1fhy

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
(New page: 200px<br /><applet load="1fhy" size="450" color="white" frame="true" align="right" spinBox="true" caption="1fhy, resolution 2.20&Aring;" /> '''PSORALEN CROSS-LINKE...)
Line 1: Line 1:
-
[[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==
Line 13: Line 13:
[[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]]
Line 25: Line 25:
[[Category: psoralen]]
[[Category: psoralen]]
-
''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Sat Nov 24 23:51:33 2007''
+
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 12:38:50 2008''

Revision as of 10:38, 21 February 2008


1fhy, resolution 2.20Å

Drag the structure with the mouse to rotate

PSORALEN CROSS-LINKED D(CCGCTAGCGG) FORMS HOLLIDAY JUNCTION

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.

About this Structure

1FHY is a Protein complex structure of sequences from [1] with and as ligands. Full crystallographic information is available from OCA.

Reference

The crystal structures of psoralen cross-linked DNAs: drug-dependent formation of Holliday junctions., Eichman BF, Mooers BH, Alberti M, Hearst JE, Ho PS, J Mol Biol. 2001 Apr 20;308(1):15-26. PMID:11302703

Page seeded by OCA on Thu Feb 21 12:38:50 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools