Fluorine in PDB, part 22 (files: 841-880),
PDB 2pdl-2q94
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: 841-880 (PDB 2pdl-2q94).
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2pdl (F: 3) - Human Aldose Reductase Mutant L301M Complexed with Tolrestat.
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2pdm (F: 3) - Human Aldose Reductase Mutant S302R Complexed with Zopolrestat.
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2pdw (F: 1) - Human Aldose Reductase Mutant C303D Complexed with Fidarestat.
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2pdx (F: 3) - Human Aldose Reductase Double Mutant S302R-C303D Complexed with Zopolrestat.
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2pdy (F: 1) - Human Aldose Reductase Double Mutant S302R-C303D Complexed with Fidarestat.
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2pev (F: 3) - Complex of Aldose Reductase with Nadp+ and Simaltaneously Bound Competetive Inhibitors Fidarestat and IDD594. Concentration of Fidarestat in Soaking Solution Exceeds Concentration of IDD594.
Other atoms:
Br (1);
Cl (1);
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2pf8 (F: 3) - Complex of Aldose Reductase with Nadp+ and Simaltaneously Bound Competetive Inhibitors Fidarestat and IDD594. Concentration of Fidarestat in Soaking Solution Is Equal to Concentration of IDD594.
Other atoms:
Br (1);
Cl (1);
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2pfh (F: 3) - Complex of Aldose Reductase with Nadp+ and Simaltaneously Bound Competetive Inhibitors Fidarestat and IDD594. Concentration of Fidarestat in Soaking Solution Is Less Than Concentration of IDD594.
Other atoms:
Br (1);
Cl (1);
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2ph6 (F: 1) - Crystal Structure of Human Beta Secretase Complexed with Inhibitor
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2phb (F: 1) - An Orally Efficacious Factor Xa Inhibitor
Other atoms:
Cl (1);
Ca (1);
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2pis (F: 12) - Efforts Toward Expansion of the Genetic Alphabet: Structure and Replication of Unnatural Base Pairs
Other atoms:
Br (12);
Mg (6);
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2pix (F: 3) - Ar Lbd with Small Molecule
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2pkk (F: 1) - Crystal Structure of M Tuberculosis Adenosine Kinase Complexed with 2-Fluro Adenosine
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2pl1 (F: 3) - Berrylium Fluoride Activated Receiver Domain of E.Coli Phop
Other atoms:
Mg (1);
Pt (3);
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2pl9 (F: 9) - Crystal Structure of Chey-Mg(2+)-Bef(3)(-) in Complex with Chez(C19) Peptide Solved From A P2(1)2(1)2 Crystal
Other atoms:
Mg (3);
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2pnu (F: 2) - Crystal Structure of Human Androgen Receptor Ligand-Binding Domain in Complex with Em-5744
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2pow (F: 3) - The Crystal Structure of the Human Carbonic Anhydrase II in Complex with 4-Amino-6-Trifluoromethyl-Benzene-1,3- Disulfonamide
Other atoms:
Zn (1);
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2pq9 (F: 2) - E. Coli Epsps Liganded with (R)-Difluoromethyl Tetrahedral Reaction Intermediate Analog
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2pqb (F: 2) - CP4 Epsps Liganded with (R)-Difluoromethyl Tetrahedral Intermediate Analog
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2pqd (F: 2) - A100G CP4 Epsps Liganded with (R)-Difluoromethyl Tetrahedral Reaction Intermediate Analog
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2pr3 (F: 1) - Factor Xa Inhibitor
Other atoms:
Cl (1);
Ca (2);
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2prh (F: 1) - The Structures of Apo- and Inhibitor Bound Human Dihydroorotate Dehydrogenase Reveal Conformational Flexibility Within the Inhibitor Binding Site
Other atoms:
Cl (1);
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2pu1 (F: 2) - Crystal Structure of the T. Brucei Enolase Complexed with Fluoro-Phosphonoacetohydroxamate (Fpah)
Other atoms:
Zn (3);
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2pxi (F: 1) - Ternary Complex of Dna Polymerase Beta with A Dideoxy Terminated Primer and 2'-Deoxyguanosine 5'-Beta, Gamma- Monofluoromethylene Triphosphate
Other atoms:
Mg (1);
Cl (5);
Na (3);
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2q0m (F: 3) - Tricarbonylmanganese(I)-Lysozyme Complex : A Structurally Characterized Organometallic Protein
Other atoms:
Mn (1);
Cl (1);
Na (1);
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2q1j (F: 1) - The Discovery of Glycine and Related Amino Acid-Based Factor Xa Inhibitors
Other atoms:
Cl (1);
Ca (1);
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2q1l (F: 8) - Design and Synthesis of Pyrrole-Based, Hepatoselective Hmg- Coa Reductase Inhibitors
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2q1o (F: 8) - Crystal Structure Analysis of the Rna Dodecamer Cgc-NF2- Aauuggcg, with An Incorporated 2,4-Difluorotoluyl Residue (NF2)
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2q2y (F: 2) - Crystal Structure of Ksp in Complex with Inhibitor 1
Other atoms:
Mg (2);
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2q2z (F: 2) - Crystal Structure of Ksp in Complex with Inhibitor 22
Other atoms:
Mg (2);
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2q59 (F: 6) - Crystal Structure of Ppargamma Lbd Bound to Full Agonist MRL20
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2q5g (F: 6) - Ligand Binding Domain of Ppar Delta Receptor in Complex with A Partial Agonist
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2q5p (F: 6) - Crystal Structure of Ppargamma Bound to Partial Agonist MRL24
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2q6b (F: 4) - Design and Synthesis of Novel, Conformationally Restricted Hmg-Coa Reductase Inhibitors
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2q6c (F: 4) - Design and Synthesis of Novel, Conformationally Restricted Hmg-Coa Reductase Inhibitors
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2q6j (F: 6) - Crystal Structure of Estrogen Receptor Alpha Complexed to A B-N Substituted Ligand
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2q6p (F: 10) - The Chemical Control of Protein Folding: Engineering A Superfolder Green Fluorescent Protein
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2q70 (F: 4) - Estrogen Receptor Alpha Ligand-Binding Domain Complxed to A Benzopyran Ligand
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2q8g (F: 3) - Structure of Pyruvate Dehydrogenase Kinase Isoform 1 in Complex with Glucose-Lowering Drug AZD7545
Other atoms:
K (1);
Cl (1);
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2q94 (F: 3) - E. Coli Methionine Aminopeptidase Mn-Form with Inhibitor A04
Other atoms:
Mn (2);
Na (1);
Page generated: Wed Nov 13 08:05:23 2024
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