J. Taira

发表

Improvement of the novel inhibitor for Mycobacterium enoyl-acyl carrier protein reductase (InhA): a structure–activity relationship study of KES4 assisted by in silico structure-based drug screening

H. Sakamoto, J. Sacchettini, F. Berenger, 2020, The Journal of Antibiotics.

Structural modification of a novel inhibitor for mycobacterium enoyl-acyl carrier protein reductase assisted by In silico structure-based drug screening

H. Sakamoto, S. Aoki, J. Taira, 2020, International journal of mycobacteriology.

In silico structure-based drug screening of novel antimycobacterial pharmacophores by DOCK-GOLD tandem screening

H. Sakamoto, S. Aoki, H. Komatsu, 2017, International journal of mycobacteriology.

Identification of a novel class of small compounds with anti-tuberculosis activity by in silico structure-based drug screening

H. Sakamoto, J. Sacchettini, S. Aoki, 2017, The Journal of Antibiotics.

Discovery of InhA inhibitors with anti-mycobacterial activity through a matched molecular pair approach.

H. Sakamoto, J. Sacchettini, S. Aoki, 2015, European journal of medicinal chemistry.

Conformational Equilibrium of NADPH–Cytochrome P450 Oxidoreductase Is Essential for Heme Oxygenase Reaction

H. Sakamoto, T. Yasunaga, K. Fukuyama, 2020, Antioxidants.

Modifications on amphiphilicity and cationicity of unnatural amino acid containing peptides for the improvement of antimicrobial activity against pathogenic bacteria

H. Yamaguchi, Y. Higashimoto, H. Kodama, 2010, Journal of Peptide Science.

Evaluation of in vitro properties of predicted kinases that phosphorylate serine residues within nuclear localization signal 1 of high mobility group box 1

Y. Higashimoto, J. Taira, 2014, Journal of peptide science : an official publication of the European Peptide Society.

EprS, an autotransporter protein of Pseudomonas aeruginosa, possessing serine protease activity induces inflammatory responses through protease‐activated receptors

Y. Higashimoto, K. Kuwano, J. Taira, 2013, Cellular microbiology.

Dephosphorylation of clustered phosphoserine residues in human Grb14 by protein phosphatase 1 and its effect on insulin receptor complex formation

H. Sakamoto, Kousuke Hanada, Keisuke Yoshida, 2019, Journal of peptide science : an official publication of the European Peptide Society.

Protein phosphatase 2A dephosphorylates phosphoserines in nucleocytoplasmic shuttling and secretion of high mobility group box 1.

Y. Higashimoto, K. Kuwano, J. Taira, 2013, Journal of biochemistry.

Phosphorylation of Grb14 BPS domain by GSK-3 correlates with complex forming of Grb14 and insulin receptor.

Y. Higashimoto, J. Taira, 2014, Journal of biochemistry.

Phosphorylation of clustered serine residues in the N-terminus of BPS domain negatively regulates formation of the complex between human Grb14 and insulin receptor

H. Sakamoto, Y. Higashimoto, H. Komatsu, 2017, Journal of biochemistry.

Antiadhesive sites present in the fibronectin type III-like repeats of human plasma fibronectin.

M. Ueki, H. Kodama, H. Yajima, 2007, Biological & pharmaceutical bulletin.

Studies on the Ion Channel Properties of Transmembrane Peptide Assemblies Associated with Electrostatic Interactions March 2008

J. Taira, 2008 .

Tenascin-C-derived Peptide TNIIIA2 Highly Enhances Cell Survival and Platelet-derived Growth Factor (PDGF)-dependent Cell Proliferation through Potentiated and Sustained Activation of Integrin α5β1

H. Kodama, H. Yajima, T. Matsunaga, 2014, The Journal of Biological Chemistry.

Pigment epithelium-derived factor (PEDF) binds to caveolin-1 and inhibits the pro-inflammatory effects of caveolin-1 in endothelial cells.

Y. Higashimoto, S. Yamagishi, T. Matsui, 2013, Biochemical and biophysical research communications.

Apoptotic Death of Hematopoietic Tumor Cells through Potentiated and Sustained Adhesion to Fibronectin via VLA-4*

H. Kodama, Y. Niitsu, H. Terada, 2009, The Journal of Biological Chemistry.

Peptaibol Derived Helix‐Kink Motif Facilitates Channel Forming of the Artificial α-Aminoisobutyric Acid Rich Helices

H. Kodama, J. Taira, Satoshi Osada, 2010, International Journal of Peptide Research and Therapeutics.

Pigment epithelium-derived factor inhibits caveolin-induced interleukin-8 gene expression and proliferation of human prostate cancer cells.

Y. Higashimoto, S. Yamagishi, T. Matsui, 2015, Oncology letters.

EprS, an autotransporter serine protease, plays an important role in various pathogenic phenotypes of Pseudomonas aeruginosa.

K. Kuwano, J. Taira, Y. Kida, 2016, Microbiology.

Establishing a parallel compound screening method and identifying dihydrofolate reductase novel antimicrobial compounds targeting Staphylococcus aureus

J. Taira, S. Kawamoto, Shunsuke Aoki, 2022 .

Complex Formation of Heme Oxygenase-2 with Heme Is Competitively Inhibited by the Cytosolic Domain of Caveolin-1.

H. Sakamoto, Y. Higashimoto, J. Taira, 2021, Biochemistry.

Protective Role of PEDF-Derived Synthetic Peptide Against Experimental Diabetic Nephropathy

Y. Higashimoto, S. Yamagishi, S. Yamagishi, 2016, Hormone and Metabolic Research.

Ion-channel formation assisted by electrostatic interhelical interactions in covalently dimerized amphiphilic helical peptides.

H. Kodama, F. Kato, J. Taira, 2008, Biochemistry.

Trans-Bilayer Ion Conduction by Proline Containing Cyclic Hexapeptides and Effects of Amino Acid Substitutions on Ion Conducting Properties

H. Kodama, H. Aoyagi, T. Ueda, 2010 .

Blockade by phosphorothioate aptamers of advanced glycation end products-induced damage in cultured pericytes and endothelial cells.

Y. Higashimoto, S. Yamagishi, T. Matsui, 2013, Microvascular research.

Caveolin-1 is a competitive inhibitor of heme oxygenase-1 (HO-1) with heme: identification of a minimum sequence in caveolin-1 for binding to HO-1.

Y. Higashimoto, M. Sugishima, M. Noguchi, 2011, Biochemistry.

Identification of novel inhibitors for mycobacterial polyketide synthase 13 via in silico drug screening assisted by the parallel compound screening with genetic algorithm-based programs

J. Taira, Shunsuke Aoki, H. Sakamoto, 2022, The Journal of Antibiotics.

Improvement of heme oxygenase-1-based heme sensor for quantifying free heme in biological samples.

H. Sakamoto, Y. Higashimoto, Toru Takahashi, 2015, Analytical biochemistry.

Modifications of Hydrophobic Value and Hydrophobic Moment Value of Cationic Model Peptides for Conversion of Peptide–Membrane Interactions

H. Kodama, H. Aoyagi, J. Taira, 2008 .

Caveolin-1 interacts with protein phosphatase 5 and modulates its activity in prostate cancer cells.

Y. Higashimoto, J. Taira, 2013, Biochemical and biophysical research communications.

Caveolin-1 interacts with protein phosphatase 5 and modulates its activity in prostate cancer cells.

Y. Higashimoto, J. Taira, Junichi Taira, 2013, Biochemical and biophysical research communications.

Protective Role of PEDF-Derived Synthetic Peptide Against Experimental Diabetic Nephropathy

Y. Higashimoto, S. Yamagishi, T. Matsui, 2016, Hormone and Metabolic Research.

Modifications on amphiphilicity and cationicity of unnatural amino acid containing peptides for the improvement of antimicrobial activity against pathogenic bacteria

H. Yamaguchi, Y. Higashimoto, H. Kodama, 2010, Journal of peptide science : an official publication of the European Peptide Society.

Tenascin-C-derived Peptide TNIIIA2 Highly Enhances Cell Survival and Platelet-derived Growth Factor (PDGF)-dependent Cell Proliferation through Potentiated and Sustained Activation of Integrin α5β1

H. Kodama, H. Yajima, T. Matsunaga, 2014, The Journal of Biological Chemistry.