5UW7
PCY1 Y481F Variant in Complex with Follower Peptide
5UW7 の概要
| エントリーDOI | 10.2210/pdb5uw7/pdb |
| 関連するPDBエントリー | 5UW3 5UW5 5UW6 5UZW |
| 分子名称 | Peptide cyclase 1, Presegetalin A1, MAGNESIUM ION, ... (4 entities in total) |
| 機能のキーワード | natural product, orbitide, cyclase, lyase |
| 由来する生物種 | Vaccaria hispanica 詳細 |
| タンパク質・核酸の鎖数 | 4 |
| 化学式量合計 | 175166.20 |
| 構造登録者 | |
| 主引用文献 | Chekan, J.R.,Estrada, P.,Covello, P.S.,Nair, S.K. Characterization of the macrocyclase involved in the biosynthesis of RiPP cyclic peptides in plants. Proc. Natl. Acad. Sci. U.S.A., 114:6551-6556, 2017 Cited by PubMed Abstract: Enzymes that can catalyze the macrocyclization of linear peptide substrates have long been sought for the production of libraries of structurally diverse scaffolds via combinatorial gene assembly as well as to afford rapid in vivo screening methods. Orbitides are plant ribosomally synthesized and posttranslationally modified peptides (RiPPs) of various sizes and topologies, several of which are shown to be biologically active. The diversity in size and sequence of orbitides suggests that the corresponding macrocyclases may be ideal catalysts for production of cyclic peptides. Here we present the biochemical characterization and crystal structures of the plant enzyme PCY1 involved in orbitide macrocyclization. These studies demonstrate how the PCY1 S9A protease fold has been adapted for transamidation, rather than hydrolysis, of acyl-enzyme intermediates to yield cyclic products. Notably, PCY1 uses an unusual strategy in which the cleaved C-terminal follower peptide from the substrate stabilizes the enzyme in a productive conformation to facilitate macrocyclization of the N-terminal fragment. The broad substrate tolerance of PCY1 can be exploited as a biotechnological tool to generate structurally diverse arrays of macrocycles, including those with nonproteinogenic elements. PubMed: 28584123DOI: 10.1073/pnas.1620499114 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.37 Å) |
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