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As with AgamOBP1 crystal structure, we observed a continuous electron density in the course of this tunnel during the refinement procedure of AaegOBP1.
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Since in both cases during the refinement procedures, practically the same residuals were obtained, a preference should be given to the more symmetric orthorhombic structure.
The general procedures include isotropic refinement from one parent cell into eight child cells and then followed by anisotropic refinement which effectively removes hanging nodes.
Figure 8 gives another perspective on the refinement procedure results.
Table 6 presents statistics of the refinement procedure.
As in RefineFast, the refinement procedure does not alter the gene contents of the leaves.
After the refinement procedure, the performance improved much as shown in Table 1.
This leads to inconsistencies in the comparisons that underlie the refinement procedure.
Figure 5 gives another point of view for the refinement procedure results.
The refinement procedure produced only two new anchors with multigenes in all strains.
Now, we estimate time complexity of one iteration in the refinement procedure.
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