+ |
EIF2AK3 | down-regulates activity
phosphorylation
|
EIF2S1 |
0.757 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-260874 |
Ser52 |
MILLSELsRRRIRSI |
Homo sapiens |
|
pmid |
sentence |
25660019 |
We now demonstrate a major role for Rheb in inhibiting protein synthesis by enhancing the phosphorylation of eIF2α by protein kinase-like ER kinase (PERK). |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-246153 |
Ser52 |
MILLSELsRRRIRSI |
Homo sapiens |
|
pmid |
sentence |
30070006 |
The integrated stress response is characterized by the phosphorylation of eukaryotic initiation factor-2α (eIF2α) on serine 51 by one out of four specific kinases (EIF2AK1 to 4) |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-260165 |
|
|
Homo sapiens |
|
pmid |
sentence |
31226023 |
Activated PERK phosphorylates the α subunit of eukaryotic initiation factor 2 (eIF2α), which inhibits the conversion of inactive GDP-bound eIF2α back to the active GTP-bound form, thereby suppressing translation initiation. |
|
Publications: |
3 |
Organism: |
Homo Sapiens |
Pathways: | COVID-19 Causal Network, SARS-CoV ER STRESS |
+ |
EIF2AK3 | down-regulates
phosphorylation
|
EIF2S1 |
0.757 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-159160 |
Ser52 |
MILLSELsRRRIRSI |
Homo sapiens |
|
pmid |
sentence |
17998206 |
The endoplasmic reticulum (er)-resident protein kinase perk attenuates protein synthesis in response to er stress through the phosphorylation of translation initiation factor eif2_ at serine 51 / a modification that blocks initiation |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | COVID-19 Causal Network, SARS-CoV ER STRESS |
+ |
JAK1 | up-regulates activity
phosphorylation
|
EIF2AK3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-276676 |
Tyr585 |
NDIKNSGyISRYLTD |
Mus musculus |
Astrocyte |
pmid |
sentence |
25113558 |
JAK1 interacts with and phosphorylates PERK. PERK-dependent activation of JAK1 and STAT3 contributes to endoplasmic reticulum stress-induced inflammation. Similarly, PERK is associated with and phosphorylated by JAK1 at Y585 and Y619 (and possibly other JAKs) during ER stress, resulting in PERK- and JAK1-dependent activation of STAT3. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-276677 |
Tyr619 |
NKVDDCNyAIKRIRL |
Mus musculus |
Astrocyte |
pmid |
sentence |
25113558 |
JAK1 interacts with and phosphorylates PERK. PERK-dependent activation of JAK1 and STAT3 contributes to endoplasmic reticulum stress-induced inflammation. Similarly, PERK is associated with and phosphorylated by JAK1 at Y585 and Y619 (and possibly other JAKs) during ER stress, resulting in PERK- and JAK1-dependent activation of STAT3. |
|
Publications: |
2 |
Organism: |
Mus Musculus |
Pathways: | COVID-19 Causal Network |
+ |
EIF2AK3 | up-regulates
phosphorylation
|
EIF2AK3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-159156 |
Tyr619 |
NKVDDCNyAIKRIRL |
Homo sapiens |
|
pmid |
sentence |
17998206 |
We show that perk is capable of autophosphorylating on tyrosine residues in vitro and in vivo. We further show that tyrosine 615, which is embedded in a highly conserved region of the kinase domain of perk, is essential for autocatalytic activity. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | COVID-19 Causal Network, SARS-CoV ER STRESS |
+ |
HSPA5 | down-regulates activity
binding
|
EIF2AK3 |
0.715 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-260164 |
|
|
Homo sapiens |
|
pmid |
sentence |
31226023 |
In the stressed ER, protein chaperone GRP78 binds to unfolded proteins and dissociates from the luminal domain of PERK, leading to oligomerization and activation of PERK by autophosphorylation. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | COVID-19 Causal Network, SARS-CoV ER STRESS |
+ |
SOD1 | up-regulates activity
binding
|
EIF2AK3 |
0.278 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-262787 |
|
|
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 |
+ |
PTPN1 | down-regulates activity
dephosphorylation
|
EIF2AK3 |
0.271 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-277051 |
|
|
Homo sapiens |
|
pmid |
sentence |
22169477 |
Finally, we demonstrated that wild-type PTP1B directly dephosphorylated myc-tagged PERK that had been isolated from tunicamycin-treated HEK293T cells by immunoprecipitation ( xref ).|The ability of PTP1B to dephosphorylate Tyr619 and inactivate PERK is fine tuned by the production of H 2 S by CSE in response to ER stress. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
S | up-regulates activity
|
EIF2AK3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-260439 |
|
|
Homo sapiens |
|
pmid |
sentence |
16940539 |
SARS-CoV S protein specifically activated PERK but did not significantly affect IRE1/XBP1 or ATF6. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | COVID-19 Causal Network, SARS-CoV ER STRESS |
+ |
DNAJC3 | down-regulates activity
binding
|
EIF2AK3 |
0.603 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-246201 |
|
|
Homo sapiens |
HeLa Cell |
pmid |
sentence |
25329545 |
The protein p58IPK {also known asDnaJ3C [DnaJ heat-shock protein (hsp) 40 homologue, subfamily C, member 3]} is known to inhibit the eIF2 kinases PKR (dsRNA-dependent protein kinase/eIF2 kinase 2) and PERK |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
PDIA6 | down-regulates activity
|
EIF2AK3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-256537 |
|
|
Rattus norvegicus |
INS-1 823/13 Cell |
pmid |
sentence |
26487694 |
Protein disulfide isomerase A6 (PDIA6) interacts with protein kinase RNA-like endoplasmic reticulum kinase (PERK) and inositol requiring enzyme (IRE)-1 and inhibits their unfolded protein response signaling. |
|
Publications: |
1 |
Organism: |
Rattus Norvegicus |
+ |
RHEB | down-regulates activity
binding
|
EIF2AK3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-260873 |
|
|
in vitro |
|
pmid |
sentence |
25660019 |
Rheb GTPase directly binds and activates PERK in vitro |
|
Publications: |
1 |
Organism: |
In Vitro |