Unknown

Dataset Information

0

The dynamic organization of fungal acetyl-CoA carboxylase.


ABSTRACT: Acetyl-CoA carboxylases (ACCs) catalyse the committed step in fatty-acid biosynthesis: the ATP-dependent carboxylation of acetyl-CoA to malonyl-CoA. They are important regulatory hubs for metabolic control and relevant drug targets for the treatment of the metabolic syndrome and cancer. Eukaryotic ACCs are single-chain multienzymes characterized by a large, non-catalytic central domain (CD), whose role in ACC regulation remains poorly characterized. Here we report the crystal structure of the yeast ACC CD, revealing a unique four-domain organization. A regulatory loop, which is phosphorylated at the key functional phosphorylation site of fungal ACC, wedges into a crevice between two domains of CD. Combining the yeast CD structure with intermediate and low-resolution data of larger fragments up to intact ACCs provides a comprehensive characterization of the dynamic fungal ACC architecture. In contrast to related carboxylases, large-scale conformational changes are required for substrate turnover, and are mediated by the CD under phosphorylation control.

SUBMITTER: Hunkeler M 

PROVIDER: S-EPMC4833862 | biostudies-literature | 2016

REPOSITORIES: biostudies-literature

altmetric image

Publications

The dynamic organization of fungal acetyl-CoA carboxylase.

Hunkeler Moritz M   Stuttfeld Edward E   Hagmann Anna A   Imseng Stefan S   Maier Timm T  

Nature communications 20160413


Acetyl-CoA carboxylases (ACCs) catalyse the committed step in fatty-acid biosynthesis: the ATP-dependent carboxylation of acetyl-CoA to malonyl-CoA. They are important regulatory hubs for metabolic control and relevant drug targets for the treatment of the metabolic syndrome and cancer. Eukaryotic ACCs are single-chain multienzymes characterized by a large, non-catalytic central domain (CD), whose role in ACC regulation remains poorly characterized. Here we report the crystal structure of the ye  ...[more]

Similar Datasets

| S-EPMC10777831 | biostudies-literature
| S-EPMC3264756 | biostudies-literature
| S-EPMC10594767 | biostudies-literature
| S-EPMC7259786 | biostudies-literature
| S-EPMC2077261 | biostudies-literature
| S-EPMC6690696 | biostudies-literature
| S-EPMC2529255 | biostudies-literature
| S-EPMC8758669 | biostudies-literature
| S-EPMC3218310 | biostudies-literature
| S-EPMC52793 | biostudies-other