2YDH
Crystal structure of the SAM-I riboswitch A94G U34 G18U G19U variant in complex with SAM
Summary for 2YDH
Entry DOI | 10.2210/pdb2ydh/pdb |
Related | 2YGH |
Descriptor | SAM-I RIBOSWITCH, BARIUM ION, S-ADENOSYLMETHIONINE, ... (4 entities in total) |
Functional Keywords | rna, k-turn |
Biological source | THERMOANAEROBACTER TENGCONGENSIS |
Total number of polymer chains | 1 |
Total formula weight | 31575.33 |
Authors | Schroeder, K.T.,Daldrop, P.,Lilley, D.M.J. (deposition date: 2011-03-21, release date: 2011-09-07, Last modification date: 2023-12-20) |
Primary citation | Schroeder, K.T.,Daldrop, P.,Lilley, D.M.J. RNA Tertiary Interactions in a Riboswitch Stabilize the Structure of a Kink Turn. Structure, 19:1233-, 2011 Cited by PubMed Abstract: The kink turn is a widespread RNA motif that introduces an acute kink into the axis of duplex RNA, typically comprising a bulge followed by a G⋅A and A⋅G pairs. The kinked conformation is stabilized by metal ions, or the binding of proteins including L7Ae. We now demonstrate a third mechanism for the stabilization of k-turn structure, involving tertiary interactions within a larger RNA structure. The SAM-I riboswitch contains an essential standard k-turn sequence that kinks a helix so that its terminal loop can make a long-range interaction. We find that some sequence variations in the k-turn within the riboswitch do not prevent SAM binding, despite preventing the folding of the k-turn in isolation. Furthermore, two crystal structures show that the sequence-variant k-turns are conventionally folded within the riboswitch. This study shows that the folded structure of the k-turn can be stabilized by tertiary interactions within a larger RNA structure. PubMed: 21893284DOI: 10.1016/J.STR.2011.07.003 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.9 Å) |
Structure validation
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