The pentameric nucleoplasmin fold is present in Drosophila FKBP39 and a large number of chromatin-related proteins

Journal of Molecular Biology

Volumn 427, Issue 10, 2015, Pages 1949-1963

  Edlich Muth, Christian ^a,f   Artero, Jean Baptiste ^b,c   Callow, Phil ^b,c   Przewloka, Marcin R ^a   Watson, Aleksandra A ^a   Zhang, Wei ^a   Glover, David M ^a   Debski, Janusz ^d   Dadlez, Michal ^d   Round, Adam R ^c,e   Forsyth, V Trevor ^b,c   Laue, Ernest D ^a  

^a UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^b INSTITUT LAUE LANGEVIN   (France)

^c KEELE UNIVERSITY   (United Kingdom)

^d POLISH ACADEMY OF SCIENCES   (Poland)

^e EUROPEAN MOLECULAR BIOLOGY LABORATORY   (France)

^f UNIVERSITY OF POTSDAM   (Germany)

Author keywords

histone chaperone; NMR; nucleoplasmin; structure determination

Indexed keywords

CHAPERONE; CHROMATIN; CROSS LINKING REAGENT; DROSOPHILA PROTEIN; FK 506 BINDING PROTEIN; FK506-BP1 PROTEIN, DROSOPHILA; FPR4 PROTEIN, S CEREVISIAE; HISTONE; HISTONE DEACETYLASE 2; NUCLEOPLASMIN; PROTEIN BINDING; RECOMBINANT PROTEIN; SACCHAROMYCES CEREVISIAE PROTEIN;

AMINO ACID SEQUENCE; ANIMAL; ARABIDOPSIS; CHEMICAL STRUCTURE; CHEMISTRY; CHROMATIN; DROSOPHILA MELANOGASTER; IMMUNOPRECIPITATION; MASS SPECTROMETRY; METABOLISM; MOLECULAR GENETICS; PHYLOGENY; PROTEIN CONFORMATION; PROTEIN TERTIARY STRUCTURE; SACCHAROMYCES CEREVISIAE; SEQUENCE HOMOLOGY; STRUCTURE ACTIVITY RELATION; X RAY CRYSTALLOGRAPHY;

AMINO ACID SEQUENCE; ANIMALS; ARABIDOPSIS; CHROMATIN; CROSS-LINKING REAGENTS; CRYSTALLOGRAPHY, X-RAY; DROSOPHILA MELANOGASTER; DROSOPHILA PROTEINS; HISTONE CHAPERONES; HISTONE DEACETYLASE 2; HISTONES; IMMUNOPRECIPITATION; MODELS, MOLECULAR; MOLECULAR SEQUENCE DATA; NUCLEOPLASMINS; PHYLOGENY; PROTEIN BINDING; PROTEIN CONFORMATION; PROTEIN STRUCTURE, TERTIARY; RECOMBINANT PROTEINS; SACCHAROMYCES CEREVISIAE; SACCHAROMYCES CEREVISIAE PROTEINS; SEQUENCE HOMOLOGY, AMINO ACID; SPECTROMETRY, MASS, MATRIX-ASSISTED LASER DESORPTION-IONIZATION; STRUCTURE-ACTIVITY RELATIONSHIP; TACROLIMUS BINDING PROTEINS;

EID: 84933034999     PISSN: 00222836     EISSN: 10898638     Source Type: Journal    
DOI: 10.1016/j.jmb.2015.03.010     Document Type: Article

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