Structural basis of the autophagy-related LC3/Atg13 LIR complex: Recognition and interaction mechanism

Structure

Volumn 22, Issue 1, 2014, Pages 47-58

  Suzuki, Hironori ^a,b   Tabata, Keisuke ^c,d   Morita, Eiji ^c   Kawasaki, Masato ^b   Kato, Ryuichi ^b   Dobson, Renwick C J ^a,e   Yoshimori, Tamotsu ^d,f   Wakatsuki, Soichi ^b,g,h  

^a UNIVERSITY OF CANTERBURY   (New Zealand)

^b INSTITUTE OF MATERIALS STRUCTURE SCIENCE   (Japan)

^c OSAKA UNIVERSITY   (Japan)

^d OSAKA UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^e UNIVERSITY OF MELBOURNE   (Australia)

^f OSAKA UNIVERSITY   (Japan)

^g SLAC NATIONAL ACCELERATOR LABORATORY   (United States)

^h STANFORD UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOPHAGY PROTEIN 13; LYSINE; MICROTUBULE ASSOCIATE PROTEIN 1 LIGHT CHAIN 3; PROTEIN; UNCLASSIFIED DRUG; LIGHT CHAIN 3 PROTEIN; LIGHT CHAIN 3A PROTEIN; LIGHT CHAIN 3B PROTEIN; LIGHT CHAIN 3C PROTEIN; MICROTUBULE ASSOCIATED PROTEIN 1;

AMINO ACID SEQUENCE; ANIMAL CELL; ARTICLE; AUTOPHAGOSOME; AUTOPHAGY; BINDING AFFINITY; CONTROLLED STUDY; CRYSTAL STRUCTURE; DISSOCIATION CONSTANT; EMBRYO; GENE REARRANGEMENT; HUMAN; HUMAN CELL; MASS SPECTROMETRY; MOUSE; NONHUMAN; POINT MUTATION; POLYACRYLAMIDE GEL ELECTROPHORESIS; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN BINDING; PROTEIN FUNCTION; PROTEIN PROTEIN INTERACTION; PROTEIN STRUCTURE; SEQUENCE ALIGNMENT; SURFACE PLASMON RESONANCE; WESTERN BLOTTING; X RAY CRYSTALLOGRAPHY; AUTOPHAGY RELATED GENE 13; CELL CULTURE; CHEMICAL STRUCTURE; GENE; MACROMOLECULE; MUTATION;

PYRONIA TITHONUS;

ADAPTOR PROTEINS, SIGNAL TRANSDUCING; AMINO ACID SEQUENCE; ANIMALS; AUTOPHAGY; BINDING SITES; CRYSTALLOGRAPHY, X-RAY; ESCHERICHIA COLI; FIBROBLASTS; GENE EXPRESSION REGULATION; HEK293 CELLS; HUMANS; LYSINE; MICE; MICROTUBULE-ASSOCIATED PROTEINS; MODELS, MOLECULAR; MOLECULAR SEQUENCE DATA; MUTATION; PHAGOSOMES; PROTEIN BINDING; PROTEIN INTERACTION DOMAINS AND MOTIFS; PROTEIN ISOFORMS; RECOMBINANT PROTEINS;

EID: 84891841002     PISSN: 09692126     EISSN: 18784186     Source Type: Journal    
DOI: 10.1016/j.str.2013.09.023     Document Type: Article

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