We have a suspicion that you are an automated web bot software, not a real user. To keep our site fast for other users, we have slowed down this page. The slowdown will gradually disappear. If you think this is a mistake, please contact us at genome-www@soe.ucsc.edu. Also note that all data for hgGeneGraph can be obtained through our public MySQL server and all our software source code is available and can be installed locally onto your own computer. If you are unsure how to use these resources, do not hesitate to contact us.
UCSC Genome Browser Gene Interaction Graph
Gene interactions and pathways from curated databases and text-mining

◀ Back to PXN

CRK — PXN

Pathways - manually collected, often from reviews:

Protein-Protein interactions - manually collected from original source literature:

Studies that report less than 10 interactions are marked with *

Text-mined interactions from Literome

Furundzija et al., Biochem Biophys Res Commun 2010 (Atherosclerosis) : Pharmacological blocking experiments with specific inhibitors of Akt, PKC and p38 MAP-kinase revealed that IGF-1 dependent activation of focal adhesion kinase ( FAK ) and paxillin , and consecutively IGF-1 facilitated migration, required IGF-1/IGF-1R mediated PI3-kinase/PKC/p38 dependent integrin inside-out signaling
Sabe et al., J Biol Chem 1995 (Cell Transformation, Viral) : In this study, we detected co-immunoprecipitation of tyrosine phosphorylated paxillin with v-Crk in CT10 transformed chicken embryo fibroblasts ( CEF ), and demonstrated that v-Crk binding to paxillin can inhibit Csk binding to paxillin ... We therefore suggest that the competitive binding of overexpressed v-Crk affects an efficient interaction of Csk with tyrosine phosphorylated paxillin in CT10 transformed CEF