Ontology highlight
ABSTRACT:
SUBMITTER: Branis J
PROVIDER: S-EPMC5390273 | biostudies-literature | 2017 Apr
REPOSITORIES: biostudies-literature
Braniš Jaroslav J Pataki Csilla C Spörrer Marina M Gerum Richard C RC Mainka Astrid A Cermak Vladimir V Goldmann Wolfgang H WH Fabry Ben B Brabek Jan J Rosel Daniel D
Scientific reports 20170413
CAS is a docking protein, which was shown to act as a mechanosensor in focal adhesions. The unique assembly of structural domains in CAS is important for its function as a mechanosensor. The tension within focal adhesions is transmitted to a stretchable substrate domain of CAS by focal adhesion-targeting of SH3 and CCH domain of CAS, which anchor the CAS protein in focal adhesions. Mechanistic models of the stretching biosensor propose equal roles for both anchoring domains. Using deletion mutan ...[more]