GW domains of the Listeria monocytogenes invasion protein InlB are SH3-like and mediate binding to host ligands

EMBO Journal

Volumn 21, Issue 21, 2002, Pages 5623-5634

  Marino, Michael ^a   Banerjee, Manidipa ^a   Jonquières, Renaud ^a   Cossart, Pascale ^a   Ghosh, Partho ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Cell invasion; GC1q R; GW domain; Internalin; SH3 domain

Indexed keywords

BACTERIAL PROTEIN; GLYCOSAMINOGLYCAN; LEUCINE; LIGAND; METHIONINE; PROLINE; PROTEIN INLB; PROTEIN TYROSINE KINASE; UNCLASSIFIED DRUG;

ARTICLE; BACTERIUM ADHERENCE; BINDING SITE; CELL INVASION; ENZYME ACTIVATION; LISTERIA MONOCYTOGENES; MOLECULAR CLONING; NONHUMAN; NUCLEOTIDE SEQUENCE; PHAGOCYTOSIS; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN DEGRADATION; PROTEIN DOMAIN; PROTEIN PURIFICATION; PROTEIN STRUCTURE;

AMINO ACID SEQUENCE; BACTERIAL PROTEINS; LISTERIA MONOCYTOGENES; MEMBRANE PROTEINS; MODELS, MOLECULAR; MOLECULAR SEQUENCE DATA; PROTEIN CONFORMATION; SEQUENCE HOMOLOGY, AMINO ACID; SRC HOMOLOGY DOMAINS;

BACTERIA (MICROORGANISMS); LISTERIA MONOCYTOGENES; MAMMALIA; POSIBACTERIA;

EID: 0036845352     PISSN: 02614189     EISSN: None     Source Type: Journal    
DOI: 10.1093/emboj/cdf558     Document Type: Article

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