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4EVH

Crystal structure of calcium-bound alpha-1 giardin

4EVH の概要
エントリーDOI10.2210/pdb4evh/pdb
関連するPDBエントリー4EVF
分子名称Giardin subunit alpha-1, CALCIUM ION (3 entities in total)
機能のキーワードannexin, calcium-binding protein, membrane-binding protein, metal binding protein
由来する生物種Giardia intestinalis (Giardia lamblia)
細胞内の位置Cytoplasm, cytoskeleton: P17063
タンパク質・核酸の鎖数1
化学式量合計34022.07
構造登録者
Weeratunga, S.,Hofmann, A. (登録日: 2012-04-26, 公開日: 2012-07-25, 最終更新日: 2023-11-08)
主引用文献Weeratunga, S.K.,Osman, A.,Hu, N.-J.,Wang, C.K.,Mason, L.,Svard, S.,Hope, G.,Jones, M.K.,Hofmann, A.
Alpha-1 giardin is an annexin with highly unusual calcium-regulated mechanisms
J.Mol.Biol., 423:169-181, 2012
Cited by
PubMed Abstract: Alpha-giardins constitute the annexin proteome (group E annexins) in the intestinal protozoan parasite Giardia and, as such, represent the evolutionary oldest eukaryotic annexins. The dominance of alpha-giardins in the cytoskeleton of Giardia with its greatly reduced actin content emphasises the importance of the alpha-giardins for the structural integrity of the parasite, which is particularly critical in the transformation stage between cyst and trophozoite. In this study, we report the crystal structures of the apo- and calcium-bound forms of α1-giardin, a protein localised to the plasma membrane of Giardia trophozoites that has recently been identified as a vaccine target. The calcium-bound crystal structure of α1-giardin revealed the presence of a type III site in the first repeat as known from other annexin structures, as well as a novel calcium binding site situated between repeats I and IV. By means of comparison, the crystal structures of three different alpha-giardins known to date indicate that these proteins engage different calcium coordination schemes, among each other, as well as compared to annexins of groups A-D. Evaluation of the calcium-dependent binding to acidic phosphoplipid membranes revealed that this process is not only mediated but also regulated by the environmental calcium concentration. Uniquely within the large family of annexins, α1-giardin disengages from the phospholipid membrane at high calcium concentrations possibly due to formation of a dimeric species. The observed behaviour is in line with changing calcium levels experienced by the parasite during excystation and may thus provide first insights into the molecular mechanisms underpinning the transformation and survival of the parasite in the host.
PubMed: 22796298
DOI: 10.1016/j.jmb.2012.06.041
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.6 Å)
構造検証レポート
Validation report summary of 4evh
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2026-02-11に公開中

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