Fluorine in PDB, part 131 (files: 5201-5240),
PDB 6b9l-6bqk
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: 5201-5240 (PDB 6b9l-6bqk).
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6b9l (F: 4) - Crystal Structure of EPHA2 with Peptide 135E2
Other atoms:
Cl (4);
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6ba2 (F: 1) - Crystal Structure of Myst Acetyltransferase Domain in Complex with Inhibitor
Other atoms:
Zn (1);
Cl (1);
Na (1);
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6bad (F: 4) - Lactate Dehydrogenase in Complex with Inhibitor (R)-3-((2- Chlorophenyl)Thio)-6-(3-((4-Fluorophenyl)Amino)Phenyl)-4-Hydroxy-6- (Thiophen-3-Yl)-5,6-Dihydro-2H-Pyran-2-One
Other atoms:
Cl (4);
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6bag (F: 4) - Lactate Dehydrogenase in Complex with Inhibitor (R)-5-((2- Chlorophenyl)Thio)-6'-((4-Fluorophenyl)Amino)-4-Hydroxy-2-(Thiophen- 3-Yl)-2,3-Dihydro-[2,2'-Bipyridin]-6(1H)-One
Other atoms:
Cl (4);
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6baz (F: 2) - Lactate Dehydrogenase in Complex with Inhibitor (S)-5-((2- Chlorophenyl)Thio)-6'-((4-Fluorophenyl)Amino)-4-Hydroxy-2-(Thiophen- 3-Yl)-2,3-Dihydro-[2,2'-Bipyridin]-6(1H)-One
Other atoms:
Cl (2);
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6bb1 (F: 6) - Lactate Dehydrogenase in Complex with Inhibitor (R)-5-((2- Chlorophenyl)Thio)-6'-(4-Fluorophenoxy)-4-Hydroxy-2-(Thiophen-3-Yl)- 2,3-Dihydro-[2,2'-Bipyridin]-6(1H)-One
Other atoms:
Cl (6);
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6bb2 (F: 3) - Lactate Dehydrogenase in Complex with Inhibitor (S)-5-((2- Chlorophenyl)Thio)-6'-(4-Fluorophenoxy)-4-Hydroxy-2-(Thiophen-3-Yl)- 2,3-Dihydro-[2,2'-Bipyridin]-6(1H)-One
Other atoms:
Cl (3);
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6bb3 (F: 4) - Lactate Dehydrogenase in Complex with Inhibitor 3-((2-Chlorophenyl) Thio)-6-(6-((4-Fluorophenyl)Amino)Pyridin-2-Yl)-4-Hydroxy-6- (Thiophen-3-Yl)-5,6-Dihydro-2H-Pyran-2-One
Other atoms:
Cl (4);
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6bba (F: 14) - Crystal Structure of Human Mitochondrial Clpp Complex with Acyldepsipeptide Adep-28
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6bcr (F: 6) - Complex of 14-3-3 Theta with An IRSP53 Peptide Phosphorylated at T340
Other atoms:
Mg (5);
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6bds (F: 3) - Schistosoma Mansoni (Blood Fluke) Sulfotransferase/Cidd-0000204 (Compound 11F) Complex
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6bel (F: 1) - Ternary Complex Crystal Structure of Dna Polymerase Beta with R-Isomer of Beta-Gamma-Chf-Dctp
Other atoms:
Mg (2);
Cl (1);
Na (3);
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6bfb (F: 1) - Crystal Structure of A F. Nucleatum Fmn Riboswitch Bound to Wg-3
Other atoms:
Mg (1);
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6bfe (F: 4) - Bace Crystal Structure with Hydroxy Pyrrolidine Inhibitor
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6bfv (F: 1) - Crystal Structure of Purine Nucleoside Phosphorylase Isoform 2 From Schistosoma Mansoni in Complex with 5-Fluoro-1,2-Dihydropyrimidin-2- One
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6bfw (F: 4) - Bace Crystal Structure with Hydroxy Morpholine Inhibitor
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6bfx (F: 4) - Bace Crystal Structure with Hydroxy Pyrrolidine Inhibitor
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6bg3 (F: 3) - Structure of (3S,4S)-1-Benzyl-4-(3-(3-(Trifluoromethyl)Phenyl)Ureido) Piperidin-3-Yl Acetate Bound to DCN1
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6bg5 (F: 3) - Structure of 1-(Benzo[D][1,3]Dioxol-5-Ylmethyl)-1-(1-Propylpiperidin- 4-Yl)-3-(3-(Trifluoromethyl)Phenyl)Urea Bound to DCN1
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6bgn (F: 15) - Crystal Structure of 4-Oxalocrotonate Tautomerase After Incubation with 5-Fluoro-2-Hydroxy-2,4-Pentadienoate
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6bgw (F: 2) - Linked KDM5A Jmj Domain Bound to the Inhibitor 2-((2-Chlorophenyl)(2- (4,4-Difluoropiperidin-1-Yl)Ethoxy)Methyl)-1H-Pyrrolo[3,2-B]Pyridine- 7-Carboxylic Acid(Compound N41)
Other atoms:
Mn (1);
Cl (1);
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6bgx (F: 2) - Linked KDM5A Jmj Domain Bound to the Inhibitor 2-((2-Chlorophenyl)((4, 4-Difluorocyclohexyl)Methoxy)Methyl)-1H-Pyrrolo[3,2-B]Pyridine-7- Carboxylic Acid(Compound N42)
Other atoms:
Mn (1);
Cl (1);
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6bkw (F: 2) - Btk Complex with Compound 12
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6bkz (F: 2) - Novel Modes of Inhibition of Wild-Type IDH1: Non-Equivalent Allosteric Inhibition with CMPD3
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6blf (F: 8) - PDE2 Complexed with 2-[6-Fluoro-8-Methylsulfonyl-9-[(1R)-1-[4- (Trifluoromethyl)Phenyl]Ethyl]-1,2,3,4-Tetrahydrocarbazol-1-Yl]Acetic Acid
Other atoms:
Mg (2);
Zn (2);
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6bln (F: 2) - Btk Complex with Compound 13
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6bmf (F: 9) - VPS4P-VTA1P Complex with Peptide Binding to the Central Pore of VPS4P
Other atoms:
Mg (4);
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6bn6 (F: 14) - Identification of Bicyclic Hexafluoroisopropyl Alcohol Sulfonamides As Rorgt/Rorc Inverse Agonists
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6bns (F: 13) - Structure of Human Pregnane X Receptor Ligand Binding Domain Bound Tethered with Src Co-Activator Peptide and Compound 25A Aka Bicyclic Hexafluoroisopropyl 2 Alcohol Sulfonamides
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6bp0 (F: 4) - Crystal Structure of the Human Vaccinia-Related Kinase 1 Bound to (R)- 2-Phenylaminopteridinone Inhibitor
Other atoms:
Cl (7);
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6bpr (F: 2) - Crystal Structure of Cysteine, Nitric Oxide-Bound Ferrous Form of the Uncrosslinked F2-TYR157 Human Cysteine Dioxygenase
Other atoms:
Fe (1);
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6bps (F: 2) - Crystal Structure of Cysteine-Bound Ferrous Form of the Uncrosslinked F2-TYR157 Human Cysteine Dioxygenase
Other atoms:
Fe (1);
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6bpt (F: 2) - Crystal Structure of Ferrous Form of the Uncrosslinked F2-TYR157 Human Cysteine Dioxygenase
Other atoms:
Fe (1);
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6bpu (F: 3) - Crystal Structure of Ferrous Form of the F2-TYR157 Human Cysteine Dioxygenase with Both Uncrosslinked and Crosslinked Cofactor
Other atoms:
Fe (1);
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6bpv (F: 1) - Crystal Structure of Cysteine-Bound Ferrous Form of the Matured F2- TYR157 Human Cysteine Dioxygenase
Other atoms:
Fe (1);
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6bq0 (F: 3) - Structure of Human Monoacylglycerol Lipase Bound to A Covalent Inhibitor
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6bq1 (F: 2) - Human PI4KIIIA Lipid Kinase Complex
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6bqh (F: 2) - Crystal Structure of 5-HT2C in Complex with Ritanserin
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6bqj (F: 6) - Crystal Structure of Hepatis C Virus Protease (NS3) Complexed with Tripeptidic Acyl Sulfonamide Inhibitor (Compound 16)
Other atoms:
Cl (3);
Zn (3);
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6bqk (F: 4) - Crystal Structure of Hepatis C Virus Protease (NS3) Complexed with Tripeptidic Acyl Sulfonamide Inhibitor (Compound 18)
Other atoms:
Cl (2);
Zn (2);
Page generated: Fri May 13 23:17:11 2022
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