2nnx: Difference between revisions

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New page: left|200px<br /> <applet load="2nnx" size="450" color="white" frame="true" align="right" spinBox="true" caption="2nnx, resolution 2.30Å" /> '''Crystal Structure o...
 
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[[Image:2nnx.gif|left|200px]]<br />
[[Image:2nnx.gif|left|200px]]<br /><applet load="2nnx" size="350" color="white" frame="true" align="right" spinBox="true"  
<applet load="2nnx" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="2nnx, resolution 2.30&Aring;" />
caption="2nnx, resolution 2.30&Aring;" />
'''Crystal Structure of the H46R, H48Q double mutant of human [Cu-Zn] Superoxide Dismutase'''<br />
'''Crystal Structure of the H46R, H48Q double mutant of human [Cu-Zn] Superoxide Dismutase'''<br />


==Overview==
==Overview==
A subset of superoxide dismutase 1 (Cu/Zn-SOD1) mutants that cause, familial amyotrophic lateral sclerosis (FALS) have heightened reactivity, with (-)ONOO and H(2)O(2) in vitro. This reactivity requires a copper ion, bound in the active site and is a suggested mechanism of motor neuron, injury. However, we have found that transgenic mice that express, SOD1-H46R/H48Q, which combines natural FALS mutations at ligands for, copper and which is inactive, develop motor neuron disease. Using a direct, radioactive copper incorporation assay in transfected cells and the, established tools of single crystal x-ray diffraction, we now demonstrate, that this variant does not stably bind copper. We find that single, mutations at copper ligands, including H46R, H48Q, and a quadruple mutant, H46R/H48Q/H63G/H120G, also diminish the binding of radioactive copper., Further, using native polyacrylamide gel electrophoresis and a yeast, two-hybrid assay, the binding of copper was found to be related to the, formation of the stable dimeric enzyme. Collectively, our data demonstrate, a relationship between copper and assembly of SOD1 into stable dimers and, also define disease-causing SOD1 mutants that are unlikely to robustly, produce toxic radicals via copper-mediated chemistry.
A subset of superoxide dismutase 1 (Cu/Zn-SOD1) mutants that cause familial amyotrophic lateral sclerosis (FALS) have heightened reactivity with (-)ONOO and H(2)O(2) in vitro. This reactivity requires a copper ion bound in the active site and is a suggested mechanism of motor neuron injury. However, we have found that transgenic mice that express SOD1-H46R/H48Q, which combines natural FALS mutations at ligands for copper and which is inactive, develop motor neuron disease. Using a direct radioactive copper incorporation assay in transfected cells and the established tools of single crystal x-ray diffraction, we now demonstrate that this variant does not stably bind copper. We find that single mutations at copper ligands, including H46R, H48Q, and a quadruple mutant H46R/H48Q/H63G/H120G, also diminish the binding of radioactive copper. Further, using native polyacrylamide gel electrophoresis and a yeast two-hybrid assay, the binding of copper was found to be related to the formation of the stable dimeric enzyme. Collectively, our data demonstrate a relationship between copper and assembly of SOD1 into stable dimers and also define disease-causing SOD1 mutants that are unlikely to robustly produce toxic radicals via copper-mediated chemistry.


==Disease==
==Disease==
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==About this Structure==
==About this Structure==
2NNX is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with ZN, SO4 and ACE as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Superoxide_dismutase Superoxide dismutase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.15.1.1 1.15.1.1] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2NNX OCA].  
2NNX is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with <scene name='pdbligand=ZN:'>ZN</scene>, <scene name='pdbligand=SO4:'>SO4</scene> and <scene name='pdbligand=ACE:'>ACE</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Superoxide_dismutase Superoxide dismutase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.15.1.1 1.15.1.1] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2NNX OCA].  


==Reference==
==Reference==
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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Superoxide dismutase]]
[[Category: Superoxide dismutase]]
[[Category: Hart, P.J.]]
[[Category: Hart, P J.]]
[[Category: Schuermann, J.P.]]
[[Category: Schuermann, J P.]]
[[Category: ACE]]
[[Category: ACE]]
[[Category: SO4]]
[[Category: SO4]]
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[[Category: oxidoreductase; human; cu-zn superoxide dismutase; superoxide acceptor; familial amyotrophic lateral sclerosis mutant]]
[[Category: oxidoreductase; human; cu-zn superoxide dismutase; superoxide acceptor; familial amyotrophic lateral sclerosis mutant]]


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