Doppel: Difference between revisions

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Doppel (Dpl), named for '''''do'''wnstream '''p'''rion '''p'''rotein like''<ref>1</ref>, is a homolog of the [[prion protein]] (PrP). It is a cell surface glycoprotein.
Doppel (Dpl), named for '''''do'''wnstream '''p'''rion '''p'''rotein-like''<ref>Moore, R ''et al.'' (1999) Ataxia in Prion Protein (PrP)-deficient mice is associated with upregulation of the novel PrP-like protein Doppel ''J. Mol. Biol.'' '''292''', 797-817</ref>, is a homolog of the [[prion protein]] (PrP). It is a cell surface glycoprotein.


==Structure of Dpl==
==Structure of Dpl==


{{STRUCTURE_1lg4 |  PDB=1lg4  |  SCENE=  }}
{{STRUCTURE_1lg4 |  PDB=1lg4  |  SCENE=  }}
Dpl has the same fold as PrP, with three alpha helices and two short beta strands, however it differs in that the third helix has a significant kink in it and it also contains two disulphide bonds.
Dpl has the same fold as PrP, with three alpha helices and two short beta strands<ref>Mo H ''et al.'' (2001) ''Proc. Natl. Acad. Sci. USA'' '''98''',2352-7</ref>.  however it differs in that the third helix has a significant kink in it and it also contains two disulphide bonds.
 
The structure mutant PrP with the additional disulphide bond was also determoned <ref>Zahn R ''et al.'' (2003) NMR structure of a variant human prion protein with two disulfide bridges '' J. Mol. Biol.'' '''326''', 225-34.
 


=Related structures=
=Related structures=
Line 14: Line 17:


=References=
=References=
  {{Reflist}} 
  </reference>
Moore ''et al.'' (1999) Ataxia in Prion Protein (PrP)-deficient Mice is
Associated with Upregulation of the Novel PrP-like
Protein Doppel ''J. Mol. Biol.'' '''292''', 797-817 </reference>
Zahn R. et al. (2003) NMR structure of a variant human prion protein with two disulfide bridges'' J. Mol. Biol.'' '''326''', 225-34.

Revision as of 09:18, 15 December 2008

Doppel (Dpl), named for downstream prion protein-like[1], is a homolog of the prion protein (PrP). It is a cell surface glycoprotein.

Structure of Dpl

Drag the structure with the mouse to rotate
1lg4, 20 NMR models (default scene)
Gene: Prnd (Homo sapiens)
Related: 1i17
Resources: FirstGlance, OCA, RCSB, PDBsum
Coordinates: save as pdb, mmCIF, xml


Dpl has the same fold as PrP, with three alpha helices and two short beta strands[2]. however it differs in that the third helix has a significant kink in it and it also contains two disulphide bonds.

The structure mutant PrP with the additional disulphide bond was also determoned <ref>Zahn R et al. (2003) NMR structure of a variant human prion protein with two disulfide bridges J. Mol. Biol. 326, 225-34.


Related structures

  • 1z65 Mouse Dpl residues 1-30
  • 1lg4 Human Dpl residues 24-152
  • 1i17 Mouse Dpl residues 51-157
  • 1h0l Human PrP residues 121-230, with an additional disulphide bond analogous to the homolog Doppel


References

</reference>
  1. Moore, R et al. (1999) Ataxia in Prion Protein (PrP)-deficient mice is associated with upregulation of the novel PrP-like protein Doppel J. Mol. Biol. 292, 797-817
  2. Mo H et al. (2001) Proc. Natl. Acad. Sci. USA 98,2352-7

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