Development of catalytic covalent biomimetic acyltransferases

Author(s)Turniansky, Baruch
Date Accessioned2023-08-21T23:21:30Z
Date Available2023-08-21T23:21:30Z
Publication Date2023
SWORD Update2023-06-26T19:10:31Z
AbstractThioesters are ubiquitous in many biochemical pathways throughout the cell, often being used as precursors for amide bond formation. Thioesters are more reactive and less stable than their (oxygen) ester counterparts but are still stable enough to hydrolysis to be used for reactions in aqueous systems. For example, the coenzyme acetyl coenzyme A (AcCoA) holds acetate equivalents as thioesters, then transfers them as part of multiple catabolic systems. Thioester acyl transfer is also key in protein ubiquination, polyketide synthesis, glutathione biosynthesis, and intein splicing, among many other pathways. In this work, we looked at intercepting these reactive thioester intermediates, utilizing both inteins and small molecule catalysts to modify proteins.
AdvisorKoh, John T.
DegreePh.D.
DepartmentUniversity of Delaware, Department of Chemistry and Biochemistry
DOIhttps://doi.org/10.58088/3erj-em41
Unique Identifier1398311557
URLhttps://udspace.udel.edu/handle/19716/33245
Languageen
PublisherUniversity of Delaware
URIhttps://login.udel.idm.oclc.org/login?url=https://www.proquest.com/dissertations-theses/development-catalytic-covalent-biomimetic/docview/2832938350/se-2?accountid=10457
KeywordsAcetylation
KeywordsCatalytic
KeywordsThioesters
KeywordsCatabolic systems
KeywordsGlutathione biosynthesis
TitleDevelopment of catalytic covalent biomimetic acyltransferases
TypeThesis
Files
Original bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
Turniansky_udel_0060D_15443.pdf
Size:
3.12 MB
Format:
Adobe Portable Document Format
License bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
2.22 KB
Format:
Item-specific license agreed upon to submission
Description: