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1NBL

NMR Structure of Hellethionin D

1NBL の概要
エントリーDOI10.2210/pdb1nbl/pdb
NMR情報BMRB: 5670
分子名称Hellethionin D (1 entity in total)
機能のキーワードgamma thionins helleborus, toxin
由来する生物種Helleborus purpurascens
タンパク質・核酸の鎖数1
化学式量合計4915.62
構造登録者
Milbradt, A.G.,Kerek, F.,Moroder, L.,Renner, C. (登録日: 2002-12-03, 公開日: 2003-03-11, 最終更新日: 2024-11-20)
主引用文献Milbradt, A.G.,Kerek, F.,Moroder, L.,Renner, C.
Structural Characterization of Hellethionins from Helleborus purpurascens
Biochemistry, 42:2404-2411, 2003
Cited by
PubMed Abstract: Thionins are relatively small-sized multiple-cystine peptides that are probably involved in the plant defense against pathogens. As such, these peptides constitute promising candidates for engineered plant resistance in the agricultural industry. More recently, thionins have been proposed as potential immunotoxins in tumor therapy. In the search for pharmacologically active natural products, a new family of thionins was recently discovered in the roots of Helleborus purpurascens that accordingly were termed hellethionins. The structural characterization by NMR of one representative member of this family, i.e., of hellethionin D, clearly reveals that thionins from different sources share a highly conserved overall fold. In fact, the well-defined 3D structure of hellethionin D is very similar to those reported so far for viscotoxins, purothionins, or crambin, although distinct differences could be detected in the C-terminal portion, especially for loop 36-39. These differences may derive from the unusual distribution of charged residues in the C-terminal half of the peptide sequence compared to other thionins and from the uncommon occurrence of four contiguous threonine residues in loop 36-39. As expected, reduction of the disulfide bonds in hellethionin D leads to complete unfolding, but upon oxidative refolding by air oxygen in the presence of glutathione the correct isomer is recovered in high yields, confirming the very robust fold of this class of bioactive cystine peptides.
PubMed: 12600207
DOI: 10.1021/bi020628h
主引用文献が同じPDBエントリー
実験手法
SOLUTION NMR
構造検証レポート
Validation report summary of 1nbl
検証レポート(詳細版)ダウンロードをダウンロード

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件を2025-12-31に公開中

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