1o3s

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(New page: 200px<br /><applet load="1o3s" size="450" color="white" frame="true" align="right" spinBox="true" caption="1o3s, resolution 3.00&Aring;" /> '''PROTEIN-DNA RECOGNIT...)
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'''PROTEIN-DNA RECOGNITION AND DNA DEFORMATION REVEALED IN CRYSTAL STRUCTURES OF CAP-DNA COMPLEXES'''<br />
'''PROTEIN-DNA RECOGNITION AND DNA DEFORMATION REVEALED IN CRYSTAL STRUCTURES OF CAP-DNA COMPLEXES'''<br />
==Overview==
==Overview==
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The catabolite activator protein (CAP) sharply bends DNA in the CAP-DNA, complex, introducing a DNA kink, with a roll angle of approximately 40, degrees and a twist angle of approximately 20 degrees, between positions 6, and 7 of the DNA half-site, 5'-A(1)A(2)A(3)T(4)G(5)T(6)G(7)A(8)T(9)C(10)T(11)-3' ("primary kink"). CAP, recognizes the base-pair immediately 5' to the primary-kink site, T:A(6), through an "indirect-readout" mechanism involving sequence effects on the, energetics of primary-kink formation. CAP recognizes the base-pair, immediately 3' to the primary-kink site, G:C(7), through a, "direct-readout" mechanism involving formation of a hydrogen bond between, Glu181 of CAP and G:C(7). Here, we report that substitution of the, carboxylate side-chain of Glu181 of CAP by the one-methylene-group-shorter, carboxylate side-chain of Asp changes DNA binding specificity at position, 6 of the DNA half site, changing specificity for T:A(6) to specificity for, C:G(6), and we report a crystallographic analysis defining the structural, basis of the change in specificity. The Glu181--&gt;Asp substitution, eliminates the primary kink and thus eliminates indirect-readout-based, specificity for T:A(6). The Glu181--&gt;Asp substitution does not eliminate, hydrogen-bond formation with G:C(7), and thus does not eliminate, direct-readout-based specificity for G:C(7).
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The catabolite activator protein (CAP) sharply bends DNA in the CAP-DNA complex, introducing a DNA kink, with a roll angle of approximately 40 degrees and a twist angle of approximately 20 degrees, between positions 6 and 7 of the DNA half-site, 5'-A(1)A(2)A(3)T(4)G(5)T(6)G(7)A(8)T(9)C(10)T(11)-3' ("primary kink"). CAP recognizes the base-pair immediately 5' to the primary-kink site, T:A(6), through an "indirect-readout" mechanism involving sequence effects on the energetics of primary-kink formation. CAP recognizes the base-pair immediately 3' to the primary-kink site, G:C(7), through a "direct-readout" mechanism involving formation of a hydrogen bond between Glu181 of CAP and G:C(7). Here, we report that substitution of the carboxylate side-chain of Glu181 of CAP by the one-methylene-group-shorter carboxylate side-chain of Asp changes DNA binding specificity at position 6 of the DNA half site, changing specificity for T:A(6) to specificity for C:G(6), and we report a crystallographic analysis defining the structural basis of the change in specificity. The Glu181--&gt;Asp substitution eliminates the primary kink and thus eliminates indirect-readout-based specificity for T:A(6). The Glu181--&gt;Asp substitution does not eliminate hydrogen-bond formation with G:C(7), and thus does not eliminate direct-readout-based specificity for G:C(7).
==About this Structure==
==About this Structure==
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1O3S is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli] with CMP as [http://en.wikipedia.org/wiki/ligand ligand]. This structure superseeds the now removed PDB entry 1DB9. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1O3S OCA].
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1O3S is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli] with <scene name='pdbligand=CMP:'>CMP</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. This structure supersedes the now removed PDB entry 1DB9. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1O3S OCA].
==Reference==
==Reference==
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[[Category: Escherichia coli]]
[[Category: Escherichia coli]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: Berman, H.M.]]
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[[Category: Berman, H M.]]
[[Category: Chen, S.]]
[[Category: Chen, S.]]
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[[Category: Ebright, R.H.]]
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[[Category: Ebright, R H.]]
[[Category: CMP]]
[[Category: CMP]]
[[Category: camp receptor protein]]
[[Category: camp receptor protein]]
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[[Category: protein-dna complex]]
[[Category: protein-dna complex]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:13:07 2008''

Revision as of 12:13, 21 February 2008


1o3s, resolution 3.00Å

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PROTEIN-DNA RECOGNITION AND DNA DEFORMATION REVEALED IN CRYSTAL STRUCTURES OF CAP-DNA COMPLEXES

Overview

The catabolite activator protein (CAP) sharply bends DNA in the CAP-DNA complex, introducing a DNA kink, with a roll angle of approximately 40 degrees and a twist angle of approximately 20 degrees, between positions 6 and 7 of the DNA half-site, 5'-A(1)A(2)A(3)T(4)G(5)T(6)G(7)A(8)T(9)C(10)T(11)-3' ("primary kink"). CAP recognizes the base-pair immediately 5' to the primary-kink site, T:A(6), through an "indirect-readout" mechanism involving sequence effects on the energetics of primary-kink formation. CAP recognizes the base-pair immediately 3' to the primary-kink site, G:C(7), through a "direct-readout" mechanism involving formation of a hydrogen bond between Glu181 of CAP and G:C(7). Here, we report that substitution of the carboxylate side-chain of Glu181 of CAP by the one-methylene-group-shorter carboxylate side-chain of Asp changes DNA binding specificity at position 6 of the DNA half site, changing specificity for T:A(6) to specificity for C:G(6), and we report a crystallographic analysis defining the structural basis of the change in specificity. The Glu181-->Asp substitution eliminates the primary kink and thus eliminates indirect-readout-based specificity for T:A(6). The Glu181-->Asp substitution does not eliminate hydrogen-bond formation with G:C(7), and thus does not eliminate direct-readout-based specificity for G:C(7).

About this Structure

1O3S is a Single protein structure of sequence from Escherichia coli with as ligand. This structure supersedes the now removed PDB entry 1DB9. Full crystallographic information is available from OCA.

Reference

Indirect readout of DNA sequence at the primary-kink site in the CAP-DNA complex: alteration of DNA binding specificity through alteration of DNA kinking., Chen S, Gunasekera A, Zhang X, Kunkel TA, Ebright RH, Berman HM, J Mol Biol. 2001 Nov 16;314(1):75-82. PMID:11724533

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