phenylalanine and dihydropyridines

phenylalanine has been researched along with dihydropyridines in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (20.00)18.2507
2000's4 (80.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Clarke, DM; Loo, TW1
Chen, KG; Cohen, D; DurĂ¡n, GE; Lacayo, NJ; Sikic, BI1
Glossmann, H; Mitterdorfer, J; Striessnig, J; Wappl, E1
Gaivin, RJ; Gonzalez-Cabrera, P; Perez, DM; Ross, SA; Waugh, DJ; Yun, J; Zuscik, MJ1
Adachi-Akahane, S; Ichijo, H; Nagao, T; Yamaguchi, S; Yoshioka, K; Zhorov, BS1

Other Studies

5 other study(ies) available for phenylalanine and dihydropyridines

ArticleYear
Functional consequences of phenylalanine mutations in the predicted transmembrane domain of P-glycoprotein.
    The Journal of biological chemistry, 1993, Sep-25, Volume: 268, Issue:27

    Topics: 3T3 Cells; Amino Acid Sequence; Animals; ATP Binding Cassette Transporter, Subfamily B, Member 1; Azides; Carrier Proteins; Cell Membrane; Cloning, Molecular; Dihydropyridines; DNA; Drug Resistance; Humans; Kinetics; Membrane Glycoproteins; Mice; Models, Structural; Molecular Sequence Data; Mutagenesis, Site-Directed; Phenylalanine; Protein Structure, Secondary; Recombinant Proteins; Transfection; Vinblastine

1993
Loss of cyclosporin and azidopine binding are associated with altered ATPase activity by a mutant P-glycoprotein with deleted phe(335).
    Molecular pharmacology, 2000, Volume: 57, Issue:4

    Topics: Adenosine Triphosphatases; Adenosine Triphosphate; Amino Acid Sequence; ATP Binding Cassette Transporter, Subfamily B, Member 1; Azides; Binding Sites; Calcium Channel Blockers; Cyclosporine; Dihydropyridines; Drug Interactions; Enzyme Activation; Humans; Molecular Sequence Data; Phenylalanine; Photoaffinity Labels; Tritium; Tumor Cells, Cultured; Vanadates; Verapamil

2000
Mechanism of dihydropyridine interaction with critical binding residues of L-type Ca2+ channel alpha 1 subunits.
    The Journal of biological chemistry, 2001, Apr-20, Volume: 276, Issue:16

    Topics: Alanine; Amino Acid Sequence; Amino Acid Substitution; Animals; Binding Sites; Calcium Channel Blockers; Calcium Channels, L-Type; Dihydropyridines; Female; Isoleucine; Isradipine; Kinetics; Methionine; Models, Molecular; Molecular Sequence Data; Mutagenesis, Site-Directed; Oocytes; Phenylalanine; Protein Structure, Secondary; Protein Subunits; Recombinant Proteins; Valine; Xenopus laevis

2001
Phe-308 and Phe-312 in transmembrane domain 7 are major sites of alpha 1-adrenergic receptor antagonist binding. Imidazoline agonists bind like antagonists.
    The Journal of biological chemistry, 2001, Jul-06, Volume: 276, Issue:27

    Topics: Adrenergic alpha-1 Receptor Antagonists; Adrenergic alpha-Antagonists; Amino Acid Sequence; Animals; Cell Membrane; Clonidine; Conserved Sequence; Cricetinae; Dihydropyridines; Dioxanes; Humans; Imidazoles; Models, Molecular; Molecular Sequence Data; Oxymetazoline; Phenylalanine; Piperazines; Prazosin; Protein Structure, Secondary; Rats; Receptors, Adrenergic, alpha-1; Structure-Activity Relationship

2001
Key roles of Phe1112 and Ser1115 in the pore-forming IIIS5-S6 linker of L-type Ca2+ channel alpha1C subunit (CaV 1.2) in binding of dihydropyridines and action of Ca2+ channel agonists.
    Molecular pharmacology, 2003, Volume: 64, Issue:2

    Topics: Alanine; Animals; Calcium Channel Agonists; Calcium Channel Blockers; Calcium Channels, L-Type; Dihydropyridines; Isradipine; Phenylalanine; Point Mutation; Protein Subunits; Pyrroles; Rats; Repetitive Sequences, Nucleic Acid; Serine

2003