Proteomics strategy to identify substrates of LNX, a PDZ domain-containing E3 ubiquitin ligase

Journal of Proteome Research

Volumn 11, Issue 10, 2012, Pages 4847-4862

  Guo, Zhengguang ^a   Song, Eli ^b   Ma, Sucan ^a   Wang, Xiaorong ^a   Gao, Shijuan ^a   Shao, Chen ^a   Hu, Siqi ^a   Jia, Lulu ^a   Tian, Rui ^a   Xu, Tao ^b   Gao, Youhe ^a  

^a PEKING UNION MEDICAL COLLEGE   (China)

^b INSTITUTE OF BIOPHYSICS   (China)

Author keywords

LNX; PDZ Domain; Protein Interaction Domain; Random Peptide Library; Ubiquitin Ligase; Ubiquitination

Indexed keywords

PROTEIN LNX; UBIQUITIN PROTEIN LIGASE E3; UNCLASSIFIED DRUG;

APOPTOSIS; ARTICLE; CELL PROLIFERATION; CONTROLLED STUDY; ENZYME ANALYSIS; ENZYME BINDING; ENZYME SUBSTRATE; HUMAN; PDZ DOMAIN; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN MOTIF; PROTEOMICS;

AMINO ACID SEQUENCE; ANTIBIOTICS, ANTINEOPLASTIC; CELL PROLIFERATION; CELL SURVIVAL; CONSENSUS SEQUENCE; DOXORUBICIN; GENE KNOCKDOWN TECHNIQUES; HEK293 CELLS; HELA CELLS; HUMANS; MCF-7 CELLS; MITOGEN-ACTIVATED PROTEIN KINASE KINASES; MOLECULAR SEQUENCE ANNOTATION; PEPTIDE FRAGMENTS; PROTEIN BINDING; PROTEIN INTERACTION DOMAINS AND MOTIFS; PROTEIN PROCESSING, POST-TRANSLATIONAL; PROTEOMICS; RNA INTERFERENCE; TWO-HYBRID SYSTEM TECHNIQUES; UBIQUITIN-PROTEIN LIGASES; UBIQUITINATION;

EID: 84867471014     PISSN: 15353893     EISSN: 15353907     Source Type: Journal    
DOI: 10.1021/pr300674c     Document Type: Article

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