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PDBsum entry 4lup

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protein dna_rna ligands Protein-protein interface(s) links
Transcription/DNA PDB id
4lup

 

 

 

 

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Contents
Protein chains
91 a.a.
DNA/RNA
Ligands
EDO
Waters ×207
PDB id:
4lup
Name: Transcription/DNA
Title: Crystal structure of the complex formed by region of e. Coli sigmae bound to its -10 element non template strand
Structure: RNA polymerase sigma factor. Chain: a, c. Fragment: unp residues 3-92. Engineered: yes. Region 2 of sigmae of e. Coli. Chain: b, d. Engineered: yes
Source: Escherichia coli. Organism_taxid: 562. Gene: rpoe, bn17_18601, ecs3439, lf82_1962. Expressed in: escherichia coli. Expression_system_taxid: 562. Synthetic: yes. Other_details: oligonucleotide synthetically generated
Resolution:
1.20Å     R-factor:   0.147     R-free:   0.165
Authors: S.Campagne,M.E.Marsh,J.A.V.Vorholt,F.H.-T.Allain,G.Capitani
Key ref: S.Campagne et al. (2014). Structural basis for -10 promoter element melting by environmentally induced sigma factors. Nat Struct Biol, 21, 269-276. PubMed id: 24531660 DOI: 10.1038/nsmb.2777
Date:
25-Jul-13     Release date:   19-Feb-14    
PROCHECK
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 Headers
 References

Protein chains
Pfam   ArchSchema ?
Q0P6M2  (Q0P6M2_ECOLX) -  RNA polymerase sigma factor from Escherichia coli
Seq:
Struc:
191 a.a.
91 a.a.*
Key:    PfamA domain  Secondary structure  CATH domain
* PDB and UniProt seqs differ at 3 residue positions (black crosses)

DNA/RNA chains
  T-G-T-C-A-A-A 7 bases
  G-T-C-A-A-A 6 bases

 

 
DOI no: 10.1038/nsmb.2777 Nat Struct Biol 21:269-276 (2014)
PubMed id: 24531660  
 
 
Structural basis for -10 promoter element melting by environmentally induced sigma factors.
S.Campagne, M.E.Marsh, G.Capitani, J.A.Vorholt, F.H.Allain.
 
  ABSTRACT  
 
Bacterial transcription is controlled by sigma factors, the RNA polymerase subunits that act as initiation factors. Although a single housekeeping sigma factor enables transcription from thousands of promoters, environmentally induced sigma factors redirect gene expression toward small regulons to carry out focused responses. Using structural and functional analyses, we determined the molecular basis of -10 promoter element recognition by Escherichia coli σ(E), which revealed an unprecedented way to achieve promoter melting. Group IV sigma factors induced strand separation at the -10 element by flipping out a single nucleotide from the nontemplate-strand DNA base stack. Unambiguous selection of this critical base was driven by a dynamic protein loop, which can be substituted to modify specificity of promoter recognition. This mechanism of promoter melting explains the increased promoter-selection stringency of environmentally induced sigma factors.
 

 

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