Fluorine in PDB, part 57 (files: 2241-2280),
PDB 460d-4az3
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: 2241-2280 (PDB 460d-4az3).
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460d (F: 2) - A "Hydrat-Ion Spine" in A B-Dna Minor Groove
Other atoms:
Rb (1);
Mg (3);
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461d (F: 2) - A "Hydrat-Ion Spine" in A B-Dna Minor Groove
Other atoms:
Rb (1);
Mg (2);
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478d (F: 2) - Crystal Structure of the B-Dna Dodecamer 5'-D(Cgcgaa(Taf) Tcgcg), Where Taf Is 2'-Deoxy-2'-Fluoro-Arabino-Furanosyl Thymine
Other atoms:
Ca (3);
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4a36 (F: 6) - Structure of Duck Rig-I Helicase Domain Bound to 19-Mer Dsrna and Atp Transition State Analogue
Other atoms:
Mg (2);
Al (2);
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4a3h (F: 1) - 2',4' Dinitrophenyl-2-Deoxy-2-Fluro-B-D-Cellobioside Complex of the Endoglucanase CEL5A From Bacillus Agaradhaerens at 1.6 A Resolution
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4a4l (F: 3) - Crystal Structure of Polo-Like Kinase 1 in Complex with A 5-(2-Amino-Pyrimidin-4-Yl)-1H-Pyrrole Inhibitor
Other atoms:
Zn (1);
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4a4o (F: 3) - Crystal Structure of Polo-Like Kinase 1 in Complex with A 2- (2-Amino-Pyrimidin-4-Yl)-1,5,6,7-Tetrahydro-Pyrrolopyridin- 4-One Inhibitor
Other atoms:
Zn (1);
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4a4x (F: 3) - NEK2-Ede Bound to CCT248662
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4a6l (F: 4) - Beta-Tryptase Inhibitor
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4a6v (F: 6) - X-Ray Structures of Oxazole Hydroxamate Ecmetap-Mn Complexes
Other atoms:
Mn (4);
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4a7c (F: 3) - Crystal Structure of PIM1 Kinase with ETP46546
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4a7s (F: 2) - Structure of Human I113T SOD1 Mutant Complexed with 5- Fluorouridine in the P21 Space Group
Other atoms:
Cu (4);
Zn (2);
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4a92 (F: 4) - Full-Length Hcv NS3-4A Protease-Helicase in Complex with A Macrocyclic Protease Inhibitor.
Other atoms:
Zn (2);
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4a98 (F: 10) - X-Ray Structure of A Pentameric Ligand Gated Ion Channel From Erwinia Chrysanthemi (Elic) in Complex with Bromoflurazepam
Other atoms:
Br (10);
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4aaa (F: 2) - Crystal Structure of the Human CDKL2 Kinase Domain
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4acu (F: 3) - Aminoimidazoles As Bace-1 Inhibitors. X-Ray Crystal Structure of Beta Secretase Complexed with Compound 14
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4acx (F: 4) - Aminoimidazoles As Bace-1 Inhibitors. X-Ray Crystal Structure of Beta Secretase Complexed with Compound 23
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4afe (F: 3) - NEK2 Bound to Hybrid Compound 21
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4agd (F: 1) - Crystal Structure of VEGFR2 (Juxtamembrane and Kinase Domains) in Complex with Sunitinib (SU11248) (N-2- Diethylaminoethyl)-5-((Z)-(5-Fluoro-2-Oxo-1H-Indol-3- Ylidene)Methyl)-2,4-Dimethyl-1H-Pyrrole-3-Carboxamide)
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4agw (F: 6) - Discovery of A Small Molecule Type II Inhibitor of Wild- Type and Gatekeeper Mutants of Bcr-Abl, Pdgfralpha, Kit, and Src Kinases
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4ajm (F: 1) - Development of A Plate-Based Optical Biosensor Methodology to Identify PDE10 Fragment Inhibitors
Other atoms:
Mg (2);
Zn (2);
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4amw (F: 4) - Crystal Structure of the Gracilariopsis Lemaneiformis Alpha- 1,4-Glucan Lyase Covalent Intermediate Complex with 5- Fluoro-Idosyl-Fluoride
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4amx (F: 4) - Crystal Structure of the Gracilariopsis Lemaneiformis Alpha-1,4-Glucan Lyase Covalent Intermediate Complex with 5-Fluoro-Glucosyl-Fluoride
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4an2 (F: 3) - Crystal Structures of Human MEK1 with Carboxamide-Based Allosteric Inhibitor XL518 (Gdc-0973), or Related Analogs.
Other atoms:
Mg (1);
I (1);
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4an3 (F: 3) - Crystal Structures of Human MEK1 with Carboxamide-Based Allosteric Inhibitor XL518 (Gdc-0973), or Related Analogs.
Other atoms:
Mg (1);
I (1);
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4an9 (F: 3) - Crystal Structures of Human MEK1 with Carboxamide-Based Allosteric Inhibitor XL518 (Gdc-0973), or Related Analogs.
Other atoms:
Mg (1);
I (1);
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4anb (F: 3) - Crystal Structures of Human MEK1 with Carboxamide-Based Allosteric Inhibitor XL518 (Gdc-0973), or Related Analogs.
Other atoms:
Mg (1);
I (1);
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4anj (F: 4) - Myosin VI (MDINSERT2-Gfp Fusion) Pre-Powerstroke State (Mg.Adp.ALF4)
Other atoms:
Mg (1);
Al (1);
Ca (3);
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4anq (F: 1) - Structure of G1269A Mutant Anaplastic Lymphoma Kinase in Complex with Crizotinib
Other atoms:
Cl (2);
-
4ans (F: 1) - Structure of L1196M,G1269A Double Mutant Anaplastic Lymphoma Kinase in Complex with Crizotinib
Other atoms:
Cl (2);
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4anw (F: 4) - Complexes of PI3KGAMMA with Isoform Selective Inhibitors.
Other atoms:
Cl (2);
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4aoj (F: 3) - Human Trka in Complex with the Inhibitor Az-23
Other atoms:
Cl (3);
Zn (6);
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4ap7 (F: 1) - Crystal Structure of C-Met Kinase Domain in Complex with 4-( (6-(4- Fluorophenyl)-(1,2,4)Triazolo(4,3-B)(1,2,4)Triazin-3-Yl)Methyl) Phenol
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4ark (F: 2) - Crystal Structure of the Catalytic Domain of Human Map Kinase Kinase 1 (MEK1) in Complex with A Small Molecule Inhibitor and Adp
Other atoms:
Mg (1);
I (1);
-
4asd (F: 3) - Crystal Structure of VEGFR2 (Juxtamembrane and Kinase Domains) in Complex with Sorafenib (Bay 43-9006)
Other atoms:
Cl (1);
-
4at4 (F: 4) - Crystal Structure of Trkb Kinase Domain in Complex with EX429
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4aw1 (F: 3) - Human PDK1 Kinase Domain in Complex with Allosteric Compound PS210 Bound to the Pif-Pocket
Other atoms:
Mn (1);
Cl (3);
Na (2);
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4axx (F: 3) - The Catalytically Active Fully Closed Conformation of Human Phosphoglycerate Kinase in Complex with Adp 3-Phosphoglycerate and Beryllium Trifluoride
Other atoms:
Mg (1);
Cl (1);
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4az0 (F: 1) - Crystal Structure of Cathepsin A, Complexed with 8A.
Other atoms:
Cd (6);
-
4az3 (F: 2) - Crystal Structure of Cathepsin A, Complexed with 15A
Other atoms:
Cd (4);
Page generated: Tue Dec 1 09:21:25 2020
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