MKKS
Gene Ontology Biological Process
- brain morphogenesis [ISS]
- cerebral cortex development [ISS]
- cilium assembly [ISS]
- cilium morphogenesis [ISS]
- convergent extension involved in gastrulation [ISS]
- detection of mechanical stimulus involved in sensory perception of sound [ISS]
- determination of left/right symmetry [ISS]
- fat cell differentiation [ISS]
- gonad development [TAS]
- heart development [TAS]
- heart looping [ISS]
- hippocampus development [ISS]
- intracellular transport [ISS]
- melanosome transport [ISS]
- negative regulation of appetite by leptin-mediated signaling pathway [ISS]
- photoreceptor cell maintenance [ISS]
- pigment granule aggregation in cell center [ISS]
- regulation of cilium beat frequency involved in ciliary motility [ISS]
- sensory perception of smell [ISS]
- social behavior [ISS]
- spermatid development [ISS]
- striatum development [ISS]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
HSPA4
Gene Ontology Biological Process
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
MKKS is a centrosome-shuttling protein degraded by disease-causing mutations via CHIP-mediated ubiquitination.
McKusick-Kaufman syndrome (MKKS) is a recessively inherited human genetic disease characterized by several developmental anomalies. Mutations in the MKKS gene also cause Bardet-Biedl syndrome (BBS), a genetically heterogeneous disorder with pleiotropic symptoms. However, little is known about how MKKS mutations lead to disease. Here, we show that disease-causing mutants of MKKS are rapidly degraded via the ubiquitin-proteasome pathway in a ... [more]
Throughput
- Low Throughput
Curated By
- BioGRID