4-coumarate--CoA ligase 3 (4CL3), Recombinant Protein
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4-coumarate--CoA ligase 3 (4CL3), Recombinant Protein

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Cat: RP00961
Species: Arabidopsis thaliana (Mouse-ear cress)
Datasheet:

Product Info

Full Product Name
Recombinant Arabidopsis thaliana 4-coumarate--CoA ligase 3 (4CL3) , partial
Product Gene Name
4CL3 recombinant protein
Product Synonym Gene Name
4CL3
Purity
Greater or equal to 85% purity as determined by SDS-PAGE. (lot specific)
Format
Lyophilized or liquid (Format to be determined during the manufacturing process)
Host
E Coli or Yeast or Baculovirus or Mammalian Cell
Molecular Weight
61,311 Da
Storage
Store at -20℃. For long-term storage, store at -20℃ or -80℃. Store working aliquots at 4℃ for up to one week. Repeated freezing and thawing is not recommended.

NCBI/Uniprot Data

NCBI Accession #
NP_176686.1
NCBI GI #
15217838
NCBI GenBank Nucleotide #
NM_105180.4
NCBI GeneID
842814
NCBI Official Full Name
4-coumarate:CoA ligase 3
NCBI Official Symbol
4CL3
NCBI Official Synonym Symbols
4-COUMARATE:COA LIGASE; 4-coumarate:CoA ligase 3; F16G16.6; F16G16_6
NCBI Protein Information
4-coumarate:CoA ligase 3
NCBI Summary
encodes an isoform of 4-coumarate:CoA ligase (4CL), which is involved in the last step of the general phenylpropanoid pathway. mRNA levels are not induced in response to wounding or to fungal infection by P. parasitica. mRNA is expressed in flowers, to a lesser degree in mature leaves and siliques and marginally in seedling roots and bolting stems of mature plants. The catalytic efficiency was in the following (descending) order: p-coumaric acid, caffeic acid, ferulic acid, cinnamic acid and 5-OH-ferulic acid. At4CL3 was unable to use sinapic acid as substrate.
UniProt Gene Name
4CL3
UniProt Synonym Gene Names
4CL 3; At4CL3
UniProt Protein Name
4-coumarate--CoA ligase 3
UniProt Synonym Protein Names
4-coumarate--CoA ligase isoform 3; At4CL3; 4-coumaroyl-CoA synthase 3
UniProt Primary Accession #
Q9S777
UniProt Secondary Accession #
Q93Z69
UniProt Related Accession #
Q9S777
UniProt Comments
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.

For research use only, not for clinical use.