2ZGO

Crystal structure of AAL mutant H59Q complex with lactose

2ZGO の概要

• エントリーDOI: 10.2210/pdb2zgo/pdb
• 関連するPDBエントリー: 2ZGK 2ZGL 2ZGM 2ZGN 2ZGP 2ZGQ 2ZGR 2ZGS 2ZGT 2ZGU
• 関連するBIRD辞書のPRD_ID: PRD_900004
• 分子名称: Anti-tumor lectin, beta-D-galactopyranose-(1-4)-beta-D-glucopyranose (3 entities in total)
• 機能のキーワード: galectin, jelly roll, apoptosis, hydrolase, nuclease
• 由来する生物種: Agrocybe aegerita (Black poplar mushroom)
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 37024.86

構造登録者

Li, D.F.,Yang, N.,Wang, D.C. (登録日: 2008-01-23, 公開日: 2009-01-20, 最終更新日: 2023-11-01)

主引用文献

Yang, N.,Li, D.F.,Feng, L.,Xiang, Y.,Liu, W.,Sun, H.,Wang, D.C.
Structural basis for the tumor cell apoptosis-inducing activity of an antitumor lectin from the edible mushroom Agrocybe aegerita
J.Mol.Biol., 387:694-705, 2009

PubMed Abstract: Lectin AAL (Agrocybe aegerita lectin) from the edible mushroom A. aegerita is an antitumor protein that exerts its tumor-suppressing function via apoptosis-inducing activity in cancer cells. The crystal structures of ligand-free AAL and its complex with lactose have been determined. The AAL structure shows a dimeric organization, and each protomer adopts a prototype galectin fold. To identify the structural determinants for antitumor effects arising from the apoptosis-inducing activity of AAL, 11 mutants were prepared and subjected to comprehensive investigations covering oligomerization detection, carbohydrate binding test, apoptosis-inducing activity assay, and X-ray crystallographic analysis. The results show that dimerization of AAL is a prerequisite for its tumor cell apoptosis-inducing activity, and both galactose and glucose are basic moieties of functional carbohydrate ligands for lectin bioactivity. Furthermore, we have identified a hydrophobic pocket that is essential for the protein's apoptosis-inducing activity but independent of its carbohydrate binding and dimer formation. This hydrophobic pocket comprises a hydrophobic cluster including residues Leu33, Leu35, Phe93, and Ile144, and is involved in AAL's function mechanism as an integrated structural motif. Single mutants such as F93G or I144G do not disrupt carbohydrate binding and homodimerization capabilities, but abolish the bioactivity of the protein. These findings reveal the structural basis for the antitumor property of AAL, which may lead to de novo designs of antitumor drugs based on AAL as a prototype model.

PubMed: 19361423
DOI: 10.1016/j.jmb.2009.02.002

実験手法

X-RAY DIFFRACTION (2 Å)