Fluorine in PDB, part 156 (files: 6201-6240),
PDB 6t5b-6u65
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: 6201-6240 (PDB 6t5b-6u65).
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6t5b (F: 2) - KRASG12C Ligand Complex
Other atoms:
Mg (1);
Cl (1);
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6t6f (F: 6) - Crystal Structure of Human Calmodulin-Dependent Protein Kinase 1D (CAMK1D) Bound to Compound 8 (CS275)
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6t8p (F: 12) - Hkatii in Complex with Ligand (2R)-N-Benzyl-1-[6-Methyl-5-(Oxan-4-Yl)- 7-Oxo-6H,7H-[1,3]Thiazolo[5,4-D]Pyrimidin-2-Yl]Pyrrolidine-2- Carboxamide
Other atoms:
I (7);
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6ta3 (F: 3) - Human Kinesin-5 Motor Domain in the Gsk-1 State Bound to Microtubules (Conformation 1)
Other atoms:
Mg (2);
-
6tam (F: 2) - X-Ray Structure of Human K-Ras G12C in Complex with Covalent Isoquinolinone Inhibitor (Compound 3)
Other atoms:
Mg (1);
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6tan (F: 1) - X-Ray Structure of Human K-Ras G12C in Complex with Covalent Isoquinolinone Inhibitor (Compound 17)
Other atoms:
Mg (1);
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6tc8 (F: 20) - 2'-F-Arabinoguanosine and 2'-F-Riboguanosine Modified Hybrid Type G- Quadruplex with V-Loop
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6tcg (F: 20) - 2'-F-Riboguanosine and 2'-F-Arabinoguanosine Modified G-Quadruplex with V-Loop and All-Syn G-Tract
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6tel (F: 4) - Crystal Structure of DOT1L in Complex with An Inhibitor (Compound 10).
Other atoms:
K (1);
Cl (2);
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6ten (F: 4) - Crystal Structure of DOT1L in Complex with An Inhibitor (Compound 11).
Other atoms:
Cl (2);
-
6teq (F: 8) - Crystal Structure of A Galactokinase From Bifidobacterium Infantis in Complex with 2-Deoxy-2-Fluoro-Galactose
Other atoms:
Cl (7);
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6tfp (F: 10) - Btk in Complex with LOU064, A Potent and Highly Selective Covalent Inhibitor
Other atoms:
Na (2);
-
6tiw (F: 3) - Human Kinesin-5 Motor Domain in the Gsk State Bound to Microtubules (Conformation 2)
Other atoms:
Mg (2);
-
6tnb (F: 1) - X-Ray Structure of MPS1 in Complex with Compound 41
Other atoms:
Cl (1);
-
6tnd (F: 5) - X-Ray Structure of MPS1 in Complex with Compound 79
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6tom (F: 2) - Crystal Structure of Human BCL6 Btb Domain in Complex with Compound 1
Other atoms:
Cl (1);
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6tos (F: 2) - Crystal Structure of the Orexin-1 Receptor in Complex with GSK1059865
Other atoms:
Br (2);
Na (1);
-
6tot (F: 4) - Crystal Structure of the Orexin-1 Receptor in Complex with Lemborexant
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6tp6 (F: 2) - Crystal Structure of the Orexin-1 Receptor in Complex with Filorexant
Other atoms:
Cl (1);
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6tpf (F: 4) - Fragment-Based Discovery of Pyrazolopyridones As JAK1 Inhibitors with Excellent Subtype Selectivity
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6tpn (F: 3) - Crystal Structure of the Orexin-2 Receptor in Complex with HTL6641 at 2.61 A Resolution
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6tq6 (F: 6) - Crystal Structure of the Orexin-1 Receptor in Complex with Compound 14
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6tq9 (F: 6) - Crystal Structure of the Orexin-1 Receptor in Complex with Sb-408124
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6tr7 (F: 2) - N-[2-(5-Fluoro-1H-Indol-3-Yl)Ethyl]Acetamide-Notum Complex
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6tti (F: 12) - PKM2 in Complex with Compound 6
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6ttz (F: 14) - Structure of the Clpp:ADEP4-Complex From Staphylococcus Aureus (Open State)
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6tu9 (F: 6) - The ROR1 Pseudokinase Domain Bound to Ponatinib
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6tug (F: 24) - Enterococcus Italicus CSM6 Bound to Cyclic Hexa-2'-Fluoro-Hexa-Damp
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6tvl (F: 3) - Hen Egg White Lysozyme in Complex with A "Half Sandwich"-Type Ru(II) Coordination Compound
Other atoms:
Ru (1);
Cl (1);
Na (1);
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6txg (F: 3) - Proteinase K in Complex with A "Half Sandwich"-Type Ru(II) Coordination Compound
Other atoms:
Ru (2);
Ca (1);
Na (1);
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6tzi (F: 15) - Adc-7 in Complex with Boronic Acid Transition State Inhibitor PFC_001
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6u15 (F: 1) - Human Thymine Dna Glycosylase N140A Mutant Bound to Dna with 2'-F-5- Carboxyl-Dc Substrate Analog
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6u17 (F: 1) - Human Thymine Dna Glycosylase Bound to Dna with 2'-F-5-Carboxyl-Dc Substrate Analog
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6u25 (F: 8) - Crystal Structure of Rar-Related Orphan Receptor C (Nhis- Rorgt(244- 487)-L6-SRC1(678-692)) in Complex with A Tricyclic Inverse Agonist
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6u26 (F: 1) - PCSK9 in Complex with Compound 16
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6u2p (F: 1) - PCSK9 in Complex with Compound 5
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6u36 (F: 1) - PCSK9 in Complex with A Fab and Compound 14
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6u38 (F: 1) - PCSK9 in Complex with A Fab and Compound 8
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6u5m (F: 10) - Discovery and Optimization of Salicyclic Acid-Derived Sulfonamide Inhibitors of the WDR5:Myc Protein-Protein Interaction
Other atoms:
Br (2);
-
6u65 (F: 4) - Mcl-1 Bound to Compound 19
Page generated: Tue Dec 1 09:28:51 2020
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