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. 2003 Apr;77(8):4818–4826. doi: 10.1128/JVI.77.8.4818-4826.2003

TABLE 2.

Other papillomavirus L2 expression constructs used in this study

Virus L2 amino acids incor- porated NCBI reference no.a Primer sequence (5′ to 3′)b
Forward Reverse
HPV6b 314-459 NC_001355 AATTCCGGATCCGGGGCCCGCATTCATTATTTTTA AATTCCGCGGCCGCCTAGGCCGCCACATCTG
HPV16 321-473 NC_001526 AATTCCGGATCCGGTGCTAAGGTACATTATTATTA AATTCCGCGGCCGCCTAGGCAGCCAAAGAGAC
HPV33 319-467 NC_001528 AATTCCGGATCCGGAGCTAGAATACATTATTATC AATTCCGCGGCCGCCTAGGCCGCCACACGGAC
HPV1a 347-507 NC_001356 AATTCCGGATCCGGGCCACAAAGCCATTTTTAC AATTCCGCGGCCGCTTAAAAAAAAAAATGTTTGCG
HPV5 376-518c NC_001531 AATCCGGATCCGGGTCGCAAGTCCATTTTTAC AATTCCGCGGCCGCTCACAAATATTTTCTT
HPV12 360-518 NC_001577 AATTCCGGATCCGGATCACAGGTTCATTTTTATAG AATTCCGCGGCCGCTCACAAATATTTTCTT
COPV1 360-513 NC_001619 AATTCCGGATCCGGGCCACAAAGCCATTTTTAC AATTCCGCGGCCGCTTAAAAAAAAAAATGTTTGCG
BPV1 316-469 NC_001522 AATTCCGGATCCGGACCACAGCTACATGTCAGG CTCGAGTTAGGCATGTTTCCGTTTTTTTCGTTTC
a

Sequences are the same as those given in the NCBI reference with the exception of the HPV5 isolate. The relevant amino acid changes within the putative L1 binding domain of HPV5 are indicated on Fig. 5.

b

Restriction sites within the primer are underlined.

c

Although primers were designed such that HPV5 amino acids 360 to 518 would be incorporated, only amino acids 376 to 518 are present due to the presence of a cryptic BamHI site at position 5472 in the HPV5 isolate used for PCR amplification.