BAIT

HTT

AI256365, C430023I11Rik, Hd, Hdh, IT15
huntingtin
GO Process (57)
GO Function (10)
GO Component (21)

Gene Ontology Biological Process

Mus musculus
PREY

NEGR1

DMML2433, IGLON4, KILON, Ntra, UNQ2433
neuronal growth regulator 1
GO Process (2)
GO Function (1)
GO Component (6)
Homo sapiens

Affinity Capture-MS

An interaction is inferred when a bait protein is affinity captured from cell extracts by either polyclonal antibody or epitope tag and the associated interaction partner is identified by mass spectrometric methods.

Publication

Huntingtin interacting proteins are genetic modifiers of neurodegeneration.

Kaltenbach LS, Romero E, Becklin RR, Chettier R, Bell R, Phansalkar A, Strand A, Torcassi C, Savage J, Hurlburt A, Cha GH, Ukani L, Chepanoske CL, Zhen Y, Sahasrabudhe S, Olson J, Kurschner C, Ellerby LM, Peltier JM, Botas J, Hughes RE

Huntington's disease (HD) is a fatal neurodegenerative condition caused by expansion of the polyglutamine tract in the huntingtin (Htt) protein. Neuronal toxicity in HD is thought to be, at least in part, a consequence of protein interactions involving mutant Htt. We therefore hypothesized that genetic modifiers of HD neurodegeneration should be enriched among Htt protein interactors. To test this idea, ... [more]

PLoS Genet. May. 11, 2007; 3(5);e82 [Pubmed: 17500595]

Throughput

  • High Throughput

Curated By

  • BioGRID