+ |
KDM1A | up-regulates activity
demethylation
|
H3-4 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-264508 |
Lys5 |
kQTARKST |
Homo sapiens |
|
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 |
+ |
KDM1A | up-regulates activity
demethylation
|
H3C1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-264507 |
Lys5 |
kQTARKST |
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 |
+ |
KDM1A | up-regulates activity
demethylation
|
H3-3A |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-264509 |
Lys5 |
kQTARKST |
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 |
+ |
CSNK2A1 | up-regulates activity
phosphorylation
|
KDM1A |
0.323 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-276902 |
Ser131 |
DESLANLsEDEYYSE |
Homo sapiens |
HEK-293T Cell |
pmid |
sentence |
25999347 |
We demonstrated here that phosphorylation and dephosphorylation of LSD1 at S131 and S137 was mediated by casein kinase 2 (CK2) and wild-type p53-induced phosphatase 1 (WIP1), respectively. LSD1, RNF168 and 53BP1 interacted with each other directly. CK2-mediated phosphorylation of LSD1 exhibited no impact on its interaction with 53BP1, but promoted its interaction with RNF168 and RNF168-dependent 53BP1 ubiquitination and subsequent recruitment to the DNA damage sites. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-276903 |
Ser137 |
LSEDEYYsEEERNAK |
Homo sapiens |
HEK-293T Cell |
pmid |
sentence |
25999347 |
We demonstrated here that phosphorylation and dephosphorylation of LSD1 at S131 and S137 was mediated by casein kinase 2 (CK2) and wild-type p53-induced phosphatase 1 (WIP1), respectively. LSD1, RNF168 and 53BP1 interacted with each other directly. CK2-mediated phosphorylation of LSD1 exhibited no impact on its interaction with 53BP1, but promoted its interaction with RNF168 and RNF168-dependent 53BP1 ubiquitination and subsequent recruitment to the DNA damage sites. |
|
Publications: |
2 |
Organism: |
Homo Sapiens |
+ |
PPM1D | down-regulates activity
dephosphorylation
|
KDM1A |
0.478 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-276904 |
Ser131 |
DESLANLsEDEYYSE |
Homo sapiens |
HEK-293T Cell |
pmid |
sentence |
25999347 |
We demonstrated here that phosphorylation and dephosphorylation of LSD1 at S131 and S137 was mediated by casein kinase 2 (CK2) and wild-type p53-induced phosphatase 1 (WIP1), respectively. LSD1, RNF168 and 53BP1 interacted with each other directly. CK2-mediated phosphorylation of LSD1 exhibited no impact on its interaction with 53BP1, but promoted its interaction with RNF168 and RNF168-dependent 53BP1 ubiquitination and subsequent recruitment to the DNA damage sites. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-276905 |
Ser137 |
LSEDEYYsEEERNAK |
Homo sapiens |
HEK-293T Cell |
pmid |
sentence |
25999347 |
We demonstrated here that phosphorylation and dephosphorylation of LSD1 at S131 and S137 was mediated by casein kinase 2 (CK2) and wild-type p53-induced phosphatase 1 (WIP1), respectively. LSD1, RNF168 and 53BP1 interacted with each other directly. CK2-mediated phosphorylation of LSD1 exhibited no impact on its interaction with 53BP1, but promoted its interaction with RNF168 and RNF168-dependent 53BP1 ubiquitination and subsequent recruitment to the DNA damage sites. |
|
Publications: |
2 |
Organism: |
Homo Sapiens |
+ |
GTF2I | up-regulates activity
relocalization, binding
|
KDM1A |
0.415 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-268540 |
|
|
Homo sapiens |
|
pmid |
sentence |
21282467 |
Moreover, the inhibitory effect of TFII-I on transcription is mediated by its ability to recruit corepressor complexes, including histone deacetylase 3 (HDAC3) (25, 133), histone H3K4-specific demethylase LSD1 (48), and components of the polycomb repressor complex |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-268539 |
|
|
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
12493763 |
We identify a new family of HDAC1,2-associated complexes containing BHC110. Moreover, we define the polypeptide composition of a novel member of this family containing the candidate gene for X-linked mental retardation XFIM and the initiator-binding protein TFII-I. |
|
Publications: |
2 |
Organism: |
Homo Sapiens |
+ |
RCOR1 | up-regulates activity
binding
|
KDM1A |
0.954 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-264506 |
|
|
in vitro |
|
pmid |
sentence |
16140033 |
CoREST protects LSD1 from proteasomal degradation and also plays an indispensable role in LSD1-mediated demethylation of nucleosomal substrates in vitro. in contrast to CoREST, which is a positive regulator of LSD1 activity, the in vitro evidence presented above suggests that BHC80 may function to inhibit LSD1 activity. |
|
Publications: |
1 |
Organism: |
In Vitro |
+ |
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 |
+ |
KDM1A | form complex
binding
|
BHC complex |
0.796 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-264501 |
|
|
Homo sapiens |
HeLa Cell, HEK-293 Cell |
pmid |
sentence |
15325272 |
BRAF–HDAC complex (BHC) consisting of six subunit proteins, BRAF35, BHC80, BHC110, HDAC1, HDAC2, and CoREST, has been purified from HeLa and HEK293 cells |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ASXL3 | down-regulates activity
binding
|
KDM1A |
0.27 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-266764 |
|
|
Homo sapiens |
|
pmid |
sentence |
25450400 |
Here, we showed that ASXL3 interacts with HP1α and LSD1, leading to transcriptional repression. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
PHF21A | down-regulates activity
binding
|
KDM1A |
0.704 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-264505 |
|
|
in vitro |
|
pmid |
sentence |
16140033 |
BHC80 Inhibits LSD1 Demethylase Activity In Vitro. in contrast to CoREST, which is a positive regulator of LSD1 activity, the in vitro evidence presented above suggests that BHC80 may function to inhibit LSD1 activity. |
|
Publications: |
1 |
Organism: |
In Vitro |
+ |
KDM4C | up-regulates activity
binding
|
KDM1A |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-263880 |
|
|
Homo sapiens |
Prostate Cancer Cell Line |
pmid |
sentence |
29207681 |
JMJD2C was found to be co-localized with AR and LSD1 in the epithelium of prostate carcinoma and normal prostate cells. For the detailed mechanism, JMJD2C, AR and LSD1 assembled on the chromatin to remove the methyl groups from mono-, di- and trimethylated H3K9. Importantly, JMJD2C specifically removed the demethylation of the trimethyl H3K9 marks and modulated the transcriptional activity of AR. Moreover, JMJD2C cooperated with LSD1 and activated AR-mediated gene expression via decreasing H3K9me3 at the promoter of AR targeting genes KLK2 and PSA. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
HIF1A | down-regulates quantity by repression
transcriptional regulation
|
KDM1A |
0.268 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-271573 |
|
|
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 |
+ |
KDM1A | down-regulates
|
Epigenetic_regulation |
0.7 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-268728 |
|
|
Homo sapiens |
|
pmid |
sentence |
28720390 |
The Lysine-specific demethylase 1, KDM1A/LSD1, plays a central role in the regulation of Pol II transcription through the removal of the activation mark (mono- and dimethyl lysine 4 of histone H3). LSD1 is often deregulated in human cancers, and it is frequently overexpressed in human solid cancers and leukemia. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
KDM1A | form complex
binding
|
CoREST-HDAC complex |
0.74 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-222121 |
|
|
Homo sapiens |
HeLa Cell |
pmid |
sentence |
11171972 |
Here we describe the components of a histone deacetylase (HDAC) complex that we term the CoREST-HDAC complex. CoREST Is a Component of an HDAC1/2 Complex. p40 is a Sox-like protein, p110b contains homology to polyamine oxidases, p110a is ZNF217, an eight-zinc finger protein, and p80 is a hypothetical protein of unknown function. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
EPAS1 | down-regulates quantity by repression
transcriptional regulation
|
KDM1A |
0.283 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-271588 |
|
|
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 |
+ |
BRMS1 | up-regulates activity
binding
|
KDM1A |
0.26 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-266409 |
|
|
Homo sapiens |
MCF-7 Cell |
pmid |
sentence |
30416854 |
Our results have showed that BRMS1 together with LSD1 are required for inhibition of breast cancer cell migration and invasion. Collectively, these findings demonstrate that BRMS1 executes transcriptional suppression of breast cancer metastasis by associating with the LSD1 and thus can be targeted for breast cancer therapy. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |