TBK1、IKKε介导的IRF3、IRF7激活的调控
中文名称
通路描述
Toll样受体3(TLR3)和TLR4配体诱导的I型干扰素基因的产生由TBK1或IKKε(IKBKE)介导,它们磷酸化干扰素调节因子3(IRF3)和IRF7。TBK1和/或IRF3、IRF7的活动受多种机制调节,包括翻译后修饰、蛋白质相互作用和蛋白质降解(Zhao W等,2013;Runde AP等,2022)。
本Reactome模块描述了TBK1和IKKε活性通过K63连接泛素化以及TBK1与OPTN相互作用而受到调节。
本Reactome模块描述了TBK1和IKKε活性通过K63连接泛素化以及TBK1与OPTN相互作用而受到调节。
英文描述
Potential therapeutics for SARS The search for drugs to prevent or reduce the severity of human infection with SARS-CoV-1 or SARS-CoV-2 has centered on ones that are effective in treatment of human infections with other RNA viruses or in diminishing cytokine storms and other pathologies due to destructive host reactions. The interactions of a large number of these candidate drugs with their known viral and human protein targets are annotated, as are some drugs that inhibit Cytochrome P450 (CYP) oxidoreductases to prolong the plasma half-lives of antiviral drugs. In addition, effects of these drugs on unrelated essential human proteins, that might limit their use in vivo, are annotated.A notable success of this search is a combination treatment, Paxlovid (NCT04960202), involving ritonavir, an inhibitor of CYP3A4 and CYP2B6 oxidoreductases, and nirmatrelvir, an inhibitor of SARS-CoV-2 3CLp protease, to block steps in maturation of viral replicase proteins (Hashemian et al. 2023).
所含基因
108 个基因
ACE2
AP2A1
AP2A2
AP2B1
AP2M1
AP2S1
ARID4A
ARID4B
ATP1A1
ATP1A2
ATP1A3
ATP1A4
ATP1B1
ATP1B2
ATP1B3
BLNK
BRD4
BRMS1
BTK
CD79A
CD79B
CHD3
CHD4
COMT
CRBN
CYSLTR1
FKBP1A
FKBP4
FNTA
FNTB
FURIN
FXYD1
FXYD2
FXYD3
FXYD4
FXYD6
FXYD7
G76-NEDD8-K712-CUL3
GATAD2A
GATAD2B
HDAC1
HDAC2
HMG20B
HSP90AA1
HSP90AB1
IFNAR1
IFNGR1
IFNGR2
IGHD
IGHM
IGHV
IGKC
IGKVA18
IGLC1
IGLC2
IGLC3
IGLC6
IGLC7
IGLV
IL1R1
IL6R
IMPDH1
IMPDH2
ITGA4
ITGB1
JAK1
JAK2
JAK3
KDM1A
KEAP1
MBD3
MTA1
MTA2
MTA3
NCK1
NFE2L2
NR3C1
NS5B
PDCD1
PHF21A
PLCG2
PTGES3
RBBP4
RBBP7
RBX1
RCOR1
REST
RIPK1
ROCK1
ROCK2
S1PR1
SAP18
SAP30
SAP30L
SH3KBP1
SIGMAR1
SOS1
STAT2
SUDS3
SYK
TBK1
TLR7
TLR9
TUBB
TYK2
VAV1
VEGFA
ZBP1