1le8

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(New page: 200px<br /><applet load="1le8" size="450" color="white" frame="true" align="right" spinBox="true" caption="1le8, resolution 2.30&Aring;" /> '''Crystal Structure of...)
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[[Image:1le8.jpg|left|200px]]<br /><applet load="1le8" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1le8, resolution 2.30&Aring;" />
caption="1le8, resolution 2.30&Aring;" />
'''Crystal Structure of the MATa1/MATalpha2-3A Heterodimer Bound to DNA Complex'''<br />
'''Crystal Structure of the MATa1/MATalpha2-3A Heterodimer Bound to DNA Complex'''<br />
==Overview==
==Overview==
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Triply mutated MATalpha2 protein, alpha2-3A, in which all three major, groove-contacting residues are mutated to alanine, is defective in binding, DNA alone or in complex with Mcm1 yet binds with MATa1 with near wild-type, affinity and specificity. To gain insight into this unexpected behavior, we determined the crystal structure of the a1/alpha2-3A/DNA complex. The, structure shows that the triple mutation causes a collapse of the, alpha2-3A/DNA interface that results in a reorganized set of alpha2-3A/DNA, contacts, thereby enabling the mutant protein to recognize the wild-type, DNA sequence. Isothermal titration calorimetry measurements reveal that a, much more favorable entropic component stabilizes the a1/alpha2-3A/DNA, complex than the alpha2-3A/DNA complex. The combined structural and, thermodynamic studies provide an explanation of how partner proteins, influence the sequence specificity of a DNA binding protein.
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Triply mutated MATalpha2 protein, alpha2-3A, in which all three major groove-contacting residues are mutated to alanine, is defective in binding DNA alone or in complex with Mcm1 yet binds with MATa1 with near wild-type affinity and specificity. To gain insight into this unexpected behavior, we determined the crystal structure of the a1/alpha2-3A/DNA complex. The structure shows that the triple mutation causes a collapse of the alpha2-3A/DNA interface that results in a reorganized set of alpha2-3A/DNA contacts, thereby enabling the mutant protein to recognize the wild-type DNA sequence. Isothermal titration calorimetry measurements reveal that a much more favorable entropic component stabilizes the a1/alpha2-3A/DNA complex than the alpha2-3A/DNA complex. The combined structural and thermodynamic studies provide an explanation of how partner proteins influence the sequence specificity of a DNA binding protein.
==About this Structure==
==About this Structure==
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1LE8 is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Saccharomyces_cerevisiae Saccharomyces cerevisiae]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1LE8 OCA].
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1LE8 is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Saccharomyces_cerevisiae Saccharomyces cerevisiae]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1LE8 OCA].
==Reference==
==Reference==
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[[Category: Saccharomyces cerevisiae]]
[[Category: Saccharomyces cerevisiae]]
[[Category: Ke, A.]]
[[Category: Ke, A.]]
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[[Category: Mathias, J.R.]]
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[[Category: Mathias, J R.]]
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[[Category: Vershon, A.K.]]
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[[Category: Vershon, A K.]]
[[Category: Wolberger, C.]]
[[Category: Wolberger, C.]]
[[Category: isothermal titration calorimetry]]
[[Category: isothermal titration calorimetry]]
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[[Category: protein-dna complex]]
[[Category: protein-dna complex]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Nov 20 20:30:33 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:44:14 2008''

Revision as of 11:44, 21 February 2008


1le8, resolution 2.30Å

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Crystal Structure of the MATa1/MATalpha2-3A Heterodimer Bound to DNA Complex

Overview

Triply mutated MATalpha2 protein, alpha2-3A, in which all three major groove-contacting residues are mutated to alanine, is defective in binding DNA alone or in complex with Mcm1 yet binds with MATa1 with near wild-type affinity and specificity. To gain insight into this unexpected behavior, we determined the crystal structure of the a1/alpha2-3A/DNA complex. The structure shows that the triple mutation causes a collapse of the alpha2-3A/DNA interface that results in a reorganized set of alpha2-3A/DNA contacts, thereby enabling the mutant protein to recognize the wild-type DNA sequence. Isothermal titration calorimetry measurements reveal that a much more favorable entropic component stabilizes the a1/alpha2-3A/DNA complex than the alpha2-3A/DNA complex. The combined structural and thermodynamic studies provide an explanation of how partner proteins influence the sequence specificity of a DNA binding protein.

About this Structure

1LE8 is a Protein complex structure of sequences from Saccharomyces cerevisiae. Full crystallographic information is available from OCA.

Reference

Structural and thermodynamic characterization of the DNA binding properties of a triple alanine mutant of MATalpha2., Ke A, Mathias JR, Vershon AK, Wolberger C, Structure. 2002 Jul;10(7):961-71. PMID:12121651

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