Protein conformation ensembles monitored by HDX reveal a structural rationale for abscisic acid signaling protein affinities and activities

Structure

Volumn 21, Issue 2, 2013, Pages 229-235

  West, Graham M ^a   Pascal, Bruce D ^a   Ng, Ley Moy ^b   Soon, Fen Fen ^b   Melcher, Karsten ^b   Xu, H Eric ^b   Chalmers, Michael J ^a   Griffin, Patrick R ^a  

^a SCRIPPS RESEARCH INSTITUTE   (United States)

^b VAN ANDEL RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ABSCISIC ACID; PHOSPHATASE; PHOSPHOTRANSFERASE;

ARTICLE; BINDING AFFINITY; CONTROLLED STUDY; CRYSTAL STRUCTURE; DEUTERIUM HYDROGEN EXCHANGE; MASS SPECTROMETRY; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN CONFORMATION; PROTEIN STABILITY; PROTEIN STRUCTURE; SIGNAL TRANSDUCTION;

ABSCISIC ACID; ADENOSINE TRIPHOSPHATE; AMINO ACID SEQUENCE; ARABIDOPSIS; ARABIDOPSIS PROTEINS; DEUTERIUM EXCHANGE MEASUREMENT; HYDROGEN BONDING; MODELS, MOLECULAR; MOLECULAR SEQUENCE DATA; PHOSPHOPROTEIN PHOSPHATASES; PROTEIN BINDING; PROTEIN INTERACTION DOMAINS AND MOTIFS; PROTEIN KINASES; PROTEIN STABILITY; PROTEIN STRUCTURE, SECONDARY; PROTEIN-SERINE-THREONINE KINASES; SIGNAL TRANSDUCTION;

EID: 84873405050     PISSN: 09692126     EISSN: 18784186     Source Type: Journal    
DOI: 10.1016/j.str.2012.12.001     Document Type: Article

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