Searching across hundreds of databases

Our searching services are busy right now. Your search will reload in five seconds.

X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

Methods to study kinase regulation of the replication fork helicase.

Methods (San Diego, Calif.) | 2010

Dbf4-Cdc7 phosphorylation of the Mcm2-7 complex is required for the activation of the replication fork helicase in budding yeast cells. There is a genetic interaction between Dbf4-Cdc7 and Mcm2, and Dbf4-Cdc7 phosphorylates Mcm2 in vitro and in vivo. We initiated a focused study of how Dbf4-Cdc7 phosphorylates Mcm2 in budding yeast, and we also investigated the in vivo implications of this kinase reaction. Described herein are detailed methods for how we conducted biochemical and genetic experiments to dissect the mechanism and function of Dbf4-Cdc7 phosphorylation of Mcm2 in budding yeast cells. The methods are likely applicable to other kinase reactions and studies of replication fork helicases from other organisms.

Pubmed ID: 20170732 RIS Download

Research resources used in this publication

None found

Additional research tools detected in this publication

Antibodies used in this publication

None found

Associated grants

None

Publication data is provided by the National Library of Medicine ® and PubMed ®. Data is retrieved from PubMed ® on a weekly schedule. For terms and conditions see the National Library of Medicine Terms and Conditions.

This is a list of tools and resources that we have found mentioned in this publication.


ClustalW (tool)

RRID:SCR_017277

Web sevice of ClustalW provided by DNA data bank of Japan.

View all literature mentions