Fluorine in PDB, part 158 (files: 6281-6320),
PDB 6ra7-6rs3
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: 6281-6320 (PDB 6ra7-6rs3).
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6ra7 (F: 1) - Human Tnik in Complex with Compound 9
Other atoms:
Mg (1);
-
6rb1 (F: 3) - Human Protein Kinase CK2 Alpha in Complex with 2-Cyano-2-Propenamide Compound 1
-
6rcg (F: 6) - Crystal Structure of Casein Kinase 1 Delta (CK1 Delta) Complexed with SR3029 Inhibitor
-
6rch (F: 2) - Crystal Structure of Casein Kinase I Isoform Delta (CK1 Delta) Complexed with SR4133 Inhibitor
Other atoms:
Na (2);
-
6rfv (F: 6) - Revisiting pH-Gated Conformational Switch. Complex HK853-RR468 pH 7
Other atoms:
Mg (2);
-
6rfw (F: 2) - Crystal Structure of T. Brucei Pde-B1 Catalytic Domain with Inhibitor Npd-1039
Other atoms:
Mg (2);
Zn (2);
-
6rgy (F: 6) - Revisiting pH-Gated Conformational Switch. Complex HK853-RR468 pH 7.5
Other atoms:
Mg (2);
-
6rgz (F: 6) - Revisiting pH-Gated Conformational Switch. Complex HK853-RR468 pH 6.5
Other atoms:
Mg (2);
Cl (1);
-
6rh0 (F: 6) - Revisiting pH-Gated Conformational Switch. Complex HK853-RR468 pH 5.5
Other atoms:
Mg (2);
-
6rhl (F: 2) - Room Temperature Data of Galectin-3C in Complex with A Pair of Enantiomeric Ligands: R Enantiomer
-
6rhm (F: 2) - Room Temperature Data of Galectin-3C in Complex with A Pair of Enantiomeric Ligands: S Enantiomer
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6ri4 (F: 2) - Single Crystal Serial Study of the Inhibition of Laccases From Steccherinum Murashkinskyi By Fluoride Anions at Sub-Atomic Resolution. First Structure of the Series with 13 Kgy Dose.
Other atoms:
Cu (6);
-
6ri6 (F: 2) - Single Crystal Serial Study of the Inhibition of Laccases From Steccherinum Murashkinskyi By Fluoride Anions at Sub-Atomic Resolution. Second Structure of the Series with 400 Kgy Dose.
Other atoms:
Cu (7);
-
6ri8 (F: 2) - Single Crystal Serial Study of the Inhibition of Laccases From Steccherinum Murashkinskyi By Fluoride Anions at Sub-Atomic Resolution. Third Structure of the Series with 800 Kgy Dose.
Other atoms:
Cu (7);
-
6rii (F: 2) - Single Crystal Serial Study of the Inhibition of Laccases From Steccherinum Murashkinskyi By Fluoride Anions at Sub-Atomic Resolution. Fourth Structure of the Series with 1200 Kgy Dose.
Other atoms:
Cu (7);
-
6rik (F: 1) - Single Crystal Serial Study of the Inhibition of Laccases From Steccherinum Murashkinskyi By Fluoride Anions at Sub-Atomic Resolution. Thirteenth Structure of the Series with 5200 Kgy Dose.
Other atoms:
Cu (4);
-
6ril (F: 2) - Single Crystal Serial Study of the Inhibition of Laccases From Steccherinum Murashkinskyi By Fluoride Anions at Sub-Atomic Resolution. Fourteenth Structure of the Series with 5600 Kgy Dose (Data Was Collected After Refreezing).
Other atoms:
Cu (7);
-
6rit (F: 2) - Human Carbonic Anhydrase II in Complex with 2-Fluorobenzenesulfonamide
Other atoms:
Hg (2);
Zn (1);
-
6rj7 (F: 6) - Crystal Structure of the 19F Labelled Oxa-48
Other atoms:
Ca (1);
Cl (1);
-
6rjj (F: 4) - Human Carbonic Anhydrase II in Complex with Fluorinated Benzenesulfonamide
Other atoms:
Hg (2);
Zn (1);
-
6rkb (F: 2) - Crystal Structure of Human Monoamine Oxidase B in Complex with Styrylpiperidine Analogue 1
-
6rkn (F: 2) - Human Carbonic Anhydrase II in Complex with A Fluorinated Benzenesulfonamide.
Other atoms:
Hg (2);
Zn (1);
-
6rkp (F: 6) - Crystal Structure of Human Monoamine Oxidase B in Complex with Styrylpiperidine Analogue 84
-
6rln (F: 4) - Crystal Structure of RIP1 Kinase in Complex with GSK3145095
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6rmx (F: 3) - Human Carbonic Anhydrase II Mutant T199V Bound By 2-[(1S)-2,3-Dihydro- 1H-Inden-1-Ylamino]-3,5,6-Trifluoro-4-[(2-Hydroxyethyl) Thio]Benzenesulfonamide
Other atoms:
Zn (1);
Na (1);
-
6rmy (F: 3) - Human Carbonic Anhydrase II Mutant T199V Bound By 3-(Cyclooctylamino)- 2,5,6-Trifluoro-4-[(2-Hydroxyethyl)Sulfonyl]Benzenesulfonamide
Other atoms:
Zn (1);
-
6rne (F: 1) - DPP1 in Complex with Inhibitor
Other atoms:
Cl (1);
-
6rnp (F: 4) - Human Carbonic Anhydrase II in Complex with Fluorinated Benzenesulfonamide
Other atoms:
Hg (2);
Zn (1);
-
6rnr (F: 3) - The Crystal Structure of A Complex Between the Llfpg Protein, A Thf- Dna and An Inhibitor
-
6rnu (F: 2) - Bcl-Xl in A Complex with A Covalent Small Molecule Inhibitor
Other atoms:
Br (1);
-
6roe (F: 6) - Human Carbonic Anhydrase II in Complex with Fluorinated Benzenesulfonamide
Other atoms:
Hg (2);
Zn (1);
-
6rof (F: 6) - Human Carbonic Anhydrase II Mutant T199V Bound By 2-(Cyclooctylamino)- 3,5,6-Trifluoro-4-[(2-Hydroxyethyl)Thio]Benzenesulfonamide
Other atoms:
Zn (1);
Na (1);
-
6roh (F: 3) - Cryo-Em Structure of the Autoinhibited DRS2P-CDC50P
Other atoms:
Mg (1);
-
6roi (F: 3) - Cryo-Em Structure of the Partially Activated DRS2P-CDC50P
Other atoms:
Mg (1);
-
6roj (F: 3) - Cryo-Em Structure of the Activated DRS2P-CDC50P
Other atoms:
Mg (1);
-
6rq6 (F: 2) - CYP121 in Complex with 3-Fluoro Dicyclotyrosine
Other atoms:
Fe (2);
-
6rqi (F: 1) - Human Carbonic Anhydrase II in Complex with Fluorinated Benzenesulfonamide
Other atoms:
Hg (2);
Zn (1);
-
6rrg (F: 4) - Human Carbonic Anhydrase II in Complex with Fluorinated Benzenesulfonamide
Other atoms:
Hg (2);
Zn (1);
-
6rri (F: 8) - Human Carbonic Anhydrase II in Complex with Fluorinated Benzenesulfonamide
Other atoms:
Hg (2);
Zn (1);
-
6rs3 (F: 20) - 2'-F-Riboguanosine Modified G-Quadruplex with V-Loop
Page generated: Fri May 13 23:24:31 2022
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