Ontology highlight
ABSTRACT:
SUBMITTER: Tsai YC
PROVIDER: S-EPMC4660213 | biostudies-literature | 2015 Nov
REPOSITORIES: biostudies-literature
Tsai Yi-Chin Candace YC Lapina Maria Claribel MC Bhushan Shashi S Mueller-Cajar Oliver O
Nature communications 20151116
Ribulose-1,5-bisphosphate carboxylase/oxygenase (rubisco) is responsible for almost all biological CO2 assimilation, but forms inhibited complexes with its substrate ribulose-1,5-bisphosphate (RuBP) and other sugar phosphates. The distantly related AAA+ proteins rubisco activase and CbbX remodel inhibited rubisco complexes to effect inhibitor release in plants and α-proteobacteria, respectively. Here we characterize a third class of rubisco activase in the chemolithoautotroph Acidithiobacillus f ...[more]