Integrins α1β1 and α2β1 are receptors for the rotavirus enterotoxin

Proceedings of the National Academy of Sciences of the United States of America

Volumn 105, Issue 26, 2008, Pages 8811-8818

  Seo, Neung Seon ^a   Zeng, Carl Q Y ^b   Hyser, Joseph M ^b   Utama, Budi ^b   Crawford, Sue E ^b   Kim, Kate J ^a   Höök, Magnus ^a   Estes, Mary K ^b  

^a TEXAS A AND M HEALTH SCIENCE CENTER   (United States)

^b BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

Diarrhea; Domain; NSP4; Signaling

Indexed keywords

ALPHA2 INTEGRIN; AMINO ACID; COLLAGEN TYPE 1; EDETIC ACID; ENTEROTOXIN; INTEGRIN RECEPTOR; LIGAND; MANGANESE; METAL ION; ROTAVIRUS NONSTRUCTURAL PROTEIN 4; VERY LATE ACTIVATION ANTIGEN 1; VERY LATE ACTIVATION ANTIGEN 2; 1 (6 ((3 METHOXYESTRA 1,3,5(10) TRIEN 17 YL)AMINO)HEXYL) 1H PYRROLE 2,5 DIONE; 1-(6-((3-METHOXYESTRA-1,3,5(10)-TRIEN-17-YL)AMINO)HEXYL)-1H-PYRROLE-2,5-DIONE; 2 PYRROLIDONE DERIVATIVE; ANDROSTANE DERIVATIVE; ESTRANE DERIVATIVE; GLYCOPROTEIN; NS28 PROTEIN, ROTAVIRUS; TOXIN; VIRUS PROTEIN; WORTMANNIN;

ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; CELL STRAIN CACO 2; CONTROLLED STUDY; DIARRHEA; LIGAND BINDING; MOUSE; MYOBLAST; NEWBORN; NONHUMAN; PATHOGENESIS; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN INTERACTION; PROTEIN LOCALIZATION; PROTEIN MOTIF; RECEPTOR BINDING; ROTAVIRUS; SIGNAL TRANSDUCTION; VIRUS VIRULENCE; ANIMAL; BINDING SITE; CELL ADHESION; CELL LINE; CELL MOTION; CHEMICALLY INDUCED DISORDER; CHEMISTRY; DRUG EFFECT; ENZYME LINKED IMMUNOSORBENT ASSAY; HUMAN; METABOLISM; PROTEIN BINDING; PROTEIN TERTIARY STRUCTURE; PROTEIN TRANSPORT; SURFACE PLASMON RESONANCE;

MUS; ROTAVIRUS;

ANDROSTADIENES; ANIMALS; BINDING SITES; CELL ADHESION; CELL LINE; CELL MOVEMENT; DIARRHEA; ENTEROTOXINS; ENZYME-LINKED IMMUNOSORBENT ASSAY; ESTRENES; GLYCOPROTEINS; HUMANS; INTEGRIN ALPHA1BETA1; INTEGRIN ALPHA2BETA1; MICE; PROTEIN BINDING; PROTEIN STRUCTURE, TERTIARY; PROTEIN TRANSPORT; PYRROLIDINONES; ROTAVIRUS; SIGNAL TRANSDUCTION; SURFACE PLASMON RESONANCE; TOXINS, BIOLOGICAL; VIRAL NONSTRUCTURAL PROTEINS;

EID: 48249150347     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.0803934105     Document Type: Article

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