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1NVP

HUMAN TFIIA/TBP/DNA COMPLEX

Summary for 1NVP
Entry DOI10.2210/pdb1nvp/pdb
Descriptor5'-D(*GP*GP*GP*GP*GP*GP*GP*CP*TP*AP*TP*AP*AP*AP*AP*GP*G)-3', 5'-D(*CP*CP*TP*TP*TP*TP*AP*TP*AP*GP*CP*CP*CP*CP*CP*CP*C)-3', TATA box binding protein, ... (7 entities in total)
Functional Keywordstranscription regulation, dna, complex, transcription-dna complex, transcription/dna
Biological sourceHomo sapiens (human)
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Cellular locationNucleus: P20226 P52655 P52655 P52657
Total number of polymer chains6
Total formula weight58370.52
Authors
Bleichenbacher, M.,Tan, S.,Richmond, T.J. (deposition date: 2003-02-04, release date: 2003-10-21, Last modification date: 2024-02-14)
Primary citationBleichenbacher, M.,Tan, S.,Richmond, T.J.
Novel interactions between the components of human and yeast TFIIA/TBP/DNA complexes.
J.Mol.Biol., 332:783-793, 2003
Cited by
PubMed Abstract: RNA polymerase II-dependent transcription requires the assembly of a multi-protein, preinitiation complex on core promoter elements. Transcription factor IID (TFIID) comprising the TATA box-binding protein (TBP) and TBP-associated factors (TAFs) is responsible for promoter recognition in this complex. Subsequent association of TFIIA and TFIIB provides enhanced complex stability. TFIIA is required for transcriptional stimulation by certain viral and cellular activators, and favors formation of the preinitiation complex in the presence of repressor NC2. The X-ray structures of human and yeast TBP/TFIIA/DNA complexes at 2.1A and 1.9A resolution, respectively, are presented here and seen to resemble each other closely. The interactions made by human TFIIA with TBP and DNA within and upstream of the TATA box, including those involving water molecules, are described and compared to the yeast structure. Of particular interest is a previously unobserved region of TFIIA that extends the binding interface with TBP in the yeast, but not in the human complex, and that further elucidates biochemical and genetic results.
PubMed: 12972251
DOI: 10.1016/S0022-2836(03)00887-8
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.1 Å)
Structure validation

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