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An interesting observation that comes from the analysis of these data is that some protease sequences are localized preferentially in specific areas of the conformational landscape of this protein.
These highly repeated sequences are localized in specific segments of the heterochromatin, which may contain different sets of satellite DNA [ 8- 11].
A recent survey of all the missense mutations and neutral polymorphisms reported in the InSIGHT mutation database for the hMLH1 and hMSH2 genes [ 15] indicates that missense mutations, but not neutral polymorphisms, tend to occur where ESE sequences are localized [ 16].
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These sequences were localized either in promoter regions or in open reading frame sequences.
Four simple repeat sequences were localized in this interval.
A total of 102 putative coding sequences were localized on the genomic sequences.
Mainly non-conserved DNA sequences were localized downstream of the gal-lac operon and the truncated galT.
To estimate distribution biases of promoter hexamer sequences, all hexamer sequences were localized in 10 000 independent promoters (from −1 to −1000) in Arabidopsis, rice, and soybean.
After that, the FLcDNA sequences were localized to the maize genome using GMAP [ 15] and correlated with maize genome transcripts using BLAST search [ 16].
Within the broad GO category 'cellular components', over a third of the sequences were localized to the plastid, 23.4% to the mitochondrion and 17% to the nucleus.
Over two-thirds of the consensus sequences were localized by cellular component to either cell or organelle, as shown in Figure 3(c).
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