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PDBsum entry 3e00
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Transcription/DNA
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PDB id
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3e00
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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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Intact ppar gamma - rxr alpha nuclear receptor complex on DNA bound with gw9662, 9-cis retinoic acid and ncoa2 peptide
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Structure:
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Retinoic acid receptor rxr-alpha. Chain: a. Fragment: unp residues 11-462. Synonym: retinoid x receptor alpha, nuclear receptor subfamily 2 group b member 1. Engineered: yes. Peroxisome proliferator-activated receptor gamma. Chain: d. Fragment: unp residues 102-505.
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Source:
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Homo sapiens. Human. Organism_taxid: 9606. Gene: nr2b1, rxra, rxralpha. Expressed in: escherichia coli. Expression_system_taxid: 562. Gene: nr1c3, pparg, ppargamma. Synthetic: yes. Other_details: synthetic DNA.
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Resolution:
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3.10Å
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R-factor:
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0.214
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R-free:
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0.276
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Authors:
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V.Chandra,P.Huang,Y.Hamuro,S.Raghuram,Y.Wang,T.P.Burris,F.Rastinejad
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Key ref:
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V.Chandra
et al.
(2008).
Structure of the intact PPAR-gamma-RXR- nuclear receptor complex on DNA.
Nature,
456,
350-356.
PubMed id:
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Date:
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30-Jul-08
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Release date:
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28-Oct-08
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PROCHECK
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Headers
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References
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Enzyme class:
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Chains A, D:
E.C.?
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Nature
456:350-356
(2008)
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PubMed id:
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Structure of the intact PPAR-gamma-RXR- nuclear receptor complex on DNA.
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V.Chandra,
P.Huang,
Y.Hamuro,
S.Raghuram,
Y.Wang,
T.P.Burris,
F.Rastinejad.
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ABSTRACT
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Nuclear receptors are multi-domain transcription factors that bind to DNA
elements from which they regulate gene expression. The peroxisome
proliferator-activated receptors (PPARs) form heterodimers with the retinoid X
receptor (RXR), and PPAR-gamma has been intensively studied as a drug target
because of its link to insulin sensitization. Previous structural studies have
focused on isolated DNA or ligand-binding segments, with no demonstration of how
multiple domains cooperate to modulate receptor properties. Here we present
structures of intact PPAR-gamma and RXR-alpha as a heterodimer bound to DNA,
ligands and coactivator peptides. PPAR-gamma and RXR-alpha form a non-symmetric
complex, allowing the ligand-binding domain (LBD) of PPAR-gamma to contact
multiple domains in both proteins. Three interfaces link PPAR-gamma and
RXR-alpha, including some that are DNA dependent. The PPAR-gamma LBD cooperates
with both DNA-binding domains (DBDs) to enhance response-element binding. The
A/B segments are highly dynamic, lacking folded substructures despite their
gene-activation properties.
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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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J.Zhang,
M.J.Chalmers,
K.R.Stayrook,
L.L.Burris,
Y.Wang,
S.A.Busby,
B.D.Pascal,
R.D.Garcia-Ordonez,
J.B.Bruning,
M.A.Istrate,
D.J.Kojetin,
J.A.Dodge,
T.P.Burris,
and
P.R.Griffin
(2011).
DNA binding alters coactivator interaction surfaces of the intact VDR-RXR complex.
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Nat Struct Mol Biol,
18,
556-563.
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N.Rochel,
F.Ciesielski,
J.Godet,
E.Moman,
M.Roessle,
C.Peluso-Iltis,
M.Moulin,
M.Haertlein,
P.Callow,
Y.Mély,
D.I.Svergun,
and
D.Moras
(2011).
Common architecture of nuclear receptor heterodimers on DNA direct repeat elements with different spacings.
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Nat Struct Mol Biol,
18,
564-570.
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D.Kim,
B.J.Blus,
V.Chandra,
P.Huang,
F.Rastinejad,
and
S.Khorasanizadeh
(2010).
Corecognition of DNA and a methylated histone tail by the MSL3 chromodomain.
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Nat Struct Mol Biol,
17,
1027-1029.
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PDB codes:
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M.L.Privalsky,
S.Lee,
J.B.Hahm,
B.M.Young,
R.N.Fong,
and
I.H.Chan
(2009).
The p160 coactivator PAS-B motif stabilizes nuclear receptor binding and contributes to isoform-specific regulation by thyroid hormone receptors.
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J Biol Chem,
284,
19554-19563.
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T.Oyama,
K.Toyota,
T.Waku,
Y.Hirakawa,
N.Nagasawa,
J.I.Kasuga,
Y.Hashimoto,
H.Miyachi,
and
K.Morikawa
(2009).
Adaptability and selectivity of human peroxisome proliferator-activated receptor (PPAR) pan agonists revealed from crystal structures.
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Acta Crystallogr D Biol Crystallogr,
65,
786-795.
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PDB codes:
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Y.Pan,
C.J.Tsai,
B.Ma,
and
R.Nussinov
(2009).
How do transcription factors select specific binding sites in the genome?
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Nat Struct Mol Biol,
16,
1118-1120.
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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
codes are
shown on the right.
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}
}
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