From Wikipedia, the free encyclopedia
2-amino-4-deoxychorismate dehydrogenase
Identifiers
EC no. 1.3.99.24
Databases
IntEnz IntEnz view
BRENDA BRENDA entry
ExPASy NiceZyme view
KEGG KEGG entry
MetaCyc metabolic pathway
PRIAM profile
PDB structures RCSB PDB PDBe PDBsum
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PMC articles
PubMed articles
NCBI proteins

2-Amino-4-deoxychorismate dehydrogenase ( EC 1.3.99.24, ADIC dehydrogenase, 2-amino-2-deoxyisochorismate dehydrogenase, SgcG) is an enzyme with systematic name (2S)-2-amino-4-deoxychorismate:FMN oxidoreductase. [1] [2] This enzyme catalyses the following chemical reaction

(2S)-2-amino-4-deoxychorismate + FMN 3-(1-carboxyvinyloxy)anthranilate + FMNH2

This enzyme participates in the formation of the benzoxazolinate moiety of the enediyne antitumour antibiotic C-1027].

References

  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.

External links

From Wikipedia, the free encyclopedia
2-amino-4-deoxychorismate dehydrogenase
Identifiers
EC no. 1.3.99.24
Databases
IntEnz IntEnz view
BRENDA BRENDA entry
ExPASy NiceZyme view
KEGG KEGG entry
MetaCyc metabolic pathway
PRIAM profile
PDB structures RCSB PDB PDBe PDBsum
Search
PMC articles
PubMed articles
NCBI proteins

2-Amino-4-deoxychorismate dehydrogenase ( EC 1.3.99.24, ADIC dehydrogenase, 2-amino-2-deoxyisochorismate dehydrogenase, SgcG) is an enzyme with systematic name (2S)-2-amino-4-deoxychorismate:FMN oxidoreductase. [1] [2] This enzyme catalyses the following chemical reaction

(2S)-2-amino-4-deoxychorismate + FMN 3-(1-carboxyvinyloxy)anthranilate + FMNH2

This enzyme participates in the formation of the benzoxazolinate moiety of the enediyne antitumour antibiotic C-1027].

References

  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.

External links


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