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Structure and interactions of NCAM modules 1 and 2, basic elements in neural cell adhesion.
- 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.
- Subjects :
- Amino Acid Substitution
Binding Sites
Cell Adhesion
Crystallization
Crystallography, X-Ray
Dimerization
Disulfides chemistry
Immunoglobulins chemistry
Models, Molecular
Molecular Sequence Data
Neural Cell Adhesion Molecules genetics
Neural Cell Adhesion Molecules metabolism
Neurons chemistry
Neurons cytology
Nuclear Magnetic Resonance, Biomolecular
Peptide Fragments chemistry
Peptide Fragments genetics
Protein Binding
Protein Conformation
Protein Structure, Secondary
Static Electricity
Thermodynamics
Neural Cell Adhesion Molecules chemistry
Neurons physiology
Peptide Fragments metabolism
Subjects
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