Gene Ontology annotation through association of InterPro records with GO terms
Annotation inferences using phylogenetic trees
Gene Ontology annotation based on UniProtKB/Swiss-Prot keyword mapping
Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping
Electronic Gene Ontology annotations created by ARBA machine learning models
Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia
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First identification of CHMP2B mutations in FTD
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CHMP2B localizes to late endosomes, lysosomes, and cytosol
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Mutations cause enlarged endosomes and neuronal dysfunction
Recycling of ESCRTs by the AAA-ATPase Vps4 is regulated by a conserved VSL region in Vta1
The ESCRT-III subunit hVps24 is required for degradation but not silencing of the epidermal growth factor receptor
A systematic analysis of human CHMP protein interactions: additional MIT domain-containing proteins bind to multiple components of the human ESCRT III complex.
ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B).
ESCRT-III dysfunction causes autophagosome accumulation and neurodegeneration.
ESCRT-III recognition by VPS4 ATPases
Functional multivesicular bodies are required for autophagic clearance of protein aggregates associated with neurodegenerative disease
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ESCRT depletion or CHMP2B mutants inhibit autophagy
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Causes accumulation of ubiquitin/p62-positive aggregates
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CHMP2B mutations disrupt TDP-43 clearance
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Links ESCRT dysfunction to neurodegeneration
Large-scale proteomics and phosphoproteomics of urinary exosomes
Membrane scission by the ESCRT-III complex
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ESCRT-III alone can drive membrane fission
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Three ESCRT-III subunits sufficient for vesicle detachment
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VPS4 required for recycling, not scission
Membrane budding and scission by the ESCRT machinery: it's all in the neck.
Human ESCRT-III and VPS4 proteins are required for centrosome and spindle maintenance
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ESCRT-III depletion inhibits abscission
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Also affects centrosome and spindle maintenance
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VPS4 localizes to spindle poles and midbodies
The role of ESCRT proteins in fusion events involving lysosomes, endosomes and autophagosomes.
ESCRT-III subunits Snf7-1 and Snf7-2 differentially regulate transmembrane cargos in hESC-derived human neurons.
The SARS-coronavirus-host interactome: identification of cyclophilins as target for pan-coronavirus inhibitors.
ESCRT-III CHMP2A and CHMP3 form variable helical polymers in vitro and act synergistically during HIV-1 budding
In-depth proteomic analyses of exosomes isolated from expressed prostatic secretions in urine
Syntaxin 13, a genetic modifier of mutant CHMP2B in frontotemporal dementia, is required for autophagosome maturation
ESCRT requirements for EIAV budding
ESCRT machinery is required for plasma membrane repair
Structure of cellular ESCRT-III spirals and their relationship to HIV budding
E-cadherin interactome complexity and robustness resolved by quantitative proteomics
Spastin and ESCRT-III coordinate mitotic spindle disassembly and nuclear envelope sealing
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ESCRT-III recruited to NE during anaphase
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Coordinates with spastin for spindle disassembly
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Localizes to kinetochores and midbody
ESCRT-III controls nuclear envelope reformation
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CHMP2A/B encircle forming daughter nuclei during telophase
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ESCRT-III localizes to sites of annular fusion
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Required for NE integrity and sealing
A human interactome in three quantitative dimensions organized by stoichiometries and abundances
Recruitment Of HIV Virion Budding Machinery
VPS4 binds ESCRT-III assemblies at nuclear envelope (NE) fenestrations
CHMP7 binds CHMP4B, which recruits other subunits of the ESCRT-III complex
SPAST (spastin) binds the IST1 subunit of ESCRT-III at the sites of microtubule attachment to chromatin
VPS4 mediates disassembly of ESCRTIII subunits to promote sealing of holes in the nuclear envelope
SPAST (spastin) mediates the severing of microtubules at chromosome attachment sites
Genome-wide YFP fluorescence complementation screen identifies new regulators for telomere signaling in human cells.
Deep research report on CHMP2B