1qm7

From Proteopedia

Revision as of 02:05, 25 November 2007 by OCA (Talk | contribs)
(diff) ←Older revision | Current revision (diff) | Newer revision→ (diff)
Jump to: navigation, search

1qm7, resolution 2.1Å

Drag the structure with the mouse to rotate

X-RAY STRUCTURE OF A THREE-FINGERED CHIMERIC PROTEIN, STABILITY OF A STRUCTURAL SCAFFOLD

Overview

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.

About this Structure

1QM7 is a Protein complex structure of sequences from [1]. Full crystallographic information is available from OCA.

Reference

Stability of a structural scaffold upon activity transfer: X-ray structure of a three fingers chimeric protein., Le Du MH, Ricciardi A, Khayati M, Menez R, Boulain JC, Menez A, Ducancel F, J Mol Biol. 2000 Mar 3;296(4):1017-26. PMID:10686100 [[Category: ]]

Page seeded by OCA on Sun Nov 25 04:13:06 2007

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools