5OL6

Crystal structure of an inactivated Npu SICLOPPS intein with CAFHPQ extein

5OL6 の概要

• エントリーDOI: 10.2210/pdb5ol6/pdb
• 関連するPDBエントリー: 5OL1 5OL5
• 分子名称: Nucleic acid binding, OB-fold, tRNA/helicase-type,DNA-directed DNA polymerase (2 entities in total)
• 機能のキーワード: intein, extein, siclopps, cyclic peptide, splicing
• 由来する生物種: Nostoc punctiforme (strain ATCC 29133 / PCC 73102); 詳細
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 34813.37

構造登録者

Kick, L.M.,Schneider, S. (登録日: 2017-07-26, 公開日: 2017-09-27, 最終更新日: 2024-11-06)

主引用文献

Kick, L.M.,Harteis, S.,Koch, M.F.,Schneider, S.
Mechanistic Insights into Cyclic Peptide Generation by DnaE Split-Inteins through Quantitative and Structural Investigation.
Chembiochem, 18:2242-2246, 2017

PubMed Abstract: Inteins carry out protein-splicing reactions, which are used in protein chemistry, protein engineering and biotechnological applications. Rearrangement of the order of the domains in split-inteins results in head-to-tail cyclisation of the target sequence, which can be used for genetic encoding and expression of libraries of cyclic peptides (CPs). The efficiency of the splicing reaction depends on the target sequence. Here we used mass spectrometry to assess in vivo cyclic peptide formation from different hexameric target sequences by the DnaE split-inteins from Synechocystis sp. and Nostoc punctiforme, revealing a strong impact of the target sequence and of the intein on the intracellular peptide concentration. Furthermore, we determined the crystal structures of their pre-splicing complexes, which allowed us to identify F-block Asp17 as crucial for the DnaE-mediated splicing reaction.

PubMed: 28914478
DOI: 10.1002/cbic.201700503

実験手法

X-RAY DIFFRACTION (2 Å)