Indole-3-acetic acid-amido synthetase GH3.17 (GH3.17), Recombinant Protein
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Indole-3-acetic acid-amido synthetase GH3.17 (GH3.17), Recombinant Protein

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Cat: RP06614
Species: Arabidopsis thaliana (Mouse-ear cress)
Datasheet:

Product Info

Full Product Name
Recombinant Arabidopsis thaliana Indole-3-acetic acid-amido synthetase GH3.17 (GH3.17) , partial
Product Gene Name
GH3.17 recombinant protein
Product Synonym Gene Name
GH3.17
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
53,095 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.
Protein Family
Indole-3-acetic acid-amido synthetase

NCBI/Uniprot Data

NCBI Accession #
NP_174134.1
NCBI GI #
15217844
NCBI GenBank Nucleotide #
NM_102578.4
NCBI GeneID
839706
NCBI Official Full Name
Auxin-responsive GH3 family protein
NCBI Official Symbol
GH3.17
NCBI Official Synonym Symbols
F3H9.21; F3H9_21
NCBI Protein Information
Auxin-responsive GH3 family protein
NCBI Summary
encodes an IAA-amido synthase that conjugates Asp and other amino acids to auxin in vitro. Lines carrying insertions in this gene are hypersensitive to auxin.
UniProt Gene Name
GH3.17
UniProt Synonym Gene Names
AtGH3-17
UniProt Protein Name
Indole-3-acetic acid-amido synthetase GH3.17
UniProt Synonym Protein Names
Auxin-responsive GH3-like protein 17; AtGH3-17
UniProt Primary Accession #
Q9FZ87
UniProt Related Accession #
Q9FZ87
UniProt Comments
Catalyzes the synthesis of indole-3-acetic acid (IAA)-amino acid conjugates, providing a mechanism for the plant to cope with the presence of excess auxin. Strongly reactive with Glu, Gln, Trp, Asp, Ala, Leu, Phe, Gly, Tyr, Met, Ile and Val. Appears to favor Glu over Asp while the other GH3 favor Asp over Glu. Little or no product formation with His, Ser, Thr, Arg, Lys, or Cys. Also active on pyruvic and butyric acid analogs of IAA, PAA and the synthetic auxin naphthaleneacetic acid (NAA). The two chlorinated synthetic auxin herbicides 2,4-D and 3,6-dichloro-o-anisic acid (dicamba) cannot be used as substrates.

For research use only, not for clinical use.