Homo sapiens Protein: KDM2A | |||||||||||||||||||
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Summary | |||||||||||||||||||
InnateDB Protein | IDBP-232539.7 | ||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
Gene Symbol | KDM2A | ||||||||||||||||||
Protein Name | lysine (K)-specific demethylase 2A | ||||||||||||||||||
Synonyms | CXXC8; FBL11; FBL7; FBXL11; JHDM1A; LILINA; | ||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||
Ensembl Protein | ENSP00000381640 | ||||||||||||||||||
InnateDB Gene | IDBG-59841 (KDM2A) | ||||||||||||||||||
Protein Structure | |||||||||||||||||||
UniProt Annotation | |||||||||||||||||||
Function | Histone demethylase that specifically demethylates 'Lys- 36' of histone H3, thereby playing a central role in histone code. Preferentially demethylates dimethylated H3 'Lys-36' residue while it has weak or no activity for mono- and tri-methylated H3 'Lys- 36'. May also recognize and bind to some phosphorylated proteins and promote their ubiquitination and degradation. Required to maintain the heterochromatic state. Associates with centromeres and represses transcription of small non-coding RNAs that are encoded by the clusters of satellite repeats at the centromere. Required to sustain centromeric integrity and genomic stability, particularly during mitosis. {ECO:0000269PubMed:16362057, ECO:0000269PubMed:19001877}. | ||||||||||||||||||
Subcellular Localization | Nucleus, nucleoplasm {ECO:0000269PubMed:19001877, ECO:0000269PubMed:20417597}. Note=Punctate expression throughout the nucleoplasm and enriched in the perinucleolar region. Specifically nucleates at CpG islands where it's presence results in chromatin depleted in H3K36me2. | ||||||||||||||||||
Disease Associations | |||||||||||||||||||
Tissue Specificity | Widely expressed, with highest levels in brain, testis and ovary, followed by lung. {ECO:0000269PubMed:10231032}. | ||||||||||||||||||
Comments | |||||||||||||||||||
Interactions | |||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 25 experimentally validated interaction(s) in this database.
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Gene Ontology | |||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Protein Structure and Domains | |||||||||||||||||||
PDB ID | |||||||||||||||||||
InterPro |
IPR001965
Zinc finger, PHD-type IPR002857 Zinc finger, CXXC-type IPR003347 JmjC domain IPR011011 Zinc finger, FYVE/PHD-type IPR019787 Zinc finger, PHD-finger |
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PFAM |
PF02008
PF02373 PF08007 PF00628 |
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PRINTS | |||||||||||||||||||
PIRSF | |||||||||||||||||||
SMART |
SM00249
SM00558 |
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TIGRFAMs | |||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||
Modification | |||||||||||||||||||
Cross-References | |||||||||||||||||||
SwissProt | Q9Y2K7 | ||||||||||||||||||
PhosphoSite | PhosphoSite-Q9Y2K7 | ||||||||||||||||||
TrEMBL | |||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||
Entrez Gene | 22992 | ||||||||||||||||||
UniGene | Hs.622131 | ||||||||||||||||||
RefSeq | |||||||||||||||||||
HUGO | HGNC:13606 | ||||||||||||||||||
OMIM | 605657 | ||||||||||||||||||
CCDS | |||||||||||||||||||
HPRD | 05741 | ||||||||||||||||||
IMGT | |||||||||||||||||||
EMBL | AB023221 AB490246 AF179221 AK024505 AL117517 AP000729 AP001885 BC001203 BC047371 BC047486 BC064360 JQ710743 JQ710744 | ||||||||||||||||||
GenPept | AAD56012 AAH01203 AAH47371 AAH47486 AAH64360 AFK81542 AFK81543 BAA76848 BAB15795 BAJ05817 CAH10721 | ||||||||||||||||||