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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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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2002
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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. |
format | Text |
id | pubmed-2173053 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2002 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
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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