Related references
Note: Only part of the references are listed.Vps13b is required for acrosome biogenesis through functions in Golgi dynamic and membrane trafficking
Romain Da Costa et al.
CELLULAR AND MOLECULAR LIFE SCIENCES (2020)
De novo phosphatidylcholine synthesis is required for autophagosome membrane formation and maintenance during autophagy
Gabriela Andrejeva et al.
AUTOPHAGY (2020)
Local Fatty Acid Channeling into Phospholipid Synthesis Drives Phagophore Expansion during Autophagy
Maximilian Schuetter et al.
CELL (2020)
A VPS13D spastic ataxia mutation disrupts the conserved adaptor-binding site in yeast Vps13
Samantha K. Dziurdzik et al.
HUMAN MOLECULAR GENETICS (2020)
Cryo-EM reconstruction of a VPS13 fragment reveals a long groove to channel lipids between membranes
PeiQi Li et al.
JOURNAL OF CELL BIOLOGY (2020)
The binding of the APT1 domains to phosphoinositides is regulated by metal ions in vitro
Damian Kolakowski et al.
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES (2020)
Vps13 is required for the packaging of the ER into autophagosomes during ER-phagy
Shuliang Chen et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2020)
XK is a partner for VPS13A: a molecular link between Chorea-Acanthocytosis and McLeod Syndrome
Jae-Sook Park et al.
MOLECULAR BIOLOGY OF THE CELL (2020)
Atg9 is a lipid scramblase that mediates autophagosomal membrane expansion
Kazuaki Matoba et al.
NATURE STRUCTURAL & MOLECULAR BIOLOGY (2020)
FFAT motif phosphorylation controls formation and lipid transfer function of inter-organelle contacts
Thomas Di Mattia et al.
EMBO JOURNAL (2020)
VPS13A is closely associated with mitochondria and is required for efficient lysosomal degradation
Sandra Munoz-Braceras et al.
DISEASE MODELS & MECHANISMS (2019)
Mdm1 maintains endoplasmic reticulum homeostasis by spatially regulating lipid droplet biogenesis
Hanaa Hariri et al.
JOURNAL OF CELL BIOLOGY (2019)
Cerebellar ataxia disease-associated Snx14 promotes lipid droplet growth at ER-droplet contacts
Sanchari Datta et al.
JOURNAL OF CELL BIOLOGY (2019)
Atg2 mediates direct lipid transfer between membranes for autophagosome formation
Takuo Osawa et al.
NATURE STRUCTURAL & MOLECULAR BIOLOGY (2019)
The Expanding and Unexpected Functions of Mitochondria Contact Sites
Laura L. Lackner
TRENDS IN CELL BIOLOGY (2019)
ATG2 transports lipids to promote autophagosome biogenesis
Diana P. Valverde et al.
JOURNAL OF CELL BIOLOGY (2019)
Human VPS13A is associated with multiple organelles and influences mitochondrial morphology and lipid droplet motility
Wondwossen M. Yeshaw et al.
ELIFE (2019)
SNAREs define targeting specificity of trafficking vesicles by combinatorial interaction with tethering factors
Seiichi Koike et al.
NATURE COMMUNICATIONS (2019)
The autophagic membrane tether ATG2A transfers lipids between membranes
Shintaro Maeda et al.
ELIFE (2019)
TOM40 Targets Atg2 to Mitochondria-Associated ER Membranes for Phagophore Expansion
Zhenyuan Tang et al.
CELL REPORTS (2019)
Lipid transfer proteins: the lipid commute via shuttles, bridges and tubes
Louise H. Wong et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2019)
Structure-function insights into direct lipid transfer between membranes by Mmm1-Mdm12 of ERMES
Shin Kawano et al.
JOURNAL OF CELL BIOLOGY (2018)
Recessive mutations in >VPS13D cause childhood onset movement disorders
Julie Gauthier et al.
ANNALS OF NEUROLOGY (2018)
Mutations in VPS13D lead to a new recessive ataxia with spasticity and mitochondrial defects
Eunju Seong et al.
ANNALS OF NEUROLOGY (2018)
Vps39 Interacts with Tom40 to Establish One of Two Functionally Distinct Vacuole-Mitochondria Contact Sites
Ayelen Gonzalez Montoro et al.
DEVELOPMENTAL CELL (2018)
SNX14 mutations affect endoplasmic reticulum-associated neutral lipid metabolism in autosomal recessive spinocerebellar ataxia 20
Dale Bryant et al.
HUMAN MOLECULAR GENETICS (2018)
Structural basis of sterol binding and transport by a yeast StARkin domain
Julian-Alexander Jentsch et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2018)
Atg9 establishes Atg2-dependent contact sites between the endoplasmic reticulum and phagophores
Ruben Gomez-Sanchez et al.
JOURNAL OF CELL BIOLOGY (2018)
Competitive organelle-specific adaptors recruit Vps13 to membrane contact sites
Bjorn D. M. Bean et al.
JOURNAL OF CELL BIOLOGY (2018)
Vacuolar protein sorting 13C is a novel lipid droplet protein that inhibits lipolysis in brown adipocytes
Vanesa D. Ramseyer et al.
MOLECULAR METABOLISM (2018)
VPS13A and VPS13C are lipid transport proteins differentially localized at ER contact sites
Nikit Kumar et al.
JOURNAL OF CELL BIOLOGY (2018)
Insights into autophagosome biogenesis from structural and biochemical analyses of the ATG2A-WIPI4 complex
Saikat Chowdhury et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2018)
The Atg2-Atg18 complex tethers pre-autophagosomal membranes to the endoplasmic reticulum for autophagosome formation
Tetsuya Kotani et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2018)
Molecular Basis and Clinical Overview of McLeod Syndrome Compared With Other Neuroacanthocytosis Syndromes A Review
Eileen Roulis et al.
JAMA NEUROLOGY (2018)
The Many Faces of Amphipathic Helices
Manuel Gimenez-Andres et al.
BIOMOLECULES (2018)
Lipid droplet biogenesis is spatially coordinated at ER-vacuole contacts under nutritional stress
Hanaa Hariri et al.
EMBO REPORTS (2018)
Differential requirement for ATG2A domains for localization to autophagic membranes and lipid droplets'
Norito Tamura et al.
FEBS LETTERS (2017)
Amino acid substitution equivalent to human chorea-acanthocytosis I2771R in yeast Vps13 protein affects its binding to phosphatidylinositol 3-phosphate
Weronika Rzepnikowska et al.
HUMAN MOLECULAR GENETICS (2017)
Vps13-Mcp1 interact at vacuole-mitochondria interfaces and bypass ER-mitochondria contact sites
Arun T. John Peter et al.
JOURNAL OF CELL BIOLOGY (2017)
The Vps13p-Cdc31p complex is directly required for TGN late endosome transport and TGN homotypic fusion
Mithu De et al.
JOURNAL OF CELL BIOLOGY (2017)
Phosphatidylserine synthesis at membrane contact sites promotes its transport out of the ER
Muthukumar Kannan et al.
JOURNAL OF LIPID RESEARCH (2017)
Lipid droplets are central organelles for meiosis II progression during yeast sporulation
Tzu-Han Hsu et al.
MOLECULAR BIOLOGY OF THE CELL (2017)
Drosophila Vps13 Is Required for Protein Homeostasis in the Brain
Jan J. Vonk et al.
PLOS ONE (2017)
Membrane contact sites, ancient and central hubs of cellular lipid logistics
Amrita Jain et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH (2017)
Loss of VPS1 3C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy
Suzanne Lesage et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2016)
A new molecular link between defective autophagy and erythroid abnormalities in chorea-acanthocytosis
Francesca Lupo et al.
BLOOD (2016)
Phosphatidylinositol-3-phosphate regulates response of cells to proteotoxic stress
Joanna Kaminska et al.
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY (2016)
Yeast Vps13 promotes mitochondrial function and is localized at membrane contact sites
Jae-Sook Park et al.
MOLECULAR BIOLOGY OF THE CELL (2016)
Structure of human Niemann-Pick C1 protein
Xiaochun Li et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2016)
Using HHsearch to tackle proteins of unknown function: A pilot study with PH domains
David R. Fidler et al.
TRAFFIC (2016)
Identification of VPS13C as a Galectin-12-Binding Protein That Regulates Galectin-12 Protein Stability and Adipogenesis
Ri-Yao Yang et al.
PLOS ONE (2016)
TipC and the chorea-acanthocytosis protein VPS13A regulate autophagy in Dictyostelium and human HeLa cells
Sandra Munoz-Braceras et al.
AUTOPHAGY (2015)
The BioPlex Network: A Systematic Exploration of the Human Interactome
Edward L. Huttlin et al.
CELL (2015)
Lipid droplets and their component triglycerides and steryl esters regulate autophagosome biogenesis
Tomer Shpilka et al.
EMBO JOURNAL (2015)
ER-mitochondrial junctions can be bypassed by dominant mutations in the endosomal protein Vps13
Alexander B. Lang et al.
JOURNAL OF CELL BIOLOGY (2015)
The I-TASSER Suite: protein structure and function prediction
Jianyi Yang et al.
NATURE METHODS (2015)
Lam6 Regulates the Extent of Contacts between Organelles
Yael Elbaz-Alon et al.
CELL REPORTS (2015)
Cohen Syndrome-associated Protein COH1 Physically and Functionally Interacts with the Small GTPase RAB6 at the Golgi Complex and Directs Neurite Outgrowth
Wenke Seifert et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2015)
Neutral Lipid Stores and Lipase PNPLA5 Contribute to Autophagosome Biogenesis
Nicolas Dupont et al.
CURRENT BIOLOGY (2014)
Exposure of Phosphatidylserine by Xk-related Protein Family Members during Apoptosis
Jun Suzuki et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2014)
SPO71 Encodes a Developmental Stage-Specific Partner for Vps13 in Saccharomyces cerevisiae
Jae-Sook Park et al.
EUKARYOTIC CELL (2013)
Xk-Related Protein 8 and CED-8 Promote Phosphatidylserine Exposure in Apoptotic Cells
Jun Suzuki et al.
SCIENCE (2013)
VPS13 regulates membrane morphogenesis during sporulation in Saccharomyces cerevisiae
Jae-Sook Park et al.
JOURNAL OF CELL SCIENCE (2012)
Mammalian Atg2 proteins are essential for autophagosome formation and important for regulation of size and distribution of lipid droplets
Anoop Kumar G. Velikkakath et al.
MOLECULAR BIOLOGY OF THE CELL (2012)
Novel Pathogenic Mutations and Copy Number Variations in the VPS13A Gene in Patients With Chorea-Acanthocytosis
Akiyuki Tomiyasu et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2011)
Cohen Syndrome-associated Protein, COH1, Is a Novel, Giant Golgi Matrix Protein Required for Golgi Integrity
Wenke Seifert et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2011)
Structure and function of WD40 domain proteins
Chao Xu et al.
PROTEIN & CELL (2011)
Homology of SMP domains to the TULIP superfamily of lipid-binding proteins provides a structural basis for lipid exchange between ER and mitochondria
Klaus O. Kopec et al.
BIOINFORMATICS (2010)
Identification of Surface Residues on Niemann-Pick C2 Essential for Hydrophobic Handoff of Cholesterol to NPC1 in Lysosomes
Michael L. Wang et al.
CELL METABOLISM (2010)
Optimized Measurement Temperature Gives Access to the Solution Structure of a 49 kDa Homohexameric β-Propeller
Ilka Varnay et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2010)
The Phagosomal Proteome in Interferon-γ-Activated Macrophages
Matthias Trost et al.
IMMUNITY (2009)
An ER-Mitochondria Tethering Complex Revealed by a Synthetic Biology Screen
Benoit Kornmann et al.
SCIENCE (2009)
Membrane lipids: where they are and how they behave
Gerrit van Meer et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2008)
Membrane proteomics of phagosomes suggests a connection to autophagy
Wenqing Shui et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
The dynamic phagosomal proteome and the contribution of the endoplasmic reticulum
Lindsay D. Rogers et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
A general amphipathic α-helical motif for sensing membrane curvature
Guillaume Drin et al.
NATURE STRUCTURAL & MOLECULAR BIOLOGY (2007)
Nucleus-vacuole junctions and piecemeal microautophagy of the nucleus in S-cerevisiae
Erik Kvam et al.
AUTOPHAGY (2007)
Mutational spectrum of COH1 and clinical heterogeneity in Cohen syndrome
W Seifert et al.
JOURNAL OF MEDICAL GENETICS (2006)
Structural mechanism for sterol sensing and transport by OSBP-related proteins
YJ Im et al.
NATURE (2005)
The HHpred interactive server for protein homology detection and structure prediction
J Söding et al.
NUCLEIC ACIDS RESEARCH (2005)
A highly conserved binding site in vesicle-associated membrane protein-associated protein (VAP) for the FFAT motif of lipid-binding proteins
CJR Loewen et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2005)
A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis
AL Nishimura et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
Cohen syndrome is caused by mutations in a novel gene, COH1, encoding a transmembrane protein with a presumed role in vesicle-mediated sorting and intracellular protein transport
J Kolehmainen et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2003)
Piecemeal microautophagy of nucleus in Saccharomyces cerevisiae
P Roberts et al.
MOLECULAR BIOLOGY OF THE CELL (2003)
Mutational spectrum of the CHAC gene in patients with chorea-acanthocytosis
C Dobson-Stone et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2002)
A conserved sorting-associated protein is mutant in chorea-acanthocytosis
L Rampoldi et al.
NATURE GENETICS (2001)
Share Paper
