3b36: Difference between revisions

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[[Image:3b36.jpg|left|200px]]<br /><applet load="3b36" size="350" color="white" frame="true" align="right" spinBox="true"
[[Image:3b36.jpg|left|200px]]
caption="3b36, resolution 1.50&Aring;" />
 
'''Structure of M26L DJ-1'''<br />
{{Structure
|PDB= 3b36 |SIZE=350|CAPTION= <scene name='initialview01'>3b36</scene>, resolution 1.50&Aring;
|SITE= <scene name='pdbsite=AC1:Cl+Binding+Site+For+Residue+A+190'>AC1</scene>, <scene name='pdbsite=AC2:Edo+Binding+Site+For+Residue+A+191'>AC2</scene>, <scene name='pdbsite=AC3:Edo+Binding+Site+For+Residue+A+192'>AC3</scene>, <scene name='pdbsite=AC4:Edo+Binding+Site+For+Residue+A+193'>AC4</scene>, <scene name='pdbsite=AC5:Edo+Binding+Site+For+Residue+A+194'>AC5</scene>, <scene name='pdbsite=AC6:Edo+Binding+Site+For+Residue+A+195'>AC6</scene>, <scene name='pdbsite=AC7:Edo+Binding+Site+For+Residue+A+196'>AC7</scene>, <scene name='pdbsite=AC8:Edo+Binding+Site+For+Residue+A+197'>AC8</scene> and <scene name='pdbsite=AC9:Edo+Binding+Site+For+Residue+A+198'>AC9</scene>
|LIGAND= <scene name='pdbligand=CL:CHLORIDE+ION'>CL</scene> and <scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene>
|ACTIVITY=
|GENE= PARK7 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
}}
 
'''Structure of M26L DJ-1'''
 


==Overview==
==Overview==
Line 7: Line 16:


==About this Structure==
==About this Structure==
3B36 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with <scene name='pdbligand=CL:'>CL</scene> and <scene name='pdbligand=EDO:'>EDO</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Known structural/functional Sites: <scene name='pdbsite=AC1:Cl+Binding+Site+For+Residue+A+190'>AC1</scene>, <scene name='pdbsite=AC2:Edo+Binding+Site+For+Residue+A+191'>AC2</scene>, <scene name='pdbsite=AC3:Edo+Binding+Site+For+Residue+A+192'>AC3</scene>, <scene name='pdbsite=AC4:Edo+Binding+Site+For+Residue+A+193'>AC4</scene>, <scene name='pdbsite=AC5:Edo+Binding+Site+For+Residue+A+194'>AC5</scene>, <scene name='pdbsite=AC6:Edo+Binding+Site+For+Residue+A+195'>AC6</scene>, <scene name='pdbsite=AC7:Edo+Binding+Site+For+Residue+A+196'>AC7</scene>, <scene name='pdbsite=AC8:Edo+Binding+Site+For+Residue+A+197'>AC8</scene> and <scene name='pdbsite=AC9:Edo+Binding+Site+For+Residue+A+198'>AC9</scene>. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3B36 OCA].  
3B36 is a [[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=3B36 OCA].  


==Reference==
==Reference==
Structural Impact of Three Parkinsonism-Associated Missense Mutations on Human DJ-1(,)., Lakshminarasimhan M, Maldonado MT, Zhou W, Fink AL, Wilson MA, Biochemistry. 2008 Feb 5;47(5):1381-92. Epub 2008 Jan 9. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=18181649 18181649]
Structural Impact of Three Parkinsonism-Associated Missense Mutations on Human DJ-1(,)., Lakshminarasimhan M, Maldonado MT, Zhou W, Fink AL, Wilson MA, Biochemistry. 2008 Feb 5;47(5):1381-92. Epub 2008 Jan 9. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/18181649 18181649]
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: ubl conjugation]]
[[Category: ubl conjugation]]


''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 19:02:59 2008''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 18:55:46 2008''

Revision as of 19:55, 20 March 2008

File:3b36.jpg


PDB ID 3b36

Drag the structure with the mouse to rotate
, resolution 1.50Å
Sites: , , , , , , , and
Ligands: and
Gene: PARK7 (Homo sapiens)
Coordinates: save as pdb, mmCIF, xml



Structure of M26L DJ-1


OverviewOverview

A number of missense mutations in the oxidative stress response protein DJ-1 are implicated in rare forms of familial Parkinsonism. The best-characterized Parkinsonian DJ-1 missense mutation, L166P, disrupts homodimerization and results in a poorly folded protein. The molecular basis by which the other Parkinsonism-associated mutations disrupt the function of DJ-1, however, is incompletely understood. In this study we show that three different Parkinsonism-associated DJ-1 missense mutations (A104T, E163K, and M26I) reduce the thermal stability of DJ-1 in solution by subtly perturbing the structure of DJ-1 without causing major folding defects or loss of dimerization. Atomic resolution X-ray crystallography shows that the A104T substitution introduces water and a discretely disordered residue into the core of the protein, E163K disrupts a key salt bridge with R145, and M26I causes packing defects in the core of the dimer. The deleterious effect of each Parkinsonism-associated mutation on DJ-1 is dissected by analysis of engineered substitutions (M26L, A104V, and E163K/R145E) that partially alleviate each of the defects introduced by the A104T, E163K and M26I mutations. In total, our results suggest that the protective function of DJ-1 can be compromised by diverse perturbations in its structural integrity, particularly near the junctions of secondary structural elements.

About this StructureAbout this Structure

3B36 is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

ReferenceReference

Structural Impact of Three Parkinsonism-Associated Missense Mutations on Human DJ-1(,)., Lakshminarasimhan M, Maldonado MT, Zhou W, Fink AL, Wilson MA, Biochemistry. 2008 Feb 5;47(5):1381-92. Epub 2008 Jan 9. PMID:18181649

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