1nzb: Difference between revisions

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|PDB= 1nzb |SIZE=350|CAPTION= <scene name='initialview01'>1nzb</scene>, resolution 3.10&Aring;
|PDB= 1nzb |SIZE=350|CAPTION= <scene name='initialview01'>1nzb</scene>, resolution 3.10&Aring;
|SITE=  
|SITE=  
|LIGAND= <scene name='pdbligand=IOD:IODIDE+ION'>IOD</scene> and <scene name='pdbligand=MG:MAGNESIUM ION'>MG</scene>
|LIGAND= <scene name='pdbligand=DA:2&#39;-DEOXYADENOSINE-5&#39;-MONOPHOSPHATE'>DA</scene>, <scene name='pdbligand=DC:2&#39;-DEOXYCYTIDINE-5&#39;-MONOPHOSPHATE'>DC</scene>, <scene name='pdbligand=DG:2&#39;-DEOXYGUANOSINE-5&#39;-MONOPHOSPHATE'>DG</scene>, <scene name='pdbligand=DT:THYMIDINE-5&#39;-MONOPHOSPHATE'>DT</scene>, <scene name='pdbligand=IOD:IODIDE+ION'>IOD</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene>, <scene name='pdbligand=UMP:2&#39;-DEOXYURIDINE+5&#39;-MONOPHOSPHATE'>UMP</scene>
|ACTIVITY=  
|ACTIVITY=  
|GENE=  
|GENE=  
|DOMAIN=
|RELATEDENTRY=[[1ouq|1OUQ]], [[1q3u|1Q3U]], [[1q3v|1Q3V]]
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1nzb FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1nzb OCA], [http://www.ebi.ac.uk/pdbsum/1nzb PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1nzb RCSB]</span>
}}
}}


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==About this Structure==
==About this Structure==
1NZB is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Enterobacteria_phage_p21 Enterobacteria phage p21]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1NZB OCA].  
1NZB is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Enterobacteria_phage_p1 Enterobacteria phage p1]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1NZB OCA].  


==Reference==
==Reference==
Crystal structure of a wild-type Cre recombinase-loxP synapse reveals a novel spacer conformation suggesting an alternative mechanism for DNA cleavage activation., Ennifar E, Meyer JE, Buchholz F, Stewart AF, Suck D, Nucleic Acids Res. 2003 Sep 15;31(18):5449-60. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/12954782 12954782]
Crystal structure of a wild-type Cre recombinase-loxP synapse reveals a novel spacer conformation suggesting an alternative mechanism for DNA cleavage activation., Ennifar E, Meyer JE, Buchholz F, Stewart AF, Suck D, Nucleic Acids Res. 2003 Sep 15;31(18):5449-60. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/12954782 12954782]
[[Category: Enterobacteria phage p21]]
[[Category: Enterobacteria phage p1]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Buchholz, F.]]
[[Category: Buchholz, F.]]
Line 27: Line 30:
[[Category: Stewart, A F.]]
[[Category: Stewart, A F.]]
[[Category: Suck, D.]]
[[Category: Suck, D.]]
[[Category: IOD]]
[[Category: MG]]
[[Category: cre]]
[[Category: cre]]
[[Category: dna]]
[[Category: dna]]
[[Category: recombinase]]
[[Category: recombinase]]


''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 13:03:40 2008''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 22:37:35 2008''

Revision as of 22:37, 30 March 2008

File:1nzb.gif


PDB ID 1nzb

Drag the structure with the mouse to rotate
, resolution 3.10Å
Ligands: , , , , , ,
Related: 1OUQ, 1Q3U, 1Q3V


Resources: FirstGlance, OCA, PDBsum, RCSB
Coordinates: save as pdb, mmCIF, xml



Crystal structure of wild type Cre recombinase-loxP synapse


OverviewOverview

Escherichia coli phage P1 Cre recombinase catalyzes the site-specific recombination of DNA containing loxP sites. We report here two crystal structures of a wild-type Cre recombinase-loxP synaptic complex corresponding to two distinct reaction states: an initial pre-cleavage complex, trapped using a phosphorothioate modification at the cleavable scissile bond that prevents the recombination reaction, and a 3'-phosphotyrosine protein-DNA intermediate resulting from the first strand cleavage. In contrast to previously determined Cre complexes, both structures contain a full tetrameric complex in the asymmetric unit, unequivocally showing that the anti-parallel arrangement of the loxP sites is an intrinsic property of the Cre-loxP recombination synapse. The conformation of the spacer is different to the one observed for the symmetrized loxS site: a kink next to the scissile phosphate in the top strand of the pre-cleavage complex leads to unstacking of the TpG step and a widening of the minor groove. This side of the spacer is interacting with a 'cleavage-competent' Cre subunit, suggesting that the first cleavage occurs at the ApT step in the top strand. This is further confirmed by the structure of the 3'-phosphotyrosine intermediate, where the DNA is cleaved in the top strands and covalently linked to the 'cleavage-competent' subunits. The cleavage is followed by a movement of the C-terminal part containing the attacking Y324 and the helix N interacting with the 'non-cleaving' subunit. This rearrangement could be responsible for the interconversion of Cre subunits. Our results also suggest that the Cre-induced kink next to the scissile phosphodiester activates the DNA for cleavage at this position and facilitates strand transfer.

About this StructureAbout this Structure

1NZB is a Single protein structure of sequence from Enterobacteria phage p1. Full crystallographic information is available from OCA.

ReferenceReference

Crystal structure of a wild-type Cre recombinase-loxP synapse reveals a novel spacer conformation suggesting an alternative mechanism for DNA cleavage activation., Ennifar E, Meyer JE, Buchholz F, Stewart AF, Suck D, Nucleic Acids Res. 2003 Sep 15;31(18):5449-60. PMID:12954782

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