The FAP motif within human ATG7, an autophagy-related E1-like enzyme, is essential for the E2-substrate reaction of LC3 lipidation

Autophagy

Volumn 8, Issue 1, 2012, Pages 88-97

  Tanida, Isei ^a,b   Yamasaki, Manabu ^b,c   Komatsu, Masaaki ^d   Ueno, Takashi ^b  

^a NATIONAL INSTITUTE OF INFECTIOUS DISEASES   (Japan)

^b JUNTENDO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^c Microbial Chemistry Research Foundation   (Japan)

^d TOKYO METROPOLITAN INSTITUTE OF MEDICAL SCIENCE   (Japan)

Author keywords

ATG12; ATG7; Autophagosomes; Autophagy; LC3; Lipidation; Modifier; Ubiquitylation like reaction

Indexed keywords

ALANINE; ASPARTIC ACID; ATG12 PROTEIN; ATG3 PROTEIN; ATG7 PROTEIN; MICROTUBULE ASSOCIATED PROTEIN 1 LIGHT CHAIN 3; PHENYLALANINE; PROLINE; PROTEIN; UNCLASSIFIED DRUG;

AMINO ACID SEQUENCE; AMINO TERMINAL SEQUENCE; ARTICLE; CONJUGATION; FAP MOTIF; GENE OVEREXPRESSION; HUMAN; IMMUNOPRECIPITATION; MUTATIONAL ANALYSIS; PROTEIN EXPRESSION; PROTEIN INTERACTION; PROTEIN MOTIF;

EID: 84856487167     PISSN: 15548627     EISSN: 15548635     Source Type: Journal    
DOI: 10.4161/auto.8.1.18339     Document Type: Article

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