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New page: left|200px<br /><applet load="1svs" size="450" color="white" frame="true" align="right" spinBox="true" caption="1svs, resolution 1.5Å" /> '''Structure of the K180...
 
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[[Image:1svs.jpg|left|200px]]<br /><applet load="1svs" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1svs.jpg|left|200px]]<br /><applet load="1svs" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1svs, resolution 1.5&Aring;" />
caption="1svs, resolution 1.5&Aring;" />
'''Structure of the K180P mutant of Gi alpha subunit bound to GppNHp.'''<br />
'''Structure of the K180P mutant of Gi alpha subunit bound to GppNHp.'''<br />


==Overview==
==Overview==
Heterotrimeric G protein alpha (G alpha) subunits possess intrinsic GTPase, activity that leads to functional deactivation with a rate constant of, approximately 2 min(-1) at 30 degrees C. GTP hydrolysis causes, conformational changes in three regions of G alpha, including Switch I and, Switch II. Mutation of G202--&gt;A in Switch II of G alpha(i1) accelerates, the rates of both GTP hydrolysis and conformational change, which is, measured by the loss of fluorescence from Trp-211 in Switch II. Mutation, of K180--&gt;P in Switch I increases the rate of conformational change but, decreases the GTPase rate, which causes transient but substantial, accumulation of a low-fluorescence G alpha(i1).GTP species. Isothermal, titration calorimetric analysis of the binding of (G202A)G alpha(i1) and, (K180P)G alpha(i1) to the GTPase-activating protein RGS4 indicates that, the G202A mutation stabilizes the pretransition state-like conformation of, G alpha(i1) that is mimicked by the complex of G alpha(i1) with GDP and, magnesium fluoroaluminate, whereas the K180P mutation destabilizes this, state. The crystal structures of (K180P)G alpha(i1) bound to a slowly, hydrolyzable GTP analog, and the GDP.magnesium fluoroaluminate complex, provide evidence that the Mg(2+) binding site is destabilized and that, Switch I is torsionally restrained by the K180P mutation. The data are, consistent with a catalytic mechanism for G alpha in which major, conformational transitions in Switch I and Switch II are obligate events, that precede the bond-breaking step in GTP hydrolysis. In (K180P)G, alpha(i1), the two events are decoupled kinetically, whereas in the native, protein they are concerted.
Heterotrimeric G protein alpha (G alpha) subunits possess intrinsic GTPase activity that leads to functional deactivation with a rate constant of approximately 2 min(-1) at 30 degrees C. GTP hydrolysis causes conformational changes in three regions of G alpha, including Switch I and Switch II. Mutation of G202--&gt;A in Switch II of G alpha(i1) accelerates the rates of both GTP hydrolysis and conformational change, which is measured by the loss of fluorescence from Trp-211 in Switch II. Mutation of K180--&gt;P in Switch I increases the rate of conformational change but decreases the GTPase rate, which causes transient but substantial accumulation of a low-fluorescence G alpha(i1).GTP species. Isothermal titration calorimetric analysis of the binding of (G202A)G alpha(i1) and (K180P)G alpha(i1) to the GTPase-activating protein RGS4 indicates that the G202A mutation stabilizes the pretransition state-like conformation of G alpha(i1) that is mimicked by the complex of G alpha(i1) with GDP and magnesium fluoroaluminate, whereas the K180P mutation destabilizes this state. The crystal structures of (K180P)G alpha(i1) bound to a slowly hydrolyzable GTP analog, and the GDP.magnesium fluoroaluminate complex provide evidence that the Mg(2+) binding site is destabilized and that Switch I is torsionally restrained by the K180P mutation. The data are consistent with a catalytic mechanism for G alpha in which major conformational transitions in Switch I and Switch II are obligate events that precede the bond-breaking step in GTP hydrolysis. In (K180P)G alpha(i1), the two events are decoupled kinetically, whereas in the native protein they are concerted.


==About this Structure==
==About this Structure==
1SVS is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Rattus_norvegicus Rattus norvegicus] with MG and GNP as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Heterotrimeric_G-protein_GTPase Heterotrimeric G-protein GTPase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.6.5.1 3.6.5.1] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1SVS OCA].  
1SVS is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Rattus_norvegicus Rattus norvegicus] with <scene name='pdbligand=MG:'>MG</scene> and <scene name='pdbligand=GNP:'>GNP</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Heterotrimeric_G-protein_GTPase Heterotrimeric G-protein GTPase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.6.5.1 3.6.5.1] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1SVS OCA].  


==Reference==
==Reference==
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[[Category: Du, X.]]
[[Category: Du, X.]]
[[Category: Li, P.]]
[[Category: Li, P.]]
[[Category: Ross, E.M.]]
[[Category: Ross, E M.]]
[[Category: Sprang, S.R.]]
[[Category: Sprang, S R.]]
[[Category: Thomas, C.J.]]
[[Category: Thomas, C J.]]
[[Category: Wang, Y.]]
[[Category: Wang, Y.]]
[[Category: GNP]]
[[Category: GNP]]
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[[Category: k180p mutation]]
[[Category: k180p mutation]]


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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:05:47 2008''