Skip to main content
. 2010 Oct 27;107(46):19748–19753. doi: 10.1073/pnas.1009999107

Fig. 4.

Fig. 4.

Molecular models for expansion segments ES3S/ES6S, ES7L, and ES27L. (A) Isolated density for ES6Sd (blue) and ES3Sa,c (gold) on the 40S subunit (Left) and transparent with a molecular model (Center). rRNA secondary structure prediction highlighting interaction between the loop of ES6Sd and the bulge in ES3Sc (Right), as proposed by ref. 59. (B) Isolated density for ES7L from T. aestivum (T. a., blue) and S. cerevisiae (S. c., gold) on the 80S ribosome (Left) and transparent with a molecular model (Center). Ribosomal proteins L28e (red) stabilizes ES7La in the T. aestivum 80S ribosome, whereas the extension of r-protein L6e appears to pass through the three-way junction formed by helices ES7Lc–e (Right). Molecular models for the Inline graphic (gold) and Inline graphic (blue) positions (Left), as observed in S. cerevisiae 80S ribosomes (Thumbnail Insets) (39) and an intermediate position (Inline graphic, gray) observed in the T. aestivum 80S ribosome. In yeast, r-protein L34e (green) and L38e (red) interact with the Inline graphic and Inline graphic positions, respectively. The tunnel exit (TE) and L1 stalk (L1) are indicated for reference. (C) Schematic (Top Right) and molecular model (Middle Right) indicating that the interchange between the Inline graphic (gold) and Inline graphic (blue) positions involves a rotation of ∼110° of ES27La–c relative to H63. Secondary structure for the junctions of S. cerevisiae ES27La–c and H63.