Amino‐acid sequence of the heterogeneous nuclear RNP G protein family and RNA‐binding SELEX consensus sequence obtained for human RBMY. (A) Sequence alignment.

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Amino‐acid sequence of the heterogeneous nuclear RNP G protein family and RNA‐binding SELEX consensus sequence obtained for human RBMY. (A) Sequence alignment of human RBMY (hRBMY) RRM, and related orthologues and paralogues. Amino‐acid sequence of the heterogeneous nuclear RNP G protein family and RNA‐binding SELEX consensus sequence obtained for human RBMY. (A) Sequence alignment of human RBMY (hRBMY) RRM, and related orthologues and paralogues. The RNP2 and RNP1 motifs are indicated by light green and dark green boxes, respectively. Amino acids of hRBMY found in contact with the RNA loop and stem are shown in blue and red, respectively. The arrows show the two non‐conserved mutated amino acids of β2–β3 loop. (B) Consensus sequence obtained after SELEX. All analysed sequences (supplementary Fig S1 online) can fold into a stable stem–loop structure with a highly conserved CWCAA loop. The table shows the statistical predominance for specific base‐pairing in the stem, including non‐canonical base pairs (G‐U or U‐G). The red box shows the core consensus sequence of the stem that we observed in 51% of sequences. RBMY, RNA‐binding motif gene on Y chromosome; SELEX, systematic evolution of ligands by exponential enrichment; Y, C or U; W, U or A; R, G or C. Lenka Skrisovska et al. EMBO Rep. 2007;8:372-379 © as stated in the article, figure or figure legend