1fhy: Difference between revisions

New page: left|200px<br /><applet load="1fhy" size="450" color="white" frame="true" align="right" spinBox="true" caption="1fhy, resolution 2.20Å" /> '''PSORALEN CROSS-LINKE...
 
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[[Image:1fhy.gif|left|200px]]<br /><applet load="1fhy" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1fhy.gif|left|200px]]<br /><applet load="1fhy" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1fhy, resolution 2.20&Aring;" />
caption="1fhy, resolution 2.20&Aring;" />
'''PSORALEN CROSS-LINKED D(CCGCTAGCGG) FORMS HOLLIDAY JUNCTION'''<br />
'''PSORALEN CROSS-LINKED D(CCGCTAGCGG) FORMS HOLLIDAY JUNCTION'''<br />


==Overview==
==Overview==
The single-crystal structures are presented for two DNA sequences with the, thymine bases covalently cross-linked across the complementary strands by, 4'-hydroxymethyl-4,5',8-trimethylpsoralen (HMT). The HMT-adduct of, d(CCGCTAGCGG) forms a psoralen-induced Holliday junction, showing for the, first time the effect of this important class of chemotheraputics on the, structure of the recombination intermediate. In contrast, HMT-d(CCGGTACCGG) forms a sequence-dependent junction. In both structures, the DNA duplex is highly distorted at the thymine base linked to the, six-member pyrone ring of the drug. The psoralen cross-link defines the, intramolecular interactions of the drug-induced junction, while the, sequence-dependent structure is nearly identical to the native Holliday, junction of d(CCGGTACCGG) alone. The two structures contrast the effects, of drug- and sequence-dependent interactions on the structure of a, Holliday junction, suggesting a role for psoralen in the mechanism to, initiate repair of psoralen-lesions in mammalian DNA.
The single-crystal structures are presented for two DNA sequences with the thymine bases covalently cross-linked across the complementary strands by 4'-hydroxymethyl-4,5',8-trimethylpsoralen (HMT). The HMT-adduct of d(CCGCTAGCGG) forms a psoralen-induced Holliday junction, showing for the first time the effect of this important class of chemotheraputics on the structure of the recombination intermediate. In contrast, HMT-d(CCGGTACCGG) forms a sequence-dependent junction. In both structures, the DNA duplex is highly distorted at the thymine base linked to the six-member pyrone ring of the drug. The psoralen cross-link defines the intramolecular interactions of the drug-induced junction, while the sequence-dependent structure is nearly identical to the native Holliday junction of d(CCGGTACCGG) alone. The two structures contrast the effects of drug- and sequence-dependent interactions on the structure of a Holliday junction, suggesting a role for psoralen in the mechanism to initiate repair of psoralen-lesions in mammalian DNA.


==About this Structure==
==About this Structure==
1FHY is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/ ] with CA and PSO as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1FHY OCA].  
1FHY is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/ ] with <scene name='pdbligand=CA:'>CA</scene> and <scene name='pdbligand=PSO:'>PSO</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1FHY OCA].  


==Reference==
==Reference==
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[[Category: Protein complex]]
[[Category: Protein complex]]
[[Category: Alberti, M.]]
[[Category: Alberti, M.]]
[[Category: Eichman, B.F.]]
[[Category: Eichman, B F.]]
[[Category: Hearst, J.E.]]
[[Category: Hearst, J E.]]
[[Category: Ho, P.S.]]
[[Category: Ho, P S.]]
[[Category: Mooers, B.H.M.]]
[[Category: Mooers, B H.M.]]
[[Category: CA]]
[[Category: CA]]
[[Category: PSO]]
[[Category: PSO]]
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[[Category: psoralen]]
[[Category: psoralen]]


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