
pmid: 23154893
AbstractSegregation of chromosomes during mitosis requires the interaction of dynamic microtubules with the kinetochore, a large protein structure established on the centromere region of sister chromatids. The core microtubule‐binding activity of the kinetochore resides in the KMN network, an outer kinetochore complex. As part of the KMN network, the Ndc80 complex, which is composed of Ndc80, Nuf2, Spc24, and Spc25, is able to bind directly to microtubules and has the ability to track with depolymerizing microtubules to produce chromosome movement. The Ndc80 complex binds directly to microtubules through a calponin homology domain and an unstructured tail in the N terminus of the Ndc80 protein. A recent flurry of papers has highlighted the importance of an internal loop region in Ndc80 in establishing end‐on attachment to microtubules. Here I discuss these recent findings that suggest that the Ndc80 internal loop functions as a binding site for proteins required for kinetochore‐microtubule interactions.
Binding Sites, Saccharomyces cerevisiae Proteins, Protein Conformation, Molecular Sequence Data, Nuclear Proteins, Cell Cycle Proteins, Microtubules, DNA-Binding Proteins, Cytoskeletal Proteins, Chromosome Segregation, Vertebrates, Animals, Humans, Amino Acid Sequence, Schizosaccharomyces pombe Proteins, Kinetochores, Microtubule-Associated Proteins
Binding Sites, Saccharomyces cerevisiae Proteins, Protein Conformation, Molecular Sequence Data, Nuclear Proteins, Cell Cycle Proteins, Microtubules, DNA-Binding Proteins, Cytoskeletal Proteins, Chromosome Segregation, Vertebrates, Animals, Humans, Amino Acid Sequence, Schizosaccharomyces pombe Proteins, Kinetochores, Microtubule-Associated Proteins
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