FBXW7: a substrate recognition component of a SCF (SKP1-CUL1-F-box protein) E3 ubiquitin-protein ligase complex which mediates the ubiquitination and subsequent proteasomal degradation of target proteins including MYC, cyclin E, NOTCH1-released notch intracellular domain (NICD), JUN, and probably PSEN1. Recognizes and binds to phosphorylated target proteins. Other components of the SCF(FBXW7) complex are sCUL1, RBX1, and SKP1A. Defects in FBXW7 may be a cause of breast cancer. The homolog of Cdc4, one of the yeast genes that regulate sister chromatid cohesion. Down-regulation or disruption of FBXW7 resulted in abnormal sister chromatid cohesion in human cells. Four alternatively spliced isoforms have been described.
Protein type: Nucleolus; Motility/polarity/chemotaxis; Ubiquitin conjugating system
Chromosomal Location of Human Ortholog: 4q31.3
Cellular Component: nucleoplasm; Golgi apparatus; protein complex; endoplasmic reticulum; cytoplasm; nucleolus; SCF ubiquitin ligase complex
Molecular Function: protein binding, bridging; identical protein binding; protein binding; cyclin binding; ubiquitin protein ligase binding; transcription factor activity
Biological Process: SCF-dependent proteasomal ubiquitin-dependent protein catabolic process; Notch signaling pathway; viral reproduction; protein stabilization; sister chromatid cohesion; protein ubiquitination; lipid homeostasis; negative regulation of DNA endoreduplication; regulation of protein localization; regulation of transcription, DNA-dependent; vasculature development; positive regulation of epidermal growth factor receptor activity; positive regulation of protein ubiquitination; positive regulation of ubiquitin-protein ligase activity; negative regulation of Notch signaling pathway; vasculogenesis; response to DNA damage stimulus; lung development
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