Fluorine in PDB, part 52 (files: 2041-2080),
PDB 3syn-3u2o
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: 2041-2080 (PDB 3syn-3u2o).
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3syn (F: 12) - Crystal Structure of Flhf in Complex with Its Activator
Other atoms:
Mg (4);
Al (4);
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3syr (F: 1) - Glycogen Phosphorylase B in Complex with Beta-D-Glucopyranonucleoside 5-Fluorouracil
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3t0l (F: 3) - Small-Molecule Inhibitors of 14-3-3 Protein-Protein Interactions From Virtual Screening
Other atoms:
Mg (2);
Cl (3);
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3t12 (F: 4) - Mgla in Complex with Mglb in Transition State
Other atoms:
Mg (3);
Al (1);
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3t34 (F: 8) - Arabidopsis Thaliana Dynamin-Related Protein 1A (ATDRP1A) in Prefission State
Other atoms:
Mg (2);
Al (2);
Na (2);
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3t3i (F: 3) - Glycogen Phosphorylase B in Complex with GLCCF3U
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3t78 (F: 1) - Crystal Structure of Mycobacterium Tuberculosis Indole Glycerol Phosphate Synthase (Igps) in Complex with 5-Fluoroanthranilate
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3t9e (F: 3) - Crystal Structure of the Catalytic Domain of Human Diphosphoinositol Pentakisphosphate Kinase 2 (PPIP5K2) in Complex with Adp, 5-(Pp)-IP5 (5-IP7) and MGF3 (Transition State Mimic)
Other atoms:
Mg (6);
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3t9t (F: 1) - Crystal Structure of Btk Mutant (F435T,K596R) Complexed with Imidazo[1,5-A]Quinoxaline
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3taf (F: 4) - 5-Fluorocytosine Paired with Ddgmp in RB69 GP43
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3tag (F: 2) - 5-Fluorocytosine Paired with Damp in RB69 GP43
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3tc5 (F: 1) - Selective Targeting of Disease-Relevant Protein Binding Domains By O- Phosphorylated Natural Product Derivatives
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3tcp (F: 2) - Crystal Structure of the Catalytic Domain of the Proto-Oncogene Tyrosine-Protein Kinase Mer in Complex with Inhibitor UNC569
Other atoms:
Cl (3);
Ca (3);
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3tdj (F: 2) - Crystal Structure of the GLUA2 Ligand-Binding Domain (S1S2J-L483Y- N754S) in Complex with Glutamate and Bpam-97 at 1.95 A Resolution
Other atoms:
Cl (5);
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3tfr (F: 2) - Ternary Complex Structure of Dna Polymerase Beta with A Gapped Dna Substrate and A, B Damp(CF2)Pp in the Active Site
Other atoms:
Mg (2);
Cl (4);
Na (2);
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3tfs (F: 1) - Ternary Complex Structure of Dna Polymerase Beta with A Gapped Dna Substrate and A, B Damp(Cfh)Pp in the Active Site: Stereoselective Binding of (S) Isomer
Other atoms:
Mg (2);
Cl (4);
Na (2);
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3tgu (F: 6) - Cytochrome BC1 Complex From Chicken with Pfvs-Designed Moa Inhibitor Bound
Other atoms:
Fe (10);
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3tgw (F: 1) - Crystal Structure of Subunit B Mutant H156A of the A1AO Atp Synthase
Other atoms:
Cl (2);
-
3th9 (F: 2) - Crystal Structure of Hiv-1 Protease Mutant Q7K V32I L63I with A Cyclic Sulfonamide Inhibitor
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3ti1 (F: 1) - CDK2 in Complex with Sunitinib
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3tik (F: 8) - Sterol 14-Alpha Demethylase (CYP51) From Trypanosoma Brucei in Complex with the Tipifarnib Derivative 6-((4-Chlorophenyl)(Methoxy)(1-Methyl- 1H-Imidazol-5-Yl)Methyl)-4-(2,6-Difluorophenyl)-1-Methylquinolin- 2(1H)-One
Other atoms:
Fe (4);
Cl (4);
-
3tiv (F: 1) - Crystal Structure of Subunit B Mutant N157A of the A1AO Atp Synthase
Other atoms:
Cl (1);
-
3tjw (F: 5) - Crystal Structure of Quasiracemic Villin Headpiece Subdomain Containing (F5PHE10) Substitution
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3tkm (F: 4) - Crystal Structure Ppar Delta Binding GW0742
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3tpx (F: 9) - Crystal Structure of Human MDM2 in Complex with A Trifluoromethylated D-Peptide Inhibitor
Other atoms:
Cl (5);
-
3trv (F: 5) - Crystal Structure of Quasiracemic Villin Headpiece Subdomain Containing (F5PHE17) Substitution
-
3tti (F: 3) - Crystal Structure of JNK3 Complexed with Cc-930, An Orally Active Anti-Fibrotic Jnk Inhibitor
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3ttj (F: 1) - Crystal Structure of JNK3 Complexed with Cc-359, A Jnk Inhibitor For the Prevention of Ischemia-Reperfusion Injury
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3ttz (F: 2) - Crystal Structure of A Topoisomerase Atpase Inhibitor
Other atoms:
Mg (5);
Cl (4);
-
3tu1 (F: 2) - Exhaustive Fluorine Scanning Towards Potent P53-MDM2 Antagonist
Other atoms:
Cl (1);
-
3tud (F: 3) - Crystal Structure of Syk Kinase Domain with N-(4-Methyl-3-(8-Methyl-7- Oxo-2-(Phenylamino)-7,8-Dihydropyrido[2,3-D]Pyrimidin-6-Yl)Phenyl)-3- (Trifluoromethyl)Benzamide
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3tv4 (F: 4) - Human B-Raf Kinase Domain in Complex with An Bromopyridine Benzamide Inhibitor
Other atoms:
Br (2);
-
3tv6 (F: 4) - Human B-Raf Kinase Domain in Complex with A Methoxypyrazolopyridinyl Benzamide Inhibitor
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3twf (F: 36) - Crystal Structure of the De Novo Designed Fluorinated Peptide ALPHA4F3A
Other atoms:
Na (1);
-
3twg (F: 60) - Crystal Structure of the De Novo Designed Fluorinated Peptide ALPHA4F3AF3D
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3tyl (F: 2) - Structure of Neuronal Nitric Oxide Synthase Heme Domain in Complex with 6-(((3S,4S)-4-(2-((2-Fluorobenzyl)Amino)Ethoxy)Pyrrolidin-3-Yl) Methyl)-4-Methylpyridin-2-Amine
Other atoms:
Fe (2);
Zn (1);
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3tyv (F: 6) - Sar Development and Discovery of Potent Indole-Based Inhibitors of the Hepatitis C Virus NS5B Polymerase
-
3u15 (F: 8) - Structure of Hdmx with Dimer Inducing Indolyl Hydantoin Ro-2443
Other atoms:
Cl (4);
-
3u2c (F: 1) - Aldose Reductase in Complex with Nsaid-Type Inhibitor at 1.0 A Resolution
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3u2o (F: 1) - Dihydroorotate Dehydrogenase (Dhodh) Crystal Structure in Complex with Small Molecule Inhibitor
Page generated: Thu Dec 28 04:02:13 2023
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