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. Author manuscript; available in PMC: 2010 May 1.
Published in final edited form as: Mol Immunol. 2009 Mar 14;46(8-9):1647–1653. doi: 10.1016/j.molimm.2009.02.021

Table 3.

Amino acid alignments of fHbp in the antigenic variant 1, 2 and 3 groupsa

Antigenic Variant Group Amino Acid Range Amino Acid Sequenceb
1 22–51 APLDHKDKGL QSLTLDQSVR KNEKLKLAAQ
2 22–51 APLDHKDKGK QSLTLDQSVR KNEKLKLAAQ
3 27–56 APLDHKDKGL KSLTLEDSIP QNGTLTLSAQ
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1 52–79 GAEKTYGNGD ---SLNTGKL KNDKVSRFDF
2 52–79 GAEKTYGNGD ---SLNTGKL KNDKVSRFDF
3 57–87 GAEKTFKAGD KDNSLNTGKL KNDKISRFDF
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a

Alignment of a region of the N-domains of fHbps in the antigenic variant 1, 2 and 3 groups (strains MC58, 8047 and M1239, respectively).

b

The positions that differed among JAR 4-postive fHbp variant 1 or 2 wildtype proteins and JAR-4 negative variant 3 wildtype proteins are indicated with an asterisk below the sequences. The consensus tripeptide sequence DHK was identified by phage display (Table 2). The DHK residues and the KDN and YGN tripeptides affecting JAR-4 binding were identified by site-specific mutagenesis (Figures 2, 3 and 4, respectively). The respective tripeptides are shown in bold.