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Kyle L Dunbar

Showing results (1-10 of 21) with videos related to

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Journal of the American Chemical Society|June 1, 2013
Insights into the mechanism of peptide cyclodehydrations achieved through the chemoenzymatic generation of amide derivativesKyle L Dunbar, Douglas A Mitchell
ACS Chemical Biology|January 5, 2013
Revealing nature's synthetic potential through the study of ribosomal natural product biosynthesisKyle L Dunbar, Douglas A Mitchell
Natural Product Reports|September 29, 2021
Ribosome-independent peptide biosynthesis: the challenge of a unifying nomenclatureMaria Dell, Kyle L Dunbar, Christian Hertweck
Angewandte Chemie (International Ed. in English)|May 15, 2024
An Enzymatic Prodrug-like Route to Thio and SelenoamidesKeishi Ishida, Agnieszka Litomska, Kyle L Dunbar, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 9, 2020
Reconstitution of polythioamide antibiotic backbone formation reveals unusual thiotemplated assembly strategyKyle L Dunbar, Maria Dell, Finn Gude, et al.
Nature Chemical Biology|April 24, 2012
YcaO domains use ATP to activate amide backbones during peptide cyclodehydrationsKyle L Dunbar, Joel O Melby, Douglas A Mitchell
Chemical Reviews|April 19, 2017
Enzymatic Carbon-Sulfur Bond Formation in Natural Product BiosynthesisKyle L Dunbar, Daniel H Scharf, Agnieszka Litomska, et al.
Angewandte Chemie (International Ed. in English)|July 6, 2019
Reconstitution of Iterative Thioamidation in Closthioamide Biosynthesis Reveals Tailoring Strategy for Nonribosomal Peptide BackbonesKyle L Dunbar, Maria Dell, Evelyn M Molloy, et al.
Journal of the American Chemical Society|March 10, 2012
Selectivity, directionality, and promiscuity in peptide processing from a Bacillus sp. Al Hakam cyclodehydrataseJoel O Melby, Kyle L Dunbar, Nhat Q Trinh, et al.
Nature Chemical Biology|July 14, 2015
A prevalent peptide-binding domain guides ribosomal natural product biosynthesisBrandon J Burkhart, Graham A Hudson, Kyle L Dunbar, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Journal of the American Chemical Society|June 1, 2013
Insights into the mechanism of peptide cyclodehydrations achieved through the chemoenzymatic generation of amide derivativesKyle L Dunbar, Douglas A Mitchell
ACS Chemical Biology|January 5, 2013
Revealing nature's synthetic potential through the study of ribosomal natural product biosynthesisKyle L Dunbar, Douglas A Mitchell
Natural Product Reports|September 29, 2021
Ribosome-independent peptide biosynthesis: the challenge of a unifying nomenclatureMaria Dell, Kyle L Dunbar, Christian Hertweck
Angewandte Chemie (International Ed. in English)|May 15, 2024
An Enzymatic Prodrug-like Route to Thio and SelenoamidesKeishi Ishida, Agnieszka Litomska, Kyle L Dunbar, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 9, 2020
Reconstitution of polythioamide antibiotic backbone formation reveals unusual thiotemplated assembly strategyKyle L Dunbar, Maria Dell, Finn Gude, et al.
Nature Chemical Biology|April 24, 2012
YcaO domains use ATP to activate amide backbones during peptide cyclodehydrationsKyle L Dunbar, Joel O Melby, Douglas A Mitchell
Chemical Reviews|April 19, 2017
Enzymatic Carbon-Sulfur Bond Formation in Natural Product BiosynthesisKyle L Dunbar, Daniel H Scharf, Agnieszka Litomska, et al.
Angewandte Chemie (International Ed. in English)|July 6, 2019
Reconstitution of Iterative Thioamidation in Closthioamide Biosynthesis Reveals Tailoring Strategy for Nonribosomal Peptide BackbonesKyle L Dunbar, Maria Dell, Evelyn M Molloy, et al.
Journal of the American Chemical Society|March 10, 2012
Selectivity, directionality, and promiscuity in peptide processing from a Bacillus sp. Al Hakam cyclodehydrataseJoel O Melby, Kyle L Dunbar, Nhat Q Trinh, et al.
Nature Chemical Biology|July 14, 2015
A prevalent peptide-binding domain guides ribosomal natural product biosynthesisBrandon J Burkhart, Graham A Hudson, Kyle L Dunbar, et al.
Pageof 3