Amino acid polymorphism among the 29 translated PGIC1 amino acid sequences from F. ovina.

NOTES.—The exon number is shown in the first row of the table header. The vertically arranged numbers in the second row of the table header indicate the location of each polymorphic amino acid site. The first row beneath the table header is the consensus sequence, where each amino acid represents the most frequent residue in the alignment at each position. Each of the subsequent rows represents a single predicted amino acid sequence; for each sequence (apart from the consensus sequence), Hap = haplotype, pI = isoelectric point (predicted from the translated haplotype sequence using Protein calculator v3.3 http://www.scripps.edu/~cdputnam/protcalc.html), Ind = the F. ovina individual from which the sequence was derived, Ind EM = the PGIC enzyme electromorph phenotype (coded for by the PgiC1 and PgiC2 loci) of the individual. Apart from the consensus sequence, all the sequences are listed in ascending order of predicted pI values. Dashes (-) within a sequence indicate that the amino acid residue at a polymorphic site is the same as in the consensus sequence. The negatively charged residues at the selected polymorphic amino acid sites 173 and 200 are shown in bold italics. In the column Ind EM, bold italics indicate: EM 1 in the sequences with negatively charged residues at both sites 173 and 200; EM 2 in sequences with negatively charged residue at either sites 173 or 200, but not at both sites.Amino acid polymorphism among the 29 translated PGIC1 amino acid sequences from F. ovina.