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5AZV

Crystal structure of hPPARgamma ligand binding domain complexed with 17-oxoDHA

Summary for 5AZV
Entry DOI10.2210/pdb5azv/pdb
Related5AZT
DescriptorPeroxisome proliferator-activated receptor gamma, (4~{Z},7~{Z},10~{Z},13~{Z},19~{Z})-17-oxidanylidenedocosa-4,7,10,13,19-pentaenoic acid (3 entities in total)
Functional Keywordsnuclear receptor, transcription regulation, ligand binding domain, zinc-finger, dna binding, transcription, obesity, nucleus, receptor, activator, oxidized fatty acid, transcription factor, agonist, dual agonist, covalent, ppre, nuclear, dna binding protein
Biological sourceHomo sapiens (Human)
Total number of polymer chains2
Total formula weight63588.02
Authors
Egawa, D.,Itoh, T.,Yamamoto, K. (deposition date: 2015-10-23, release date: 2016-07-06, Last modification date: 2024-10-23)
Primary citationEgawa, D.,Itoh, T.,Akiyama, Y.,Saito, T.,Yamamoto, K.
17-OxoDHA Is a PPAR alpha/gamma Dual Covalent Modifier and Agonist
Acs Chem.Biol., 2016
Cited by
PubMed Abstract: 17-Hydroxy docosahexaenoic acid (17-HDHA) is an oxidized form of docosahexaenoic acid (DHA) and known as a specialized proresolving mediator. We found that a further oxidized product, 17-oxodocosahexaenoic acid (17-oxoDHA), activates peroxisome proliferator-activated receptors γ (PPARγ) and PPARα in transcriptional assays and thus can be classified as an α/γ dual agonist. ESI mass spectroscopy and X-ray crystallographic analysis showed that 17-oxoDHA binds to PPARγ and PPARα covalently, making 17-oxoDHA the first of a novel class of PPAR agonists, the PPARα/γ dual covalent agonist. Furthermore, the covalent binding sites were identified as Cys285 for PPARγ and Cys275 for PPARα.
PubMed: 27337155
DOI: 10.1021/acschembio.6b00338
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.7 Å)
Structure validation

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