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The resulting proximity of G-proteins could produce FRET between subunits of different G-proteins as well as between subunits within the same G-protein and changes in FRET may be due to conformational changes within an individual G-protein, between different G-proteins or a combination of both.
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It is clear that none of our experiments have actually determined that the interactions between the Ccr4-Not complex and either the exosome or TRAMP are directly mediated by interactions between subunits of these different complexes.
All these enzymes share a common structural feature; they are composed of three subunits of different size whereby each subunit holds a different cofactor.
The system is a powerful tool in studies of different aspects of interactions between subunits of the homodimeric proteins since it makes possible separate genetic manipulations on each subunit of the dimer.
This observation cannot be explained on the basis of thermodynamic stability, because interactions between mtDNA-encoded subunits contribute more weakly to the complex stability than those interactions between subunits encoded by different genomes.
This differential behavior cannot be explained on the basis of predicted thermodynamic stability, as interactions between mtDNA-encoded subunits contribute more weakly to the complex stability than those interactions between subunits encoded by different genomes.
Evolution has clearly shaped multiple contact possibilities between subunits involved in different processes.
Thus, some linking cross interactions implying interactions between the subunits of the two different liquids must be possible either between the side chains or between the polar groups, which then allow interconnection of both liquids with a fluctuating network, that is, either dispersive forces or hydrogen bonding.
The interaction between different subunits of TRPP2 helps maintaining the channel stability and this cooperativity between neighboring chains are contributed by the interaction between their PMD and the pore turret of adjacent chain.
Thus, there was a clear distinction in responses even between different subunits of PP6.
A series of C C biflavones was designed to investigate the relationship between structural array of different flavone flavone subunit linkage and the inhibitory activity against phospholipase A2 (PLA2).
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