The Molecular Biology Society of Japan

4:47 PM - 5:02 PM

[2PW-13-5(3P-0044)] Human rare disease caused by genetic mutation provides insights into structural rearrangement in GPCR

〇Yukiko Kurihara1, Toru Ekimoto2, Chris T. Gordon3, Taro Kitazawa1, Ryo Sugiyama1, Risa Kotani1, Yasunobu Uchijima1, Mitsunori Ikeguchi2, Amiel Jeanne3, Hiroki Kurihara1 (1.Dept. of Physiol. Chem. and Metab., Grad. Sch. of Med., Univ. of Tokyo , 2.Grad. Sch. of Med. Life Sci., Yokohama City Univ., 3.Institut Imagine)

GPCR, Endothelin A receptor, MD simulation

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