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1cf1

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(New page: 200px<br /><applet load="1cf1" size="450" color="white" frame="true" align="right" spinBox="true" caption="1cf1, resolution 2.8&Aring;" /> '''ARRESTIN FROM BOVINE ...)
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[[Image:1cf1.gif|left|200px]]<br /><applet load="1cf1" size="450" color="white" frame="true" align="right" spinBox="true"
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[[Image:1cf1.gif|left|200px]]<br /><applet load="1cf1" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1cf1, resolution 2.8&Aring;" />
caption="1cf1, resolution 2.8&Aring;" />
'''ARRESTIN FROM BOVINE ROD OUTER SEGMENTS'''<br />
'''ARRESTIN FROM BOVINE ROD OUTER SEGMENTS'''<br />
==Overview==
==Overview==
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G protein-coupled signaling is utilized by a wide variety of eukaryotes, for communicating information from the extracellular environment. Signal, termination is achieved by the action of the arrestins, which bind to, activated, phosphorylated G protein-coupled receptors. We describe here, crystallographic studies of visual arrestin in its basal conformation. The, salient features of the structure are a bipartite molecule with an unusual, polar core. This core is stabilized in part by an extended, carboxy-terminal tail that locks the molecule into an inactive state. In, addition, arrestin is found to be a dimer of two asymmetric molecules, suggesting an intrinsic conformational plasticity. In conjunction with, biochemical and mutagenesis data, we propose a molecular mechanism by, which arrestin is activated for receptor binding.
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G protein-coupled signaling is utilized by a wide variety of eukaryotes for communicating information from the extracellular environment. Signal termination is achieved by the action of the arrestins, which bind to activated, phosphorylated G protein-coupled receptors. We describe here crystallographic studies of visual arrestin in its basal conformation. The salient features of the structure are a bipartite molecule with an unusual polar core. This core is stabilized in part by an extended carboxy-terminal tail that locks the molecule into an inactive state. In addition, arrestin is found to be a dimer of two asymmetric molecules, suggesting an intrinsic conformational plasticity. In conjunction with biochemical and mutagenesis data, we propose a molecular mechanism by which arrestin is activated for receptor binding.
==About this Structure==
==About this Structure==
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1CF1 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Bos_taurus Bos taurus]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1CF1 OCA].
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1CF1 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Bos_taurus Bos taurus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1CF1 OCA].
==Reference==
==Reference==
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[[Category: Bos taurus]]
[[Category: Bos taurus]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: Gurevich, V.V.]]
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[[Category: Gurevich, V V.]]
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[[Category: Hirsch, J.A.]]
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[[Category: Hirsch, J A.]]
[[Category: Schubert, C.]]
[[Category: Schubert, C.]]
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[[Category: Sigler, P.B.]]
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[[Category: Sigler, P B.]]
[[Category: binding to acticated and phosphorylated rhodopsin]]
[[Category: binding to acticated and phosphorylated rhodopsin]]
[[Category: desensitisation of the visual transduction cascade]]
[[Category: desensitisation of the visual transduction cascade]]
[[Category: visual arrestin]]
[[Category: visual arrestin]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Nov 20 12:24:21 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 12:05:28 2008''

Revision as of 10:05, 21 February 2008


1cf1, resolution 2.8Å

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ARRESTIN FROM BOVINE ROD OUTER SEGMENTS

Overview

G protein-coupled signaling is utilized by a wide variety of eukaryotes for communicating information from the extracellular environment. Signal termination is achieved by the action of the arrestins, which bind to activated, phosphorylated G protein-coupled receptors. We describe here crystallographic studies of visual arrestin in its basal conformation. The salient features of the structure are a bipartite molecule with an unusual polar core. This core is stabilized in part by an extended carboxy-terminal tail that locks the molecule into an inactive state. In addition, arrestin is found to be a dimer of two asymmetric molecules, suggesting an intrinsic conformational plasticity. In conjunction with biochemical and mutagenesis data, we propose a molecular mechanism by which arrestin is activated for receptor binding.

About this Structure

1CF1 is a Single protein structure of sequence from Bos taurus. Full crystallographic information is available from OCA.

Reference

The 2.8 A crystal structure of visual arrestin: a model for arrestin's regulation., Hirsch JA, Schubert C, Gurevich VV, Sigler PB, Cell. 1999 Apr 16;97(2):257-69. PMID:10219246

Page seeded by OCA on Thu Feb 21 12:05:28 2008

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