Structural and functional comparison of fumarylacetoacetate domain containing protein 1 in human and mouse.


Journal

Bioscience reports
ISSN: 1573-4935
Titre abrégé: Biosci Rep
Pays: England
ID NLM: 8102797

Informations de publication

Date de publication:
27 03 2020
Historique:
received: 23 12 2019
revised: 14 02 2020
accepted: 17 02 2020
pubmed: 19 2 2020
medline: 26 3 2021
entrez: 19 2 2020
Statut: ppublish

Résumé

FAH domain containing protein 1 (FAHD1) is a mammalian mitochondrial protein, displaying bifunctionality as acylpyruvate hydrolase (ApH) and oxaloacetate decarboxylase (ODx) activity. We report the crystal structure of mouse FAHD1 and structural mapping of the active site of mouse FAHD1. Despite high structural similarity with human FAHD1, a rabbit monoclonal antibody (RabMab) could be produced that is able to recognize mouse FAHD1, but not the human form, whereas a polyclonal antibody recognized both proteins. Epitope mapping in combination with our deposited crystal structures revealed that the epitope overlaps with a reported SIRT3 deacetylation site in mouse FAHD1.

Identifiants

pubmed: 32068790
pii: 222164
doi: 10.1042/BSR20194431
pmc: PMC7056447
pii:
doi:

Substances chimiques

Acetoacetates 0
Mitochondrial Proteins 0
fumarylacetoacetate 28613-33-4
FAHD1 protein, human EC 3.-
Fahd2a protein, mouse EC 3.-
Hydrolases EC 3.-
Carboxy-Lyases EC 4.1.1.-
oxaloacetate decarboxylase EC 4.1.1.112

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Austrian Science Fund FWF
ID : P 28395
Pays : Austria
Organisme : Austrian Science Fund FWF
ID : P 31582
Pays : Austria

Informations de copyright

© 2020 The Author(s).

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Auteurs

Alexander K H Weiss (AKH)

University of Innsbruck, Research Institute for Biomedical Aging Research, Rennweg 10, Innsbruck A-6020, Austria.
University of Innsbruck, Center for Molecular Biosciences Innsbruck (CMBI), Innrain 80-82, Innsbruck A-6020, Austria.

Andreas Naschberger (A)

Medical University of Innsbruck, Division of Genetic Epidemiology, Schöpfstrasse 41, Innsbruck A-6020, Austria.

Elia Cappuccio (E)

University of Innsbruck, Research Institute for Biomedical Aging Research, Rennweg 10, Innsbruck A-6020, Austria.
University of Innsbruck, Center for Molecular Biosciences Innsbruck (CMBI), Innrain 80-82, Innsbruck A-6020, Austria.

Christina Metzger (C)

University of Innsbruck, Research Institute for Biomedical Aging Research, Rennweg 10, Innsbruck A-6020, Austria.
University of Innsbruck, Center for Molecular Biosciences Innsbruck (CMBI), Innrain 80-82, Innsbruck A-6020, Austria.

Lorenza Mottes (L)

University of Innsbruck, Research Institute for Biomedical Aging Research, Rennweg 10, Innsbruck A-6020, Austria.
University of Innsbruck, Center for Molecular Biosciences Innsbruck (CMBI), Innrain 80-82, Innsbruck A-6020, Austria.

Max Holzknecht (M)

University of Innsbruck, Research Institute for Biomedical Aging Research, Rennweg 10, Innsbruck A-6020, Austria.
University of Innsbruck, Center for Molecular Biosciences Innsbruck (CMBI), Innrain 80-82, Innsbruck A-6020, Austria.

Jill von Velsen (J)

European Molecular Biology Laboratory, Grenoble Outstation, 71 Avenue des Martyrs, CS 90181, Grenoble 38042, France.

Matthew W Bowler (MW)

European Molecular Biology Laboratory, Grenoble Outstation, 71 Avenue des Martyrs, CS 90181, Grenoble 38042, France.

Bernhard Rupp (B)

Medical University of Innsbruck, Division of Genetic Epidemiology, Schöpfstrasse 41, Innsbruck A-6020, Austria.

Pidder Jansen-Dürr (P)

University of Innsbruck, Research Institute for Biomedical Aging Research, Rennweg 10, Innsbruck A-6020, Austria.
University of Innsbruck, Center for Molecular Biosciences Innsbruck (CMBI), Innrain 80-82, Innsbruck A-6020, Austria.

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Classifications MeSH