1s8e

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(New page: 200px<br /><applet load="1s8e" size="450" color="white" frame="true" align="right" spinBox="true" caption="1s8e, resolution 2.3&Aring;" /> '''Crystal structure of ...)
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[[Image:1s8e.jpg|left|200px]]<br /><applet load="1s8e" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1s8e, resolution 2.3&Aring;" />
caption="1s8e, resolution 2.3&Aring;" />
'''Crystal structure of Mre11-3'''<br />
'''Crystal structure of Mre11-3'''<br />
==Overview==
==Overview==
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The Mre11, Rad50 and Nbs1 proteins make up the conserved multi-functional, Mre11 (MRN) complex involved in multiple, critical DNA metabolic processes, including double-strand break repair and telomere maintenance. The Mre11, protein is a nuclease with broad substrate recognition, but MRN-dependent, processes requiring the nuclease activity are not clearly defined. Here, we report the functional and structural characterization of a, nuclease-deficient Mre11 protein termed mre11-3. Importantly, the hmre11-3, protein has wild-type ability to bind DNA, Rad50 and Nbs1; however, nuclease activity was completely abrogated. When expressed in cell lines, from patients with ataxia telangiectasia-like disorder (ATLD), hmre11-3, restored the formation of ionizing radiation-induced foci. Consistent with, the biochemical results, the 2.3 A crystal structure of mre11-3 from, Pyrococcus furiosus revealed an active site structure with a, wild-type-like metal-binding environment. The structural analysis of the, H85L mutation provides a detailed molecular basis for the ability of, mre11-3 to bind but not hydrolyze DNA. Together, these results establish, that the mre11-3 protein provides an excellent system for dissecting, nuclease-dependent and independent functions of the Mre11 complex.
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The Mre11, Rad50 and Nbs1 proteins make up the conserved multi-functional Mre11 (MRN) complex involved in multiple, critical DNA metabolic processes including double-strand break repair and telomere maintenance. The Mre11 protein is a nuclease with broad substrate recognition, but MRN-dependent processes requiring the nuclease activity are not clearly defined. Here, we report the functional and structural characterization of a nuclease-deficient Mre11 protein termed mre11-3. Importantly, the hmre11-3 protein has wild-type ability to bind DNA, Rad50 and Nbs1; however, nuclease activity was completely abrogated. When expressed in cell lines from patients with ataxia telangiectasia-like disorder (ATLD), hmre11-3 restored the formation of ionizing radiation-induced foci. Consistent with the biochemical results, the 2.3 A crystal structure of mre11-3 from Pyrococcus furiosus revealed an active site structure with a wild-type-like metal-binding environment. The structural analysis of the H85L mutation provides a detailed molecular basis for the ability of mre11-3 to bind but not hydrolyze DNA. Together, these results establish that the mre11-3 protein provides an excellent system for dissecting nuclease-dependent and independent functions of the Mre11 complex.
==About this Structure==
==About this Structure==
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1S8E is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Pyrococcus_furiosus Pyrococcus furiosus] with MN as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1S8E OCA].
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1S8E is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Pyrococcus_furiosus Pyrococcus furiosus] with <scene name='pdbligand=MN:'>MN</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1S8E OCA].
==Reference==
==Reference==
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[[Category: Pyrococcus furiosus]]
[[Category: Pyrococcus furiosus]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: Hopfner, K.P.]]
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[[Category: Hopfner, K P.]]
[[Category: MN]]
[[Category: MN]]
[[Category: dna double-strand break]]
[[Category: dna double-strand break]]
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[[Category: rad50]]
[[Category: rad50]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Wed Nov 21 02:12:00 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:59:03 2008''

Revision as of 12:59, 21 February 2008


1s8e, resolution 2.3Å

Drag the structure with the mouse to rotate

Crystal structure of Mre11-3

Overview

The Mre11, Rad50 and Nbs1 proteins make up the conserved multi-functional Mre11 (MRN) complex involved in multiple, critical DNA metabolic processes including double-strand break repair and telomere maintenance. The Mre11 protein is a nuclease with broad substrate recognition, but MRN-dependent processes requiring the nuclease activity are not clearly defined. Here, we report the functional and structural characterization of a nuclease-deficient Mre11 protein termed mre11-3. Importantly, the hmre11-3 protein has wild-type ability to bind DNA, Rad50 and Nbs1; however, nuclease activity was completely abrogated. When expressed in cell lines from patients with ataxia telangiectasia-like disorder (ATLD), hmre11-3 restored the formation of ionizing radiation-induced foci. Consistent with the biochemical results, the 2.3 A crystal structure of mre11-3 from Pyrococcus furiosus revealed an active site structure with a wild-type-like metal-binding environment. The structural analysis of the H85L mutation provides a detailed molecular basis for the ability of mre11-3 to bind but not hydrolyze DNA. Together, these results establish that the mre11-3 protein provides an excellent system for dissecting nuclease-dependent and independent functions of the Mre11 complex.

About this Structure

1S8E is a Single protein structure of sequence from Pyrococcus furiosus with as ligand. Full crystallographic information is available from OCA.

Reference

Structural and functional analysis of Mre11-3., Arthur LM, Gustausson K, Hopfner KP, Carson CT, Stracker TH, Karcher A, Felton D, Weitzman MD, Tainer J, Carney JP, Nucleic Acids Res. 2004 Mar 26;32(6):1886-93. Print 2004. PMID:15047855

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