2aqx

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(New page: 200px<br /><applet load="2aqx" size="450" color="white" frame="true" align="right" spinBox="true" caption="2aqx, resolution 2.50&Aring;" /> '''Crystal Structure of...)
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[[Image:2aqx.gif|left|200px]]<br /><applet load="2aqx" size="450" color="white" frame="true" align="right" spinBox="true"
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[[Image:2aqx.gif|left|200px]]<br /><applet load="2aqx" size="350" color="white" frame="true" align="right" spinBox="true"
caption="2aqx, resolution 2.50&Aring;" />
caption="2aqx, resolution 2.50&Aring;" />
'''Crystal Structure of the Catalytic and CaM-Binding domains of Inositol 1,4,5-Trisphosphate 3-Kinase B'''<br />
'''Crystal Structure of the Catalytic and CaM-Binding domains of Inositol 1,4,5-Trisphosphate 3-Kinase B'''<br />
==Overview==
==Overview==
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D-Myoinositol 1,4,5-trisphophate 3-kinases (IP(3)-3Ks) play important, roles in metazoan cellular signaling. It has been demonstrated that mice, without a functional version of IP(3)-3K isoform B are deficient in, peripheral T-cells, indicating that IP(3)-3KB is essential to the, developing immune system. The recent apo IP(3)-3KA structure exhibited a, helix at the catalytic domain N-terminus exhibited a helix at the, N-terminus of the catalytic domain, with a tryptophan indole moiety, mimicking the binding mode of the substrate ATP purine ring, suggesting a, mechanism of autoinhibition. Here we present the structure of the complete, catalytic domain of IP(3)-3KB, including the CaM binding domain in complex, with Mg(2+) and ATP. The crystal structure reveals a homodimeric, arrangement of IP(3)-3KB catalytic domains, mediated via an intermolecular, antiparallel beta-sheet formed from part of the CaM binding region., Residues from the putative autoinhibitory helix are rearranged into a loop, configuration, with extensive interactions with the bound ATP. Mutagenesis, of residues from this region reveals that substitution of the putative, autoinhibitory tryptophan generates a hyperactive enzyme which retains, Ca(2+)/CaM sensitivity. The IP(3)-3KB structure suggests a mechanism of, enzyme activation, and raises the possibility that an interaction between, IP(3)-3KB molecules may occur as part of the catalytic or regulatory, cycle.
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D-Myoinositol 1,4,5-trisphophate 3-kinases (IP(3)-3Ks) play important roles in metazoan cellular signaling. It has been demonstrated that mice without a functional version of IP(3)-3K isoform B are deficient in peripheral T-cells, indicating that IP(3)-3KB is essential to the developing immune system. The recent apo IP(3)-3KA structure exhibited a helix at the catalytic domain N-terminus exhibited a helix at the N-terminus of the catalytic domain, with a tryptophan indole moiety mimicking the binding mode of the substrate ATP purine ring, suggesting a mechanism of autoinhibition. Here we present the structure of the complete catalytic domain of IP(3)-3KB, including the CaM binding domain in complex with Mg(2+) and ATP. The crystal structure reveals a homodimeric arrangement of IP(3)-3KB catalytic domains, mediated via an intermolecular antiparallel beta-sheet formed from part of the CaM binding region. Residues from the putative autoinhibitory helix are rearranged into a loop configuration, with extensive interactions with the bound ATP. Mutagenesis of residues from this region reveals that substitution of the putative autoinhibitory tryptophan generates a hyperactive enzyme which retains Ca(2+)/CaM sensitivity. The IP(3)-3KB structure suggests a mechanism of enzyme activation, and raises the possibility that an interaction between IP(3)-3KB molecules may occur as part of the catalytic or regulatory cycle.
==About this Structure==
==About this Structure==
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2AQX is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Mus_musculus Mus musculus] with MG and ATP as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Inositol-trisphosphate_3-kinase Inositol-trisphosphate 3-kinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.1.127 2.7.1.127] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2AQX OCA].
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2AQX is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Mus_musculus Mus musculus] with <scene name='pdbligand=MG:'>MG</scene> and <scene name='pdbligand=ATP:'>ATP</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Inositol-trisphosphate_3-kinase Inositol-trisphosphate 3-kinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.1.127 2.7.1.127] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2AQX OCA].
==Reference==
==Reference==
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[[Category: Mus musculus]]
[[Category: Mus musculus]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: Chamberlain, P.P.]]
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[[Category: Chamberlain, P P.]]
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[[Category: Cooke, M.P.]]
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[[Category: Cooke, M P.]]
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[[Category: Lesley, S.A.]]
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[[Category: Lesley, S A.]]
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[[Category: Sandberg, M.L.]]
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[[Category: Sandberg, M L.]]
[[Category: Sauer, K.]]
[[Category: Sauer, K.]]
[[Category: Spraggon, G.]]
[[Category: Spraggon, G.]]
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[[Category: kinase]]
[[Category: kinase]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Wed Nov 21 08:18:44 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 16:29:58 2008''

Revision as of 14:30, 21 February 2008


2aqx, resolution 2.50Å

Drag the structure with the mouse to rotate

Crystal Structure of the Catalytic and CaM-Binding domains of Inositol 1,4,5-Trisphosphate 3-Kinase B

Overview

D-Myoinositol 1,4,5-trisphophate 3-kinases (IP(3)-3Ks) play important roles in metazoan cellular signaling. It has been demonstrated that mice without a functional version of IP(3)-3K isoform B are deficient in peripheral T-cells, indicating that IP(3)-3KB is essential to the developing immune system. The recent apo IP(3)-3KA structure exhibited a helix at the catalytic domain N-terminus exhibited a helix at the N-terminus of the catalytic domain, with a tryptophan indole moiety mimicking the binding mode of the substrate ATP purine ring, suggesting a mechanism of autoinhibition. Here we present the structure of the complete catalytic domain of IP(3)-3KB, including the CaM binding domain in complex with Mg(2+) and ATP. The crystal structure reveals a homodimeric arrangement of IP(3)-3KB catalytic domains, mediated via an intermolecular antiparallel beta-sheet formed from part of the CaM binding region. Residues from the putative autoinhibitory helix are rearranged into a loop configuration, with extensive interactions with the bound ATP. Mutagenesis of residues from this region reveals that substitution of the putative autoinhibitory tryptophan generates a hyperactive enzyme which retains Ca(2+)/CaM sensitivity. The IP(3)-3KB structure suggests a mechanism of enzyme activation, and raises the possibility that an interaction between IP(3)-3KB molecules may occur as part of the catalytic or regulatory cycle.

About this Structure

2AQX is a Single protein structure of sequence from Mus musculus with and as ligands. Active as Inositol-trisphosphate 3-kinase, with EC number 2.7.1.127 Full crystallographic information is available from OCA.

Reference

Structural insights into enzyme regulation for inositol 1,4,5-trisphosphate 3-kinase B., Chamberlain PP, Sandberg ML, Sauer K, Cooke MP, Lesley SA, Spraggon G, Biochemistry. 2005 Nov 8;44(44):14486-93. PMID:16262249

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