Proteins
Curated comments from UniProt
Type | Comment | Proteins |
---|---|---|
4CL1_ARATH-2 4CL1_ARATH | function | Produces CoA thioesters of a variety of hydroxy- and methoxy-substituted cinnamic acids, which are used to synthesize several phenylpropanoid-derived compounds, including anthocyanins, flavonoids, isoflavonoids, coumarins, lignin, suberin and wall-bound phenolics (PubMed:10417722). Follows a two-step reaction mechanism, wherein the carboxylate substrate first undergoes adenylation by ATP, followed by a thioesterification in the presence of CoA to yield the final CoA thioesters (By similarity). |
4CL1_ARATH-2 4CL1_ARATH | pathway | Phytoalexin biosynthesis; 3,4',5-trihydroxystilbene biosynthesis; 3,4',5-trihydroxystilbene from trans-4-coumarate: step 1/2. |
4CL1_ARATH-2 A8MS69_ARATH 4CL1_ARATH | similarity | Belongs to the ATP-dependent AMP-binding enzyme family. |
4CL1_ARATH-2 4CL1_ARATH | tissue specificity | Preferentially expressed in roots, bolting stems and siliques. Also detected in leaves. |
Function
Gene Ontology
cellular component | |
---|---|
cytoplasm | ECO |
molecular function | |
ATP binding | ECO |
(E)-caffeate-CoA ligase activity | ECO |
4-coumarate-CoA ligase activity | ECO |
biological process | |
phenylpropanoid metabolic process | ECO |
Interactions
Interaction Network
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