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. Author manuscript; available in PMC: 2010 Jan 5.

Published in final edited form as: Microbiology (Reading). 2009 Sep 3;155(Pt 12):4155–4169. doi: 10.1099/mic.0.027995-0

Fig. 5 — Structure of the fH-fHbp complex (Schneider et al., 2009) with temperature colouring using per-site point estimate of ω for (a) subfamily B/variant 1 sequences, (b) subfamily A/variant 2 and (c) subfamily A/variant 3 sequences. Peptides indicated in (a) are putative bactericidal epitopes previously identified (Giuliani et al., 2005; Scarselli et al., 2008; Welsch et al., 2004). In (b) and (c) positively selected sites are indicated. Note: subfamily A/variant 2 and subfamily A/variant 3 differ from subfamily B/variant 1 in length by +4 bp (e.g. Glu¹⁵¹ is equivalent to Glu¹⁴⁷ in variant 1) and +7 bp (e.g. Glu¹⁵⁴ is equivalent to Glu¹⁴⁷ in variant 1) in length respectively.

Fig. 5 — Structure of the fH-fHbp complex (Schneider et al., 2009) with temperature colouring using per-site point estimate of ω for (a) subfamily B/variant 1 sequences, (b) subfamily A/variant 2 and (c) subfamily A/variant 3 sequences. Peptides indicated in (a) are putative bactericidal epitopes previously identified (Giuliani et al., 2005; Scarselli et al., 2008; Welsch et al., 2004). In (b) and (c) positively selected sites are indicated. Note: subfamily A/variant 2 and subfamily A/variant 3 differ from subfamily B/variant 1 in length by +4 bp (e.g. Glu¹⁵¹ is equivalent to Glu¹⁴⁷ in variant 1) and +7 bp (e.g. Glu¹⁵⁴ is equivalent to Glu¹⁴⁷ in variant 1) in length respectively.