Structural Characterization of the Chaetomium thermophilum TREX-2 Complex and its Interaction with the mRNA Nuclear Export Factor Mex67:Mtr2

Structure

Volumn 23, Issue 7, 2015, Pages 1246-1257

  Dimitrova, Lyudmila ^a,b   Valkov, Eugene ^a,c   Aibara, Shintaro ^a   Flemming, Dirk ^b   McLaughlin, Stephen H ^a   Hurt, Ed ^b   Stewart, Murray ^a  

^a MRC LABORATORY OF MOLECULAR BIOLOGY   (United Kingdom)

^b UNIVERSITY OF HEIDELBERG   (Germany)

^c MAX PLANCK INSTITUTE FOR DEVELOPMENTAL BIOLOGY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CHAETOMIUM THERMOPHILUM TREX 2 COMPLEX; GLUTATHIONE TRANSFERASE; KARYOPHERIN BETA; MESSENGER RNA; MOLECULAR SCAFFOLD; MTR2 PROTEIN; NUCLEAR EXPORT FACTOR MEX67; NUCLEAR FACTOR; NUCLEAR PROTEIN; NUCLEOPORIN; PHENYLALANINE; UNCLASSIFIED DRUG; FUNGAL PROTEIN; NUCLEOCYTOPLASMIC TRANSPORT PROTEIN; PROTEIN BINDING; RNA BINDING PROTEIN;

AMINO TERMINAL SEQUENCE; ARTICLE; ASSOCIATION RATE CONSTANT; BINDING SITE; CARBOXY TERMINAL SEQUENCE; CONTROLLED STUDY; CRYSTAL STRUCTURE; CRYSTALLIZATION; CRYSTALLOGRAPHY; ELECTRON MICROSCOPY; IN VITRO STUDY; NONHUMAN; NUCLEAR PORE; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN MOTIF; PROTEIN RNA BINDING; PROTEIN TRANSPORT; SACCHAROMYCES CEREVISIAE; STRUCTURE ANALYSIS; YEAST CELL; ACTIVE TRANSPORT; AMINO ACID SEQUENCE; CHAETOMIUM; CHEMISTRY; MOLECULAR GENETICS; MOLECULAR MODEL; PROTEIN DOMAIN; PROTEIN QUATERNARY STRUCTURE; PROTEIN SECONDARY STRUCTURE; RNA TRANSPORT; SEQUENCE HOMOLOGY; ULTRASTRUCTURE; X RAY CRYSTALLOGRAPHY;

CHAETOMIUM THERMOPHILUM; SACCHAROMYCES CEREVISIAE;

ACTIVE TRANSPORT, CELL NUCLEUS; AMINO ACID SEQUENCE; CHAETOMIUM; CRYSTALLOGRAPHY, X-RAY; FUNGAL PROTEINS; MODELS, MOLECULAR; MOLECULAR SEQUENCE DATA; NUCLEOCYTOPLASMIC TRANSPORT PROTEINS; PROTEIN BINDING; PROTEIN INTERACTION DOMAINS AND MOTIFS; PROTEIN STRUCTURE, QUATERNARY; PROTEIN STRUCTURE, SECONDARY; RNA TRANSPORT; RNA-BINDING PROTEINS; SEQUENCE HOMOLOGY, AMINO ACID;

EID: 84936847063     PISSN: 09692126     EISSN: 18784186     Source Type: Journal    
DOI: 10.1016/j.str.2015.05.002     Document Type: Article

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