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3C46

X-ray crystal structure of the N4 mini-vRNAP P2_7a promoter complex soaked with MgCl2

Summary for 3C46
Entry DOI10.2210/pdb3c46/pdb
Related3C2P 3C3L 3C42 3C47
DescriptorVirion RNA polymerase, P2_7a Promoter DNA, DIHYDROGENPHOSPHATE ION, ... (4 entities in total)
Functional Keywordsprotein-dna complex, nucleotidyltransferase, promoter binary complex, dna-hairpin, virion rna polymerase, phosphate ion, transferase-dna complex, transferase/dna
Biological sourceBacteriophage N4
Cellular locationVirion : Q859P9
Total number of polymer chains4
Total formula weight268280.78
Authors
Gleghorn, M.L.,Murakami, K.S. (deposition date: 2008-01-29, release date: 2008-12-09, Last modification date: 2024-02-21)
Primary citationGleghorn, M.L.,Davydova, E.K.,Rothman-Denes, L.B.,Murakami, K.S.
Structural basis for DNA-hairpin promoter recognition by the bacteriophage N4 virion RNA polymerase.
Mol.Cell, 32:707-717, 2008
Cited by
PubMed Abstract: Coliphage N4 virion-encapsidated RNA polymerase (vRNAP) is a member of the phage T7-like single-subunit RNA polymerase (RNAP) family. Its central domain (mini-vRNAP) contains all RNAP functions of the full-length vRNAP, which recognizes a 5 to 7 base pair stem and 3 nucleotide loop hairpin DNA promoter. Here, we report the X-ray crystal structures of mini-vRNAP bound to promoters. Mini-vRNAP uses four structural motifs to recognize DNA sequences at the hairpin loop and stem and to unwind DNA. Despite their low sequence similarity, three out of four motifs are shared with T7 RNAP that recognizes a double-stranded DNA promoter. The binary complex structure and results of engineered disulfide linkage experiments reveal that the plug and motif B loop, which block the access of template DNA to the active site in the apo-form mini-vRNAP, undergo a large-scale conformational change upon promoter binding, explaining the restricted promoter specificity that is critical for N4 phage early transcription.
PubMed: 19061645
DOI: 10.1016/j.molcel.2008.11.010
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2 Å)
Structure validation

227344

數據於2024-11-13公開中

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