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1ile

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(New page: 200px<br /><applet load="1ile" size="450" color="white" frame="true" align="right" spinBox="true" caption="1ile, resolution 2.5&Aring;" /> '''ISOLEUCYL-TRNA SYNTHE...)
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[[Image:1ile.gif|left|200px]]<br /><applet load="1ile" size="450" color="white" frame="true" align="right" spinBox="true"
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[[Image:1ile.gif|left|200px]]<br /><applet load="1ile" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1ile, resolution 2.5&Aring;" />
caption="1ile, resolution 2.5&Aring;" />
'''ISOLEUCYL-TRNA SYNTHETASE'''<br />
'''ISOLEUCYL-TRNA SYNTHETASE'''<br />
==Overview==
==Overview==
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High-fidelity transfers of genetic information in the central dogma can be, achieved by a reaction called editing. The crystal structure of an enzyme, with editing activity in translation is presented here at 2.5 angstroms, resolution. The enzyme, isoleucyl-transfer RNA synthetase, activates not, only the cognate substrate L-isoleucine but also the minimally distinct, L-valine in the first, aminoacylation step. Then, in a second, "editing", step, the synthetase itself rapidly hydrolyzes only the valylated, products. For this two-step substrate selection, a "double-sieve", mechanism has already been proposed. The present crystal structures of the, synthetase in complexes with L-isoleucine and L-valine demonstrate that, the first sieve is on the aminoacylation domain containing the Rossmann, fold, whereas the second, editing sieve exists on a globular beta-barrel, domain that protrudes from the aminoacylation domain.
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High-fidelity transfers of genetic information in the central dogma can be achieved by a reaction called editing. The crystal structure of an enzyme with editing activity in translation is presented here at 2.5 angstroms resolution. The enzyme, isoleucyl-transfer RNA synthetase, activates not only the cognate substrate L-isoleucine but also the minimally distinct L-valine in the first, aminoacylation step. Then, in a second, "editing" step, the synthetase itself rapidly hydrolyzes only the valylated products. For this two-step substrate selection, a "double-sieve" mechanism has already been proposed. The present crystal structures of the synthetase in complexes with L-isoleucine and L-valine demonstrate that the first sieve is on the aminoacylation domain containing the Rossmann fold, whereas the second, editing sieve exists on a globular beta-barrel domain that protrudes from the aminoacylation domain.
==About this Structure==
==About this Structure==
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1ILE is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Thermus_thermophilus Thermus thermophilus] 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=1ILE OCA].
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1ILE is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Thermus_thermophilus Thermus thermophilus] 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=1ILE OCA].
==Reference==
==Reference==
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[[Category: Nakama, T.]]
[[Category: Nakama, T.]]
[[Category: Nureki, O.]]
[[Category: Nureki, O.]]
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[[Category: RSGI, RIKEN.Structural.Genomics/Proteomics.Initiative.]]
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[[Category: RSGI, RIKEN Structural Genomics/Proteomics Initiative.]]
[[Category: Schimmel, P.]]
[[Category: Schimmel, P.]]
[[Category: Shimada, A.]]
[[Category: Shimada, A.]]
[[Category: Tateno, M.]]
[[Category: Tateno, M.]]
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[[Category: Vassylyev, D.G.]]
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[[Category: Vassylyev, D G.]]
[[Category: Yokoyama, S.]]
[[Category: Yokoyama, S.]]
[[Category: ZN]]
[[Category: ZN]]
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[[Category: structural genomics]]
[[Category: structural genomics]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Nov 20 17:29:13 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:13:01 2008''

Revision as of 11:13, 21 February 2008


1ile, resolution 2.5Å

Drag the structure with the mouse to rotate

ISOLEUCYL-TRNA SYNTHETASE

Overview

High-fidelity transfers of genetic information in the central dogma can be achieved by a reaction called editing. The crystal structure of an enzyme with editing activity in translation is presented here at 2.5 angstroms resolution. The enzyme, isoleucyl-transfer RNA synthetase, activates not only the cognate substrate L-isoleucine but also the minimally distinct L-valine in the first, aminoacylation step. Then, in a second, "editing" step, the synthetase itself rapidly hydrolyzes only the valylated products. For this two-step substrate selection, a "double-sieve" mechanism has already been proposed. The present crystal structures of the synthetase in complexes with L-isoleucine and L-valine demonstrate that the first sieve is on the aminoacylation domain containing the Rossmann fold, whereas the second, editing sieve exists on a globular beta-barrel domain that protrudes from the aminoacylation domain.

About this Structure

1ILE is a Single protein structure of sequence from Thermus thermophilus with as ligand. Full crystallographic information is available from OCA.

Reference

Enzyme structure with two catalytic sites for double-sieve selection of substrate., Nureki O, Vassylyev DG, Tateno M, Shimada A, Nakama T, Fukai S, Konno M, Hendrickson TL, Schimmel P, Yokoyama S, Science. 1998 Apr 24;280(5363):578-82. PMID:9554847

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