Fluorine in PDB, part 218 (files: 8681-8720),
PDB 7zk3-8a2r
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: 8681-8720 (PDB 7zk3-8a2r).
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7zk3 (F: 6) - Structure of 1PBC- and Calcium-Bound MTMEM16A(Ac) Chloride Channel at 2.85 A Resolution
Other atoms:
Ca (6);
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7zke (F: 3) - MOT1:Tbp:Dna - Pre-Hydrolysis State
Other atoms:
Mg (1);
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7zkf (F: 1) - Crystal Structure of Human Brachyury G177D Variant in Complex with Cf- 5-86
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7zks (F: 1) - SRPK1 in Complex with Inhibitor
Other atoms:
Cl (2);
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7zku (F: 2) - Crystal Structure of Human Sting in Complex with 3',3'-C-(2'F,2'Damp- 2'DGmp)
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7zkx (F: 1) - SRPK2 in Complex with Inhibitor
Other atoms:
Cl (1);
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7zl3 (F: 6) - Signal Peptide Mimicry Primes SEC61 For Client-Selective Inhibition
Other atoms:
Br (1);
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7zlm (F: 4) - Crystal Structure of SOCS2:Elonginb:Elonginc in Complex with Compound MN551
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7zln (F: 2) - Crystal Structure of SOCS2:Elonginb:Elonginc in Complex with Compound 11
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7zlo (F: 2) - Crystal Structure of SOCS2:Elonginb:Elonginc in Complex with Compound 12
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7zlp (F: 2) - Crystal Structure of SOCS2:Elonginb:Elonginc in Complex with Compound 9
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7zlr (F: 2) - Crystal Structure of SOCS2:Elonginb:Elonginc in Complex with Compound 13
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7zls (F: 8) - Co-Crystal Structure of SOCS2:Elonginb:Elonginc in Complex with Compound 13
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7zlu (F: 3) - Catalytic Domain of Udp-Glucose Glycoprotein Glucosyltransferase From Chaetomium Thermophilum in Complex with Udp-2-Deoxy-2-Fluoro-D- Glucose
Other atoms:
Ca (3);
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7znt (F: 2) - Crystal Structure of AT7 in Complex with the Second Bromodomain of Human BRD4 and Pvhl:Elonginc:Elonginb
Other atoms:
Cl (2);
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7zog (F: 4) - Crystal Structure of Cryptosporidium Parvum -Plasmodium Falciparum Mutant Lysyl Trna Synthetase in Complex with Inhibitor
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7zqx (F: 3) - Human Galectin-3C in Complex with A Galactose Derivative
Other atoms:
Br (1);
Cl (3);
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7zs7 (F: 4) - Crystal Structure of Human Cathepsin L with Covalently Bound Calpain Inhibitor VI
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7zso (F: 15) - Human Purine Nucleoside Phosphorylase in Complex with Js-554
Other atoms:
Na (2);
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7zsp (F: 5) - Human Purine Nucleoside Phosphorylase in Complex with Js-555
Other atoms:
Na (1);
W (18);
Te (3);
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7zun (F: 3) - Crystal Structure of PIM1 in Complex with A Pyrrolo-Pyrazinone Compound
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7zv0 (F: 2) - Crystal Structure of Human Sting in Complex with 3',3'-C-(2'F,2'Damp- 2'F,2'DAmp)
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7zvk (F: 2) - Crystal Structure of Human Sting in Complex with 3',3'-C-(2'F,2'Damp- Imp)
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7zwl (F: 2) - Crystal Structure of Human Sting in Complex with 3',3'-C-Di-(2'F, 2'DAmp)
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7zwq (F: 2) - Crystal Structure of Human BCL6 Btb Domain in Complex with Compound 10
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7zwr (F: 3) - Crystal Structure of Human BCL6 Btb Domain in Complex with Compound 11
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7zws (F: 3) - Crystal Structure of Human BCL6 Btb Domain in Complex with Compound 13
Other atoms:
Cl (1);
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7zwz (F: 1) - Crystal Structure of Human BCL6 Btb Domain in Complex with Compound 22
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7zxb (F: 1) - Crystal Structure of Human Sting in Complex with 3',3'-C-(2'Damp-2'F, 2'DAmp)
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7zyx (F: 100) - Dimeric I-Motif From 2'Farabinocytidine-Modified TC5
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7zzo (F: 3) - HDAC2 in Complex with An Inhibitor
Other atoms:
Na (3);
Ca (3);
Zn (3);
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8a19 (F: 1) - Structure of A Leucinostatin Derivative Determined By Host Lattice Display : L1E4V1 Construct
Other atoms:
Mn (4);
Cl (5);
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8a1a (F: 1) - Structure of A Leucinostatin Derivative Determined By Host Lattice Display : L1F11V1 Construct
Other atoms:
Cl (4);
Mn (4);
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8a1m (F: 2) - Crystal Structure of the Transpeptidase LDTMT2 From Mycobacterium Tuberculosis in Complex with Maleimide Analogue 4
Other atoms:
Cl (4);
Na (3);
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8a27 (F: 3) - Egfr Kinase Domain in Complex with 2-(6,7-Dihydro-5H-Pyrrolo[1,2- C]Imidazol-1-Yl)-2-[6-[2-[4-[[4-(Hydroxymethyl)-1- Piperidyl]Methyl]Phenyl]Ethynyl]-1-Oxo-4-(Trifluoromethyl)Isoindolin- 2-Yl]-N-Thiazol-2-Yl-Acetamide
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8a2a (F: 3) - Egfr Kinase Domain in Complex with 2-(6,7-Dihydro-5H-Pyrrolo[1,2- C]Imidazol-1-Yl)-2-[6-[2-[4-[[4-(Hydroxymethyl)-1- Piperidyl]Methyl]Phenyl]Ethynyl]-1-Oxo-4-(Trifluoromethyl)Isoindolin- 2-Yl]-N-Thiazol-2-Yl-Acetamide (Form 2)
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8a2b (F: 3) - Egfr Kinase Domain (L858R/V948R) in Complex with 2-(6,7-Dihydro-5H- Pyrrolo[1,2-C]Imidazol-1-Yl)-2-[6-[2-[4-[[4-(Hydroxymethyl)-1- Piperidyl]Methyl]Phenyl]Ethynyl]-1-Oxo-4-(Trifluoromethyl)Isoindolin- 2-Yl]-N-Thiazol-2-Yl-Acetamide
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8a2d (F: 2) - Egfr Kinase Domain (L858R/V948R) in Complex with 2-[4- (Difluoromethyl)-6-[2-[4-[[4-(Hydroxymethyl)-1- Piperidyl]Methyl]Phenyl]Ethynyl]-7-Methyl-Indazol-2-Yl]-2-Spiro[6,7- Dihydropyrrolo[1,2-C]Imidazole-5,1'-Cyclopropane]-1-Yl-N-Thiazol-2- Yl-Acetamide
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8a2p (F: 2) - Room-Temperature Structure of the Stabilised A2A-LUAA47070 Complex Determined By Synchrotron Serial Crystallography
Other atoms:
Na (1);
-
8a2r (F: 15) - Cryo-Em Structure of F-Actin in the MG2+-Adp-BEF3- Nucleotide State.
Other atoms:
Mg (5);
Page generated: Thu Dec 28 04:19:47 2023
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