PDB ID: 3PEQ
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Code | Name | Style | Show | Link | |
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3EQ | [(4-{butyl[2-methyl-4'-(methylsulfanyl)biphenyl-3-yl]sulfamoyl}naphthalen-1-yl)oxy]acetic acid | PoSSuM | |||
IOD | Iodide ion | PoSSuM | |||
JZR | Hexyl beta-D-glucopyranoside | PoSSuM |
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Download interaction data: 3PEQ
Structure summary
Code : | 3PEQ PDBj RCSB PDB PDBe | ||||||||||||
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Header : | TRANSCRIPTION/TRANSCRIPTION agonist | ||||||||||||
Title : | PPARd complexed with a phenoxyacetic acid partial agonist | ||||||||||||
Release Data : | 2011-10-12 | ||||||||||||
Compound : |
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Source : |
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Authors : | Lambert, M.H., Evans, K.A., Shearer, B.G., Wisnoski, D.D., Shi, D., Jin, J., Rivero, R.A., Sparks, S.M., Winegar, D.A., Billin, A.N., Britt, C., Way, J.M., Leesnitzer, L.M., Merrihew, R.V. | ||||||||||||
Keywords : | PPAR nuclear receptor, TRANSCRIPTION-TRANSCRIPTION agonist complex | ||||||||||||
Exp. method : | X-RAY DIFFRACTION ( 2.40 Å ) | ||||||||||||
Citation : |
Phenoxyacetic acid PPARd partial agonists for the treatment of type 2 diabetes: synthesis, optimization, and in vivo efficacy
Evans, K.A.,Shearer, B.G.,Wisnoski, D.D.
et al.
PubMed: 21414782 |
Reaction
Chain : | A, B |
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UniProt : | Q03181 (PPARD_HUMAN) |
Reaction : | - |