5.3.3.19: 3-[(4R)-4-hydroxycyclohexa-1,5-dien-1-yl]-2-oxopropanoate isomerase

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For detailed information about 3-[(4R)-4-hydroxycyclohexa-1,5-dien-1-yl]-2-oxopropanoate isomerase, go to the full flat file.

Reaction

Synonyms

BacB

ECTree

     5 Isomerases

         5.3 Intramolecular oxidoreductases

             5.3.3 Transposing C=C bonds

                5.3.3.19 3-[(4R)-4-hydroxycyclohexa-1,5-dien-1-yl]-2-oxopropanoate isomerase

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Results	in table
18	AA Sequence
6	Cloned(Commentary)
2	Crystallization (Commentary)
6	General Information
1	General Stability
1	Inhibitors
1	KM Value [mM]
2	Metals/Ions
2	Natural Substrates/ Products (Substrates)
32	Organism
6	Pathway
2	pH Optimum
2	Protein Variants
5	Purification (Commentary)
3	Reaction
11	Reference
16	Substrates and Products (Substrate)
6	Synonyms
1	Systematic Name
3	Temperature Optimum [°C]
1	Turnover Number [1/s]

Systematic Name

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Systematic Name on EC 5.3.3.19 - 3-[(4R)-4-hydroxycyclohexa-1,5-dien-1-yl]-2-oxopropanoate isomerase

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SYSTEMATIC NAME

IUBMB Comments

3-[(4R)-4-hydroxycyclohexa-1,5-dien-1-yl]-2-oxopropanoate isomerase

The enzyme, characterized from the bacterium Bacillus subtilis, is involved in the biosynthesis of the nonribosomally synthesized dipeptide antibiotic bacilysin, composed of L-alanine and L-anticapsin. The enzyme can interconvert the (E) isomer formed in the reaction into the (Z) isomer [2], although this isomerization is not part of the pathway leading to bacilysin [3].