2bgw

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==Overview==
==Overview==
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The XPF/Mus81 structure-specific endonucleases cleave double-stranded DNA, (dsDNA) within asymmetric branched DNA substrates and play an essential, role in nucleotide excision repair, recombination and genome integrity. We, report the structure of an archaeal XPF homodimer alone and bound to, dsDNA. Superposition of these structures reveals a large domain movement, upon binding DNA, indicating how the (HhH)(2) domain and the nuclease, domain are coupled to allow the recognition of, double-stranded/single-stranded DNA junctions. We identify two, nonequivalent DNA-binding sites and propose a model in which XPF distorts, the 3' flap substrate in order to engage both binding sites and promote, strand cleavage. The model rationalises published biochemical data and, implies a novel role for the ERCC1 subunit of eukaryotic XPF complexes.
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The XPF/Mus81 structure-specific endonucleases cleave double-stranded DNA (dsDNA) within asymmetric branched DNA substrates and play an essential role in nucleotide excision repair, recombination and genome integrity. We report the structure of an archaeal XPF homodimer alone and bound to dsDNA. Superposition of these structures reveals a large domain movement upon binding DNA, indicating how the (HhH)(2) domain and the nuclease domain are coupled to allow the recognition of double-stranded/single-stranded DNA junctions. We identify two nonequivalent DNA-binding sites and propose a model in which XPF distorts the 3' flap substrate in order to engage both binding sites and promote strand cleavage. The model rationalises published biochemical data and implies a novel role for the ERCC1 subunit of eukaryotic XPF complexes.
==About this Structure==
==About this Structure==
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[[Category: Knowles, P.]]
[[Category: Knowles, P.]]
[[Category: Lally, J.]]
[[Category: Lally, J.]]
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[[Category: Mcdonald, N.Q.]]
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[[Category: Mcdonald, N Q.]]
[[Category: Murray-Rust, J.]]
[[Category: Murray-Rust, J.]]
[[Category: Newman, M.]]
[[Category: Newman, M.]]
[[Category: Rudolf, J.]]
[[Category: Rudolf, J.]]
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[[Category: White, M.F.]]
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[[Category: White, M F.]]
[[Category: MG]]
[[Category: MG]]
[[Category: SO4]]
[[Category: SO4]]
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[[Category: structure specific endonuclease]]
[[Category: structure specific endonuclease]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Feb 3 10:23:54 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 16:37:40 2008''

Revision as of 14:37, 21 February 2008


2bgw, resolution 2.80Å

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XPF FROM AEROPYRUM PERNIX, COMPLEX WITH DNA

Overview

The XPF/Mus81 structure-specific endonucleases cleave double-stranded DNA (dsDNA) within asymmetric branched DNA substrates and play an essential role in nucleotide excision repair, recombination and genome integrity. We report the structure of an archaeal XPF homodimer alone and bound to dsDNA. Superposition of these structures reveals a large domain movement upon binding DNA, indicating how the (HhH)(2) domain and the nuclease domain are coupled to allow the recognition of double-stranded/single-stranded DNA junctions. We identify two nonequivalent DNA-binding sites and propose a model in which XPF distorts the 3' flap substrate in order to engage both binding sites and promote strand cleavage. The model rationalises published biochemical data and implies a novel role for the ERCC1 subunit of eukaryotic XPF complexes.

About this Structure

2BGW is a Single protein structure of sequence from Aeropyrum pernix with and as ligands. Known structural/functional Site: . Full crystallographic information is available from OCA.

Reference

Structure of an XPF endonuclease with and without DNA suggests a model for substrate recognition., Newman M, Murray-Rust J, Lally J, Rudolf J, Fadden A, Knowles PP, White MF, McDonald NQ, EMBO J. 2005 Mar 9;24(5):895-905. Epub 2005 Feb 17. PMID:15719018

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