Skip to main content
. 2007 Mar 30;7:49. doi: 10.1186/1471-2148-7-49

Table 1.

Paralog sequence similarity of fugu protocadherin subclusters

5' low homology region 3' high homology region


Paralog subclustersa Pcdh protein sequenceb Amino acid identityc (%) Nucleotide identityd (%) Pcdh protein sequenceb Amino acid identityc (%) Nucleotide identityd (%)
FrPcdh2α2–7 1–331 80.0 ± 13.4 79.0 ± 13.9 332–777 99.3 ± 0.3 99.3 ± 0.2
FrPcdh2α8–25 1–507 67.6 ± 10.8 69.9 ± 9.9 508–759 99.4 ± 0.3 99.1 ± 0.2
FrPcdh2α26–36 1–487 57.5 ± 6.6 60.7 ± 5.1 488–770 99.4 ± 0.3 99.4 ± 0.3
FrPcdh2γ1–17 1–356 70.0 ± 10.8 72.7 ± 10.0 357–764 99.6 ± 0.3 99.3 ± 0.3
FrPcdh2γ19–32' 1–507 66.4 ± 9.0 68.2 ± 8.5 508–781 99.3 ± 0.3 99.3 ± 0.2
FrPcdh2γ33'-36' 1–449 66.5 ± 9.5 68.7 ± 7.3 450–792 99.3 ± 0.6 99.6 ± 0.3

a The fugu Pcdh sequences used for this analysis do not include the coding sequences for the signal peptide.

b The numbers refer to the consensus of the amino acid sequence alignment without the signal peptide sequence

c The amino acid sequence identity is calculated by average of the pair-wise comparison of paralog members in the same subcluster and expressed as mean ± standard deviation.

d Nucleotide sequences were aligned according to the amino acid alignment and the percentage identity is calculated by average of the pair-wise comparison and expressed as mean ± standard deviation.