3AWK
Crystal structure of the polyketide synthase 1 from huperzia serrata
3AWK の概要
| エントリーDOI | 10.2210/pdb3awk/pdb |
| 関連するPDBエントリー | 3AWJ |
| 分子名称 | Chalcone synthase-like polyketide synthase, GLYCEROL, SULFATE ION, ... (4 entities in total) |
| 機能のキーワード | type iii polyketide synthase, chalcone synthase, transferase |
| 由来する生物種 | Huperzia serrata (toothed club-moss) |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 43943.24 |
| 構造登録者 | |
| 主引用文献 | Morita, H.,Yamashita, M.,Shi, S.P.,Wakimoto, T.,Kondo, S.,Kato, R.,Sugio, S.,Kohno, T.,Abe, I. Synthesis of unnatural alkaloid scaffolds by exploiting plant polyketide synthase. Proc.Natl.Acad.Sci.USA, 108:13504-13509, 2011 Cited by PubMed Abstract: HsPKS1 from Huperzia serrata is a type III polyketide synthase (PKS) with remarkable substrate tolerance and catalytic potential. Here we present the synthesis of unnatural unique polyketide-alkaloid hybrid molecules by exploiting the enzyme reaction using precursor-directed and structure-based approaches. HsPKS1 produced novel pyridoisoindole (or benzopyridoisoindole) with the 6.5.6-fused (or 6.6.5.6-fused) ring system by the condensation of 2-carbamoylbenzoyl-CoA (or 3-carbamoyl-2-naphthoyl-CoA), a synthetic nitrogen-containing nonphysiological starter substrate, with two molecules of malonyl-CoA. The structure-based S348G mutant not only extended the product chain length but also altered the cyclization mechanism to produce a biologically active, ring-expanded 6.7.6-fused dibenzoazepine, by the condensation of 2-carbamoylbenzoyl-CoA with three malonyl-CoAs. Thus, the basic nitrogen atom and the structure-based mutagenesis enabled additional C─C and C─N bond formation to generate the novel polyketide-alkaloid scaffold. PubMed: 21825160DOI: 10.1073/pnas.1107782108 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2 Å) |
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