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. 2000 Jul;74(13):5796–5801. doi: 10.1128/jvi.74.13.5796-5801.2000

FIG. 2.

FIG. 2

Deduced amino acid sequence comparison of the midregion of the SU gene of the in vivo-derived rFeLV clones with those of parent enFeLVs, various FeLV-B isolates, and F6A. Clones representative of recombination sites E, F/G, and >G (sites marked above the CFE-6 sequence) are shown. Numbers in parentheses indicate the total number of such clones examined. Amino acid sequences are presented relative to that of CFE-6, with dots indicating identity. Four consistent amino acid sequences differences observed in all in vivo-derived rFeLV clones as well as three isolates of FeLV-B, Gardner-Arnstein (GA), Snyder-Theilen (ST), and Rickard (R), are highlighted by boldface type (with the exception of the last position, for which only clones of recombinant site >G are highlighted) under the corresponding amino acid in CFE-6 (underlined). Numbers at both ends of the CFE-6 sequence depict the relative positions of these amino acids from the start point of the mature SU peptide. CFE-16 has a truncated SU peptide sequence because of a natural deletion. The reference F6A sequence is shown at the bottom, with gaps (dashes) introduced to maintain the sequence alignment.