1t3s

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 1: Line 1:
-
[[Image:1t3s.jpg|left|200px]]<br /><applet load="1t3s" size="350" color="white" frame="true" align="right" spinBox="true"
+
[[Image:1t3s.jpg|left|200px]]
-
caption="1t3s, resolution 2.30&Aring;" />
+
 
-
'''Structural Analysis of the Voltage-Dependent Calcium Channel Beta Subunit Functional Core'''<br />
+
{{Structure
 +
|PDB= 1t3s |SIZE=350|CAPTION= <scene name='initialview01'>1t3s</scene>, resolution 2.30&Aring;
 +
|SITE=
 +
|LIGAND= <scene name='pdbligand=HG:MERCURY (II) ION'>HG</scene>
 +
|ACTIVITY=
 +
|GENE= CACNB2, CACNLB2 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9986 Oryctolagus cuniculus])
 +
}}
 +
 
 +
'''Structural Analysis of the Voltage-Dependent Calcium Channel Beta Subunit Functional Core'''
 +
 
==Overview==
==Overview==
Line 7: Line 16:
==About this Structure==
==About this Structure==
-
1T3S is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Oryctolagus_cuniculus Oryctolagus cuniculus] with <scene name='pdbligand=HG:'>HG</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1T3S OCA].
+
1T3S is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Oryctolagus_cuniculus Oryctolagus cuniculus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1T3S OCA].
==Reference==
==Reference==
-
Mutant huntingtin directly increases susceptibility of mitochondria to the calcium-induced permeability transition and cytochrome c release., Choo YS, Johnson GV, MacDonald M, Detloff PJ, Lesort M, Hum Mol Genet. 2004 Jul 15;13(14):1407-20. Epub 2004 May 26. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=15163634 15163634]
+
Mutant huntingtin directly increases susceptibility of mitochondria to the calcium-induced permeability transition and cytochrome c release., Choo YS, Johnson GV, MacDonald M, Detloff PJ, Lesort M, Hum Mol Genet. 2004 Jul 15;13(14):1407-20. Epub 2004 May 26. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/15163634 15163634]
[[Category: Oryctolagus cuniculus]]
[[Category: Oryctolagus cuniculus]]
[[Category: Single protein]]
[[Category: Single protein]]
Line 21: Line 30:
[[Category: sh3 domain]]
[[Category: sh3 domain]]
-
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:09:40 2008''
+
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 14:13:22 2008''

Revision as of 12:13, 20 March 2008


PDB ID 1t3s

Drag the structure with the mouse to rotate
, resolution 2.30Å
Ligands:
Gene: CACNB2, CACNLB2 (Oryctolagus cuniculus)
Coordinates: save as pdb, mmCIF, xml



Structural Analysis of the Voltage-Dependent Calcium Channel Beta Subunit Functional Core


Overview

Huntington's disease (HD) is initiated by an abnormally expanded polyglutamine stretch in the huntingtin protein, conferring a novel property on the protein that leads to the loss of striatal neurons. Defects in mitochondrial function have been implicated in the pathogenesis of HD. Here, we have examined the hypothesis that the mutant huntingtin protein may directly interact with the mitochondrion and affect its function. In human neuroblastoma cells and clonal striatal cells established from HdhQ7 (wild-type) and HdhQ111 (mutant) homozygote mouse knock-in embryos, huntingtin was present in a purified mitochondrial fraction. Subfractionation of the mitochondria and limited trypsin digestion of the organelle demonstrated that huntingtin was associated with the outer mitochondrial membrane. We further demonstrated that a recombinant truncated mutant huntingtin protein, but not a wild-type, directly induced mitochondrial permeability transition (MPT) pore opening in isolated mouse liver mitochondria, an effect that was prevented completely by cyclosporin A (CSA) and ATP. Importantly, the mutant huntingtin protein significantly decreased the Ca2+ threshold necessary to trigger MPT pore opening. We found a similar increased susceptibility to the calcium-induced MPT in liver mitochondria isolated from a knock-in HD mouse model. The mutant huntingtin protein-induced MPT pore opening was accompanied by a significant release of cytochrome c, an effect completely inhibited by CSA. These findings suggest that the development of specific MPT inhibitors may be an interesting therapeutic avenue to delay the onset of HD.

About this Structure

1T3S is a Single protein structure of sequence from Oryctolagus cuniculus. Full crystallographic information is available from OCA.

Reference

Mutant huntingtin directly increases susceptibility of mitochondria to the calcium-induced permeability transition and cytochrome c release., Choo YS, Johnson GV, MacDonald M, Detloff PJ, Lesort M, Hum Mol Genet. 2004 Jul 15;13(14):1407-20. Epub 2004 May 26. PMID:15163634

Page seeded by OCA on Thu Mar 20 14:13:22 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools