1gef: Difference between revisions

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[[Image:1gef.gif|left|200px]]
[[Image:1gef.gif|left|200px]]


{{Structure
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|GENE= HJC ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=2261 Pyrococcus furiosus])
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1gef FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1gef OCA], [http://www.ebi.ac.uk/pdbsum/1gef PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1gef RCSB]</span>
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'''CRYSTAL STRUCTURE OF THE ARCHAEAL HOLLIDAY JUNCTION RESOLVASE HJC'''
'''CRYSTAL STRUCTURE OF THE ARCHAEAL HOLLIDAY JUNCTION RESOLVASE HJC'''
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[[Category: Nishino, T.]]
[[Category: Nishino, T.]]
[[Category: Tsuchiya, D.]]
[[Category: Tsuchiya, D.]]
[[Category: hjc]]
[[Category: Hjc]]
[[Category: holliday junction resolvase]]
[[Category: Holliday junction resolvase]]
 
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 20:42:26 2008''

Revision as of 17:28, 2 May 2008

File:1gef.gif

Template:STRUCTURE 1gef

CRYSTAL STRUCTURE OF THE ARCHAEAL HOLLIDAY JUNCTION RESOLVASE HJC


OverviewOverview

BACKGROUND: Homologous recombination is a crucial mechanism in determining genetic diversity and repairing damaged chromosomes. Holliday junction is the universal DNA intermediate whose interaction with proteins is one of the major events in the recombinational process. Hjc is an archaeal endonuclease, which specifically resolves the junction DNA to produce two separate recombinant DNA duplexes. The atomic structure of Hjc should clarify the mechanisms of the specific recognition with Holliday junction and the catalytic reaction. RESULTS: The crystal structure of Hjc from the hyperthermophilic archaeon Pyrococcus furiosus has been determined at 2.0 A resolution. The active Hjc molecule forms a homodimer, where an extensive hydrophobic interface tightly assembles two subunits of a single compact domain. The folding of the Hjc subunit is clearly different from any other Holliday junction resolvases thus far known. Instead, it resembles those of type II restriction endonucleases, including the configurations of the active site residues, which constitute the canonical catalytic motifs. The dimeric Hjc molecule displays an extensive basic surface on one side, which contains many conserved amino acids, including those in the active site. CONCLUSIONS: The architectural similarity of Hjc to restriction endonucleases allowed us to construct a putative model of the complex with Holliday junction. This model accounts for how Hjc recognizes and resolves the junction DNA in a specific manner. Mutational and biochemical analyses highlight the importance of some loops and the amino terminal region in interaction with DNA.

About this StructureAbout this Structure

1GEF is a Single protein structure of sequence from Pyrococcus furiosus. Full crystallographic information is available from OCA.

ReferenceReference

Crystal structure of the archaeal holliday junction resolvase Hjc and implications for DNA recognition., Nishino T, Komori K, Tsuchiya D, Ishino Y, Morikawa K, Structure. 2001 Mar 7;9(3):197-204. PMID:11286886 Page seeded by OCA on Fri May 2 17:28:16 2008

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