Ontology highlight
ABSTRACT:
SUBMITTER: Yao NY
PROVIDER: S-EPMC8794833 | biostudies-literature | 2022 Jan
REPOSITORIES: biostudies-literature

Proceedings of the National Academy of Sciences of the United States of America 20220101 4
The adenosine triphosphate (ATP) analog ATPγS often greatly slows or prevents enzymatic ATP hydrolysis. The eukaryotic CMG (Cdc45, Mcm2 to 7, GINS) replicative helicase is presumed unable to hydrolyze ATPγS and thus unable to perform DNA unwinding, as documented for certain other helicases. Consequently, ATPγS is often used to "preload" CMG onto forked DNA substrates without unwinding before adding ATP to initiate helicase activity. We find here that CMG does hydrolyze ATPγS and couples it to DN ...[more]