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The system was simulated in explicit water model at several temperatures by using isobaric-isothermal ensemble to better understand the behaviour of each monomer and its tetramer form.
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The kinetics of each monomer was determined by plotting the conversion of each monomer to polymer over time.
Additional experiments about the phase behaviour of the starting monomer for the synthesis of PBO3O4, reveal that a highly ordered mesophase is also obtained for the monomer, with a diffractogram rather similar to that exhibited by the ordered mesophase of the polymer.
Figure 2b demonstrates the behaviour of the RB monomer absorbance following bacteria addition (5.1 × 107 CFU/mL).
Helices E and F protrude from the core region of each monomer.
The four ACT domains of each monomer interact together and do not make any contact with those of the second monomer.
Although there is no loss or gain in the NCIs, the electron density of each monomer changes because of the interaction between monomers.
Indeed, "dimerization" is accompanied by burial of 9.4% of each monomer's total accessible surface (1332.2Å2).
However, in the case of hTLR10, homodimer formation occurs between LRR11-17 of each monomer.
The coordinated actions of each monomer result in efficient introduction of a topoII-linked DSB.
In the oomycetes, a single exon contains the four motifs characteristic of each monomer.
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