Inhibitors | Comment | Organism | Structure |
---|---|---|---|
2-bromodecanoic acid | - |
Meyerozyma guilliermondii | |
2-bromooctanoic acid | - |
Meyerozyma guilliermondii | |
2-bromopalmitic acid | potent inhibitor | Meyerozyma guilliermondii | |
chlorpromazine | - |
Meyerozyma guilliermondii | |
tetradecylglycidic acid | - |
Meyerozyma guilliermondii |
Localization | Comment | Organism | GeneOntology No. | Textmining |
---|---|---|---|---|
cytosol | - |
Rattus norvegicus | 5829 | - |
cytosol | - |
Meyerozyma guilliermondii | 5829 | - |
peroxisome | - |
Rattus norvegicus | 5777 | - |
peroxisome | - |
Meyerozyma guilliermondii | 5777 | - |
Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
---|---|---|---|---|---|---|
acyl-CoA + L-carnitine | Rattus norvegicus | - |
acyl-L-carnitine + CoA | - |
r | |
acyl-CoA + L-carnitine | Meyerozyma guilliermondii | metabolic pathway of peroxisomal beta-oxidation in yeasts | acyl-L-carnitine + CoA | - |
r | |
acyl-L-carnitine + CoA | Rattus norvegicus | - |
acyl-CoA + L-carnitine | - |
r | |
acyl-L-carnitine + CoA | Meyerozyma guilliermondii | - |
acyl-CoA + L-carnitine | - |
r |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Meyerozyma guilliermondii | - |
yeast | - |
Rattus norvegicus | - |
rat | - |
Source Tissue | Comment | Organism | Textmining |
---|---|---|---|
hepatocyte | - |
Rattus norvegicus | - |
Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|
acyl-CoA + L-carnitine | - |
Rattus norvegicus | acyl-L-carnitine + CoA | - |
r | |
acyl-CoA + L-carnitine | - |
Meyerozyma guilliermondii | acyl-L-carnitine + CoA | - |
r | |
acyl-CoA + L-carnitine | metabolic pathway of peroxisomal beta-oxidation in yeasts | Meyerozyma guilliermondii | acyl-L-carnitine + CoA | - |
r | |
acyl-L-carnitine + CoA | - |
Rattus norvegicus | acyl-CoA + L-carnitine | - |
r | |
acyl-L-carnitine + CoA | - |
Meyerozyma guilliermondii | acyl-CoA + L-carnitine | - |
r |