CUL5

Protein-coding gene in humans From Wikipedia, the free encyclopedia

Cullin-5 is a protein that in humans is encoded by the CUL5 gene.[5][6][7]

PDBOrtholog search: PDBe RCSB
AliasesCUL5, VACM-1, VACM1, cullin 5, CUL-5
Quick facts Available structures, PDB ...
CUL5
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesCUL5, VACM-1, VACM1, cullin 5, CUL-5
External IDsOMIM: 601741; MGI: 1922967; HomoloGene: 2597; GeneCards: CUL5; OMA:CUL5 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_003478

NM_001161618
NM_027807

RefSeq (protein)

NP_003469

NP_001155090
NP_082083

Location (UCSC)Chr 11: 108.01 – 108.11 MbChr 9: 53.53 – 53.58 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse
Close

Discovery

The mammalian gene product was originally discovered by expression cloning, due to the protein's ability to mobilize intracellular calcium in response to the peptide hormone arginine vasopressin. It was first titled VACM-1, for vasopressin-activated, calcium-mobilizing receptor.[8] Since then, VACM-1 has been shown to be homologous to the Cullin family of proteins, and was subsequently dubbed cul5.

Tissue distribution

Studies have shown that the cul5 protein is expressed at its highest levels in heart and skeletal tissue, and is specifically expressed in vascular endothelium and renal collecting tubules.[9]

Function

Cul5 inhibits cellular proliferation, potentially through its involvement in the SOCS/ BC-box/ eloBC/ cul5/ RING E3 ligase complex, which functions as part of the ubiquitin system for protein degradation.[10]

One study have shown that Cul5 plays a role in Reelin signaling cascade, participating in the DAB1 degradation and thus ensuring the negative feedback mechanism of Reelin signaling during corticogenesis.[11]

Interactions

CUL5 has been shown to interact with RBX1.[12][13]

References

Further reading

Related Articles

Wikiwand AI