2K32

Truncated AcrA from Campylobacter jejuni for glycosylation studies

2K32 の概要

• エントリーDOI: 10.2210/pdb2k32/pdb
• 関連するPDBエントリー: 2K33
• NMR情報: BMRB: 15735
• 分子名称: A (1 entity in total)
• 機能のキーワード: nonglycosylated acra, membrane protein, transport protein
• 由来する生物種: Campylobacter jejuni
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 12748.24

構造登録者

Slynko, V.,Schubert, M.,Numao, S.,Kowarik, M.,Aebi, M.,Allain, F. (登録日: 2008-04-17, 公開日: 2009-02-03, 最終更新日: 2024-05-08)

主引用文献

Slynko, V.,Schubert, M.,Numao, S.,Kowarik, M.,Aebi, M.,Allain, F.H.
NMR structure determination of a segmentally labeled glycoprotein using in vitro glycosylation.
J.Am.Chem.Soc., 131:1274-1281, 2009

PubMed Abstract: Although there is great interest in three-dimensional structures of glycoproteins and complex oligosaccharides, their structural determination have been hampered by inhomogeneous and incomplete glycosylation, poor expression, low tendency to crystallize, and severe chemical shift overlap. Using segmental labeling of the glycan and the protein component by in vitro glycosylation, we developed a novel method of NMR structural determination that overcomes some of these problems. Highly homogeneously glycosylated proteins in milligram amounts can be obtained. This allowed the determination of the structure of an N-linked glycoprotein from Campylobacter jejuni. The glycosylation acceptor site was found to be in a flexible loop. The presented methodology extends the observable NOE distance limit of oligosaccharides significantly over 4 A, resulting in a high number of distance restraints per glycosidic linkage. A well-defined glycan structure was obtained.

PubMed: 19154179
DOI: 10.1021/ja808682v

実験手法

SOLUTION NMR