Fluorine in PDB, part 202 (files: 8041-8080),
PDB 7ovf-7pmq
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: 8041-8080 (PDB 7ovf-7pmq).
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7ovf (F: 1) - Crystal Structure of the Vim-2 Acquired Metallo-Beta-Lactamase in Complex with Compound 8 (Jmv-7207)
Other atoms:
Zn (3);
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7ovj (F: 2) - Protein Kinase MKK7 in Complex with Difluoro-Phenethyltriazole- Substituted Pyrazolopyrimidine
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7oyf (F: 3) - Crystal Structure of Depupylase Dop in Complex with Pup and Adp/Trifluoromagnesate
Other atoms:
Mg (4);
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7oyh (F: 4) - Crystal Structure of Depupylase Dop in Complex with Pup and Adp/Tetrafluoromagnesate
Other atoms:
Mg (6);
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7ozk (F: 3) - Cryoem Structure of Human Enterovirus 70 in Complex with Pleconaril
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7ozx (F: 4) - Structure of Human Galactokinase 1 Bound with Azepan-1-Yl(2,6- Difluorophenyl)Methanone
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7p1e (F: 3) - Structure of Kdnase From Aspergillus Terrerus in Complex with 2,3- Difluoro-2-Keto-3-Deoxynononic Acid
Other atoms:
Ca (1);
Cl (1);
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7p1r (F: 4) - Structure of Trichophyton Rubrum Kdnase in Complex with 2,3-Difluoro- Kdn
Other atoms:
Na (4);
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7p2s (F: 1) - Crystal Structure of Schistosoma Mansoni HDAC8 in Complex with A Tricyclic Thieno[3,2-B]Indole Capped Hydroxamate-Based Inhibitor, Chlorine Derivative
Other atoms:
K (2);
Zn (1);
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7p3c (F: 2) - Eed in Complex with Compound 4
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7p3g (F: 1) - Eed in Complex with Compound 4
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7p3j (F: 1) - Eed in Complex with Compound 4
Other atoms:
Mg (3);
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7p3v (F: 6) - B-Raf V600E Structure Bound to A New Inhibitor
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7p4e (F: 4) - Crystal Structure of Ppargamma in Complex with Compound FL217
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7p4k (F: 8) - Soluble Epoxide Hydrolase in Complex with FL217
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7p4u (F: 3) - Crystal Structure of Pqsr (Mvfr) Ligand-Binding Domain in Complex with 3-Pyridin-4-Yl-2,4-Dihydro-Indeno[1,2-.C.]Pyrazole
Other atoms:
Cl (1);
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7p58 (F: 3) - Pyrazole Carboxylic Acid Inhibitors of KEAP1:NRF2 Interaction
Other atoms:
Cl (1);
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7p5e (F: 3) - Pyrazole Carboxylic Acid Inhibitors of KEAP1:NRF2 Interaction
Other atoms:
Cl (1);
-
7p5k (F: 1) - Pyrazole Carboxylic Acid Inhibitors of KEAP1:NRF2 Interaction
Other atoms:
Cl (1);
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7p80 (F: 4) - Crystal Structure of Clpp From Bacillus Subtilis in Complex with ADEP2 (Compressed State)
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7p81 (F: 40) - Crystal Structure of Clpp From Bacillus Subtilis in Complex with ADEP2 (Compact State)
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7pav (F: 6) - MALT1 in Complex with Compound 1
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7paw (F: 3) - MALT1 in Complex with Compound 1
Other atoms:
Cl (1);
-
7pcd (F: 1) - HER2 in Complex with A Covalent Inhibitor
Other atoms:
Cl (2);
-
7pg6 (F: 3) - Crystal Structure of PI3KALPHA in Complex with the Inhibitor Nvp- BYL719
Other atoms:
Na (1);
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7ph1 (F: 1) - Trypsin in Complex with Bpti Mutant (2S)-2-Amino-4-Monofluorobutanoic Acid
Other atoms:
Ca (1);
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7phj (F: 1) - Lpxc Inhibitors with Fluoroproline As A Novel Zinc-Binding Group Can Serve As A Novel Class of Antibiotic with Activity Against Multidrug- Resistant Gram-Negative Bacteria
Other atoms:
Zn (1);
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7phn (F: 1) - Lpxc Inhibitors with Fluoroproline As A Novel Zinc-Binding Group Can Serve As A Novel Class of Antibiotic with Activity Against Multidrug- Resistant Gram-Negative Bacteria
Other atoms:
Zn (1);
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7pj2 (F: 1) - Lpxc Inhibitors with Fluoroproline As A Novel Zinc-Binding Group Can Serve As A Novel Class of Antibiotic with Activity Against Multidrug- Resistant Gram-Negative Bacteria
Other atoms:
Zn (1);
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7pjc (F: 2) - The Structure of Candida Albicans Phosphoglucomutase with Isothiazolone Modification on CYS359
Other atoms:
Cl (2);
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7pjn (F: 4) - Crystal Structure of Ivosidenib-Resistant IDH1 Variant R132C S280F in Complex with Nadph and Inhibitor Ds-1001B
Other atoms:
Cl (12);
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7pjr (F: 6) - NOTUM_ARUK3000438
Other atoms:
Cl (2);
-
7pk3 (F: 3) - NOTUM_ARUK3001185
Other atoms:
Cl (2);
-
7pk8 (F: 1) - Lpxc Inhibitors with Fluoroproline As A Novel Zinc-Binding Group Can Serve As A Novel Class of Antibiotic with Activity Against Multidrug- Resistant Gram-Negative Bacteria
Other atoms:
Zn (1);
-
7pkk (F: 1) - Lpxc Inhibitors with Fluoroproline As A Novel Zinc-Binding Group Can Serve As A Novel Class of Antibiotic with Activity Against Multidrug- Resistant Gram-Negative Bacteria
Other atoms:
Zn (1);
-
7pkm (F: 1) - Lpxc Inhibitors with Fluoroproline As A Novel Zinc-Binding Group Can Serve As A Novel Class of Antibiotic with Activity Against Multidrug- Resistant Gram-Negative Bacteria
Other atoms:
Zn (1);
-
7pkv (F: 3) - NOTUM_INHIBITOR ARUK3000223
Other atoms:
Cl (1);
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7pli (F: 18) - Dead-Box Helicase Dbpa Bound to Single Stranded Rna and Adp/BEF3
Other atoms:
Mg (6);
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7pmm (F: 6) - Dead-Box Helicase Dbpa in the Active Conformation Bound to A Ss/Dsrna Junction and Adp/BEF3
Other atoms:
Mg (2);
-
7pmq (F: 12) - Dead-Box Helicase Dbpa in the Active Conformation Bound to A Hairpin Loop Rna and Adp/BEF3
Other atoms:
Mg (4);
Page generated: Sun Dec 15 10:28:06 2024
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