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Phosphoproteomic identification of ULK substrates reveals VPS15-dependent ULK/VPS34 interplay in the regulation of autophagy.

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第一作者： Thomas John,Mercer

第一单位： Molecular Cell Biology of Autophagy, The Francis Crick Institute, London, UK.

作者： Thomas John,Mercer ^[1] ; Yohei,Ohashi ^[2] ; Stefan,Boeing ^[3] ; Harold B J,Jefferies ^[1] ; Stefano,De Tito ^[4] ; Helen,Flynn ^[5] ; Shirley,Tremel ^[2] ; Wenxin,Zhang ^[1] ; Martina,Wirth ^[1] ; David,Frith ^[6] ; Ambrosius P,Snijders ^[6] ; Roger Lee,Williams ^[2] ; Sharon A,Tooze ^[1]

作者单位： Molecular Cell Biology of Autophagy, The Francis Crick Institute, London, UK. ^[1] MRC Laboratory of Molecular Biology, Cambridge, UK. ^[2] Bioinformatics and Biostatistics, The Francis Crick Institute, London, UK. ^[3] Molecular Cell Biology of Autophagy, The Francis Crick Institute, London, UK.;Institute of Experimental Endocrinology and Oncology (IEOS), National Research Council, Naples, Italy. ^[4] Institute of Experimental Endocrinology and Oncology (IEOS), National Research Council, Naples, Italy. ^[5] Proteomics, The Francis Crick Institute, London, UK. ^[6]

关键词 PIK3R4 PRKAG2 ULK1 VPS15 p62