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5WQH

Structure of fungal meroterpenoid isomerase Trt14 complexed with substrate analog and endo-terretonin D

Summary for 5WQH
Entry DOI10.2210/pdb5wqh/pdb
Related5WQF 5WQG 5WQI
DescriptorIsomerase trt14, CALCIUM ION, methyl (2S,4aR,4bS,5S,6aS,10aS,10bS,12aS)-2,4b,7,7,10a,12,12a-heptamethyl-5-oxidanyl-1,4,6,8-tetrakis(oxidanylidene)-4a,5,6a,9,10,10b-hexahydronaphtho[1,2-h]isochromene-2-carboxylate, ... (5 entities in total)
Functional Keywordsisomerase, meroterpenoid, terretonin
Biological sourceAspergillus terreus NIH 2624
Total number of polymer chains6
Total formula weight113069.20
Authors
Mori, T.,Matsuda, Y.,Abe, I. (deposition date: 2016-11-26, release date: 2017-07-26, Last modification date: 2023-11-08)
Primary citationMori, T.,Iwabuchi, T.,Hoshino, S.,Wang, H.,Matsuda, Y.,Abe, I.
Molecular basis for the unusual ring reconstruction in fungal meroterpenoid biogenesis
Nat. Chem. Biol., 13:1066-1073, 2017
Cited by
PubMed Abstract: Trt14 from Aspergillus terreus is involved in unusual skeletal reconstruction during the biosynthesis of the fungal meroterpenoid terretonin. Detailed in vitro characterization revealed that this novel multifunctional enzyme catalyzes not only the D-ring expansion via intramolecular methoxy rearrangement, but also the hydrolysis of the expanded D-ring. The X-ray crystal structures of Trt14, in complex with substrate or product, and two Trt14 homologs, AusH and PrhC from Aspergillus nidulans and Penicillium brasilianum, respectively, indicated similar overall structures to those of the NTF2-like superfamily of enzymes, despite lacking sequence and functional similarities. Moreover, we gained structural insight into the mechanism of the Trt14-catalyzed ring reconstruction from the in-crystal enzyme reaction and site-directed mutagenesis to show that this reaction involves sequential ester bond cleavage and formation. Structural comparison of Trt14 and its homologs suggests that the enzymes in this new superfamily employ similar acid-base chemistry to diversify the molecular architecture of fungal meroterpenoids.
PubMed: 28759016
DOI: 10.1038/nchembio.2443
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.102 Å)
Structure validation

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건을2025-07-02부터공개중

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