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Journal of Korean Medical Science ; : 1-7, 2004.
Article in English | WPRIM | ID: wpr-60901

ABSTRACT

Intracellular organelle transport is essential for morphogenesis and functioning of the cell. Kinesins and kinesin-related proteins make up a large superfamily of molecular motors that transport cargoes such as vesicles, organelles (e.g. mitochondria, peroxisomes, lysosomes), protein complexes (e.g. elements of the cytoskeleton, virus particles), and mRNAs in a microtubule- and ATP-dependent manner in neuronal and non-neuronal cells. Until now, more than 45 kinesin superfamily proteins (KIFs) have been identified in the mouse and human genomes. Elucidating the transport pathways mediated by kinesins, the identities of the cargoes moved, and the nature of the proteins that link kinesin motors to cargoes are areas of intense investigation. This review focuses on the structure, the binding partners of kinesins and kinesin-based human diseases.


Subject(s)
Animals , Humans , Mice , Adenosine Triphosphate/metabolism , Alzheimer Disease/metabolism , Biological Transport , Cytoplasm/metabolism , Diabetes Mellitus/metabolism , Kinesins/chemistry , Microtubule-Associated Proteins/chemistry , Microtubules/metabolism , Models, Biological , Neurons/metabolism , Protein Binding
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