BAIT

SMU2

SUPPRESSORS OF MEC-8 AND UNC-52 2, T9J22.13, T9J22_13, AT2G26460
RNA splicing protein SMU2
GO Process (1)
GO Function (0)
GO Component (1)

Gene Ontology Biological Process

Gene Ontology Cellular Component

Arabidopsis thaliana (Columbia)
PREY

SMU1

F25P22.14, F25P22_14, SUPPRESSORS OF MEC-8 AND UNC-52 1, AT1G73720
RNA splicing protein SMU1
GO Process (1)
GO Function (1)
GO Component (2)

Gene Ontology Biological Process

Gene Ontology Molecular Function

Gene Ontology Cellular Component

Arabidopsis thaliana (Columbia)

Reconstituted Complex

An interaction is inferred between proteins in vitro. This can include proteins in recombinant form or proteins isolated directly from cells with recombinant or purified bait. For example, GST pull-down assays where a GST-tagged protein is first isolated and then used to fish interactors from cell lysates are considered reconstituted complexes (e.g. PUBMED: 14657240, Fig. 4A or PUBMED: 14761940, Fig. 5). This can also include gel-shifts, surface plasmon resonance, isothermal titration calorimetry (ITC) and bio-layer interferometry (BLI) experiments. The bait-hit directionality may not be clear for 2 interacting proteins. In these cases the directionality is up to the discretion of the curator.

Publication

Plant SMU-1 and SMU-2 homologues regulate pre-mRNA splicing and multiple aspects of development.

Chung T, Wang D, Kim CS, Yadegari R, Larkins BA

In eukaryotes, alternative splicing of pre-mRNAs contributes significantly to the proper expression of the genome. However, the functions of many auxiliary spliceosomal proteins are still unknown. Here, we functionally characterized plant homologues of nematode suppressors of mec-8 and unc-52 (smu). We compared transcript profiles of maize (Zea mays) smu2 endosperm with those of wild-type plants and identified pre-mRNA splicing events ... [more]

Plant Physiol. Nov. 01, 2009; 151(3);1498-512 [Pubmed: 19734266]

Throughput

  • Low Throughput

Curated By

  • BioGRID