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1iyr

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(New page: 200px<br /> <applet load="1iyr" size="450" color="white" frame="true" align="right" spinBox="true" caption="1iyr" /> '''NMR Structure Ensemble Of Dff-C Domain'''<b...)
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'''NMR Structure Ensemble Of Dff-C Domain'''<br />
'''NMR Structure Ensemble Of Dff-C Domain'''<br />
==Overview==
==Overview==
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DFF45/ICAD has dual functions in the final stage of apoptosis, by acting, as both a folding chaperone and a DNase inhibitor of DFF40/CAD. Here, we, present the solution structure of the C-terminal domain of DFF45, which is, essential for its chaperone-like activity. The structure of this domain, (DFF-C) consists of four alpha helices, which are folded in a novel, helix-packing arrangement. The 3D structure reveals a large cluster of, negatively charged residues on the molecular surface of DFF-C. This, observation suggests that charge complementation plays an important role, in the interaction of DFF-C with the positively charged catalytic domain, of DFF40, and thus for the chaperone activity of DFF45. The structure of, DFF-C also provides a rationale for the loss of the chaperone activity in, DFF35, a short isoform of DFF45. Indeed, in DFF35, the amino acid sequence, is truncated in the middle of the second alpha helix constituting the, structure of DFF-C, and thus both the hydrophobic core and the cluster of, negative charges are disrupted.
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DFF45/ICAD has dual functions in the final stage of apoptosis, by acting as both a folding chaperone and a DNase inhibitor of DFF40/CAD. Here, we present the solution structure of the C-terminal domain of DFF45, which is essential for its chaperone-like activity. The structure of this domain (DFF-C) consists of four alpha helices, which are folded in a novel helix-packing arrangement. The 3D structure reveals a large cluster of negatively charged residues on the molecular surface of DFF-C. This observation suggests that charge complementation plays an important role in the interaction of DFF-C with the positively charged catalytic domain of DFF40, and thus for the chaperone activity of DFF45. The structure of DFF-C also provides a rationale for the loss of the chaperone activity in DFF35, a short isoform of DFF45. Indeed, in DFF35, the amino acid sequence is truncated in the middle of the second alpha helix constituting the structure of DFF-C, and thus both the hydrophobic core and the cluster of negative charges are disrupted.
==About this Structure==
==About this Structure==
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1IYR 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=1IYR OCA].
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1IYR 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=1IYR OCA].
==Reference==
==Reference==
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[[Category: Koshiba, S.]]
[[Category: Koshiba, S.]]
[[Category: Kuroda, Y.]]
[[Category: Kuroda, Y.]]
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[[Category: RSGI, RIKEN.Structural.Genomics/Proteomics.Initiative.]]
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[[Category: RSGI, RIKEN Structural Genomics/Proteomics Initiative.]]
[[Category: Yokoyama, S.]]
[[Category: Yokoyama, S.]]
[[Category: apoptosis]]
[[Category: apoptosis]]
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[[Category: structural genomics]]
[[Category: structural genomics]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 17:36:01 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:17:08 2008''

Revision as of 11:17, 21 February 2008


1iyr

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NMR Structure Ensemble Of Dff-C Domain

Overview

DFF45/ICAD has dual functions in the final stage of apoptosis, by acting as both a folding chaperone and a DNase inhibitor of DFF40/CAD. Here, we present the solution structure of the C-terminal domain of DFF45, which is essential for its chaperone-like activity. The structure of this domain (DFF-C) consists of four alpha helices, which are folded in a novel helix-packing arrangement. The 3D structure reveals a large cluster of negatively charged residues on the molecular surface of DFF-C. This observation suggests that charge complementation plays an important role in the interaction of DFF-C with the positively charged catalytic domain of DFF40, and thus for the chaperone activity of DFF45. The structure of DFF-C also provides a rationale for the loss of the chaperone activity in DFF35, a short isoform of DFF45. Indeed, in DFF35, the amino acid sequence is truncated in the middle of the second alpha helix constituting the structure of DFF-C, and thus both the hydrophobic core and the cluster of negative charges are disrupted.

About this Structure

1IYR is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Solution structure of the DFF-C domain of DFF45/ICAD. A structural basis for the regulation of apoptotic DNA fragmentation., Fukushima K, Kikuchi J, Koshiba S, Kigawa T, Kuroda Y, Yokoyama S, J Mol Biol. 2002 Aug 9;321(2):317-27. PMID:12144788

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