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New page: left|200px<br /><applet load="2isz" size="450" color="white" frame="true" align="right" spinBox="true" caption="2isz, resolution 2.403Å" /> '''Crystal structure o...
 
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[[Image:2isz.gif|left|200px]]<br /><applet load="2isz" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:2isz.gif|left|200px]]<br /><applet load="2isz" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="2isz, resolution 2.403&Aring;" />
caption="2isz, resolution 2.403&Aring;" />
'''Crystal structure of a two-domain IdeR-DNA complex crystal form I'''<br />
'''Crystal structure of a two-domain IdeR-DNA complex crystal form I'''<br />


==Overview==
==Overview==
The iron-dependent regulator IdeR is a key transcriptional regulator of, iron uptake in Mycobacterium tuberculosis. In order to increase our, insight into the role of the SH3-like third domain of this essential, regulator, the metal-binding and DNA-binding properties of two-domain IdeR, (2D-IdeR) whose SH3-like domain has been truncated were characterized. The, equilibrium dissociation constants for Co2+ and Ni2+ activation of 2D-IdeR, for binding to the fxbA operator and the DNA-binding affinities of 2D-IdeR, in the presence of excess metal ions were estimated using fluorescence, spectroscopy. 2D-IdeR binds to fxbA operator DNA with similar affinity as, full-length IdeR in the presence of excess metal ion. However, the Ni2+, concentrations required to activate 2D-IdeR for DNA binding appear to be, smaller than that for full-length IdeR while the concentration of Co2+, required for activation remains the same. We have determined the crystal, structures of Ni2+-activated 2D-IdeR at 1.96 A resolution and its double, dimer complex with the mbtA-mbtB operator DNA in two crystal forms at 2.4, A and 2.6 A, the highest resolutions for DNA complexes for any structures, of iron-dependent regulator family members so far. The 2D-IdeR-DNA complex, structures confirm the specificity of Ser37 and Pro39 for thymine bases, and suggest preferential contacts of Gln43 to cytosine bases of the DNA., In addition, our 2D-IdeR structures reveal a remarkable property of the, TEV cleavage sequence remaining after removal of the C-terminal His6. This, C-terminal tail promotes crystal contacts by forming a beta-sheet with the, corresponding tail of neighboring subunits in two unrelated structures of, 2D-IdeR, one with and one without DNA. The contact-promoting properties of, this C-terminal TEV cleavage sequence may be beneficial for crystallizing, other proteins.
The iron-dependent regulator IdeR is a key transcriptional regulator of iron uptake in Mycobacterium tuberculosis. In order to increase our insight into the role of the SH3-like third domain of this essential regulator, the metal-binding and DNA-binding properties of two-domain IdeR (2D-IdeR) whose SH3-like domain has been truncated were characterized. The equilibrium dissociation constants for Co2+ and Ni2+ activation of 2D-IdeR for binding to the fxbA operator and the DNA-binding affinities of 2D-IdeR in the presence of excess metal ions were estimated using fluorescence spectroscopy. 2D-IdeR binds to fxbA operator DNA with similar affinity as full-length IdeR in the presence of excess metal ion. However, the Ni2+ concentrations required to activate 2D-IdeR for DNA binding appear to be smaller than that for full-length IdeR while the concentration of Co2+ required for activation remains the same. We have determined the crystal structures of Ni2+-activated 2D-IdeR at 1.96 A resolution and its double dimer complex with the mbtA-mbtB operator DNA in two crystal forms at 2.4 A and 2.6 A, the highest resolutions for DNA complexes for any structures of iron-dependent regulator family members so far. The 2D-IdeR-DNA complex structures confirm the specificity of Ser37 and Pro39 for thymine bases and suggest preferential contacts of Gln43 to cytosine bases of the DNA. In addition, our 2D-IdeR structures reveal a remarkable property of the TEV cleavage sequence remaining after removal of the C-terminal His6. This C-terminal tail promotes crystal contacts by forming a beta-sheet with the corresponding tail of neighboring subunits in two unrelated structures of 2D-IdeR, one with and one without DNA. The contact-promoting properties of this C-terminal TEV cleavage sequence may be beneficial for crystallizing other proteins.


==About this Structure==
==About this Structure==
2ISZ is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Mycobacterium_tuberculosis Mycobacterium tuberculosis] with NI and NA as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2ISZ OCA].  
2ISZ is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Mycobacterium_tuberculosis Mycobacterium tuberculosis] with <scene name='pdbligand=NI:'>NI</scene> and <scene name='pdbligand=NA:'>NA</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2ISZ OCA].  


==Reference==
==Reference==
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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Beeson, C.]]
[[Category: Beeson, C.]]
[[Category: Chou, C.J.]]
[[Category: Chou, C J.]]
[[Category: Hol, W.G.]]
[[Category: Hol, W G.]]
[[Category: Holmes, R.K.]]
[[Category: Holmes, R K.]]
[[Category: Rice, A.E.]]
[[Category: Rice, A E.]]
[[Category: Roach, C.]]
[[Category: Roach, C.]]
[[Category: Wisedchaisri, G.]]
[[Category: Wisedchaisri, G.]]
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[[Category: dna-binding protein]]
[[Category: dna-binding protein]]


''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Nov 20 15:30:52 2007''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 17:55:35 2008''