2jvy

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[[Image:2jvy.jpg|left|200px]]
[[Image:2jvy.jpg|left|200px]]
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{{Structure
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|PDB= 2jvy |SIZE=350|CAPTION= <scene name='initialview01'>2jvy</scene>
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The line below this paragraph, containing "STRUCTURE_2jvy", creates the "Structure Box" on the page.
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|SITE= <scene name='pdbsite=AC1:Zn+Binding+Site+For+Residue+A+29'>AC1</scene>
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You may change the PDB parameter (which sets the PDB file loaded into the applet)
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|LIGAND= <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene>
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or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
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|ACTIVITY=
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|GENE=
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{{STRUCTURE_2jvy| PDB=2jvy | SCENE= }}
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|RELATEDENTRY=[[2jvx|2JVX]]
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2jvy FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2jvy OCA], [http://www.ebi.ac.uk/pdbsum/2jvy PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2jvy RCSB]</span>
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}}
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'''Solution Structure of the EDA-ID-related C417F mutant of human NEMO zinc finger'''
'''Solution Structure of the EDA-ID-related C417F mutant of human NEMO zinc finger'''
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==About this Structure==
==About this Structure==
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2JVY is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/ ]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2JVY OCA].
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2JVY is a [[Single protein]] structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2JVY OCA].
==Reference==
==Reference==
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[[Category: Veron, M.]]
[[Category: Veron, M.]]
[[Category: Vinolo, E.]]
[[Category: Vinolo, E.]]
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[[Category: beta-beta-alpha fold]]
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[[Category: Beta-beta-alpha fold]]
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[[Category: cchc classical zinc finger]]
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[[Category: Cchc classical zinc finger]]
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[[Category: cchf mutant zinc finger]]
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[[Category: Cchf mutant zinc finger]]
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[[Category: coiled coil]]
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[[Category: Coiled coil]]
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[[Category: cytoplasm]]
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[[Category: Cytoplasm]]
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[[Category: disease mutation]]
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[[Category: Disease mutation]]
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[[Category: ectodermal dysplasia]]
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[[Category: Ectodermal dysplasia]]
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[[Category: eda-id c417f mutant of nemo zinc finger]]
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[[Category: Eda-id c417f mutant of nemo zinc finger]]
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[[Category: host-virus interaction]]
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[[Category: Host-virus interaction]]
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[[Category: metal binding protein]]
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[[Category: Metal binding protein]]
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[[Category: nucleus]]
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[[Category: Nucleus]]
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[[Category: transcription]]
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[[Category: Transcription]]
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[[Category: transcription regulation]]
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[[Category: Transcription regulation]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Apr 9 14:39:49 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 04:02:09 2008''
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Revision as of 11:39, 9 April 2008

Template:STRUCTURE 2jvy

Solution Structure of the EDA-ID-related C417F mutant of human NEMO zinc finger


Overview

The regulatory NEMO (NF-kappaB essential modulator) protein has a crucial role in the canonical NF-kappaB signaling pathway notably involved in immune and inflammatory responses, apoptosis and oncogenesis. The regulatory domain is located in the C-terminal half of NEMO and contains a classical CCHC-type zinc finger (ZF). We have investigated the structural and functional effects of a cysteine to phenylalanine point mutation (C417F) in the ZF motif, identified in patients with anhidrotic ectodermal dysplasia with immunodeficiency. The solution structures of the wild type and mutant ZF were determined by NMR. Remarkably, the mutant adopts a global betabetaalpha fold similar to that of the wild type and retains thermodynamic stability, i.e., the ability to bind zinc with a native-like affinity, although the last zinc-chelating residue is missing. However, the mutation induces enhanced dynamics in the motif and leads to an important loss of stability. A detailed analysis of the wild type solution structure and experimental evidences led to the identification of two possible protein-binding surfaces that are largely destabilized in the mutant. This is sufficient to alter NEMO function, since functional complementation assays using NEMO-deficient pre-B and T lymphocytes show that full-length C417F pathogenic NEMO leads to a partial to strong defect in LPS, IL-1beta and TNF-alpha-induced NF-kappaB activation, respectively, as compared to wild type NEMO. Altogether, these results shed light onto the role of NEMO ZF as a protein-binding motif and show that a precise structural integrity of the ZF should be preserved to lead to a functional protein-recognition motif triggering full NF-kappaB activation.

About this Structure

2JVY is a Single protein structure. Full crystallographic information is available from OCA.

Reference

Solution Structure of NEMO Zinc Finger and Impact of an Anhidrotic Ectodermal Dysplasia with Immunodeficiency-related Point Mutation., Cordier F, Vinolo E, Veron M, Delepierre M, Agou F, J Mol Biol. 2008 Jan 30;. PMID:18313693 Page seeded by OCA on Wed Apr 9 14:39:49 2008

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