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These two sequences differ by rearrangement around two pairs of large repeats (6.5 and 4.3 kb), an inversion at a 205-bp repeat, a novel junction, and an insertion in Col-0 of 1.8 kb of fragmented genes (Forner et al. 2005; Davila et al. 2011).
The rate constant calculated by accounting for the electrostatic repulsion only is in excellent agreement with this value, thus the inner and outer sphere rearrangement around the ions is likely less significant in the activation process of this reaction.
We have further suggested that these additional capsomers bind at a lower affinity than the nucleation center, allowing their rearrangement around the minichromosome, as required for capsid geometry.
By following the dynamic evolution of lipid rearrangement around the macroion, we can identify two timescales corresponding to two processes.
One exception to this was the large rearrangement around the terminus that is present in the N. lactamica isolate and one gonococcal isolate (FA1090).
If, as indicated by the above results, the CED-1 pathway regulates CHC-1 localization during engulfment through EPN-1, inactivating CED-1, CED-6 or DYN-1 should impair actin rearrangement around cell corpses.
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Independently, Das et al. ([2010]) also identified rearrangements around the regions of atp6 and orfB.
Several other authors suggested similar taxonomic rearrangements around the same time.
Functionality of this TAS was maintained even in cases where severe rearrangements around the relBE2Spn region were found.
Physical mapping and pastime sequencing unra-veled a set of genome rearrangements around psbA gene in "higher" fern lineages [ 8- 10].
It is also possible, however, that rearrangements around the internal metal site could create interfaces for oligomerization.
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