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IID00443
UniprotP19525
ProteinInterferon-induced, double-stranded RNA-activated protein kinase
GeneEIF2AK2
OrganismHomo sapiens
Sequence LLPS PhaSepDB
PhaSePro
LLPSDB
DrLLPS
Network xml rdf
Structure
Experiment
  :order   disorder   conflict   PDB cluster   ProS   Pfam Domain   SEG
551
 order/disorder by at least rule
     disorder by at least rule
     order by at least rule
 order/disorder by majority rule
Seq 1-170 Monomer :
 Evidence NMR 1qu6 A Reference
       Region 1qu6 A 1-170 order
       Region 1qu6 A 5-6 high_rmsd
       Region 1qu6 A 33-38 high_rmsd
       Region 1qu6 A 79-100 high_rmsd
       Region 1qu6 A 107-113 high_rmsd
       Region 1qu6 A 123-130 high_rmsd
       Region 1qu6 A 167-170 high_rmsd
Seq 254-551 Monomer :
 Evidence X-RAY 3uiu B Reference
       Region 3uiu B 254-336 order
       Region 3uiu B 337-354 disorder
       Region 3uiu B 355-439 order
       Region 3uiu B 440-450 disorder
       Region 3uiu B 451-460 order
       Region 3uiu B 461-464 disorder
       Region 3uiu B 465-541 order
       Region 3uiu B 542-551 disorder
 Evidence X-RAY 3uiu A Reference
       Region 3uiu A 254-336 order
       Region 3uiu A 337-354 disorder
       Region 3uiu A 355-439 order
       Region 3uiu A 440-450 disorder
       Region 3uiu A 451-460 order
       Region 3uiu A 461-464 disorder
       Region 3uiu A 465-541 order
       Region 3uiu A 542-551 disorder
Seq 258-337,351-550 Hetero tetramer : IID50184Complex
 Evidence X-RAY 2a1a B Reference
       Region 2a1a B 258-337 order
       Region 2a1a B 351-354 disorder
       Region 2a1a B 355-541 order
       Region 2a1a B 542-550 disorder
Seq 258-337,351-550 Hetero trimer : IID50184Complex
 Evidence X-RAY 2a19 C Reference
       Region 2a19 C 258-337 order
       Region 2a19 C 351-357 disorder
       Region 2a19 C 358-374 order
       Region 2a19 C 375-389 disorder
       Region 2a19 C 390-436 order
       Region 2a19 C 437-465 disorder
       Region 2a19 C 466-482 order
       Region 2a19 C 483-500 disorder
       Region 2a19 C 501-541 order
       Region 2a19 C 542-550 disorder
 Evidence X-RAY 2a19 B Reference
       Region 2a19 B 258-333 order
       Region 2a19 B 334-337 disorder
       Region 2a19 B 351-355 disorder
       Region 2a19 B 356-541 order
       Region 2a19 B 542-550 disorder
Seqphosphorylation
    542-542 Phosphoserine
    451-451 Phosphothreonine; by autocatalysis
    456-456 Phosphoserine
    293-293 Phosphotyrosine; by autocatalysis
    446-446 Phosphothreonine; by autocatalysis
    258-258 Phosphothreonine; by autocatalysis
    255-255 Phosphothreonine; by autocatalysis
    242-242 Phosphoserine; by autocatalysis
    162-162 Phosphotyrosine; by autocatalysis
    101-101 Phosphotyrosine; by autocatalysis
    90-90 Phosphothreonine; by autocatalysis
    89-89 Phosphothreonine; by autocatalysis
    88-88 Phosphothreonine; by autocatalysis
    83-83 Phosphoserine
Seqacetylation
    2-2 N-acetylalanine
 
Prediction
NeProc
Disorder 1-5,80-97,170-260,333-356,545-551
Order 6-79,98-169,261-332,357-544
ProS 170-182,229-235,240-249,256-260,333-356,545-551
AlphaFold
Disorder 1-8,80-99,122-129,170-254,337-355,441-444,447-450,543-551
Order 9-79,100-121,130-169,255-336,356-440,445-446,451-542
Pfam Hmmer
PF00035 10-75 5e-19
PF00035 101-165 1.2e-14
PF00069 267-536 5.7e-60
SEG 60-71 ,150-164 ,216-235 ,471-482
Function
Function in SwissProt
IFN-induced dsRNA-dependent serine/threonine-protein kinase that phosphorylates the alpha subunit of eukaryotic translation initiation factor 2 (EIF2S1/eIF-2-alpha) and plays a key role in the innate immune response to viral infection (PubMed:18835251, PubMed:19507191, PubMed:19189853, PubMed:21123651, PubMed:21072047, PubMed:22948139, PubMed:23229543, PubMed:22381929). Inhibits viral replication via the integrated stress response (ISR): EIF2S1/eIF-2-alpha phosphorylation in response to viral infection converts EIF2S1/eIF-2-alpha in a global protein synthesis inhibitor, resulting to a shutdown of cellular and viral protein synthesis, while concomitantly initiating the preferential translation of ISR-specific mRNAs, such as the transcriptional activator ATF4 (PubMed:19189853, PubMed:21123651, PubMed:22948139, PubMed:23229543). Exerts its antiviral activity on a wide range of DNA and RNA viruses including hepatitis C virus (HCV), hepatitis B virus (HBV), measles virus (MV) and herpes simplex virus 1 (HHV-1) (PubMed:11836380, PubMed:19189853, PubMed:20171114, PubMed:19840259, PubMed:21710204, PubMed:23115276, PubMed:23399035). Also involved in the regulation of signal transduction, apoptosis, cell proliferation and differentiation: phosphorylates other substrates including p53/TP53, PPP2R5A, DHX9, ILF3, IRS1 and the HHV-1 viral protein US11 (PubMed:11836380, PubMed:22214662, PubMed:19229320). In addition to serine/threonine-protein kinase activity, also has tyrosine-protein kinase activity and phosphorylates CDK1 at 'Tyr-4' upon DNA damage, facilitating its ubiquitination and proteosomal degradation (PubMed:20395957). Either as an adapter protein and/or via its kinase activity, can regulate various signaling pathways (p38 MAP kinase, NF-kappa-B and insulin signaling pathways) and transcription factors (JUN, STAT1, STAT3, IRF1, ATF3) involved in the expression of genes encoding proinflammatory cytokines and IFNs (PubMed:22948139, PubMed:23084476, PubMed:23372823). Activates the NF-kappa-B pathway via interaction with IKBKB and TRAF family of proteins and activates the p38 MAP kinase pathway via interaction with MAP2K6 (PubMed:10848580, PubMed:15121867, PubMed:15229216). Can act as both a positive and negative regulator of the insulin signaling pathway (ISP) (PubMed:20685959). Negatively regulates ISP by inducing the inhibitory phosphorylation of insulin receptor substrate 1 (IRS1) at 'Ser-312' and positively regulates ISP via phosphorylation of PPP2R5A which activates FOXO1, which in turn up-regulates the expression of insulin receptor substrate 2 (IRS2) (PubMed:20685959). Can regulate NLRP3 inflammasome assembly and the activation of NLRP3, NLRP1, AIM2 and NLRC4 inflammasomes (PubMed:22801494). Plays a role in the regulation of the cytoskeleton by binding to gelsolin (GSN), sequestering the protein in an inactive conformation away from actin (By similarity).