Skip to Content
Merck
CN
  • Identification of FAH domain-containing protein 1 (FAHD1) as oxaloacetate decarboxylase.

Identification of FAH domain-containing protein 1 (FAHD1) as oxaloacetate decarboxylase.

The Journal of biological chemistry (2015-01-13)
Haymo Pircher, Susanne von Grafenstein, Thomas Diener, Christina Metzger, Eva Albertini, Andrea Taferner, Hermann Unterluggauer, Christian Kramer, Klaus R Liedl, Pidder Jansen-Dürr
ABSTRACT

Fumarylacetoacetate hydrolase (FAH) domain-containing proteins occur in both prokaryotes and eukaryotes, where they carry out diverse enzymatic reactions, probably related to structural differences in their respective FAH domains; however, the precise relationship between structure of the FAH domain and the associated enzyme function remains elusive. In mammals, three FAH domain-containing proteins, FAHD1, FAHD2A, and FAHD2B, are known; however, their enzymatic function, if any, remains to be demonstrated. In bacteria, oxaloacetate is subject to enzymatic decarboxylation; however, oxaloacetate decarboxylases (ODx) were so far not identified in eukaryotes. Based on molecular modeling and subsequent biochemical investigations, we identified FAHD1 as a eukaryotic ODx enzyme. The results presented here indicate that dedicated oxaloacetate decarboxylases exist in eukaryotes.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Monoclonal Anti-α-Tubulin antibody produced in mouse, ascites fluid, clone B-5-1-2