The predicted secondary structures of the human spliceosomal snRNAs. The binding sites for Sm proteins are shaded in gray, and the sequences interacting with the 5′ss or BPS in cyan. Sequences involved in various U2/U6 or U12/U6atac interactions are indicated by green (helix I), purple (helix II), and yellow shading (helix III), similar to . Nucleotide modifications are omitted. (Structures are based on data originally published in Ref for U1, U2, and U5, Ref for U11, Ref for U12, and Ref for U4, U6, U4atac, and U6atac). The locations and identities of the Taybi-Linder syndrome or microcephalic osteodysplastic primordial dwarfism type I (TALS/MOPD1) mutations in the U4atac snRNA are from Ref and are indicated in red.