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5N5Y

Cryo-EM structure of RNA polymerase I in complex with Rrn3 and Core Factor (Orientation III)

Summary for 5N5Y
Entry DOI10.2210/pdb5n5y/pdb
EMDB information3590
DescriptorDNA-directed RNA polymerase I subunit RPA190, DNA-directed RNA polymerases I, II, and III subunit RPABC5, DNA-directed RNA polymerases I and III subunit RPAC2, ... (21 entities in total)
Functional Keywordstranscription, rna polymerase i initiation
Biological sourceSaccharomyces cerevisiae (Baker's yeast)
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Total number of polymer chains18
Total formula weight885697.37
Authors
Engel, C.,Gubbey, T.,Neyer, S.,Sainsbury, S.,Oberthuer, C.,Baejen, C.,Bernecky, C.,Cramer, P. (deposition date: 2017-02-14, release date: 2017-04-05, Last modification date: 2018-10-03)
Primary citationEngel, C.,Gubbey, T.,Neyer, S.,Sainsbury, S.,Oberthuer, C.,Baejen, C.,Bernecky, C.,Cramer, P.
Structural Basis of RNA Polymerase I Transcription Initiation.
Cell, 169:120-131.e22, 2017
Cited by
PubMed Abstract: Transcription initiation at the ribosomal RNA promoter requires RNA polymerase (Pol) I and the initiation factors Rrn3 and core factor (CF). Here, we combine X-ray crystallography and cryo-electron microscopy (cryo-EM) to obtain a molecular model for basal Pol I initiation. The three-subunit CF binds upstream promoter DNA, docks to the Pol I-Rrn3 complex, and loads DNA into the expanded active center cleft of the polymerase. DNA unwinding between the Pol I protrusion and clamp domains enables cleft contraction, resulting in an active Pol I conformation and RNA synthesis. Comparison with the Pol II system suggests that promoter specificity relies on a distinct "bendability" and "meltability" of the promoter sequence that enables contacts between initiation factors, DNA, and polymerase.
PubMed: 28340337
DOI: 10.1016/j.cell.2017.03.003
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (7.7 Å)
Structure validation

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