1pib

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[[Image:1pib.gif|left|200px]]
[[Image:1pib.gif|left|200px]]
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{{Structure
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|PDB= 1pib |SIZE=350|CAPTION= <scene name='initialview01'>1pib</scene>
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The line below this paragraph, containing "STRUCTURE_1pib", 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>
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{{STRUCTURE_1pib| PDB=1pib | SCENE= }}
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|RELATEDENTRY=[[1snh|1SNH]]
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1pib FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1pib OCA], [http://www.ebi.ac.uk/pdbsum/1pib PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1pib RCSB]</span>
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'''Solution structure of DNA containing CPD opposited by GA'''
'''Solution structure of DNA containing CPD opposited by GA'''
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==About this Structure==
==About this Structure==
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1PIB 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=1PIB OCA].
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Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1PIB OCA].
==Reference==
==Reference==
NMR structure of the DNA decamer duplex containing double T*G mismatches of cis-syn cyclobutane pyrimidine dimer: implications for DNA damage recognition by the XPC-hHR23B complex., Lee JH, Park CJ, Shin JS, Ikegami T, Akutsu H, Choi BS, Nucleic Acids Res. 2004 Apr 30;32(8):2474-81. Print 2004. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/15121904 15121904]
NMR structure of the DNA decamer duplex containing double T*G mismatches of cis-syn cyclobutane pyrimidine dimer: implications for DNA damage recognition by the XPC-hHR23B complex., Lee JH, Park CJ, Shin JS, Ikegami T, Akutsu H, Choi BS, Nucleic Acids Res. 2004 Apr 30;32(8):2474-81. Print 2004. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/15121904 15121904]
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[[Category: Protein complex]]
 
[[Category: Choi, B S.]]
[[Category: Choi, B S.]]
[[Category: Lee, J H.]]
[[Category: Lee, J H.]]
[[Category: Park, C J.]]
[[Category: Park, C J.]]
[[Category: Shin, J S.]]
[[Category: Shin, J S.]]
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[[Category: cis-syn cyclobutane pyrimidine dimer]]
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[[Category: Cis-syn cyclobutane pyrimidine dimer]]
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[[Category: cpd containing dna]]
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[[Category: Cpd containing dna]]
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[[Category: helical distortion]]
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[[Category: Helical distortion]]
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[[Category: thyminedimer]]
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[[Category: Thyminedimer]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 05:06:45 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 22:59:58 2008''
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Revision as of 02:06, 3 May 2008

Template:STRUCTURE 1pib

Solution structure of DNA containing CPD opposited by GA


Overview

The cis-syn cyclobutane pyrimidine dimer (CPD) is a cytotoxic, mutagenic and carcinogenic DNA photoproduct and is repaired by the nucleotide excision repair (NER) pathway in mammalian cells. The XPC-hHR23B complex as the initiator of global genomic NER binds to sites of certain kinds of DNA damage. Although CPDs are rarely recognized by the XPC-hHR23B complex, the presence of mismatched bases opposite a CPD significantly increased the binding affinity of the XPC-hHR23B complex to the CPD. In order to decipher the properties of the DNA structures that determine the binding affinity for XPC-hHR23B to DNA, we carried out structural analyses of the various types of CPDs by NMR spectroscopy. The DNA duplex which contains a single 3' T*G wobble pair in a CPD (CPD/GA duplex) induces little conformational distortion. However, severe distortion of the helical conformation occurs when a CPD contains double T*G wobble pairs (CPD/GG duplex) even though the T residues of the CPD form stable hydrogen bonds with the opposite G residues. The helical bending angle of the CPD/GG duplex was larger than those of the CPD/GA duplex and properly matched CPD/AA duplex. The fluctuation of the backbone conformation and significant changes in the widths of the major and minor grooves at the double T*G wobble paired site were also observed in the CPD/GG duplex. These structural features were also found in a duplex that contains the (6-4) adduct, which is efficiently recognized by the XPC-hHR23B complex. Thus, we suggest that the unique structural features of the DNA double helix (that is, helical bending, flexible backbone conformation, and significant changes of the major and/or minor grooves) might be important factors in determining the binding affinity of the XPC-hHR23B complex to DNA.

About this Structure

Full crystallographic information is available from OCA.

Reference

NMR structure of the DNA decamer duplex containing double T*G mismatches of cis-syn cyclobutane pyrimidine dimer: implications for DNA damage recognition by the XPC-hHR23B complex., Lee JH, Park CJ, Shin JS, Ikegami T, Akutsu H, Choi BS, Nucleic Acids Res. 2004 Apr 30;32(8):2474-81. Print 2004. PMID:15121904 Page seeded by OCA on Sat May 3 05:06:45 2008

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