BAIT

SMN1

BCD541, GEMIN1, SMA, SMA1, SMA2, SMA3, SMA4, SMA@, SMN, SMNT, T-BCD541, TDRD16A
survival of motor neuron 1, telomeric
Homo sapiens
PREY

KIAA1841

KIAA1841
GO Process (0)
GO Function (0)
GO Component (0)
Homo sapiens

Proximity Label-MS

An interaction is inferred when a bait-enzyme fusion protein selectively modifies a vicinal protein with a diffusible reactive product, followed by affinity capture of the modified protein and identification by mass spectrometric methods.

Publication

SMA-linked SMN mutants prevent phase separation properties and SMN interactions with FMRP family members.

Binda O, Juillard F, Ducassou JN, Kleijwegt C, Paris G, Didillon A, Baklouti F, Corpet A, Coute Y, Cote J, Lomonte P

Although recent advances in gene therapy provide hope for spinal muscular atrophy (SMA) patients, the pathology remains the leading genetic cause of infant mortality. SMA is a monogenic pathology that originates from the loss of the SMN1 gene in most cases or mutations in rare cases. Interestingly, several SMN1 mutations occur within the TUDOR methylarginine reader domain of SMN. We ... [more]

Life Sci Alliance Jan. 01, 2023; 6(1); [Pubmed: 36375840]

Throughput

  • High Throughput

Additional Notes

  • BioID
  • FDR less than 1%
  • Fold change greater or equal to 1.5 and P less than or equal to 0.0025
  • Proteins significantly enriched in BirA-SMN-Y109C eluates compared to BirA eluates

Curated By

  • BioGRID