Charakterisierung der Substratspezifität von Protein-Methyltransferasen
| dc.contributor.author | Schnee, Philipp | |
| dc.contributor.author | Weirich, Sara | |
| dc.contributor.author | Jeltsch, Albert | |
| dc.date.accessioned | 2024-11-20T11:48:20Z | |
| dc.date.available | 2024-11-20T11:48:20Z | |
| dc.date.issued | 2023 | de |
| dc.date.updated | 2024-11-02T08:44:22Z | |
| dc.description.abstract | The regulation of cellular activities is a key hallmark in the development of complex life forms. Among other factors, it is facilitated by protein lysine methyltransferases (PKMTs), which modify proteins in a highly specific manner and regulate their biological activities. Here, we describe methods to decipher the PKMT-substrate specificity by biochemical experiments and molecular dynamics simulations. This led to the discovery of novel PKMT substrates and rational design of even better non-natural substrates, which represent a promising starting point for the design of novel PKMT inhibitors. | en |
| dc.identifier.issn | 1868-6249 | |
| dc.identifier.issn | 0947-0867 | |
| dc.identifier.other | 1913062937 | |
| dc.identifier.uri | http://nbn-resolving.de/urn:nbn:de:bsz:93-opus-ds-152976 | de |
| dc.identifier.uri | http://elib.uni-stuttgart.de/handle/11682/15297 | |
| dc.identifier.uri | http://dx.doi.org/10.18419/opus-15278 | |
| dc.language.iso | de | de |
| dc.relation.uri | doi:10.1007/s12268-023-1930-y | de |
| dc.rights | info:eu-repo/semantics/openAccess | de |
| dc.rights.uri | https://creativecommons.org/licenses/by/4.0/deed.en | de |
| dc.subject.ddc | 540 | de |
| dc.title | Charakterisierung der Substratspezifität von Protein-Methyltransferasen | en |
| dc.type | article | de |
| ubs.fakultaet | Chemie | de |
| ubs.institut | Institut für Biochemie und Technische Biochemie | de |
| ubs.publikation.seiten | 249-251 | de |
| ubs.publikation.source | BIOspektrum 29 (2023), S. 249-251 | de |
| ubs.publikation.typ | Zeitschriftenartikel | de |