Fluorine in PDB, part 203 (files: 8081-8120),
PDB 7pva-7qm4
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: 8081-8120 (PDB 7pva-7qm4).
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7pva (F: 24) - 1.9 Angstrom Crystal Structure of Dimeric Porx, Co-Crystallized in the Presence of Zinc
Other atoms:
Mg (11);
Cl (2);
Zn (6);
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7pvk (F: 12) - X-Ray Structure of Dimeric Porx (T272A Mutant), in Complex with Pgpg.
Other atoms:
Mg (4);
Zn (10);
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7pvu (F: 1) - Crystal Structure of P38ALPHA C162S in Complex with CAS2094511-69-8, P 1 21 1
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7px6 (F: 1) - PARP15 Catalytic Domain in Complex with OUL241
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7py4 (F: 3) - Cryo-Em Structure of ATP8B1-CDC50A in E2P Autoinhibited State
Other atoms:
Mg (1);
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7pzs (F: 1) - Lpxc Inhibitors with Fluoroproline As A Novel Zinc-Binding Group Can Serve As A Novel Class of Antibiotic with Activity Against Multidrug- Resistant Gram-Negative Bacteria
Other atoms:
Zn (1);
Cl (1);
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7pzu (F: 2) - Lpxc Inhibitors with Fluoroproline As A Novel Zinc-Binding Group Can Serve As A Novel Class of Antibiotic with Activity Against Multidrug- Resistant Gram-Negative Bacteria
Other atoms:
Zn (1);
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7pzv (F: 1) - Lpxc Inhibitors with Fluoroproline As A Novel Zinc-Binding Group Can Serve As A Novel Class of Antibiotic with Activity Against Multidrug- Resistant Gram-Negative Bacteria
Other atoms:
Zn (1);
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7pzw (F: 1) - Lpxc Inhibitors with Fluoroproline As A Novel Zinc-Binding Group Can Serve As A Novel Class of Antibiotic with Activity Against Multidrug- Resistant Gram-Negative Bacteria
Other atoms:
Zn (1);
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7pzx (F: 1) - Lpxc Inhibitors with Fluoroproline As A Novel Zinc-Binding Group Can Serve As A Novel Class of Antibiotic with Activity Against Multidrug- Resistant Gram-Negative Bacteria
Other atoms:
Zn (1);
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7q01 (F: 1) - Lpxc Inhibitors with Fluoroproline As A Novel Zinc-Binding Group Can Serve As A Novel Class of Antibiotic with Activity Against Multidrug- Resistant Gram-Negative Bacteria
Other atoms:
Zn (1);
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7q2j (F: 3) - Quaternary Complex of Human WDR5 and Pvhl:Elonginc:Elonginb Bound to Protac Homer
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7q2x (F: 6) - Cryo-Em Structure of Clamped S.Cerevisiae Condensin-Dna Complex (Form I)
Other atoms:
Mg (2);
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7q2y (F: 6) - Cryo-Em Structure of Clamped S.Cerevisiae Condensin-Dna Complex (Form II)
Other atoms:
Mg (2);
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7q3b (F: 1) - Crystal Structure of Human Sting in Complex with 3'3'-C-(2'F,2'Da- Isonuca)Mp
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7q4a (F: 6) - Toxoplasma Gondii PRP4K Kinase Domain (L715F) Bound to Altiratinib
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7q6p (F: 32) - Crystal Structure of Bacterial Prolyl Peptidyl Isomerase with 5,5'- Difluoroleucines
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7q6t (F: 1) - Crystal Structure of the Bromodomain of ATAD2 with AZ13824374
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7q7l (F: 1) - JAK2 in Complex with 4-(2-Amino-8-{[(2S)-1-Hydroxypropan-2- Yl]Amino}Quinazolin-6-Yl)-5-Ethyl-2-Fluorophenol
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7q7r (F: 2) - Crystal Structure of Human BCL6 Btb Domain in Complex with Compound 1
Other atoms:
Cl (2);
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7q7w (F: 1) - JAK2 in Complex with 4-(2-{[5-(Dimethylamino)Pentyl]Amino}-8-{[(2S)-1- Hydroxypropan-2-Yl]Amino}Quinazolin-6-Yl)-5-Ethyl-2-Fluorophenol
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7q85 (F: 2) - Crystal Structure of Human Sting in Complex with MD1193
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7qa0 (F: 6) - Crystal Structure of Pqsr (Mvfr) Ligand-Binding Domain in Complex with Compound 1456
Other atoms:
Cl (2);
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7qa3 (F: 6) - Crystal Structure of Pqsr (Mvfr) Ligand-Binding Domain in Complex with Compound N-((2-(4-Phenoxyphenyl)Thiazol-5-Yl)Methyl)-2- (Trifluoromethyl)Pyridin-4-Amine
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7qav (F: 6) - Crystal Structure of Pqsr (Mvfr) Ligand-Binding Domain in Complex with Compound N-((2-(4-Cyclopropylphenyl)Thiazol-5-Yl)Methyl)-2- (Trifluoromethyl)Pyridin-4-Amine
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7qbz (F: 4) - Crystal Structure Cadmium Translocating P-Type Atpase
Other atoms:
Al (1);
Mg (1);
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7qc0 (F: 3) - Crystal Structure of Cadmium Translocating P-Type Atpase
Other atoms:
Mg (1);
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7qc5 (F: 2) - Crystal Structure of Human Wild Type Transthyretin in Complex with (3, 4-Dihydroxy-5-Nitrophenyl)-(3-Fluoro-5-Hydroxyphenyl)Methanone Compound
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7qg3 (F: 2) - IRAK4 in Complex with Inhibitor
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7qh1 (F: 8) - Discovery and Development of A Novel Inhaled Antivirulence Therapy For the Treatment of Pseudomonas Aeruginosa Infections in Patients with Chronic Respiratory Disease
Other atoms:
Ca (8);
Zn (4);
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7qhn (F: 1) - Crystal Structure of Lysyl-Trna Synthetase From Mycobacterium Tuberculosis Complexed with L-Lysine and An Inhibitor
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7qi8 (F: 2) - Crystal Structure of Lysyl-Trna Synthetase From Mycobacterium Tuberculosis Complexed with L-Lysine and Inhibitor
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7qir (F: 2) - Crystal Structure of the P1 Monofluorethylglycine(Mfegly) Bpti Mutant- Bovine Chymotrypsin Complex
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7qis (F: 4) - Crystal Structure of the P1 Difluoroethylglycine (Dfegly) Bpti Mutant- Bovine Chymotrypsin Complex
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7qit (F: 6) - Crystal Structure of the P1 Trifluoroethylglycine (Tfegly) Bpti Mutant- Bovine Chymotrypsin Complex
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7qk0 (F: 2) - Crystal Structure of Human BCL6 Btb Domain in Complex with Compound 12A
Other atoms:
Cl (2);
-
7qk4 (F: 1) - Eed in Complex with PRC2 Allosteric Inhibitor Compound 22 (MAK683)
Other atoms:
Cl (3);
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7qlt (F: 3) - Endothiapepsin in Complex with Ligand TL00150 in 10% Dmso at 100K
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7qm3 (F: 3) - Endothiapepsin in Complex with Compound TL00150 in 5% Dmso at 298 K
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7qm4 (F: 3) - Endothiapepsin in Complex with Compound TL00150 in 8% Dmso at 298 K
Page generated: Wed Nov 13 08:12:59 2024
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