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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/15023
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dc.contributor.authorSingh, Shashi Prakash-
dc.date.accessioned2024-07-30T09:58:25Z-
dc.date.available2024-07-30T09:58:25Z-
dc.date.issued2020-12-
dc.identifier.urihttps://www.tandfonline.com/doi/full/10.1080/19420889.2020.1855854-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/15023-
dc.description.abstractThe Scar/WAVE complex catalyzes the protrusion of pseudopods and lamellipods, and is therefore a principal regulator of cell migration. However, it is unclear how its activity is regulated, beyond a dependence on Rac. Phosphorylation of the proline-rich region, by kinases such as Erk2, has been suggested as an upstream activator. We have recently reported that phosphorylation is not required for complex activation. Rather, it occurs after Scar/WAVE has been activated, and acts as a modulator. Neither chemoattractant signaling nor Erk2 affects the amount of phosphorylation, though in Dictyostelium it is promoted by cell-substrate adhesion. We now report that cell-substrate adhesion also promotes Scar/WAVE2 phosphorylation in mammalian cells, suggesting that the process is evolutionarily conserved.en_US
dc.language.isoenen_US
dc.publisherTaylor & Francisen_US
dc.subjectBiologyen_US
dc.subjectScar/WAVEen_US
dc.subjectPhosphorylationen_US
dc.subjectCell migrationen_US
dc.subjectAdhesionen_US
dc.titleAdhesion stimulates Scar/WAVE phosphorylation in mammalian cellsen_US
dc.typeArticleen_US
Appears in Collections:Department of Biological Sciences

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