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NCIR: a database of non-canonical interactions in known RNA structures

By Uma Nagaswamy, Maia Larios-Sanz, James Hury, Shakaala Collins, Zhengdong Zhang, Qin Zhao and George E. Fox


The secondary and tertiary structure of an RNA molecule typically includes a number of non-canonical base–base interactions. The known occurrences of these interactions are tabulated in the NCIR database, which can be accessed from The number of examples is now over 1400, which is an increase of >700% since the database was first published. This dramatic increase reflects the addition of data from the recently published crystal structures of the 50S (2.4 Å) and 30S (3.0 Å) ribosomal subunits. In addition, non-canonical interactions observed in published crystal and NMR structures of tRNAs, group I introns, ribozymes, RNA aptamers and synthetic oligonucleotides are included. Properties associated with these interactions, such as sequence context, sugar pucker conformation, glycosidic angle conformation, melting temperature, chemical shift and free energy, are also reported when available. Out of the 29 anticipated pairs with at least two hydrogen bonds, 28 have been observed to date. In addition, several novel examples, not generally predicted, have also been encountered, bringing the total of such pairs to 36. Added to this list are a variety of single, bifurcated, triple and quadruple interactions. The most common non-canonical pairs are the sheared GA, GA imino, AU reverse Hoogsteen, and the GU and AC wobble pairs. The most frequent triple interaction connects N3 of an A with the amino of a G that is also involved in a standard Watson–Crick pair

Topics: Article
Publisher: Oxford University Press
Year: 2002
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Provided by: PubMed Central
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