1svo

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(New page: 200px<br /><applet load="1svo" size="450" color="white" frame="true" align="right" spinBox="true" caption="1svo, resolution 2.6&Aring;" /> '''Structure of SV40 lar...)
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[[Image:1svo.gif|left|200px]]<br /><applet load="1svo" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1svo, resolution 2.6&Aring;" />
caption="1svo, resolution 2.6&Aring;" />
'''Structure of SV40 large T antigen helicase domain'''<br />
'''Structure of SV40 large T antigen helicase domain'''<br />
==Overview==
==Overview==
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The large tumor antigen (LTag) of simian virus 40, an AAA(+) protein, is a, hexameric helicase essential for viral DNA replication in eukaryotic, cells. LTag functions as an efficient molecular machine powered by ATP, binding and hydrolysis for origin DNA melting and replication fork, unwinding. To understand how ATP binding and hydrolysis are coupled to, conformational changes, we have determined high-resolution structures (, approximately 1.9 A) of LTag hexamers in distinct nucleotide binding, states. The structural differences of LTag in various nucleotide states, detail the molecular mechanisms of conformational changes triggered by ATP, binding/hydrolysis and reveal a potential mechanism of concerted, nucleotide binding and hydrolysis. During these conformational changes, the angles and orientations between domains of a monomer alter, creating, an "iris"-like motion in the hexamer. Additionally, six unique beta, hairpins on the channel surface move longitudinally along the central, channel, possibly serving as a motor for pulling DNA into the LTag double, hexamer for unwinding.
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The large tumor antigen (LTag) of simian virus 40, an AAA(+) protein, is a hexameric helicase essential for viral DNA replication in eukaryotic cells. LTag functions as an efficient molecular machine powered by ATP binding and hydrolysis for origin DNA melting and replication fork unwinding. To understand how ATP binding and hydrolysis are coupled to conformational changes, we have determined high-resolution structures ( approximately 1.9 A) of LTag hexamers in distinct nucleotide binding states. The structural differences of LTag in various nucleotide states detail the molecular mechanisms of conformational changes triggered by ATP binding/hydrolysis and reveal a potential mechanism of concerted nucleotide binding and hydrolysis. During these conformational changes, the angles and orientations between domains of a monomer alter, creating an "iris"-like motion in the hexamer. Additionally, six unique beta hairpins on the channel surface move longitudinally along the central channel, possibly serving as a motor for pulling DNA into the LTag double hexamer for unwinding.
==About this Structure==
==About this Structure==
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1SVO is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Simian_virus_40 Simian virus 40] with ZN as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1SVO OCA].
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1SVO is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Simian_virus_40 Simian virus 40] with <scene name='pdbligand=ZN:'>ZN</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1SVO OCA].
==Reference==
==Reference==
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[[Category: Simian virus 40]]
[[Category: Simian virus 40]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: Chen, X.S.]]
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[[Category: Chen, X S.]]
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[[Category: Finkielstein, C.V.]]
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[[Category: Finkielstein, C V.]]
[[Category: Gai, D.]]
[[Category: Gai, D.]]
[[Category: Zhao, R.]]
[[Category: Zhao, R.]]
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[[Category: aaa+ fold]]
[[Category: aaa+ fold]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Wed Nov 21 02:45:59 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:05:41 2008''

Revision as of 13:05, 21 February 2008


1svo, resolution 2.6Å

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Structure of SV40 large T antigen helicase domain

Overview

The large tumor antigen (LTag) of simian virus 40, an AAA(+) protein, is a hexameric helicase essential for viral DNA replication in eukaryotic cells. LTag functions as an efficient molecular machine powered by ATP binding and hydrolysis for origin DNA melting and replication fork unwinding. To understand how ATP binding and hydrolysis are coupled to conformational changes, we have determined high-resolution structures ( approximately 1.9 A) of LTag hexamers in distinct nucleotide binding states. The structural differences of LTag in various nucleotide states detail the molecular mechanisms of conformational changes triggered by ATP binding/hydrolysis and reveal a potential mechanism of concerted nucleotide binding and hydrolysis. During these conformational changes, the angles and orientations between domains of a monomer alter, creating an "iris"-like motion in the hexamer. Additionally, six unique beta hairpins on the channel surface move longitudinally along the central channel, possibly serving as a motor for pulling DNA into the LTag double hexamer for unwinding.

About this Structure

1SVO is a Single protein structure of sequence from Simian virus 40 with as ligand. Full crystallographic information is available from OCA.

Reference

Mechanisms of conformational change for a replicative hexameric helicase of SV40 large tumor antigen., Gai D, Zhao R, Li D, Finkielstein CV, Chen XS, Cell. 2004 Oct 1;119(1):47-60. PMID:15454080

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