Fluorine in PDB, part 210 (files: 8361-8400),
PDB 7s4c-7sq2
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: 8361-8400 (PDB 7s4c-7sq2).
-
7s4c (F: 3) - Crystal Structure of Inhibitor-Bound Galactokinase
Other atoms:
Cl (3);
Na (2);
-
7s4e (F: 2) - Crystal Structure of Ligand ACBI1 in Complex with Bromodomain of Human SMARCA2 and Pvhl:Elonginc:Elonginb Complex
Other atoms:
Na (5);
-
7s5g (F: 1) - PCSK9 in Complex with Compound 19
-
7s5h (F: 1) - PCSK9(Deltacrd) in Complex with Cyclic Peptide 35
-
7s76 (F: 6) - Hbv Capsid Y132A with Compound 10B at 2.5A Resolution
Other atoms:
Cl (6);
-
7s7a (F: 3) - Crystal Structure of CDK2 Liganded with Compound EF3019
-
7s84 (F: 3) - Crystal Structure of CDK2 Liganded with Compound TW8972
-
7s85 (F: 3) - Crystal Structure of CDK2 Liganded with Compound WN316
-
7s9x (F: 3) - Crystal Structure of CDK2 Liganded with Compound WN378
-
7sa0 (F: 6) - Crystal Structure of CDK2 Liganded with Compound EF4195
-
7sdc (F: 3) - Structure of the Sars-Cov-2 Main Protease in Complex with Inhibitor Mi-09
-
7se8 (F: 6) - Crystal Structure of Human Fibrillarin in Complex with Fragment 1 From Cocktail Soak
-
7se9 (F: 6) - Crystal Structure of Human Fibrillarin in Complex with Compound 1 From Single Soak
-
7sea (F: 3) - Crystal Structure of Human Fibrillarin in Complex with Compound 2 From Cocktail Soak
-
7seb (F: 3) - Crystal Structure of Human Fibrillarin in Complex with Compound 2 From Single Soak
-
7sec (F: 6) - Crystal Structure of Human Fibrillarin in Complex with Compound 1A
-
7sed (F: 3) - Crystal Structure of Human Fibrillarin in Complex with Compound 2A
-
7sel (F: 2) - E. Coli Msba in Complex with Lps and Inhibitor G7090 (Compound 3)
Other atoms:
Cl (4);
-
7sf3 (F: 3) - Sars-Cov-2 Main Protease (Mpro) in Complex with ML1006M
Other atoms:
Cl (1);
-
7sff (F: 3) - Human DNMT1(729-1600) Bound to Zebularine-Containing 12MER Dsdna and Inhibitor GSK3852279B
Other atoms:
Zn (2);
-
7sfi (F: 3) - Sars-Cov-2 Main Protease (Mpro) in Complex with ML104
Other atoms:
Cl (1);
Ca (1);
-
7sfq (F: 40) - Emre S64V Mutant Bound to Tetra(4-Fluorophenyl)Phosphonium at pH 8.0
-
7sgh (F: 12) - Sars-Cov-2 Main Protease (Mpro) in Complex with ML124N
-
7si3 (F: 4) - Consensus Structure of ATP7B
Other atoms:
Mg (1);
Al (1);
-
7si4 (F: 1) - Crystal Structure of Eed with Mrtx-2219
-
7si5 (F: 1) - Crystal Structure of Eed with Mrtx-1919
Other atoms:
Na (2);
-
7si6 (F: 4) - Structure of ATP7B in State 1
Other atoms:
Mg (1);
Al (1);
-
7si7 (F: 4) - Structure of ATP7B in State 2
Other atoms:
Mg (1);
Al (1);
-
7si9 (F: 3) - Room Temperature X-Ray Structure of Sars-Cov-2 Main Protease (Mpro) in Complex with Pf-07321332
-
7sii (F: 8) - Human Sting Bound to Both Cgamp and 1-[(2-Chloro-6-Fluorophenyl) Methyl]-3,3-Dimethyl-2-Oxo-N-[(2,4,6-Trifluorophenyl)Methyl]-2,3- Dihydro-1H-Indole-6-Carboxamide (Compound 53)
Other atoms:
Cl (2);
-
7sj3 (F: 2) - Structure of CDK4-Cyclin D3 Bound to Abemaciclib
-
7slr (F: 7) - Hiv Reverse Transcriptase with Compound PYR01
-
7sls (F: 7) - Hiv Reverse Transcriptase with Compound PYR02
-
7snl (F: 5) - Disulfide Stabilized Hiv-1 Ca Hexamer in Complex with Capsid Inhibitor N-(1-(3-(4-Chloro-1-Methyl-3-(Methylsulfonamido)-1H-Indazol-7-Yl)-4- Oxo-3,4-Dihydropyrido[2,3-D]Pyrimidin-2-Yl)-2-(3,5-Difluorophenyl) Ethyl)-2-(3-(Trifluoromethyl)-4,5,6,7-Tetrahydro-1H-Indazol-1-Yl) Acetamide
Other atoms:
I (4);
Cl (8);
-
7snn (F: 4) - Disulfide Stabilized Hiv-1 Ca Hexamer in Complex with Capsid Inhibitor N-(1-(3-(4-Chloro-1-Methyl-3-(Methylsulfonamido)-1H-Indazol-7-Yl)-4- Oxo-3,4-Dihydropyrido[2,3-D]Pyrimidin-2-Yl)-2-(3,5-Difluorophenyl) Ethyl)-2-(3-(Difluoromethyl)-5,6-Dihydrocyclopenta[C]Pyrazol-1(4H)- Yl)Acetamide
Other atoms:
I (3);
Cl (8);
-
7so4 (F: 1) - Crystal Structure of Hiv-1 Y181C Mutant Reverse Transcriptase in Complex with 5-(2-(2-(2,4-Dioxo-3,4-Dihydropyrimidin-1(2H)-Yl) Ethoxy)Phenoxy)-7-Fluoro-2-Naphthonitrile (JLJ635), A Non-Nucleoside Inhibitor
-
7so6 (F: 1) - Crystal Structure of Hiv-1 K103N, Y181C Mutant Reverse Transcriptase in Complex with 5-(2-(2-(2,4-Dioxo-3,4-Dihydropyrimidin-1(2H)-Yl) Ethoxy)Phenoxy)-7-Fluoro-2-Naphthonitrile (JLJ635), A Non-Nucleoside Inhibitor
Other atoms:
Mg (1);
-
7sp3 (F: 1) - E. Coli Rpph Bound to AP4A
Other atoms:
Mg (3);
Cl (1);
-
7sps (F: 4) - Crystal Structure of Human Glucose Transporter GLUT3 Bound with Exofacial Inhibitor SA47
-
7sq2 (F: 4) - Reprocessed and Refined Structure of Phospholipase C-Beta and Gq Signaling Complex
Other atoms:
Al (1);
Ca (1);
Mg (2);
Page generated: Tue Feb 25 09:27:17 2025
|
