Biology:MARK3

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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

MAP/microtubule affinity-regulating kinase 3 is an enzyme that in humans is encoded by the MARK3 gene.[1][2]

Interactions

MARK3 has been shown to interact with Stratifin.[3][4]

It has been linked to a form of genetic blindness, believed to be a genetic recessive disease that progressively destroys the eyes.[5]

References

  1. "Assignment of MARK3 alias KP78 to human chromosome band 14q32.3 by in situ hybridization". Cytogenet Cell Genet 79 (1–2): 101–2. April 1998. doi:10.1159/000134692. PMID 9533022. 
  2. "Entrez Gene: MARK3 MAP/microtubule affinity-regulating kinase 3". https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=4140. 
  3. "Towards a proteome-scale map of the human protein–protein interaction network". Nature 437 (7062): 1173–8. October 2005. doi:10.1038/nature04209. PMID 16189514. Bibcode2005Natur.437.1173R. 
  4. "Targeted proteomic analysis of 14-3-3 sigma, a p53 effector commonly silenced in cancer". Mol. Cell. Proteomics 4 (6): 785–95. June 2005. doi:10.1074/mcp.M500021-MCP200. PMID 15778465. 
  5. "Découverte d'un gène provoquant une cécité - Communiqués de presse - UNIGE". 23 July 2018. https://www.unige.ch/communication/communiques/2018/cdp180723/. 

Further reading