1I17: NMR STRUCTURE OF MOUSE DOPPEL 51-157

Citation:
Abstract
The downstream prion-like protein (doppel, or Dpl) is a paralog of the cellular prion protein, PrP(C). The two proteins have approximately 25% sequence identity, but seem to have distinct physiologic roles. Unlike PrP(C), Dpl does not support prion replication; instead, overexpression of Dpl in the brain seems to cause a completely different neurodegenerative disease. We report the solution structure of a fragment of recombinant mouse Dpl (residues 26-157) containing a globular domain with three helices and a small amount of beta-structure. Overall, the topology of Dpl is very similar to that of PrP(C). Significant differences include a marked kink in one of the helices in Dpl, and a different orientation of the two short beta-strands. Although the two proteins most likely arose through duplication of a single ancestral gene, the relationship is now so distant that only the structures retain similarity; the functions have diversified along with the sequence.
PDB ID: 1I17Download
MMDB ID: 15561
PDB Deposition Date: 2001/1/31
Updated in MMDB: 2007/11
Experimental Method:
solution nmr
Source Organism:
Similar Structures:
Molecular Components in 1I17
Label Count Molecule
Protein (1 molecule)
1
Prion-like Protein(Gene symbol: Prnd)
Molecule annotation
* Click molecule labels to explore molecular sequence information.

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