Fluorine in PDB, part 60 (files: 2361-2400),
PDB 4c6l-4cqj
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: 2361-2400 (PDB 4c6l-4cqj).
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4c6l (F: 1) - Crystal Structure of the Dihydroorotase Domain of Human Cad Bound to the Inhibitor Fluoroorotate at pH 6.0
Other atoms:
Zn (2);
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4c6m (F: 1) - Crystal Structure of the Dihydroorotase Domain of Human Cad Bound to the Inhibitor Fluoroorotate at pH 7.0
Other atoms:
Zn (3);
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4c73 (F: 6) - Crystal Structure of M. Tuberculosis C171Q Kasa in Complex with TLM6
Other atoms:
K (2);
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4c7o (F: 16) - The Structural Basis of Ftsy Recruitment and Gtpase Activation By Srp Rna
Other atoms:
Mg (4);
Al (4);
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4c8b (F: 6) - Structure of the Kinase Domain of Human RIPK2 in Complex with Ponatinib
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4c9w (F: 1) - Crystal Structure of NUDT1 (MTH1) with R-Crizotinib
Other atoms:
Cl (3);
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4c9x (F: 1) - Crystal Structure of NUDT1 (MTH1) with S-Crizotinib
Other atoms:
Cl (3);
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4cam (F: 2) - Structure of Rat Neuronal Nitric Oxide Synthase Heme Domain in Complex with 7-((3-Fluorophenethylamino)Methyl)Quinolin-2-Amine
Other atoms:
Fe (2);
Zn (1);
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4can (F: 2) - Structure of Rat Neuronal Nitric Oxide Synthase Heme Domain in Complex with 7-(2-(3-Fluorobenzylamino)Ethyl)Quinolin-2-Amine
Other atoms:
Fe (2);
Zn (1);
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4cao (F: 2) - Structure of Rat Neuronal Nitric Oxide Synthase Heme Domain in Complex with 7-(2-(3-(3-Fluorophenyl(Propylamino)Ethyl)) Quinolin-2-Amine
Other atoms:
Fe (2);
Zn (1);
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4cap (F: 2) - Structure of Rat Neuronal Nitric Oxide Synthase Heme Domain in Complex with 7-(2-(3-(3-Fluorophenyl(Propylamino)Methyl) )Quinolin-2-Amine
Other atoms:
Fe (2);
Zn (1);
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4car (F: 2) - Structure of Bovine Endothelial Nitric Oxide Synthase Heme Domain in Complex with 7-((3-Fluorophenethylamino)Methyl) Quinolin-2-Amine
Other atoms:
As (2);
Fe (2);
Zn (1);
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4cav (F: 3) - Crystal Structure of Aspergillus Fumigatus N-Myristoyl Transferase in Complex with Myristoyl Coa and A Benzofuran Ligand R0-09-4879
Other atoms:
Cl (1);
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4cbt (F: 3) - Design, Synthesis, and Biological Evaluation of Potent and Selective Class Iia Hdac Inhibitors As A Potential Therapy For Huntingtons Disease
Other atoms:
Zn (6);
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4cc6 (F: 3) - Fragment-Based Discovery of 6 Azaindazoles As Inhibitors of Bacterial Dna Ligase
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4ccb (F: 1) - Structure of the Human Anaplastic Lymphoma Kinase in Complex with 3-((R)-1-(5-Fluoro-2-(2H-1,2,3-Triazol-2-Yl) Phenyl)Ethoxy)-5-(5-Methyl-1H-Pyrazol-4-Yl)Pyridin-2-Amine
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4ccu (F: 1) - Structure of the Human Anaplastic Lymphoma Kinase in Complex with 2-(5-(6-Amino-5-((R)-1-(5-Fluoro-2-(2H-1,2,3-Triazol-2-Yl) Phenyl)Ethoxy)Pyridin-3-Yl)-4-Methylthiazol-2-Yl)Propan-2-Ol
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4cd0 (F: 1) - Structure of L1196M Mutant Human Anaplastic Lymphoma Kinase in Complex with 2-(5-(6-Amino-5-((R)-1-(5-Fluoro-2-(2H-1,2,3-Triazol-2-Yl) Phenyl)Ethoxy)Pyridin-3-Yl)-4-Methylthiazol-2-Yl)Propane-1,2-Diol
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4cdt (F: 2) - Structure of Rat Neuronal Nitric Oxide Synthase Heme Domain in Complex with 7-((3-Fluorophenethylamino)Ethyl)Quinolin- 2-Amine
Other atoms:
Fe (2);
Zn (1);
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4cex (F: 2) - 1.59 A Resolution Fluoride Inhibited Sporosarcina Pasteurii Urease
Other atoms:
Ni (2);
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4cfn (F: 6) - Structure-Based Design of C8-Substituted O6-Cyclohexylmethoxyguanine CDK1 and 2 Inhibitors.
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4cft (F: 2) - Structure of Bovine Endothelial Nitric Oxide Synthase Heme Domain in Complex with 7-((3-Fluorophenethylamino)Ethyl) Quinolin-2-Amine
Other atoms:
As (1);
Fe (2);
Zn (1);
-
4cgn (F: 1) - Leishmania Major N-Myristoyltransferase in Complex with A Piperidinylindole Inhibitor
Other atoms:
Mg (1);
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4ck6 (F: 3) - Pseudo-Atomic Model of Microtubule-Bound Human Kinesin-5 Motor Domain in the Adp.Alfx State, Based on Cryo-Electron Microscopy Experiment.
Other atoms:
Mg (2);
Al (1);
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4ck7 (F: 3) - Pseudo-Atomic Model of Microtubule-Bound Human Kinesin-5 Motor Domain in Presence of Adp.Alfx (Neck-Linker in Its Disconnected Conformation, Based on Cryo-Electron Microscopy Experiment
Other atoms:
Mg (2);
Al (1);
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4cka (F: 1) - Sterol 14-Alpha Demethylase (CYP51)From Trypanosoma Cruzi in Complex with (S)-1-(4-Fluorophenyl)-2-(1H-Imidazol-1-Yl) Ethyl 4-Isopropylphenylcarbamate (Lfs)
Other atoms:
Fe (1);
-
4ckr (F: 3) - Crystal Structure of the Human DDR1 Kinase Domain in Complex with DDR1-in-1
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4cli (F: 1) - Structure of the Human Anaplastic Lymphoma Kinase in Complex with Pf-06463922 ((10R)-7-Amino-12-Fluoro-2,10,16-Trimethyl-15 -Oxo-10,15,16,17-Tetrahydro-2H-8,4-(Metheno)Pyrazolo(4,3-H) (2,5,11)Benzoxadiazacyclotetradecine-3-Carbonitrile).
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4clj (F: 1) - Structure of L1196M Mutant Human Anaplastic Lymphoma Kinase in Complex with Pf-06463922 ((10R)-7-Amino-12-Fluoro-2,10, 16-Trimethyl-15-Oxo-10,15,16,17-Tetrahydro-2H-8,4-(Metheno) Pyrazolo(4,3-H)(2,5,11)Benzoxadiazacyclotetradecine-3- Carbonitrile).
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4cm4 (F: 4) - Crystal Structure of Pteridine Reductase 1 (PTR1) From Trypanosoma Brucei in Ternary Complex with Cofactor and Inhibitor
-
4cmb (F: 4) - Crystal Structure of Pteridine Reductase 1 (PTR1) From Trypanosoma Brucei in Ternary Complex with Cofactor and Inhibitor
-
4cmg (F: 4) - Crystal Structure of Pteridine Reductase 1 (PTR1) From Trypanosoma Brucei in Ternary Complex with Cofactor and Inhibitor
-
4cmo (F: 1) - Structure of the Human Anaplastic Lymphoma Kinase in Complex with the Inhibitor 2-((1R)-1-((3-Amino-6-(2- Methoxypyridin- -Yl)Pyrazin-2-Yl)Oxy)Ethyl)-4-Fluoro-N-Methylbenzamide
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4cmt (F: 1) - Structure of the Human Anaplastic Lymphoma Kinase in Complex with the Inhibitor 3-((1R)-1-(5-Fluoro-2-(2H-1,2,3-Triazol-2-Yl) Phenyl)Ethoxy)-5-(3-(Methylsulfonyl)Phenyl)Pyridin-2-Amine
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4cmu (F: 1) - Structure of the Human Anaplastic Lymphoma Kinase in Complex with the Inhibitor (10R)-7-Amino-12-Fluoro-1,3,10, 16-Tetramethyl-16,17-Dihydro-1H-8,4-(Metheno)Pyrazolo(4,3- H)(2,5,11)Benzoxadiazacyclotetradecin-15(10H)-One
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4cn4 (F: 2) - Glge Isoform 1 From Streptomyces Coelicolor E423A Mutant with 2-Deoxy-2-Fluoro-Beta-Maltosyl Modification
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4cnh (F: 3) - Structure of the Human Anaplastic Lymphoma Kinase in Complex with the Inhibitor 3-((1R)-1-(5-Fluoro-2- Methoxyphenyl)Ethoxy)-5-(1-Methyl-1H-1,2,3-Triazol-5-Yl) Pyridin-2-Amine
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4coh (F: 3) - Crystal Structure of Trypanosoma Cruzi CYP51 Bound to the Sulfonamide Derivative of the 4-Aminopyridyl-Based Inhibitor
Other atoms:
Fe (2);
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4cqe (F: 6) - B-Raf Kinase V600E Mutant in Complex with A Diarylthiazole B-Raf Inhibitor
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4cqj (F: 3) - Fluorinase Substrate Flexibility Enables Last Step Aqueous and Ambient 18F Fluorination of A Rgd Peptide For Positron Emission Tomography
Page generated: Wed Nov 13 08:06:47 2024
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