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• W2001045944 abstract "Selective autophagy ensures recognition and removal of various cytosolic cargoes. Hence, aggregated proteins, damaged organelles, or pathogens are enclosed into the double-membrane vesicle, the autophagosome, and delivered to the lysosome for degradation. This process is mediated by selective autophagy receptors, such as p62/SQSTM1. These proteins recognize autophagic cargo and, via binding to small ubiquitin-like modifiers (UBLs)--Atg8/LC3/GABARAPs and ATG5--mediate formation of selective autophagosomes. Recently, it was found that UBLs can directly engage the autophagosome nucleation machinery. Here, we review recent findings on selective autophagy and propose a model for selective autophagosome formation in close proximity to cargo." @default.
• W2001045944 created "2016-06-24" @default.
• W2001045944 creator A5025286296 @default.
• W2001045944 creator A5035695744 @default.
• W2001045944 creator A5035924475 @default.
• W2001045944 creator A5072603201 @default.
• W2001045944 date "2014-01-01" @default.
• W2001045944 modified "2023-10-16" @default.
• W2001045944 title "Interactions between Autophagy Receptors and Ubiquitin-like Proteins Form the Molecular Basis for Selective Autophagy" @default.
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• W2001045944 doi "https://doi.org/10.1016/j.molcel.2013.12.014" @default.
• W2001045944 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/24462201" @default.
• W2001045944 hasPublicationYear "2014" @default.
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