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6SMO

AntDE:AntF (apo): type II PKS acyl-carrier protein in complex with its ketosynthase bound to the hexaketide

Summary for 6SMO
Entry DOI10.2210/pdb6smo/pdb
Related1TQY 6SM4
DescriptorAcyl carrier protein, PKS_KS domain-containing protein, Ketoacyl_synth_N domain-containing protein, ... (7 entities in total)
Functional Keywordsnatural product biosynthesis, polyketides, minimal pks system, anthraquinone, chain elongation, catalysis, protein binding
Biological sourcePhotorhabdus luminescens
More
Total number of polymer chains7
Total formula weight276168.93
Authors
Braeuer, A.,Zhou, Q.,Grammbitter, G.L.C.,Schmalhofer, M.,Ruehl, M.,Kaila, V.R.I.,Bode, H.,Groll, M. (deposition date: 2019-08-22, release date: 2020-05-27, Last modification date: 2024-01-24)
Primary citationBrauer, A.,Zhou, Q.,Grammbitter, G.L.C.,Schmalhofer, M.,Ruhl, M.,Kaila, V.R.I.,Bode, H.B.,Groll, M.
Structural snapshots of the minimal PKS system responsible for octaketide biosynthesis.
Nat.Chem., 12:755-763, 2020
Cited by
PubMed Abstract: Type II polyketide synthases (PKSs) are multi-enzyme complexes that produce secondary metabolites of medical relevance. Chemical backbones of such polyketides are produced by minimal PKS systems that consist of a malonyl transacylase, an acyl carrier protein and an α/β heterodimeric ketosynthase. Here, we present X-ray structures of all ternary complexes that constitute the minimal PKS system for anthraquinone biosynthesis in Photorhabdus luminescens. In addition, we characterize this invariable core using molecular simulations, mutagenesis experiments and functional assays. We show that malonylation of the acyl carrier protein is accompanied by major structural rearrangements in the transacylase. Principles of an ongoing chain elongation are derived from the ternary complex with a hexaketide covalently linking the heterodimeric ketosynthase with the acyl carrier protein. Our results for the minimal PKS system provide mechanistic understanding of PKSs and a fundamental basis for engineering PKS pathways for future applications.
PubMed: 32632186
DOI: 10.1038/s41557-020-0491-7
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.7 Å)
Structure validation

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