- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
1 Online-Ressource.
- Language
-
Englisch
- Bibliographic citation
-
Decrypting the programming of β-methylation in virginiamycin M biosynthesis ; volume:14 ; number:1 ; day:10 ; month:3 ; year:2023 ; pages:1-18 ; date:12.2023
Nature Communications ; 14, Heft 1 (10.3.2023), 1-18, 12.2023
- Creator
-
Collin, Sabrina
Cox, Russell
Paris, Cédric
Jacob, Christophe
Chagot, Benjamin
Weissman, Kira J.
Gruez, Arnaud
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1038/s41467-023-36974-3
- URN
-
urn:nbn:de:101:1-2503051020082.002715465613
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:20 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Collin, Sabrina
- Cox, Russell
- Paris, Cédric
- Jacob, Christophe
- Chagot, Benjamin
- Weissman, Kira J.
- Gruez, Arnaud
- SpringerLink (Online service)
Other Objects (12)
Oxidative rearrangements during fungal biosynthesis
Investigating and engineering fungal tropolone meroterpenoid biosynthesis
Reductive Release from a Hybrid PKS‐NRPS during the Biosynthesis of Pyrichalasin H
Curiouser and curiouser: progress in understanding the programming of iterative highly-reducing polyketide synthases
Decrypting the programming of β-methylation in virginiamycin M biosynthesis
The molecular steps of citrinin biosynthesis in fungi
Oxidative steps during the biosynthesis of squalestatin S1
Diels–Alder Reactions During the Biosynthesis of Sorbicillinoids
Diels–Alder Reactions During the Biosynthesis of Sorbicillinoids
Reengineering the programming of a functional domain of an iterative highly reducing polyketide synthase
Biosynthesis of 6‐Hydroxymellein Requires a Collaborating Polyketide Synthase‐like Enzyme
Biosynthesis of 6‐Hydroxymellein Requires a Collaborating Polyketide Synthase‐like Enzyme
Oxidative rearrangements during fungal biosynthesis
Investigating and engineering fungal tropolone meroterpenoid biosynthesis
Reductive Release from a Hybrid PKS‐NRPS during the Biosynthesis of Pyrichalasin H
Curiouser and curiouser: progress in understanding the programming of iterative highly-reducing polyketide synthases
Decrypting the programming of β-methylation in virginiamycin M biosynthesis
The molecular steps of citrinin biosynthesis in fungi
Oxidative steps during the biosynthesis of squalestatin S1
Diels–Alder Reactions During the Biosynthesis of Sorbicillinoids
Diels–Alder Reactions During the Biosynthesis of Sorbicillinoids
Reengineering the programming of a functional domain of an iterative highly reducing polyketide synthase
Biosynthesis of 6‐Hydroxymellein Requires a Collaborating Polyketide Synthase‐like Enzyme
Biosynthesis of 6‐Hydroxymellein Requires a Collaborating Polyketide Synthase‐like Enzyme
Oxidative rearrangements during fungal biosynthesis
Investigating and engineering fungal tropolone meroterpenoid biosynthesis
Reductive Release from a Hybrid PKS‐NRPS during the Biosynthesis of Pyrichalasin H
Curiouser and curiouser: progress in understanding the programming of iterative highly-reducing polyketide synthases
Decrypting the programming of β-methylation in virginiamycin M biosynthesis
The molecular steps of citrinin biosynthesis in fungi
Oxidative steps during the biosynthesis of squalestatin S1
Diels–Alder Reactions During the Biosynthesis of Sorbicillinoids
Diels–Alder Reactions During the Biosynthesis of Sorbicillinoids
Reengineering the programming of a functional domain of an iterative highly reducing polyketide synthase
Biosynthesis of 6‐Hydroxymellein Requires a Collaborating Polyketide Synthase‐like Enzyme