KAT8

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

K(lysine) acetyltransferase 8 (KAT8) is an enzyme that in humans is encoded by the KAT8 gene.[5][6]

PDBOrtholog search: PDBe RCSB
AliasesKAT8, MOF, MYST1, ZC2HC8, hMOF, lysine acetyltransferase 8, LIGOWS
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KAT8
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesKAT8, MOF, MYST1, ZC2HC8, hMOF, lysine acetyltransferase 8, LIGOWS
External IDsOMIM: 609912; MGI: 1915023; HomoloGene: 41676; GeneCards: KAT8; OMA:KAT8 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_032188
NM_182958

NM_026370
NM_001360699

RefSeq (protein)

NP_115564
NP_892003

NP_080646
NP_001347628

Location (UCSC)Chr 16: 31.11 – 31.13 MbChr 7: 127.51 – 127.53 Mb
PubMed search[3][4]
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Function

The MYST family of histone acetyltransferases, which includes KAT8, was named for the founding members MOZ (MYST3; MIM 601408), yeast YBF2 and SAS2, and TIP60 (HTATIP; MIM 601409). All members of this family contain a MYST region of about 240 amino acids with a canonical acetyl-CoA-binding site and a C2HC-type zinc finger motif. Most MYST proteins also have a chromodomain involved in protein-protein interactions and targeting transcriptional regulators to chromatin.[6]

KAT8 is also known as MOF, and in humans hMOF. Given its fundamental role in modulating higher-order chromatin structure, hMOF is involved in many of the steps of the DNA damage response.[7] The human hMOF gene encodes an enzyme that specifically acetylates histone H4 at lysine 16.[7][8] The depletion of hMOF greatly decreases DNA double-strand break repair by both non-homologous end joining and homologous recombination.[8] Thus MOF activity is critical for double-strand break repair.[8]

Interactions

KAT8 has been shown to interact with MORF4L1.[9]

References

Further reading

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