Biology:KDM3A

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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

Lysine demethylase 3A is a protein that in humans is encoded by the KDM3A gene.[1]

Function

This gene encodes a zinc finger protein that contains a jumonji C (JmjC) domain and may play a role in hormone-dependent transcriptional activation. Alternative splicing results in multiple transcript variants. KDM3A catalyzes the demethylation of H3K9me1 and H3K9me2 residues. Its function is dependent on the presence of cofactors Fe(II) and α-Ketoglutarate.[2]

References

  1. "Entrez Gene: Lysine demethylase 3A". https://www.ncbi.nlm.nih.gov/gene/55818. 
  2. "JHDM2A, a JmjC-containing H3K9 demethylase, facilitates transcription activation by androgen receptor". Cell 125 (3): 483–495. May 2006. doi:10.1016/j.cell.2006.03.027. PMID 16603237. 

Further reading

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