1xcy

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[[Image:1xcy.gif|left|200px]]
[[Image:1xcy.gif|left|200px]]
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{{Structure
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<!--
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|PDB= 1xcy |SIZE=350|CAPTION= <scene name='initialview01'>1xcy</scene>
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The line below this paragraph, containing "STRUCTURE_1xcy", 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=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=DXD:(1S,3S,4R)-4-(PHOSPHOOXYMETHYL)-CYCLOPENTANE-1,3-DIOL'>DXD</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=
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or leave the SCENE parameter empty for the default display.
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|GENE=
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|DOMAIN=
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{{STRUCTURE_1xcy| PDB=1xcy | SCENE= }}
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|RELATEDENTRY=[[1xcz|1xcz]]
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1xcy FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1xcy OCA], [http://www.ebi.ac.uk/pdbsum/1xcy PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1xcy RCSB]</span>
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}}
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'''Structure of DNA containing the alpha-anomer of a carbocyclic abasic site'''
'''Structure of DNA containing the alpha-anomer of a carbocyclic abasic site'''
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==About this Structure==
==About this Structure==
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1XCY is a [[Protein complex]] structure of sequences from [http://en.wikipedia.org/wiki/ ]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1XCY OCA].
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Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1XCY OCA].
==Reference==
==Reference==
Impact of the C1' configuration of abasic sites on DNA duplex structure., de Los Santos C, El-Khateeb M, Rege P, Tian K, Johnson F, Biochemistry. 2004 Dec 14;43(49):15349-57. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/15581347 15581347]
Impact of the C1' configuration of abasic sites on DNA duplex structure., de Los Santos C, El-Khateeb M, Rege P, Tian K, Johnson F, Biochemistry. 2004 Dec 14;43(49):15349-57. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/15581347 15581347]
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[[Category: Protein complex]]
 
[[Category: El-khateeb, M.]]
[[Category: El-khateeb, M.]]
[[Category: Johnson, F.]]
[[Category: Johnson, F.]]
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[[Category: Santos, C de los.]]
[[Category: Santos, C de los.]]
[[Category: Tian, K.]]
[[Category: Tian, K.]]
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[[Category: abasic site]]
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[[Category: Abasic site]]
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[[Category: double helix]]
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[[Category: Double helix]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 14:52:13 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 00:47:53 2008''
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Revision as of 11:52, 3 May 2008

Template:STRUCTURE 1xcy

Structure of DNA containing the alpha-anomer of a carbocyclic abasic site


Overview

Naturally occurring abasic sites in DNA exist as an equilibrium mixture of the aldehyde, the hydrated aldehyde, and the hemiacetal forms (dominant). The influence of the configuration of the C1' hydroxyl group of the hemiacetal form on duplex structure and abasic site repair has been examined using novel carbocyclic analogues. Both the alpha- and beta-forms of this novel abasic site were introduced into oligomeric DNA using the standard DMT-phosphoramidite approach in an automated solid-phase synthesizer. Solution structures of the d(CGTACXCATGC).d(GCATGAGTACG) duplex (where X is the alpha- or beta-anomer of the carbocyclic abasic site analogue) were determined by NMR spectroscopy and restrained molecular dynamics simulations. The structures were only minimally perturbed by the presence of either anomer of the abasic site. All residues adopted an anti conformation, and Watson-Crick alignments were observed on all base pairs of the duplexes. At the lesion site, the abasic residues and their partner adenines showed increased dynamic behavior but adopted intrahelical positions in the final refined structures. Incision of duplexes having the alpha- or beta-anomer of the carbocyclic abasic site by human AP endonuclease showed that the enzyme recognizes both configurations of the lesion and nicks the DNA backbone with similar efficiency. Our results challenge the suggestion that Ape1 is stereoselective and imply a plasticity at the active site of the enzyme for accommodating either anomer of the lesion.

About this Structure

Full crystallographic information is available from OCA.

Reference

Impact of the C1' configuration of abasic sites on DNA duplex structure., de Los Santos C, El-Khateeb M, Rege P, Tian K, Johnson F, Biochemistry. 2004 Dec 14;43(49):15349-57. PMID:15581347 Page seeded by OCA on Sat May 3 14:52:13 2008

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