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Cited by 306

The DOI matches its Crossref record; 33 of the 33 references it cites were found in a registry or an index.

Kinetic Intermediates in RNA Folding

Zarrinkar, Patrick P., Williamson, James R.·1994·Science

Abstract

The folding pathways of large, highly structured RNA molecules are largely unexplored. Insight into both the kinetics of folding and the presence of intermediates was provided in a study of the Mg 2+ -induced folding of the Tetrahymena ribozyme by hybridization of complementary oligodeoxynucleotide probes. This RNA folds via a complex mechanism involving both Mg 2+ -dependent and Mg 2+ -independent steps. A hierarchical model for the folding pathway is proposed in which formation of one helical domain (P4-P6) precedes that of a second helical domain (P3-P7). The overall rate-limiting step is formation of P3-P7, and takes place with an observed rate constant of 0.72 ± 0.14 minute -1 . The folding mechanism of large RNAs appears similar to that of many multidomain proteins in that formation of independently stable substructures precedes their association into the final conformation.

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Metadata

Authors
Zarrinkar, P. P., & Williamson, J. R.
Venue
Science
Published
1994-08-12
Volume
265
Issue
5174
Pages
918-924
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W1969476076
Cited by
306
References
33
FWCI
6.50
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Kinetic Intermediates in RNA Folding. https://app.cochat.ai/papers/10.1126/science.8052848
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Zarrinkar, P. P., & Williamson, J. R. (1994). Kinetic Intermediates in RNA Folding. Science. https://doi.org/10.1126/science.8052848

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.