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Motor protein mitotic kinesin

Certain proteins endow cells with unique capabilities for movement. Cell division, muscle contraction, and cell motility represent some of the ways in which cells execute motion. The contractile and motile proteins underlying these motions share a common property they are filamentous or polymerize to form filaments. Examples include actin and myosin, the filamentous proteins forming the contractile systems of cells, and tubulin, the major component of microtubules (the filaments involved in the mitotic spindle of cell division as well as in flagella and cilia). Another class of proteins involved in movement includes dynein and kinesin, so-called motor proteins that drive the movement of vesicles, granules, and organelles along microtubules serving as established cytoskeletal tracks. ... [Pg.124]

Eg5 (Motor Protein and Mitotic Kinesin) -Accessible Active Site, More Amenable Cryptic Binding Site... [Pg.72]

Figure 1.9 Identification of monastrol (an inhibitor of the normal mitotic spindle formation) and its molecular target (a molecular motor protein, kinesin, Eg5) using chemical genomics. Figure 1.9 Identification of monastrol (an inhibitor of the normal mitotic spindle formation) and its molecular target (a molecular motor protein, kinesin, Eg5) using chemical genomics.
In a pioneering forward chemical genetic screen (whole-cell mitotic arrest assay detected by fluorescence microscopy), a cell-permeable small molecule, monastrol (Figure 1.9), was identified, as it caused inhibition of the normal mitotic spindle formation but did not affect normal tubulin formation. In subsequent studies, testing the inhibition of the formation of the mutant phenotype led to the identification of the primary molecular target in the signaling cascade, a molecular motor protein, kinesin, Eg5. Monastrol treatment showed a phenotype identical to the blocking of Eg5 function by microinjection of Eg5-specific antibodies (Kapoor et al., 2000). [Pg.16]


See other pages where Motor protein mitotic kinesin is mentioned: [Pg.314]    [Pg.314]    [Pg.199]    [Pg.14]    [Pg.73]    [Pg.833]    [Pg.841]    [Pg.338]    [Pg.25]    [Pg.70]    [Pg.16]    [Pg.1503]    [Pg.196]    [Pg.569]   
See also in sourсe #XX -- [ Pg.5 , Pg.314 ]




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