1b63

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(New page: 200px<br /><applet load="1b63" size="450" color="white" frame="true" align="right" spinBox="true" caption="1b63, resolution 1.9&Aring;" /> '''MUTL COMPLEXED WITH A...)
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[[Image:1b63.gif|left|200px]]<br /><applet load="1b63" size="450" color="white" frame="true" align="right" spinBox="true"
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[[Image:1b63.gif|left|200px]]<br /><applet load="1b63" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1b63, resolution 1.9&Aring;" />
caption="1b63, resolution 1.9&Aring;" />
'''MUTL COMPLEXED WITH ADPNP'''<br />
'''MUTL COMPLEXED WITH ADPNP'''<br />
==Overview==
==Overview==
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The MutL DNA mismatch repair protein has recently been shown to be an, ATPase and to belong to an emerging ATPase superfamily that includes DNA, topoisomerase II and Hsp90. We report here the crystal structures of a 40, kDa ATPase fragment of E. coli MutL (LN40) complexed with a substrate, analog, ADPnP, and with product ADP. More than 60 residues that are, disordered in the apoprotein structure become ordered and contribute to, both ADPnP binding and dimerization of LN40. Hydrolysis of ATP, signified, by subsequent release of the gamma-phosphate, releases two key loops and, leads to dissociation of the LN40 dimer. Dimerization of the LN40 region, is required for and is the rate-limiting step in ATP hydrolysis by MutL., The ATPase activity of MutL is stimulated by DNA and likely acts as a, switch to coordinate DNA mismatch repair.
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The MutL DNA mismatch repair protein has recently been shown to be an ATPase and to belong to an emerging ATPase superfamily that includes DNA topoisomerase II and Hsp90. We report here the crystal structures of a 40 kDa ATPase fragment of E. coli MutL (LN40) complexed with a substrate analog, ADPnP, and with product ADP. More than 60 residues that are disordered in the apoprotein structure become ordered and contribute to both ADPnP binding and dimerization of LN40. Hydrolysis of ATP, signified by subsequent release of the gamma-phosphate, releases two key loops and leads to dissociation of the LN40 dimer. Dimerization of the LN40 region is required for and is the rate-limiting step in ATP hydrolysis by MutL. The ATPase activity of MutL is stimulated by DNA and likely acts as a switch to coordinate DNA mismatch repair.
==About this Structure==
==About this Structure==
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1B63 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli] with MG, EDO and ANP as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1B63 OCA].
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1B63 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli] with <scene name='pdbligand=MG:'>MG</scene>, <scene name='pdbligand=EDO:'>EDO</scene> and <scene name='pdbligand=ANP:'>ANP</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1B63 OCA].
==Reference==
==Reference==
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[[Category: dna mismatch repair]]
[[Category: dna mismatch repair]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Nov 20 11:23:32 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 11:51:52 2008''

Revision as of 09:51, 21 February 2008


1b63, resolution 1.9Å

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MUTL COMPLEXED WITH ADPNP

Overview

The MutL DNA mismatch repair protein has recently been shown to be an ATPase and to belong to an emerging ATPase superfamily that includes DNA topoisomerase II and Hsp90. We report here the crystal structures of a 40 kDa ATPase fragment of E. coli MutL (LN40) complexed with a substrate analog, ADPnP, and with product ADP. More than 60 residues that are disordered in the apoprotein structure become ordered and contribute to both ADPnP binding and dimerization of LN40. Hydrolysis of ATP, signified by subsequent release of the gamma-phosphate, releases two key loops and leads to dissociation of the LN40 dimer. Dimerization of the LN40 region is required for and is the rate-limiting step in ATP hydrolysis by MutL. The ATPase activity of MutL is stimulated by DNA and likely acts as a switch to coordinate DNA mismatch repair.

About this Structure

1B63 is a Single protein structure of sequence from Escherichia coli with , and as ligands. Full crystallographic information is available from OCA.

Reference

Transformation of MutL by ATP binding and hydrolysis: a switch in DNA mismatch repair., Ban C, Junop M, Yang W, Cell. 1999 Apr 2;97(1):85-97. PMID:10199405

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