Original Literature | Model OverView |
---|---|
Publication
Title
The interferon signaling network and transcription factor C/EBP-beta.
Affiliation
Department of Microbiology & Immunology, Greenebaum Cancer Center, University ofMaryland School of Medicine, 660 W. Redwood Street, Baltimore, MD 21201, USA.
Abstract
Cytokines like interferons (IFNs) play a central role in regulating innate andspecific immunities against the pathogens and neoplastic cells. A number ofsignaling pathways are induced in response to IFN in various cells. One classicmechanism employed by IFNs is the JAK-STAT signaling pathway for inducingcellular responses. Here we describe the non-STAT pathways that participate inIFN-induced responses. In particular, we will focus on the role played bytranscription factor C/EBP-beta in mediating these responses.
PMID
18163952
|
Entity
Process
C/EBPbeta
--
G010787
cso30:c:mRNA
cso30:i:CC_Nucleoplasm
--
csml-variable:Double
m93693
10
infinite
0
TRANSFAC | G010787 |
--
Ras family
--
MO000000003
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m80
10
infinite
0
TRANSPATH | MO000000003 |
--
Raf
--
MO000000009
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m82
10
infinite
0
TRANSPATH | MO000000009 |
--
JNK
--
MO000000023
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m97
10
infinite
0
TRANSPATH | MO000000023 |
--
Elk-1
--
MO000000038
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m85
10
infinite
0
InterPro | IPR002341 |
TRANSPATH | MO000000038 |
--
c-Jun
--
MO000000049
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m86
10
infinite
0
InterPro | IPR002112 |
TRANSPATH | MO000000049 |
--
NF-kappaB
--
MO000000058
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m39
10
infinite
0
TRANSPATH | MO000000058 |
--
MEKKs
--
MO000000060
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m91
10
infinite
0
TRANSPATH | MO000000060 |
--
MEK1
--
MO000000078
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m84
10
infinite
0
InterPro | IPR000719 |
TRANSPATH | MO000000078 |
--
IL-1
--
MO000000214
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m185
10
infinite
0
TRANSPATH | MO000000214 |
--
c-Fos
--
MO000000279
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m221
10
infinite
0
InterPro | IPR002114 |
TRANSPATH | MO000000279 |
--
TNF-alpha
--
MO000000289
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m230
10
infinite
0
InterPro | IPR003636 |
TRANSPATH | MO000000289 |
--
ERK1
--
MO000004670
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m549
10
infinite
0
InterPro | IPR000719 |
TRANSPATH | MO000004670 |
--
p38gamma
--
MO000004690
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m567
10
infinite
0
InterPro | IPR000719 |
TRANSPATH | MO000004690 |
--
IL-6
--
MO000007384
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m871
10
infinite
0
InterPro | IPR003573 |
TRANSPATH | MO000007384 |
--
STAT1
--
MO000013119
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m1357
10
infinite
0
InterPro | IPR008967 |
TRANSPATH | MO000013119 |
--
STAT2
--
MO000013120
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m1358
10
infinite
0
InterPro | IPR008967 |
TRANSPATH | MO000013120 |
--
C/EBPbeta
--
MO000016580
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m1576
10
infinite
0
InterPro | IPR004827 |
TRANSPATH | MO000016580 |
--
IFNgamma
--
MO000016665
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m1639
10
infinite
0
InterPro | IPR002069 |
TRANSPATH | MO000016665 |
--
STAT2{pY}:STAT1{pY}
--
MO000016845
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m1780
10
infinite
0
TRANSPATH | MO000016845 |
--
STAT2{pY}
--
MO000016849
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m1783
10
infinite
0
TRANSPATH | MO000016849 |
--
MLK3
--
MO000016913
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m1828
10
infinite
0
InterPro | IPR001452 |
TRANSPATH | MO000016913 |
--
MKK4
--
MO000016917
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m1832
10
infinite
0
InterPro | IPR000719 |
TRANSPATH | MO000016917 |
--
p38alpha
--
MO000016958
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m1867
10
infinite
0
InterPro | IPR000719 |
TRANSPATH | MO000016958 |
--
p38beta
--
MO000016959
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m1868
10
infinite
0
InterPro | IPR000719 |
TRANSPATH | MO000016959 |
--
p38delta
--
MO000016961
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m1870
10
infinite
0
InterPro | IPR000719 |
TRANSPATH | MO000016961 |
--
Egr-1
--
MO000017190
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m2058
10
infinite
0
InterPro | IPR007087 |
TRANSPATH | MO000017190 |
--
C/EBPalpha
--
MO000019417
cso30:c:Protein
cso30:i:CC_CellComponent
--
--
csml-variable:Double
m3982
10
infinite
0
InterPro | IPR000217 |
TRANSPATH | MO000019417 |
--
IFNAR1:Tyk2
--
MO000019457
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m4019
10
infinite
0
TRANSPATH | MO000019457 |
--
IFNGR1:Jak1
--
MO000019460
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m4021
10
infinite
0
TRANSPATH | MO000019460 |
--
STAT1{p}
--
MO000019704
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m4238
10
infinite
0
TRANSPATH | MO000019704 |
--
Elk-1{p}
--
MO000038364
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m16574
10
infinite
0
TRANSPATH | MO000038364 |
--
p38alpha{p}
--
MO000038368
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m16578
10
infinite
0
TRANSPATH | MO000038368 |
--
p38beta{p}
--
MO000038382
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m16592
10
infinite
0
TRANSPATH | MO000038382 |
--
IFNAR1:Tyk2:IFNAR2:Jak1
--
MO000038483
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m16693
10
infinite
0
TRANSPATH | MO000038483 |
--
IFNAR2:Jak1
--
MO000038484
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m16694
10
infinite
0
TRANSPATH | MO000038484 |
--
c-Jun{p}
--
MO000038589
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m16780
10
infinite
0
TRANSPATH | MO000038589 |
--
MEK1{p}
--
MO000038670
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m16860
10
infinite
0
TRANSPATH | MO000038670 |
--
ERK1{p}
--
MO000038672
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m16862
10
infinite
0
TRANSPATH | MO000038672 |
--
ERK2{p}
--
MO000038692
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m16878
10
infinite
0
TRANSPATH | MO000038692 |
--
p38gamma{p}
--
MO000042106
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m19920
10
infinite
0
TRANSPATH | MO000042106 |
--
p38delta{p}
--
MO000042108
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m19922
10
infinite
0
TRANSPATH | MO000042108 |
--
--
e1
cso30:c:EntityBiologicalCompartment
cso30:i:CC_PlasmaMembrane
--
--
--
csml-variable:Double
m1
0
infinite
0
--
--
e10
cso30:c:EntityBiologicalCompartment
cso30:i:CC_Cytosol
--
--
--
csml-variable:Double
m10
0
infinite
0
--
csml-variable:Double
m11
0
infinite
0
--
IFNbeta:IFNAR1:Tyk2:IFNAR2:Jak1
--
e12
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m12
10
infinite
0
TRANSPATH | MO000038483 |
--
STAT1{p}:STAT2{p}:IRF9
--
e13
cso30:c:Complex
cso30:i:CC_Cytosol
--
csml-variable:Double
m13
0
infinite
0
--
csml-variable:Double
m14
0
infinite
0
--
ISRE:STAT1{p}:STAT2{p}:IRF9
--
e15
cso30:c:Complex
cso30:i:CC_Nucleoplasm
--
csml-variable:Double
m15
0
infinite
0
--
IFN inducible genes
--
e16
cso30:c:mRNA
cso30:i:CC_Nucleoplasm
--
csml-variable:Double
m16
0
infinite
0
--
IFNGR1:JAK1:IFNGR2:JAK2
--
e18
cso30:c:Complex
cso30:i:CC_Cytosol
--
csml-variable:Double
m18
0
infinite
0
--
IFNGR1:JAK1:IFNGR2:JAK2:IFNgamma
--
e19
cso30:c:Complex
cso30:i:CC_Cytosol
--
csml-variable:Double
m19
0
infinite
0
--
--
e2
cso30:c:EntityBiologicalCompartment
cso30:i:CC_PlasmaMembrane_ExternalSideOfPlasmaMembrane_
--
--
--
csml-variable:Double
m2
0
infinite
0
--
(STAT1{p})2
--
e20
cso30:c:Complex
cso30:i:CC_Cytosol
--
csml-variable:Double
m20
0
infinite
0
--
(STAT1{p})2
--
e21
cso30:c:Complex
cso30:i:CC_Cytosol
--
csml-variable:Double
m21
0
infinite
0
--
csml-variable:Double
m22
0
infinite
0
--
csml-variable:Double
m23
0
infinite
0
--
IFNgamma inducible genes
--
e24
cso30:c:mRNA
cso30:i:CC_Nucleoplasm
--
--
csml-variable:Double
m24
0
infinite
0
--
type III IFN:type III IFN receptor
--
e25
cso30:c:Complex
cso30:i:CC_Cytosol
--
csml-variable:Double
m25
0
infinite
0
--
type III IFN receptor
--
e26
cso30:c:Protein
cso30:i:CC_Cytosol
--
--
csml-variable:Double
m26
0
infinite
0
--
type III IFN
--
e27
cso30:c:Protein
cso30:i:CC_Cytosol
--
--
csml-variable:Double
m27
0
infinite
0
--
PI3K{active}
--
e28
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m29
10
infinite
0
TRANSPATH | MO000000030 |
--
--
e3
cso30:c:EntityBiologicalCompartment
cso30:i:CC_PlasmaMembrane_IntegralToPlasmaMembrane_
--
--
--
csml-variable:Double
m3
0
infinite
0
--
C/EBPbeta
--
e31
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m32
10
infinite
0
InterPro | IPR004827 |
TRANSPATH | MO000016580 |
--
IL-1
--
e32
cso30:c:mRNA
cso30:i:CC_Cytosol
--
--
csml-variable:Double
m33
0
infinite
0
--
IL8
--
e33
cso30:c:mRNA
cso30:i:CC_Nucleoplasm
--
--
csml-variable:Double
m34
0
infinite
0
--
CRP
--
e34
cso30:c:mRNA
cso30:i:CC_Nucleoplasm
--
--
csml-variable:Double
m35
0
infinite
0
--
alpha2-microglobulin
--
e35
cso30:c:mRNA
cso30:i:CC_Nucleoplasm
--
--
csml-variable:Double
m36
0
infinite
0
--
¦Á1-acid glycoprotein
--
e36
cso30:c:mRNA
cso30:i:CC_Nucleoplasm
--
--
csml-variable:Double
m37
0
infinite
0
--
C/EBPbeta:STAT3
--
e37
cso30:c:Complex
cso30:i:CC_Cytosol
--
--
csml-variable:Double
m38
0
infinite
0
--
C/EBPbeta:NF-kappaB
--
e38
cso30:c:Complex
cso30:i:CC_Cytosol
--
--
csml-variable:Double
m40
0
infinite
0
--
C/EBPbeta:SP1
--
e39
cso30:c:Complex
cso30:i:CC_Cytosol
--
--
csml-variable:Double
m41
0
infinite
0
--
--
e4
cso30:c:EntityBiologicalCompartment
cso30:i:CC_PlasmaMembrane_InternalSideOfPlasmaMembrane_
--
--
--
csml-variable:Double
m4
0
infinite
0
--
C/EBPbeta:pRb
--
e40
cso30:c:Complex
cso30:i:CC_Cytosol
--
--
csml-variable:Double
m42
0
infinite
0
--
LIP
--
e41
cso30:c:Protein
cso30:i:CC_Cytosol
--
--
csml-variable:Double
m43
0
infinite
0
--
C/EBPbeta:LIP
--
e42
cso30:c:Complex
cso30:i:CC_Cytosol
--
--
csml-variable:Double
m44
0
infinite
0
--
csml-variable:Double
m46
0
infinite
0
--
C/EBPzeta:C/ebpbeta
--
e44
cso30:c:Complex
cso30:i:CC_Cytosol
--
--
csml-variable:Double
m47
0
infinite
0
--
C/EBPzeta:C/EBPalpha
--
e45
cso30:c:Complex
cso30:i:CC_Cytosol
--
--
csml-variable:Double
m48
0
infinite
0
--
Dexamethasone
--
e46
cso30:c:SmallMolecule
cso30:i:CC_Cytosol
--
--
csml-variable:Double
m49
0
infinite
0
--
C?EBPbeta{p}
--
e47
cso30:c:Protein
cso30:i:CC_Cytosol
--
csml-variable:Double
m63
0
infinite
0
--
csml-variable:Double
m64
0
infinite
0
--
csml-variable:Double
m65
0
infinite
0
--
IFNalpha:IFNAR1:Tyk2:IFNAR2:Jak1
--
e5
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m5
10
infinite
0
TRANSPATH | MO000038483 |
--
--
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
--
IFNalpha
--
e6
cso30:c:Protein
cso30:i:CC_Cytosol
--
--
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
--
PKA
--
e63
cso30:c:Protein
cso30:i:CC_Cytosol
--
--
csml-variable:Double
m68
0
infinite
0
--
pu.1:C/EBPbeta
--
e64
cso30:c:Complex
cso30:i:CC_Cytosol
--
--
csml-variable:Double
m69
0
infinite
0
--
C/EBPbeta:c-myb
--
e65
cso30:c:Complex
cso30:i:CC_Cytosol
--
--
csml-variable:Double
m70
0
infinite
0
--
IRF9
--
e66
cso30:c:mRNA
cso30:i:CC_Nucleoplasm
--
csml-variable:Double
m71
0
infinite
0
--
2-5A synthatase
--
e67
cso30:c:mRNA
cso30:i:CC_Nucleoplasm
--
--
csml-variable:Double
m72
0
infinite
0
--
MHC I
--
e68
cso30:c:mRNA
cso30:i:CC_Cytosol
--
--
csml-variable:Double
m73
0
infinite
0
--
--
e7
cso30:c:EntityBiologicalCompartment
cso30:i:CC_Cell
--
--
--
csml-variable:Double
m7
0
infinite
0
--
growth factor
--
e70
cso30:c:Protein
cso30:i:CC_Extracellular
--
--
csml-variable:Double
m75
0
infinite
0
--
growth factor:growth factor receptor
--
e71
cso30:c:Complex
cso30:i:CC_Cytosol
--
csml-variable:Double
m76
0
infinite
0
--
growth factor receptor
--
e72
cso30:c:Protein
cso30:i:CC_PlasmaMembrane_IntegralToPlasmaMembrane_
--
--
csml-variable:Double
m77
0
infinite
0
--
growth factor:growth factor receptor:GRB2:SOS
--
e73
cso30:c:Complex
cso30:i:CC_PlasmaMembrane_IntegralToPlasmaMembrane_
--
csml-variable:Double
m79
0
infinite
0
--
c-fos{p}
--
e76
cso30:c:Protein
cso30:i:CC_Cytosol
--
csml-variable:Double
m87
0
infinite
0
--
Egr-1{p}
--
e77
cso30:c:Protein
cso30:i:CC_Cytosol
--
csml-variable:Double
m88
0
infinite
0
--
MEKKs{active}
--
e79
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m93
10
infinite
0
TRANSPATH | MO000000060 |
--
--
e8
cso30:c:EntityBiologicalCompartment
cso30:i:CC_Cell_WithoutCellWall_
--
--
--
csml-variable:Double
m8
0
infinite
0
--
MKK4{active}
--
e80
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m94
10
infinite
0
InterPro | IPR000719 |
TRANSPATH | MO000016917 |
--
SEK2{active}
--
e81
cso30:c:Protein
cso30:i:CC_Cytosol
--
csml-variable:Double
m95
0
infinite
0
--
SEK2
--
e82
cso30:c:Protein
cso30:i:CC_Cytosol
--
--
csml-variable:Double
m96
0
infinite
0
--
JNK
--
e83
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m98
10
infinite
0
TRANSPATH | MO000000023 |
--
MEKK1{active}
--
e84
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m100
10
infinite
0
InterPro | IPR000719 |
TRANSPATH | MO000000047 |
--
MEKK1:MEk1:ERK1:ERK2
--
e86
cso30:c:Complex
cso30:i:CC_Cytosol
--
--
csml-variable:Double
m102
0
infinite
0
--
NF-kappaB{active}
--
e87
cso30:c:Protein
cso30:i:CC_CellComponent
--
csml-variable:Double
m103
10
infinite
0
TRANSPATH | MO000000058 |
--
IFN-beta
--
e88
cso30:c:mRNA
cso30:i:CC_Nucleoplasm
--
--
csml-variable:Double
m104
0
infinite
0
--
transcription mediator complex
--
e89
cso30:c:Complex
cso30:i:CC_Cytosol
--
--
csml-variable:Double
m105
0
infinite
0
--
--
e9
cso30:c:EntityBiologicalCompartment
cso30:i:CC_Cytoplasm
--
--
--
csml-variable:Double
m9
0
infinite
0
--
C/EBPbeta:transcription mediator complex
--
e90
cso30:c:Complex
cso30:i:CC_Cytosol
--
--
csml-variable:Double
m106
0
infinite
0
--
csml-variable:Double
m107
0
infinite
0
--
GBF1
--
e92
cso30:c:Protein
cso30:i:CC_Cytosol
--
csml-variable:Double
m108
0
infinite
0
--
C/EBPbeta{p}:GBF1
--
e93
cso30:c:Complex
cso30:i:CC_Cytosol
--
csml-variable:Double
m109
0
infinite
0
--
IRF9
--
e94
cso30:c:Dna
cso30:i:CC_Nucleoplasm
--
--
csml-variable:Double
m110
0
infinite
0
--
C/EBPbeta:GBF1:IRF9
--
e95
cso30:c:Complex
cso30:i:CC_Nucleoplasm
--
--
csml-variable:Double
m111
0
infinite
0
--
MLKs:Cdc42
--
e96
cso30:c:Complex
cso30:i:CC_Cytosol
--
csml-variable:Double
m113
0
infinite
0
--
MLKs
--
e97
cso30:c:Protein
cso30:i:CC_Cytosol
--
csml-variable:Double
m114
0
infinite
0
--
(MLKs)2:Cdc42
--
e98
cso30:c:Complex
cso30:i:CC_Cytosol
--
csml-variable:Double
m115
0
infinite
0
--
(MLKs{p})2:Cdc42
--
e99
cso30:c:Complex
cso30:i:CC_Cytosol
--
--
csml-variable:Double
m116
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
m898*m132*0.1
nodelay
--
0
PMID: 18163952 From fig.1
p10
p10
cso30:i:ME_Binding
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c28 : 1
stoichiometry:c29 : 1
stoichiometry:c30 : 1
m4238*m1783*0.1
nodelay
--
0
PMID: 18163952, 8417326 After being activated (i.e. tyrosyl phosphorylated) STAT1 and STAT2 heterodimers associate with the non-STAT DNA-binding protein, IFN gene regulatory factor-9 (IRF-9/p48/ISGF3-¦Ã)
p100
p100
cso30:i:ME_Phosphorylation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c273 : 1
stoichiometry:c278 : 1
stoichiometry:c274 : 1
m567*m94*0.1
nodelay
--
0
PMID: 18163952 MEKKs then activate stress responsive kinases, such as the various isoforms of p38 MAPK (¦Á, ¦Â, ¦Ã, ¦Ä) and c-Jun N-terminal kinases (JNK), using the intermediate enzymes SEK1/2.
p101
p101
cso30:i:ME_Phosphorylation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c281 : 1
stoichiometry:c283 : 1
stoichiometry:c282 : 1
m1870*m95*0.1
nodelay
--
0
PMID: 18163952 MEKKs then activate stress responsive kinases, such as the various isoforms of p38 MAPK (¦Á, ¦Â, ¦Ã, ¦Ä) and c-Jun N-terminal kinases (JNK), using the intermediate enzymes SEK1/2.
p102
p102
cso30:i:ME_Phosphorylation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c279 : 1
stoichiometry:c284 : 1
stoichiometry:c280 : 1
m1870*m94*0.1
nodelay
--
0
PMID: 18163952 MEKKs then activate stress responsive kinases, such as the various isoforms of p38 MAPK (¦Á, ¦Â, ¦Ã, ¦Ä) and c-Jun N-terminal kinases (JNK), using the intermediate enzymes SEK1/2.
p103
p103
cso30:i:ME_UnknownActivation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c285 : 1
stoichiometry:c287 : 1
stoichiometry:c286 : 1
m99*m1639*0.1
nodelay
--
0
PMID: 18163952, 12048245 Instead of Raf, MEKK1 was required for IFN-¦Ã-induced ERK activation and the induction IRF-9 gene
p104
p104
cso30:i:ME_UnknownActivation
cso30:i:CC_Extracellular
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c288 : 1
stoichiometry:c290 : 1
stoichiometry:c289 : 1
m101*m100*0.1
nodelay
--
0
PMID: 18163952, 12048245 Instead of Raf, MEKK1 was required for IFN-¦Ã-induced ERK activation and the induction IRF-9 gene
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c292 : 1
stoichiometry:c291 : 1
m100*0.1
nodelay
--
0
PMID: 18163952, 12048245 Instead of Raf, MEKK1 was required for IFN-¦Ã-induced ERK activation and the induction IRF-9 gene
p106
p106
cso30:i:ME_Binding
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c293 : 1
stoichiometry:c294 : 1
stoichiometry:c295 : 1
stoichiometry:c296 : 1
stoichiometry:c297 : 1
m100*m84*m554*m549*0.1
nodelay
--
0
PMID: 18163952, 10969079 This domain acts as a scaffold for the binding of MEK1 and ERK1/2, which permits the juxtaposition of the kinases and their activation.
p107
p107
cso30:i:ME_Phosphorylation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c298 : 1
stoichiometry:c300 : 1
stoichiometry:c299 : 1
m84*m100*0.1
nodelay
--
0
PMID: 18163952, 7624324 MEKK1 phosphorylates MEK1 on the same residue as does Raf
p108
p108
cso30:i:ME_UnknownActivation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c301 : 1
stoichiometry:c303 : 1
stoichiometry:c302 : 1
m39*m100*0.1
nodelay
--
0
PMID: 18163952, 10346818, 9689078, 10805784 MEKK1 is also required for the activation of NF-¦ÊB and c-Jun N-terminal kinases
p109
p109
cso30:i:ME_UnknownActivation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c304 : 1
stoichiometry:c306 : 1
stoichiometry:c305 : 1
m97*m100*0.1
nodelay
--
0
PMID: 18163952, 10346818, 9689078, 10805784 MEKK1 is also required for the activation of NF-¦ÊB and c-Jun N-terminal kinases
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c31 : 1
stoichiometry:c32 : 1
stoichiometry:c33 : 1
m1780*m11*0.1
nodelay
--
0
PMID: 18163952, 8417326 After being activated (i.e. tyrosyl phosphorylated) STAT1 and STAT2 heterodimers associate with the non-STAT DNA-binding protein, IFN gene regulatory factor-9 (IRF-9/p48/ISGF3-¦Ã)
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c308 : 1
stoichiometry:c307 : 1
m100*0.1
nodelay
--
0
PMID: 18163952, 10747925 It also plays a major role in IFN-¦Â gene induction
p111
p111
cso30:i:ME_Phosphorylation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c309 : 1
stoichiometry:c311 : 1
stoichiometry:c310 : 1
m1576*m80*0.1
nodelay
--
0
PMID: 18163952, 14759369 One recent study showed that Ras induces phosphorylation of C/EBP-¦Â and activated C/EBP-¦Â interacts with the transcriptional mediator complex
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c312 : 1
stoichiometry:c314 : 1
stoichiometry:c313 : 1
m105*m63*0.1
nodelay
--
0
PMID: 18163952, 14759369 One recent study showed that Ras induces phosphorylation of C/EBP-¦Â and activated C/EBP-¦Â interacts with the transcriptional mediator complex
p113
p113
cso30:i:ME_DNABinding
cso30:i:CC_Nucleoplasm
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c315 : 1
stoichiometry:c316 : 1
stoichiometry:c318 : 1
stoichiometry:c317 : 1
m64*m108*m1639*0.1
nodelay
--
0
PMID: 18163952, 12050152 GATE also binds another transcriptional activator, GBF1, in response to IFN-¦Ã
p114
p114
cso30:i:ME_Phosphorylation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c319 : 1
stoichiometry:c321 : 1
stoichiometry:c320 : 1
m1799*m1639*0.1
nodelay
--
0
PMID: 18163952, 10657627 CRKL is tyrosine phosphorylated during IFN-treatment
p115
p115
cso30:i:ME_Binding
cso30:i:CC_Nucleoplasm
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c322 : 1
stoichiometry:c323 : 1
stoichiometry:c325 : 1
stoichiometry:c324 : 1
m108*m63*m1639*0.1
nodelay
--
0
PMID: 18163952 Mutation of this motif and/or interference with the ERK1/2 activation prevented the IFN-¦Ã-induced association between GBF1 and C/EBP-¦Â.
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c326 : 1
stoichiometry:c327 : 1
stoichiometry:c328 : 1
m110*m109*0.1
nodelay
--
0
PMID: 18163952, 15879117 Our subsequent studies have shown that GBF1 recruitment to the IRF-9 promoter is dependent on C/EBP-¦Â.
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c329 : 1
stoichiometry:c331 : 1
stoichiometry:c330 : 1
m112*m114*0.1
nodelay
--
0
PMID: 18163952, 10799501 Signal induced binding of Cdc42/Rac to the CRIB causes MLK dimerization, leading to their autophosphorylation
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c332 : 1
stoichiometry:c333 : 1
m113*0.1
nodelay
--
0
PMID: 18163952, 10799501 Signal induced binding of Cdc42/Rac to the CRIB causes MLK dimerization, leading to their autophosphorylation
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c334 : 1
stoichiometry:c335 : 1
m115*0.1
nodelay
--
0
PMID: 18163952, 10799501 Signal induced binding of Cdc42/Rac to the CRIB causes MLK dimerization, leading to their autophosphorylation
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c34 : 1
stoichiometry:c36 : 1
stoichiometry:c35 : 1
m14*m13*0.1
nodelay
--
0
PMID: 18163952 The resultant trimeric transcription factor, ISGF3, binds to the IFN-stimulated regulatory elements (ISREs) to induce the expression of many IFN-¦Á/¦Â-regulated genes.
p120
p120
cso30:i:ME_UnknownActivation
cso30:i:CC_Extracellular
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c336 : 1
stoichiometry:c338 : 1
stoichiometry:c337 : 1
m39*m114*0.1
nodelay
--
0
PMID: 18163952, 9003778, 11432832 MLKs function as MKKKs and have been implicated in the activation of JNK and SEK1 and transcription factor NF-¦ÊB
p121
p121
cso30:i:ME_UnknownActivation
cso30:i:CC_Extracellular
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c340 : 1
stoichiometry:c341 : 1
stoichiometry:c339 : 1
m97*m114*0.1
nodelay
--
0
PMID: 18163952, 9003778, 11432832 MLKs function as MKKKs and have been implicated in the activation of JNK and SEK1 and transcription factor NF-¦ÊB
p122
p122
cso30:i:ME_UnknownActivation
cso30:i:CC_Extracellular
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c342 : 1
stoichiometry:c344 : 1
stoichiometry:c343 : 1
m1832*m114*0.1
nodelay
--
0
PMID: 18163952, 9003778, 11432832 MLKs function as MKKKs and have been implicated in the activation of JNK and SEK1 and transcription factor NF-¦ÊB
p123
p123
cso30:i:ME_UnknownActivation
cso30:i:CC_Extracellular
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c345 : 1
stoichiometry:c347 : 1
stoichiometry:c346 : 1
m117*m114*0.1
nodelay
--
0
PMID: 18163952, 9003778, 11432832 MLKs function as MKKKs and have been implicated in the activation of JNK and SEK1 and transcription factor NF-¦ÊB
p124
p124
cso30:i:ME_GeneExpression
cso30:i:CC_Nucleoplasm
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c349 : 1
stoichiometry:c350 : 1
stoichiometry:c348 : 1
m1639*m1828*0.1
nodelay
--
0
PMID: 18163952 co-expression of MLK3, but not MLK2, significantly stimulated the IFN-¦Ã-induced expression of IRF-9.
p125
p125
cso30:i:ME_Phosphorylation
cso30:i:CC_Extracellular
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c351 : 1
stoichiometry:c353 : 1
stoichiometry:c354 : 1
stoichiometry:c352 : 1
m1576*m2337*0.1
nodelay
--
0
PMID: 18163952, 15314150 One likely candidate is Cdk2, which phosphorylates C/EBP-¦Â in vitro at S64 and T189 PMID: 18163952, 8755534 IFN-¦Ã treatment has been shown to cause a decrease in Cdk2 activity
p126
p126
cso30:i:ME_Phosphorylation
cso30:i:CC_Extracellular
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c355 : 1
stoichiometry:c357 : 1
stoichiometry:c358 : 1
stoichiometry:c356 : 1
m1576*0.1
nodelay
--
0
PMID: 18163952 IFN-¦Ã treatment decreased S64 phosphorylation. Surprisingly, MLK3 caused a decrease in phosphorylation of C/EBP-¦Â instead of its stimulation in an IFN-¦Ã dependent manner.
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c37 : 1
stoichiometry:c38 : 1
m15*0.1
nodelay
--
0
PMID: 18163952 The resultant trimeric transcription factor, ISGF3, binds to the IFN-stimulated regulatory elements (ISREs) to induce the expression of many IFN-¦Á/¦Â-regulated genes.
p14
p14
cso30:i:ME_Binding
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c39 : 1
stoichiometry:c41 : 1
stoichiometry:c40 : 1
m1772*m129*0.1
nodelay
--
0
PMID: 18163952 From fig.1
p15
p15
cso30:i:ME_Binding
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c42 : 1
stoichiometry:c43 : 1
stoichiometry:c44 : 1
m881*m130*0.1
nodelay
--
0
PMID: 18163952 From fig.1
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c45 : 1
stoichiometry:c46 : 1
stoichiometry:c47 : 1
m17*m4021*0.1
nodelay
--
0
PMID: 18163952 From fig.1
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c48 : 1
stoichiometry:c49 : 1
stoichiometry:c50 : 1
m18*m1639*0.1
nodelay
--
0
PMID: 18163952 From fig.1
p18
p18
cso30:i:ME_Phosphorylation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c51 : 1
stoichiometry:c53 : 1
stoichiometry:c52 : 1
m1357*m19*0.1
nodelay
--
0
PMID: 18163952 Only the STAT1 protein is tyrosyl phosphorylated by JAK1 and JAK2 at the ligand engaged type II IFN receptor.
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c54 : 1
stoichiometry:c55 : 1
m4238*0.1
nodelay
--
0
PMID: 18163952, 7690989 STAT1 dimers, thus formed, migrate to the nucleus, bind to the ¦Ã-IFN-activated sequence (GAS) to drive ¦Ã-IFN-induced gene expression
p2
p2
cso30:i:ME_Binding
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c4 : 1
stoichiometry:c6 : 1
stoichiometry:c5 : 1
m901*m129*0.1
nodelay
--
0
PMID: 18163952 From fig.1
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c56 : 1
stoichiometry:c57 : 1
m20*0.1
nodelay
--
0
PMID: 18163952, 7690989 STAT1 dimers, thus formed, migrate to the nucleus, bind to the ¦Ã-IFN-activated sequence (GAS) to drive ¦Ã-IFN-induced gene expression
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c58 : 1
stoichiometry:c60 : 1
stoichiometry:c59 : 1
m22*m21*0.1
nodelay
--
0
PMID: 18163952, 7690989 STAT1 dimers, thus formed, migrate to the nucleus, bind to the ¦Ã-IFN-activated sequence (GAS) to drive ¦Ã-IFN-induced gene expression
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c61 : 1
stoichiometry:c62 : 1
m23*0.1
nodelay
--
0
PMID: 18163952, 7690989 STAT1 dimers, thus formed, migrate to the nucleus, bind to the ¦Ã-IFN-activated sequence (GAS) to drive ¦Ã-IFN-induced gene expression
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c63 : 1
stoichiometry:c64 : 1
stoichiometry:c65 : 1
m27*m26*0.1
nodelay
--
0
PMID: 18163952, 15166220 The ligand-bound type III IFN receptor, although activated in a manner similar to the type I receptor, activates multiple STATs-STAT1, STAT2, STAT3, STAT4 and STAT5
p24
p24
cso30:i:ME_Phosphorylation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c66 : 1
stoichiometry:c68 : 1
stoichiometry:c67 : 1
m1357*m25*0.1
nodelay
--
0
PMID: 18163952, 15166220 The ligand-bound type III IFN receptor, although activated in a manner similar to the type I receptor, activates multiple STATs-STAT1, STAT2, STAT3, STAT4 and STAT5
p25
p25
cso30:i:ME_Phosphorylation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c69 : 1
stoichiometry:c71 : 1
stoichiometry:c70 : 1
m1358*m25*0.1
nodelay
--
0
PMID: 18163952, 15166220 The ligand-bound type III IFN receptor, although activated in a manner similar to the type I receptor, activates multiple STATs-STAT1, STAT2, STAT3, STAT4 and STAT5
p26
p26
cso30:i:ME_Phosphorylation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c72 : 1
stoichiometry:c74 : 1
stoichiometry:c73 : 1
m1360*m25*0.1
nodelay
--
0
PMID: 18163952, 15166220 The ligand-bound type III IFN receptor, although activated in a manner similar to the type I receptor, activates multiple STATs-STAT1, STAT2, STAT3, STAT4 and STAT5
p27
p27
cso30:i:ME_Phosphorylation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c75 : 1
stoichiometry:c77 : 1
stoichiometry:c76 : 1
m2053*m25*0.1
nodelay
--
0
PMID: 18163952, 15166220 The ligand-bound type III IFN receptor, although activated in a manner similar to the type I receptor, activates multiple STATs-STAT1, STAT2, STAT3, STAT4 and STAT5
p28
p28
cso30:i:ME_Phosphorylation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c78 : 1
stoichiometry:c80 : 1
stoichiometry:c79 : 1
m1798*m25*0.1
nodelay
--
0
PMID: 18163952, 15166220 The ligand-bound type III IFN receptor, although activated in a manner similar to the type I receptor, activates multiple STATs-STAT1, STAT2, STAT3, STAT4 and STAT5
p29
p29
cso30:i:ME_Phosphorylation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c81 : 1
stoichiometry:c85 : 1
stoichiometry:c82 : 1
m1867*m5*0.1
nodelay
--
0
PMID: 18163952, 10878008, 10523304 some studies have shown p38¦Á is phosphorylated and activated in a type-I-IFN-dependent manner in several IFN-sensitive cell lines.
p3
p3
cso30:i:ME_Binding
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c7 : 1
stoichiometry:c8 : 1
stoichiometry:c9 : 1
m16694*m4019*0.1
nodelay
--
0
--
p30
p30
cso30:i:ME_Phosphorylation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c83 : 1
stoichiometry:c86 : 1
stoichiometry:c84 : 1
m1867*m12*0.1
nodelay
--
0
PMID: 18163952, 10878008, 10523304 some studies have shown p38¦Á is phosphorylated and activated in a type-I-IFN-dependent manner in several IFN-sensitive cell lines.
p31
p31
cso30:i:ME_UnknownActivation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c87 : 1
stoichiometry:c89 : 1
stoichiometry:c88 : 1
m28*m12*0.1
nodelay
--
0
PMID: 18163952, 15864272 The PI3K-signaling cascade also regulates IFN inducible activation of the mammalian target of rapamycin (mTOR), via Akt, which mediates the initiation of mRNA translation
p32
p32
cso30:i:ME_UnknownActivation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c90 : 1
stoichiometry:c92 : 1
stoichiometry:c91 : 1
m28*m5*0.1
nodelay
--
0
PMID: 18163952, 15864272 The PI3K-signaling cascade also regulates IFN inducible activation of the mammalian target of rapamycin (mTOR), via Akt, which mediates the initiation of mRNA translation
p33
p33
cso30:i:ME_UnknownActivation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c93 : 1
stoichiometry:c95 : 1
stoichiometry:c94 : 1
m45*m29*0.1
nodelay
--
0
PMID: 18163952, 15864272 The PI3K-signaling cascade also regulates IFN inducible activation of the mammalian target of rapamycin (mTOR), via Akt, which mediates the initiation of mRNA translation
p34
p34
cso30:i:ME_UnknownActivation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c96 : 1
stoichiometry:c98 : 1
stoichiometry:c97 : 1
m2018*m30*0.1
nodelay
--
0
PMID: 18163952, 15864272 The PI3K-signaling cascade also regulates IFN inducible activation of the mammalian target of rapamycin (mTOR), via Akt, which mediates the initiation of mRNA translation
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c99 : 1
stoichiometry:c100 : 1
m16*m31*0.1
nodelay
--
0
PMID: 18163952, 15864272 The PI3K-signaling cascade also regulates IFN inducible activation of the mammalian target of rapamycin (mTOR), via Akt, which mediates the initiation of mRNA translation
p36
p36
cso30:i:ME_UnknownActivation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c101 : 1
stoichiometry:c103 : 1
stoichiometry:c102 : 1
m1576*m871*0.1
nodelay
--
0
PMID: 18163952, 9238507 C/EBP-¦Â also regulates IL-6 and IL-6-induced expression of the cytokines IL-1, IL-8, tumor necrosis factor-¦Á (TNF-¦Á), and granulocyte colony-stimulating factor (G-CSF), as well acute phase response proteins such as ¦Á1-acid glycoprotein, ¦Á2-microglobulin, and C-reactive protein
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c104 : 1
stoichiometry:c105 : 1
m32*0.1
nodelay
--
0
PMID: 18163952, 9238507 C/EBP-¦Â also regulates IL-6 and IL-6-induced expression of the cytokines IL-1, IL-8, tumor necrosis factor-¦Á (TNF-¦Á), and granulocyte colony-stimulating factor (G-CSF), as well acute phase response proteins such as ¦Á1-acid glycoprotein, ¦Á2-microglobulin, and C-reactive protein
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c112 : 1
stoichiometry:c113 : 1
m32*0.1
nodelay
--
0
PMID: 18163952, 9238507 C/EBP-¦Â also regulates IL-6 and IL-6-induced expression of the cytokines IL-1, IL-8, tumor necrosis factor-¦Á (TNF-¦Á), and granulocyte colony-stimulating factor (G-CSF), as well acute phase response proteins such as ¦Á1-acid glycoprotein, ¦Á2-microglobulin, and C-reactive protein
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c107 : 1
stoichiometry:c106 : 1
m32*0.1
nodelay
--
0
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c10 : 1
stoichiometry:c11 : 1
stoichiometry:c12 : 1
m16693*m6*0.1
nodelay
--
0
PMID: 18163952 From fig.1
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c108 : 1
stoichiometry:c109 : 1
m32*0.1
nodelay
--
0
PMID: 18163952, 9238507 C/EBP-¦Â also regulates IL-6 and IL-6-induced expression of the cytokines IL-1, IL-8, tumor necrosis factor-¦Á (TNF-¦Á), and granulocyte colony-stimulating factor (G-CSF), as well acute phase response proteins such as ¦Á1-acid glycoprotein, ¦Á2-microglobulin, and C-reactive protein
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c110 : 1
stoichiometry:c111 : 1
m32*0.1
nodelay
--
0
PMID: 18163952, 9238507 C/EBP-¦Â also regulates IL-6 and IL-6-induced expression of the cytokines IL-1, IL-8, tumor necrosis factor-¦Á (TNF-¦Á), and granulocyte colony-stimulating factor (G-CSF), as well acute phase response proteins such as ¦Á1-acid glycoprotein, ¦Á2-microglobulin, and C-reactive protein
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c115 : 1
stoichiometry:c114 : 1
m32*0.1
nodelay
--
0
PMID: 18163952, 9238507 C/EBP-¦Â also regulates IL-6 and IL-6-induced expression of the cytokines IL-1, IL-8, tumor necrosis factor-¦Á (TNF-¦Á), and granulocyte colony-stimulating factor (G-CSF), as well acute phase response proteins such as ¦Á1-acid glycoprotein, ¦Á2-microglobulin, and C-reactive protein
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c117 : 1
stoichiometry:c116 : 1
m32*0.1
nodelay
--
0
PMID: 18163952, 9238507 C/EBP-¦Â also regulates IL-6 and IL-6-induced expression of the cytokines IL-1, IL-8, tumor necrosis factor-¦Á (TNF-¦Á), and granulocyte colony-stimulating factor (G-CSF), as well acute phase response proteins such as ¦Á1-acid glycoprotein, ¦Á2-microglobulin, and C-reactive protein
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c118 : 1
stoichiometry:c119 : 1
stoichiometry:c120 : 1
m32*m1360*0.1
nodelay
--
0
PMID: 18163952, 8321203, 8552662, 9121452, 11238899 C/EBP-¦Â can interact with transcription factors outside its family, such as NF-¦ÊB (84), retinoblastoma (pRb) tumor suppressor protein (85), Sp1 (86), STAT3 (87) to regulate cellular functions.
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c121 : 1
stoichiometry:c122 : 1
stoichiometry:c123 : 1
m32*m39*0.1
nodelay
--
0
PMID: 18163952, 8321203, 8552662, 9121452, 11238899 C/EBP-¦Â can interact with transcription factors outside its family, such as NF-¦ÊB (84), retinoblastoma (pRb) tumor suppressor protein (85), Sp1 (86), STAT3 (87) to regulate cellular functions. PMID: 18163952, 7959007, 8756629, 8552662, 9121452 C/EBP-¦Â binds to a variety of response elements and forms heteromeric complexes with other transcription factors, such as pRb, NF-¦ÊB, Sp1, Myb and PU.1
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c124 : 1
stoichiometry:c125 : 1
stoichiometry:c126 : 1
m32*m11975*0.1
nodelay
--
0
PMID: 18163952, 8321203, 8552662, 9121452, 11238899 C/EBP-¦Â can interact with transcription factors outside its family, such as NF-¦ÊB (84), retinoblastoma (pRb) tumor suppressor protein (85), Sp1 (86), STAT3 (87) to regulate cellular functions. PMID: 18163952, 7959007, 8756629, 8552662, 9121452 C/EBP-¦Â binds to a variety of response elements and forms heteromeric complexes with other transcription factors, such as pRb, NF-¦ÊB, Sp1, Myb and PU.1
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c127 : 1
stoichiometry:c128 : 1
stoichiometry:c129 : 1
m1320*m32*0.1
nodelay
--
0
PMID: 18163952, 8321203, 8552662, 9121452, 11238899 C/EBP-¦Â can interact with transcription factors outside its family, such as NF-¦ÊB (84), retinoblastoma (pRb) tumor suppressor protein (85), Sp1 (86), STAT3 (87) to regulate cellular functions. PMID: 18163952, 7959007, 8756629, 8552662, 9121452 C/EBP-¦Â binds to a variety of response elements and forms heteromeric complexes with other transcription factors, such as pRb, NF-¦ÊB, Sp1, Myb and PU.1
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c130 : 1
stoichiometry:c131 : 1
stoichiometry:c132 : 1
m32*m43*0.1
nodelay
--
0
PMID: 18163952, 1934061 LIP dominantly inhibits the transcriptional activity of the full-length C/EBP-beta by dimerizing with it.
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c133 : 1
stoichiometry:c134 : 1
stoichiometry:c135 : 1
m32*m46*0.1
nodelay
--
0
PMID: 18163952, 1547942 It can form heterodimers with C/EBP-¦Á and C/EBP-¦Â, and attenuate their transcriptional activity
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c13 : 1
stoichiometry:c14 : 1
stoichiometry:c15 : 1
m1636*m16693*0.1
nodelay
--
0
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c136 : 1
stoichiometry:c137 : 1
stoichiometry:c138 : 1
m46*m3982*0.1
nodelay
--
0
PMID: 18163952, 1547942 It can form heterodimers with C/EBP-¦Á and C/EBP-¦Â, and attenuate their transcriptional activity
p51
p51
cso30:i:ME_GeneExpression
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c141 : 1
stoichiometry:c139 : 1
m157177*0.1
nodelay
--
0
PMID: 18163952, 2112087 LPS, IL-6, IL-1, dexamethasone, and glucagon can strongly up-regulate the expression of C/EBP-¦Â
p52
p52
cso30:i:ME_GeneExpression
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c142 : 1
stoichiometry:c140 : 1
m740*0.1
nodelay
--
0
PMID: 18163952, 2112087 LPS, IL-6, IL-1, dexamethasone, and glucagon can strongly up-regulate the expression of C/EBP-¦Â
p53
p53
cso30:i:ME_GeneExpression
cso30:i:CC_Nucleoplasm
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c145 : 1
stoichiometry:c143 : 1
m871*0.1
nodelay
--
0
PMID: 18163952, 2112087 LPS, IL-6, IL-1, dexamethasone, and glucagon can strongly up-regulate the expression of C/EBP-¦Â
p54
p54
cso30:i:ME_GeneExpression
cso30:i:CC_Nucleoplasm
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c146 : 1
stoichiometry:c144 : 1
m185*0.1
nodelay
--
0
PMID: 18163952, 2112087 LPS, IL-6, IL-1, dexamethasone, and glucagon can strongly up-regulate the expression of C/EBP-¦Â
p55
p55
cso30:i:ME_GeneExpression
cso30:i:CC_Nucleoplasm
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c150 : 1
stoichiometry:c148 : 1
m1639*0.1
nodelay
--
0
PMID: 18163952, 10777554 We have shown that IFN-¦Ã not only induces the expression of C/EBP-¦Â but also enhances its transcriptional activity
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c149 : 1
stoichiometry:c147 : 1
m49*0.1
nodelay
--
0
PMID: 18163952, 2112087 LPS, IL-6, IL-1, dexamethasone, and glucagon can strongly up-regulate the expression of C/EBP-¦Â
p57
p57
cso30:i:ME_Phosphorylation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c151 : 1
stoichiometry:c164 : 1
stoichiometry:c152 : 1
m1576*m66*0.1
nodelay
--
0
PMID: 18163952, 8336793, 8384717, 10635333, 11684016 Posttranscriptional modifications of C/EBP by protein kinases PKA, PKC,ribosomal S6 kinase (RSK), and extracellular signal-related kinase (ERK) appear to modulate its activity in different cells
p58
p58
cso30:i:ME_Phosphorylation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c153 : 1
stoichiometry:c166 : 1
stoichiometry:c154 : 1
m1576*m68*0.1
nodelay
--
0
PMID: 18163952, 8336793, 8384717, 10635333, 11684016 Posttranscriptional modifications of C/EBP by protein kinases PKA, PKC,ribosomal S6 kinase (RSK), and extracellular signal-related kinase (ERK) appear to modulate its activity in different cells
p59
p59
cso30:i:ME_Phosphorylation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c155 : 1
stoichiometry:c165 : 1
stoichiometry:c156 : 1
m1576*m67*0.1
nodelay
--
0
PMID: 18163952, 8336793, 8384717, 10635333, 11684016 Posttranscriptional modifications of C/EBP by protein kinases PKA, PKC,ribosomal S6 kinase (RSK), and extracellular signal-related kinase (ERK) appear to modulate its activity in different cells
p6
p6
cso30:i:ME_Phosphorylation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c16 : 1
stoichiometry:c18 : 1
stoichiometry:c17 : 1
m1357*m5*0.1
nodelay
--
0
PMID: 18163952, 9759489, 7532278, 9726434 The STAT1 and STAT2 proteins have been reported to be activated by the IFN-¦Á/¦Â via tyrosyl phosphorylation at critical residues, using tyrosine kinases Tyk2 and JAK1.
p60
p60
cso30:i:ME_Phosphorylation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c157 : 1
stoichiometry:c159 : 1
stoichiometry:c158 : 1
m1576*m92*0.1
nodelay
--
0
PMID: 18163952, 8336793, 8384717, 10635333, 11684016 Posttranscriptional modifications of C/EBP by protein kinases PKA, PKC,ribosomal S6 kinase (RSK), and extracellular signal-related kinase (ERK) appear to modulate its activity in different cells
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c160 : 1
stoichiometry:c162 : 1
stoichiometry:c161 : 1
m64*m32*0.1
nodelay
--
0
PMID: 18163952, 10777554, 11312260 We have shown that C/EBP-¦Â binds to GATE and stimulates transcription
PMID: 18163952, 10777554, 11312260 We have shown that C/EBP-¦Â binds to GATE and stimulates transcription
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c167 : 1
stoichiometry:c168 : 1
stoichiometry:c169 : 1
m32*m15836*0.1
nodelay
--
0
PMID: 18163952, 7959007, 8756629, 8552662, 9121452 C/EBP-¦Â binds to a variety of response elements and forms heteromeric complexes with other transcription factors, such as pRb, NF-¦ÊB, Sp1, Myb and PU.1
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c170 : 1
stoichiometry:c171 : 1
stoichiometry:c172 : 1
m1158*m32*0.1
nodelay
--
0
PMID: 18163952, 7959007, 8756629, 8552662, 9121452 C/EBP-¦Â binds to a variety of response elements and forms heteromeric complexes with other transcription factors, such as pRb, NF-¦ÊB, Sp1, Myb and PU.1
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c173 : 1
stoichiometry:c174 : 1
m32*0.1
nodelay
--
0
PMID: 18163952, 11004486 IL-6 induces IRF-9 gene expression through GATE using C/EBP-¦Â
p66
p66
cso30:i:ME_GeneExpression
cso30:i:CC_Nucleoplasm
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c175 : 1
stoichiometry:c176 : 1
m871*0.1
nodelay
--
0
PMID: 18163952, 1888886 IL-6 induces the expression of 2-5A synthetase and MHC class I genes
p67
p67
cso30:i:ME_GeneExpression
cso30:i:CC_Nucleoplasm
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c178 : 1
stoichiometry:c177 : 1
m871*0.1
nodelay
--
0
PMID: 18163952, 1888886 IL-6 induces the expression of 2-5A synthetase and MHC class I genes
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c179 : 1
stoichiometry:c181 : 1
stoichiometry:c180 : 1
m77*m75*0.1
nodelay
--
0
--
p69
p69
cso30:i:ME_Binding
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c182 : 1
stoichiometry:c183 : 1
stoichiometry:c184 : 1
stoichiometry:c185 : 1
m76*m78*m1720*0.1
nodelay
--
0
PMID: 18163952, 11057895 Ras activation is dependent on the recruitment of the adaptor proteins Grb and Sos to the growth factor receptors
p7
p7
cso30:i:ME_Phosphorylation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c19 : 1
stoichiometry:c21 : 1
stoichiometry:c20 : 1
m1357*m12*0.1
nodelay
--
0
PMID: 18163952, 9759489, 7532278, 9726434 The STAT1 and STAT2 proteins have been reported to be activated by the IFN-¦Á/¦Â via tyrosyl phosphorylation at critical residues, using tyrosine kinases Tyk2 and JAK1.
p70
p70
cso30:i:ME_UnknownActivation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c186 : 1
stoichiometry:c188 : 1
stoichiometry:c187 : 1
m81*m79*0.1
nodelay
--
0
PMID: 18163952, 11057895 Ras activation is dependent on the recruitment of the adaptor proteins Grb and Sos to the growth factor receptors
p71
p71
cso30:i:ME_UnknownActivation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c189 : 1
stoichiometry:c191 : 1
stoichiometry:c190 : 1
m82*m80*0.1
nodelay
--
0
PMID: 18163952 Raf, a serine-threonine kinase, responds to Ras and phosphorylates MAP kinase kinase 1 (MEK1).
p72
p72
cso30:i:ME_Phosphorylation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c192 : 1
stoichiometry:c194 : 1
stoichiometry:c193 : 1
m84*m83*0.1
nodelay
--
0
PMID: 18163952 Raf, a serine-threonine kinase, responds to Ras and phosphorylates MAP kinase kinase 1 (MEK1).
p73
p73
cso30:i:ME_Phosphorylation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c195 : 1
stoichiometry:c197 : 1
stoichiometry:c196 : 1
m549*m16860*0.1
nodelay
--
0
PMID: 18163952 MEK1, a dual specificity kinase, phosphorylates at the conserved threonine and tyrosine residues present in the activation loop of ERKs: ERK1 (p44) and ERK2 (p42).
p74
p74
cso30:i:ME_Phosphorylation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c198 : 1
stoichiometry:c200 : 1
stoichiometry:c199 : 1
m554*m16860*0.1
nodelay
--
0
PMID: 18163952 MEK1, a dual specificity kinase, phosphorylates at the conserved threonine and tyrosine residues present in the activation loop of ERKs: ERK1 (p44) and ERK2 (p42).
p75
p75
cso30:i:ME_Phosphorylation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c201 : 1
stoichiometry:c203 : 1
stoichiometry:c204 : 1
m16862*m85*0.1
nodelay
--
0
PMID: 18163952 ERKs1/2 are known to phosphorylate members of the AP1 family, such as Elk1, Egr1, Fos, and Jun.
p76
p76
cso30:i:ME_Phosphorylation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c202 : 1
stoichiometry:c205 : 1
stoichiometry:c206 : 1
m16878*m85*0.1
nodelay
--
0
PMID: 18163952 ERKs1/2 are known to phosphorylate members of the AP1 family, such as Elk1, Egr1, Fos, and Jun.
p77
p77
cso30:i:ME_Phosphorylation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c207 : 1
stoichiometry:c209 : 1
stoichiometry:c210 : 1
m16862*m86*0.1
nodelay
--
0
PMID: 18163952 ERKs1/2 are known to phosphorylate members of the AP1 family, such as Elk1, Egr1, Fos, and Jun.
p78
p78
cso30:i:ME_Phosphorylation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c208 : 1
stoichiometry:c211 : 1
stoichiometry:c212 : 1
m16878*m86*0.1
nodelay
--
0
PMID: 18163952 ERKs1/2 are known to phosphorylate members of the AP1 family, such as Elk1, Egr1, Fos, and Jun.
p79
p79
cso30:i:ME_Phosphorylation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c213 : 1
stoichiometry:c215 : 1
stoichiometry:c217 : 1
m16878*m221*0.1
nodelay
--
0
PMID: 18163952 ERKs1/2 are known to phosphorylate members of the AP1 family, such as Elk1, Egr1, Fos, and Jun.
p8
p8
cso30:i:ME_Phosphorylation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c22 : 1
stoichiometry:c27 : 1
stoichiometry:c23 : 1
m1358*m5*0.1
nodelay
--
0
PMID: 18163952, 9759489, 7532278, 9726434 The STAT1 and STAT2 proteins have been reported to be activated by the IFN-¦Á/¦Â via tyrosyl phosphorylation at critical residues, using tyrosine kinases Tyk2 and JAK1.
p80
p80
cso30:i:ME_Phosphorylation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c214 : 1
stoichiometry:c216 : 1
stoichiometry:c218 : 1
m16862*m221*0.1
nodelay
--
0
PMID: 18163952 ERKs1/2 are known to phosphorylate members of the AP1 family, such as Elk1, Egr1, Fos, and Jun.
p81
p81
cso30:i:ME_Phosphorylation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c220 : 1
stoichiometry:c222 : 1
stoichiometry:c224 : 1
m16878*m2058*0.1
nodelay
--
0
PMID: 18163952 ERKs1/2 are known to phosphorylate members of the AP1 family, such as Elk1, Egr1, Fos, and Jun.
p82
p82
cso30:i:ME_Phosphorylation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c219 : 1
stoichiometry:c221 : 1
stoichiometry:c223 : 1
m16862*m2058*0.1
nodelay
--
0
PMID: 18163952 ERKs1/2 are known to phosphorylate members of the AP1 family, such as Elk1, Egr1, Fos, and Jun.
p83
p83
cso30:i:ME_UnknownActivation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c225 : 1
stoichiometry:c227 : 1
stoichiometry:c226 : 1
m82*m1636*0.1
nodelay
--
0
PMID: 18163952, 9199317, 9668040 Raf activation by IFN-¦Ã and IFN-¦Â has been reported
p84
p84
cso30:i:ME_UnknownActivation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c228 : 1
stoichiometry:c230 : 1
stoichiometry:c229 : 1
m82*m1639*0.1
nodelay
--
0
PMID: 18163952, 9199317, 9668040 Raf activation by IFN-¦Ã and IFN-¦Â has been reported
p85
p85
cso30:i:ME_UnknownActivation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c231 : 1
stoichiometry:c233 : 1
stoichiometry:c232 : 1
m2203*m230*0.1
nodelay
--
0
PMID: 18163952, 9305638 Rho and Rac, the G proteins similar to Ras, are activated first
p86
p86
cso30:i:ME_UnknownActivation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c234 : 1
stoichiometry:c236 : 1
stoichiometry:c235 : 1
m89*m230*0.1
nodelay
--
0
PMID: 18163952, 9305638 Rho and Rac, the G proteins similar to Ras, are activated first
p87
p87
cso30:i:ME_UnknownActivation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c237 : 1
stoichiometry:c239 : 1
stoichiometry:c238 : 1
m89*m185*0.1
nodelay
--
0
PMID: 18163952, 9305638 Rho and Rac, the G proteins similar to Ras, are activated first
p88
p88
cso30:i:ME_UnknownActivation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c240 : 1
stoichiometry:c242 : 1
stoichiometry:c241 : 1
m2203*m185*0.1
nodelay
--
0
--
p89
p89
cso30:i:ME_UnknownActivation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c243 : 1
stoichiometry:c245 : 1
stoichiometry:c244 : 1
m91*m74*0.1
nodelay
--
0
PMID: 18163952 These G-proteins then activate MAP kinase kinase kinases (MEKKs)
p9
p9
cso30:i:ME_Phosphorylation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c24 : 1
stoichiometry:c26 : 1
stoichiometry:c25 : 1
m1358*m12*0.1
nodelay
--
0
PMID: 18163952, 9759489, 7532278, 9726434 The STAT1 and STAT2 proteins have been reported to be activated by the IFN-¦Á/¦Â via tyrosyl phosphorylation at critical residues, using tyrosine kinases Tyk2 and JAK1.
p90
p90
cso30:i:ME_UnknownActivation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c246 : 1
stoichiometry:c248 : 1
stoichiometry:c247 : 1
m91*m90*0.1
nodelay
--
0
PMID: 18163952 These G-proteins then activate MAP kinase kinase kinases (MEKKs)
p91
p91
cso30:i:ME_UnknownActivation
cso30:i:CC_Extracellular
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c249 : 1
stoichiometry:c251 : 1
stoichiometry:c250 : 1
m1832*m93*0.1
nodelay
--
0
PMID: 18163952 MEKKs then activate stress responsive kinases, such as the various isoforms of p38 MAPK (¦Á, ¦Â, ¦Ã, ¦Ä) and c-Jun N-terminal kinases (JNK), using the intermediate enzymes SEK1/2.
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c252 : 1
stoichiometry:c254 : 1
stoichiometry:c253 : 1
m96*m93*0.1
nodelay
--
0
PMID: 18163952 MEKKs then activate stress responsive kinases, such as the various isoforms of p38 MAPK (¦Á, ¦Â, ¦Ã, ¦Ä) and c-Jun N-terminal kinases (JNK), using the intermediate enzymes SEK1/2.
p93
p93
cso30:i:ME_UnknownActivation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c257 : 1
stoichiometry:c259 : 1
stoichiometry:c258 : 1
m97*m95*0.1
nodelay
--
0
PMID: 18163952 MEKKs then activate stress responsive kinases, such as the various isoforms of p38 MAPK (¦Á, ¦Â, ¦Ã, ¦Ä) and c-Jun N-terminal kinases (JNK), using the intermediate enzymes SEK1/2.
p94
p94
cso30:i:ME_UnknownActivation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c255 : 1
stoichiometry:c260 : 1
stoichiometry:c256 : 1
m97*m94*0.1
nodelay
--
0
PMID: 18163952 MEKKs then activate stress responsive kinases, such as the various isoforms of p38 MAPK (¦Á, ¦Â, ¦Ã, ¦Ä) and c-Jun N-terminal kinases (JNK), using the intermediate enzymes SEK1/2.
p95
p95
cso30:i:ME_Phosphorylation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c264 : 1
stoichiometry:c266 : 1
stoichiometry:c265 : 1
m1867*m95*0.1
nodelay
--
0
PMID: 18163952 MEKKs then activate stress responsive kinases, such as the various isoforms of p38 MAPK (¦Á, ¦Â, ¦Ã, ¦Ä) and c-Jun N-terminal kinases (JNK), using the intermediate enzymes SEK1/2.
p96
p96
cso30:i:ME_Phosphorylation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c261 : 1
stoichiometry:c263 : 1
stoichiometry:c262 : 1
m1867*m94*0.1
nodelay
--
0
PMID: 18163952 MEKKs then activate stress responsive kinases, such as the various isoforms of p38 MAPK (¦Á, ¦Â, ¦Ã, ¦Ä) and c-Jun N-terminal kinases (JNK), using the intermediate enzymes SEK1/2.
p97
p97
cso30:i:ME_Phosphorylation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c269 : 1
stoichiometry:c272 : 1
stoichiometry:c270 : 1
m1868*m95*0.1
nodelay
--
0
PMID: 18163952 MEKKs then activate stress responsive kinases, such as the various isoforms of p38 MAPK (¦Á, ¦Â, ¦Ã, ¦Ä) and c-Jun N-terminal kinases (JNK), using the intermediate enzymes SEK1/2.
p98
p98
cso30:i:ME_Phosphorylation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c267 : 1
stoichiometry:c271 : 1
stoichiometry:c268 : 1
m1868*m94*0.1
nodelay
--
0
PMID: 18163952 MEKKs then activate stress responsive kinases, such as the various isoforms of p38 MAPK (¦Á, ¦Â, ¦Ã, ¦Ä) and c-Jun N-terminal kinases (JNK), using the intermediate enzymes SEK1/2.
p99
p99
cso30:i:ME_Phosphorylation
cso30:i:CC_Cytosol
--
--
and
mass
coefficient1:0.1
coefficient2:1.0
stoichiometry:c275 : 1
stoichiometry:c277 : 1
stoichiometry:c276 : 1
m567*m95*0.1
nodelay
--
0
PMID: 18163952 MEKKs then activate stress responsive kinases, such as the various isoforms of p38 MAPK (¦Á, ¦Â, ¦Ã, ¦Ä) and c-Jun N-terminal kinases (JNK), using the intermediate enzymes SEK1/2.
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
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:OutputProcess
threshold
--
0
1,
--
cso30:c:InputAssociation
threshold
--
0
1,
--
cso30:c:InputAssociation
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: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: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: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: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:InputAssociation
threshold
--
0
1,
--
cso30:c:InputAssociation
threshold
--
0
1,
--
cso30:c:OutputProcess
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: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:InputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:OutputProcess
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:InputAssociation
threshold
--
0
1,
--
cso30:c:InputAssociation
threshold
--
0
1,
--
cso30:c:InputAssociation
threshold
--
0
1,
--
cso30:c:InputAssociation
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:OutputProcess
threshold
--
0
1,
--
cso30:c:InputAssociation
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:InputAssociation
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:InputAssociation
threshold
--
0
1,
--
cso30:c:InputProcess
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:InputAssociation
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:InputAssociation
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:InputAssociation
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:InputAssociation
threshold
--
0
1,
--
cso30:c:OutputProcess
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:InputAssociation
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:InputAssociation
threshold
--
0
1,
--
cso30:c:InputAssociation
threshold
--
0
1,
--
cso30:c:InputProcess
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:InputProcess
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:InputAssociation
threshold
--
0
1,
--
cso30:c:InputProcess
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: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:InputAssociation
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:InputAssociation
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:InputAssociation
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:InputAssociation
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:InputAssociation
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:InputAssociation
threshold
--
0
1,
--
cso30:c:InputProcess
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:InputAssociation
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:InputAssociation
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:InputAssociation
threshold
--
0
1,
--
cso30:c:InputProcess
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: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:OutputProcess
threshold
--
0
1,
--
cso30:c:InputAssociation
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:InputAssociation
threshold
--
0
1,
--
cso30:c:OutputProcess
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:OutputProcess
threshold
--
0
1,
--
cso30:c:InputAssociation
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:OutputProcess
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:OutputProcess
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:InputProcess
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: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:InputAssociation
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:InputAssociation
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:InputAssociation
threshold
--
0
1,
--
cso30:c:InputProcess
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:InputProcess
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:InputAssociation
threshold
--
0
1,
--
cso30:c:InputInhibitor
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:OutputProcess
threshold
--
0
1,
--
cso30:c:InputInhibitor
threshold
--
0
1,
--
cso30:c:InputInhibitor
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,
--
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:InputAssociation
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:OutputProcess
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: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:InputAssociation
threshold
--
0
1,
--
cso30:c:InputProcess
threshold
--
0
1,
--
cso30:c:InputAssociation
threshold
--
0
1,
--
cso30:c:InputAssociation
threshold
--
0
1,
--
cso30:c:InputAssociation
threshold
--
0
1,
--
cso30:c:InputAssociation
threshold
--
0
1,
--