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In eukaryotic cells, it works as a proton-translocating machinery driven by ATP hydrolysis, and it is responsible for the acidification of lysosome lumens, chromaffin granules and vacuoles.
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Within all of these sites, the molecular clock machinery drives rhythmic transcriptional and metabolic pathways in a tissue-specific manner, a process critical to proper tissue function1,2,3.
How does the ESCRT machinery drive membrane scission, and how does virus budding bypass the need for ESCRT-II in the budding process?
Machinery drives for offshore installations range in size from fractional horsepower cabin ventilation fans to the 15 MW or more machines required for gas injection compressors.
Although the precise mechanism by which the ESCRT machinery drives membrane scission remains to be fully defined, it is clear that ESCRT-III plays a central part in this process.
Furthermore, with the development of the machinery industry driven by FDI, the export of machinery products has also increased since the late 1980s and early 1990s.
Large agricultural machinery is driven fast to cut and pick up grass in this rare dry interlude.
To cope with the detrimental effects of UV exposure, the cellular machinery is driven by mounting a rapid, inducible, and transient response termed the 'UV stress response.' The first genetic response is the DNA damage repair system.
In V4, agricultural machinery is driven with biomethane from catch crops.
Exploitation of the ESCRT machinery is driven by virally encoded proteins that recruit one or more ESCRT subunits to the membrane microdomain where new viruses are being packaged, the goal being to nucleate a protein interaction network that mediates recruitment of ESCRT-III.
Given the biochemical characteristics, the molecular machinery behind intra-chloroplast vesicular transport could be evolutionary related to the machinery that drives vesicle trafficking in the secretory pathway.
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CEO of Professional Science Editing for Scientists @ prosciediting.com