The DOI matches its Crossref record; 39 of the 39 references it cites were found in a registry or an index.
Translation initiation in Escherichia coli: sequences within the ribosome‐binding site
Abstract
Summary: The translational roles of the Shine‐Dalgarno sequence, the initiation codon, the space between them, and the second codon have been studied. The Shine Dalgarno sequence UAAGGAGG initiated translation roughly four times more efficiently than did the shorter AAGGA sequence. Each Shine‐Dalgarno sequence required a minimum distance to the initiation codon in order to drive translation; spacing, however, could be rather long. Initiation at AUG was more efficient than at GUG or UUG at each spacing examined; initiation at GUG was only slightly better than UUG. Translation was also affected by residues 3′ to the initiation codon. The second codon can influence the rate of initiation, with the magnitude depending on the initiation codon. The data are consistent with a simple kinetic model in which a variety of rate constants contribute to the process of translation initiation.
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Continuous evolution of base editors with expanded target compatibility and improved activity
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Production of Biopharmaceuticals in E. coli: Current Scenario and Future Perspectives
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Metadata
- Authors
- Ringquist, S., Shinedling, S., Barrick, D., Green, L., Binkley, J., Stormo, G. D., & Gold, L.
- Venue
- Molecular Microbiology
- Publisher
- Wiley
- Published
- 1992-05
- Volume
- 6
- Issue
- 9
- Pages
- 1219-1229
- ISSN
- 0950-382X (ISSN-L)
- 1365-2958
- OpenAlex
- W2094333855
- Cited by
- 351
- References
- 39
- FWCI
- 5.09
- Type
- journal article
- Language
- en
- Open access
- closed
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- Ringquist, S., Shinedling, S., Barrick, D., Green, L., Binkley, J., Stormo, G. D., & Gold, L. (1992). Translation initiation in Escherichia coli: sequences within the ribosome‐binding site. Molecular Microbiology. https://doi.org/10.1111/j.1365-2958.1992.tb01561.x
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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