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Endosomal sorting complexes required for transport by
Codex 0 Created 2026-10-20 Updated 2026-11-05
The LacY transporter importing lactose in Escherichia coli. Binding of dephosphorylated EIIA glucose can inhibit transport and reduce inducer accumulation.
A bacterial sugar-uptake system coupling transport to phosphorylation using a phosphoenolpyruvate-derived phosphoryl relay. Its phosphorylation state also contributes to carbon-source regulation.
A substance facilitating proton transfer across a membrane and dissipating the proton electrochemical gradient. It can uncouple respiration from ATP synthesis without directly inhibiting every electron-transfer reaction.
An ATP-regulated anion channel whose phosphorylation-dependent activity contributes to epithelial chloride transport. Its activation downstream of cyclic AMP is important in cholera-associated secretion.
Movement of proteins and lipids between cellular compartments by vesicles, tubules, membrane fusion and selective retrieval.
hydrophobic mismatch is an energetic incompatibility between a membrane protein's hydrophobic span and the hydrophobic thickness of its surrounding lipid bilayer. Local deformation, altered conformation or changed association can partly accommodate it.
In kidney podocytes, it is a component of the specialized filtration-slit architecture. Its intracellular signalling interactions can recruit Nck and actin-regulatory partners, connecting a membrane contact to cytoskeletal organization. [ref]
Molecular Biology of the Cell, 4th edition by Bruce Alberts and others. Chapters 3, 6 and 15, protein function, translation and cell signalling
An iron-export protein. IRE-containing transcripts can be regulated at biological translation, while protein-level and systemic regulation provide additional controls.
A SNARE protein contributes a helical segment to a membrane-fusion assembly. Complementary SNARE proteins on opposing membranes form a SNARE complex whose assembly helps pull the membranes together. Syntaxins, SNAP-25 and synaptobrevin illustrate different components of the neuronal machinery. Purified components reconstituted into separate liposomes can promote fusion, showing that these proteins participate directly in membrane rearrangement. Cellular control additionally involves targeting and regulatory factors. [ref]
SNAREpins: minimal machinery for membrane fusion by T. Weber and others. Weber and others, 1998, abstract: recombinant v- and t-SNARE reconstitution
Membrane fusion intermediate in which contacting membrane leaflets have merged while the aqueous compartments remain separate. A lipid mixing assay therefore need not establish full membrane fusion.
A readout of lipid redistribution between membrane biological populations, for example through fluorescence dequenching. It must be distinguished from aqueous content mixing and leakage.
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