Phosphatidylethanolamine deficiency in Mammalian mitochondria impairs oxidative phosphorylation and alters mitochondrial morphology. - Wikidata - wikimedia - TriplyDB

Phosphatidylethanolamine deficiency in Mammalian mitochondria impairs oxidative phosphorylation and alters mitochondrial morphology.

Phosphatidylethanolamine deficiency in Mammalian mitochondria impairs oxidative phosphorylation and alters mitochondrial morphology.

http://www.wikidata.org/entity/Q36596263

about

Phosphatidylserine decarboxylase 1 autocatalysis and function does not require a mitochondrial-specific factor.An assembly of proteins and lipid domains regulates transport of phosphatidylserine to phosphatidylserine decarboxylase 2 in Saccharomyces cerevisiae.Aim24 and MICOS modulate respiratory function, tafazzin-related cardiolipin modification and mitochondrial architecture Phosphatidylserine transport by Ups2-Mdm35 in respiration-active mitochondria Role of mitochondrial lipids in guiding fission and fusion Mitochondrial lipids in neurodegeneration IDH1 regulates phospholipid metabolism in developing astrocytes LACTB is a tumour suppressor that modulates lipid metabolism and cell state.Role of phosphatidylethanolamine in the biogenesis of mitochondrial outer membrane proteins Mouse mitochondrial lipid composition is defined by age in brain and muscle.Mitochondria hyperfusion and elevated autophagic activity are key mechanisms for cellular bioenergetic preservation in centenarians.Metabolic determinants of cancer cell sensitivity to glucose limitation and biguanides.Role of choline deficiency in the Fatty liver phenotype of mice fed a low protein, very low carbohydrate ketogenic diet.Impaired cardiac energy metabolism in embryos lacking adrenergic stimulation.The complex I subunit NDUFA10 selectively rescues Drosophila pink1 mutants through a mechanism independent of mitophagy.A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity.Phosphatidylethanolamine Metabolism in Health and Disease.Early structural and metabolic cardiac remodelling in response to inducible adipose triglyceride lipase ablation.Specific requirements of nonbilayer phospholipids in mitochondrial respiratory chain function and formation.Meclizine inhibits mitochondrial respiration through direct targeting of cytosolic phosphoethanolamine metabolism.Genome-wide transcriptome analysis revealed organelle specific responses to temperature variations in algae.Of yeast, mice and men: MAMs come in two flavors.Phosphatidylethanolamine synthesis in the parasite mitochondrion is required for efficient growth but dispensable for survival of Toxoplasma gondii Regulation of mitochondrial morphology by lipids.Lipid metabolism in mitochondrial membranes.Mitochondrial phospholipids: role in mitochondrial function.How lipids modulate mitochondrial protein import.Respiratory chain supercomplexes: Structures, function and biogenesis.StarD7 Protein Deficiency Adversely Affects the Phosphatidylcholine Composition, Respiratory Activity, and Cristae Structure of Mitochondria.ORP5/ORP8 localize to endoplasmic reticulum-mitochondria contacts and are involved in mitochondrial function.The coming of age of the mitochondria-ER contact: a matter of thickness.Cardiolipin and mitochondrial cristae organization.Looking Beyond Structure: Membrane Phospholipids of Skeletal Muscle Mitochondria.Phospholipids in mitochondrial dysfunction during hemorrhagic shock.Interaction of MDM33 with mitochondrial inner membrane homeostasis pathways in yeast.MAMs are attractive targets for bacterial repurposing of the host cell: MAM-functions might be key for undermining an infected cell.Phosphatidylcholine Affects Inner Membrane Protein Translocases of Mitochondria.Ethanolamine and Phosphatidylethanolamine: Partners in Health and Disease.From masochistic enzymology to mechanistic physiology and disease.Phosphatidylcholine affects the role of the sorting and assembly machinery in the biogenesis of mitochondrial β-barrel proteins.

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P2860

Phosphatidylethanolamine deficiency in Mammalian mitochondria impairs oxidative phosphorylation and alters mitochondrial morphology.

http://www.wikidata.org/entity/Q36596263

description

2012 nî lūn-bûn

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Phosphatidylethanolamine defic ...... ters mitochondrial morphology.

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Phosphatidylethanolamine defic ...... ters mitochondrial morphology.

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Phosphatidylethanolamine defic ...... ters mitochondrial morphology.

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JBC.M112.434183

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Journal of Biological Chemistry

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Phosphatidylethanolamine defic ...... ters mitochondrial morphology.

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Alois Haromy

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Evangelos Michelakis

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Guergana Tasseva

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Helin Daniel Bai

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Jean E Vance

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Magdalena Davidescu

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P2860

Defective remodeling of cardiolipin and phosphatidylglycerol in Barth syndrome

Dynamin-related protein Drp1 is required for mitochondrial division in mammalian cells

Mitochondrial respiratory chain supercomplexes are destabilized in Barth Syndrome patients

Parkin is recruited selectively to impaired mitochondria and promotes their autophagy

Loss of OPA1 perturbates the mitochondrial inner membrane structure and integrity, leading to cytochrome c release and apoptosis

Isolation of phosphatidylethanolamine as a solitary cofactor for prion formation in the absence of nucleic acids

Disruption of the phosphatidylserine decarboxylase gene in mice causes embryonic lethality and mitochondrial defects

Redistribution of phosphatidylethanolamine at the cleavage furrow of dividing cells during cytokinesis

Fission and selective fusion govern mitochondrial segregation and elimination by autophagy

A RAPID METHOD OF TOTAL LIPID EXTRACTION AND PURIFICATION

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6

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phosphorylation

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