+ |
PDHX | down-regulates activity
binding
|
PAX6 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-254903 |
|
|
Homo sapiens |
BHK-21 Cell |
pmid |
sentence |
12783165 |
In the heterologous cell line BHK-21, Pdx1 inhibited by 60 to 80% the activation of the alpha-cell specific element G1 conferred by Pax-6 and/or Cdx-2/3. Although Pdx1 could bind three AT-rich motifs within G1, two of which are binding sites for Pax-6 and Cdx-2/3, the affinity of Pdx1 for G1 was much lower as compared to Pax-6. In addition, Pdx1 inhibited Pax-6 mediated activation through G3, to which Pdx1 was unable to bind. Moreover, a mutation impairing DNA binding of Pdx1 had no effect on its inhibition on Cdx-2/3. Since Pdx1 interacts directly with Pax-6 and Cdx-2/3 forming heterodimers, we suggest that Pdx1 inhibits glucagon gene transcription through protein to protein interactions with Pax-6 and Cdx-2/3. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
PDHX | down-regulates quantity by repression
transcriptional regulation
|
GCG |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-254901 |
|
|
Homo sapiens |
Glucagonoma Cell |
pmid |
sentence |
12783165 |
In glucagonoma cells transduced with a Pdx1-encoding lentiviral vector, insulin gene expression was induced while glucagon mRNA levels were reduced by 50 to 60%. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
PDHX | up-regulates quantity by expression
transcriptional regulation
|
INS |
0.293 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-254902 |
|
|
Homo sapiens |
Glucagonoma Cell |
pmid |
sentence |
12783165 |
In glucagonoma cells transduced with a Pdx1-encoding lentiviral vector, insulin gene expression was induced while glucagon mRNA levels were reduced by 50 to 60%. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
PDHX | down-regulates activity
binding
|
CDX2 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-254904 |
|
|
Homo sapiens |
BHK-21 Cell |
pmid |
sentence |
12783165 |
In the heterologous cell line BHK-21, Pdx1 inhibited by 60 to 80% the activation of the alpha-cell specific element G1 conferred by Pax-6 and/or Cdx-2/3. Although Pdx1 could bind three AT-rich motifs within G1, two of which are binding sites for Pax-6 and Cdx-2/3, the affinity of Pdx1 for G1 was much lower as compared to Pax-6. In addition, Pdx1 inhibited Pax-6 mediated activation through G3, to which Pdx1 was unable to bind. Moreover, a mutation impairing DNA binding of Pdx1 had no effect on its inhibition on Cdx-2/3. Since Pdx1 interacts directly with Pax-6 and Cdx-2/3 forming heterodimers, we suggest that Pdx1 inhibits glucagon gene transcription through protein to protein interactions with Pax-6 and Cdx-2/3. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
PDHX | form complex
binding
|
PDH |
0.809 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-266543 |
|
|
Homo sapiens |
|
pmid |
sentence |
20160912 |
The human (h) pyruvate dehydrogenase complex (hPDC) consists of multiple copies of several components: pyruvate dehydrogenase (E1), dihydrolipoamide acetyltransferase (E2), dihydrolipoamide dehydrogenase (E3), E3-binding protein (BP), and specific kinases and phosphatases. Mammalian PDC has a well organized structure with an icosahedral symmetry of the central E2/BP core to which the other component proteins bind non-covalently. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |