+ |
KDM5C | up-regulates activity
demethylation
|
H3-4 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-264306 |
Lys5 |
kQTARKST |
Homo sapiens |
|
pmid |
sentence |
30246379 |
KDM5 subfamily is capable of removing tri†and di†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 |
+ |
KDM5C | up-regulates activity
demethylation
|
H3C1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-264305 |
Lys5 |
kQTARKST |
Homo sapiens |
|
pmid |
sentence |
30246379 |
KDM5 subfamily is capable of removing tri‐ and di‐ 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 |
+ |
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 |
+ |
EPAS1 | up-regulates quantity by expression
transcriptional regulation
|
KDM5C |
0.282 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-271579 |
|
|
Homo sapiens |
|
pmid |
sentence |
32938217 |
To this end, we confirm that KDM3A, KDM4B, KDM4C, KDM5B, KDM5C, and KDM62 are direct targets of HIF-1a while extent the list of known targets to KDM2A, KDM2B, KDM4D, KDM5A, and KDM6A. The results demonstrated that majority of the KDMs were similarly induced (KDM2A, KDM2B, KDM3A, KDM4B, KDM4C, KDM4D, KDM5A, KDM5B, KDM5C, KDM6B, and KDM7A) or repressed (KDM NO66 and KDM1A) by both HIF-1a and HIF-2a. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
KDM5C | down-regulates quantity by repression
transcriptional regulation
|
SYN1 |
0.353 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-264314 |
|
|
Mus musculus |
|
pmid |
sentence |
31691806 |
The KDM5C decrease was associated with a lack of repression of downstream target genes Scn2a, Syn1 and Bdnf in the embryonic brain of Arx-null mice. |
|
Publications: |
1 |
Organism: |
Mus Musculus |
+ |
KDM5C | down-regulates quantity by repression
transcriptional regulation
|
BDNF |
0.278 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-264315 |
|
|
Mus musculus |
|
pmid |
sentence |
31691806 |
The KDM5C decrease was associated with a lack of repression of downstream target genes Scn2a, Syn1 and Bdnf in the embryonic brain of Arx-null mice. |
|
Publications: |
1 |
Organism: |
Mus Musculus |
+ |
CNOT4 | down-regulates quantity by destabilization
ubiquitination
|
KDM5C |
0.561 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-271468 |
|
|
Homo sapiens |
|
pmid |
sentence |
19346402 |
In our study, we show that the protein level of the yeast histone H3 Lys 4 (H3 K4) demethylase Jhd2/Kdm5 is modulated through polyubiquitination by the E3 ubiquitin ligase Not4 and turnover by the proteasome. Finally, we show that human NOT4 can polyubiquitinate human JARID1C/SMCX, a homolog of Jhd2, suggesting that this is likely a conserved mechanism. We propose that Not4 is an E3 ubiquitin ligase that monitors and controls a precise amount of Jhd2 protein so that the proper balance between histone demethylase and histone methyltransferase activities occur in the cell, ensuring appropriate levels of H3 K4 trimethylation and gene expression. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
KDM5C | down-regulates quantity by repression
transcriptional regulation
|
SCN2A |
0.336 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-264313 |
|
|
Mus musculus |
|
pmid |
sentence |
31691806 |
The KDM5C decrease was associated with a lack of repression of downstream target genes Scn2a, Syn1 and Bdnf in the embryonic brain of Arx-null mice. |
|
Publications: |
1 |
Organism: |
Mus Musculus |
+ |
2-oxoglutarate(2-) | up-regulates activity
chemical activation
|
KDM5C |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-273468 |
|
|
|
|
pmid |
sentence |
29981745 |
Histone lysine demethylases (KDMs) are 2-oxoglutarate-dependent dioxygenases (2-OGDDs) that regulate gene expression by altering chromatin structure. |2-OG is a central intermediate of the Krebs cycle, where it is produced by isocitrate dehydrogenase (IDH) isoenzymes 2 and 3. |
|
Publications: |
1 |
+ |
HIF1A | up-regulates quantity by expression
transcriptional regulation
|
KDM5C |
0.262 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-271564 |
|
|
Homo sapiens |
|
pmid |
sentence |
32938217 |
To this end, we confirm that KDM3A, KDM4B, KDM4C, KDM5B, KDM5C, and KDM62 are direct targets of HIF-1a while extent the list of known targets to KDM2A, KDM2B, KDM4D, KDM5A, and KDM6A. The results demonstrated that majority of the KDMs were similarly induced (KDM2A, KDM2B, KDM3A, KDM4B, KDM4C, KDM4D, KDM5A, KDM5B, KDM5C, KDM6B, and KDM7A) or repressed (KDM NO66 and KDM1A) by both HIF-1a and HIF-2a. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
BRD4 | up-regulates quantity by expression
transcriptional regulation
|
KDM5C |
0.334 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-264311 |
|
|
Homo sapiens |
|
pmid |
sentence |
30921702 |
 KDM5C was transcriptionally upregulated by bromodomain-containing protein 4 (BRD4), and knockdown KDM5C sensitized the therapeutic effects of CRPC cells to the bromodomain and extraterminal (BET) inhibitor. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
RNF4 | up-regulates activity
sumoylation
|
KDM5C |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-271576 |
|
|
Homo sapiens |
|
pmid |
sentence |
33859667 |
Hendriks and coworkers showed that, in response to alkylation damage by methyl methanesulfonate (MMS), SUMOylated JARID1B (KDM5B) is ubiquitylated by the SUMOtargeted ubiquitin ligase RNF4 and degraded by the proteasome, whereas JARID1C (KDM5C) is SUMOylated and recruited to the chromatin to demethylate histone H3K4 (Hendriks et al., 2015). |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
KDM5C | down-regulates quantity by repression
transcriptional regulation
|
PTEN |
0.343 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-264312 |
|
|
Homo sapiens |
|
pmid |
sentence |
30921702 |
KDM5C performs its oncogenic function by suppressing PTEN epigenetically. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |