Simple molecule NO
NO@Cytosol
Identifiers
CHEBI:16480 KEGGCOMPOUND:C00533 CAS:10102-43-9
References
PMID:10792026
Nitric oxide inhibits tumor necrosis factor-alpha-induced apoptosis by reducing the generation of ceramide.
rc_re1550( Regulated Cell Death
):
PMID:12387875
PMID:9841888
rc_re1562( Regulated Cell Death
):
PMID:12404124
NO was found to be mediated through stimulation of guanylate cyclase and to require activation of protein kinase G
NO@Mitochondrial intermembrane space
Identifiers
CHEBI:16480 KEGGCOMPOUND:C00533 CAS:10102-43-9
References
rc_re834( Regulated Cell Death
):
PMID:7544575
in vitro
in RAW 264.7 upon NOS2 induction (LPS+IFNg)
proposed mechanise: loss of iron sulfur cluster
NO@Mitochondrial inner membrane
Identifiers
CHEBI:16480 KEGGCOMPOUND:C00533 CAS:10102-43-9
References
rc_re90( Regulated Cell Death
):
PMID:8194600
cytochrome oxidase inhibition by nitric oxide
NO@default
Identifiers
CHEBI:16480 KEGGCOMPOUND:C00533 CAS:10102-43-9
References
NATURAL_KILLER
PMID:22006996, PMID:18559521
Nitric oxide inhibits the hypoxia-induced expression of ADAM10 and the hypoxia-induced accumulation of HIF1A
and decrease MIC shedding.
NO attenuates in vivo tumor growth by sensitizing tumor cells to recognition and elimination by the innate immune system.
NO@INNATE_IMMUNE_CELL_Cytosol
References
PMID:15644117, PMID:17260466
HMGB1 induces NO production probably via NFkB dependent upregulation of INOS expression in rodent macrophage
PMID:24092389
TANs from early tumors are more cytotoxic toward tumor cells and produce higher levels of TNF-??, NO, and H2O2 and, in established tumors, these functions are downregulated and TAN acquire a more protumorigenic phenotype
NO@TUMOR_CELL_AS_INDUCTOR
Identifiers
CHEBI:16480 KEGGCOMPOUND:C00533 CAS:10102-43-9
References
NATURAL_KILLER
PMID:22006996, PMID:18559521
Nitric oxide inhibits the hypoxia-induced expression of ADAM10 and the hypoxia-induced accumulation of HIF1A
and decrease MIC shedding.
NO attenuates in vivo tumor growth by sensitizing tumor cells to recognition and elimination by the innate immune system.
Modifications:
In compartment: Cytosol
- NO@Cytosol
In compartment: INNATE_IMMUNE_CELL_Cytosol
- NO@INNATE_IMMUNE_CELL_Cytosol
In compartment: Mitochondrial inner membrane
- NO@Mitochondrial inner membrane
In compartment: Mitochondrial intermembrane space
- NO@Mitochondrial intermembrane space
In compartment: TUMOR_CELL_AS_INDUCTOR
- NO@TUMOR_CELL_AS_INDUCTOR
In compartment: default
- NO@default
Participates in complexes:
Participates in reactions:
As Reactant or Product:- NO@default
→
NO_production@default
- L-arginine@INNATE_IMMUNE_CELL_Cytosol
+ O_sub_2_endsub_@INNATE_IMMUNE_CELL_Cytosol
+ NADPH@INNATE_IMMUNE_CELL_Cytosol
→
NO@INNATE_IMMUNE_CELL_Cytosol
+ L-citrulin@INNATE_IMMUNE_CELL_Cytosol
+ NADP+@INNATE_IMMUNE_CELL_Cytosol
- NO@INNATE_IMMUNE_CELL_Cytosol
→
NO@default
- Caspase3*@Cytosol
+ NO@Cytosol
→
Caspase3*|-SNO@Cytosol
- IKK_beta_*@Cytosol
+ NO@Cytosol
→
IKK_beta_*|-SNO@Cytosol
- Caspase9*|S196_unk|T125_unk|S144_unk|Y153_unk@Cytosol
+ NO@Cytosol
→
Caspase9*|S196_unk|T125_unk|S144_unk|Y153_unk|-SNO@Cytosol
- NO@Cytosol
→
NO@Mitochondrial inner membrane
- NO@Mitochondrial inner membrane
→
NO@Mitochondrial intermembrane space
- L-arginine@Cytosol
+ O_sub_2_endsub_@Cytosol
+ NADPH@Cytosol
→
NO@Cytosol
+ L-citrulline@Cytosol
+ NADP_super_+_endsuper_@Cytosol
- FECH|hm2|[2FE-2S]@Mitochondrial intermembrane space
+ NO@Mitochondrial intermembrane space
→
FECH@Mitochondrial intermembrane space
As Catalyser:- HIF1A@TUMOR_CELL_AS_INDUCTOR
→
HIF1A@TUMOR_CELL_AS_INDUCTOR
- gADAM10@TUMOR_CELL_AS_INDUCTOR
→
rADAM10@TUMOR_CELL_AS_INDUCTOR
- Sphingomyelin@Cytosol
+ H2O@Cytosol
→
Ceramide@Cytosol
+ Choline Phosphate@Cytosol
- GUCY*@Cytosol
→
GUCY*@Cytosol
- ACER*@Cytosol
→
ACER*|ubi@Cytosol
- Cytochrome_C*|ferroheme:cardiolipin@Mitochondrial inner membrane
+ H+@Mitochondrial Matrix
+ O_sub_2_endsub_@Mitochondrial inner membrane
→
Cytochrome_C*|ferriheme:cardiolipin@Mitochondrial inner membrane
+ H+@Mitochondrial intermembrane space