7OC6

Selenomethionine derivative of alpha-humulene synthase AsR6 from Sarocladium schorii

Summary for 7OC6

• Entry DOI: 10.2210/pdb7oc6/pdb
• Descriptor: Alpha-humulene synthase asR6, GLYCEROL, SULFATE ION, ... (5 entities in total)
• Functional Keywords: cyclase, terpene cyclase, 2e-humulene, alpha-humulene, humulene, xenovulene, tropolone sesquiterpenoid, biosynthetic protein
• Biological source: Sarocladium schorii (Acremonium strictum (strain IMI 501407))
• Total number of polymer chains: 1
• Total formula weight: 54150.57

Authors

Schotte, C.,Lukat, P.,Deuschmann, A.,Blankenfeldt, W.,Cox, R.J. (deposition date: 2021-04-26, release date: 2021-07-07, Last modification date: 2024-10-23)

Primary citation

Schotte, C.,Lukat, P.,Deuschmann, A.,Blankenfeldt, W.,Cox, R.J.
Understanding and Engineering the Stereoselectivity of Humulene Synthase.
Angew.Chem.Int.Ed.Engl., 60:20308-20312, 2021

PubMed Abstract: The non-canonical terpene cyclase AsR6 is responsible for the formation of 2E,6E,9E-humulene during the biosynthesis of the tropolone sesquiterpenoid (TS) xenovulene A. The structures of unliganded AsR6 and of AsR6 in complex with an in crystallo cyclized reaction product and thiolodiphosphate reveal a new farnesyl diphosphate binding motif that comprises a unique binuclear Mg -cluster and an essential K289 residue that is conserved in all humulene synthases involved in TS formation. Structure-based site-directed mutagenesis of AsR6 and its homologue EupR3 identify a single residue, L285/M261, that controls the production of either 2E,6E,9E- or 2Z,6E,9E-humulene. A possible mechanism for the observed stereoselectivity was investigated using different isoprenoid precursors and results demonstrate that M261 has gatekeeping control over product formation.

PubMed: 34180566
DOI: 10.1002/anie.202106718

Experimental method

X-RAY DIFFRACTION (2.01 Å)