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4OKZ

Selinadiene Synthase in complex with dihydrofarnesyl pyrophosphate

Summary for 4OKZ
Entry DOI10.2210/pdb4okz/pdb
Related1PS1 4MC0 4MC3 4OKM
DescriptorTerpene synthase metal-binding domain-containing protein, MAGNESIUM ION, (3S,6E)-3,7,11-trimethyldodeca-6,10-dien-1-yl trihydrogen diphosphate, ... (4 entities in total)
Functional Keywordssesquiterpene, cyclase, terpenoid, induced fit, closed conformation, dihydrofarnesyl pyrophosphate, pyrophosphate sensor, transferase
Biological sourceStreptomyces pristinaespiralis
Total number of polymer chains4
Total formula weight166962.84
Authors
Baer, P.,Rabe, P.,Fischer, K.,Citron, C.A.,Klapschinski, T.,Groll, M.,Dickschat, J.S. (deposition date: 2014-01-23, release date: 2014-06-11, Last modification date: 2023-09-20)
Primary citationBaer, P.,Rabe, P.,Fischer, K.,Citron, C.A.,Klapschinski, T.A.,Groll, M.,Dickschat, J.S.
Induced-fit mechanism in class i terpene cyclases.
Angew.Chem.Int.Ed.Engl., 53:7652-7656, 2014
Cited by
PubMed Abstract: We present crystallographic and functional data of selina-4(15),7(11)-diene synthase (SdS) from Streptomyces pristinaespiralis in its open and closed (ligand-bound) conformation. We could identify an induced-fit mechanism by elucidating a rearrangement of the G1/2 helix-break motif upon substrate binding. This rearrangement highlights a novel effector triad comprising the pyrophosphate sensor Arg178, the linker Asp181, and the effector Gly182-O. This structural motif is strictly conserved in class I terpene cyclases from bacteria, fungi, and plants, including epi-isozizaene synthase (3KB9), aristolochene synthase (4KUX), bornyl diphosphate synthase (1N20), limonene synthase (2ONG), 5-epi-aristolochene synthase (5EAT), and taxa-4(5),11(12)-diene synthase (3P5R). An elaborate structure-based mutagenesis in combination with analysis of the distinct product spectra confirmed the mechanistic models of carbocation formation and stabilization in SdS.
PubMed: 24890698
DOI: 10.1002/anie.201403648
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.9 Å)
Structure validation

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