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Sequence variability (haplotypes) was observed in all species.
The results are found to be consistent with the sequence variability of the tetrapeptide substrate.
The high sequence variability suggests that somatic diversification of these nonself recognition molecules could have occurred.
The sequence variability in the ComX peptide is evident in both B. subtilis and non-B.
A major challenge is the extreme viral sequence variability among strains.
Information of sequence variability in each partition is summarized in Table 1.
It finds regions with unusually high sequence variability.
Due to satellite sequence variability it is probably present in many PRAT monomers.
The inflexion point (Figure 4B), is correlated with the sequence variability within each group.
The C-terminal region, flexible and unstructured, shows sequence variability with a polar tendency.
At 75d, greater sequence variability was observed in the UD-UD condition.
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