 1-(2-Amino-4-Phenylimidazol-1-Yl)-3-(2-Fluorophenyl) Urea at 2.7A Resolution
-
4bpm (F: 3) - Crystal Structure of A Human Integral Membrane Enzyme
Other atoms:
Cl (2);
-
4bpv (F: 30) - Mouse Cathepsin S with Covalent Ligand
Other atoms:
Cl (5);
-
4bqp (F: 12) - Mtb Inha Complex with Methyl-Thiazole Compound 7
Other atoms:
Na (1);
-
4bqr (F: 2) - Complex with Methyl-Thiazole Compound 11
-
4bqv (F: 48) - Mouse Cathepsin S with Covalent Ligand
-
4bs5 (F: 3) - Mouse Cathepsin S with Covalent Ligand
-
4bs6 (F: 6) - Mouse Cathepsin S with Covalent Ligand
Other atoms:
Cl (2);
-
4bti (F: 4) - Factor Xa in Complex with the Dual Thrombin-Fxa Inhibitor 58.
Other atoms:
Cl (2);
Ca (2);
-
4btu (F: 4) - Factor Xa in Complex with the Dual Thrombin-Fxa Inhibitor 57.
Other atoms:
Cl (8);
Ca (2);
-
4bul (F: 2) - Novel Hydroxyl Tricyclics (E.G. GSK966587) As Potent Inhibitors of Bacterial Type Iia Topoisomerases
Other atoms:
Mn (4);
-
4bvc (F: 3) - Identification of Small Molecule Inhibitors Selective For Apo(A) Kringles Kiv-7, Kiv-10 and Kv.
Other atoms:
Cl (1);
-
4bvd (F: 1) - Identification of Small Molecule Inhibitors Selective For Apo(A) Kringles Kiv-7, Kiv-10 and Kv.
Other atoms:
Cl (2);
-
4bvv (F: 1) - Identification of Small Molecule Inhibitors Selective For Apo(A) Kringles Kiv-7, Kiv-10 and Kv.
-
4bw4 (F: 3) - The First Bromodomain of Human BRD4 in Complex with 3,5 Dimethylisoxaxole Ligand
-
4bx2 (F: 6) - Crystal Structure of Murine Chronophin (Pyridoxal Phosphate Phosphatase) in Complex with Beryllium Trifluoride
Other atoms:
Mg (2);
-
4by0 (F: 4) - Crystal Structure of Trypanosoma Cruzi CYP51 Bound to the Inhibitor (R)-N-(3-(1H-Indol-3-Yl)-1-Oxo-1-(Pyridin-4- Ylamino)Propan-2-Yl)-3,3'-Difluoro-(1,1'-Biphenyl)-4- Carboxamide
Other atoms:
Fe (2);
-
4byg (F: 4) - Atpase Crystal Structure
Other atoms:
Mg (1);
Al (1);
K (1);
-
4bzo (F: 1) - Crystal Structure of PIM1 in Complex with A Pyrrolo- Pyrazinone Inhibitor
-
4c0c (F: 3) - Crystal Structure of Trypanosoma Cruzi CYP51 Bound to the Inhibitor (R)-N-(3-(1H-Indol-3-Yl)-1-Oxo-1-(Pyridin-4- Ylamino)Propan-2-Yl)-4-(4-(2,4-Difluorophenyl)Piperazin-1- Yl)-2-Fluorobenzamide.
Other atoms:
Fe (1);
-
4c1m (F: 12) - Myeloperoxidase in Complex with the Revesible Inhibitor HX1
Other atoms:
Fe (2);
Ca (2);
Cl (2);
-
4c27 (F: 12) - Crystal Structure of Trypanosoma Cruzi CYP51 Bound to the Inhibitor (R)-N-(3-(1H-Indol-3-Yl)-1-Oxo-1-(Pyridin-4- 4-Ylamino)Propan-2-Yl)-2-Fluoro-4-(4-(4-(Trifluoromethyl) Phenyl)Piperazin-1-Yl)Benzamide
Other atoms:
Fe (2);
Cl (1);
-
4c28 (F: 4) - Crystal Structure of Trypanosoma Cruzi CYP51 Bound to the Inhibitor (R)-N-(3-(1H-Indol-3-Yl)-1-Oxo-1-(Pyridin-4- Ylamino)Propan-2-Yl)-4-(4-(4-Chlorophenyl)Piperazin-1-Yl)- 2-Fluorobenzamide.
Other atoms:
Fe (2);
Cl (5);
-
4c2v (F: 2) - Aurora B Kinase in Complex with the Specific Inhibitor Barasertib
-
4c4d (F: 1) - Covalent Glycosyl-Enzyme Intermediate of Hypocrea Jecorina CEL7A E217Q Mutant Trapped Using Dnp-2-Deoxy-2-Fluoro-Cellotrioside
Other atoms:
Co (3);
-
4c4r (F: 3) - Structure of Beta-Phosphoglucomutase in Complex with A Phosphonate Analogue of Beta-Glucose-1-Phosphate and Magnesium Trifluoride
Other atoms:
Mg (2);
-
4c4s (F: 4) - Structure of Beta-Phosphoglucomutase in Complex with An Alpha-Fluorophosphonate Analogue of Beta-Glucose-1-Phosphate and Magnesium Trifluoride
Other atoms:
Mg (2);
-
4c4t (F: 5) - Structure of Beta-Phosphoglucomutase in Complex with A Phosphonate Analogue of Beta-Glucose-1-Phosphate and Aluminium Tetrafluoride
Other atoms:
Mg (1);
Al (1);
-
4c52 (F: 4) - Crystal Structure of Bcl-Xl in Complex with Benzoylurea Compound (39B)
-
4c5d (F: 4) - Crystal Structure of Bcl-Xl in Complex with Benzoylurea Compound (42)
Other atoms:
Br (2);
-
4c5r (F: 8) - Structural Investigations Into the Stereochemistry and Activity of A Phenylalanine-2,3-Aminomutase From Taxus Chinensis
-
4c5s (F: 8) - Structural Investigations Into the Stereochemistry and Activity of A Phenylalanine-2,3-Aminomutase From Taxus Chinensis
-
4c61 (F: 2) - Inhibitors of JAK2 Kinase Domain
-
4c62 (F: 2) - Inhibitors of JAK2 Kinase Domain
Page generated: Wed Nov 13 08:06:45 2024
|
