SEC63

From Wikipedia, the free encyclopedia

SEC63 homolog (S. cerevisiae)

Identifiers

SEC63; ERdj2; PRO2507; SEC63L

External IDs

OMIM: 608648 MGI: 2155302 HomoloGene: 5220

Gene ontology
Molecular Function:	• receptor activity • heat shock protein binding • unfolded protein binding
Cellular Component:	• endoplasmic reticulum • microsome • membrane • integral to membrane
Biological Process:	• protein folding • protein targeting to membrane • protein transport

RNA expression pattern

More reference expression data

Orthologs

Human

Mouse

Refseq

NM_007214 (mRNA)
NP_009145 (protein)

NM_153055 (mRNA)
NP_694695 (protein)

Location

Chr 6: 108.3 - 108.39 Mb

Chr 10: 42.45 - 42.52 Mb

Pubmed search

[1]

[2]

SEC63 homolog (S. cerevisiae), also known as SEC63, is a human gene.^[1]

The Sec61 complex is the central component of the protein translocation apparatus of the endoplasmic reticulum (ER) membrane. The protein encoded by this gene and SEC62 protein are found to be associated with ribosome-free SEC61 complex. It is speculated that Sec61-Sec62-Sec63 may perform post-translational protein translocation into the ER. The Sec61-Sec62-Sec63 complex might also perform the backward transport of ER proteins that are subject to the ubiquitin-proteasome-dependent degradation pathway. The encoded protein is an integral membrane protein located in the rough ER.^[1]

[edit] References

^ ^a ^b Entrez Gene: SEC63 SEC63 homolog (S. cerevisiae).

[edit] Further reading

Woollatt E, Pine KA, Shine J, et al. (1999). "Human Sec63 endoplasmic reticulum membrane protein, map position 6q21.". Chromosome Res. 7 (1): 77. PMID 10219736.
Skowronek MH, Rotter M, Haas IG (1999). "Molecular characterization of a novel mammalian DnaJ-like Sec63p homolog.". Biol. Chem. 380 (9): 1133-8. PMID 10543453.
Meyer HA, Grau H, Kraft R, et al. (2000). "Mammalian Sec61 is associated with Sec62 and Sec63.". J. Biol. Chem. 275 (19): 14550-7. PMID 10799540.
Ponting CP (2001). "Proteins of the endoplasmic-reticulum-associated degradation pathway: domain detection and function prediction.". Biochem. J. 351 Pt 2: 527-35. PMID 11023840.
Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899-903. doi:10.1073/pnas.242603899. PMID 12477932.
Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs.". Nat. Genet. 36 (1): 40-5. doi:10.1038/ng1285. PMID 14702039.
Davila S, Furu L, Gharavi AG, et al. (2004). "Mutations in SEC63 cause autosomal dominant polycystic liver disease.". Nat. Genet. 36 (6): 575-7. doi:10.1038/ng1357. PMID 15133510.
Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).". Genome Res. 14 (10B): 2121-7. doi:10.1101/gr.2596504. PMID 15489334.
Otsuki T, Ota T, Nishikawa T, et al. (2007). "Signal sequence and keyword trap in silico for selection of full-length human cDNAs encoding secretion or membrane proteins from oligo-capped cDNA libraries.". DNA Res. 12 (2): 117-26. doi:10.1093/dnares/12.2.117. PMID 16303743.
Ewing RM, Chu P, Elisma F, et al. (2007). "Large-scale mapping of human protein-protein interactions by mass spectrometry.". Mol. Syst. Biol. 3: 89. doi:10.1038/msb4100134. PMID 17353931.
You KT, Li LS, Kim NG, et al. (2007). "Selective translational repression of truncated proteins from frameshift mutation-derived mRNAs in tumors.". PLoS Biol. 5 (5): e109. doi:10.1371/journal.pbio.0050109. PMID 17456004.