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1iq1

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(New page: 200px<br /><applet load="1iq1" size="450" color="white" frame="true" align="right" spinBox="true" caption="1iq1, resolution 2.8&Aring;" /> '''CRYSTAL STRUCTURE OF ...)
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[[Image:1iq1.jpg|left|200px]]<br /><applet load="1iq1" size="450" color="white" frame="true" align="right" spinBox="true"
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[[Image:1iq1.jpg|left|200px]]<br /><applet load="1iq1" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1iq1, resolution 2.8&Aring;" />
caption="1iq1, resolution 2.8&Aring;" />
'''CRYSTAL STRUCTURE OF THE IMPORTIN-ALPHA(44-54)-IMPORTIN-ALPHA(70-529) COMPLEX'''<br />
'''CRYSTAL STRUCTURE OF THE IMPORTIN-ALPHA(44-54)-IMPORTIN-ALPHA(70-529) COMPLEX'''<br />
==Overview==
==Overview==
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Proteins containing the classical nuclear localization sequences (NLSs), are imported into the nucleus by the importin-alpha/beta heterodimer., Importin-alpha contains the NLS binding site, whereas importin-beta, mediates the translocation through the nuclear pore. We characterized the, interactions involving importin-alpha during nuclear import using a, combination of biophysical techniques (biosensor, crystallography, sedimentation equilibrium, electrophoresis, and circular dichroism)., Importin-alpha is shown to exist in a monomeric autoinhibited state, (association with NLSs undetectable by biosensor). Association with, importin-beta (stoichiometry, 1:1; K(D) = 1.1 x 10(-8) m) increases the, affinity for NLSs; the importin-alpha/beta complex binds representative, monopartite NLS (simian virus 40 large T-antigen) and bipartite NLS, (nucleoplasmin) with affinities (K(D) = 3.5 x 10(-8) m and 4.8 x 10(-8) m, respectively) comparable with those of a truncated importin-alpha lacking, the autoinhibitory domain (T-antigen NLS, K(D) = 1.7 x 10(-8) m;, nucleoplasmin NLS, K(D) = 1.4 x 10(-8) m). The autoinhibitory domain (as a, separate peptide) binds the truncated importin-alpha, and the crystal, structure of the complex resembles the structure of full-length, importin-alpha. Our results support the model of regulation of nuclear, import mediated by the intrasteric autoregulatory sequence of, importin-alpha and provide a quantitative description of the binding and, regulatory steps during nuclear import.
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Proteins containing the classical nuclear localization sequences (NLSs) are imported into the nucleus by the importin-alpha/beta heterodimer. Importin-alpha contains the NLS binding site, whereas importin-beta mediates the translocation through the nuclear pore. We characterized the interactions involving importin-alpha during nuclear import using a combination of biophysical techniques (biosensor, crystallography, sedimentation equilibrium, electrophoresis, and circular dichroism). Importin-alpha is shown to exist in a monomeric autoinhibited state (association with NLSs undetectable by biosensor). Association with importin-beta (stoichiometry, 1:1; K(D) = 1.1 x 10(-8) m) increases the affinity for NLSs; the importin-alpha/beta complex binds representative monopartite NLS (simian virus 40 large T-antigen) and bipartite NLS (nucleoplasmin) with affinities (K(D) = 3.5 x 10(-8) m and 4.8 x 10(-8) m, respectively) comparable with those of a truncated importin-alpha lacking the autoinhibitory domain (T-antigen NLS, K(D) = 1.7 x 10(-8) m; nucleoplasmin NLS, K(D) = 1.4 x 10(-8) m). The autoinhibitory domain (as a separate peptide) binds the truncated importin-alpha, and the crystal structure of the complex resembles the structure of full-length importin-alpha. Our results support the model of regulation of nuclear import mediated by the intrasteric autoregulatory sequence of importin-alpha and provide a quantitative description of the binding and regulatory steps during nuclear import.
==About this Structure==
==About this Structure==
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1IQ1 is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Mus_musculus Mus musculus]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1IQ1 OCA].
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1IQ1 is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Mus_musculus Mus musculus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1IQ1 OCA].
==Reference==
==Reference==
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[[Category: Protein complex]]
[[Category: Protein complex]]
[[Category: Catimel, B.]]
[[Category: Catimel, B.]]
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[[Category: Fontes, M.R.M.]]
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[[Category: Fontes, M R.M.]]
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[[Category: Jennings, I.G.]]
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[[Category: Jennings, I G.]]
[[Category: Kobe, B.]]
[[Category: Kobe, B.]]
[[Category: Teh, T.]]
[[Category: Teh, T.]]
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[[Category: solenoid]]
[[Category: solenoid]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Nov 20 17:34:17 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:14:20 2008''

Revision as of 11:14, 21 February 2008


1iq1, resolution 2.8Å

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CRYSTAL STRUCTURE OF THE IMPORTIN-ALPHA(44-54)-IMPORTIN-ALPHA(70-529) COMPLEX

Overview

Proteins containing the classical nuclear localization sequences (NLSs) are imported into the nucleus by the importin-alpha/beta heterodimer. Importin-alpha contains the NLS binding site, whereas importin-beta mediates the translocation through the nuclear pore. We characterized the interactions involving importin-alpha during nuclear import using a combination of biophysical techniques (biosensor, crystallography, sedimentation equilibrium, electrophoresis, and circular dichroism). Importin-alpha is shown to exist in a monomeric autoinhibited state (association with NLSs undetectable by biosensor). Association with importin-beta (stoichiometry, 1:1; K(D) = 1.1 x 10(-8) m) increases the affinity for NLSs; the importin-alpha/beta complex binds representative monopartite NLS (simian virus 40 large T-antigen) and bipartite NLS (nucleoplasmin) with affinities (K(D) = 3.5 x 10(-8) m and 4.8 x 10(-8) m, respectively) comparable with those of a truncated importin-alpha lacking the autoinhibitory domain (T-antigen NLS, K(D) = 1.7 x 10(-8) m; nucleoplasmin NLS, K(D) = 1.4 x 10(-8) m). The autoinhibitory domain (as a separate peptide) binds the truncated importin-alpha, and the crystal structure of the complex resembles the structure of full-length importin-alpha. Our results support the model of regulation of nuclear import mediated by the intrasteric autoregulatory sequence of importin-alpha and provide a quantitative description of the binding and regulatory steps during nuclear import.

About this Structure

1IQ1 is a Protein complex structure of sequences from Mus musculus. Full crystallographic information is available from OCA.

Reference

Biophysical characterization of interactions involving importin-alpha during nuclear import., Catimel B, Teh T, Fontes MR, Jennings IG, Jans DA, Howlett GJ, Nice EC, Kobe B, J Biol Chem. 2001 Sep 7;276(36):34189-98. Epub 2001 Jul 11. PMID:11448961

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