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PDBsum entry 2xyx

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Transcription PDB id
2xyx

 

 

 

 

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Contents
Protein chains
261 a.a. *
Ligands
Z00 ×2
BOG ×2
Waters ×31
* Residue conservation analysis
PDB id:
2xyx
Name: Transcription
Title: Novel sulfonylthiadiazoles with an unusual binding mode as partial dual peroxisome proliferator-activated receptor (ppar) gamma-delta agonists with high potency and in-vivo efficacy
Structure: Peroxisome proliferator-activated receptor delta. Chain: a, b. Fragment: ligand binding domain, residues 165-441. Synonym: nuci, nuclear hormone receptor 1, nuclear receptor subfamily 1 group c member 2, peroxisome proliferator-activated receptor beta, ppar-delta, nuc1, ppar-beta. Engineered: yes
Source: Homo sapiens. Human. Organism_taxid: 9606. Expressed in: escherichia coli. Expression_system_taxid: 469008.
Resolution:
2.70Å     R-factor:   0.216     R-free:   0.264
Authors: J.-P.Marquette,M.Mathieu
Key ref: S.Keil et al. (2011). Sulfonylthiadiazoles with an unusual binding mode as partial dual peroxisome proliferator-activated receptor (PPAR) γ/δ agonists with high potency and in vivo efficacy. Chemmedchem, 6, 633-653. PubMed id: 21400663
Date:
19-Nov-10     Release date:   23-Feb-11    
PROCHECK
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 Headers
 References

Protein chains
Pfam   ArchSchema ?
Q03181  (PPARD_HUMAN) -  Peroxisome proliferator-activated receptor delta from Homo sapiens
Seq:
Struc:
441 a.a.
261 a.a.
Key:    PfamA domain  Secondary structure  CATH domain

 Enzyme reactions 
   Enzyme class: E.C.?
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]

 

 
Chemmedchem 6:633-653 (2011)
PubMed id: 21400663  
 
 
Sulfonylthiadiazoles with an unusual binding mode as partial dual peroxisome proliferator-activated receptor (PPAR) γ/δ agonists with high potency and in vivo efficacy.
S.Keil, H.Matter, K.Schönafinger, M.Glien, M.Mathieu, J.P.Marquette, N.Michot, S.Haag-Diergarten, M.Urmann, W.Wendler.
 
  ABSTRACT  
 
No abstract given.

 

 

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