Literature summary extracted from
Roach, P.L.; Clifton, I.J.; Fulop, V.; Harlos, K.; Barton, G.J.; Hajdu, J.; Andersson, I.; Schofield, C.J.; Baldwin, J.E.
Crystal structure of isopenicillin N synthase is the first from a new structural family of enzymes (1995), Nature, 375, 700-704.
Activating Compound
EC Number |
Activating Compound |
Comment |
Organism |
Structure |
---|
1.21.3.1 |
O2 |
required |
Aspergillus nidulans |
|
Crystallization (Commentary)
EC Number |
Crystallization (Comment) |
Organism |
---|
1.21.3.1 |
enzyme complexed with manganese instead of iron in the active site, more stable |
Aspergillus nidulans |
1.21.3.1 |
structure analysis |
Aspergillus nidulans |
Metals/Ions
EC Number |
Metals/Ions |
Comment |
Organism |
Structure |
---|
1.21.3.1 |
Fe2+ |
- |
Aspergillus nidulans |
|
Natural Substrates/ Products (Substrates)
EC Number |
Natural Substrates |
Organism |
Comment (Nat. Sub.) |
Natural Products |
Comment (Nat. Pro.) |
Rev. |
Reac. |
---|
1.21.3.1 |
N-[(5S)-5-amino-5-carboxypentanoyl]-L-cysteinyl-D-valine + O2 |
Aspergillus nidulans |
common step in the biosynthesis of penicillins, cephalosporins and cephamycins |
isopenicillin N + 2 H2O |
product has antibiotic activity |
? |
|
Organism
EC Number |
Organism |
UniProt |
Comment |
Textmining |
---|
1.21.3.1 |
Aspergillus nidulans |
P05326 |
accession number SwissProt |
- |
Reaction
EC Number |
Reaction |
Comment |
Organism |
Reaction ID |
---|
1.21.3.1 |
N-[(5S)-5-amino-5-carboxypentanoyl]-L-cysteinyl-D-valine + O2 = isopenicillin N + 2 H2O |
structure and mechanism |
Aspergillus nidulans |
|
1.21.3.1 |
N-[(5S)-5-amino-5-carboxypentanoyl]-L-cysteinyl-D-valine + O2 = isopenicillin N + 2 H2O |
active site with conserved jelly-roll motif, cysteine residues are not directly involved in the coordination of the metal ion |
Aspergillus nidulans |
|
Substrates and Products (Substrate)
EC Number |
Substrates |
Comment Substrates |
Organism |
Products |
Comment (Products) |
Rev. |
Reac. |
---|
1.21.3.1 |
N-[(5S)-5-amino-5-carboxypentanoyl]-L-cysteinyl-D-valine + O2 |
- |
Aspergillus nidulans |
isopenicillin N + 2 H2O |
- |
? |
|
1.21.3.1 |
N-[(5S)-5-amino-5-carboxypentanoyl]-L-cysteinyl-D-valine + O2 |
common step in the biosynthesis of penicillins, cephalosporins and cephamycins |
Aspergillus nidulans |
isopenicillin N + 2 H2O |
product has antibiotic activity |
? |
|
Synonyms
EC Number |
Synonyms |
Comment |
Organism |
---|
1.21.3.1 |
IPNS |
- |
Aspergillus nidulans |