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EC Number Substrates Commentary Substrates Organism Products Commentary (Products) Reversibility
Show all pathways known for 5.3.3.19Display the reaction diagram Show all sequences 5.3.3.193-[(4R)-4-hydroxycyclohexa-1,5-dien-1-yl]-2-oxopropanoate - Bacillus subtilis (3Z)-3-[(4R)-4-hydroxycyclohex-2-en-1-ylidene]-2-oxopropanoate - ?
Show all pathways known for 5.3.3.19Display the reaction diagram Show all sequences 5.3.3.193-[(4R)-4-hydroxycyclohexa-1,5-dien-1-yl]-2-oxopropanoate the enzyme from the bacterium Bacillus subtilis is involved in the biosynthesis of the nonproteinogenic amino acid tetrahydrotyrosine a component of the dipeptide antibiotic bacilysin Bacillus subtilis (3Z)-3-[(4R)-4-hydroxycyclohex-2-en-1-ylidene]-2-oxopropanoate - ?
Show all pathways known for 5.3.3.19Display the reaction diagram Show all sequences 5.3.3.193-[(4R)-4-hydroxycyclohexa-1,5-dien-1-yl]-2-oxopropanoate 3-[(4S)-4-hydroxycyclohexa-1,5-dien-1-yl]-2-oxopropanoate also undergoes a nonenzymatic isomerization Bacillus subtilis (3Z)-3-[(4R)-4-hydroxycyclohex-2-en-1-ylidene]-2-oxopropanoate - ?
Show all pathways known for 5.3.3.19Display the reaction diagram Show all sequences 5.3.3.193-[(4R)-4-hydroxycyclohexa-1,5-dien-1-yl]-2-oxopropanoate nonenzymatic isomerization gives (3E)-3-[(4S)-4-hydroxycyclohex-2-en-1-ylidene]-2-oxopropanoate and (3Z)-3-[(4S)-4-hydroxycyclohex-2-en-1-ylidene]-2-oxopropanoate in the ratio 50:1. Isomerization by BacB gives a 3:1 mixture of the E- and Z-isomers Bacillus subtilis (3Z)-3-[(4R)-4-hydroxycyclohex-2-en-1-ylidene]-2-oxopropanoate - ?
Show all pathways known for 5.3.3.19Display the reaction diagram Show all sequences 5.3.3.193-[(4R)-4-hydroxycyclohexa-1,5-dien-1-yl]-2-oxopropanoate the enzyme generates a mixture of 3E- and 3Z-isomers. It equilibrates the more stable 3E and less stable 3Z geometric isomers to give up to 25% of the 3Z isomer, which on subsequent reduction by BacG gives the desired 4S stereochemistry of the cyclohexanol scaffold Bacillus subtilis (3Z)-3-[(4R)-4-hydroxycyclohex-2-en-1-ylidene]-2-oxopropanoate - ?
Show all pathways known for 5.3.3.19Display the reaction diagram Show all sequences 5.3.3.193-[(4R)-4-hydroxycyclohexa-1,5-dien-1-yl]-2-oxopropanoate the enzyme from the bacterium Bacillus subtilis is involved in the biosynthesis of the nonproteinogenic amino acid tetrahydrotyrosine a component of the dipeptide antibiotic bacilysin Bacillus subtilis 168 (3Z)-3-[(4R)-4-hydroxycyclohex-2-en-1-ylidene]-2-oxopropanoate - ?
Show all pathways known for 5.3.3.19Display the reaction diagram Show all sequences 5.3.3.193-[(4R)-4-hydroxycyclohexa-1,5-dien-1-yl]-2-oxopropanoate 3-[(4S)-4-hydroxycyclohexa-1,5-dien-1-yl]-2-oxopropanoate also undergoes a nonenzymatic isomerization Bacillus subtilis 168 (3Z)-3-[(4R)-4-hydroxycyclohex-2-en-1-ylidene]-2-oxopropanoate - ?
Show all pathways known for 5.3.3.19Display the reaction diagram Show all sequences 5.3.3.193-[(4R)-4-hydroxycyclohexa-1,5-dien-1-yl]-2-oxopropanoate nonenzymatic isomerization gives (3E)-3-[(4S)-4-hydroxycyclohex-2-en-1-ylidene]-2-oxopropanoate and (3Z)-3-[(4S)-4-hydroxycyclohex-2-en-1-ylidene]-2-oxopropanoate in the ratio 50:1. Isomerization by BacB gives a 3:1 mixture of the E- and Z-isomers Bacillus subtilis 168 (3Z)-3-[(4R)-4-hydroxycyclohex-2-en-1-ylidene]-2-oxopropanoate - ?
Show all pathways known for 5.3.3.19Display the reaction diagram Show all sequences 5.3.3.193-[(4R)-4-hydroxycyclohexa-1,5-dien-1-yl]-2-oxopropanoate the enzyme generates a mixture of 3E- and 3Z-isomers. It equilibrates the more stable 3E and less stable 3Z geometric isomers to give up to 25% of the 3Z isomer, which on subsequent reduction by BacG gives the desired 4S stereochemistry of the cyclohexanol scaffold Bacillus subtilis 168 (3Z)-3-[(4R)-4-hydroxycyclohex-2-en-1-ylidene]-2-oxopropanoate - ?
Show all pathways known for 5.3.3.19Display the reaction diagram Show all sequences 5.3.3.193-[(4R)-4-hydroxycyclohexa-1,5-dien-1-yl]-2-oxopropanoate - Bacillus subtilis 168 (3Z)-3-[(4R)-4-hydroxycyclohex-2-en-1-ylidene]-2-oxopropanoate - ?
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