TUBG1
Gene Ontology Biological Process
Gene Ontology Molecular Function
Gene Ontology Cellular Component
NDE1
Gene Ontology Biological Process
- G2/M transition of mitotic cell cycle [TAS]
- cell migration [IBA]
- centrosome duplication [ISS]
- centrosome localization [IBA]
- cerebral cortex development [IMP]
- chromosome segregation [IBA]
- establishment of chromosome localization [IMP]
- establishment of mitotic spindle orientation [IMP]
- microtubule nucleation [IBA]
- mitotic cell cycle [TAS]
- mitotic centrosome separation [IBA]
- vesicle transport along microtubule [IBA]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
Affinity Capture-Western
An interaction is inferred when a bait protein is affinity captured from cell extracts by either polyclonal antibody or epitope tag and the associated interaction partner identified by Western blot with a specific polyclonal antibody or second epitope tag. This category is also used if an interacting protein is visualized directly by dye stain or radioactivity. Note that this differs from any co-purification experiment involving affinity capture in that the co-purification experiment involves at least one extra purification step to get rid of potential contaminating proteins.
Publication
LIS1 regulates CNS lamination by interacting with mNudE, a central component of the centrosome.
LIS1, a microtubule-associated protein, is required for neuronal migration, but the precise mechanism of LIS1 function is unknown. We identified a LIS1 interacting protein encoded by a mouse homolog of NUDE, a nuclear distribution gene in A. nidulans and a multicopy suppressor of the LIS1 homolog, NUDF. mNudE is located in the centrosome or microtubule organizing center (MTOC), and interacts ... [more]
Throughput
- Low Throughput
Curated By
- BioGRID