Erratum
for Helm, Nucl. Acids Res. 34 (2) 721-733.
Nucleic Acids Research Advance Access originally published online on October 11, 2007
Nucleic Acids Research 2007 35(20):7041; doi:10.1093/nar/gkm819
Nucleic Acids Research, 2007, Vol. 35, No. 20 7041
© 2007 The Author(s)
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Post-transcriptional nucleotide modification and alternative folding of RNA
Mark Helm
Nucleic Acids Res., (2006) 34, 721–733
The author wishes it to be known that there was a print error in Figure 4 of the above mentioned article. A corrected figure is shown below with its legend.

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Figure 4. Rearrangement on the secondary structure level induced by double methylation of human cytosolic tRNAAsn. The calculated structure of the unmodified transcript on the left side features an aberrant D-stem without G10, but including G26. Double methylation on N6 of G26 impedes its Watson–Crick pairing with Cytidines and thus renders the base pair G26-C11, which is highlighted by a box, impossible. The fully modified tRNAAsn may thus adopt the classical cloverleaf structure as shown on the right. U? denoted an unknown modified uridine, likely a derivative of ribothymidine, at position 54.
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