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21IG

Crystal structure of terpeniod cyclase SpSODS from rhizobacterium Serratia plymuthica

Summary for 21IG
Entry DOI10.2210/pdb21ig/pdb
DescriptorTerpene synthase, GLYCEROL (3 entities in total)
Functional Keywordsterpeniod cyclase, sodorifen synthase, spsods, lyase
Biological sourceSerratia plymuthica 4Rx13
Total number of polymer chains2
Total formula weight84703.52
Authors
Li, X.Q.,Zheng, Y.,Zhang, L.L.,Huang, J.-W.,Chen, C.-C.,Guo, R.-T. (deposition date: 2025-12-13, release date: 2026-03-18, Last modification date: 2026-03-25)
Primary citationLi, X.,Zhang, L.,Zheng, Y.,Pan, N.,Zhou, Z.,Huang, Y.,Liang, Q.,Huang, J.W.,Chen, C.C.,Guo, R.T.
Structure and catalytic mechanism of C 16 terpenoid cyclase SpSODS from Serratia plymuthica.
Int.J.Biol.Macromol., 352:151065-151065, 2026
Cited by
PubMed Abstract: Terpenoid cyclases (TCs) utilize acyclic linear C precursors as substrates to synthesize structurally diverse terpenoids that contain mono- or polycyclic carbon skeletons. A C terpenoid cyclase SpSODS from Rhizobacterium Serratia plymuthica 4R×13 transforms the monocyclic α-pre-sodorifen pyrophosphate (α-PSPP, C) to homoterpenoid sodorifen with a bicyclo[3.2.1]octadiene skeleton. Here, we report the crystal structure of SpSODS and its complexes with pyrophosphate (PPi) and substrate analogue geranyl pyrophosphate (GPP) in a closed conformation. These structures reveal the conformational transitions between the open and closed states, and demonstrate the residues involved in the substrate-interaction network. Combining the mutagenesis experiments and the docking assays, we inferred key residues that could play an essential role in each step of the previously proposed sodorifen synthesis process. Notably, a water molecule that is stabilized by Y318, N241, and R237, and invariantly seen in all resolved structures might involve in the deprotonation at the final stage of the reaction. These findings provide insight into the structure and catalytic mechanism of SpSODS and lay an important foundation for future investigations of this type of non-canonical TCs.
PubMed: 41747984
DOI: 10.1016/j.ijbiomac.2026.151065
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.22 Å)
Structure validation

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