1svs: Difference between revisions
From Proteopedia
Jump to navigationJump to search
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... |
No edit summary |
||
| Line 1: | Line 1: | ||
[[Image:1svs.jpg|left|200px]]<br /><applet load="1svs" size=" | [[Image:1svs.jpg|left|200px]]<br /><applet load="1svs" size="350" color="white" frame="true" align="right" spinBox="true" | ||
caption="1svs, resolution 1.5Å" /> | caption="1svs, resolution 1.5Å" /> | ||
'''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 | 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-->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-->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:// | 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== | ||
| Line 16: | Line 16: | ||
[[Category: Du, X.]] | [[Category: Du, X.]] | ||
[[Category: Li, P.]] | [[Category: Li, P.]] | ||
[[Category: Ross, E | [[Category: Ross, E M.]] | ||
[[Category: Sprang, S | [[Category: Sprang, S R.]] | ||
[[Category: Thomas, C | [[Category: Thomas, C J.]] | ||
[[Category: Wang, Y.]] | [[Category: Wang, Y.]] | ||
[[Category: GNP]] | [[Category: GNP]] | ||
| Line 26: | Line 26: | ||
[[Category: k180p mutation]] | [[Category: k180p mutation]] | ||
''Page seeded by [http:// | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:05:47 2008'' | ||