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Status: Bibliographieeintrag

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Verfasst von:Bezerra, Gustavo A. [VerfasserIn]   i
 Foster, William R. [VerfasserIn]   i
 Bailey, Henry J. [VerfasserIn]   i
 Hicks, Kevin G. [VerfasserIn]   i
 Sauer, Sven [VerfasserIn]   i
 Dimitrov, Bianca [VerfasserIn]   i
 McCorvie, Thomas J. [VerfasserIn]   i
 Okun, Jürgen G. [VerfasserIn]   i
 Rutter, Jared [VerfasserIn]   i
 Kölker, Stefan [VerfasserIn]   i
 Yue, Wyatt W. [VerfasserIn]   i
Titel:Crystal structure and interaction studies of human DHTKD1 provide insight into a mitochondrial megacomplex in lysine catabolism
Verf.angabe:Gustavo A. Bezerra, William R. Foster, Henry J. Bailey, Kevin G. Hicks, Sven W. Sauer, Bianca Dimitrov, Thomas J. McCorvie, Jürgen G. Okun, Jared Rutter, Stefan Kölker and Wyatt W. Yue
E-Jahr:2020
Jahr:10 June 2020
Umfang:14 S.
Fussnoten:Gesehen am 11.08.2020
Titel Quelle:Enthalten in: IUCrJ
Ort Quelle:Chester, 2014
Jahr Quelle:2020
Band/Heft Quelle:7(2020), Seite 693-706
ISSN Quelle:2052-2525
Abstract:DHTKD1 is a lesser-studied E1 enzyme among the family of 2-oxoacid dehydrogenases. In complex with E2 (dihydrolipoamide succinyltransferase, DLST) and E3 (dihydrolipoamide dehydrogenase, DLD) components, DHTKD1 is involved in lysine and tryptophan catabolism by catalysing the oxidative decarboxylation of 2-oxoadipate (2OA) in mitochondria. Here, the 1.9 angstrom resolution crystal structure of human DHTKD1 is solved in complex with the thiamine diphosphate co-factor. The structure reveals how the DHTKD1 active site is modelled upon the well characterized homologue 2-oxoglutarate (2OG) dehydrogenase but engineered specifically to accommodate its preference for the longer substrate of 2OA over 2OG. A 4.7 angstrom resolution reconstruction of the human DLST catalytic core is also generated by single-particle electron microscopy, revealing a 24-mer cubic scaffold for assembling DHTKD1 and DLD protomers into a megacomplex. It is further demonstrated that missense DHTKD1 variants causing the inborn error of 2-aminoadipic and 2-oxoadipic aciduria impact on the complex formation, either directly by disrupting the interaction with DLST, or indirectly through destabilizing the DHTKD1 protein. This study provides the starting framework for developing DHTKD1 modulators to probe the intricate mitochondrial energy metabolism.
DOI:doi:10.1107/S205225252000696X
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: https://doi.org/10.1107/S205225252000696X
 DOI: https://doi.org/10.1107/S205225252000696X
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:2-oxoacid dehydrogenase
 2-oxoadipate
 2-oxoglutarate dehydrogenase
 acid
 alpha-ketoacid dehydrogenase
 complex
 cryo-EM
 cubic-core
 enzyme mechanisms
 generation
 human DHTKD1
 ketoglutarate dehydrogenase
 lysine catabolism
 multi-protein complexes
 subunit
 superoxide/hydrogen peroxide
 thiamine diphosphate
K10plus-PPN:1726772144
Verknüpfungen:→ Zeitschrift

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