Detail Information for IndEnz0016000028
IED ID IndEnz0016000028
Enzyme Type ID tyrosinase000028
Protein Name Aureusidin synthase
AmAS1
EC 1.21.3.6
Gene Name AS1
Organism Antirrhinum majus (Garden snapdragon)
Taxonomic Lineage cellular organisms Eukaryota Viridiplantae Streptophyta Streptophytina Embryophyta Tracheophyta Euphyllophyta Spermatophyta Magnoliopsida Mesangiospermae eudicotyledons Gunneridae Pentapetalae asterids lamiids Lamiales Plantaginaceae Antirrhineae Antirrhinum (snapdragons) Antirrhinum majus (Garden snapdragon)
Enzyme Sequence MFKNPNIRYHKLSSKSNDNDQESSHRCKHILLFIITLFLLIVGLYIANSLAYARFASTSTGPIAAPDVTKCGQPDLPPGTAPINCCPPIPAKIIDFELPPPSTTMRVRRAAHLVDDAYIAKFKKAVELMRALPEDDPRSFKQQANVHCAYCAGAYNQAGFTNLKLQIHRSWLFFPFHRYYIYFFERILGKLINDTTFALPFWNYDSPGGMTIPSMFIDTNSSLYDSLRDSNHQPPTIVDLNYAFSDSDNTTTPEEQMIINLKIVYRQMVSSAKTPQLFFGRPYRRGDQEFPGVGSIELVPHGMIHLWTGSENTPYGENMGAFYSTARDPIFFAHHSNVDRMWSIWKTLGGPRRTDLTDPDFLDASFVFYDENAEMVRVKVRDCLDEKKLGYVYQDVEIPWLNTRPTPKVSPSLLKKFHRTNTANPRQVFPAILDRVLKVIVTRPKKTRSRKEKDELEEILVIEGIELERDHGHVKFDVYINADEDDLAVISPENAEFAGSFVSLWHKPIKGKRTKTQLLTLSICDILEDLDADEDDYVLVTLVPRNAGDAIKIHNVKIELDG
Enzyme Length 562
Uniprot Accession Number Q9FRX6
Absorption
Active Site
Activity Regulation ACTIVITY REGULATION: H(2)O(2) activates the 3-hydroxylation and oxidative cyclization of tetrahydroxychalcone but inhibits reaction with pentahydroxychalcone. Inhibited by phenylthiourea. {ECO:0000269|PubMed:11073455, ECO:0000269|PubMed:11418122}.
Binding Site
Calcium Binding
catalytic Activity CATALYTIC ACTIVITY: Reaction=2',4,4',6'-tetrahydroxychalcone 4'-O-beta-D-glucoside + H(+) + O2 = aureusidin 6-O-beta-glucoside + H2O; Xref=Rhea:RHEA:34203, ChEBI:CHEBI:15377, ChEBI:CHEBI:15378, ChEBI:CHEBI:15379, ChEBI:CHEBI:66905, ChEBI:CHEBI:77978; EC=1.21.3.6; Evidence={ECO:0000269|PubMed:11073455, ECO:0000269|PubMed:11418122}; CATALYTIC ACTIVITY: Reaction=2 2',3,4,4',6'-pentahydroxychalcone 4'-O-beta-D-glucoside + 2 H(+) + O2 = 2 aureusidin 6-O-beta-glucoside + 2 H2O; Xref=Rhea:RHEA:34195, ChEBI:CHEBI:15377, ChEBI:CHEBI:15378, ChEBI:CHEBI:15379, ChEBI:CHEBI:66905, ChEBI:CHEBI:77622; EC=1.21.3.6; Evidence={ECO:0000269|PubMed:11073455, ECO:0000269|PubMed:11418122}; CATALYTIC ACTIVITY: Reaction=2',3,4,4',6'-pentahydroxychalcone 4'-O-beta-D-glucoside + H(+) + O2 = bracteatin 6-O-beta-glucoside + H2O; Xref=Rhea:RHEA:34199, ChEBI:CHEBI:15377, ChEBI:CHEBI:15378, ChEBI:CHEBI:15379, ChEBI:CHEBI:66907, ChEBI:CHEBI:77622; EC=1.21.3.6; Evidence={ECO:0000269|PubMed:11073455, ECO:0000269|PubMed:11418122};
DNA Binding
EC Number 1.21.3.6
Enzyme Function FUNCTION: Involved in the biosynthesis of aurones, plant flavonoids that provide yellow coloration to flowers. Can use tetrahydroxychalcone (THC), pentahydroxychalcone (PHC), THC 4'-glucoside and PHC 4'-glucoside as substrates, but not 2'-hydroxychalcone, 4-hydroxychalcone, PHC 3-glucoside, 2',6'-dihydroxy-4,4'-dimethoxychalcone, naringenin, eriodictyol and 4,4',6-trihydroxyaurone. Can also produce bracteatin from PHC. {ECO:0000269|PubMed:11073455, ECO:0000269|PubMed:16832053}.
Temperature Dependency
PH Dependency BIOPHYSICOCHEMICAL PROPERTIES: pH dependence: Optimum pH is 5.4 for the reaction with tetrahydroxychalcone and 5.0 - 7.0 for the reaction with pentahydroxychalcone. {ECO:0000269|PubMed:11073455, ECO:0000269|PubMed:11418122};
Pathway
nucleotide Binding
Features Chain (1); Cross-link (1); Disulfide bond (2); Metal binding (6); Mutagenesis (2)
Keywords Copper;Direct protein sequencing;Disulfide bond;Glycoprotein;Metal-binding;Oxidoreductase;Thioether bond;Vacuole
Interact With
Induction
Subcellular Location SUBCELLULAR LOCATION: Vacuole lumen {ECO:0000269|PubMed:16367960, ECO:0000269|PubMed:16832053}.
Modified Residue
Post Translational Modification PTM: Glycosylated. {ECO:0000269|PubMed:11073455}.; PTM: Contains probably N- and C-terminal propeptides.
Signal Peptide
Structure 3D
Cross Reference PDB -
Mapped Pubmed ID -
Motif
Gene Encoded By
Mass 64,044
Kinetics BIOPHYSICOCHEMICAL PROPERTIES: Kinetic parameters: KM=4.3 uM for 2',4,4',6'-tetrahydroxychalcone {ECO:0000269|PubMed:11073455, ECO:0000269|PubMed:11418122}; KM=3.9 uM for 2',4,4',6'-tetrahydroxychalcone 4'-glucoside {ECO:0000269|PubMed:11073455, ECO:0000269|PubMed:11418122}; KM=2.5 uM for isoliquiritigenin {ECO:0000269|PubMed:11073455, ECO:0000269|PubMed:11418122}; KM=15.7 uM for 2',3,4,4',6'-pentahydroxychalcone {ECO:0000269|PubMed:11073455, ECO:0000269|PubMed:11418122}; KM=8.1 uM for 2',3,4,4',6'-pentahydroxychalcone 4'-glucoside {ECO:0000269|PubMed:11073455, ECO:0000269|PubMed:11418122}; KM=14.7 uM for butein {ECO:0000269|PubMed:11073455, ECO:0000269|PubMed:11418122};
Metal Binding METAL 147; /note=Copper A; /evidence=ECO:0000250|UniProtKB:Q9ZP19; METAL 168; /note=Copper A; /evidence=ECO:0000250|UniProtKB:Q9ZP19; METAL 177; /note=Copper A; /evidence=ECO:0000250|UniProtKB:Q9ZP19; METAL 301; /note=Copper B; /evidence=ECO:0000250|UniProtKB:Q9ZP19; METAL 305; /note=Copper B; /evidence=ECO:0000250|UniProtKB:Q9ZP19; METAL 335; /note=Copper B; /evidence=ECO:0000250|UniProtKB:Q9ZP19
Rhea ID RHEA:34203; RHEA:34195; RHEA:34199
Cross Reference Brenda 1.14.18.1;1.21.3.6;