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. 2012 Nov;86(21):11441–11456. doi: 10.1128/JVI.00439-12

Table 3.

Sequence and detection of insertions cloned into the WT to validate the profiling

Protein Nucleotide position Strain Amino acid sequencea Profiling detectionb
Input Passage 3
NS1-2 84 WT SSKASV 4358 31032
Mutant SSKVRPHKASV
NS1-2 218c WT LAGLPV
Mutant LAGCGRTGLPV
NS1-2 382 WT SHAEDA 407 23352
Mutant SHAAAAAHADEA
NS4 2600 WT DDGWYH 6348 31617
Mutant DDGCGRNGWYH
VP2 6686 WT MAGALF 9181 17900
Mutant MAGAAAAGALF
VP2 6688d WT MAGALF 618
Mutant MAGAAAAGALF
VP2 6722 WT GLMGII 4736
Mutant GLMCGRMMGII
VP2 7229 WT PRDHTP 308 3399
Mutant PRDCGRSDHTP
VP2 7239 WT TPATQG 283 4262
Mutant TPVRPQPATQG
a

Underlined residues correspond to the inserted residues; residues in italics indicate a change in residue identity due to insertion within a codon.

b

Numbers reflect detection of the insertion to within 1 nt and refer to fluorescence intensity of the corresponding peak.

c

Insertions were not detected in the profiling but were isolated by limiting dilution.

d

Insertion 6688 was not identified in the input profile.