Detail Information

P450 Protein:

P450 SymbolttmP
Protein NameTtmP
Uniprot IDA0A0P0FVK8
SpeciesStreptomyces afghaniensis
Txid 66865
P450 Protein Structure
Model Confidence (pLDDT)
Very high (>90)
High (90 > 70)
Low (70 > 50)
Very low (<50)
Subcellular Location
Protein Sequence GO

Reaction Scheme:

Chemical Conversion C13H18O2S → C13H16O4S
Reaction TypeOxidation
Chemical BondCH3

(5R)-3,5-diethyl-4-hydroxy-5-[(1E)-2-methylbuta-1,3-dienyl]-2,5-dihydrothiophen-2-one

ttmP

[(2R)-4-ethyl-3-hydroxy-2-[(1E)-2-methylbuta-1,3-dienyl]-5-oxo-2,5-dihydrothiophen-2-yl]acetic acid

Substrate Information:

Substrate Name (5R)-3,5-diethyl-4-hydroxy-5-[(1E)-2-methylbuta-1,3-dienyl]-2,5-dihydrothiophen-2-one
Substrate Chemical FormulaC13H18O2S
Substrate PubChem CID135754258
Substrate SmilesO=C1C(CC)=C([C@@](CC)(/C=C(/C=C)C)S1)O
Substrate Structure

Product Information:

Product Name [(2R)-4-ethyl-3-hydroxy-2-[(1E)-2-methylbuta-1,3-dienyl]-5-oxo-2,5-dihydrothiophen-2-yl]acetic acid
Product Chemical FormulaC13H16O4S
Product SmilesO=C(C[C@]1(C(=C(CC)C(=O)S1)O)/C=C(C)/C=C)O
Product Structure

References:

Title: Synthesis, bioactivity, and enzymatic modification of antibacterial thiotetromycin derivatives.
PMID: 30869693
Journal: Organic & Biomolecular Chemistry
Year: 2019/3/11

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