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Component of the HBO1 complex which has a histone H4- specific acetyltransferase activity, a reduced activity toward histone H3 and is responsible for the bulk of histone H4 acetylation in vivo.
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Hbo1 is another ERalpha (show ESR1 Proteins) coactivator that ubiquitinates ERalpha (show ESR1 Proteins)
Histone acetyltransferase binding to ORC1 (HBO1) is upregulated in bladder cancer.
The results demonstrate some connections between KAT7 upregulated in RA SFs and RA progression and present the inhibition of KAT7 activity as a novel therapeutic target for interfering RA disease.
Structural and mechanistic insights into regulation of HBO1 histone acetyltransferase activity by BRPF2 (show BRD1 Proteins) have been presented.
KAT7-containing acetyltransferases associating with the Mis18 complex provides competence for histone turnover/exchange activity on alphoid DNA and prevents Suv39h1 (show SUV39H1 Proteins)-mediated heterochromatin invasion into centromeres.
the possible binding sites and biological functions of HBO1, were identified.
Data show that HTLV-1 basic leucine zipper (bZIP) factor (HBZ) represses p53 activity by direct inhibition of the histone acetyltransferase (HAT) activity of p300/CBP and the HAT activity of HBO1: [HBZ]
This study demonstrates that CRL4(DDB2 (show DDB2 Proteins)) is a novel ubiquitin ligase of HBO1.
Taken together, MYST2 is a repressed growth suppressor in AML (show RUNX1 Proteins) mediating reduced acetylation of histone 4 at residue 5 and is associated with inferior AML patient survival.
Myst2-mediated histone acetylation may be required for recruitment of Oct4 to the Nanog promoter
MYST2 gene was cloned; results demonstrated that 2872G > A substitution was significantly associated with the litter size of all parities in Large White sows and Landrace sows
a nonredundant role for KAT7 in the maintenance of Histone h 3 lusine 14 acetylation, which is intimately linked with the ability to develop a normal immune system, is reported.
These results indicate that BRPF3 forms a functional tetrameric complex with HBO1 but is not required for mouse development and survival
Taken together, MYST2 is a repressed growth suppressor in AML (show RUNX1 Proteins) mediating reduced acetylation of histone 4 at residue 5
Brd1 (show BRD1 Proteins)-mediated Hbo1 activity is crucial for efficient activation of CD8 (show CD8A Proteins) expression via acetylation at H3K14, which serves as an epigenetic mark that promotes the recruitment of transcription machinery to the CD8 (show CD8A Proteins) enhancers.
Modulation of Fbxw15 levels was able to differentially regulate histone H3K14 acetylation and cellular proliferation by altering HBO1 levels.
The Hbo1-Brd1 (show BRD1 Proteins) complex is the major H3K14 HAT required for transcriptional activation of erythroid developmental regulator (show GIPC1 Proteins) genes.
the primary role of HBO1 in development is that of a transcriptional activator, which is indispensable for H3K14 acetylation and for the normal expression of essential genes regulating embryonic development
reveal a direct regulatory connection between p53 (show TP53 Proteins)-responsive stress signaling and Hbo1-dependent chromatin pathways
FAD24 (show NOC3L Proteins) controls DNA replication by recruiting HBO1 to origins of DNA replication and is required for MCE during adipocyte differentiation.
Component of the HBO1 complex which has a histone H4- specific acetyltransferase activity, a reduced activity toward histone H3 and is responsible for the bulk of histone H4 acetylation in vivo. Through chromatin acetylation it may regulate DNA replication and act as a coactivator of TP53-dependent transcription. Specifically represses AR-mediated transcription (By similarity).
MOZ, YBF2/SAS3, SAS2 and TIP60 protein 2
, MYST histone acetyltransferase 2
, MYST protein 2
, histone acetyltransferase KAT7
, histone acetyltransferase MYST2
, histone acetyltransferase binding to ORC1
, lysine acetyltransferase 7