CDC23

CDC23
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
Aliases CDC23, ANAPC8, APC8, CUT23, cell division cycle 23
External IDs MGI: 1098815 HomoloGene: 3426 GeneCards: CDC23
RNA expression pattern
More reference expression data
Orthologs
Species Human Mouse
Entrez

8697

52563

Ensembl

ENSG00000094880

ENSMUSG00000024370

UniProt

Q9UJX2

Q8BGZ4

RefSeq (mRNA)

NM_004661

NM_178347

RefSeq (protein)

NP_004652.2

NP_848124.1

Location (UCSC) Chr 5: 138.19 – 138.21 Mb Chr 18: 34.63 – 34.65 Mb
PubMed search [1] [2]
Wikidata
View/Edit HumanView/Edit Mouse

Cell division cycle 23 homolog (S. cerevisiae), also known as CDC23, is a protein that, in humans, is encoded by the CDC23 gene.[3]

Function

The CDC23 protein shares strong similarity with Saccharomyces cerevisiae Cdc23, a protein essential for cell cycle progression through the G2/M transition. This protein is a component of anaphase-promoting complex (APC), which is composed of eight protein subunits and highly conserved in eukaryotic cells. APC catalyzes the formation of cyclin B-ubiquitin conjugate that is responsible for the ubiquitin-mediated proteolysis of B-type cyclins. This protein and 3 other members of the APC complex contain the TPR (tetratricopeptide repeat), a protein domain important for protein-protein interaction.[3]

Interactions

CDC23 has been shown to interact with CDC27.[4][5]

References

  1. "Human PubMed Reference:".
  2. "Mouse PubMed Reference:".
  3. 1 2 "Entrez Gene: CDC23 cell division cycle 23 homolog (S. cerevisiae)".
  4. Vodermaier HC, Gieffers C, Maurer-Stroh S, Eisenhaber F, Peters JM (Sep 2003). "TPR subunits of the anaphase-promoting complex mediate binding to the activator protein CDH1". Current Biology. 13 (17): 1459–68. doi:10.1016/S0960-9822(03)00581-5. PMID 12956947.
  5. Gmachl M, Gieffers C, Podtelejnikov AV, Mann M, Peters JM (Aug 2000). "The RING-H2 finger protein APC11 and the E2 enzyme UBC4 are sufficient to ubiquitinate substrates of the anaphase-promoting complex". Proceedings of the National Academy of Sciences of the United States of America. 97 (16): 8973–8. doi:10.1073/pnas.97.16.8973. PMC 16806Freely accessible. PMID 10922056.

Further reading


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