AP-4 vesicles contribute to spatial control of autophagy via RUSC-dependent peripheral delivery of ATG9A.

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Title: AP-4 vesicles contribute to spatial control of autophagy via RUSC-dependent peripheral delivery of ATG9A.
Authors: Davies AK; Cambridge Institute for Medical Research, University of Cambridge, Cambridge, CB2 0XY, UK., Itzhak DN; Department of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, Martinsried, 82152, Germany., Edgar JR; Cambridge Institute for Medical Research, University of Cambridge, Cambridge, CB2 0XY, UK., Archuleta TL; Department of Biological Sciences, Vanderbilt University, Nashville, TN, 37235, USA.; Center for Structural Biology, Vanderbilt University, Nashville, TN, 37235, USA., Hirst J; Cambridge Institute for Medical Research, University of Cambridge, Cambridge, CB2 0XY, UK., Jackson LP; Department of Biological Sciences, Vanderbilt University, Nashville, TN, 37235, USA.; Center for Structural Biology, Vanderbilt University, Nashville, TN, 37235, USA., Robinson MS; Cambridge Institute for Medical Research, University of Cambridge, Cambridge, CB2 0XY, UK. msr12@cam.ac.uk., Borner GHH; Department of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, Martinsried, 82152, Germany. borner@biochem.mpg.de.
Source: Nature communications [Nat Commun] 2018 Sep 27; Vol. 9 (1), pp. 3958. Date of Electronic Publication: 2018 Sep 27.
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-1723 (Electronic) Linking ISSN: 20411723 NLM ISO Abbreviation: Nat Commun Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: AP-4 vesicles contribute to spatial control of autophagy via RUSC-dependent peripheral delivery of ATG9A.
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  Data: <searchLink fieldCode="AU" term="%22Davies+AK%22">Davies AK</searchLink>; Cambridge Institute for Medical Research, University of Cambridge, Cambridge, CB2 0XY, UK.<br /><searchLink fieldCode="AU" term="%22Itzhak+DN%22">Itzhak DN</searchLink>; Department of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, Martinsried, 82152, Germany.<br /><searchLink fieldCode="AU" term="%22Edgar+JR%22">Edgar JR</searchLink>; Cambridge Institute for Medical Research, University of Cambridge, Cambridge, CB2 0XY, UK.<br /><searchLink fieldCode="AU" term="%22Archuleta+TL%22">Archuleta TL</searchLink>; Department of Biological Sciences, Vanderbilt University, Nashville, TN, 37235, USA.; Center for Structural Biology, Vanderbilt University, Nashville, TN, 37235, USA.<br /><searchLink fieldCode="AU" term="%22Hirst+J%22">Hirst J</searchLink>; Cambridge Institute for Medical Research, University of Cambridge, Cambridge, CB2 0XY, UK.<br /><searchLink fieldCode="AU" term="%22Jackson+LP%22">Jackson LP</searchLink>; Department of Biological Sciences, Vanderbilt University, Nashville, TN, 37235, USA.; Center for Structural Biology, Vanderbilt University, Nashville, TN, 37235, USA.<br /><searchLink fieldCode="AU" term="%22Robinson+MS%22">Robinson MS</searchLink>; Cambridge Institute for Medical Research, University of Cambridge, Cambridge, CB2 0XY, UK. msr12@cam.ac.uk.<br /><searchLink fieldCode="AU" term="%22Borner+GHH%22">Borner GHH</searchLink>; Department of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, Martinsried, 82152, Germany. borner@biochem.mpg.de.
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  Data: <searchLink fieldCode="JN" term="%22101528555%22">Nature communications</searchLink> [Nat Commun] 2018 Sep 27; Vol. 9 (1), pp. 3958. <i>Date of Electronic Publication: </i>2018 Sep 27.
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              Text: 2018 Sep 27
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