Detail Information

P450 Protein:

P450 SymbolCYP79A1
Protein NameTyrosine N-monooxygenase
Uniprot IDQ43135
EC Number1.14.14.36
Gene ID 8061413
SpeciesSorghum bicolor (Sorghum) (Sorghum vulgare)
Txid 4558
P450 Protein Structure
Model Confidence (pLDDT)
Very high (>90)
High (90 > 70)
Low (70 > 50)
Very low (<50)
Subcellular LocationEndoplasmic reticulum membrane; Single-pass membrane protein
Protein Sequence GO

Reaction Scheme:

Chemical Conversion C9H11NO5 + H+ → C8H9NO2 + CO2 + H2O
Reaction TypeOxidoreduction
Chemical BondCH-NH2;Carboxyl
RheaID 23044

N,N-dihydroxy-L-tyrosine

+

H+

CYP79A1

(E)-4-Hydroxyphenylacetaldehyde Oxime

+

CO2

+

H2O

Substrate Information:

Substrate Name N,N-dihydroxy-L-tyrosine
Substrate Chemical FormulaC9H11NO5
Substrate PubChem CID5461147
Substrate SmilesC1=CC(=CC=C1C[C@@H](C(=O)O)N(O)O)O
Substrate Structure
Substrate Name H+
Substrate Chemical FormulaH+
Substrate PubChem CID1038
Substrate CAS Number12408-02-5
Substrate Smiles[H+]
Substrate Structure

Product Information:

Product Name (E)-4-Hydroxyphenylacetaldehyde Oxime
Product Chemical FormulaC8H9NO2
Product PubChem CID5460411
Product SmilesC1=CC(=CC=C1C/C=N/O)O
Product Structure
Product Name CO2
Product Chemical FormulaCO2
Product PubChem CID280
Product CAS Number124-38-9
Product SmilesO=C=O
Product Structure
Product Name H2O
Product Chemical FormulaH2O
Product PubChem CID962
Product CAS Number7732-18-5
Product SmilesO
Product Structure

References:

Title: Isolation of the heme-thiolate enzyme cytochrome P-450TYR, which catalyzes the committed step in the biosynthesis of the cyanogenic glucoside dhurrin in Sorghum bicolor (L.) Moench.
PMID: 7937883
Journal: Proceedings of the National Academy of Sciences of the United States of America
Year: 1994/10/11

Contact zhy1001@alu.uestc.edu.cn or yangzhang@cdutcm.edu.cn
© Department of Bioinformatics