Fluorine in PDB, part 49 (files: 1921-1960),
PDB 3qrj-3rgf
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: 1921-1960 (PDB 3qrj-3rgf).
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3qrj (F: 2) - The Crystal Structure of Human ABL1 Kinase Domain T315I Mutant in Complex with Dcc-2036
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3qrm (F: 6) - Hiv-1 Protease (Mutant Q7K L33I L63I) in Complex with A Three-Armed Pyrrolidine-Based Inhibitor
Other atoms:
Cl (3);
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3qro (F: 3) - Hiv-1 Protease (Mutant Q7K L33I L63I) in Complex with A Three-Armed Pyrrolidine-Based Inhibitor
Other atoms:
Cl (3);
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3qrs (F: 3) - Hiv-1 Protease (Mutant Q7K L33I L63I) in Complex with A Three-Armed Pyrrolidine-Based Inhibitor
Other atoms:
Cl (3);
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3qsa (F: 6) - Anthranilate Phosphoribosyltransferase (Trpd) From Mycobacterium Tuberculosis (Complex with Inhibitor Tamu-A7)
Other atoms:
Mg (4);
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3qsb (F: 2) - Structure of E. Coli Poliiibeta with (Z)-5-(1-((4'-Fluorobiphenyl-4- Yl)Methoxyimino)Butyl)-2,2-Dimethyl-4,6-Dioxocyclohexanecarbonitrile
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3qsc (F: 2) - The First Crystal Structure of A Human Telomeric G-Quadruplex Dna Bound to A Metal-Containing Ligand (A Copper Complex)
Other atoms:
K (3);
Br (1);
Cu (1);
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3qsf (F: 2) - The First Crystal Structure of A Human Telomeric G-Quadruplex Dna Bound to A Metal-Containing Ligand (A Nickel Complex)
Other atoms:
Ni (1);
K (3);
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3qt7 (F: 2) - Crystal Structure of Staphylococcus Epidermidis Mevalonate Diphosphate Decarboxylase Complexed with Inhibitor 6-Fmvapp
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3qt8 (F: 2) - Crystal Structure of Mutant S192A Staphylococcus Epidermidis Mevalonate Diphosphate Decarboxylase Complexed with Inhibitor 6- Fmvapp
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3qtk (F: 18) - The Crystal Structure of Chemically Synthesized Vegf-A
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3qtz (F: 1) - CDK2 in Complex with Inhibitor Rc-2-36
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3que (F: 2) - Human P38 Map Kinase in Complex with Skepinone-L
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3qup (F: 1) - Inhibitor Bound Structure of the Kinase Domain of the Murine Receptor Tyrosine Kinase TYRO3 (Sky)
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3qzg (F: 1) - CDK2 in Complex with Inhibitor Jws-6-76
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3qzq (F: 4) - Human Enterovirus 71 3C Protease Mutant E71D in Complex with Rupintrivir
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3qzr (F: 2) - Human Enterovirus 71 3C Protease Mutant E71A in Complex with Rupintrivir
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3r0f (F: 2) - Human Enterovirus 71 3C Protease Mutant H133G in Complex with Rupintrivir
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3r0i (F: 4) - Ispc in Complex with An N-Methyl-Substituted Hydroxamic Acid
Other atoms:
Mn (2);
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3r0t (F: 3) - Crystal Structure of Human Protein Kinase CK2 Alpha Subunit in Complex with the Inhibitor Cx-5279
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3r17 (F: 1) - Hcarbonic Anhydrase II Bound to N-(2-Fluoro.4-Sulfamoylphenyl)-2- (Thiophen-2-Yl) Acetamide
Other atoms:
Zn (1);
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3r28 (F: 3) - CDK2 in Complex with Inhibitor Kvr-1-140
Other atoms:
Cl (1);
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3r2f (F: 8) - Crystal Structure of Beta-Site App-Cleaving Enzyme 1 (Bace-Wt) Complex with Bms-693391 Aka (2S)-2-((3R)-3-Acetamido-3-Isobutyl-2-Oxo-1- Pyrrolidinyl)-N-((1S,2R)-1-(3,5-Difluorobenzyl)-2-Hydroxy-2-((2R,4R)- 4-Propoxy-2-Pyrrolidinyl)Ethyl)-4-Phenylbutanamide
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3r3v (F: 1) - Crystal Structure of the Fluoroacetate Dehalogenase RPA1163 - ASP110ASN/Fluoroacetate
Other atoms:
Cl (4);
Ca (1);
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3r4n (F: 6) - Optimization of Potent, Selective, and Orally Bioavailable Pyrrolodinopyrimidine-Containing Inhibitors of Heat Shock Protein 90. Identification of Development Candidate 2-Amino-4-{4-Chloro-2-[2-(4- Fluoro-1H-Pyrazol-1-Yl)Ethoxy]-6-Methylphenyl}-N-(2,2- Difluoropropyl)-5,7-Dihydro-6H-Pyrrolo[3,4-D]Pyrimidine-6-Carboxamide
Other atoms:
Cl (2);
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3r4o (F: 6) - Optimization of Potent, Selective, and Orally Bioavailable Pyrrolodinopyrimidine-Containing Inhibitors of Heat Shock Protein 90. Identification of Development Candidate 2-Amino-4-{4-Chloro-2-[2-(4- Fluoro-1H-Pyrazol-1-Yl)Ethoxy]-6-Methylphenyl}-N-(2,2- Difluoropropyl)-5,7-Dihydro-6H-Pyrrolo[3,4-D]Pyrimidine-6-Carboxamide
Other atoms:
Cl (4);
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3r4p (F: 4) - Optimization of Potent, Selective, and Orally Bioavailable Pyrrolodinopyrimidine-Containing Inhibitors of Heat Shock Protein 90. Identification of Development Candidate 2-Amino-4-{4-Chloro-2-[2-(4- Fluoro-1H-Pyrazol-1-Yl)Ethoxy]-6-Methylphenyl}-N-(2,2- Difluoropropyl)-5,7-Dihydro-6H-Pyrrolo[3,4-D]Pyrimidine-6-Carboxamide
Other atoms:
Cl (4);
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3r6t (F: 1) - Rat Catechol O-Methyltransferase in Complex with the Bisubstrate Inhibitor 4'-Fluoro-4,5-Dihydroxy-Biphenyl-3-Carboxylic Acid {(E)-3- [(2S,4R,5R)-4-Hydroxy-5-(6-Methyl-Purin-9-Yl)-Tetrahydro-Furan-2-Yl]- Allyl}-Amide
Other atoms:
Mg (1);
Cl (3);
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3r7m (F: 1) - AKR1C3 Complex with Sulindac
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3r94 (F: 1) - AKR1C3 Complex with Flurbiprofen
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3r9d (F: 1) - CDK2 in Complex with Inhibitor Rc-2-135
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3r9h (F: 2) - CDK2 in Complex with Inhibitor Rc-2-142
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3r9o (F: 2) - CDK2 in Complex with Inhibitor Rc-2-143
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3rad (F: 2) - Quinolone(Clinafloxacin)-Dna Cleavage Complex of Type IV Topoisomerase From S. Pneumoniae
Other atoms:
Mg (6);
Cl (2);
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3rae (F: 2) - Quinolone(Levofloxacin)-Dna Cleavage Complex of Type IV Topoisomerase From S. Pneumoniae
Other atoms:
Mg (6);
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3raf (F: 2) - Quinazolinedione-Dna Cleavage Complex of Type IV Topoisomerase From S. Pneumoniae
Other atoms:
Mg (4);
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3rcd (F: 6) - HER2 Kinase Domain Complexed with Tak-285
Other atoms:
Cl (2);
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3rdp (F: 2) - Crystal Structure of Thymidine Kinase From Herpes Simplex Virus Type 1 in Complex with N-Methyl-Fhbt
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3rfu (F: 16) - Crystal Structure of A Copper-Transporting Pib-Type Atpase
Other atoms:
Mg (4);
Al (4);
K (4);
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3rgf (F: 3) - Crystal Structure of Human CDK8/Cycc
Other atoms:
Cl (1);
Page generated: Wed Nov 13 08:06:23 2024
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