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Protein Name: Cullin-7

UniprotKB/SwissProt ID: CUL7_HUMAN (Q14999)

Gene Name: CUL7

Synonyms: KIAA0076

Organism: Homo sapiens (Human).

Function: Component of a probable SCF-like E3 ubiquitin-protein ligase complex, which mediates the ubiquitination and subsequent proteasomal degradation of target proteins. Probably plays a role in the degradation of proteins involved in endothelial proliferation and/or differentiation (By similarity). Seems not to promote polyubiquitination and proteasomal degradation of TP53. In vitro, complexes of CUL7 with either CUL9 or FBXW8 or TP53 contain E3 ubiquitin-protein ligase activity. In complex with FBXW8, mediates ubiquitination and consequent degradation of GORASP1, acting as a component of the ubiquitin ligase pathway that regulates Golgi morphogenesis and dendrite patterning in brain.

Other Modifications: View all modification sites in dbPTM

Protein Subcellular Localization: Cytoplasm. Cytoplasm, perinuclear region. Golgi apparatus. Note=Colocalizes with FBXW8 at the Golgi apparatus in neurons; localization to Golgi is mediated by OBSL1.

PDB :
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Graphical Visualization of Ubiquitination Sites:
Overview of Protein Ubiquitination Sites with Functional and Structural Information
InterPro ID Domain
IPR001373
IPR004939
IPR008979


The ubiquitination sites of CUL7_HUMAN

No. Position Ubiquitinated Peptide Secondary Structure Solvent Accessibility Substrate Motifs PubMed ID
1255VLFSLV K RYLHVT HHHHHH H HHHHHH 40.39%21890473
2610AAKVEA K EPPSQS HHHCCC C CCCCCC 58.19%21906983
31153WRAVVE K QVNNFL HHHHHH H HHHHHH 48.19%21906983
41312QSLSTS K ELQRQF HHCCCC H HHHHHH 63.63%21906983
51431YSNFYN K SQSHPA HHHHHC C CCCCCC 38.19%21890473

The interacting network mediated by proteins: CUL7_HUMAN


Disease:
Disease database Database Entry Disease information
HPRD099013@m syndrome
Metabolic pathway:
Kegg map ID Pathway
map03008Ribosome biogenesis in eukaryotes