Fluorine in PDB, part 110 (files: 4361-4400),
PDB 5olw-5p92
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: 4361-4400 (PDB 5olw-5p92).
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5olw (F: 6) - 5-Fluorotryptophan Labeled Beta-Phosphoglucomutase in An Open Conformation
Other atoms:
Ca (5);
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5olx (F: 5) - 5-Fluorotryptophan Labeled Beta-Phosphoglucomutase in A Closed Conformation, Orthorhomic Crystal Form
Other atoms:
Mg (3);
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5oly (F: 10) - 5-Fluorotryptophan Labeled Beta-Phosphoglucomutase in A Closed Conformation, Monoclinic Crystal Form
Other atoms:
Mg (6);
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5omg (F: 1) - P38ALPHA in Complex with Pyrazolobenzothiazine Inhibitor COXP4M12
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5onl (F: 2) - Yndl-Apo (Zinc-Free)
-
5op4 (F: 4) - Structure of CHK1 10-Pt. Mutant Complex with Aminopyrimidine LRRK2 Inhibitor
-
5opa (F: 1) - The Crystal Structure of P450 CYP121 in Complex with Lead Compound 7B
Other atoms:
Fe (2);
-
5opx (F: 42) - Crystal Structure of the Groel Mutant A109C in Complex with Groes and Adp BEF2
Other atoms:
Mg (14);
K (14);
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5oq4 (F: 3) - PQR309 - A Potent, Brain-Penetrant, Orally Bioavailable, Pan-Class I PI3K/Mtor Inhibitor As Clinical Candidate in Oncology
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5oqw (F: 2) - Xiap in Complex with Small Molecule
Other atoms:
Zn (2);
Na (1);
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5or6 (F: 3) - Crystal Structures of PYR1/HAB1 in Complex with Synthetic Analogues of Abscisic Acid
Other atoms:
Mn (3);
-
5or8 (F: 1) - Crystal Structure of BAZ2A Bromodomain in Complex with 1,3-Dimethyl- Benzimidazolone Compound 1
-
5or9 (F: 1) - Crystal Structure of BAZ2B Bromodomain in Complex with 1-Methyl- Cyclopentapyrazole Compound 13
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5ork (F: 1) - The Crystal Structure of CK2ALPHA in Complex with Compound 6
Other atoms:
Mg (2);
Cl (2);
-
5orl (F: 1) - Crystal Structure of Aurora-A Kinase in Complex with An Allosterically Binding Fragment
Other atoms:
Mg (2);
Cl (4);
-
5orp (F: 3) - Crystal Structure of Aurora-A Kinase in Complex with An Allosterically Binding Fragment
Other atoms:
Mg (2);
Cl (1);
-
5orr (F: 3) - Crystal Structure of Aurora-A Kinase in Complex with An Allosterically Binding Fragment
Other atoms:
Mg (2);
Cl (2);
-
5orw (F: 1) - Crystal Structure of Aurora-A Kinase in Complex with An Allosterically Binding Fragment
Other atoms:
Mg (2);
-
5ory (F: 2) - Crystal Structure of Aurora-A Kinase in Complex with An Allosterically Binding Fragment
Other atoms:
Mg (2);
Cl (3);
-
5os8 (F: 4) - The Crystal Structure of CK2ALPHA in Complex with Compound 11
Other atoms:
Cl (4);
-
5osu (F: 3) - The Crystal Structure of CK2ALPHA in Complex with Analogues of Compound 1
Other atoms:
Cl (1);
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5oty (F: 3) - The Crystal Structure of CK2ALPHA in Complex with CAM4712
Other atoms:
Cl (2);
-
5otz (F: 3) - The Crystal Structure of CK2ALPHA in Complex with Compound 1
Other atoms:
Cl (4);
-
5ouj (F: 1) - Crystal Structure of Human AKR1B1 Complexed with Nadp+ and Compound 39
Other atoms:
Cl (1);
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5ouk (F: 1) - Crystal Structure of Human AKR1B1 Complexed with Nadp+ and Compound 41
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5oul (F: 11) - The Crystal Structure of CK2ALPHA in Complex with Compound 9
Other atoms:
Cl (8);
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5ov2 (F: 30) - 2'F-Ana-G Modified Quadruplex with A Flipped Tetrad
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5ow1 (F: 2) - X-Ray Characterization of Striatal-Enriched Protein Tyrosine Phosphatase Inhibitors
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5ow8 (F: 6) - Indole-2 Carboxamides As Selective Secreted Phospholipase A2 Type X (SPLA2-X) Inhibitors
Other atoms:
Cl (4);
Ca (2);
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5owc (F: 6) - Indole-2 Carboxamides As Selective Secreted Phospholipase A2 Type X (SPLA2-X) Inhibitors
Other atoms:
Ca (2);
-
5owp (F: 1) - Crystal Structure of Glycopeptide "Gvtsafpdt*Rpap" in Complex with Scfv-SM3
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5owq (F: 2) - Human STK10 Bound to Dovitinib
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5owz (F: 3) - Glycogen Phosphorylase in Complex with KS172
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5oxd (F: 3) - Complex of A C. Perfringens O-Glcnacase with A Fragment Hit
Other atoms:
Cd (22);
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5p8x (F: 2) - Humanized Rat Catechol O-Methyltransferase in Complex with N-[2-[5- (1H-Benzimidazol-5-Yl)-4H-1,2,4-Triazol-3-Yl]Ethyl]-5-(4- Fluorophenyl)-2,3-Dihydroxybenzamide at 1.31A
Other atoms:
Mg (1);
Cl (2);
-
5p8y (F: 1) - Humanized Rat Catechol O-Methyltransferase in Complex with 5-(4- Fluorophenyl)-2,3-Dihydroxy-N-[3-(Pyrrolo[3,2-C]Pyridin-1-Ylmethoxy) Propyl]Benzamide at 1.42A
Other atoms:
Mg (1);
Cl (2);
-
5p8z (F: 1) - Humanized Rat Catechol O-Methyltransferase in Complex with 5-(4- Fluorophenyl)-2,3-Dihydroxy-N-(4-Thieno[3,2-C]Pyridin-2-Ylbutyl) Benzamide at 1.42A
Other atoms:
Mg (1);
Cl (2);
-
5p90 (F: 1) - Humanized Rat Catechol O-Methyltransferase in Complex with 5-(4- Fluorophenyl)-2,3-Dihydroxy-N-[(E)-5-Pyrrolo[3,2-C]Pyridin-1-Ylpent- 3-Enyl]Benzamide at 1.24A
Other atoms:
Mg (1);
Cl (2);
-
5p91 (F: 2) - Humanized Rat Catechol O-Methyltransferase in Complex with 5-(4- Fluorophenyl)-2,3-Dihydroxy-N-[2-[5-(2-Methylpyridin-4-Yl)-4H-1,2,4- Triazol-3-Yl]Ethyl]Benzamide at 1.20A
Other atoms:
Mg (1);
Cl (2);
-
5p92 (F: 1) - Humanized Rat Catechol O-Methyltransferase in Complex with 5-(4- Fluorophenyl)-2,3-Dihydroxy-N-(4-Thieno[2,3-C]Pyridin-2-Ylbutyl) Benzamide at 1.61A
Other atoms:
Mg (1);
Cl (2);
Page generated: Sun Dec 15 10:24:41 2024
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