BAIT

CCDC8

3M3, PPP1R20, p90
coiled-coil domain containing 8
GO Process (3)
GO Function (0)
GO Component (4)
Homo sapiens
PREY

TUBB2A

CDCBM5, TUBB, TUBB2, dJ40E16.7
tubulin, beta 2A class IIa
GO Process (3)
GO Function (0)
GO Component (4)
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

Impaired plasma membrane localization of ubiquitin ligase complex underlies 3-M syndrome development.

Wang P, Yan F, Li Z, Yu Y, Parnell SE, Xiong Y

3-M primordial dwarfism is an inherited disease characterized by severe pre- and postnatal growth retardation and by mutually exclusive mutations in three genes, CUL7, OBSL1, and CCDC8. The mechanism underlying 3-M dwarfism is not clear. We showed here that CCDC8, derived from a retrotransposon Gag protein in placental mammals, exclusively localized on the plasma membrane and was phosphorylated by CK2 ... [more]

J. Clin. Invest. Jul. 25, 2019; 130();4393-4407 [Pubmed: 31343991]

Throughput

  • High Throughput

Curated By

  • BioGRID