EC Number | Activating Compound | Comment | Organism | Structure |
---|---|---|---|---|
7.1.1.9 | 3-Amino-1,2,4-triazole | - |
Arabidopsis thaliana | |
7.1.1.9 | salicylic acid | produces a slight and transient increase in transcript levels of COX19 | Arabidopsis thaliana | |
7.1.1.9 | sodium nitroprusside | produces a several fold increase in COX19 expression after 4 h of treatment, but transcript levels return to normal values after higher incubation times | Arabidopsis thaliana |
EC Number | Application | Comment | Organism |
---|---|---|---|
7.1.1.9 | additional information | Arabidopsis thaliana COX19 genes encode functional homologues of the yeast metal chaperone. Smaller COX19-1 isoform, but not the larger one, is able to restore growth on non-fermentable carbon sources when expressed in a yeast cox19 null mutant. Induction by biotic and abiotic stress factors may indicate a relevant role of this protein in the biogenesis of cytochrome c oxidase to replace damaged forms of the enzyme. COX19 has additional functions besides its participation in COX assembly as, for example, metal transport, detoxification, or general protection against oxidative stress | Arabidopsis thaliana |
EC Number | Cloned (Comment) | Organism |
---|---|---|
7.1.1.9 | cDNAs from both COX19-1 splice variants cloned in the sense and antisense orientations in plasmid pYPGE15, containing a constitutive phosphoglycerate kinase gene promoter and a CYC1 terminator. Expressed in a yeast cox19 null mutant | Arabidopsis thaliana |
EC Number | Inhibitors | Comment | Organism | Structure |
---|---|---|---|---|
7.1.1.9 | additional information | import of COX19 is not inhibited by the ionophore valinomycin indicating that an electrical membrane potential is not required | Arabidopsis thaliana |
EC Number | Localization | Comment | Organism | GeneOntology No. | Textmining |
---|---|---|---|---|---|
7.1.1.9 | inner membrane | AtCOX19 isoforms are imported into mitochondria in vitro and are attached to the inner membrane facing the intermembrane space | Arabidopsis thaliana | - |
- |
7.1.1.9 | mitochondrion | - |
Arabidopsis thaliana | 5739 | - |
EC Number | Metals/Ions | Comment | Organism | Structure |
---|---|---|---|---|
7.1.1.9 | Cu2+ | increases COX19 transcript levels | Arabidopsis thaliana | |
7.1.1.9 | Fe2+ | - |
Arabidopsis thaliana | |
7.1.1.9 | Zn2+ | - |
Arabidopsis thaliana |
EC Number | Organism | UniProt | Comment | Textmining |
---|---|---|---|---|
7.1.1.9 | Arabidopsis thaliana | - |
ecotype Columbia | - |
EC Number | Source Tissue | Comment | Organism | Textmining |
---|---|---|---|---|
7.1.1.9 | anther | highly stained in AtCOX19-1::GUS plants | Arabidopsis thaliana | - |
7.1.1.9 | leaf | expression in leaves is only observed when cuts are produced, suggesting an induction by wounding | Arabidopsis thaliana | - |
7.1.1.9 | additional information | infection of plants with the pathogenic bacterium Pseudomonas syringae pv. tomato induces COX19 gene expression | Arabidopsis thaliana | - |
7.1.1.9 | root | highly stained in AtCOX19-1::GUS plants. Activity in roots is already evident at very early stages of development (1-2 days after imbibition), but not in embryos at late stages of embryogenesis and is higher in the root meristem, the vascular cylinder and nascent secondary roots | Arabidopsis thaliana | - |
EC Number | Synonyms | Comment | Organism |
---|---|---|---|
7.1.1.9 | COX19 | - |
Arabidopsis thaliana |
7.1.1.9 | cytochrome c oxidase | - |
Arabidopsis thaliana |