Original Literature | Model OverView |
---|---|
Publication
Title
Type I interferon receptors: biochemistry and biological functions.
Affiliation
Centre for Functional Genomics and Human Disease, Monash Institute of MedicalResearch, Monash University, Clayton, Victoria 3168, Australia.
Abstract
PMID
17502368
|
Entity
IFNAR1
--
MO000007545
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m898
10
infinite
0
InterPro | IPR003961 |
TRANSPATH | MO000007545 |
--
IFNAR2
--
MO000007548
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m901
10
infinite
0
InterPro | IPR000282 |
TRANSPATH | MO000007548 |
--
STAT2
--
MO000013120
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m1358
10
infinite
0
InterPro | IPR008967 |
TRANSPATH | MO000013120 |
--
IFNbeta
--
MO000016660
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m1636
10
infinite
0
InterPro | IPR000471 |
TRANSPATH | MO000016660 |
--
SOCS-1
--
MO000017004
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m1906
10
infinite
0
InterPro | IPR001496 |
TRANSPATH | MO000017004 |
--
IFNAR1:Tyk2
--
MO000019457
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m4019
10
infinite
0
TRANSPATH | MO000019457 |
--
--
e1
cso30:c:EntityBiologicalCompartment
cso30:i:CC_PlasmaMembrane
--
--
--
csml-variable:Double
m1
0
infinite
0
--
degradants
--
e10
cso30:c:EntityBiological
cso30:i:CC_Cytoplasm
--
--
csml-variable:Double
m10
0
infinite
0
--
IFN-alpha
--
e11
cso30:c:Protein
cso30:i:CC_Cytosol
--
--
csml-variable:Double
m11
0
infinite
0
--
IFNAR2:Jak1
--
e12
cso30:c:Complex
cso30:i:CC_Cytosol
--
csml-variable:Double
m12
0
infinite
0
--
IFN:IFNAR1{p}:Tyk2{p}:SOCS-1
--
e13
cso30:c:Complex
cso30:i:CC_Extracellular
--
csml-variable:Double
m13
0
infinite
0
--
IFN:IFNAR2c{p}:Jak1{p}:SOCS-1
--
e14
cso30:c:Complex
cso30:i:CC_Extracellular
--
csml-variable:Double
m14
0
infinite
0
--
--
e2
cso30:c:EntityBiologicalCompartment
cso30:i:CC_PlasmaMembrane_ExternalSideOfPlasmaMembrane_
--
--
--
csml-variable:Double
m2
0
infinite
0
--
UBP43
--
e20
cso30:c:Protein
cso30:i:CC_Cytosol
--
csml-variable:Double
m20
0
infinite
0
--
IFNAR1:UBP43
--
e21
cso30:c:Complex
cso30:i:CC_Cytosol
--
--
csml-variable:Double
m21
0
infinite
0
--
IFNAR1:SHP
--
e23
cso30:c:Complex
cso30:i:CC_Cytosol
--
--
csml-variable:Double
m23
0
infinite
0
--
SHP
--
e24
cso30:c:Protein
cso30:i:CC_Cytosol
--
csml-variable:Double
m24
0
infinite
0
--
IFNAR2:UBP43
--
e25
cso30:c:Complex
cso30:i:CC_Cytosol
--
csml-variable:Double
m25
0
infinite
0
--
IFNAR2:SHP
--
e26
cso30:c:Complex
cso30:i:CC_Cytosol
--
--
csml-variable:Double
m26
0
infinite
0
--
E3 ubiquitin ligase
--
e29
cso30:c:Protein
cso30:i:CC_Cytosol
--
csml-variable:Double
m29
0
infinite
0
--
--
e3
cso30:c:EntityBiologicalCompartment
cso30:i:CC_PlasmaMembrane_IntegralToPlasmaMembrane_
--
--
--
csml-variable:Double
m3
0
infinite
0
--
IFNAR1:Tyk2:E3 ubiquitin ligase
--
e30
cso30:c:Complex
cso30:i:CC_Cytosol
--
csml-variable:Double
m30
0
infinite
0
--
IFNAR1{ub}:Tyk2:E3 ubiquitin ligase
--
e31
cso30:c:Complex
cso30:i:CC_Cytosol
--
csml-variable:Double
m31
0
infinite
0
--
sIFNAR2a:IFN-alpha
--
e33
cso30:c:Complex
cso30:i:CC_Cytoplasm
--
--
csml-variable:Double
m33
0
infinite
0
--
sIFNAR2a:IFNbeta
--
e34
cso30:c:Complex
cso30:i:CC_Cytoplasm
--
--
csml-variable:Double
m34
0
infinite
0
--
IFN
--
e35
cso30:c:Protein
cso30:i:CC_Extracellular
--
csml-variable:Double
m35
0
infinite
0
--
IFN:IFNAR1:Tyk2
--
e36
cso30:c:Complex
cso30:i:CC_Extracellular
--
csml-variable:Double
m36
0
infinite
0
--
IFNAR2c:Jak1
--
e37
cso30:c:Complex
cso30:i:CC_Extracellular
--
--
csml-variable:Double
m37
0
infinite
0
--
IFN:IFNAR2c:Jak1
--
e38
cso30:c:Complex
cso30:i:CC_Extracellular
--
csml-variable:Double
m38
0
infinite
0
--
IFN:IFNAR1{p}:Tyk2{p}
--
e39
cso30:c:Complex
cso30:i:CC_Extracellular
--
csml-variable:Double
m39
0
infinite
0
--
--
e4
cso30:c:EntityBiologicalCompartment
cso30:i:CC_PlasmaMembrane_InternalSideOfPlasmaMembrane_
--
--
--
csml-variable:Double
m4
0
infinite
0
--
IFN:IFNAR2c{p}:Jak1{p}
--
e40
cso30:c:Complex
cso30:i:CC_Extracellular
--
csml-variable:Double
m40
0
infinite
0
--
IFN:IFNAR1{p}:Tyk2{p}:STAT1
--
e41
cso30:c:Complex
cso30:i:CC_Extracellular
--
csml-variable:Double
m41
0
infinite
0
--
IFN:IFNAR2c{p}:Jak1{p}:STAT2
--
e42
cso30:c:Complex
cso30:i:CC_Extracellular
--
csml-variable:Double
m42
0
infinite
0
--
IFN:IFNAR1{p}:Tyk2{p}:STAT1{p}
--
e43
cso30:c:Complex
cso30:i:CC_Extracellular
--
csml-variable:Double
m43
0
infinite
0
--
IFN:IFNAR2c{p}:Jak1{p}:STAT2{p}
--
e44
cso30:c:Complex
cso30:i:CC_Extracellular
--
csml-variable:Double
m44
0
infinite
0
--
IFN:IFNAR1{p}:Tyk2{p}:STAT1{p}(2)
--
e45
cso30:c:Complex
cso30:i:CC_Cytoplasm
--
csml-variable:Double
m45
0
infinite
0
--
IFN:IFNAR2c{p}:Jak1{p}:STAT2{p}(2)
--
e46
cso30:c:Complex
cso30:i:CC_Cytoplasm
--
csml-variable:Double
m46
0
infinite
0
--
IFN:IFNAR2c{p}:IFNAR1:Tyk2:Jak1{p}:STAT2{p}:STAT1{p}
--
e47
cso30:c:Complex
cso30:i:CC_Cytoplasm
--
csml-variable:Double
m47
0
infinite
0
--
STAT1{p}:STAT1{p}
--
e48
cso30:c:Protein
cso30:i:CC_Cytoplasm
--
csml-variable:Double
m48
0
infinite
0
--
STAT2{p}:STAT2{p}
--
e49
cso30:c:Protein
cso30:i:CC_Cytoplasm
--
csml-variable:Double
m49
0
infinite
0
--
IFN:IFNAR1{p}:Tyk2{p}:STAT2
--
e5
cso30:c:Complex
cso30:i:CC_Extracellular
--
--
csml-variable:Double
m5
0
infinite
0
--
--
e50
cso30:c:EntityBiologicalCompartment
cso30:i:CC_NuclearEnvelopeLumen
--
--
--
csml-variable:Double
m50
0
infinite
0
--
--
e51
cso30:c:EntityBiologicalCompartment
cso30:i:CC_NuclearPore
--
--
--
csml-variable:Double
m51
0
infinite
0
--
--
e52
cso30:c:EntityBiologicalCompartment
cso30:i:CC_NuclearInnerMembrane
--
--
--
csml-variable:Double
m52
0
infinite
0
--
--
e53
cso30:c:EntityBiologicalCompartment
cso30:i:CC_NuclearLumen
--
--
--
csml-variable:Double
m53
0
infinite
0
--
--
e54
cso30:c:EntityBiologicalCompartment
cso30:i:CC_NuclearOuterMembrane
--
--
--
csml-variable:Double
m54
0
infinite
0
--
--
e55
cso30:c:EntityBiologicalCompartment
cso30:i:CC_Nucleus
--
--
--
csml-variable:Double
m55
0
infinite
0
--
--
e56
cso30:c:EntityBiologicalCompartment
cso30:i:CC_Nucleoplasm
--
--
--
csml-variable:Double
m56
0
infinite
0
--
--
e57
cso30:c:EntityBiologicalCompartment
cso30:i:CC_NuclearBody
--
--
--
csml-variable:Double
m57
0
infinite
0
--
--
e58
cso30:c:EntityBiologicalCompartment
cso30:i:CC_Nucleolus
--
--
--
csml-variable:Double
m58
0
infinite
0
--
--
e59
cso30:c:EntityBiologicalCompartment
cso30:i:CC_NuclearEnvelope
--
--
--
csml-variable:Double
m59
0
infinite
0
--
IFNAR2:Jak1:STAT1
--
e6
cso30:c:Complex
cso30:i:CC_Extracellular
--
csml-variable:Double
m6
0
infinite
0
--
--
e60
cso30:c:EntityBiologicalCompartment
cso30:i:CC_Chromatin
--
--
--
csml-variable:Double
m60
0
infinite
0
--
--
e61
cso30:c:EntityBiologicalCompartment
cso30:i:CC_NuclearChromosome
--
--
--
csml-variable:Double
m61
0
infinite
0
--
--
e62
cso30:c:EntityBiologicalCompartment
cso30:i:CC_NuclearCentromere
--
--
--
csml-variable:Double
m62
0
infinite
0
--
STAT1{p}:STAT2{p}
--
e63
cso30:c:Complex
cso30:i:CC_Cytoplasm
--
csml-variable:Double
m63
0
infinite
0
--
STAT1{p}:STAT2{p}
--
e64
cso30:c:Complex
cso30:i:CC_Cytoplasm
--
csml-variable:Double
m64
0
infinite
0
--
STAT1{p}:STAT1{p}
--
e65
cso30:c:Protein
cso30:i:CC_Cytoplasm
--
csml-variable:Double
m65
0
infinite
0
--
STAT2{p}:STAT2{p}
--
e66
cso30:c:Protein
cso30:i:CC_Cytoplasm
--
csml-variable:Double
m66
0
infinite
0
--
IFN gene
--
e67
cso30:c:Dna
cso30:i:CC_Nucleoplasm
--
csml-variable:Double
m67
0
infinite
0
--
STAT1{p}:STAT2{p}:IFN gene
--
e68
cso30:c:Complex
cso30:i:CC_Nucleoplasm
--
csml-variable:Double
m68
0
infinite
0
--
STAT1{p}:STAT1{p}:IFN gene
--
e69
cso30:c:Complex
cso30:i:CC_Nucleoplasm
--
csml-variable:Double
m69
0
infinite
0
--
--
e7
cso30:c:EntityBiologicalCompartment
cso30:i:CC_Cell
--
--
--
csml-variable:Double
m7
0
infinite
0
--
STAT2{p}:STAT2{p}:IFN gene
--
e70
cso30:c:Complex
cso30:i:CC_Nucleoplasm
--
csml-variable:Double
m70
0
infinite
0
--
csml-variable:Double
m71
0
infinite
0
--
IFNA2:IFNAR1
--
e72
cso30:c:Complex
cso30:i:CC_Extracellular
--
--
csml-variable:Double
m72
0
infinite
0
--
IFNA2:IFNAR2
--
e73
cso30:c:Complex
cso30:i:CC_Extracellular
--
--
csml-variable:Double
m73
0
infinite
0
--
IFNAR2:IFNbeta
--
e74
cso30:c:Complex
cso30:i:CC_Cytoplasm
--
--
csml-variable:Double
m74
0
infinite
0
--
Intramembrane proteases
--
e75
cso30:c:Protein
cso30:i:CC_Cytoplasm
--
--
csml-variable:Double
m75
0
infinite
0
--
sIL-6Ralpha
--
e76
cso30:c:Protein
cso30:i:CC_Extracellular
--
csml-variable:Double
m76
0
infinite
0
--
IL-6Ralpha
--
e77
cso30:c:Protein
cso30:i:CC_Extracellular
--
csml-variable:Double
m77
0
infinite
0
--
--
e8
cso30:c:EntityBiologicalCompartment
cso30:i:CC_Cell_WithoutCellWall_
--
--
--
csml-variable:Double
m8
0
infinite
0
--
IFNAR2:Jak1:STAT1:STAT2
--
e9
cso30:c:Complex
cso30:i:CC_PlasmaMembrane_IntegralToPlasmaMembrane_
--
--
csml-variable:Double
m9
0
infinite
0
--
p1
p1
cso30:i:ME_Binding
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c1 : 1
stoichiometry:c2 : 1
stoichiometry:c3 : 1
m132*m898*0.1
nodelay
--
0
PMID: 17502368,8628273,16551269 IFNAR1 is preassociated with Tyk2, , which also stabilizes IFNAR1 cell surface expression levels.
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c36 : 1
stoichiometry:c17 : 1
stoichiometry:c18 : 1
m1906*m39*0.1
nodelay
--
0
PMID: 17502368,16311601,10022928,16710296 Thus, IFNARs also interact with a number of negative regulatory molecules, including SOCS-1 (suppressor of cytokine signaling), UBP43, and SHP , to limit the extent of signaling
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c39 : 1
stoichiometry:c38 : 1
stoichiometry:c40 : 1
m20*m898*0.1
nodelay
--
0
PMID: 17502368,16311601,10022928,16710296 Thus, IFNARs also interact with a number of negative regulatory molecules, including SOCS-1 (suppressor of cytokine signaling), UBP43, and SHP , to limit the extent of signaling
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c42 : 1
stoichiometry:c37 : 1
stoichiometry:c41 : 1
m1906*m40*0.1
nodelay
--
0
PMID: 17502368,16311601,10022928,16710296 Thus, IFNARs also interact with a number of negative regulatory molecules, including SOCS-1 (suppressor of cytokine signaling), UBP43, and SHP , to limit the extent of signaling
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c44 : 1
stoichiometry:c45 : 1
stoichiometry:c46 : 1
m898*m24*0.1
nodelay
--
0
PMID: 17502368,16311601,10022928,16710296 Thus, IFNARs also interact with a number of negative regulatory molecules, including SOCS-1 (suppressor of cytokine signaling), UBP43, and SHP , to limit the extent of signaling
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c47 : 1
stoichiometry:c48 : 1
stoichiometry:c49 : 1
m901*m20*0.1
nodelay
--
0
PMID: 17502368,16311601,10022928,16710296 Thus, IFNARs also interact with a number of negative regulatory molecules, including SOCS-1 (suppressor of cytokine signaling), UBP43, and SHP , to limit the extent of signaling
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c50 : 1
stoichiometry:c51 : 1
stoichiometry:c52 : 1
m901*m24*0.1
nodelay
--
0
PMID: 17502368,16311601,10022928,16710296 Thus, IFNARs also interact with a number of negative regulatory molecules, including SOCS-1 (suppressor of cytokine signaling), UBP43, and SHP , to limit the extent of signaling
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c57 : 1
stoichiometry:c15 : 1
stoichiometry:c58 : 1
m29*m4019*0.1
nodelay
--
0
PMID: 17502368,15337770 Residues within this region are also essential for the recruitment of E3 ubiquitin ligases and ubiquitination and degradation of the receptor
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c59 : 1
stoichiometry:c60 : 1
m30*0.1
nodelay
--
0
PMID: 17502368, 15337770 Residues within this region are also essential for the recruitment of E3 ubiquitin ligases and ubiquitination and degradation of the receptor
p21
p21
cso30:i:ME_UnknownDegradation
cso30:i:CC_Cytoplasm
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c61 : 1
stoichiometry:c62 : 1
stoichiometry:c63 : 1
stoichiometry:c64 : 1
m31*0.1
nodelay
--
0
PMID: 17502368, 15337770 Residues within this region are also essential for the recruitment of E3 ubiquitin ligases and ubiquitination and degradation of the receptor
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c66 : 1
stoichiometry:c67 : 1
stoichiometry:c68 : 1
m11*m32*0.1
nodelay
--
0
PMID: 17502368,11154225 We have demonstrated in vitro that sIFNAR2a can bind IFN{alpha} or -beta and transduce a signal through IFNAR1
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c69 : 1
stoichiometry:c70 : 1
stoichiometry:c71 : 1
m1636*m32*0.1
nodelay
--
0
PMID: 17502368,11154225 We have demonstrated in vitro that sIFNAR2a can bind IFN{alpha} or -beta and transduce a signal through IFNAR1
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c72 : 1
stoichiometry:c73 : 1
stoichiometry:c74 : 1
m35*m4019*0.1
nodelay
--
0
PMID: 17502368 Figure 1B PMID: 17502368 conventional signaling occurs when IFN binds to IFNAR1 and tmIFNAR2c resulting in cross-phosphorylation of receptors and associated Janus kinases (Tyk2 and Jak1)
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c76 : 1
stoichiometry:c75 : 1
stoichiometry:c77 : 1
m35*m37*0.1
nodelay
--
0
PMID: 17502368 Figure 1B PMID: 17502368 conventional signaling occurs when IFN binds to IFNAR1 and tmIFNAR2c resulting in cross-phosphorylation of receptors and associated Janus kinases (Tyk2 and Jak1)
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c78 : 1
stoichiometry:c79 : 1
m36*0.1
nodelay
--
0
PMID: 17502368 Figure 1B PMID: 17502368 conventional signaling occurs when IFN binds to IFNAR1 and tmIFNAR2c resulting in cross-phosphorylation of receptors and associated Janus kinases (Tyk2 and Jak1)
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c80 : 1
stoichiometry:c81 : 1
m38*0.1
nodelay
--
0
PMID: 17502368 Figure 1B PMID: 17502368 conventional signaling occurs when IFN binds to IFNAR1 and tmIFNAR2c resulting in cross-phosphorylation of receptors and associated Janus kinases (Tyk2 and Jak1)
p28
p28
cso30:i:ME_Binding
cso30:i:CC_Cytoplasm
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c82 : 1
stoichiometry:c83 : 1
stoichiometry:c21 : 1
stoichiometry:c22 : 1
stoichiometry:c84 : 1
m39*m1357*0.1
nodelay
--
0
PMID: 17502368 This provides docking sites on the receptor complex for STAT proteins. PMID: 17502368,9121453,15864272 HuIFNAR1 also bound STAT1 and STAT2 via phospho-Tyr466 and phospho-Tyr48 when overexpressed in heterologous cells PMID: 17502368,16311601 This may occur by binding a negative regulator such as SOCS-1 to inhibit JAK/STAT signaling
p28
p29
cso30:i:ME_Binding
cso30:i:CC_Cytoplasm
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c85 : 1
stoichiometry:c86 : 1
stoichiometry:c23 : 1
stoichiometry:c24 : 1
stoichiometry:c87 : 1
m1358*m40*0.1
nodelay
--
0
PMID: 17502368 This provides docking sites on the receptor complex for STAT proteins. PMID: 17502368,16311601 This may occur by binding a negative regulator such as SOCS-1 to inhibit JAK/STAT signaling
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c8 : 1
stoichiometry:c4 : 1
stoichiometry:c5 : 1
m1358*m39*0.1
nodelay
--
0
PMID: 17502368,9121453,15864272 HuIFNAR1 also bound STAT1 and STAT2 via phospho-Tyr466 and phospho-Tyr48 when overexpressed in heterologous cells
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c88 : 1
stoichiometry:c89 : 1
m41*0.1
nodelay
--
0
PMID: 17502368 STAT proteins are in turn phosphorylated and form homo- and heterodimeric complexes, which dissociate from the receptor and then translocate to the nucleus and bind to an ISRE or GAS element within the promoters of interferon-regulated genes, leading to their transcription.
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c90 : 1
stoichiometry:c91 : 1
m42*0.1
nodelay
--
0
PMID: 17502368 STAT proteins are in turn phosphorylated and form homo- and heterodimeric complexes, which dissociate from the receptor and then translocate to the nucleus and bind to an ISRE or GAS element within the promoters of interferon-regulated genes, leading to their transcription.
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c92 : 1
stoichiometry:c93 : 1
m43*0.1
nodelay
--
0
PMID: 17502368 STAT proteins are in turn phosphorylated and form homo- and heterodimeric complexes, which dissociate from the receptor and then translocate to the nucleus and bind to an ISRE or GAS element within the promoters of interferon-regulated genes, leading to their transcription.
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c94 : 1
stoichiometry:c95 : 1
m44*0.1
nodelay
--
0
PMID: 17502368 STAT proteins are in turn phosphorylated and form homo- and heterodimeric complexes, which dissociate from the receptor and then translocate to the nucleus and bind to an ISRE or GAS element within the promoters of interferon-regulated genes, leading to their transcription.
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c96 : 1
stoichiometry:c97 : 1
stoichiometry:c98 : 1
m43*m44*0.1
nodelay
--
0
PMID: 17502368 STAT proteins are in turn phosphorylated and form homo- and heterodimeric complexes, which dissociate from the receptor and then translocate to the nucleus and bind to an ISRE or GAS element within the promoters of interferon-regulated genes, leading to their transcription.
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c99 : 1
stoichiometry:c100 : 1
stoichiometry:c101 : 1
m45*0.1
nodelay
--
0
PMID: 17502368 STAT proteins are in turn phosphorylated and form homo- and heterodimeric complexes, which dissociate from the receptor and then translocate to the nucleus and bind to an ISRE or GAS element within the promoters of interferon-regulated genes, leading to their transcription. are in turn phosphorylated and form homo- and heterodimeric complexes, which dissociate from the receptor and then translocate to the nucleus and bind to an ISRE or GAS element within the promoters of interferon-regulated genes, leading to their transcription.
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c105 : 1
stoichiometry:c106 : 1
stoichiometry:c107 : 1
stoichiometry:c108 : 1
m47*0.1
nodelay
--
0
PMID: 17502368 STAT proteins are in turn phosphorylated and form homo- and heterodimeric complexes, which dissociate from the receptor and then translocate to the nucleus and bind to an ISRE or GAS element within the promoters of interferon-regulated genes, leading to their transcription. are in turn phosphorylated and form homo- and heterodimeric complexes, which dissociate from the receptor and then translocate to the nucleus and bind to an ISRE or GAS element within the promoters of interferon-regulated genes, leading to their transcription.
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c102 : 1
stoichiometry:c103 : 1
stoichiometry:c104 : 1
m46*0.1
nodelay
--
0
PMID: 17502368 STAT proteins are in turn phosphorylated and form homo- and heterodimeric complexes, which dissociate from the receptor and then translocate to the nucleus and bind to an ISRE or GAS element within the promoters of interferon-regulated genes, leading to their transcription. are in turn phosphorylated and form homo- and heterodimeric complexes, which dissociate from the receptor and then translocate to the nucleus and bind to an ISRE or GAS element within the promoters of interferon-regulated genes, leading to their transcription.
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c109 : 1
stoichiometry:c110 : 1
m63*0.1
nodelay
--
0
PMID: 17502368 STAT proteins are in turn phosphorylated and form homo- and heterodimeric complexes, which dissociate from the receptor and then translocate to the nucleus and bind to an ISRE or GAS element within the promoters of interferon-regulated genes, leading to their transcription. are in turn phosphorylated and form homo- and heterodimeric complexes, which dissociate from the receptor and then translocate to the nucleus and bind to an ISRE or GAS element within the promoters of interferon-regulated genes, leading to their transcription.
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c111 : 1
stoichiometry:c112 : 1
m48*0.1
nodelay
--
0
PMID: 17502368 STAT proteins are in turn phosphorylated and form homo- and heterodimeric complexes, which dissociate from the receptor and then translocate to the nucleus and bind to an ISRE or GAS element within the promoters of interferon-regulated genes, leading to their transcription. are in turn phosphorylated and form homo- and heterodimeric complexes, which dissociate from the receptor and then translocate to the nucleus and bind to an ISRE or GAS element within the promoters of interferon-regulated genes, leading to their transcription.
p4
p4
cso30:i:ME_Binding
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c10 : 1
stoichiometry:c11 : 1
stoichiometry:c65 : 1
stoichiometry:c12 : 1
m901*m129*0.1
nodelay
--
0
PMID: 17502368,9121453 Jak1, STAT1, and STAT2 may also be preassociated with IFNAR2 PMID: 17502368,16710296 Recently, a type I IFN-inducible cysteine protease, UBP43, was shown to interact directly with IFNAR2, blocking the interaction between Jak1 and the receptor
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c113 : 1
stoichiometry:c114 : 1
m49*0.1
nodelay
--
0
PMID: 17502368 STAT proteins are in turn phosphorylated and form homo- and heterodimeric complexes, which dissociate from the receptor and then translocate to the nucleus and bind to an ISRE or GAS element within the promoters of interferon-regulated genes, leading to their transcription. are in turn phosphorylated and form homo- and heterodimeric complexes, which dissociate from the receptor and then translocate to the nucleus and bind to an ISRE or GAS element within the promoters of interferon-regulated genes, leading to their transcription.
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c115 : 1
stoichiometry:c116 : 1
stoichiometry:c121 : 1
m64*m67*0.1
nodelay
--
0
PMID: 17502368 STAT proteins are in turn phosphorylated and form homo- and heterodimeric complexes, which dissociate from the receptor and then translocate to the nucleus and bind to an ISRE or GAS element within the promoters of interferon-regulated genes, leading to their transcription. are in turn phosphorylated and form homo- and heterodimeric complexes, which dissociate from the receptor and then translocate to the nucleus and bind to an ISRE or GAS element within the promoters of interferon-regulated genes, leading to their transcription.
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c117 : 1
stoichiometry:c118 : 1
stoichiometry:c122 : 1
m65*m67*0.1
nodelay
--
0
PMID: 17502368 STAT proteins are in turn phosphorylated and form homo- and heterodimeric complexes, which dissociate from the receptor and then translocate to the nucleus and bind to an ISRE or GAS element within the promoters of interferon-regulated genes, leading to their transcription. are in turn phosphorylated and form homo- and heterodimeric complexes, which dissociate from the receptor and then translocate to the nucleus and bind to an ISRE or GAS element within the promoters of interferon-regulated genes, leading to their transcription.
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c119 : 1
stoichiometry:c120 : 1
stoichiometry:c123 : 1
m66*m67*0.1
nodelay
--
0
PMID: 17502368 STAT proteins are in turn phosphorylated and form homo- and heterodimeric complexes, which dissociate from the receptor and then translocate to the nucleus and bind to an ISRE or GAS element within the promoters of interferon-regulated genes, leading to their transcription. are in turn phosphorylated and form homo- and heterodimeric complexes, which dissociate from the receptor and then translocate to the nucleus and bind to an ISRE or GAS element within the promoters of interferon-regulated genes, leading to their transcription.
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c124 : 1
stoichiometry:c125 : 1
m68*0.1
nodelay
--
0
PMID: 17502368 STAT proteins are in turn phosphorylated and form homo- and heterodimeric complexes, which dissociate from the receptor and then translocate to the nucleus and bind to an ISRE or GAS element within the promoters of interferon-regulated genes, leading to their transcription. are in turn phosphorylated and form homo- and heterodimeric complexes, which dissociate from the receptor and then translocate to the nucleus and bind to an ISRE or GAS element within the promoters of interferon-regulated genes, leading to their transcription.
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c126 : 1
stoichiometry:c127 : 1
m69*0.1
nodelay
--
0
PMID: 17502368 STAT proteins are in turn phosphorylated and form homo- and heterodimeric complexes, which dissociate from the receptor and then translocate to the nucleus and bind to an ISRE or GAS element within the promoters of interferon-regulated genes, leading to their transcription. are in turn phosphorylated and form homo- and heterodimeric complexes, which dissociate from the receptor and then translocate to the nucleus and bind to an ISRE or GAS element within the promoters of interferon-regulated genes, leading to their transcription.
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c128 : 1
stoichiometry:c129 : 1
m70*0.1
nodelay
--
0
PMID: 17502368 STAT proteins are in turn phosphorylated and form homo- and heterodimeric complexes, which dissociate from the receptor and then translocate to the nucleus and bind to an ISRE or GAS element within the promoters of interferon-regulated genes, leading to their transcription. are in turn phosphorylated and form homo- and heterodimeric complexes, which dissociate from the receptor and then translocate to the nucleus and bind to an ISRE or GAS element within the promoters of interferon-regulated genes, leading to their transcription.
p47
p47
cso30:i:ME_Binding
cso30:i:CC_Extracellular
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c130 : 1
stoichiometry:c131 : 1
stoichiometry:c132 : 1
m898*m41221*0.1
nodelay
--
0
PMID: 17502368,15449939,11125298,15312780 The binding site of IFN{alpha}2 on IFNAR1 has been predicted from site-directed mutagenesis and epitope mapping with an anti-IFNAR1-neutralizing antibody , albeit the latter may be inaccurate because of steric hindrances
p48
p48
cso30:i:ME_Binding
cso30:i:CC_Cytoplasm
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c133 : 1
stoichiometry:c134 : 1
stoichiometry:c135 : 1
m41221*m901*0.1
nodelay
--
0
PMID: 17502368,12842042,15312780,9737924,10556041 Numerous studies have investigated the residues of IFNAR2 involved in ligand interactions with IFN{alpha}2 and IFNbeta
p48
p49
cso30:i:ME_Binding
cso30:i:CC_Cytoplasm
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c136 : 1
stoichiometry:c137 : 1
stoichiometry:c138 : 1
m901*m1636*0.1
nodelay
--
0
PMID: 17502368,12842042,15312780,9737924,10556041 Numerous studies have investigated the residues of IFNAR2 involved in ligand interactions with IFN{alpha}2 and IFNbeta
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c13 : 1
stoichiometry:c6 : 1
stoichiometry:c19 : 1
stoichiometry:c20 : 1
stoichiometry:c7 : 1
m1357*m12*0.1
nodelay
--
0
PMID: 17502368,9121453 Jak1, STAT1, and STAT2 may also be preassociated with IFNAR2 PMID: 17502368,16311601 This may occur by binding a negative regulator such as SOCS-1 to inhibit JAK/STAT signaling
p50
p50
cso30:i:ME_Cleavage
cso30:i:CC_Extracellular
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c139 : 1
stoichiometry:c141 : 1
stoichiometry:c142 : 1
stoichiometry:c140 : 1
m901*m75*m35*0.1
nodelay
--
0
PMID: 17502368,15286706 In vitro studies demonstrate that a soluble IFNAR2 can also be generated by cleavage of transmembrane IFNAR2 by intramembrane proteases in response to IFNs and other stimuli, but there is no definitive in vivo evidence for this effect
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c143 : 1
stoichiometry:c145 : 1
stoichiometry:c144 : 1
m77*m20522*0.1
nodelay
--
0
PMID: 17502368,15871661 Nevertheless, there is a precedent in the IL6 receptor system where the soluble IL6R{alpha} is generated both by alternative splicing and by cleavage by ADAM 10 and 17 proteases
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c146 : 1
stoichiometry:c147 : 1
stoichiometry:c148 : 1
m2428*m77*0.1
nodelay
--
0
PMID: 17502368,15871661 Nevertheless, there is a precedent in the IL6 receptor system where the soluble IL6R{alpha} is generated both by alternative splicing and by cleavage by ADAM 10 and 17 proteases
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c16 : 1
stoichiometry:c9 : 1
stoichiometry:c25 : 1
stoichiometry:c26 : 1
stoichiometry:c14 : 1
m1358*m6*0.1
nodelay
--
0
PMID: 17502368,9121453 Jak1, STAT1, and STAT2 may also be preassociated with IFNAR2 PMID: 17502368,16311601 This may occur by binding a negative regulator such as SOCS-1 to inhibit JAK/STAT signaling
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:InputAssociation
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:InputAssociation
threshold
--
0
1,
--
cso30:c:InputAssociation
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:InputAssociation
threshold
--
0
1,
--
cso30:c:InputAssociation
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:InputAssociation
threshold
--
0
1,
--
cso30:c:InputAssociation
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:InputInhibitor
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:InputInhibitor
threshold
--
0
1,
--
cso30:c:InputInhibitor
threshold
--
0
1,
--
cso30:c:InputInhibitor
threshold
--
0
1,
--
cso30:c:InputInhibitor
threshold
--
0
1,
--
cso30:c:InputInhibitor
threshold
--
0
1,
--
cso30:c:InputInhibitor
threshold
--
0
1,
--
cso30:c:InputInhibitor
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:InputInhibitor
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:InputAssociation
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--