+ |
KMT2A | up-regulates
binding
|
KAT8 |
0.465 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-138245 |
|
|
Homo sapiens |
|
pmid |
sentence |
15960975 |
Mll1 and mof can form a stable complex in vivo / given that an interaction of dmof with msl1 through its zinc finger is essential for correct targeting of mof to the male x chromosome |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
KAT8 | form complex
binding
|
MSL acetyltransferase |
0.803 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-263943 |
|
|
Homo sapiens |
|
pmid |
sentence |
16227571 |
We describe a stable, multisubunit human histone acetyltransferase complex (hMSL) that contains homologs of the Drosophila dosage compensation proteins MOF, MSL1, MSL2, and MSL3. This complex shows strong specificity for histone H4 lysine 16 in chromatin in vitro, and RNA interference-mediated knockdown experiments reveal that it is responsible for the majority of H4 acetylation at lysine 16 in the cell. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Tissue: |
HeLa Cell |
+ |
KAT8 | down-regulates quantity by destabilization
acetylation
|
FASN |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-267366 |
|
|
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
27758890 |
Overexpression of Myc-KAT8 increased the acetylation level of endogenous FASN by 2.2-fold (Fig. 3C). In contrast, knockdown of KAT8 decreased endogenous FASN acetylation by as much as 55% |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
KAT8 | form complex
binding
|
NSL histone acetyltransferase |
0.638 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-267160 |
|
|
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
20018852 |
Here we report an analysis of the subunit composition and substrate specificity of the NSL complex. Proteomic analyses of complexes purified through multiple candidate subunits reveal that NSL is composed of nine subunits. Two of its subunits, WD repeat domain 5 (WDR5) and host cell factor 1 (HCF1), are shared with members of the MLL/SET family of histone H3 lysine 4 (H3K4) methyltransferase complexes, and a third subunit, MCRS1, is shared with the human INO80 chromatin-remodeling complex. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |