Takuji Oyama

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Professor

University of Yamanashi

Japan

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Recent Grants

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Structural biology on the interaction between archaeal CMG helicase and DNA polymerase D

Open Date: 2018-04-01

Close Date: 2021-03-31

Grant: Close

Structural biology studies of clamp PCNA loading mechanism by the clamp loader RFC

Open Date: 2014-04-01

Close Date: 2017-03-31

Grant: Close

Attempt of unification by the graph of biomolecular structure data

Open Date: 2013-04-01

Close Date: 2016-03-31

Grant: Close

A study of the function structure association of the control mechanism of replisome by the clamp

Open Date: 2012-04-01

Close Date: 2016-03-31

Grant: Close

Structural basis of functional coupling between transcription and cellular metabolism

Open Date: 2006-01-01

Close Date: 2010-12-31

Articles (10)

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2023

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2022

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2022

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2022

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2022

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2022

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2022

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2021

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2021

Year:

2021

Collaborators (4)

Shotaro Kamata

Assistant professor

Showa Pharmaceutical University

JAPAN

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Yoshizumi Ishino

Professor

Kyushu Daigaku

JAPAN

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Masayuki Oda

Kyoto University

JAPAN

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Isao Ishii

Professor

Showa Pharmaceutical University

JAPAN

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Takuji Oyama

Research Interests

Explore related searches

Contact this professor

Recent Grants

Articles (10)

Functional and Structural Insights into the Human PPARα/δ/γ Targeting Preferences of Anti-NASH Investigational Drugs, Lanifibranor, Seladelpar, and Elafibranor

Pivotal role of a conserved histidine in Escherichia coli ribonuclease HI as proposed by X-ray crystallography

Functional and Structural Insights into Human PPARα/δ/γ Subtype Selectivity of Bezafibrate, Fenofibric Acid, and Pemafibrate

Family D DNA polymerase interacts with GINS to promote CMG-helicase in the archaeal replisome

Toward High-throughput Crystal Structure Determination of PPAR Ligand-binding Domains in Complexes with Less Soluble Ligands

Carboxyl Terminus of HOATZ is Intrinsically Disordered and Interacts with Heat Shock Protein A Families

Crystal structures of the ligand-binding domain of human peroxisome proliferator-activated receptor δ in complexes with phenylpropanoic acid derivatives and a pyridine carboxylic acid derivative

Preparation of co-crystals of human PPAR<b>α</b>-LBD and ligand for high-resolution X-ray crystallography.

Crystal Structures of the Human Peroxisome Proliferator-Activated Receptor (PPAR)α Ligand-Binding Domain in Complexes with a Series of Phenylpropanoic Acid Derivatives Generated by a Ligand-Exchange Soaking Method.

Structural Basis for Anti-non-alcoholic Fatty Liver Disease and Diabetic Dyslipidemia Drug Saroglitazar as a PPAR α/γ Dual Agonist.

Collaborators (4)

Shotaro Kamata

Yoshizumi Ishino

Masayuki Oda

Isao Ishii

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