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- W2028642981 abstract "Type I myosins are highly conserved actin-based molecular motors that localize to the actin-rich cortex and participate in motility functions such as endocytosis, polarized morphogenesis, and cell migration. The COOH-terminal tail of yeast myosin-I proteins, Myo3p and Myo5p, contains an Src homology domain 3 (SH3) followed by an acidic domain. The myosin-I SH3 domain interacted with both Bee1p and Vrp1p, yeast homologues of human WASP and WIP, adapter proteins that link actin assembly and signaling molecules. The myosin-I acidic domain interacted with Arp2/3 complex subunits, Arc40p and Arc19p, and showed both sequence similarity and genetic redundancy with the COOH-terminal acidic domain of Bee1p (Las17p), which controls Arp2/3-mediated actin nucleation. These findings suggest that myosin-I proteins may participate in a diverse set of motility functions through a role in actin assembly." @default.
- W2028642981 created "2016-06-24" @default.
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- W2028642981 date "2000-01-24" @default.
- W2028642981 modified "2023-10-03" @default.
- W2028642981 title "A Role for Myosin-I in Actin Assembly through Interactions with Vrp1p, Bee1p, and the Arp2/3 Complex" @default.
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- W2028642981 doi "https://doi.org/10.1083/jcb.148.2.353" @default.
- W2028642981 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/2174279" @default.
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