Fluorine in PDB, part 43 (files: 1681-1720),
PDB 3lz3-3n0n
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: 1681-1720 (PDB 3lz3-3n0n).
-
3lz3 (F: 1) - Human Aldose Reductase Mutant T113S Complexed with IDD388
Other atoms:
Br (2);
Cl (1);
-
3lz5 (F: 2) - Human Aldose Reductase Mutant T113V Complexed with IDD594
Other atoms:
Br (1);
-
3lz9 (F: 1) - The Crystal Structure of 5-Epi-Aristolochene Synthase M4 Mutant Complexed with (2-Trans,6-Trans)-2-Fluorofarnesyl Diphosphate
Other atoms:
Mg (3);
-
3m00 (F: 1) - Crystal Structure of 5-Epi-Aristolochene Synthase M4 Mutant Complexed with (2-Cis,6-Trans)-2-Fluorofarnesyl Diphosphate
Other atoms:
Mg (3);
-
3m01 (F: 1) - The Crystal Structure of 5-Epi-Aristolochene Synthase Complexed with (2-Trans,6-Trans)-2-Fluorofarnesyl Diphosphate
Other atoms:
Mg (3);
-
3m02 (F: 1) - The Crystal Structure of 5-Epi-Aristolochene Synthase Complexed with (2-Cis,6-Trans)-2-Fluorofarnesyl Diphosphate
Other atoms:
Mg (3);
-
3m0i (F: 3) - Human Aldose Reductase Mutant T113V in Complex with Zopolrestat
-
3m0j (F: 2) - Structure of Oxaloacetate Acetylhydrolase in Complex with the Inhibitor 3,3-Difluorooxalacetate
Other atoms:
Mn (1);
Ca (1);
-
3m2w (F: 1) - Crystal Structure of Mapkak Kinase 2 (MK2) Complexed with A Spiroazetidine-Tetracyclic Atp Site Inhibitor
Other atoms:
Mg (1);
-
3m35 (F: 4) - Trypsin in Complex with the Inhibitor 1-[3-(Aminomethyl) Phenyl]-N-[3-Fluoro-2'-(Methylsulfonyl)Biphenyl-4-Yl]-3- (Trifluoromethyl)-1H-Pyrazole-5-Carboxamide (DPC423)
Other atoms:
Ca (1);
-
3m36 (F: 4) - Factor Xa in Complex with the Inhibitor 1-[3-(Aminomethyl) Phenyl]-N-[3-Fluoro-2'-(Methylsulfonyl)Biphenyl-4-Yl]-3- (Trifluoromethyl)-1H-Pyrazole-5-Carboxamide (DPC423)
Other atoms:
Ca (1);
-
3m37 (F: 4) - Factor Xa in Complex with the Inhibitor 1-[2-(Aminomethyl) Phenyl]-N-(3-Fluoro-2'-Sulfamoylbiphenyl-4-Yl)-3- (Trifluoromethyl)-1H-Pyrazole-5-Carboxamide (DPC602)
Other atoms:
Ca (1);
-
3m3f (F: 4) - Pepa Bound to the Ligand Binding Domain of GLUA3 (Flop Form)
Other atoms:
Zn (2);
-
3m3l (F: 6) - Pepa Bound to the Ligand Binding Domain of GLUA2 (Flop Form)
Other atoms:
Zn (5);
-
3m4h (F: 1) - Human Aldose Reductase Mutant T113V Complexed with IDD388
Other atoms:
Br (2);
Cl (1);
-
3m5l (F: 2) - Crystal Structure of Hcv NS3/4A Protease in Complex with Itmn-191
Other atoms:
Zn (1);
-
3mb9 (F: 3) - Human Aldose Reductase Mutant T113A Complexed with Zopolrestat
-
3mba (F: 1) - Aplysia Limacina Myoglobin. Crystallographic Analysis at 1.6 Angstroms Resolution
Other atoms:
Fe (1);
-
3mbl (F: 1) - Crystal Structure of the Human Mitogen-Activated Protein Kinase Kinase 1 (Mek 1) in Complex with Ligand and Mgadp
Other atoms:
Mg (1);
I (1);
-
3mdc (F: 2) - Dna Polymerase Lambda in Complex with Dfdctp
Other atoms:
Mg (2);
Na (4);
-
3mdt (F: 6) - Voriconazole Complex of Cytochrome P450 46A1
Other atoms:
Fe (2);
-
3mhj (F: 6) - Human Tankyrase 2 - Catalytic Parp Domain in Complex with 1-Methyl-3- (Trifluoromethyl)-5H-Benzo[C][1,8]Naphtyridine-6-One
Other atoms:
Zn (2);
-
3mhz (F: 7) - 1.7A Structure of 2-Fluorohistidine Labeled Protective Antigen
Other atoms:
Ca (2);
-
3miy (F: 2) - X-Ray Crystal Structure of Itk Complexed with Sunitinib
-
3mne (F: 1) - Crystal Structure of the Agonist Form of Mouse Glucocorticoid Receptor Stabilized By F608S Mutation at 1.96A
-
3mno (F: 1) - Crystal Structure of the Agonist Form of Mouse Glucocorticoid Receptor Stabilized By (A611V, F608S) Mutations at 1.55A
-
3mnp (F: 1) - Crystal Structure of the Agonist Form of Mouse Glucocorticoid Receptor Stabilized By (A611V, V708A, E711G) Mutations at 1.50A
-
3mo7 (F: 1) - Crystal Structure of Human Orotidine 5'-Monophosphate Decarboxylase Covalently Modified By 2'-Fluoro-6-Iodo-Ump
-
3mpa (F: 1) - Conformational Plasticity of P38 Map Kinase Dfg Motif Mutants in Response to Inhibitor Binding
-
3mqe (F: 12) - Structure of Sc-75416 Bound at the Cox-2 Active Site
Other atoms:
Fe (4);
Cl (4);
-
3mqf (F: 2) - Glycogen Phosphorylase Complexed with 4-Fluorobenzaldehyde-4-(Beta-D- Glucopyranosyl)-Thiosemicarbazone
-
3ms4 (F: 6) - Glycogen Phosphorylase Complexed with 4-Trifluoromethylbenzaldehyde-4- (Beta-D-Glucopyranosyl)-Thiosemicarbazone
-
3msx (F: 3) - Crystal Structure of Rhoa.Gdp.MGF3 in Complex with Gap Domain of ARHGAP20
Other atoms:
Mg (2);
-
3mvh (F: 2) - Crystal Structure of Akt-1-Inhibitor Complexes
Other atoms:
Mn (1);
-
3mw1 (F: 2) - P38 Kinase Crystal Structure in Complex with Small Molecule Inhibitor
Other atoms:
Cl (2);
-
3mw7 (F: 2) - Crystal Structure of Human Orotidine 5'-Monophosphate Decarboxylase Complexed with 5-Fluoro-Ump, Produced From 5-Fluoro-6-Amino-Ump
-
3mwa (F: 2) - Crystal Structure of Plasmodium Falciparum Orotidine 5'-Monophosphate Decarboxylase Covalently Modified By 2'-Fluoro-6-Iodo-Ump
-
3mxe (F: 3) - Crystal Structure of Hiv-1 Protease Inhibitor, KC32 Complexed with Wild-Type Protease
-
3myy (F: 12) - Structure of E. Coli Chey Mutant A113P Bound to Beryllium Fluoride
Other atoms:
Mn (7);
-
3n0n (F: 10) - Crystal Structure of Human Carbonic Anhydrase II in Complex with A Benzenesulfonamide Inhibitor
Other atoms:
Zn (1);
Page generated: Thu Dec 28 04:01:30 2023
|
