2agv: Difference between revisions

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New page: left|200px<br /><applet load="2agv" size="450" color="white" frame="true" align="right" spinBox="true" caption="2agv, resolution 2.40Å" /> '''Crystal structure of...
 
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[[Image:2agv.gif|left|200px]]<br /><applet load="2agv" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:2agv.gif|left|200px]]<br /><applet load="2agv" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="2agv, resolution 2.40&Aring;" />
caption="2agv, resolution 2.40&Aring;" />
'''Crystal structure of the SR CA2+-ATPASE with BHQ and TG'''<br />
'''Crystal structure of the SR CA2+-ATPASE with BHQ and TG'''<br />


==Overview==
==Overview==
Ca(2+)-ATPase of sarcoplasmic reticulum is an ATP-powered Ca(2+) pump but, also a H(+) pump in the opposite direction with no demonstrated functional, role. Here, we report a 2.4-A-resolution crystal structure of the, Ca(2+)-ATPase in the absence of Ca(2+) stabilized by two inhibitors, dibutyldihydroxybenzene, which bridges two transmembrane helices, and, thapsigargin, also bound in the membrane region. Now visualized are water, and several phospholipid molecules, one of which occupies a cleft between, two transmembrane helices. Atomic models of the Ca(2+) binding sites with, explicit hydrogens derived by continuum electrostatic calculations show, how water and protons fill the space and compensate charge imbalance, created by Ca(2+)-release. They suggest that H(+) countertransport is a, consequence of a requirement for maintaining structural integrity of the, empty Ca(2+)-binding sites. For this reason, cation countertransport is, probably mandatory for all P-type ATPases and possibly accompanies, transport of water as well.
Ca(2+)-ATPase of sarcoplasmic reticulum is an ATP-powered Ca(2+) pump but also a H(+) pump in the opposite direction with no demonstrated functional role. Here, we report a 2.4-A-resolution crystal structure of the Ca(2+)-ATPase in the absence of Ca(2+) stabilized by two inhibitors, dibutyldihydroxybenzene, which bridges two transmembrane helices, and thapsigargin, also bound in the membrane region. Now visualized are water and several phospholipid molecules, one of which occupies a cleft between two transmembrane helices. Atomic models of the Ca(2+) binding sites with explicit hydrogens derived by continuum electrostatic calculations show how water and protons fill the space and compensate charge imbalance created by Ca(2+)-release. They suggest that H(+) countertransport is a consequence of a requirement for maintaining structural integrity of the empty Ca(2+)-binding sites. For this reason, cation countertransport is probably mandatory for all P-type ATPases and possibly accompanies transport of water as well.


==About this Structure==
==About this Structure==
2AGV is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Oryctolagus_cuniculus Oryctolagus cuniculus] with NA, TG1, BHQ and PTY as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Calcium-transporting_ATPase Calcium-transporting ATPase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.6.3.8 3.6.3.8] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2AGV OCA].  
2AGV is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Oryctolagus_cuniculus Oryctolagus cuniculus] with <scene name='pdbligand=NA:'>NA</scene>, <scene name='pdbligand=TG1:'>TG1</scene>, <scene name='pdbligand=BHQ:'>BHQ</scene> and <scene name='pdbligand=PTY:'>PTY</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Calcium-transporting_ATPase Calcium-transporting ATPase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.6.3.8 3.6.3.8] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2AGV OCA].  


==Reference==
==Reference==
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[[Category: p-type atpase]]
[[Category: p-type atpase]]


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