The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
Geometric nomenclature and classification of RNA base pairs
Open accessAbstract
Non-Watson-Crick base pairs mediate specific interactions responsible for RNA-RNA self-assembly and RNA-protein recognition. An unambiguous and descriptive nomenclature with well-defined and nonoverlapping parameters is needed to communicate concisely structural information about RNA base pairs. The definitions should reflect underlying molecular structures and interactions and, thus, facilitate automated annotation, classification, and comparison of new RNA structures. We propose a classification based on the observation that the planar edge-to-edge, hydrogen-bonding interactions between RNA bases involve one of three distinct edges: the Watson-Crick edge, the Hoogsteen edge, and the Sugar edge (which includes the 2'-OH and which has also been referred to as the Shallow-groove edge). Bases can interact in either of two orientations with respect to the glycosidic bonds, cis or trans relative to the hydrogen bonds. This gives rise to 12 basic geometric types with at least two H bonds connecting the bases. For each geometric type, the relative orientations of the strands can be easily deduced. High-resolution examples of 11 of the 12 geometries are presently available. Bifurcated pairs, in which a single exocyclic carbonyl or amino group of one base directly contacts the edge of a second base, and water-inserted pairs, in which single functional groups on each base interact directly, are intermediate between two of the standard geometries. The nomenclature facilitates the recognition of isosteric relationships among base pairs within each geometry, and thus facilitates the recognition of recurrent three-dimensional motifs from comparison of homologous sequences. Graphical conventions are proposed for displaying non-Watson-Crick interactions on a secondary structure diagram. The utility of the classification in homology modeling of RNA tertiary motifs is illustrated.
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Citations
Cites
Structure of the 30S ribosomal subunit
Wimberly, B. T., Brodersen, D. E., Clemons, W. M., Morgan-Warren, R. J., Carter, A. P., Vonrhein, C., Hartsch, T., & Ramakrishnan, V. (2000) · Nature · doi:10.1038/35030006 · Cited by 2,035
Structure of Functionally Activated Small Ribosomal Subunit at 3.3 Å Resolution
Schluenzen, F., Tocilj, A., Zarivach, R., Harms, J., Gluehmann, M., Janell, D., Bashan, A., Bartels, H., Agmon, I., Franceschi, F., et al. (2000) · Cell · doi:10.1016/s0092-8674(00)00084-2 · Cited by 979
Cited by
The non-Watson-Crick base pairs and their associated isostericity matrices
Leontis, N. B. (2002) · Nucleic Acids Research · doi:10.1093/nar/gkf481 · Cited by 796
Self-citationRohloff, J. C., Gelinas, A. D., Jarvis, T. C., Ochsner, U. A., Schneider, D. J., Gold, L., & Janjic, N. (2014) · Molecular Therapy - Nucleic Acids · doi:10.1038/mtna.2014.49 · Cited by 533
Automated de novo prediction of native-like RNA tertiary structures
Das, R., & Baker, D. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0703836104 · Cited by 438
Sequence elements outside the hammerhead ribozyme catalytic core enable intracellular activity
Khvorova, A., Lescoute, A., Westhof, E., & Jayasena, S. D. (2003) · Nature Structural & Molecular Biology · doi:10.1038/nsb959 · Cited by 438
Self-citationAdvancement of the emerging field of RNA nanotechnology
Jasinski, D., Haque, F., Binzel, D. W., & Guo, P. (2017) · ACS Nano · doi:10.1021/acsnano.6b05737 · Cited by 352
Metadata
- Authors
- LEONTIS, N. B., & WESTHOF, E.
- Venue
- RNA
- Publisher
- Cold Spring Harbor Laboratory
- Published
- 2001-04
- Volume
- 7
- Issue
- 4
- Pages
- 499-512
- ISSN
- 1355-8382 (ISSN-L)
- OpenAlex
- W2106478835
- Cited by
- 1,073
- References
- 2
- FWCI
- 5.43
- Type
- journal article
- Language
- en
- Open access
- bronze
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