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The face of TSR revealed: an extracellular signaling domain is exposed

In this issue, Tan et al. (2002) report the first high resolution (1.9 Å) structural data for thrombospondin (TSP)-1, a large multifunctional protein that regulates cell adhesion, angiogenesis, cell proliferation and survival, TGFβ activation, and protease function (for review see Chen et al., 2000)...

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Detalles Bibliográficos
Autor principal: Silverstein, Roy L.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2173053/
https://www.ncbi.nlm.nih.gov/pubmed/12403807
http://dx.doi.org/10.1083/jcb.200209138
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author Silverstein, Roy L.
author_facet Silverstein, Roy L.
author_sort Silverstein, Roy L.
collection PubMed
description In this issue, Tan et al. (2002) report the first high resolution (1.9 Å) structural data for thrombospondin (TSP)-1, a large multifunctional protein that regulates cell adhesion, angiogenesis, cell proliferation and survival, TGFβ activation, and protease function (for review see Chen et al., 2000). Because TSP-1 has multiple binding partners and many functions, precise structural information is crucial to understanding its biology. The structure now reported, derived from crystals of the second and third type I repeats of TSP-1 is of particular interest because of the specific functions attributed to these repeats and because domains homologous to the repeats appear in many other proteins in nature. The novel layered fold motif described brings great insight into how the complicated functions of TSP-1 and related molecules are affected.
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spelling pubmed-21730532008-05-01 The face of TSR revealed: an extracellular signaling domain is exposed Silverstein, Roy L. J Cell Biol Comment In this issue, Tan et al. (2002) report the first high resolution (1.9 Å) structural data for thrombospondin (TSP)-1, a large multifunctional protein that regulates cell adhesion, angiogenesis, cell proliferation and survival, TGFβ activation, and protease function (for review see Chen et al., 2000). Because TSP-1 has multiple binding partners and many functions, precise structural information is crucial to understanding its biology. The structure now reported, derived from crystals of the second and third type I repeats of TSP-1 is of particular interest because of the specific functions attributed to these repeats and because domains homologous to the repeats appear in many other proteins in nature. The novel layered fold motif described brings great insight into how the complicated functions of TSP-1 and related molecules are affected. The Rockefeller University Press 2002-10-28 /pmc/articles/PMC2173053/ /pubmed/12403807 http://dx.doi.org/10.1083/jcb.200209138 Text en Copyright © 2002, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Comment
Silverstein, Roy L.
The face of TSR revealed: an extracellular signaling domain is exposed
title The face of TSR revealed: an extracellular signaling domain is exposed
title_full The face of TSR revealed: an extracellular signaling domain is exposed
title_fullStr The face of TSR revealed: an extracellular signaling domain is exposed
title_full_unstemmed The face of TSR revealed: an extracellular signaling domain is exposed
title_short The face of TSR revealed: an extracellular signaling domain is exposed
title_sort face of tsr revealed: an extracellular signaling domain is exposed
topic Comment
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2173053/
https://www.ncbi.nlm.nih.gov/pubmed/12403807
http://dx.doi.org/10.1083/jcb.200209138
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