+ |
KDM2B | up-regulates activity
binding
|
RNF2 |
0.628 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-252242 |
|
|
Homo sapiens |
|
pmid |
sentence |
17296600 |
BcoR and Fbxl10/Jhdm1B are among the most abundant Ring1B/Rnf2 interactors identified with the highest confidence, and their association has been validated by coimmunoprecipitation studies; hence we call this the Fbxl10-BcoR complex. The assembly of Fbxl10-BcoR complex(es), the associations among its various subunits, and its functional significance remain to be characterized but are presently under investigation. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
2-oxoglutarate(2-) | up-regulates activity
chemical activation
|
KDM2B |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-273472 |
|
|
|
|
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
|
KDM2B |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-271567 |
|
|
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 |
+ |
KDM2B | up-regulates activity
binding
|
Noncanonical PRC1 |
0.675 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-252247 |
|
|
Mus musculus |
3T3-L1 Cell |
pmid |
sentence |
25533466 |
We show that FBXL10/KDM2B is an anti-adipogenic factor that is up-regulated during the early phase of 3T3-L1 preadipocyte differentiation and in adipose tissue in a diet-induced model of obesity. Interestingly, inhibition of adipogenesis does not require the JmjC demethylase domain of FBXL10, but it does require the F-box and leucine-rich repeat domains, which we show recruit a noncanonical polycomb repressive complex 1 (PRC1) containing RING1B, SKP1, PCGF1, and BCOR. |
|
Publications: |
1 |
Organism: |
Mus Musculus |
+ |
KDM2B | down-regulates quantity by repression
transcriptional regulation
|
UHRF1 |
0.288 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-252245 |
|
|
Mus musculus |
3T3-L1 Cell |
pmid |
sentence |
25533466 |
We concluded that FBXL10 recruits the noncanonical PRC1 complex to directly repress Cdk1, Uhrf1, and Pparg that may account for the FBXL10-mediated inhibition of adipogenesis. |
|
Publications: |
1 |
Organism: |
Mus Musculus |
+ |
KDM2B | down-regulates quantity by repression
transcriptional regulation
|
PPARG |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-252246 |
|
|
Mus musculus |
3T3-L1 Cell |
pmid |
sentence |
25533466 |
We concluded that FBXL10 recruits the noncanonical PRC1 complex to directly repress Cdk1, Uhrf1, and Pparg that may account for the FBXL10-mediated inhibition of adipogenesis. |
|
Publications: |
1 |
Organism: |
Mus Musculus |
+ |
KDM2B | down-regulates
|
Adipogenesis |
0.7 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-252243 |
|
|
Mus musculus |
3T3-L1 Cell |
pmid |
sentence |
25533466 |
Here, we show that FBXL10/KDM2B is an anti-adipogenic factor that is up-regulated during the early phase of 3T3-L1 preadipocyte differentiation and in adipose tissue in a diet-induced model of obesity. These results suggest that FBXL10 represses adipogenesis by targeting a noncanonical PRC1 complex to repress key genes (e.g. Pparg) that control conversion of pluripotent cells into the adipogenic lineage. |
|
Publications: |
1 |
Organism: |
Mus Musculus |
+ |
EPAS1 | up-regulates quantity by expression
transcriptional regulation
|
KDM2B |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-271582 |
|
|
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 |
+ |
KDM2B | down-regulates quantity by repression
transcriptional regulation
|
CDK1 |
0.283 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-252244 |
|
|
Mus musculus |
3T3-L1 Cell |
pmid |
sentence |
25533466 |
We concluded that FBXL10 recruits the noncanonical PRC1 complex to directly repress Cdk1, Uhrf1, and Pparg that may account for the FBXL10-mediated inhibition of adipogenesis. |
|
Publications: |
1 |
Organism: |
Mus Musculus |