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Research Paper
RAB33B recruits the ATG16L1 complex to the phagophore via a noncanonical RAB binding protein
Supansa Pantooma Department of Chemistry, Umeå Centre for Microbial Research, Umeå University, Umeå, Sweden;b Translational Neurodegeneration Section
“Albrecht-kossel”, Department of Neurology, University Medical Center Rostock , Rostock, Germany
https://orcid.org/0000-0001-9630-1999View further author information
Georgios Konstantinidisa Department of Chemistry, Umeå Centre for Microbial Research, Umeå University, Umeå, Sweden;c Institute of Molecular Biology and Biotechnology,Foundation for Research and Technology-Hellas , Crete, Greece
https://orcid.org/0000-0002-9306-2483View further author information
Stephanie Vossd Chemical Genomics Centre of the Max Planck Society, Dortmund, Germany;e Max-Planck-Institute of Molecular Physiology, Dortmund, GermanyView further author information
, Hongmei Hane Max-Planck-Institute of Molecular Physiology, Dortmund, GermanyView further author information
, Oliver Hofnagele Max-Planck-Institute of Molecular Physiology, Dortmund, GermanyView further author information
, Zhiyu Lif National Cancer Center, National Clinical Research Center for Cancer, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China
https://orcid.org/0000-0003-1666-9115View further author information
Yao-Wen Wua Department of Chemistry, Umeå Centre for Microbial Research, Umeå University, Umeå, SwedenCorrespondence[email protected] [email protected]
https://orcid.org/0000-0002-2573-8736View further author information
Pages 2290-2304
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Received 13 May 2020, Accepted 08 Sep 2020, Published online: 22 Sep 2020
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RAB33B recruits the ATG16L1 complex to the phagophore via a noncanonical RAB binding protein
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