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作 者:Jean-Charles Liévens Tangui Maurice
机构地区:[1]MMDN,Univ Montpellier,INSERM,EPHE,Montpellier,France
出 处:《Neural Regeneration Research》2021年第1期106-107,共2页中国神经再生研究(英文版)
摘 要:Initially,the Sigma-1 receptor(S1R)was incorrectly categorized as one of the opioid receptors.But it has since become clear that S1R is a non-opioid non-phencyclidine receptor with molecular chaperone activity.S1R is a 223 amino-acid long protein that shares no clear homology with any other known mammalian proteins,its closest homolog being the fungal ERG2 sterol isomerase.Even its pharmacological counterpart,the Sigma-2 receptor that was only recently cloned,is genetically distinct.S1R is more likely considered as an atypical ligand-modulated chaperone protein.S1R is widely expressed in many organs including brain where its function has mainly been explored.
分 类 号:R744.8[医药卫生—神经病学与精神病学]
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