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Structure and interactions of NCAM modules 1 and 2, basic elements in neural cell adhesion.

Authors :
Jensen PH
Soroka V
Thomsen NK
Ralets I
Berezin V
Bock E
Poulsen FM
Source :
Nature structural biology [Nat Struct Biol] 1999 May; Vol. 6 (5), pp. 486-93.
Publication Year :
1999

Abstract

The structure in solution of the second Ig-module fragment of residues 117-208 of NCAM has been determined. Like the first Ig-module of residues 20-116, it belongs to the I set of the immunogloblin superfamily. Module 1 and module 2 interact weakly, and the binding sites of this interaction have been identified. The two-module fragment NCAM(20-208) is a stable dimer. Removal of the charged residues in these sites in NCAM(20-208) abolishes the dimerization. Modeling the dimer of NCAM(20-208) to fit the interactions of these charges produces one coherent binding site for the formation of two antiparallel strands of the first two NCAM modules. This mode of binding could be a major element in trans-cellular interactions in neural cell adhesion.

Details

Language :
English
ISSN :
1072-8368
Volume :
6
Issue :
5
Database :
MEDLINE
Journal :
Nature structural biology
Publication Type :
Academic Journal
Accession number :
10331878
Full Text :
https://doi.org/10.1038/8292