Molecular structure of human TFIIH

Cell

Volumn 102, Issue 5, 2000, Pages 599-607

  Schultz, Patrick ^a   Fribourg, Sébastien ^a   Poterszman, Arnaud ^a   Mallouh, Véronique ^a   Moras, Dino ^a   Egly, Jean Marc ^a  

^a CNRS   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLINE; HELICASE; TRANSCRIPTION FACTOR;

ANTIBODY LABELING; ARTICLE; CELL DENSITY; CHEMICAL STRUCTURE; CYTOARCHITECTURE; DNA TRANSCRIPTION; ELECTRON MICROSCOPY; EXCISION; HUMAN; HUMAN CELL; PRIORITY JOURNAL; YEAST;

EID: 0034268691     PISSN: 00928674     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0092-8674(00)00082-9     Document Type: Article

References (53)

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4. Distinct regions of MAT1 regulate cdk7 kinase and TFIIH transcription activities
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6. Electron crystal structure of the transcription factor and DNA repair complex, core TFIIH
7. Mutations in the XPD helicase gene result in XP and TTD phenotypes, preventing interaction between XPD and the p44 subunit of TFIIH
8. Mutations in XPB and XPD helicases found in xeroderma pigmentosum patients impair the transcription function of TFIIH
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22. Opening of an RNA polymerase II promoter occurs in two distinct steps and requires the basal transcription factors IIE and IIH
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31. A role for the TFIIH XPB DNA helicase in promoter escape by RNA polymerase II
32. Similarity of the yeast RAD51 filament to the bacterial RecA filament
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34. A mammalian RNA polymerase II holoenzyme containing all components required for promoter-specific transcription initiation
35. Structure of a multisubunit complex that promotes DNA branch migration
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40. Substrate specificity of the cdk-activating kinase (CAK) is altered upon association with TFIIH
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42. Six molecules of SV40 large T antigen assemble in a propeller-shaped particle around a channel
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53. A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndrome