BAIT

CAX1

ATCAX1, F16M14.10, F16M14_10, HIGH AFFINITY CALCIUM ANTIPORTER CAX1, RARE COLD INDUCIBLE 4, RCI4, cation exchanger 1, AT2G38170
vacuolar cation/proton exchanger 1
Arabidopsis thaliana (Columbia)
PREY

CAX3

ATCAX3, ATHCX1, CALCIUM/PROTON EXCHANGER CAX1-LIKE PROTEIN, CAX1-LIKE, cation exchanger 3, AT3G51860
vacuolar cation/proton exchanger 3
Arabidopsis thaliana (Columbia)

Co-fractionation

Interaction inferred from the presence of two or more protein subunits in a partially purified protein preparation. If co-fractionation is demonstrated between 3 or more proteins, then add them as a complex.

Publication

Functional studies of split Arabidopsis Ca2+/H+ exchangers.

Zhao J, Connorton JM, Guo Y, Li X, Shigaki T, Hirschi KD, Pittman JK

In plants, high capacity tonoplast cation/H(+) antiport is mediated in part by a family of cation exchanger (CAX) transporters. Functional association between CAX1 and CAX3 has previously been shown. In this study we further examine the interactions between CAX protein domains through the use of nonfunctional halves of CAX transporters. We demonstrate that a protein coding for an N-terminal half ... [more]

J. Biol. Chem. Dec. 04, 2009; 284(49);34075-83 [Pubmed: 19819871]

Throughput

  • Low Throughput

Related interactions

InteractionExperimental Evidence CodeDatasetThroughputScoreCurated ByNotes
CAX1 CAX3
Affinity Capture-Western
Affinity Capture-Western

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 identified by Western blot with a specific polyclonal antibody or second epitope tag. This category is also used if an interacting protein is visualized directly by dye stain or radioactivity. Note that this differs from any co-purification experiment involving affinity capture in that the co-purification experiment involves at least one extra purification step to get rid of potential contaminating proteins.

Low-BioGRID
-
CAX1 CAX3
PCA
PCA

A Protein-Fragment Complementation Assay (PCA) is a protein-protein interaction assay in which a bait protein is expressed as fusion to one of the either N- or C- terminal peptide fragments of a reporter protein and prey protein is expressed as fusion to the complementary N- or C- terminal fragment of the same reporter protein. Interaction of bait and prey proteins bring together complementary fragments, which can then fold into an active reporter, e.g. the split-ubiquitin assay.

Low-BioGRID
431886
CAX1 CAX3
PCA
PCA

A Protein-Fragment Complementation Assay (PCA) is a protein-protein interaction assay in which a bait protein is expressed as fusion to one of the either N- or C- terminal peptide fragments of a reporter protein and prey protein is expressed as fusion to the complementary N- or C- terminal fragment of the same reporter protein. Interaction of bait and prey proteins bring together complementary fragments, which can then fold into an active reporter, e.g. the split-ubiquitin assay.

Low-BioGRID
430582

Curated By

  • BioGRID