1ig4: Difference between revisions

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New page: left|200px<br /> <applet load="1ig4" size="450" color="white" frame="true" align="right" spinBox="true" caption="1ig4" /> '''Solution Structure of the Methyl-CpG-Bindin...
 
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[[Image:1ig4.gif|left|200px]]<br />
[[Image:1ig4.gif|left|200px]]<br /><applet load="1ig4" size="350" color="white" frame="true" align="right" spinBox="true"  
<applet load="1ig4" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="1ig4" />
caption="1ig4" />
'''Solution Structure of the Methyl-CpG-Binding Domain of Human MBD1 in Complex with Methylated DNA'''<br />
'''Solution Structure of the Methyl-CpG-Binding Domain of Human MBD1 in Complex with Methylated DNA'''<br />


==Overview==
==Overview==
In vertebrates, the biological consequences of DNA methylation are often, mediated by protein factors containing conserved methyl-CpG binding, domains (MBDs). Mutations in the MBD protein MeCP2 cause the, neurodevelopmental disease Rett syndrome. We report here the solution, structure of the MBD of the human methylation-dependent transcriptional, regulator MBD1 bound to methylated DNA. DNA binding causes a loop in MBD1, to fold into a major and novel DNA binding interface. Recognition of the, methyl groups and CG sequence at the methylation site is due to five, highly conserved residues that form a hydrophobic patch. The structure, indicates how MBD may access nucleosomal DNA without encountering steric, interference from core histones, and provides a basis to interpret, mutations linked to Rett syndrome in MeCP2.
In vertebrates, the biological consequences of DNA methylation are often mediated by protein factors containing conserved methyl-CpG binding domains (MBDs). Mutations in the MBD protein MeCP2 cause the neurodevelopmental disease Rett syndrome. We report here the solution structure of the MBD of the human methylation-dependent transcriptional regulator MBD1 bound to methylated DNA. DNA binding causes a loop in MBD1 to fold into a major and novel DNA binding interface. Recognition of the methyl groups and CG sequence at the methylation site is due to five highly conserved residues that form a hydrophobic patch. The structure indicates how MBD may access nucleosomal DNA without encountering steric interference from core histones, and provides a basis to interpret mutations linked to Rett syndrome in MeCP2.


==Disease==
==Disease==
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==About this Structure==
==About this Structure==
1IG4 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1IG4 OCA].  
1IG4 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1IG4 OCA].  


==Reference==
==Reference==
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[[Category: Fujita, N.]]
[[Category: Fujita, N.]]
[[Category: Ikegami, T.]]
[[Category: Ikegami, T.]]
[[Category: Jee, J.G.]]
[[Category: Jee, J G.]]
[[Category: Nakao, M.]]
[[Category: Nakao, M.]]
[[Category: Ohki, I.]]
[[Category: Ohki, I.]]
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[[Category: recognition via beta-sheet]]
[[Category: recognition via beta-sheet]]


''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 17:29:30 2007''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:11:29 2008''