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PDBsum entry 2han

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protein dna_rna metals Protein-protein interface(s) links
Transcription/DNA PDB id
2han

 

 

 

 

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Contents
Protein chains
78 a.a. *
87 a.a. *
DNA/RNA
Metals
_ZN ×4
Waters ×222
* Residue conservation analysis
PDB id:
2han
Name: Transcription/DNA
Title: Structural basis of heterodimeric ecdysteroid receptor interaction with natural response element hsp27 gene promoter
Structure: 5'-d( Cp Ap Ap Gp Gp Gp Tp Tp Cp Ap Ap Tp Gp Cp Ap Cp Tp Tp Gp T)-3'. Chain: c. Engineered: yes. Other_details: natural ecdysone response element. 5'-d( Gp Ap Cp Ap Ap Gp Tp Gp Cp Ap Tp Tp Gp Ap Ap Cp Cp Cp Tp T)-3'. Chain: d. Engineered: yes.
Source: Synthetic: yes. Drosophila melanogaster. Fruit fly. Organism_taxid: 7227. Gene: usp, cf1, nr2b4. Expressed in: escherichia coli. Expression_system_taxid: 562. Gene: ecr, nr1h1.
Resolution:
1.95Å     R-factor:   0.182     R-free:   0.217
Authors: M.Jakob,R.Kolodziejczyk,M.Orlowski,S.Krzywda,A.Kowalska,J.Dutko- Gwozdz,T.Gwozdz,M.Kochman,M.Jaskolski,A.Ozyhar
Key ref: M.Jakób et al. (2007). Novel DNA-binding element within the C-terminal extension of the nuclear receptor DNA-binding domain. Nucleic Acids Res, 35, 2705-2718. PubMed id: 17426125
Date:
13-Jun-06     Release date:   22-May-07    
PROCHECK
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 Headers
 References

Protein chain
Pfam   ArchSchema ?
P20153  (USP_DROME) -  Protein ultraspiracle from Drosophila melanogaster
Seq:
Struc:
508 a.a.
78 a.a.
Protein chain
Pfam   ArchSchema ?
P34021  (ECR_DROME) -  Ecdysone receptor from Drosophila melanogaster
Seq:
Struc:
 
Seq:
Struc:
878 a.a.
87 a.a.
Key:    PfamA domain  Secondary structure  CATH domain

DNA/RNA chains
  C-A-A-G-G-G-T-T-C-A-A-T-G-C-A-C-T-T-G-T 20 bases
  G-A-C-A-A-G-T-G-C-A-T-T-G-A-A-C-C-C-T-T 20 bases

 

 
Nucleic Acids Res 35:2705-2718 (2007)
PubMed id: 17426125  
 
 
Novel DNA-binding element within the C-terminal extension of the nuclear receptor DNA-binding domain.
M.Jakób, R.Kołodziejczyk, M.Orłowski, S.Krzywda, A.Kowalska, J.Dutko-Gwóźdź, T.Gwóźdź, M.Kochman, M.Jaskólski, A.Ozyhar.
 
  ABSTRACT  
 
The heterodimer of the ecdysone receptor (EcR) and ultraspiracle (Usp), members of the nuclear receptors superfamily, is considered as the functional receptor for ecdysteroids initiating molting and metamorphosis in insects. Here we report the 1.95 A structure of the complex formed by the DNA-binding domains (DBDs) the EcR and the Usp, bound to the natural pseudopalindromic response element. Comparison of the structure with that obtained previously, using an idealized response element, shows how the EcRDBD, which has been previously reported to possess extraordinary flexibility, accommodates DNA-induced structural changes. Part of the C-terminal extension (CTE) of the EcRDBD folds into an alpha-helix whose location in the minor groove does not match any of the locations previously observed for nuclear receptors. Mutational analyses suggest that the alpha-helix is a component of EcR-box, a novel element indispensable for DNA-binding and located within the nuclear receptor CTE. This element seems to be a general feature of all known EcRs.
 

Literature references that cite this PDB file's key reference

  PubMed id Reference
20139421 T.Krusiński, A.Ozyhar, and P.Dobryszycki (2010).
Dual FRET assay for detecting receptor protein interaction with DNA.
  Nucleic Acids Res, 38, e108.  
19388025 O.Sénèque, E.Bonnet, F.L.Joumas, and J.M.Latour (2009).
Cooperative metal binding and helical folding in model peptides of treble-clef zinc fingers.
  Chemistry, 15, 4798-4810.  
18829458 P.Lu, G.B.Rha, M.Melikishvili, G.Wu, B.C.Adkins, M.G.Fried, and Y.I.Chi (2008).
Structural basis of natural promoter recognition by a unique nuclear receptor, HNF4alpha. Diabetes gene product.
  J Biol Chem, 283, 33685-33697.
PDB code: 3cbb
18049881 T.Krusiński, M.Wietrzych, I.Grad, A.Ozyhar, and P.Dobryszycki (2008).
Equilibrium Analysis of the DNA Binding Domain of the Ultraspiracle Protein Interaction with the Response Element from the hsp27 Gene Promoter-the Application of Molecular Beacon Technology.
  J Fluoresc, 18, 1.  
The most recent references are shown first. Citation data come partly from CiteXplore and partly from an automated harvesting procedure. Note that this is likely to be only a partial list as not all journals are covered by either method. However, we are continually building up the citation data so more and more references will be included with time. Where a reference describes a PDB structure, the PDB code is shown on the right.

 

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