Fluorine in PDB, part 72 (files: 2841-2880),
PDB 4l3o-4luv
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: 2841-2880 (PDB 4l3o-4luv).
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4l3o (F: 12) - Crystal Structure of SIRT2 in Complex with the Macrocyclic Peptide S2IL5
Other atoms:
Zn (4);
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4l42 (F: 3) - Crystal Structures of Human P70S6K1-Pif
Other atoms:
Zn (1);
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4l43 (F: 3) - Crystal Structures of Human P70S6K1-T389A (Form I)
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4l44 (F: 3) - Crystal Structures of Human P70S6K1-T389A (Form II)
Other atoms:
Zn (1);
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4l45 (F: 3) - Crystal Structures of Human P70S6K1-T389E
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4l46 (F: 3) - Crystal Structures of Human P70S6K1-Wt
Other atoms:
Zn (1);
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4l4l (F: 4) - Structural Analysis of A Phosphoribosylated Inhibitor in Complex with Human Nicotinamide Phosphoribosyltransferase
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4l4m (F: 4) - Structural Analysis of A Phosphoribosylated Inhibitor in Complex with Human Nicotinamide Phosphoribosyltransferase
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4l6q (F: 2) - ROCK2 in Complex with Benzoxaborole
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4l7f (F: 1) - Co-Crystal Structure of JNK1 and AX13587
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4l7h (F: 4) - Diethylaminosulfur Trifluoride-Mediated Intramolecular Cyclization of 2-Hydroxy-Benzylureas to Fused Bicyclic Aminooxazoline Compounds and Evaluation of Their Biochemical Activity Against Beta-Secretase-1 (Bace-1)
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4l7j (F: 2) - Diethylaminosulfur Trifluoride-Mediated Intramolecular Cyclization of 2-Hydroxy-Benzylureas to Fused Bicyclic Aminooxazoline Compounds and Evaluation of Their Biochemical Activity Against Beta-Secretase-1 (Bace-1)
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4l7s (F: 6) - Kinase Domain Mutant of Human Itk in Complex with An Aminobenzothiazole Inhibitor
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4l8m (F: 1) - Human P38 Map Kinase in Complex with A Dibenzoxepinone
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4l9i (F: 2) - Bovine G Protein Coupled Receptor Kinase 1 in Complex with Paroxetine
Other atoms:
Cl (2);
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4la0 (F: 8) - X-Ray Study of Human Serum Albumin Complexed with Bicalutamide
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4la6 (F: 1) - Crystal Structure of 2-Methylisoborneol Synthase From Streptomyces Coelicolor A3(2) in Complex with MG2+ and 2-Fluoroneryl Diphosphate
Other atoms:
Mg (2);
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4lb3 (F: 1) - Crystal Structure of Human Ar Complexed with Nadp+ and {5-Chloro-2- [(2-Fluoro-4-Iodobenzyl)Carbamoyl]Phenoxy}Acetic Acid
Other atoms:
I (1);
Cl (1);
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4lb4 (F: 4) - Crystal Structure of Human Ar Complexed with Nadp+ and {2-[(4-Bromo-2, 3,5,6-Tetrafluorobenzyl)Carbamoyl]-5-Chlorophenoxy}Acetic Acid
Other atoms:
Br (1);
Cl (1);
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4lbd (F: 1) - Ligand-Binding Domain of the Human Retinoic Acid Receptor Gamma Bound to the Synthetic Agonist BMS961
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4lbr (F: 2) - Crystal Structure of Human Ar Complexed with Nadp+ and {5-Chloro-2- [(2,6-Difluoro-4-Iodobenzyl)Carbamoyl]Phenoxy}Acetic Acid
Other atoms:
I (1);
Cl (1);
-
4lbs (F: 2) - Crystal Structure of Human Ar Complexed with Nadp+ and {2-[(4-Bromo-2, 6-Difluorobenzyl)Carbamoyl]-5-Chlorophenoxy}Acetic Acid
Other atoms:
Br (1);
Cl (1);
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4ldz (F: 6) - Crystal Structure of the Full-Length Response Regulator Desr in the Active State
Other atoms:
Mg (2);
Na (2);
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4le0 (F: 6) - Crystal Structure of the Receiver Domain of Desr in Complex with Beryllofluoride and Magnesium
Other atoms:
Mg (2);
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4lgt (F: 2) - Crystal Structure of the Catalytic Domain of Rlub in Complex with A 21-Nucleotide Rna Substrate
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4li7 (F: 2) - Tankyrase-1 Complexed with Small Molecule Inhibitor 4-Chloro-5-Cyano- N-{2-[4-(4-Fluorobenzoyl)Piperidin-1-Yl]Ethyl}-2-Methoxybenzamide
Other atoms:
Cl (2);
Na (2);
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4li8 (F: 2) - Tankyrase-1 Complexed with Small Molecule Inhibitor 2-[4-(4- Fluorobenzoyl)Piperidin-1-Yl]-N-[(4-Oxo-3,5,7,8-Tetrahydro-4H- Pyrano[4,3-D]Pyrimidin-2-Yl)Methyl]-N-(Thiophen-2-Ylmethyl)Acetamide
Other atoms:
Zn (2);
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4ll5 (F: 1) - Crystal Structure of Pim-1 in Complex with the Fluorescent Compound SKF86002
Other atoms:
Ca (1);
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4lmn (F: 3) - Crystal Structure of MEK1 Kinase Bound to GDC0973
Other atoms:
Mg (1);
I (1);
-
4ln7 (F: 2) - 5,6-Bis(4-Fluorophenyl)-3-Hydroxy-2,5-Dihydropyridin-2-One Bound to Influenza 2009 PH1N1 Endonuclease
Other atoms:
Mg (1);
Mn (2);
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4loo (F: 1) - Structural Basis of Autoactivation of P38 Alpha Induced By TAB1 (Monoclinic Crystal Form)
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4lop (F: 4) - Structural Basis of Autoactivation of P38 Alpha Induced By TAB1 (Tetragonal Crystal Form)
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4loq (F: 4) - Structural Basis of Autoactivation of P38 Alpha Induced By TAB1 (Tetragonal Crystal Form with Bound Sulphate)
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4loy (F: 1) - Crystal Structure Analysis of Thrombin in Complex with Compound D57, 5-Chlorothiophene-2-Carboxylic Acid [(S)-2-[2-Methyl-3-(2- Oxopyrrolidin-1-Yl)Benzenesulfonylamino]-3-(4-Methylpiperazin-1- Yl)- 3-Oxopropyl]Amide (SAR107375)
Other atoms:
Cl (2);
Na (2);
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4lp0 (F: 3) - Crystal Structure of A Topoisomerase Atp Inhibitor
-
4lpb (F: 3) - Crystal Structure of A Topoisomerase Atpase Inhibitor
-
4lqg (F: 1) - X-Ray Structure of Human Glutamate Carboxypeptidase II (Gcpii) in Complex with A Phosphoramidate Inhibitor CTT1056
Other atoms:
Zn (2);
Ca (1);
Cl (1);
-
4lts (F: 6) - Discovery of Potent and Efficacious Cyanoguanidine-Containing Nicotinamide Phosphoribosyltransferase (Nampt) Inhibitors
-
4lud (F: 2) - Crystal Structure of Hck in Complex with the Fluorescent Compound SKF86002
Other atoms:
Ca (3);
Cl (2);
-
4luv (F: 1) - Fragment-Based Discovery of A Potent Inhibitor of Replication Protein A Protein-Protein Interactions
Other atoms:
Cl (1);
Page generated: Sun Dec 15 10:23:17 2024
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