The DOI matches its Crossref record; 20 of the 20 references it cites were found in a registry or an index.
Dual Native Chemical Ligation at Lysine
Abstract
A thiol group introduced on the gamma-carbon of lysine mediates robust native chemical ligation at both the alpha- and epsilon-amines in two consecutive steps. Desulfurization then affords the final product, in which the lysine residue at the ligation site has an isopeptide bond on its side chain. The method is useful for the synthesis of proteins containing special post-translational modifications on lysine.
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Citations
Cites
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Cited by
Native Chemical Ligation and Extended Methods: Mechanisms, Catalysis, Scope, and Limitations
Agouridas, V., El Mahdi, O., Diemer, V., Cargoët, M., Monbaliu, J.-C. M., & Melnyk, O. (2019) · Chemical Reviews · doi:10.1021/acs.chemrev.8b00712 · Cited by 650
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Histones: At the Crossroads of Peptide and Protein Chemistry
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Chemical Synthesis of Circular Proteins
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Metadata
- Authors
- Yang, R., Pasunooti, K. K., Li, F., Liu, X.-W., & Liu, C.-F.
- Venue
- Journal of the American Chemical Society
- Publisher
- American Chemical Society (ACS)
- Published
- 2009-09-03
- Volume
- 131
- Issue
- 38
- Pages
- 13592-13593
- ISSN
- 0002-7863 (ISSN-L)
- 1520-5126
- OpenAlex
- W2030818842
- Cited by
- 260
- References
- 20
- FWCI
- 10.56
- Type
- journal article
- Language
- en
- Open access
- closed
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