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EC Number Substrates Commentary Substrates Organism Products Commentary (Products) Reversibility
Display the word mapDisplay the reaction diagram Show all sequences 3.5.2.B2(+)-2-azabicyclo[2.2.1]hept-5-en-3-one + H2O - Saccharolobus solfataricus + (+)-4-amino-cyclopent-2-enecarboxylic acid - ?
Display the word mapDisplay the reaction diagram Show all sequences 3.5.2.B2(+)-2-azabicyclo[2.2.1]hept-5-en-3-one + H2O - Saccharolobus solfataricus ATCC 35092 + (+)-4-amino-cyclopent-2-enecarboxylic acid - ?
Display the word mapDisplay the reaction diagram Show all sequences 3.5.2.B2(1S,4R)-2-azabicyclo[2.2.1]hept-5-en-3-one + H2O - Microbacterium hydrocarbonoxydans (1R,4S)-4-aminocyclopent-2-ene-1-carbaldehyde - ?
Display the word mapDisplay the reaction diagram Show all sequences 3.5.2.B2(1S,4R)-2-azabicyclo[2.2.1]hept-5-en-3-one + H2O - Saccharolobus solfataricus (1R,4S)-4-aminocyclopent-2-ene-1-carbaldehyde - ?
Display the word mapDisplay the reaction diagram Show all sequences 3.5.2.B2(1S,4R)-2-azabicyclo[2.2.1]hept-5-en-3-one + H2O - Delftia acidovorans (1R,4S)-4-aminocyclopent-2-ene-1-carbaldehyde - ?
Display the word mapDisplay the reaction diagram Show all sequences 3.5.2.B2(1S,4R)-2-azabicyclo[2.2.1]hept-5-en-3-one + H2O - Saccharolobus solfataricus (1R,4S)-4-aminocyclopent-2-ene-1-carbaldehyde 50% yield. When racemic 2-azabicyclo[2.2.1]hept-5-en-3-one is used, (1R,4S)-2-azabicyclo[2.2.1]hept-5-en-3-one is produced with 99% enantiomeric excess ?
Display the word mapDisplay the reaction diagram Show all sequences 3.5.2.B2(1S,4R)-2-azabicyclo[2.2.1]hept-5-en-3-one + H2O - Aeropyrum pernix (1R,4S)-4-aminocyclopent-2-ene-1-carbaldehyde enzyme specifically hydrolyzes the (+)-lactam, (1S,4R)-2-azabicyclo[2.2.1]hept-5-en-3-one, without any actin against the (-)-isomer. Yield is 48%, 97% enantiomeric excess ?
Display the word mapDisplay the reaction diagram Show all sequences 3.5.2.B2(1S,4R)-2-azabicyclo[2.2.1]hept-5-en-3-one + H2O enantiospecific cleavage of (1S,4R)-isomer Bradyrhizobium japonicum (1R,4S)-4-aminocyclopent-2-ene-1-carbaldehyde 99.8% enantiomeric excess ?
Display the word mapDisplay the reaction diagram Show all sequences 3.5.2.B2(1S,4R)-2-azabicyclo[2.2.1]hept-5-en-3-one + H2O - Delftia acidovorans DSM 14801 (1R,4S)-4-aminocyclopent-2-ene-1-carbaldehyde - ?
Display the word mapDisplay the reaction diagram Show all sequences 3.5.2.B2(1S,4R)-2-azabicyclo[2.2.1]hept-5-en-3-one + H2O enantiospecific cleavage of (1S,4R)-isomer Bradyrhizobium japonicum USDA 6 (1R,4S)-4-aminocyclopent-2-ene-1-carbaldehyde 99.8% enantiomeric excess ?
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