Fluorine in PDB, part 107 (files: 4241-4280),
PDB 5msb-5njh
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: 4241-4280 (PDB 5msb-5njh).
-
5msb (F: 20) - Crystal Structure of Human Carbonic Anhydrase Isozyme XII with 2,3,5, 6-Tetrafluoro-4[(2-Hydroxyethyl)Sulfonyl]Benzenesulfonamide
Other atoms:
Zn (4);
-
5mt0 (F: 1) - Complement Factor D in Complex with A Reversible Indole Carboxylic Acid Based Inhibitor
-
5mtx (F: 1) - Dibenzooxepinone Inhibitor 12B in Complex with P38 Mapk
-
5mty (F: 2) - Dibenzosuberone Inhibitor 8E in Complex with P38 Mapk
-
5mu6 (F: 4) - Human N-Myristoyltransferase (NMT1) with Myristoyl-Coa and Imp-1088 Inhibitor Bound
Other atoms:
Mg (2);
-
5mut (F: 4) - Crystal Structure of Potent Human Dihydroorotate Dehydrogenase Inhibitors Based on Hydroxylated Azole Scaffolds
Other atoms:
Cl (3);
-
5mvc (F: 4) - Crystal Structure of Potent Human Dihydroorotate Dehydrogenase Inhibitors Based on Hydroxylated Azole Scaffolds
Other atoms:
Cl (5);
-
5mvd (F: 4) - Crystal Structure of Potent Human Dihydroorotate Dehydrogenase Inhibitors Based on Hydroxylated Azole Scaffolds
Other atoms:
Cl (3);
-
5mwp (F: 1) - The Structure of Mr in Complex with AZD9977.
-
5mxv (F: 1) - Structure of Transcriptional Regulatory Repressor Protein - Ethr From Mycobacterium Tuberculosis in Complex with Compound GSK1107112A at 1.63A Resolution
Other atoms:
Cl (1);
-
5mxx (F: 3) - Crystal Structure of Human Sr Protein Kinase 1 (SRPK1) in Complex with Compound 1
Other atoms:
Ca (4);
-
5my8 (F: 3) - Crystal Structure of SRPK1 in Complex with SPHINX31
-
5myl (F: 1) - Structure of Transcriptional Regulatory Repressor Protein - Ethr From Mycobacterium Tuberculosis in Complex with Compound GSK1570606A at 1.72A Resolution
-
5myr (F: 1) - Structure of Transcriptional Regulatory Repressor Protein - Ethr From Mycobacterium Tuberculosis in Complex with Compound GSK735816A at 1.83A Resolution
-
5mys (F: 1) - Structure of Transcriptional Regulatory Repressor Protein - Ethr From Mycobacterium Tuberculosis in Complex with Compound GSK920684A at 1.59A Resolution
-
5myv (F: 12) - Crystal Structure of SRPK2 in Complex with Compound 1
-
5mz3 (F: 3) - P38 Alpha Mutant C162S in Complex with CMPD2 [N-(4-Methyl-3-(4,4,5,5- Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenyl)-3-(Trifluoromethyl) Benzamide]
-
5n1k (F: 3) - Camp-Dependent Protein Kinase A From Cricetulus Griseus in Complex with Fragment Like Molecule 2-Amino-1-(4-Fluorophenyl)Ethanol
-
5n2f (F: 2) - Structure of Pd-L1/Small-Molecule Inhibitor Complex
-
5n2n (F: 3) - Crystal Structure of the Receiver Domain of the Histidine Kinase CKI1 From Arabidopsis Thaliana Complexed with MG2+ and BEF3-
Other atoms:
Mg (1);
-
5n33 (F: 3) - Camp-Dependent Protein Kinase A From Cricetulus Griseus in Complex with Fragment Like Molecule 3-Amino-5-(Trifluoromethyl)-1H-Pyridin-2- One
-
5n3d (F: 3) - Camp-Dependent Protein Kinase A From Cricetulus Griseus in Complex with Fragment Like Molecule 4-(Trifluoromethyl)Benzenecarboximidamide
-
5n63 (F: 1) - Crystal Structure of P38ALPHA in Complex with Lipid Pocket Ligand 9C
-
5n69 (F: 2) - Cardiac Muscle Myosin S1 Fragment in the Pre-Powerstroke State Co- Crystallized with the Activator Omecamtiv Mecarbil
Other atoms:
Mg (2);
V (2);
-
5n7o (F: 6) - ETHR2 in Complex with Smart-420 Compound
-
5n9s (F: 1) - Ttk Kinase Domain in Complex with Bay 1161909
-
5n9t (F: 6) - Crystal Structure of USP7 in Complex with A Potent, Selective and Reversible Small-Molecule Inhibitor
-
5nad (F: 5) - Ttk Kinase Domain in Complex with Bay 1217389
-
5nai (F: 2) - Mono-Zinc Vim-5 Metallo-Beta-Lactamase in Complex with (1-Chloro-4- Hydroxyisoquinoline-3-Carbonyl)-D-Tryptophan (Compound 1)
Other atoms:
Cl (1);
Zn (3);
-
5nar (F: 3) - Complement Factor D in Complex with the Inhibitor (S)-Pyrrolidine-1,2- Dicarboxylic Acid 1-[(1-Carbamoyl-1H-Indol-3-Yl)-Amide] 2-[(3- Trifluoromethoxy-Phenyl)-Amide]
-
5nat (F: 3) - Complement Factor D in Complex with the Inhibitor (S)-Pyrrolidine-1,2- Dicarboxylic Acid 1-[(1-Methyl-1H-Indol-3-Yl)-Amide] 2-[(3- Trifluoromethoxy-Phenyl)-Amide]
-
5naw (F: 3) - Complement Factor D in Complex with the Inhibitor (1R,3S,5R)-2-Aza- Bicyclo[3.1.0]Hexane-2,3-Dicarboxylic Acid 2-[(1-Carbamoyl-1H-Indol- 3-Yl)-Amide] 3-[(3-Trifluoromethoxy-Phenyl)-Amide]
-
5nb6 (F: 3) - Complement Factor D in Complex with the Inhibitor (2S,4S)-4-Amino- Pyrrolidine-1,2-Dicarboxylic Acid 1-[(1-Carbamoyl-1H-Indol-3-Yl)- Amide] 2-[(3-Trifluoromethoxy-Phenyl)-Amide]
-
5nba (F: 4) - Complement Factor D in Complex with the Inhibitor (2S,4R)-4-Fluoro- Pyrrolidine-1,2-Dicarboxylic Acid 1-[(1-Carbamoyl-1H-Indol-3-Yl)- Amide] 2-[(3-Trifluoromethoxy-Phenyl)-Amide]
-
5ncq (F: 3) - Structure of the (Sr) CA2+-Atpase Bound to A Tetrahydrocarbazole and Tnp-Atp
Other atoms:
K (1);
Br (2);
-
5nd4 (F: 4) - Microtubule-Bound MKLP2 Motor Domain in the Presence of Adp.Alfx
Other atoms:
Mg (2);
Al (1);
-
5ndd (F: 1) - Crystal Structure of A Thermostabilised Human Protease-Activated Receptor-2 (PAR2) in Complex with AZ8838 at 2.8 Angstrom Resolution
Other atoms:
Na (1);
-
5nft (F: 4) - Glucocorticoid Receptor in Complex with AZD5423
-
5nge (F: 8) - Crystal Structure of USP7 in Complex with the Non-Covalent Inhibitor, FT671
-
5njh (F: 3) - Triazolopyrimidines Stabilize Microtubules By Binding to the Vinca Inhibitor Site of Tubulin
Other atoms:
Mg (5);
Cl (1);
Page generated: Wed Nov 13 08:08:31 2024
|
