The potent inhibitory activity of histone H1.2 C-terminal fragments on furin

FEBS Journal

Volumn 273, Issue 19, 2006, Pages 4459-4469

  Han, Jinbo ^a   Zhang, Ling ^b   Shao, Xiaoxia ^b   Shi, Jiahao ^a   Chi, Chengwu ^a,b  

^a INSTITUTE OF BIOCHEMISTRY AND CELL BIOLOGY   (China)

^b TONGJI UNIVERSITY   (China)

Author keywords

Furin; Gene expression; Histone H1; Inhibitory activity; Limited proteolysis; Peptide synthesis

Indexed keywords

CARBOXY TERMINAL TELOPEPTIDE; ENZYME INHIBITOR; FURIN; FURIN INHIBITOR; HISTONE H1; LYSINE; PROLYLALANYLALANYLALANYLTHREONYLVALYLTHREONYLLYSYLLYSYLVALYLALANYL LYSYLSERYLPROLYLLYSYLLYSYLALANYLLYSYLALANYLALANYLLYSYLPROLYLLYSYL LYSYLALANYLALANYLLYSYLSERYLALANYLALANYLLYSYLALANYLVALYLLYSYLPROLYLLYSINE; UNCLASSIFIED DRUG;

ANIMAL TISSUE; ARTICLE; CARBOXY TERMINAL SEQUENCE; CONTROLLED STUDY; DRUG ACTIVITY; DRUG POTENCY; DRUG PURIFICATION; DRUG SYNTHESIS; GENE SEQUENCE; MOLECULAR CLONING; NONHUMAN; NUCLEOTIDE SEQUENCE; PEPTIDE SYNTHESIS; PRIORITY JOURNAL;

AMINO ACID SEQUENCE; ANIMALS; BINDING SITES; FURIN; HISTONES; LIVER; MOLECULAR SEQUENCE DATA; PEPTIDE FRAGMENTS; PROTEASE INHIBITORS; PROTEIN STRUCTURE, SECONDARY; RECOMBINANT FUSION PROTEINS; SWINE;

BACTERIA (MICROORGANISMS); MAMMALIA; SUIDAE;

EID: 33748746123     PISSN: 1742464X     EISSN: 17424658     Source Type: Journal    
DOI: 10.1111/j.1742-4658.2006.05451.x     Document Type: Article

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