2-Amino-4-deoxychorismate synthase

2-amino-4-deoxychorismate synthase (EC 2.6.1.86, ADIC synthase, 2-amino-2-deoxyisochorismate synthase, SgcD) is an enzyme with systematic name (2S)-2-amino-4-deoxychorismate:2-oxoglutarate aminotransferase.[1][2][3][4] This enzyme catalyses the following chemical reaction

2-amino-4-deoxychorismate synthase
Identifiers
EC no.2.6.1.86
Databases
IntEnzIntEnz view
BRENDABRENDA entry
ExPASyNiceZyme view
KEGGKEGG entry
MetaCycmetabolic pathway
PRIAMprofile
PDB structuresRCSB PDB PDBe PDBsum
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PMCarticles
PubMedarticles
NCBIproteins
(2S)-2-amino-4-deoxychorismate + L-glutamate chorismate + L-glutamine

This enzyme requires Mg2+. The reaction occurs in the reverse direction.

References

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  1. ^ Van Lanen SG, Lin S, Shen B (January 2008). "Biosynthesis of the enediyne antitumor antibiotic C-1027 involves a new branching point in chorismate metabolism". Proceedings of the National Academy of Sciences of the United States of America. 105 (2): 494–9. Bibcode:2008PNAS..105..494V. doi:10.1073/pnas.0708750105. PMC 2206564. PMID 18182490.
  2. ^ Yu, L.; Mah, S.; Otani, T.; Dedon, P. (1995). "The benzoxazolinate of C-1027 confers intercalative DNA binding". J. Am. Chem. Soc. 117 (34): 8877–8878. doi:10.1021/ja00139a032.
  3. ^ McDonald M, Mavrodi DV, Thomashow LS, Floss HG (September 2001). "Phenazine biosynthesis in Pseudomonas fluorescens: branchpoint from the primary shikimate biosynthetic pathway and role of phenazine-1,6-dicarboxylic acid". Journal of the American Chemical Society. 123 (38): 9459–60. doi:10.1021/ja011243. PMID 11562236.
  4. ^ Laursen JB, Nielsen J (March 2004). "Phenazine natural products: biosynthesis, synthetic analogues, and biological activity". Chemical Reviews. 104 (3): 1663–86. doi:10.1021/cr020473j. PMID 15008629.
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