Biology:CD8A

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Short description: Protein-coding gene in the species Homo sapiens


A representation of the 3D structure of the protein myoglobin showing turquoise α-helices.
Generic protein structure example

CD8a (Cluster of Differentiation 8a), is a human gene.[1]

Function

The CD8 antigen is a cell surface glycoprotein found on most cytotoxic T lymphocytes that mediates efficient cell-cell interactions within the immune system. The CD8 antigen, acting as a coreceptor, and the T-cell receptor on the T lymphocyte recognize antigen displayed by an antigen-presenting cell (APC) in the context of class I MHC molecules. The functional coreceptor is either a homodimer composed of two alpha chains, or a heterodimer composed of one alpha and one beta chain. Both alpha and beta chains share significant homology to immunoglobulin variable light chains. This gene encodes the CD8 alpha chain isoforms. Two alternative transcripts encoding distinct isoforms, one membrane associated and one secreted, have been identified.[1]

Interactions

CD8A has been shown to interact with:

See also

References

  1. 1.0 1.1 "Entrez Gene: CD8A CD8a molecule". https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=925. 
  2. "CD3 delta establishes a functional link between the T cell receptor and CD8". J. Biol. Chem. 278 (5): 3257–64. January 2003. doi:10.1074/jbc.M208119200. PMID 12215456. 
  3. 3.0 3.1 "Classical and nonclassical class I major histocompatibility complex molecules exhibit subtle conformational differences that affect binding to CD8alphaalpha". J. Biol. Chem. 275 (20): 15232–8. May 2000. doi:10.1074/jbc.275.20.15232. PMID 10809759. 
  4. "Crystal structure of the complex between human CD8alpha(alpha) and HLA-A2". Nature 387 (6633): 630–4. June 1997. doi:10.1038/42523. PMID 9177355. Bibcode1997Natur.387..630G. 
  5. "Cell-cell adhesion mediated by CD8 and human histocompatibility leukocyte antigen G, a nonclassical major histocompatibility complex class 1 molecule on cytotrophoblasts". J. Exp. Med. 174 (3): 737–40. September 1991. doi:10.1084/jem.174.3.737. PMID 1908512. 

Further reading

External links


This article incorporates text from the United States National Library of Medicine, which is in the public domain.