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PDBsum entry 2han
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Transcription/DNA
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PDB id
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2han
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Contents |
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* Residue conservation analysis
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PDB id:
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Transcription/DNA
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Title:
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Structural basis of heterodimeric ecdysteroid receptor interaction with natural response element hsp27 gene promoter
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Structure:
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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.
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Source:
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Synthetic: yes. Drosophila melanogaster. Fruit fly. Organism_taxid: 7227. Gene: usp, cf1, nr2b4. Expressed in: escherichia coli. Expression_system_taxid: 562. Gene: ecr, nr1h1.
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Resolution:
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1.95Å
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R-factor:
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0.182
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R-free:
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0.217
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Authors:
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M.Jakob,R.Kolodziejczyk,M.Orlowski,S.Krzywda,A.Kowalska,J.Dutko- Gwozdz,T.Gwozdz,M.Kochman,M.Jaskolski,A.Ozyhar
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Key ref:
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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:
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Date:
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13-Jun-06
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Release date:
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22-May-07
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PROCHECK
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Headers
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References
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Nucleic Acids Res
35:2705-2718
(2007)
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PubMed id:
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Novel DNA-binding element within the C-terminal extension of the nuclear receptor DNA-binding domain.
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M.Jakób,
R.Kołodziejczyk,
M.Orłowski,
S.Krzywda,
A.Kowalska,
J.Dutko-Gwóźdź,
T.Gwóźdź,
M.Kochman,
M.Jaskólski,
A.Ozyhar.
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ABSTRACT
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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.
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Literature references that cite this PDB file's key reference
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PubMed id
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Reference
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T.Krusiński,
A.Ozyhar,
and
P.Dobryszycki
(2010).
Dual FRET assay for detecting receptor protein interaction with DNA.
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Nucleic Acids Res,
38,
e108.
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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.
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Chemistry,
15,
4798-4810.
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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.
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J Biol Chem,
283,
33685-33697.
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PDB code:
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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.
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J Fluoresc,
18,
1.
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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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