Crystal structure of negative cofactor 2 recognizing the TBP-DNA transcription complex (Q27633373)

2

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H Chen

3

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S Malik

4

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G Stelzer

5

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R G Roeder

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M Meisterernst

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S K Burley

The histone fold: a ubiquitous architectural motif utilized in DNA compaction and protein dimerization

8

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language of work or name

English

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publication date

13 July 2001

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published in

Cell

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volume

106

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issue

1

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page(s)

71-81

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cites work

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A variety of DNA-binding and multimeric proteins contain the histone fold motif.

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Human TAF(II)28 and TAF(II)18 interact through a histone fold encoded by atypical evolutionary conserved motifs also found in the SPT3 family

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The downstream core promoter element, DPE, is conserved from Drosophila to humans and is recognized by TAFII60 of Drosophila

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The C-terminal domain-phosphorylated IIO form of RNA polymerase II is associated with the transcription repressor NC2 (Dr1/DRAP1) and is required for transcription activation in human nuclear extracts

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Crystal structure of yeast TATA-binding protein and model for interaction with DNA

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The crystal structure of a hyperthermophilic archaeal TATA-box binding protein

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Functional antagonism between RNA polymerase II holoenzyme and global negative regulator NC2 in vivo

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The histone fold is a key structural motif of transcription factor TFIID.

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Crystal structure of the yeast TFIIA/TBP/DNA complex

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Yeast NC2 associates with the RNA polymerase II preinitiation complex and selectively affects transcription in vivo

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TBP-associated factors (TAFIIs): multiple, selective transcriptional mediators in common complexes

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A histone octamer-like structure within TFIID

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How proteins recognize the TATA box

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Co-crystal structure of TBP recognizing the minor groove of a TATA element

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Crystal structure of a yeast TBP/TATA-box complex

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A negative cofactor containing Dr1/p19 modulates transcription with TFIIA in a promoter-specific fashion

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The Dr1/DRAP1 heterodimer is a global repressor of transcription in vivo

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Genetic analysis of the YDR1-BUR6 repressor complex reveals an intricate balance among transcriptional regulatory proteins in yeast

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The 2.1-A crystal structure of an archaeal preinitiation complex: TATA-box-binding protein/transcription factor (II)B core/TATA-box

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Interplay of positive and negative regulators in transcription initiation by RNA polymerase II holoenzyme

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The NC2 repressor is dispensable in yeast mutated for the Sin4p component of the holoenzyme and plays roles similar to Mot1p in vivo

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Solution structure of a TBP-TAF(II)230 complex: protein mimicry of the minor groove surface of the TATA box unwound by TBP

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A dynamic model for PC4 coactivator function in RNA polymerase II transcription

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Cap-dependent translation initiation in eukaryotes is regulated by a molecular mimic of eIF4G

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Family of proteins that interact with TFIID and regulate promoter activity

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Protein folding and association: insights from the interfacial and thermodynamic properties of hydrocarbons

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Crystal structure of TFIID TATA-box binding protein

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Crystal structure of a TFIIB-TBP-TATA-element ternary complex

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Crystal structure of a human TATA box-binding protein/TATA element complex

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TATA element recognition by the TATA box-binding protein has been conserved throughout evolution

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Saccharomyces cerevisiae BUR6 encodes a DRAP1/NC2alpha homolog that has both positive and negative roles in transcription in vivo

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TFIID sequence recognition of the initiator and sequences farther downstream in Drosophila class II genes.

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SIR repression of a yeast heat shock gene: UAS and TATA footprints persist within heterochromatin

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Crystal structure of a yeast TFIIA/TBP/DNA complex

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