2crx

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==Overview==
==Overview==
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We have determined the X-ray crystal structures of two DNA Holliday, junctions (HJs) bound by Cre recombinase. The HJ is a four-way branched, structure that occurs as an intermediate in genetic recombination, pathways, including site-specific recombination by the lambda-integrase, family. Cre recombinase is an integrase family member that recombines 34, bp loxP sites in the absence of accessory proteins or auxiliary DNA, sequences. The 2.7 A structure of Cre recombinase bound to an immobile HJ, and the 2.5 A structure of Cre recombinase bound to a symmetric, nicked HJ, reveal a nearly planar, twofold-symmetric DNA intermediate that shares, features with both the stacked-X and the square conformations of the HJ, that exist in the unbound state. The structures support a protein-mediated, crossover isomerization of the junction that acts as the switch, responsible for activation and deactivation of recombinase active sites., In this model, a subtle isomerization of the Cre recombinase-HJ quaternary, structure dictates which strands are cleaved during resolution of the, junction via a mechanism that involves neither branch migration nor, helical restacking.
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We have determined the X-ray crystal structures of two DNA Holliday junctions (HJs) bound by Cre recombinase. The HJ is a four-way branched structure that occurs as an intermediate in genetic recombination pathways, including site-specific recombination by the lambda-integrase family. Cre recombinase is an integrase family member that recombines 34 bp loxP sites in the absence of accessory proteins or auxiliary DNA sequences. The 2.7 A structure of Cre recombinase bound to an immobile HJ and the 2.5 A structure of Cre recombinase bound to a symmetric, nicked HJ reveal a nearly planar, twofold-symmetric DNA intermediate that shares features with both the stacked-X and the square conformations of the HJ that exist in the unbound state. The structures support a protein-mediated crossover isomerization of the junction that acts as the switch responsible for activation and deactivation of recombinase active sites. In this model, a subtle isomerization of the Cre recombinase-HJ quaternary structure dictates which strands are cleaved during resolution of the junction via a mechanism that involves neither branch migration nor helical restacking.
==About this Structure==
==About this Structure==
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[[Category: Bacteriophage p1]]
[[Category: Bacteriophage p1]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: Gopaul, D.N.]]
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[[Category: Gopaul, D N.]]
[[Category: Guo, F.]]
[[Category: Guo, F.]]
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[[Category: Vanduyne, G.D.]]
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[[Category: Vanduyne, G D.]]
[[Category: cre recombinase]]
[[Category: cre recombinase]]
[[Category: holliday junction]]
[[Category: holliday junction]]
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[[Category: recombination]]
[[Category: recombination]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Feb 3 10:37:29 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 16:51:48 2008''

Revision as of 14:51, 21 February 2008


2crx, resolution 2.5Å

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STRUCTURE OF THE HOLLIDAY JUNCTION INTERMEDIATE IN CRE-LOXP SITE-SPECIFIC RECOMBINATION

Overview

We have determined the X-ray crystal structures of two DNA Holliday junctions (HJs) bound by Cre recombinase. The HJ is a four-way branched structure that occurs as an intermediate in genetic recombination pathways, including site-specific recombination by the lambda-integrase family. Cre recombinase is an integrase family member that recombines 34 bp loxP sites in the absence of accessory proteins or auxiliary DNA sequences. The 2.7 A structure of Cre recombinase bound to an immobile HJ and the 2.5 A structure of Cre recombinase bound to a symmetric, nicked HJ reveal a nearly planar, twofold-symmetric DNA intermediate that shares features with both the stacked-X and the square conformations of the HJ that exist in the unbound state. The structures support a protein-mediated crossover isomerization of the junction that acts as the switch responsible for activation and deactivation of recombinase active sites. In this model, a subtle isomerization of the Cre recombinase-HJ quaternary structure dictates which strands are cleaved during resolution of the junction via a mechanism that involves neither branch migration nor helical restacking.

About this Structure

2CRX is a Single protein structure of sequence from Bacteriophage p1. Known structural/functional Sites: and . Full crystallographic information is available from OCA.

Reference

Structure of the Holliday junction intermediate in Cre-loxP site-specific recombination., Gopaul DN, Guo F, Van Duyne GD, EMBO J. 1998 Jul 15;17(14):4175-87. PMID:9670032

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