Skip Navigation

This Article
Right arrow Print PDF (632K)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Kan, L. S.
Right arrow Articles by Ts'o, P. O.P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kan, L. S.
Right arrow Articles by Ts'o, P. O.P.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, 1977, Vol. 4, No. 5 1633-1648
© 1977


Articles

1H NMR studies of transfer RNA III: the observed and the computed spectra of the hydrogen-bonded NH resonances of baker's yeast transfer-RNAPhe1

Lou S. Kan and Paul O.P. Ts'o

The Division of Biophysics, School of Hygiene and Public Health, The Johns Hopkins University Baltimore, MD 21205, USA

Received February 4, 1977. The hydrogen-bonded NH resonances of Baker's yeast tRNAPhe in H20 solution with Mg++ have been measured by a 360 MHz spectrometer at 23°C. Totally, fifteen peaks and one shoulder can be resolved which represent 25±1 protons. Based on the refined atomic coordinates of the tRNAPhe in the or-thorhombic crystal, on the recent advances in the distance dependence of the ring-current magnetic field effects2 and on the adopted values for the isolated hydrogen-bonded NH resonances, a computed spectrum consisting of 23 protons was constructed. A quantitative comparison by computer was made between the computed spectrum and the spectrum simulated from the observed spectrum. These two spectra are closely similar but not identical. We suggest that the conformation of yeast tRNAPhe in aqueous solution is closely similar but not identical to that found in the crystal, especially in the T{psi}C region and D region. Also the NH resonances in 3–4 proposed hydrogen bonds (most likely for tertiary structure) may exchange very rapidly in aqueous solution.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.