Allosteric regulation of E-cadherin adhesion

Journal of Biological Chemistry

Volumn 290, Issue 35, 2015, Pages 21749-21761

  Shashikanth, Nitesh ^a   Petrova, Yuliya I ^d   Park, Seongjin ^b   Chekan, Jillian ^c   Maiden, Stephanie ^d   Spano, Martha ^a   Ha, Taekjip ^a,b,e   Gumbiner, Barry M ^d,f   Leckband, Deborah E ^a,b,c  

^a UNIVERSITY OF ILLINOIS AT URBANA CHAMPAIGN   (United States)

^b United States of America   (United States)

^c UNIVERSITY OF ILLINOIS AT URBANA CHAMPAIGN   (United States)

^d UNIVERSITY OF VIRGINIA   (United States)

^e HOWARD HUGHES MEDICAL INSTITUTE   (United States)

^f UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADHESION; BINDING ENERGY; CELL ADHESION; CELL MEMBRANES; TISSUE;

ADHESION PROTEINS; ALLOSTERIC REGULATION; BINDING AFFINITIES; CYTOPLASMIC BINDING; DEPHOSPHORYLATIONS; HOMOPHILIC BINDING; INTERCELLULAR ADHESION; TISSUE REMODELING;

GLYCOPROTEINS;

CELL SURFACE PROTEIN; PROTEIN ANTIBODY; PROTEIN P120; UVOMORULIN; CADHERIN; CATENIN; DELTA CATENIN; LITHIUM CHLORIDE; MUTANT PROTEIN; NEUTRALIZING ANTIBODY; PROTEIN BINDING; STAUROSPORINE;

ALLOSTERISM; ANIMAL CELL; ARTICLE; BINDING AFFINITY; BINDING SITE; CELL AGGREGATION; CELL LINE; COLO 205 CELL; CONTROLLED STUDY; CYTOPLASM; KINETICS; NONHUMAN; PRIORITY JOURNAL; PROTEIN AGGREGATION; PROTEIN BINDING; PROTEIN DEPHOSPHORYLATION; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN PROTEIN INTERACTION; QUANTITATIVE ANALYSIS; REGULATORY MECHANISM; ANIMAL; BIOLOGICAL MODEL; CELL ADHESION; DOG; DRUG EFFECTS; HUMAN; MCF 7 CELL LINE; METABOLISM; MOUSE; PHOSPHORYLATION; PROTEIN MULTIMERIZATION; RAT; THREE DIMENSIONAL IMAGING;

ALLOSTERIC REGULATION; ANIMALS; ANTIBODIES, NEUTRALIZING; CADHERINS; CATENINS; CELL ADHESION; DOGS; HUMANS; IMAGING, THREE-DIMENSIONAL; KINETICS; LITHIUM CHLORIDE; MCF-7 CELLS; MICE; MODELS, BIOLOGICAL; MUTANT PROTEINS; PHOSPHORYLATION; PROTEIN BINDING; PROTEIN MULTIMERIZATION; RATS; STAUROSPORINE;

EID: 84940513064     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M115.657098     Document Type: Article

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