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2YDH

Crystal structure of the SAM-I riboswitch A94G U34 G18U G19U variant in complex with SAM

Summary for 2YDH
Entry DOI10.2210/pdb2ydh/pdb
Related2YGH
DescriptorSAM-I RIBOSWITCH, BARIUM ION, S-ADENOSYLMETHIONINE, ... (4 entities in total)
Functional Keywordsrna, k-turn
Biological sourceTHERMOANAEROBACTER TENGCONGENSIS
Total number of polymer chains1
Total formula weight31575.33
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 citationSchroeder, 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: 21893284
DOI: 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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