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资源简介：
IP-MS interactome of FAM134B1 and FAM134B2 in C2C12 cells differentiated into myotubes
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创建时间：
2024-12-27
相关数据集
FAM134B oligomerization drives endoplasmic reticulum membrane scission for ER-phagy
Degradation of Endoplasmic Reticulum (ER) by selective autophagy (ER-phagy) is crucial for ER homeostasis. However, it remains unclear how ER scission is regulated for subsequent autophagosomal seques
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A cross-kingdom conserved ER-phagy receptor maintains endoplasmic reticulum homeostasis during stress
Eukaryotes have evolved various quality control mechanisms to promote proteostasis in the ER. Selective removal of certain ER domains via autophagy (termed as ER-phagy) has emerged as a major quality
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Binding partners of FAM134B WT and 17KR oligomers
FAM134B is a reticulon-homology domain (RHD)-containing protein that participates in membrane-shaping of the endoplasmic reticulum (ER)8 13. It also functions as a mammalian ER-phagy receptor, mediati
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FAM134B oligomerization drives ER membrane scission for ER-phagy
ER degradation by selective autophagy (ER-phagy) is crucial for ER homeostasis. However, it remains unclear how ER scission is regulated for subsequent autophagosomal sequestration and lysosomal degra
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A cross-kingdom conserved ER-phagy receptor maintains endoplasmic reticulum homeostasis during stress
We have identified a potential selective autophagy receptor protein in Arabidopsis thaliana, C53/AT5G06830/ERP1, that is recruited to ER upon ER-stress activation and induces autophagosome formation.
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