Histone deacetylase
From Proteopedia
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*Sir2 | *Sir2 | ||
- | **[[2hjh]] – yHDAC Sir2 - yeast<br /> | + | **[[2hjh]] – yHDAC Sir2 + pseudosubstrate + nicotinamide - yeast<br /> |
- | **[[4iao]] – yHDAC Sir2 + Sir4<br /> | + | **[[4iao]] – yHDAC Sir2 + Sir4 + adenosine diphosphoribose<br /> |
}} | }} | ||
== References == | == References == | ||
<references/> | <references/> | ||
[[Category:Topic Page]] | [[Category:Topic Page]] |
Revision as of 08:57, 23 March 2016
Contents |
Function
Histone deacetylase (HDAC) catalyzes the removal of acetyl group from ε-N-acetyl lysine in histones[1]. HDAC contains Zn. DNA expression is regulated by acetylation and de-acetylation. HDAC are classified according to their domain organization to 4 classes. SAHA is a common inhibitor of HDAC. For additional details see
- Understanding of the Recruitment of HDACs by MEF2, Based on Their Structure
- Transcription and RNA Processing.
Relevance
HDAC inhibitors are used in cancer therapy[2].
3D Structures of histone deacetylase
Updated on 23-March-2016
References
- ↑ Joshi P, Greco TM, Guise AJ, Luo Y, Yu F, Nesvizhskii AI, Cristea IM. The functional interactome landscape of the human histone deacetylase family. Mol Syst Biol. 2013;9:672. doi: 10.1038/msb.2013.26. PMID:23752268 doi:http://dx.doi.org/10.1038/msb.2013.26
- ↑ Marks P, Rifkind RA, Richon VM, Breslow R, Miller T, Kelly WK. Histone deacetylases and cancer: causes and therapies. Nat Rev Cancer. 2001 Dec;1(3):194-202. PMID:11902574 doi:http://dx.doi.org/10.1038/35106079