+ |
ERN1 | up-regulates activity
phosphorylation
|
ERN1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-275417 |
Tyr628 |
EHPNVIRyFCTEKDR |
in vitro |
|
pmid |
sentence |
25968568 |
IRE1 transduces the unfolded protein response by splicing XBP1 through its C-terminal cytoplasmic kinase-RNase region. IRE1 autophosphorylation is coupled to RNase activity through formation of a back-to-back dimer, although the conservation of the underlying molecular mechanism is not clear from existing structures. |
|
Publications: |
1 |
Organism: |
In Vitro |
Pathways: | COVID-19 Causal Network, SARS-CoV ER STRESS |
+ |
E | down-regulates activity
|
ERN1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-260347 |
|
|
Chlorocebus aethiops |
Vero Cell |
pmid |
sentence |
22028656 |
SARS-CoV E protein down-regulated the signaling pathway inositol-requiring enzyme 1 (IRE-1) of the unfolded protein response, but not the PKR-like ER kinase (PERK) or activating transcription factor 6 (ATF-6) pathways, and reduced cell apoptosis. |
|
Publications: |
1 |
Organism: |
Chlorocebus Aethiops |
Pathways: | COVID-19 Causal Network, SARS-CoV ER STRESS |
+ |
PPM1L | up-regulates activity
dephosphorylation
|
ERN1 |
0.315 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-277074 |
|
|
Homo sapiens |
|
pmid |
sentence |
24327956 |
Overall, our study establishes that PP2Ce mediated IRE1 regulation in ER stress signaling is a potentially important molecular basis for its genetic contribution to metabolic syndrome.Lin et al. [36] have reported that different durations and composition of ER stress signaling pathways can dictate cell fate and the balance between survival and death.|Recombinant wildtype PP2Ce, but not a phosphatase-dead mutant (PP2Ce-D302A), effectively dephosphorylated the phosphor-Ser724 site of IRE1\u03b1 protein (p-IRE1\u03b1) (A). |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
HSPA5 | down-regulates activity
binding
|
ERN1 |
0.815 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-260176 |
|
|
Homo sapiens |
|
pmid |
sentence |
31226023 |
Besides being activated like PERK via dissociation of GRP78, IRE1 is also activated by direct binding of the unfolded protein to its N-terminal luminal domain |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | COVID-19 Causal Network, SARS-CoV ER STRESS |
+ |
PDIA6 | down-regulates activity
|
ERN1 |
0.322 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-256536 |
|
|
Mus musculus |
NIH-3T3 Cell |
pmid |
sentence |
24508390 |
A resident ER protein disulfide isomerase, PDIA6, limits the duration of IRE1α activity by direct binding to cysteine148 in the luminal domain of the sensor, |
|
Publications: |
1 |
Organism: |
Mus Musculus |
+ |
P4HB | down-regulates activity
binding
|
ERN1 |
0.44 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-275573 |
|
|
|
|
pmid |
sentence |
32149426 |
The secretory pathway kinase Fam20C phosphorylates Ser357 of PDI and responds rapidly to various ER stressors. Phosphorylation of Ser357 induces an open conformation of PDI and turns it from a "foldase" into a "holdase", which is critical for preventing protein misfolding in the ER. Phosphorylated PDI also binds to the lumenal domain of IRE1α, a major UPR signal transducer, and attenuates excessive IRE1α activity. |
|
Publications: |
1 |
+ |
ERN1 | up-regulates quantity by expression
post transcriptional regulation
|
XBP1 (isoform 2) |
0.638 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-260183 |
|
|
Homo sapiens |
|
pmid |
sentence |
31226023 |
Upon activation by oligomerization and autophosphorylation, the cytosolic RNase domain of IRE1 mediates an unconventional splicing of the mRNA of X-box-binding protein 1 (XBP1). The spliced and frameshifted transcript encodes XBP1S, a bZIP transcription factor inducing the expression of numerous UPR effector genes that enhance ER folding capacity. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | COVID-19 Causal Network, SARS-CoV ER STRESS |
+ |
ERN1 | up-regulates activity
binding
|
TRAF2 |
0.667 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-262790 |
|
|
Mus musculus |
|
pmid |
sentence |
18519638 |
Activated IRE1 has been demonstrated to recruit TRAF2 and ASK1 on the ER membrane and thus to activate ASK1|ASK1 was found to associate with IRE1 only in the presence of TRAF2 and SOD1mut (Fig. 4B), suggesting that SOD1mut induces formation of an IRE1–TRAF2–ASK1 complex on the ER membrane and thus activates ASK1 by triggering ER stress-induced IRE1 activation. |
|
Publications: |
1 |
Organism: |
Mus Musculus |
+ |
ERN1 | up-regulates quantity by expression
transcriptional regulation
|
OS9 |
0.435 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-261063 |
|
|
Homo sapiens |
|
pmid |
sentence |
18417469 |
Here we characterize the function in ER quality control of two proteins derived from alternative splicing of the OS-9 gene. OS-9.1 and OS-9.2 are ubiquitously expressed in human tissues and are amplified in tumors. They are transcriptionally induced upon activation of the Ire1/Xbp1 ER-stress pathway. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ERN1 | up-regulates
|
JUN |
0.394 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-253146 |
|
|
Homo sapiens |
Neuro-2a Cell |
pmid |
sentence |
18065414 |
The induction of MTHFR was also observed after overexpression of inositol-requiring enzyme-1 (IRE1) and was inhibited by a dominant-negative mutant of IRE1. Because IRE1 triggers c-Jun signaling, we examined the possible involvement of c-Jun in up-regulation of MTHFR. Transfection of c-Jun and two activators of c-Jun (LiCl and sodium valproate) increased MTHFR expression |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
DAB2IP | up-regulates activity
binding
|
ERN1 |
0.376 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-254749 |
|
|
Homo sapiens |
Endothelial Cell |
pmid |
sentence |
27858941 |
DAB2IP binds IRE1α, and was shown to be required for activation of this signaling cascade in endothelial cells. IRE1α can trigger pro-apoptotic JNK signaling through recruitment of the TRAF2–ASK1 complex. DAB2IP facilitates IRE1α activation, and participates in a signaling complex required to induce TRAF2-dependent ASK1 activation and JNK phosphorylation. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ERN1 | down-regulates activity
|
JNK |
0.323 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-260177 |
|
|
Homo sapiens |
|
pmid |
sentence |
31226023 |
The kinase activity of IRE1 also activates a signaling cascade that ultimately activates c-Jun N-terminal kinase (JNK) |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | COVID-19 Causal Network, SARS-CoV ER STRESS |
+ |
ER stress | up-regulates
|
ERN1 |
0.7 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-253145 |
|
|
Homo sapiens |
|
pmid |
sentence |
18065414 |
Our findings suggest that MTHFR is up-regulated by ER stress and that this effect is mediated by IRE1 and c-Jun. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | COVID-19 Causal Network |
+ |
Unfolded_Proteins | up-regulates
|
ERN1 |
0.7 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-260175 |
|
|
Homo sapiens |
|
pmid |
sentence |
31226023 |
Besides being activated like PERK via dissociation of GRP78, IRE1 is also activated by direct binding of the unfolded protein to its N-terminal luminal domain |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | COVID-19 Causal Network, SARS-CoV ER STRESS |
+ |
SOD1 | up-regulates activity
binding
|
ERN1 |
0.322 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-262786 |
|
|
Mus musculus |
NSC-34 Cell |
pmid |
sentence |
18519638 |
SOD1mut-induced ER stress |we first examined whether SOD1mut induces ER stress in NSC34 motor neurons, as assessed by band-shift analyses of the ER transmembrane kinase receptors IRE1 and PERK. Adenovirus (Ad)-mediated expression of ALS-linked SOD1mut (SOD1G93A) was detectable within 48 h of infection (Supplemental Fig. S1A). SOD1mut (SOD1A4V, SOD1G85R, and SOD1G93A) but not wild-type SOD1 (SOD1wt) activated IRE1 and PERK |
|
Publications: |
1 |
Organism: |
Mus Musculus |