SLK-mediated phosphorylation of paxillin is required for focal adhesion turnover and cell migration

Oncogene

Volumn 32, Issue 39, 2013, Pages 4656-4663

  Quizi, J L ^a,b   Baron, K ^a,b   Al Zahrani, K N ^a,b   O'Reilly, P ^a   Sriram, R K ^a,b   Conway, J ^b   Laurin, A A ^b   Sabourin, L A ^a,b  

^a UNIVERSITY OF OTTAWA   (Canada)

^b OTTAWA HOSPITAL RESEARCH INSTITUTE   (Canada)

Author keywords

kinase; migration; paxillin; phosphorylation; Ste20

Indexed keywords

PAXILLIN; PHOSPHOTRANSFERASE; SERINE; STE20 LIKE KINASE; UNCLASSIFIED DRUG;

ARTICLE; CELL MIGRATION; CELL MOTILITY; CELLULAR PARAMETERS; CONTROLLED STUDY; FOCAL ADHESION; FOCAL ADHESION TURNOVER; GENE MUTATION; HUMAN; HUMAN CELL; IN VITRO STUDY; IN VIVO STUDY; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN FUNCTION; PROTEIN LOCALIZATION; PROTEIN PHOSPHORYLATION;

3T3 CELLS; AMINO ACID SEQUENCE; ANIMALS; CELL MOVEMENT; FOCAL ADHESIONS; HUMANS; MICE; MOLECULAR SEQUENCE DATA; MUTAGENESIS, SITE-DIRECTED; PAXILLIN; PHOSPHORYLATION; PHOSPHOSERINE; PROTEIN PROCESSING, POST-TRANSLATIONAL; PROTEIN STRUCTURE, TERTIARY; PROTEIN-SERINE-THREONINE KINASES; RECOMBINANT FUSION PROTEINS; SEQUENCE DELETION; SUBSTRATE SPECIFICITY;

EID: 84884902823     PISSN: 09509232     EISSN: 14765594     Source Type: Journal    
DOI: 10.1038/onc.2012.488     Document Type: Article

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