The SH3 domain of HS1 protein recognizes lysine-rich polyproline motifs

Amino Acids

Volumn 42, Issue 4, 2012, Pages 1361-1370

  Siligardi, Giuliano ^a   Ruzza, Paolo ^b   Hussain, Rohanah ^a   Cesaro, Luca ^c   Brunati, Anna Maria ^c   Pinna, Lorenzo A ^c   Donella Deana, Arianna ^c  

^a DIAMOND LIGHT SOURCE LTD   (United Kingdom)

^b CNR   (Italy)

^c UNIVERSITY OF PADOVA   (Italy)

Author keywords

HS1; Pro rich peptides; Protein protein interaction; SH3 domain

Indexed keywords

LYSINE; PROLINE; PROTEIN HS1; PROTEIN SH3; UNCLASSIFIED DRUG;

AMINO ACID SEQUENCE; ARTICLE; BINDING AFFINITY; CARBOXY TERMINAL SEQUENCE; CIRCULAR DICHROISM; COMPLEX FORMATION; COMPUTER MODEL; CONTROLLED STUDY; LIGAND BINDING; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN DOMAIN; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN INTERACTION; PROTEIN LOCALIZATION; PROTEIN MOTIF; PROTEIN STABILITY; PROTEIN SYNTHESIS; STRUCTURE ANALYSIS; SUBSTITUTION REACTION;

AMINO ACID SEQUENCE; BLOOD PROTEINS; HUMANS; KINETICS; LYSINE; MOLECULAR SEQUENCE DATA; PEPTIDES; PROTEIN BINDING; PROTEIN STRUCTURE, SECONDARY; SRC HOMOLOGY DOMAINS;

EID: 84862692314     PISSN: 09394451     EISSN: 14382199     Source Type: Journal    
DOI: 10.1007/s00726-011-0831-4     Document Type: Article

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