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αSNAP binds to these complexes and recruits N-ethylmaleimide-sensitive factor (NSF), an ATPase that catalyzes the disruption of the complexes rendering active monomeric SNARE proteins.
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Once bound to these complexes it exerts tolloid-independent anti-chordin activity, weakening chordin-BMP affinity promoting release of BMPs [ 28].
Moreover, it was shown that carotenoids bound to Lhca polypeptides are very efficient in quenching Chl triplets, suggesting that the pigments bound to these complexes are well protected from radiation damages [ 32, 33].
Furthermore, we observed that the nonhydrolyzable ATP analog adenylylimidodiphosphate (AMP-PNP) did not promote Smc3 acetylation above "background" levels, although it efficiently inhibited ATP hydrolysis by WT cohesin, suggesting that AMP-PNP bound to these cohesin complexes.
Finally, a streptavidin-horseradish peroxidase conjugate binds to this complex.
When oxygen binds to this complex, it becomes 6-coordinate.
The p52 Bcl3 complex binds to these two classes of κB sites in distinct modes, permitting the recruitment of coactivator, corepressor, or both coactivator and corepressor complexes in promoters that contain G/C-, A/T-, or both G/C- and A/T-centric sites.
(4) In vitro experiments reveal that the p52 Bcl3 complex binds to these κB sites in distinct modes, presumably because of the distinct structural states imposed by the sequence difference.
In particular, electron paramagnetic resonance (EPR) characterization of Co II)rrinoids bound to these enzymes complexed with ATP revealed unusually large g shifts and A Co) hyperfine coupling constants, consistent with the Co II) ion residing in an effectively square planar, four-coordinate (4c) ligand environment.
To acquire haem, the parasites have a protein called HpHbR that binds to these haptoglobin-haemoglobin 'complexes'complexes
As each of these subunits is bound to the complex by two strong interactions, subunit turnover may be impossible.
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