Structural basis of LSD1-CoREST selectivity in histone H3 recognition

Journal of Biological Chemistry

Volumn 282, Issue 28, 2007, Pages 20070-20074

  Forneris, Federico ^a   Binda, Claudia ^a   Adamo, Antonio ^b   Battaglioli, Elena ^b   Mattevi, Andrea ^a  

^a UNIVERSITY OF PAVIA   (Italy)

^b UNIVERSITY OF MILAN   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

INTRAMOLECULAR HYDROGEN BONDS; PEPTIDE INHIBITORS;

AMINO ACIDS; CRYSTAL STRUCTURE; ENZYME KINETICS; HYDROGEN BONDS; TRANSCRIPTION;

PROTEINS;

HISTONE H3; ISOENZYME; LYSINE SPECIFIC DEMETHYLASE 1; METHYL GROUP; PROTEIN COREST; QUERCETIN; SOLVENT; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG;

ARTICLE; CRYSTAL STRUCTURE; ELECTRICITY; ENZYME ACTIVE SITE; ENZYME ACTIVITY; ENZYME CONFORMATION; ENZYME SPECIFICITY; ENZYME STRUCTURE; ENZYME SUBSTRATE; HYDROGEN BOND; METHYLATION; MOLECULAR INTERACTION; NONHUMAN; NUCLEOTIDE SEQUENCE; OXIDATION; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN FOLDING; PROTEIN FUNCTION; STRUCTURE ANALYSIS;

ANIMALS; BINDING SITES; CRYSTALLOGRAPHY, X-RAY; DNA-BINDING PROTEINS; ENZYME INHIBITORS; FLAVINS; HISTONES; MICE; MULTIENZYME COMPLEXES; NERVE TISSUE PROTEINS; OXIDATION-REDUCTION; OXIDOREDUCTASES, N-DEMETHYLATING; PEPTIDES; PROTEIN BINDING; PROTEIN STRUCTURE, QUATERNARY; REPRESSOR PROTEINS; SUBSTRATE SPECIFICITY;

EID: 34547132094     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.C700100200     Document Type: Article

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