BAIT

KEU

F5O11.8, F5O11_8, keule, AT1G12360
SNARE-interacting protein KEULE
GO Process (1)
GO Function (2)
GO Component (4)

Gene Ontology Biological Process

Gene Ontology Molecular Function

Arabidopsis thaliana (Columbia)
PREY

SNAP33

ATSNAP33, ATSNAP33B, MAF19.2, MAF19_2, SNP33, soluble N-ethylmaleimide-sensitive factor adaptor protein 33, AT5G61210
soluble N-ethylmaleimide-sensitive factor adaptor protein 33
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

Binding of SEC11 Indicates Its Role in SNARE Recycling after Vesicle Fusion and Identifies Two Pathways for Vesicular Traffic to the Plasma Membrane.

Karnik R, Zhang B, Waghmare S, Aderhold C, Grefen C, Blatt MR

SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein receptor) proteins drive vesicle fusion in all eukaryotes and contribute to homeostasis, pathogen defense, cell expansion, and growth in plants. Two homologous SNAREs, SYP121 (=SYR1/PEN1) and SYP122, dominate secretory traffic to the Arabidopsis thaliana plasma membrane. Although these proteins overlap functionally, differences between SYP121 and SYP122 have surfaced, suggesting that they mark two discrete ... [more]

Plant Cell Mar. 01, 2015; 27(3);675-94 [Pubmed: 25747882]

Throughput

  • Low Throughput

Curated By

  • BioGRID