Spartin recruits PKC-ζ via the PKC-ζ-interacting proteins ZIP1 and ZIP3 to lipid droplets (Q28589177)

Journal of Neurochemistry

GOA release 2020-03-11

author name string

Andreas Urbanczyk

series ordinal

1

1 reference

31 January 2017

Ralf Enz

series ordinal

2

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31 January 2017

language of work or name

English

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publication date

1 September 2011

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31 January 2017

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31 January 2017

118

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31 January 2017

5

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31 January 2017

737–748

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31 January 2017

PLD1 and ERK2 regulate cytosolic lipid droplet formation

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Dynamic activity of lipid droplets: protein phosphorylation and GTP-mediated protein translocation.

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Lipid droplets: a dynamic organelle moves into focus

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ZIP3, a new splice variant of the PKC-zeta-interacting protein family, binds to GABAC receptors, PKC-zeta, and Kv beta 2

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A role for ubiquitin ligases and Spartin/SPG20 in lipid droplet turnover

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Endogenous spartin (SPG20) is recruited to endosomes and lipid droplets and interacts with the ubiquitin E3 ligases AIP4 and AIP5

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GABAC receptor rho subunits are heterogeneously expressed in the human CNS and form homo- and heterooligomers with distinct physical properties.

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Fld1p, a functional homologue of human seipin, regulates the size of lipid droplets in yeast

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Structure and functional properties of the ubiquitin binding protein p62

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Differential stimulation of PKC phosphorylation of potassium channels by ZIP1 and ZIP2

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1 reference

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Spartin activates atrophin-1-interacting protein 4 (AIP4) E3 ubiquitin ligase and promotes ubiquitination of adipophilin on lipid droplets

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Seipinopathy: a novel endoplasmic reticulum stress-associated disease

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SPG20 protein spartin associates with cardiolipin via its plant-related senescence domain and regulates mitochondrial Ca2+ homeostasis

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Cholesterol-induced caveolin targeting to lipid droplets in adipocytes: a role for caveolar endocytosis

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p62 at the crossroads of autophagy, apoptosis, and cancer

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Signal integration and diversification through the p62 scaffold protein

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Interaction of protein kinase C zeta with ZIP, a novel protein kinase C-binding protein

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Neuropathy target esterase gene mutations cause motor neuron disease

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Genetic inactivation of p62 leads to accumulation of hyperphosphorylated tau and neurodegeneration.

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Endogenous spartin, mutated in hereditary spastic paraplegia, has a complex subcellular localization suggesting diverse roles in neurons.

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Mature-onset obesity and insulin resistance in mice deficient in the signaling adapter p62.

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PNUTS forms a trimeric protein complex with GABA(C) receptors and protein phosphatase 1.

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Autophagy regulates lipid metabolism

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ATGL has a key role in lipid droplet/adiposome degradation in mammalian cells

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Rhodopsin's carboxy-terminal cytoplasmic tail acts as a membrane receptor for cytoplasmic dynein by binding to the dynein light chain Tctex-1

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Cellular strategies for controlling protein aggregation

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PKCζ-interacting protein ZIP3 is generated by intronic polyadenylation, and is expressed in the brain and retina of the rat.

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Signaling, polyubiquitination, trafficking, and inclusions: sequestosome 1/p62's role in neurodegenerative disease.

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p62 Is a common component of cytoplasmic inclusions in protein aggregation diseases

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