Jun-ichi Kishikawa

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Associated Professor

Kyoto Institute of Technology

Japan

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About

Jun-ichi Kishikawa is an Associate Professor at the Kyoto Institute of Technology, Japan. His research focuses on structural biology, particularly in understanding the mechanisms of cytotoxicity and drug actions, as evidenced by his recent articles on the Clostridium perfringens binary toxin and the ghrelin receptor. He has also explored the structural insights of various bacterial systems, including the flagellar motor complex and the human Pannexin-3 channel.

Recent Grants

Grant: Close

The mechanism of rotary ATPase for energy conversion of Proton motive force to rotation.

Open Date: 2020-04-01

Close Date: 2023-03-01

Grant: Close

Structural analysis of ATP release channel, pannexin.

Open Date: 2019-12-01

Close Date: 2022-03-01

Grant: Close

Cryo-ET analysis of membrane protein supercomplex.

Open Date: 2018-05-01

Close Date: 2023-03-01

Grant: Close

Structural and functional analysis of hexametric ATPases.

Open Date: 2016-04-01

Close Date: 2018-03-01

Articles (19)

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2025

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2022

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2021

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2020

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2020

Collaborators (21)

Makoto Fujikawa

Assistant Professor

Aichi Medical University

JAPAN

Jun-ichi Kishikawa

Research Interests

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About

Recent Grants

Articles (19)

Serine clamp of Clostridium perfringens binary toxin BECb (CPILEb)-pore confers cytotoxicity and enterotoxicity

Structural Elucidation of the Mechanism for Inhibitor Resistance in the Na+-Translocating NADH-Ubiquinone Oxidoreductase from Vibrio cholerae.

Cryo-EM Structure of the Flagellar Motor Complex from Paenibacillus sp. TCA20

The structure and function of the ghrelin receptor coding for drug actions

Structural analysis of S-ring composed of FliFG fusion proteins in marine Vibrio polar flagellar motor

Structural insight into sodium ion pathway in the bacterial flagellar stator from marine Vibrio.

Cryo-EM structure of the human Pannexin-3 channel.

The Thermal-Stable LH1-RC Complex of a Hot Spring Purple Bacterium Powers Photosynthesis with Extremely Low-Energy Near-Infrared Light.

Rotary mechanism of the prokaryotic Vo motor driven by proton motive force

Neurotransmitter recognition by human vesicular monoamine transporter 2

An inhaled ACE2 decoy confers protection against SARS-CoV-2 infection in preclinical models

Mechanism of ATP hydrolysis dependent rotation of bacterial ATP synthase

Structure of MotA, a flagellar stator protein, from hyperthermophile

Cryo-EM structures of Na+-pumping NADH-ubiquinone oxidoreductase from Vibrio cholerae

Structures of Multisubunit Membrane Complexes With the CRYO ARM 200

Structural snapshots of V/A-ATPase reveal the rotary catalytic mechanism of rotary ATPases

An infectivity-enhancing site on the SARS-CoV-2 spike protein targeted by antibodies.

Identification of chemical compounds as an inhibitor of mitochondrial ATP synthesis, leading to an increased stress resistance and an extended lifespan in C. elegans.

Mechanical inhibition of isolated Vo from V/A-ATPase for proton conductance

Collaborators (21)

Makoto Fujikawa

Yukihiko Sugita

Takeshi Ito

Seiji Kojima

Wai Tuck Soh

Toru Yoshida

Hideaki Tsuge

Hideto Miyoshi

Hiroyuki Mino

AKATSUKI SAITO

Norihiro Takekawa

Duy Tran

Takayuki Kato

Kazutoshi Tani

Toru Okamoto

Miwa Sasai

Ken Yokoyama

Masatoshi Murai

Katsumi Imada

Akio Kitao

Shuya Mitoma

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