User:Wayne Decatur/Gal 4

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Gal4p is a transcriptional activator in ''Saccharomyces cerevisiae'' that regulates the expression of genes to coordinate the response to the carbon source galactose.
Gal4p is a transcriptional activator in ''Saccharomyces cerevisiae'' that regulates the expression of genes to coordinate the response to the carbon source galactose.
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<StructureSection load='1d66' size='500' frame='true' side='right' caption='The N-terminal amino acids of Gal4p bound to DNA ([[1d66]])' scene='70/701975/1d66_firstglance/2' >
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<!-- important to note you need to use 'side' in a StructureSEction instead of 'align'. If you leave 'align' it doesn't work.-->
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<Structure load='Insert PDB code or filename here' size='550' frame='true' align='right' caption='The N-terminal amino acids of Gal4p bound to DNA ([[1d66]])' scene='70/701975/1d66_firstglance/2' />
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==Background==
==Background==
Gal4p is a transcriptional activator in ''Saccharomyces cerevisiae'' that regulates the expression of genes to coordinate the response to the carbon source galactose.
Gal4p is a transcriptional activator in ''Saccharomyces cerevisiae'' that regulates the expression of genes to coordinate the response to the carbon source galactose.
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The structure of the DNA-binding domain([[1d66]]), the dimerization domain ([[1hbw]]), and the activation domain ([[3bts]]) has been solved separately. There is a structure of the DNA-binding and dimerization domains as one unit as well ([[3coq]]).
The structure of the DNA-binding domain([[1d66]]), the dimerization domain ([[1hbw]]), and the activation domain ([[3bts]]) has been solved separately. There is a structure of the DNA-binding and dimerization domains as one unit as well ([[3coq]]).
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Pioneering studies on Gal4p from the Ptashne laboratory shaped our understanding of transcriptional activation in eukaryotes, and Gal4p derivatives, along with their cognate promoters, continue to be used as tools by investigators preforming research in yeast.
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Pioneering studies on Gal4p from the Ptashne laboratory shaped our understanding of eukaryotic transcriptional activation, and Gal4p derivatives, along with their cognate promoters, continue to be used as tools by investigators preforming research in yeast.
==DNA Recognition by Gal4p==
==DNA Recognition by Gal4p==
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<jmol>
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<br/>
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The protein <scene name='70/701975/1d66_firstglance/2'>binds as a dimer to a symmetrical 17-base-pair sequence</scene>. Specifically, the consensus Gal4p-binding site is a 17-mer of sequence conforming to the motif below.<br>
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<scene name='70/701975/1d66_firstglance_secondary/2'>Each monomer</scene> of the protein dimer has 3 '''<font color='#f00080'> alpha helices</font>'''.
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The protein <scene name='70/701975/1d66_firstglance/2'>binds as a dimer to a symmetrical 17-base-pair sequence</scene>. Specifically, the consensus Gal4p-binding site is a 17-mer of sequence conforming to the motif below, which has the key feature of CGG triplets at the 5' ends, separated by 11 bps, or 5′-CGG-N11-CCG-3′.<br>
&nbsp;<br>
&nbsp;<br>
<span style="font-weight: bold;font-family: Courier New; font-size: 14pt">
<span style="font-weight: bold;font-family: Courier New; font-size: 14pt">
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&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<span style="color:#551a8b">5'-CGGNNNNNNNNNNNCCG-3'</span><br>&nbsp;&nbsp;
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&nbsp;&nbsp;<span style="background:black;color:#FFC0C8">5'-CGGNNNNNNNNNNNCCG-3'</span><br>&nbsp;&nbsp;
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&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;|||||||||||||||||<br>
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&nbsp;&nbsp;<font style='background:black;color:#ffffff;'>|||||||||||||||||</font><br>
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&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<span style="color:#6060ff">3'-CGGNNNNNNNNNNNGGC-5'</span></span>
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&nbsp;&nbsp;<span style="background:black;color:#FFFF80">3'-CGGNNNNNNNNNNNGGC-5'</span></span>
<br>
<br>
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The DNA binding domain <scene name='70/701975/1d66_firstglance_zn_binding/2'>uses six Cys residues to coordinate the binding of two ions of zinc (Zn(II))</scene>. In the crystal structure [[1d66]], the zinc ions are represented by other members of the same group on the periodic table, the heavier cadmium ions. The Zn-binding motif lets the structure accomplish more with fewer amino acids, the metals lending an "economy of structure", arranging two small helices to recognize a specific DNA site.
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The DNA binding domain <scene name='70/701975/1d66_firstglance_zn_binding/2'>uses six Cys residues to coordinate the binding of two ions of zinc (Zn(II))</scene>. (In the crystal structure [[1d66]], the zinc ions are actually represented by other members of the same group on the periodic table, the heavier cadmium ions.) The Zn-binding motif lets the structure accomplish more with fewer amino acids, the metals lending an "economy of structure", arranging two small helices to recognize a specific DNA site. <scene name='70/701975/1d66_base_conctacts/2'>Two lysines (17 and 18) make direct base contacts in the DNA major groove with the specified CGG triplets</scene>.<br>
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<script>select A,ADE,DA; color [x5050FF]; color cartoon [x5050FF]; select C, CYT,DC; color [xE00000]; color cartoon [xE00000]; select G,GUA,DG; color [x00C000]; color cartoon [x00C000]; select T,THY,DT; color [xE6E600]; color cartoon [xE6E600]; select U,URA; color [xCC9900]; color cartoon [xCC9900];</script>
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<text>Color Structure by Nucleotide</text>
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{{ColorKey Bases DNA}}
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The third large helix of each dimer subunit interacts with the other <scene name='70/701975/1d66_firstglance_slab/2'>by arranging hydrophobic residues in the contact region</scene>. Note the abundance of gray residues in the central stem protruding from a site roughly the center of the DNA binding site. The dimer interface is more fully explored in a later publication with an expanded structure, see [[3coq]].
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Despite only making base-specific contacts at the ends, <scene name='70/701975/Spacefill/1'>Ga14p is mostly in contact with the DNA for its entire span of the binding site.</scene>
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The third, large helix of each dimer subunit interacts with the other <scene name='70/701975/1d66_firstglance_slab/3'>by arranging hydrophobic residues in the contact region</scene>. Note the abundance of gray residues in the central stem protruding from a site roughly above the center of the DNA binding site. The dimer interface is more fully explored in a later publication with an expanded structure, see [[3coq]].
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The conformation of the linker connecting each dimerization helix and the metal-binding domains determines the preferred total number of bases between the triplets.
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</StructureSection>
==Reference==
==Reference==
<ref group="xtra">PMID:1557122</ref><references group="xtra"/>
<ref group="xtra">PMID:1557122</ref><references group="xtra"/>
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==Related==
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==Impetus==
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This page accompanies a [http://fenglabwkshopmay2015.readthedocs.org/en/latest/ hands-on workshop for ChIP-Seq] being given by Wayne Decatur May 14th, 2015.
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==See Also==
* [[Gal3-Gal80-Gal4]]
* [[Gal3-Gal80-Gal4]]

Current revision

Gal4p is a transcriptional activator in Saccharomyces cerevisiae that regulates the expression of genes to coordinate the response to the carbon source galactose.

The N-terminal amino acids of Gal4p bound to DNA (1d66)

Drag the structure with the mouse to rotate

Reference

Impetus

This page accompanies a hands-on workshop for ChIP-Seq being given by Wayne Decatur May 14th, 2015.

See Also

Proteopedia Page Contributors and Editors (what is this?)

Wayne Decatur

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