5EAU

5-EPI-ARISTOLOCHENE SYNTHASE FROM NICOTIANA TABACUM

Summary for 5EAU

• Entry DOI: 10.2210/pdb5eau/pdb
• Descriptor: 5-EPI-ARISTOLOCHENE SYNTHASE, MAGNESIUM ION, TRIFLUOROFURNESYL DIPHOSPHATE, ... (4 entities in total)
• Functional Keywords: isoprenoid synthase, 5-epi-aristolochene synthase, natural products biosynthesis, isoprenoid cyclase
• Biological source: Nicotiana tabacum (common tobacco)
• Cellular location: Cytoplasm: Q40577
• Total number of polymer chains: 1
• Total formula weight: 63528.39

Authors

Starks, C.M.,Back, K.,Chappell, J.,Noel, J.P. (deposition date: 1997-12-11, release date: 1998-04-08, Last modification date: 2024-05-22)

Primary citation

Starks, C.M.,Back, K.,Chappell, J.,Noel, J.P.
Structural basis for cyclic terpene biosynthesis by tobacco 5-epi-aristolochene synthase.
Science, 277:1815-1820, 1997

PubMed Abstract: Terpene cyclases catalyze the synthesis of cyclic terpenes with 10-, 15-, and 20-carbon acyclic isoprenoid diphosphates as substrates. Plants have been a source of these natural products by providing a homologous set of terpene synthases. The crystal structures of 5-epi-aristolochene synthase, a sesquiterpene cyclase from tobacco, alone and complexed separately with two farnesyl diphosphate analogs were analyzed. These structures reveal an unexpected enzymatic mechanism for the synthesis of the bicyclic product, 5-epi-aristolochene, and provide a basis for understanding the stereochemical selectivity displayed by other cyclases in the biosynthesis of pharmacologically important cyclic terpenes. As such, these structures provide templates for the engineering of novel terpene cyclases.

PubMed: 9295271
DOI: 10.1126/science.277.5333.1815

Experimental method

X-RAY DIFFRACTION (2.15 Å)