+ |
Histone H3 | form complex
binding
|
Nucleosome |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265308 |
|
|
in vitro |
|
pmid |
sentence |
21812398 |
The elemental repeating unit of chromatin is the nucleosome core particle (NCP), which consists of 146 base pairs of DNA wrapped in 1.65 left-handed superhelical turns around the histone octamer. The histone octamer comprises two each of the core histones, H2A, H2B, H3 and H4, which form two H2A/H2B dimers and an H3/H4 tetramer, respectively, in the NCP. |
|
Publications: |
1 |
Organism: |
In Vitro |
+ |
PRKACA | up-regulates
phosphorylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265344 |
|
|
Homo sapiens |
|
pmid |
sentence |
10464286 |
Identification of a novel phosphorylation site on histone h3 coupled with mitotic chromosome condensation. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
PBK |
phosphorylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265364 |
|
|
Homo sapiens |
|
pmid |
sentence |
16982762 |
Pbk/topk could phosphorylate histone h3 at ser10 in vitro and in vivo, and mediated its growth-promoting effect through histone h3 modification. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
FYN |
phosphorylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265330 |
|
|
Homo sapiens |
|
pmid |
sentence |
15537652 |
Here we provide evidence that fyn kinase, a member of the src kinase family, is involved in the uvb-induced phosphorylation of histone h3 at serine 10 |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
KAT2B | down-regulates activity
acetylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-269610 |
|
|
Homo sapiens |
|
pmid |
sentence |
34811519 |
The HAT module within the SAGA and ADA complexes acetylates histone H3, mainly on residues K9 and K14. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
AURKA |
phosphorylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265356 |
|
|
Mus musculus |
|
pmid |
sentence |
12234980 |
In the present study, chromosome number instability and increased tumor invasiveness were noted in constitutively AIM-1-overexpressing cells in vivo. Increased mitotic Ser-10 phosphorylation was also observed in various colorectal tumor cells with high AIM-1 expression levels. These data suggest that increased H3 histone phosphorylation as a result of AIM-1 overexpression is a major precipitating factor of chromosome instability and, thus, may play a role in carcinogenesis. |
|
Publications: |
1 |
Organism: |
Mus Musculus |
+ |
RPS6KA1 | down-regulates activity
phosphorylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265346 |
|
|
Homo sapiens |
|
pmid |
sentence |
14625384 |
Phosphorylation at ser-11 (h3s10ph) by rps6ka4 and rps6ka5 is important during interphase because it enables the transcription of genes following external stimulation, like mitogens, stress, growth factors or uv irradiation and result in the activation of genes, such as c-fos and c-jun. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
AURKC | up-regulates
phosphorylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265357 |
|
|
Homo sapiens |
|
pmid |
sentence |
12588998 |
Phosphorylation at ser-11 (h3s10ph) by aurkb is crucial for chromosome condensation and cell-cycle progression during mitosis and meiosis. Phosphorylation at ser-11 (h3s10ph) by aurkb is crucial for chromosome condensation and cell-cycle progression during mitosis and meiosis. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
CTNNB1 | down-regulates activity
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265358 |
|
|
Homo sapiens |
|
pmid |
sentence |
16510874 |
Beta-cat promotes h3k4 trimethylation at the c-myc gene in vivo. H3k4 trimethylation in vivo requires prior ubiquitination of h2b, and we find that ubiquitin is necessary for transcription initiation on chromatin but not nonchromatin templates in vitro. Chromatin immunoprecipitation experiments reveal that beta-cat recruits pygopus, bcl-9/legless, and mll/set1-type complexes to the c-myc enhancertogether with the negative wnt regulators, apc, and betatrcp. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
KDM6A | down-regulates activity
demethylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265360 |
|
|
Homo sapiens |
|
pmid |
sentence |
24561908 |
Ubiquitously Transcribed Tetratricopeptide Repeat on chromosome X (UTX) and Jumonji D3 (JMJD3) as novel histone demethylases that catalyze the removal of di- and trimethyl groups on histone H3 lysine 27, thereby promoting target gene activation. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
RPS6K | down-regulates activity
phosphorylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265345 |
|
|
Homo sapiens |
|
pmid |
sentence |
10464286 |
Phosphorylation at ser-11 (h3s10ph) by rps6ka4 and rps6ka5 is important during interphase because it enables the transcription of genes following external stimulation, like mitogens, stress, growth factors or uv irradiation and result in the activation of genes, such as c-fos and c-jun. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
JMJD1C | down-regulates activity
demethylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265331 |
|
|
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
32034158 |
We now determine that JMJD1C is recruited by USF-1 to various lipogenic genes for H3K9 demethylation to enhance chromatin accessibility in the fed state. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
KDM5A | up-regulates activity
demethylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265334 |
|
|
Homo sapiens |
|
pmid |
sentence |
30246379 |
KDM5 subfamily is capable of removing tri‚Äê and di‚Äê methyl marks from lysine 4 on histone H3 (H3K4). Depending on the methylation site, its effect on transcription can be either activating or repressing. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
CBP/p300 | down-regulates activity
acetylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265322 |
|
|
Homo sapiens |
|
pmid |
sentence |
21131905 |
These results highlight the substrate and site specificities of hats in cells, demonstrate the distinct roles of gcn5/pcaf- and cbp/p300-mediated histone acetylations in gene activation, and suggest an important role of cbp/p300-mediated h3k18/27ac in nr-dependent transcription. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
SAGA complex | down-regulates activity
acetylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-269627 |
|
|
Homo sapiens |
|
pmid |
sentence |
34811519 |
The HAT module within the SAGA and ADA complexes acetylates histone H3, mainly on residues K9 and K14. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
SETD5 | up-regulates activity
methylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265350 |
|
|
in vitro |
|
pmid |
sentence |
31515109 |
SETD5 Exhibits Intrinsic Methyltransferase Activity on H3K36. This assay showed that SETD5 has specific histone methyltransferase activity toward K36 but not for other residues such as K4 and K27 (Figure 8B). we revealed that SETD5 is endowed with H3K36 methyltransferase, which is necessary for RNA elongation and processing and, ultimately, correct gene transcription. |
|
Publications: |
1 |
Organism: |
In Vitro |
+ |
KDM5C | up-regulates activity
demethylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265354 |
|
|
Homo sapiens |
|
pmid |
sentence |
30246379 |
KDM5 subfamily is capable of removing tri‚Äê and di‚Äê methyl marks from lysine 4 on histone H3 (H3K4). Depending on the methylation site, its effect on transcription can be either activating or repressing. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
MAML1 | down-regulates activity
acetylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265362 |
|
|
Homo sapiens |
|
pmid |
sentence |
17300219 |
The n-terminal domain of maml1 directly interacts with both p300 and histones, and the p300-maml1 complex specifically acetylates histone h3 and h4 tails in chromatin. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
RPS6KA3 | down-regulates activity
phosphorylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265347 |
|
|
Homo sapiens |
|
pmid |
sentence |
10464286 |
Phosphorylation at ser-11 (h3s10ph) by rps6ka4 and rps6ka5 is important during interphase because it enables the transcription of genes following external stimulation, like mitogens, stress, growth factors or uv irradiation and result in the activation of genes, such as c-fos and c-jun. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
AKT1 |
phosphorylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265320 |
|
|
Homo sapiens |
|
pmid |
sentence |
12588998 |
Additionally, active akt1 kinase strongly phosphorylates histone h3 at serine 10 in vitro |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
UNII-XH2662798I | down-regulates
|
Histone H3 |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265352 |
|
|
Homo sapiens |
|
pmid |
sentence |
20068082 |
Pf-00477736 also significantly enhances docetaxel efficacy in vitro and in vivo, in association with decreased cdc25c cytoplasmic phosphorylation (ser216) and histone h3 phosphorylation (ser10)(42). |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
SLBP | up-regulates quantity by expression
translation regulation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265373 |
|
|
Homo sapiens |
U2-OS Cell |
pmid |
sentence |
19155325 |
Synthesis of mature histone mRNA requires only a single processing reaction: an endonucleolytic cleavage between a conserved stem-loop and a purine-rich downstream element to form the 3' end. The stem-loop binding protein (SLBP) is required for processing, and following processing, histone mRNA is transported to the cytoplasm, where SLBP participates in translation of the histone mRNA|We used radiolabeled probes generated by PCR targeting the open reading frame (ORF) to detect histones H2A, H2B, H3, H4, and H1 and used 7SK snRNA as a loading control (Fig. 2A). The abundance of histone H2A, H2B, H3, and H4 mRNAs is reduced to 37% to 70% of control levels in the SLBP knockdown cells when compared to the C2 control. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
AURKB | up-regulates
phosphorylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265321 |
|
|
Homo sapiens |
|
pmid |
sentence |
10464286 |
Phosphorylation at ser-11 (h3s10ph) by aurkb is crucial for chromosome condensation and cell-cycle progression during mitosis and meiosis. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
TGM2 |
phosphorylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265369 |
|
|
Homo sapiens |
|
pmid |
sentence |
16407273 |
Tg2 is able to phosphorylate purified histone proteins, and h3 and h1 in chromatin preparations, and it is associated with chromatin in breast cancer cells. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
TLK1 | up-regulates activity
phosphorylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265370 |
|
|
in vitro |
|
pmid |
sentence |
11314006 |
Purified tlk1b phosphorylated histone h3 at s(10) with high specificity both in a mix of core histones and in isolated chromatin, suggesting that histone h3 is a physiological substrate for tlk1b. Phosphorylation of H3 has been linked to the activation of the immediate-early genes upon mitogenic stimulation, and to chromatin condensation during mitotic/meiotic events. |
|
Publications: |
1 |
Organism: |
In Vitro |
+ |
PHF2 | down-regulates activity
demethylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265343 |
|
|
Homo sapiens |
|
pmid |
sentence |
21532585 |
PHF2, a jmjC demethylase, is enzymatically inactive by itself, but becomes an active H3K9Me2 demethylase through PKA-mediated phosphorylation. This modification leads to targeting of the PHF2–ARID5B complex to its target promoters, where it removes the repressive H3K9Me2 mark. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
CBX3 | up-regulates activity
binding
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265324 |
|
|
Homo sapiens |
|
pmid |
sentence |
19111658 |
A core characteristic of heterochromatin is its association with heterochromatin protein 1 (HP1) proteins, a highly conserved family of chromosomal proteins that bind to di- and trimethylated H3K9 via a conserved N-terminal domain called the chromodomain (CD) HP1 proteins are a highly conserved family of eukaryotic proteins that bind to methylated histone H3 lysine 9 (H3K9) and are required for heterochromatic gene silencing. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
VRK1 |
phosphorylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265371 |
|
|
Homo sapiens |
|
pmid |
sentence |
17938195 |
We show that histone h3 is phosphorylated by vaccinia-related kinase 1 (vrk1). Direct phosphorylation of thr3 and ser10 in h3 by vrk1 both in vitro and in vivo was observed. Loss of vrk1 activity was associated with a marked decrease in h3 phosphorylation during mitosis. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
CBX1 | up-regulates activity
binding
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265323 |
|
|
Homo sapiens |
|
pmid |
sentence |
19111658 |
A core characteristic of heterochromatin is its association with heterochromatin protein 1 (HP1) proteins, a highly conserved family of chromosomal proteins that bind to di- and trimethylated H3K9 via a conserved N-terminal domain called the chromodomain (CD) HP1 proteins are a highly conserved family of eukaryotic proteins that bind to methylated histone H3 lysine 9 (H3K9) and are required for heterochromatic gene silencing. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
KAT2A | down-regulates activity
acetylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-269593 |
|
|
Homo sapiens |
|
pmid |
sentence |
34811519 |
The HAT module within the SAGA and ADA complexes acetylates histone H3, mainly on residues K9 and K14. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
MAPK14 |
phosphorylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265338 |
|
|
Homo sapiens |
|
pmid |
sentence |
10806218 |
More importantly, incubation of active erk2 or p38 kinase with h3 protein resulted in phosphorylation of h3 at serine 10 in vitro. These results suggest that erk and p38 kinase are at least two important mediators of phosphorylation of h3 at serine 10. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
KDM1A | up-regulates activity
demethylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265332 |
|
|
Homo sapiens |
HeLa Cell |
pmid |
sentence |
15620353 |
Here, we provide evidence that LSD1 (KIAA0601), a nuclear homolog of amine oxidases, functions as a histone demethylase and transcriptional corepressor. LSD1 specifically demethylates histone H3 lysine 4, which is linked to active transcription. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
KDM4B | down-regulates activity
demethylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265359 |
|
|
Homo sapiens |
|
pmid |
sentence |
30759871 |
The KDM4 family of Jumonj domain histone demethylases specifically target di- and tri-methylated lysine 9 on histone H3 (H3K9me3), removing a modification central to defining heterochromatin and gene repression. The majority of studies regarding its function describe it as an activator that removes repressive H3K9me3 and H3K9me2 at or near regulated promoters in order to facilitate expression of the indicated pathways. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
EP300 | down-regulates activity
acetylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265328 |
|
|
Homo sapiens |
|
pmid |
sentence |
21131905 |
These results highlight the substrate and site specificities of hats in cells, demonstrate the distinct roles of gcn5/pcaf- and cbp/p300-mediated histone acetylations in gene activation, and suggest an important role of cbp/p300-mediated h3k18/27ac in nr-dependent transcription. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
Set1-Ash2 HMT complex | down-regulates activity
methylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265349 |
|
|
Homo sapiens |
|
pmid |
sentence |
12670868 |
The Set1/Ash2 HMT methylates histone H3 at Lys 4 (K4), but not if the neighboring K9 residue is already methylated. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
AKT |
phosphorylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265319 |
|
|
Homo sapiens |
|
pmid |
sentence |
12588998 |
Additionally, active akt1 kinase strongly phosphorylates histone h3 at serine 10 in vitro |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
PIM | down-regulates activity
phosphorylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265365 |
|
|
Homo sapiens |
|
pmid |
sentence |
17643117 |
Pim1-dependent phosphorylation of histone h3 at serine 10 is required for myc-dependent transcriptional activation and oncogenic transformation. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
Sin3B_complex | down-regulates activity
binding
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-269844 |
|
|
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
21041486 |
We report here the identification of a mammalian complex containing the corepressor Sin3B, the histone deacetylase HDAC1, Mrg15, and the PHD finger-containing Pf1 and show that this complex plays important roles in regulation of transcription. Sin3B, Pf1, Mrg15, and HDAC1 associate within a stable complex that binds H3K4me3/H3K36me3-enriched nucleosomes. We identify mammalian Pf1, a PHD finger protein, as a homologue of Rco1, and show that all four components, Sin3B, HDAC1, Mrg15, and Pf1, can form a stable complex, which is recruited downstream of the transcriptional start site through complex interactions with histones. these results indicate that the Pf1/Sin3B-containing complex is recruited at discrete sites within actively transcribed loci, likely through its interaction with H3K4me3/H3K36me3-enriched chromatin. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
CHEK1 | down-regulates activity
phosphorylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265326 |
|
|
Homo sapiens |
|
pmid |
sentence |
18243098 |
We identify chk1 as the kinase responsible for h3-t11 phosphorylation. H3-t11 phosphorylation occurs throughout the cell cycle and is chk1 dependent in vivo.Phosphorylation at thr-12 (h3t11ph) by pkn1 is a specific tag for epigenetic transcriptional activation that promotes demethylation of lys-10 (h3k9me) by kdm4c/jmjd2c. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ZMYND11 | up-regulates activity
binding
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265353 |
|
|
|
|
pmid |
sentence |
24675531 |
We found that full-length BS69 specifically interacted with H3K36me3 in native nucleosome co-immunoprecipitation (co-IP) experiments. We propose that BS69 specifically associates with H3K36me3-enriched chromatin through the PWWP domain, which facilitates the recruitment of MYND-bound transcription and chromatin remodeling factors including EZH2, HDAC1, Brg1 and E2F6 to target gene loci, thereby repressing target gene transcription. |
|
Publications: |
1 |
+ |
PAK1 |
phosphorylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265363 |
|
|
Homo sapiens |
|
pmid |
sentence |
12151336 |
Histone h3 is a substrate of pak1 both in vitro and in vivo, and it specifically interacted with pak1 but not pak2 or pak3. Site-directed mutagenesis indicated that pak1 phosphorylates histone h3 on ser10. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
SETDB2 | up-regulates activity
methylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265351 |
|
|
Homo sapiens |
|
pmid |
sentence |
20404330 |
Here, we have characterized a previously undescribed member of the histone H3K9 methyltransferase family named CLLD8 (or SETDB2 or KMT1F). This protein contributes to the trimethylation of both interspersed repetitive elements and centromere-associated repeats and participates in the recruitment of heterochromatin protein 1 to centromeres. Methylation of histone H3 at lysine 9 (H3K9) has emerged as an important player in the formation of heterochromatin, chromatin condensation, and transcriptional repression. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
Polycomb repressive complex 2 | up-regulates activity
methylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265367 |
|
|
Homo sapiens |
|
pmid |
sentence |
24987060 |
The presence of trimethylation of H3K27 (H3K27me3) at promoter regions is associated with gene repression. This modification is generated by the Polycomb repressive complex 2 (PRC2), composed of the SET domain-containing histone methyltransferase (HMT) EZH2 (enhancer of zeste homolog 2) or its functional homologue EZH1, and core accessory proteins (EED, SUZ12, and RbAp48) (Fig. 1A). |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
CBX5 | up-regulates activity
binding
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265325 |
|
|
Homo sapiens |
|
pmid |
sentence |
19111658 |
A core characteristic of heterochromatin is its association with heterochromatin protein 1 (HP1) proteins, a highly conserved family of chromosomal proteins that bind to di- and trimethylated H3K9 via a conserved N-terminal domain called the chromodomain (CD) HP1 proteins are a highly conserved family of eukaryotic proteins that bind to methylated histone H3 lysine 9 (H3K9) and are required for heterochromatic gene silencing. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
KDM5D | up-regulates activity
demethylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265336 |
|
|
Homo sapiens |
|
pmid |
sentence |
30246379 |
KDM5 subfamily is capable of removing tri‚Äê and di‚Äê methyl marks from lysine 4 on histone H3 (H3K4). Depending on the methylation site, its effect on transcription can be either activating or repressing. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
PRKCD | up-regulates activity
phosphorylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265368 |
|
|
Homo sapiens |
|
pmid |
sentence |
19363025 |
We identify protein kinase c-delta as the kinase responsible for h3t45ph in vitro and in vivo. Given the nucleosomal position of h3t45, we postulate that h3t45ph induces structural change within the nucleosome to facilitate dna nicking and/or fragmentation. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
RPS6KA4 |
phosphorylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265355 |
|
|
Mus musculus |
|
pmid |
sentence |
12773393 |
The results presented here show that MSK2 and, to a lesser extent, MSK1 are the major protein kinases required for the phosphorylation of histone H3 at both Ser10 and Ser28 |
|
Publications: |
1 |
Organism: |
Mus Musculus |
+ |
RPS6KA5 | down-regulates activity
phosphorylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265348 |
|
|
Homo sapiens |
|
pmid |
sentence |
10464286 |
Phosphorylation at ser-11 (h3s10ph) by rps6ka4 and rps6ka5 is important during interphase because it enables the transcription of genes following external stimulation, like mitogens, stress, growth factors or uv irradiation and result in the activation of genes, such as c-fos and c-jun. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
KDM6B | down-regulates activity
demethylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265361 |
|
|
Homo sapiens |
|
pmid |
sentence |
24561908 |
Ubiquitously Transcribed Tetratricopeptide Repeat on chromosome X (UTX) and Jumonji D3 (JMJD3) as novel histone demethylases that catalyze the removal of di- and trimethyl groups on histone H3 lysine 27, thereby promoting target gene activation. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
KDM5B | up-regulates activity
demethylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265335 |
|
|
Homo sapiens |
|
pmid |
sentence |
30246379 |
KDM5 subfamily is capable of removing tri‚Äê and di‚Äê methyl marks from lysine 4 on histone H3 (H3K4). Depending on the methylation site, its effect on transcription can be either activating or repressing. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
P2RY2 | up-regulates activity
demethylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265342 |
|
|
Homo sapiens |
|
pmid |
sentence |
30246379 |
KDM5 subfamily is capable of removing tri‚Äê and di‚Äê methyl marks from lysine 4 on histone H3 (H3K4). Depending on the methylation site, its effect on transcription can be either activating or repressing. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
KDM4C | down-regulates activity
demethylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265333 |
|
|
Homo sapiens |
|
pmid |
sentence |
29207681 |
As one member of the Jumonji-C histone demethylase family, JMJD2C has the ability to demethylate tri- or di-methylated histone 3 and 2 in either K9 (lysine residue 9) or K36 (lysine residue 36) sites by an oxidative reaction, thereby affecting heterochromatin formation, genomic imprinting, X-chromosome inactivation, and transcriptional regulation of genes.JMJD2C has been proved to be a demethylase for H3K9 methylation, in the manner of catalyzing the demethylation of H3K9me3/me2 (the known repressive markers of gene regulation), a histone mark found in heterochromatin associated with euchromatic transcriptional silencing and heterochromatin formation |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
PIM1 | down-regulates activity
phosphorylation
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265366 |
|
|
Homo sapiens |
|
pmid |
sentence |
17643117 |
Pim1-dependent phosphorylation of histone h3 at serine 10 is required for myc-dependent transcriptional activation and oncogenic transformation. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
BAZ2B | down-regulates activity
binding
|
Histone H3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-269843 |
|
|
Homo sapiens |
|
pmid |
sentence |
31999386 |
The BAZ2B bromodomain has been shown to bind to acetylated H3K14 (H3K14ac), whose presence at promoter regions is generally associated with gene activation. This suggests a potential role for BAZ2B in transcriptional activation. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |