BAIT

ELAVL4

HUD, PNEM
ELAV like neuron-specific RNA binding protein 4
GO Process (2)
GO Function (3)
GO Component (0)

Gene Ontology Biological Process

Gene Ontology Molecular Function

Homo sapiens
PREY

SMN1

AI849087, Gemin1, Smn, RP23-333E24.4
survival motor neuron 1
Mus musculus

FRET

An interaction is inferred when close proximity of interaction partners is detected by fluorescence resonance energy transfer between pairs of fluorophore-labeled molecules, such as occurs between CFP (donor) and YFP (acceptor) fusion proteins.

Publication

Dynamics of survival of motor neuron (SMN) protein interaction with the mRNA-binding protein IMP1 facilitates its trafficking into motor neuron axons.

Fallini C, Rouanet JP, Donlin-Asp PG, Guo P, Zhang H, Singer RH, Rossoll W, Bassell GJ

Spinal muscular atrophy (SMA) is a lethal neurodegenerative disease specifically affecting spinal motor neurons. SMA is caused by the homozygous deletion or mutation of the survival of motor neuron 1 (SMN1) gene. The SMN protein plays an essential role in the assembly of spliceosomal ribonucleoproteins. However, it is still unclear how low levels of the ubiquitously expressed SMN protein lead ... [more]

Dev Neurobiol Mar. 01, 2014; 74(3);319-332 [Pubmed: 23897586]

Throughput

  • Low Throughput

Additional Notes

  • Bimolecular Fluorescence Complementation. Species of bait is unclear

Curated By

  • BioGRID