Fluorine in PDB, part 123 (files: 4881-4920),
PDB 5v5e-5vo4
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: 4881-4920 (PDB 5v5e-5vo4).
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5v5e (F: 9) - Room Temperature (280K) Crystal Structure of Kaposi'S Sarcoma- Associated Herpesvirus Protease in Complex with Allosteric Inhibitor (Compound 733)
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5v6s (F: 1) - Crystal Structure of Small Molecule Acrylamide 1 Covalently Bound to K-Ras G12C
Other atoms:
Mg (1);
Cl (1);
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5v6v (F: 2) - Crystal Structure of Small Molecule Aziridine 3 Covalently Bound to K- Ras G12C
Other atoms:
Ca (6);
Cl (2);
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5v71 (F: 6) - Kras G12C in Bound to Quinazoline Based Switch II Pocket (Swiip) Binder
Other atoms:
Mg (6);
Cl (6);
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5v7i (F: 6) - Crystal Structure of Homo Sapiens Serine Hydroxymethyltransferase 2 (Mitochondrial) (SHMT2), in Complex with Glycine, Plp and Folate- Competitive Pyrazolopyran Inhibitor: 6-Amino-4-Isopropyl-3-Methyl-4- (3-(Pyrrolidin-1-Yl)-5-(Trifluoromethyl)Phenyl)-1,4-Dihydropyrano[2, 3-C]Pyrazole-5-Carbonitrile
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5v7y (F: 9) - Prolyl 4-Hydroxylase Interacts with and Modifies Elongation Factor Tu
Other atoms:
Co (4);
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5v82 (F: 2) - PIM1 Kinase in Complex with CPD17 (1-(6-(4,4-Difluoropiperidin-3-Yl) Pyridin-2-Yl)-6-(6-Methylpyrazin-2-Yl)-1H-Pyrazolo[4,3-C]Pyridine)
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5v83 (F: 3) - Structure of DCN1 Bound to Nacm-Hit
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5v88 (F: 3) - Structure of DCN1 Bound to Nacm-Cov
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5v8q (F: 6) - Synthesis and Biological Evaluation of Novel Selective Androgen Receptor Modulators (Sarms): Part III
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5v8r (F: 2) - Small Molecule Inhibitor Abs-143 Bound to the Botulinum Neurotoxin Serotype A Light Chain
Other atoms:
Zn (2);
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5v8u (F: 2) - Small Molecule Inhibitor Abs-143 Bound to the Botulinum Neurotoxin Serotype A Light Chain
Other atoms:
Zn (2);
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5v8v (F: 4) - Crystal Structure of Human Renin in Complex with A Biphenylpipderidinylcarbinol
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5v9l (F: 3) - Kras G12C in Bound to Quinazoline Based Switch II Pocket (Swiip) Binder
Other atoms:
Mg (3);
Cl (3);
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5v9u (F: 4) - Crystal Structure of Small Molecule Ars-1620 Covalently Bound to K-Ras G12C
Other atoms:
Ca (8);
Cl (2);
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5vam (F: 6) - Braf in Complex with RAF709
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5vbe (F: 3) - Crystal Structure of Small Molecule Disulfide 2C07 Bound to H-Ras M72C Gdp
Other atoms:
Mg (1);
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5vbm (F: 3) - Crystal Structure of Small Molecule Disulfide 2C07 Bound to K-Ras Cys Light M72C Gdp
Other atoms:
Mg (1);
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5vbp (F: 4) - Crystal Structure of the First Bromodomain of Human BRD4 in Complex with RO3280
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5vbz (F: 3) - Crystal Structure of Small Molecule Disulfide 2C07 Bound to H-Ras M72C Gppnhp
Other atoms:
Mg (3);
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5vcw (F: 2) - Crystal Structure of Human MYT1 Kinase Domain in Complex with Pelitinib
Other atoms:
Cl (2);
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5vd2 (F: 3) - Crystal Structure of Human WEE1 Kinase Domain in Complex with Pf- 03814735
Other atoms:
Cl (2);
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5vd4 (F: 3) - Crystal Structure of Human WEE1 Kinase Domain in Complex with Rac-IV- 016, A MK1775 Analougue
Other atoms:
Cl (1);
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5vd7 (F: 1) - Crystal Structure of Human WEE1 Kinase Domain in Complex with Rac-IV- 098, A MK1775 Analogue
Other atoms:
Cl (1);
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5vee (F: 1) - PAK4 Kinase Domain in Complex with FRAX486
Other atoms:
Cl (2);
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5vej (F: 1) - High Resolution Crystal Structure of A Fluoride-Inhibited Organo- Phosphate-Degrading Metallohydrolase
Other atoms:
Co (2);
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5vew (F: 6) - Structure of the Human Glp-1 Receptor Complex with Pf-06372222
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5vhc (F: 3) - DHX36 with An N-Terminal Truncation Bound to Adp-BEF3
Other atoms:
Mg (1);
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5vhd (F: 4) - DHX36 with An N-Terminal Truncation Bound to Adp-ALF4
Other atoms:
Al (1);
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5vhw (F: 12) - GLUA2-0XGSG1L Bound to Zk
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5vhx (F: 12) - GLUA2-1XGSG1L Bound to Zk
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5vhy (F: 12) - GLUA2-2XGSG1L Bound to Zk
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5vi9 (F: 1) - Crystal Structure of Protein Kinase A in Complex with the Pki Peptide and Aminobenzothiazole Based Inhibitors
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5vih (F: 1) - Crystal Structure of GLUN1/GLUN2A Nmda Receptor Agonist Binding Domains with Glycine and Antagonist, 4-Fluorophenyl-Acepc
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5vii (F: 1) - Crystal Structure of GLUN1/GLUN2A Nmda Receptor Agonist Binding Domains with Glycine and Antagonist, 4-(3-Fluoropropyl)Phenyl-Acepc
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5vj3 (F: 3) - Hiv Protease (Pr) in Open Form with MG2+ in Active Site and Hive-9 in Eye Site
Other atoms:
Mg (1);
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5vlr (F: 3) - Crystal Structure of PI3K Delta in Complex with A Trifluoro-Ethyl- Pyrazol-Pyrolotriazine Inhibitor
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5vo1 (F: 3) - Dlk in Complex with Compound 10 (5-(1-Isopropyl-5-(3-(Oxetan-3-Yl)-3- Azabicyclo[3.1.0]Hexan-6-Yl)-1H-Pyrazol-3-Yl)-3-(Trifluoromethyl) Pyridin-2-Amine)
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5vo2 (F: 3) - Dlk in Complex with Inhibitor 5-(1-Isopropyl-5-(1-(Oxetan-3-Yl) Piperidin-4-Yl)-1H-Pyrazol-3-Yl)-3-(Trifluoromethyl)Pyridin-2-Amine (Compound 7)
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5vo4 (F: 1) - Crystal Structure of the Androgen Receptor Ligand Binding Domain in Complex with 5-(2-Fluoro-4-Hydroxyphenyl)-1-Methyl-1H-Pyrrole-2- Carbonitrile
Page generated: Fri May 13 23:15:01 2022
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