Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/2997
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Type: Journal article
Title: Binding site for the C-domain of insulin-like growth factor (IGF) binding protein-6 on IGF-II; implications for inhibition of IGF actions
Author: Headey, S.
Keizer, D.
Yao, S.
Wallace, J.
Bach, L.
Norton, R.
Citation: FEBS Letters, 2004; 568(1-3):19-22
Publisher: Elsevier Science BV
Issue Date: 2004
ISSN: 0014-5793
1873-3468
Statement of
Responsibility: 
Stephen J. Headey, David W. Keizer, Shenggen Yao, John C. Wallace, Leon A. Bach, and Raymond S. Norton
Abstract: Insulin-like growth factors (IGFs) are important mediators of growth and IGF-binding proteins (IGFBPs) 1–6 regulate IGF actions. As IGFBP C-terminal domains contribute to high-affinity IGF binding, we have defined the binding site for the C-domain of IGFBP-6 on IGF-II using NMR. This site lies adjacent to and between the binding sites for the IGFBP N-domain and IGF-I receptor (IGFIR), which have previously been found on opposite sides of the IGF molecule. The C-domain is therefore likely to interfere with IGF binding to the IGFIR, providing a structural basis for the potent inhibitory effects of intact IGFBPs on IGF actions.
Keywords: Insulin-like growth factor
Binding protein
Structure
Nuclear magnetic resonance
Interaction surface
Description: Copyright © 2004 Federation of European Biochemical Societies
DOI: 10.1016/j.febslet.2004.04.091
Published version: http://dx.doi.org/10.1016/j.febslet.2004.04.091
Appears in Collections:Aurora harvest 6
Molecular and Biomedical Science publications

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