Fluorine in PDB, part 140 (files: 5561-5600),
PDB 6ho3-6ic6
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: 5561-5600 (PDB 6ho3-6ic6).
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6ho3 (F: 3) - Transcriptional Repressor Ethr From Mycobacterium Tuberculosis in Complex with BDM43265
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6ho4 (F: 3) - Transcriptional Repressor Ethr From Mycobacterium Tuberculosis in Complex with BDM44693
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6ho6 (F: 3) - Transcriptional Repressor Ethr From Mycobacterium Tuberculosis in Complex with BDM44725
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6ho7 (F: 3) - Transcriptional Repressor Ethr From Mycobacterium Tuberculosis in Complex with BDM44814
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6ho8 (F: 3) - Transcriptional Repressor Ethr From Mycobacterium Tuberculosis in Complex with BDM44815
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6ho9 (F: 3) - Transcriptional Repressor Ethr From Mycobacterium Tuberculosis in Complex with BDM44825
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6hoa (F: 3) - Transcriptional Repressor Ethr From Mycobacterium Tuberculosis in Complex with BDM44830
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6hob (F: 3) - Transcriptional Repressor Ethr From Mycobacterium Tuberculosis in Complex with BDM44831
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6hoc (F: 3) - Transcriptional Repressor Ethr From Mycobacterium Tuberculosis in Complex with BDM44847
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6hoe (F: 3) - Transcriptional Repressor Ethr From Mycobacterium Tuberculosis in Complex with BDM44850
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6hof (F: 6) - Transcriptional Repressor Ethr From Mycobacterium Tuberculosis in Complex with BDM44852
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6hoo (F: 1) - Crystal Structure of Rationally Designed Oxa-48LOOP18 Beta-Lactamase
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6hp9 (F: 6) - Structure of the Kinase Domain of Human DDR1 in Complex with A 2- Amino-2,3-Dihydro-1H-Indene-5-Carboxamide-Based Inhibitor
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6hpu (F: 8) - Crystal Structure of Human PIF1 Helicase in Complex with Adp-ALF4
Other atoms:
Mg (2);
Al (2);
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6hr2 (F: 2) - Crystal Structure of Protac 2 in Complex with the Bromodomain of Human SMARCA4 and Pvhl:Elonginc:Elonginb
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6hrj (F: 2) - Apo - Yndl
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6hrp (F: 1) - Crystal Structure of Btk Kinase Domain Complexed with 6- (Dimethylamino)-2-[2-(Hydroxymethyl)-3-[1-Methyl-5-[[5-(Morpholine-4- Carbonyl)-2-Pyridyl]Amino]-6-Oxo-3-Pyridyl]Phenyl]-3,4- Dihydroisoquinolin-1-One
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6hrt (F: 1) - Crystal Structure of Btk Kinase Domain Complexed with 12-(6-Tert- Butyl-8-Fluoro-1-Oxo-Phthalazin-2-Yl)-9-Hydroxy-6-Methyl-4-[[5- (Morpholine-4-Carbonyl)-2-Pyridyl]Amino]-6-Azatricyclo[9.4.0.02, 7]Pentadeca-1(15),2(7),3,11,13-Pentaen-5-One
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6hs2 (F: 3) - ETHR2 in Complex with Compound 31 (BDM76150)
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6hu3 (F: 4) - Crystal Structure of Schistosoma Mansoni HDAC8 Complexed with A Triazole Hydroxamate Inhibitor
Other atoms:
K (8);
Zn (4);
Cl (4);
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6hwt (F: 1) - Crystal Structure of P38ALPHA in Complex with A Reduced Photoswitchable 2-Azothiazol-Based Inhibitor (Compound 31)
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6hwu (F: 1) - Crystal Structure of P38ALPHA in Complex with A Photoswitchable 2- Azothiazol-Based Inhibitor (Compound 2)
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6hwv (F: 2) - Crystal Structure of P38ALPHA in Complex with A Photoswitchable 2- Azoimidazol-Based Inhibitor (Compound 3)
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6i03 (F: 4) - D10N Variant of Beta-Phosphoglucomutase From Lactococcus Lactis Complexed with Tetrafluoroaluminate and Beta-G6P to 1.02 A
Other atoms:
Mg (1);
Al (1);
Na (1);
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6i0j (F: 6) - Crystal Structure of Human Carbonic Anhydrase I in Complex with the 4- ({[4-Chloro-3-(Trifluoromethyl)Phenyl]Carbamoyl}Amino)Phenyl Sulfamate Inhibitor
Other atoms:
Cl (2);
Zn (2);
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6i0l (F: 3) - Crystal Structure of Human Carbonic Anhydrase I in Complex with the 1- [4-Chloro-3-(Trifluoromethyl)Phenyl]-3-[2-(4-Sulfamoylphenyl) Ethyl]Urea Inhibitor
Other atoms:
Cl (1);
Zn (2);
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6i15 (F: 2) - Crystal Structure of Fascin in Complex with Compound 11
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6i2y (F: 4) - Human STK10 Bound to Foretinib
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6i3s (F: 1) - Crystal Structure of MDM2 in Complex with Compound 13.
Other atoms:
Cl (2);
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6i4b (F: 6) - Plasmodium Falciparum Dihydroorotate Dehydrogenase (Dhodh) Co- Crystallized with 3-Hydroxy-1-Methyl-5-((3-(Trifluoromethyl)Phenoxy) Methyl)-1H-Pyrazole-4-Carboxylic Acid
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6i4i (F: 3) - Crystal Structure of Plasmodium Falciparum Actin I (F54Y Mutant) in the Mg-K-Adp-Alfn State
Other atoms:
Mg (1);
Al (1);
K (2);
Ca (2);
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6i74 (F: 5) - Galectin-3C in Complex with Substituted Polyfluoroaryl Monothiogalactoside Derivative 1
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6i75 (F: 4) - Galectin-3C in Complex with Substituted Polyfluoroaryl Monothiogalactoside Derivative 2
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6i76 (F: 4) - Galectin-3C in Complex with Substituted Polyfluoroaryl Monothiogalactoside Derivative-3
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6i77 (F: 4) - Galectin-3C in Complex with Substituted Polyfluoroaryl Monothiogalactoside Derivative-4
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6i78 (F: 4) - Galectin-3C in Complex with Substituted Polyfluoroaryl Monothiogalactoside Derivative 5
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6i8z (F: 3) - Crystal Structure of PTK2 in Complex with Bi-4464.
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6ibf (F: 12) - Crystal Structure of Human Phosphodiesterase 4D2 Catalytic Domain with Inhibitor Npd-417
Other atoms:
Mg (4);
Zn (4);
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6ic2 (F: 1) - Polypharmacology of Epacadostat: A Potent and Selective Inhibitor of the Tumor Associated Carbonic Anhydrases IX and XII
Other atoms:
Br (1);
Zn (1);
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6ic6 (F: 3) - Human Cathepsin-C in Complex with Cyclopropyl Peptidyl Nitrile Inhibitor 1
Other atoms:
Cl (1);
Page generated: Tue Dec 1 09:27:41 2020
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