4OKZ
Selinadiene Synthase in complex with dihydrofarnesyl pyrophosphate
Summary for 4OKZ
| Entry DOI | 10.2210/pdb4okz/pdb |
| Related | 1PS1 4MC0 4MC3 4OKM |
| Descriptor | Terpene 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 Keywords | sesquiterpene, cyclase, terpenoid, induced fit, closed conformation, dihydrofarnesyl pyrophosphate, pyrophosphate sensor, transferase |
| Biological source | Streptomyces pristinaespiralis |
| Total number of polymer chains | 4 |
| Total formula weight | 166962.84 |
| 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 citation | Baer, 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: 24890698DOI: 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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