1QM7

X-ray structure of a three-fingered chimeric protein, stability of a structural scaffold

1QM7 の概要

• エントリーDOI: 10.2210/pdb1qm7/pdb
• 関連するPDBエントリー: 1FAS 1FSC 1FSS 1MAH 1NEA
• 分子名称: R-CHII (2 entities in total)
• 機能のキーワード: toxin, stability of a structural scaffold
• 由来する生物種: SYNTHETIC CONSTRUCT
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 6694.86

構造登録者

Le Du, M.H.,Ricciardi, A.,Khayati, M.,Menez, R.,Boulain, J.C.,Menez, A.,Ducancel, F. (登録日: 1999-09-21, 公開日: 2000-03-15, 最終更新日: 2024-10-23)

主引用文献

Le Du, M.H.,Ricciardi, A.,Khayati, M.,Menez, R.,Boulain, J.C.,Menez, A.,Ducancel, F.
Stability of a Structural Scaffold Upon Activity Transfer : X-Ray Structure of a Three Fingers Chimeric Protein.
J.Mol.Biol., 296:1017-, 2000

PubMed Abstract: Fasciculin 2 and toxin alpha proteins belong to the same structural family of three-fingered snake toxins. They act on different targets, but in each case the binding region involves residues from loops I and II. The superimposition of the two structures suggests that these functional regions correspond to structurally distinct zones. Loop I, half of loop II and the C-terminal residue of fasciculin 2 were therefore transferred into the toxin alpha. The inhibition constant of the resulting chimera is only 15-fold lower than that of fasciculin 2, and as expected the potency of binding to the toxin alpha target has been lost. In order to understand the structure-function relationship between the chimera and its "parent" molecules, we solved its structure by X-ray crystallography. The protein crystallized in space group P3(1)21 with a=b=58.5 A, and c=62.3 A. The crystal structure was solved by molecular replacement and refined to 2.1 A resolution. The structure belongs to the three-fingered snake toxin family with a core of four disulphide bridges from which emerge the three loops I, II and III. Superimposition of the chimera on fasciculin 2 or toxin alpha revealed an overall fold intermediate between those of the two parent molecules. The regions corresponding to toxin alpha and to fasciculin 2 retained their respective geometries. In addition, the chimera protein displayed a structural behaviour similar to that of fasciculin 2, i.e. dimerization in the crystal structure of fasciculin 2, and the geometry of the region that binds to acetylcholinesterase. In conclusion, this structure shows that the chimera retains the general structural characteristics of three-fingered toxins, and the structural specificity of the transferred function.

PubMed: 10686100
DOI: 10.1006/JMBI.2000.3510

実験手法

X-RAY DIFFRACTION (2.1 Å)