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Human peroxisome proliferator-activated receptor (ppar) delta ligand binding domain in complex with a synthetic agonist TIPP204
Analyse Human peroxisome proliferator-activated receptor (ppar) delta ligand binding… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 7VWF
- Type
- protein
- Length
- 516 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- UniProt
- Q03181
- Ligands
- B7G, K55
Structure
x-ray diffraction · 2 distinct chains.
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | — | protein | 258 | — | Q03181 |
| B | — | protein | 258 | — | Q03181 |
Ligands and binding sites
- B7G · heptyl beta-D-glucopyranoside · ligand · 2 copies · chains A, B
- K55 · (2S)-2-{4-butoxy-3-[({[2-fluoro-4-(trifluoromethyl) phenyl]carbonyl}amino)methyl]benzyl}butanoic acid · ligand · 2 copies · chains A, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Compared structures
- 7VWF · Human peroxisome proliferator-activated receptor (PPAR) delta ligand binding domain in… · the same entry in another collection · chain A against A, TM-score 1.00
Analyse
- Open in the research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides and crosslinks on the 3D structure
- Every structure of UniProt Q03181
- Elsewhere: RCSB PDB 7VWF · PDBe 7VWF · UniProt Q03181
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