Fluorine in PDB, part 226 (files: 9001-9040),
PDB 8c41-8cqk
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 8c41-8cqk).
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8c41 (F: 6) - High Resolution Structure of the Streptococcus Pneumoniae Topoisomerase IV-Dna Complex with the Novel Fluoroquinolone Delafloxacin
Other atoms:
Mg (6);
Cl (4);
-
8c48 (F: 1) - Crystal Structure of Thermothelomyces Thermophila GH30 (Double Mutant Ee) in Complex with Xylopentaose
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8c5q (F: 2) - CK2 Kinase Bound to Inhibitor AB668
Other atoms:
Cl (1);
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8c6q (F: 3) - Fragment Screening Hit II Bound to Endothiapepsin
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8c78 (F: 3) - Crystal Structure of Human BCL6 Btb Domain in Complex with Compound CCT374705
Other atoms:
Cl (3);
-
8c7x (F: 4) - Crystal Structure of Braf in Complex with A Hybrid Compound 6
Other atoms:
Cl (2);
Br (3);
-
8c7y (F: 4) - Crystal Structure of Braf V600E in Complex with A Hybrid Compound 6
Other atoms:
Cl (2);
-
8caa (F: 14) - Crystal Structure of TEAD4 in Complex with Ytp-13
Other atoms:
Cl (6);
-
8cae (F: 3) - Crystal Structure of Sars-Cov-2 Mpro-H172Y Mutant in Complex with Nirmatrelvir
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8cbv (F: 2) - Hiv-1 Integrase Catalytic Core Domain and C-Terminal Domain in Complex with Allosteric Integrase Inhibitor Mut-148916
Other atoms:
Cl (1);
Mg (2);
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8cc4 (F: 6) - Lasb Bound to Phosphonic Acid Based Inhibitor
Other atoms:
Zn (2);
Ca (2);
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8cd8 (F: 4) - Ulilysin - C269A with Aebsf Complex
Other atoms:
Zn (2);
Ca (5);
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8cex (F: 1) - Structure of the Mouse 8-Oxoguanine Dna Glycosylase MOGG1 in Complex with Ligand TH11227
Other atoms:
Ni (1);
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8cf2 (F: 14) - Solution Structure of the Rna Helix Formed By the 5'-End of U1 Snrna and An A-1 Bulged 5'-Splice Site in Complex with Smn-Cy
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8cf8 (F: 1) - Eravacycline Bound to the 30S Head
Other atoms:
K (12);
Mg (32);
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8cfb (F: 2) - Crystal Structure of S-Adenosyl-L-Homocysteine Hydrolase From P. Aeruginosa in Complex with F2X-Entry Library Fragment D02
Other atoms:
K (4);
-
8cfi (F: 1) - Crystal Structure of S-Adenosyl-L-Homocysteine Hydrolase From P. Aeruginosa in Complex with F2X-Entry Library Fragment D07
Other atoms:
K (4);
-
8cfn (F: 2) - Crystal Structure of S-Adenosyl-L-Homocysteine Hydrolase From P. Aeruginosa in Complex with F2X-Entry Library Fragment F03
Other atoms:
K (2);
-
8cfq (F: 3) - Crystal Structure of S-Adenosyl-L-Homocysteine Hydrolase From P. Aeruginosa in Complex with F2X-Entry Library Fragment F11
Other atoms:
K (4);
-
8cgi (F: 1) - Pentacycline TP038 Bound to the 30S Head
Other atoms:
Mg (32);
K (10);
-
8cgo (F: 1) - Structure of Human Butyrylcholinesterase in Complex with N-{[2- (Benzyloxy)-3-Methoxyphenyl]Methyl}-N-[3-(2-Fluorophenyl) Propyl]Cyclobutanamine
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8cgv (F: 2) - Tiamulin Bound to the 50S Subunit
Other atoms:
Mg (219);
Zn (1);
K (83);
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8cie (F: 2) - Crystal Structure of the Human CDKL5 Kinase Domain with Compound Yl- 354
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8cij (F: 1) - Crystal Structure of Human HPK1 (MAP4K1) Complex with 2-[8-Amino-7- Fluoro-6-(8-Methyl-2,3-Dihydro-1H-Pyrido[2,3-B][1,4]Oxazin-7-Yl)- Isoquinolin-3-Ylamino]-6-Isopropyl-5,6-Dihydro-4H-1,6,8A-Triaza- Azulen-7-One
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8cjo (F: 1) - Crystal Structure of Human Tryptophan Hydroxylase 1 in Complex with Inhibitor Km-06-004
Other atoms:
Cl (1);
Fe (1);
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8ck3 (F: 4) - Structure of HIF2A-Arnt Heterodimer in Complex with (S)-1-(3,5- Difluoro-Phenyl)-5,5-Difluoro-3-Methanesulfonyl-5,6-Dihydro-4H- Cyclopenta[C]Thiophen-4-Ol
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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);
-
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);
-
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);
-
8cnn (F: 3) - BEF3 Phospho-Hras Gsa Complex
Other atoms:
Mg (1);
-
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);
-
8cow (F: 2) - Mycobacterium Tuberculosis Dihydrofolate Reductase in Complex with 5- (Cyclopropylethynyl)-6-(2-Fluorophenyl)Pyrimidine-2,4-Diamine
Other atoms:
Co (2);
-
8cq9 (F: 3) - Mycobacterium Tuberculosis Dihydrofolate Reductase in Complex with 5- (Cyclopropylethynyl)-6-(4-(Trifluoromethyl)Phenyl)Pyrimidine-2,4- Diamine
Other atoms:
Co (2);
-
8cqb (F: 6) - Cryo-Em Structure of the Human GBP1 Dimer Bound to Gdp-ALF3
Other atoms:
Al (2);
Mg (2);
-
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);
-
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);
Page generated: Tue Aug 26 20:23:54 2025
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