CDC5L

Cell division cycle 5-like

PDB rendering based on 2dim.
Available structures
PDB Ortholog search: PDBe, RCSB
Identifiers
Symbols CDC5L ; CDC5; CDC5-LIKE; CEF1; PCDC5RP; dJ319D22.1
External IDs OMIM: 602868 MGI: 1918952 HomoloGene: 13291 GeneCards: CDC5L Gene
RNA expression pattern
More reference expression data
Orthologs
Species Human Mouse
Entrez 988 71702
Ensembl ENSG00000096401 ENSMUSG00000023932
UniProt Q99459 Q6A068
RefSeq (mRNA) NM_001253 NM_152810
RefSeq (protein) NP_001244 NP_690023
Location (UCSC) Chr 6:
44.39 – 44.45 Mb
Chr 17:
45.39 – 45.43 Mb
PubMed search

Cell division cycle 5-like protein is a protein that in humans is encoded by the CDC5L gene.[1][2][3]

Function

The protein encoded by this gene shares a significant similarity with Schizosaccharomyces pombe cdc5 gene product, which is a cell cycle regulator important for G2/M transition. This protein has been demonstrated to act as a positive regulator of cell cycle G2/M progression. It was also found to be an essential component of a non-snRNA spliceosome, which contains at least five additional protein factors and is required for the second catalytic step of pre-mRNA splicing.[3]

Interactions

CDC5L has been shown to interact with:

References

  1. Groenen PM, Vanderlinden G, Devriendt K, Fryns JP, Van de Ven WJ (Apr 1998). "Rearrangement of the human CDC5L gene by a t(6;19)(p21;q13.1) in a patient with multicystic renal dysplasia". Genomics 49 (2): 218–29. doi:10.1006/geno.1998.5254. PMID 9598309.
  2. Bernstein HS, Coughlin SR (Feb 1997). "Pombe Cdc5-related protein. A putative human transcription factor implicated in mitogen-activated signaling". The Journal of Biological Chemistry 272 (9): 5833–7. doi:10.1074/jbc.272.9.5833. PMID 9038199.
  3. 1 2 "Entrez Gene: CDC5L CDC5 cell division cycle 5-like (S. pombe)".
  4. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 Ajuh P, Kuster B, Panov K, Zomerdijk JC, Mann M, Lamond AI (Dec 2000). "Functional analysis of the human CDC5L complex and identification of its components by mass spectrometry". The EMBO Journal 19 (23): 6569–81. doi:10.1093/emboj/19.23.6569. PMC 305846. PMID 11101529.
  5. Ewing RM, Chu P, Elisma F, Li H, Taylor P, Climie S, McBroom-Cerajewski L, Robinson MD, O'Connor L, Li M, Taylor R, Dharsee M, Ho Y, Heilbut A, Moore L, Zhang S, Ornatsky O, Bukhman YV, Ethier M, Sheng Y, Vasilescu J, Abu-Farha M, Lambert JP, Duewel HS, Stewart II, Kuehl B, Hogue K, Colwill K, Gladwish K, Muskat B, Kinach R, Adams SL, Moran MF, Morin GB, Topaloglou T, Figeys D (2007). "Large-scale mapping of human protein-protein interactions by mass spectrometry". Molecular Systems Biology 3: 89. doi:10.1038/msb4100134. PMC 1847948. PMID 17353931.
  6. Ajuh P, Lamond AI (Nov 2003). "Identification of peptide inhibitors of pre-mRNA splicing derived from the essential interaction domains of CDC5L and PLRG1". Nucleic Acids Research 31 (21): 6104–16. doi:10.1093/nar/gkg817. PMC 275459. PMID 14576297.
  7. Ajuh P, Sleeman J, Chusainow J, Lamond AI (Nov 2001). "A direct interaction between the carboxyl-terminal region of CDC5L and the WD40 domain of PLRG1 is essential for pre-mRNA splicing". The Journal of Biological Chemistry 276 (45): 42370–81. doi:10.1074/jbc.M105453200. PMID 11544257.
  8. Leonard D, Ajuh P, Lamond AI, Legerski RJ (Sep 2003). "hLodestar/HuF2 interacts with CDC5L and is involved in pre-mRNA splicing". Biochemical and Biophysical Research Communications 308 (4): 793–801. doi:10.1016/s0006-291x(03)01486-4. PMID 12927788.

Further reading

This article is issued from Wikipedia - version of the Wednesday, February 10, 2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.