Fluorine in PDB, part 226 (files: 9001-9040),
PDB 8ck4-8d7w
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: 9001-9040 (PDB 8ck4-8d7w).
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8ck4 (F: 4) - Structure of HIF2A-Arnt Heterodimer in Complex with (4S)-1-(3,5- Difluorophenyl)-5,5-Difluoro-3-Methanesulfonyl-4,5,6,7-Tetrahydro-2- Benzothiophen-4-Ol
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8ck8 (F: 2) - Structure of HIF2A-Arnt Heterodimer in Complex with (S)-1- Cyclohexyloxy-5,5-Difluoro-3-Methanesulfonyl-5,6-Dihydro-4H- Cyclopenta[C]Thiophen-4-Ol
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8ckt (F: 3) - Crystal Structure of Maize Cytokinin Oxidase/Dehydrogenase 4 (Cko/CKX4) in Complex with Inhibitor 2-[(3,5-Dichlorophenyl) Carbamoylamino]-4-(Trifluoromethoxy)Benzamide
Other atoms:
Cl (2);
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8cm2 (F: 3) - Crystal Structure of Maize Cytokinin Oxidase/Dehydrogenase 4 (Cko/CKX4) in Complex with Inhibitor 2-[[3,5-Dichloro-2-(2- Hydroxyethyl)Phenyl]Carbamoylamino]-4-(Trifluoromethoxy)Benzamide
Other atoms:
Cl (2);
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8cnf (F: 1) - Human Aldose Reductase Mutant L300G in Complex with A Ligand with An Idd Structure ({5-Fluoro-2-[(3-Nitrobenzyl)Carbamoyl]Phenoxy}Acetic Acid)
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8cnj (F: 6) - Hras(1-166) in Complex with Gdp and BEF3-
Other atoms:
Mg (2);
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8cnn (F: 3) - BEF3 Phospho-Hras Gsa Complex
Other atoms:
Mg (1);
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8cnp (F: 1) - Human Aldose Reductase Mutant L300G in Complex with A Ligand with An Idd Structure (3-({[2-(Carboxymethoxy)-4-Fluorobenzoyl]Amino}Methyl) Benzoic Acid)
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8coj (F: 1) - Crystal Structure of Human Soluble Adenylyl Cyclase Catalytic Domain in Complex with the Inhibitor Tdi-10228
Other atoms:
Cl (1);
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8cow (F: 2) - Mycobacterium Tuberculosis Dihydrofolate Reductase in Complex with 5- (Cyclopropylethynyl)-6-(2-Fluorophenyl)Pyrimidine-2,4-Diamine
Other atoms:
Co (2);
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8cq9 (F: 3) - Mycobacterium Tuberculosis Dihydrofolate Reductase in Complex with 5- (Cyclopropylethynyl)-6-(4-(Trifluoromethyl)Phenyl)Pyrimidine-2,4- Diamine
Other atoms:
Co (2);
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8cqb (F: 6) - Cryo-Em Structure of the Human GBP1 Dimer Bound to Gdp-ALF3
Other atoms:
Al (2);
Mg (2);
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8cqe (F: 8) - Pvhl:Elob:Eloc in Complex with (2S,4R)-1-((S)-2-(1-Fluorocyclopropane- 1-Carboxamido)-3,3-Dimethylbutanoyl)-4-Hydroxy-N-((S)-1-(2-Methyl-4- (4-Methylthiazol-5-Yl)Phenyl)Ethyl)Pyrrolidine-2-Carboxamide (Compound 37)
Other atoms:
As (12);
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8cqk (F: 4) - Pvhl:Elob:Eloc in Complex with (2S,4R)-1-((S)-2-(1-Fluorocyclopropane- 1-Carboxamido)-3,3-Dimethylbutanoyl)-4-Hydroxy-N-((S)-1-(2-Methyl-4- (4-Methylthiazol-5-Yl)Phenyl)Ethyl)Pyrrolidine-2-Carboxamide (Compound 30)
Other atoms:
As (12);
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8cql (F: 8) - Pvhl:Elob:Eloc in Complex with (2S,4R)-N-((S)-1-(5-Fluoro-2-Methoxy-4- (4-Methylthiazol-5-Yl)Phenyl)Ethyl)-1-((S)-2-(1-Fluorocyclopropane-1- Carboxamido)-3,3-Dimethylbutanoyl)-4-Hydroxypyrrolidine-2-Carboxamide (Compound 33)
Other atoms:
As (12);
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8cr0 (F: 1) - Crystal Structure of Human Carbonic Anhydrase II in Complex with A Triazolyl Benzoxaborole Inhibitor
Other atoms:
Zn (1);
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8cu7 (F: 3) - Crystal Structure of A2AAR-STAR2-Bril in Complex with A Novel A2A Antagonist, Lj-4517
Other atoms:
Na (1);
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8cx5 (F: 2) - Crystal Structure of Small Molecule Alpha,Beta-Ketoamide 4 Covalently Bound to K-Ras(G12R)
Other atoms:
Cl (2);
Mg (2);
Na (1);
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8cza (F: 6) - Crystal Structure of the First Bromodomain (BD1) of Human Brdt Bound to Gxh-IV-075
Other atoms:
Na (2);
Cl (3);
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8czv (F: 4) - Structure of Mers 3CL Protease in Complex with the Cyclopropane Based Inhibitor 17D
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8czx (F: 4) - Structure of Sars-Cov-2 3CL Protease in Complex with the Cyclopropane Based Inhibitor 17D
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8d0c (F: 6) - Human SARM1 Tir Domain Bound to Nb-3-Adpr
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8d0f (F: 6) - Human SARM1 Tir Domain Bound to Nb-2-Adpr
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8d0g (F: 6) - Human SARM1 Tir Domain Bound to Nb-3-Adprp
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8d0h (F: 6) - Human SARM1 Tir Domain Bound to Nb-3-Gdpr
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8d0i (F: 6) - Human SARM1 Bound to An Nb-3 Eadpr Adduct
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8d0q (F: 3) - Human FUT9 Bound to Gdp-CF3-Fucose and H-Type 2
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8d1c (F: 3) - Crystal Structure of T252E-CYP199A4 in Complex with 4- (Trifluoromethoxy)Benzoic Acid
Other atoms:
Fe (1);
Cl (1);
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8d3e (F: 1) - Crystal Structure of Human Apoptosis-Inducing Factor (Aif) W196A Mutant Complexed with 6-Fluoroquinolin-4-Amine
Other atoms:
Cl (1);
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8d3j (F: 2) - Crystal Structure of Human Apoptosis-Inducing Factor (Aif) Complexed with 6-Fluoro-2-Methylquinolin-4-Amine
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8d3k (F: 2) - Crystal Structure of Human Apoptosis-Inducing Factor (Aif) Complexed with 8-Fluoro-2-Methylquinolin-4-Amine
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8d3u (F: 4) - Human ALPHA3 Na+/K+-Atpase in Its Na+-Occluded State
Other atoms:
Al (1);
-
8d3x (F: 4) - Human ALPHA3 Na+/K+-Atpase in Its K+-Occluded State
Other atoms:
Mg (1);
-
8d3y (F: 3) - Human ALPHA3 Na+/K+-Atpase in Its Exoplasmic Side-Open State
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8d4p (F: 6) - Crystal Structure of the Sars-Cov-2 (Covid-19) Main Protease in Complex with Inhibitor JUN10-90-3-C1
Other atoms:
Cl (1);
-
8d73 (F: 2) - Crystal Structure of Egfr Lrtm with Compound 7
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8d76 (F: 2) - Crystal Structure of Egfr Lrtm with Compound 24
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8d7u (F: 1) - Cereblon~DDB1 Bound to Cc-92480 with DDB1 in the Linear Conformation
Other atoms:
Zn (1);
-
8d7v (F: 1) - Cereblon~DDB1 Bound to Cc-92480 with DDB1 in the Twisted Conformation
Other atoms:
Zn (1);
-
8d7w (F: 1) - Cereblon~DDB1 Bound to Cc-92480 with DDB1 in the Hinged Conformation
Other atoms:
Zn (1);
Page generated: Mon Aug 4 22:15:54 2025
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