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The Kin I kinesins are microtubule-destabilizing enzymes important for neuronal transport, spindle assembly, and chromosome segregation. Hunter et al. (2003) now show that the Kin I MCAK is a microtubule end-stimulated ATPase that can catalytically depolymerize MT's.

1999年1月8日 · Using in vitro assays with purified proteins, we show that XKCM1 and XKIF2, two distinct members of the internal catalytic domain (Kin I) kinesin subfamily, catalytically destabilize microtubules using a novel mechanism.

Kin I kinesins are members of the diverse kinesin superfamily of molecular motors. Whereas most kinesins use ATP to move along microtubules, Kin I kinesins depolymerize microtubules rather than walk along them. Functionally, this distinct subfamily of kinesins is …

Kin I kinesins are MT-destabilizing enzymes. The three more divergent members of the Kin I subfamily are DSK1, a diatom kinesin implicated in spindle elongation (Wein et al., 1996), and two kinesins identified by geno-mics, C. elegans 11d9 and Leishmania MCAK.

1999年1月8日 · Using in vitro assays with purified proteins, we show that XKCM1 and XKIF2, two distinct members of the internal catalytic domain (Kin I) kinesin subfamily, catalytically destabilize microtubules using a novel mechanism. Both XKCM1 and XKIF2 influence microtubule stability by targeting directly to m …

The Kin I kinesins are microtubule-destabilizing enzymes important for neuronal transport, spindle assembly, and chromosome segregation. now show that the Kin I MCAK is a microtubule end-stimulated ATPase that can catalytically depolymerize MT's.

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