1en7

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[[Image:1en7.jpg|left|200px]]
[[Image:1en7.jpg|left|200px]]
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{{Structure
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<!--
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|PDB= 1en7 |SIZE=350|CAPTION= <scene name='initialview01'>1en7</scene>, resolution 2.4&Aring;
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The line below this paragraph, containing "STRUCTURE_1en7", creates the "Structure Box" on the page.
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|SITE=
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You may change the PDB parameter (which sets the PDB file loaded into the applet)
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|LIGAND= <scene name='pdbligand=CA:CALCIUM+ION'>CA</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene>
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or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
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|ACTIVITY= <span class='plainlinks'>[http://en.wikipedia.org/wiki/Crossover_junction_endodeoxyribonuclease Crossover junction endodeoxyribonuclease], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.22.4 3.1.22.4] </span>
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or leave the SCENE parameter empty for the default display.
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|GENE= GP49 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=10665 Enterobacteria phage T4])
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-->
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|DOMAIN=
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{{STRUCTURE_1en7| PDB=1en7 | SCENE= }}
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|RELATEDENTRY=
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1en7 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1en7 OCA], [http://www.ebi.ac.uk/pdbsum/1en7 PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1en7 RCSB]</span>
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}}
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'''ENDONUCLEASE VII (ENDOVII) FROM PHAGE T4'''
'''ENDONUCLEASE VII (ENDOVII) FROM PHAGE T4'''
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[[Category: Toro, I.]]
[[Category: Toro, I.]]
[[Category: Vix, O.]]
[[Category: Vix, O.]]
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[[Category: dnase]]
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[[Category: Dnase]]
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[[Category: endonuclease]]
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[[Category: Endonuclease]]
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[[Category: holliday junction]]
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[[Category: Holliday junction]]
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[[Category: resolvase]]
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[[Category: Resolvase]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May 2 15:18:23 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 20:05:56 2008''
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Revision as of 12:18, 2 May 2008

Template:STRUCTURE 1en7

ENDONUCLEASE VII (ENDOVII) FROM PHAGE T4


Overview

Phage T4 endonuclease VII (Endo VII), the first enzyme shown to resolve Holliday junctions, recognizes a broad spectrum of DNA substrates ranging from branched DNAs to single base mismatches. We have determined the crystal structures of the Ca2+-bound wild-type and the inactive N62D mutant enzymes at 2.4 and 2.1 A, respectively. The Endo VII monomers form an elongated, highly intertwined molecular dimer exhibiting extreme domain swapping. The major dimerization elements are two pairs of antiparallel helices forming a novel 'four-helix cross' motif. The unique monomer fold, almost completely lacking beta-sheet structure and containing a zinc ion tetrahedrally coordinated to four cysteines, does not resemble any of the known junction-resolving enzymes, including the Escherichia coli RuvC and lambda integrase-type recombinases. The S-shaped dimer has two 'binding bays' separated by approximately 25 A which are lined by positively charged residues and contain near their base residues known to be essential for activity. These include Asp40 and Asn62, which function as ligands for the bound calcium ions. A pronounced bipolar charge distribution suggests that branched DNA substrates bind to the positively charged face with the scissile phosphates located near the divalent cations. A model for the complex with a four-way DNA junction is presented.

About this Structure

1EN7 is a Single protein structure of sequence from Enterobacteria phage t4. Full crystallographic information is available from OCA.

Reference

X-ray structure of T4 endonuclease VII: a DNA junction resolvase with a novel fold and unusual domain-swapped dimer architecture., Raaijmakers H, Vix O, Toro I, Golz S, Kemper B, Suck D, EMBO J. 1999 Mar 15;18(6):1447-58. PMID:10075917 Page seeded by OCA on Fri May 2 15:18:23 2008

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