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Comparative Molecular Simulation of Pparg Protein Interactions with Omega-3 and Omega-6 Lipid Mediators
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Outgoing claims: the papers this work cites, builds on, or argues with.
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CHARMM‐GUI: A web‐based graphical user interface for CHARMM
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Extension of the CHARMM general force field to sulfonyl‐containing compounds and its utility in biomolecular simulations
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Verification of protein structures: Patterns of nonbonded atomic interactions
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Rational discovery of a novel interface for a coactivator in the peroxisome proliferator‐activated receptor γ: Theoretical implications of impairment in type 2 diabetes mellitus
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VMD: Visual molecular dynamics
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Peroxisome proliferator-activated receptors (PPARs)
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Peroxisome proliferator-activated receptor structures: Ligand specificity, molecular switch and interactions with regulators
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Study of new interactions of glitazone’s stereoisomers and the endogenous ligand 15d-PGJ2 on six different PPAR gamma proteins
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Identification of putative metabolites of docosahexaenoic acid as potent PPARγ agonists and antidiabetic agents
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Design of PPAR-γ agonist based on algal metabolites and the endogenous ligand 15-deoxy-Δ12, 14-prostaglandin J2
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Fatty acids, eicosanoids and PPAR gamma
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Structural basis of the activation of PPARγ by the plasticizer metabolites MEHP and MINCH
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Atomic structure of mutant PPARγ LBD complexed with 15d‐PGJ 2 : Novel modulation mechanism of PPARγ/RXRα function by covalently bound ligands
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A dynamic niching genetic algorithm strategy for docking highly flexible ligands
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The role of nitrated fatty acids and peroxisome proliferator-activated receptor gamma in modulating inflammation
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Structural Insight into PPARγ Activation Through Covalent Modification with Endogenous Fatty Acids
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Identification of antidiabetic inhibitors from Allophylus villosus and Mycetia sinensis by targeting α-glucosidase and PPAR-γ: In-vitro, in-vivo, and computational evidence
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Partial Agonists Activate PPARγ Using a Helix 12 Independent Mechanism
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PPARs at the crossroads of lipid signaling and inflammation
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Dietary n-3 fatty acids and therapy for rheumatoid arthritis
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Characterization of Covalent Bond Formation between PPARγ and Oxo-Fatty Acids
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A Selective Modulator of Peroxisome Proliferator-Activated Receptor γ with an Unprecedented Binding Mode
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Prediction of Accurate Binding Modes Using Combination of Classical and Accelerated Molecular Dynamics and Free-Energy Perturbation Calculations: An Application to Toxicity Studies
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Differential Potencies of Naturally Occurring Regioisomers of Nitrolinoleic Acid in PPARγ Activation
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Automation of the CHARMM General Force Field (CGenFF) II: Assignment of Bonded Parameters and Partial Atomic Charges
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g_mmpbsa —A GROMACS Tool for High-Throughput MM-PBSA Calculations
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PPARs and Lipid Ligands in Inflammation and Metabolism
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A Second Generation Force Field for the Simulation of Proteins, Nucleic Acids, and Organic Molecules
inferredcites →https://doi.org/10.1021/jm060663copenalex-extracted
Structural Basis for the Structure−Activity Relationships of Peroxisome Proliferator-Activated Receptor Agonists
inferredcites →https://doi.org/10.1021/jm800733hopenalex-extracted
Crystal Structure of the Peroxisome Proliferator-Activated Receptor γ (PPARγ) Ligand Binding Domain Complexed with a Novel Partial Agonist: A New Region of the Hydrophobic Pocket Could Be Exploited for Drug Design
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The nuclear receptor PPARγ individually responds to serotonin‐ and fatty acid‐metabolites
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Pharmacological repression of PPARγ promotes osteogenesis
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Nuclear receptor transrepression pathways that regulate inflammation in macrophages and T cells
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Structural basis for the activation of PPARγ by oxidized fatty acids
inferredcites →https://doi.org/10.1038/s41467-018-07133-wopenalex-extracted
A structural mechanism for directing corepressor-selective inverse agonism of PPARγ
inferredcites →https://doi.org/10.1038/srep19940openalex-extracted
Allosteric Pathways in the PPARγ-RXRα nuclear receptor complex
inferredcites →https://doi.org/10.1038/srep34792openalex-extracted
Structural basis for PPAR partial or full activation revealed by a novel ligand binding mode
inferredcites →https://doi.org/10.1046/j.1432-1033.2003.03937.xopenalex-extracted
Binding analyses between Human PPARγ–LBD and ligands
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Polymorphic transitions in single crystals: A new molecular dynamics method
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Electrostatics of nanosystems: Application to microtubules and the ribosome
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Structural determinants of ligand binding selectivity between the peroxisome proliferator-activated receptors
inferredcites →https://doi.org/10.1074/jbc.m111.294785openalex-extracted
Identification and Mechanism of 10-Carbon Fatty Acid as Modulating Ligand of Peroxisome Proliferator-activated Receptors
inferredcites →https://doi.org/10.1074/jbc.m802040200openalex-extracted
Structural and Biochemical Basis for the Binding Selectivity of Peroxisome Proliferator-activated Receptor γ to PGC-1α
inferredcites →https://doi.org/10.1079/pns2002173openalex-extracted
A role for the peroxisome proliferator-activated receptor α in T-cell physiology and ageing immunobiology
inferredcites →https://doi.org/10.1080/07315724.2001.10719008openalex-extracted
Types of Dietary Fat and Risk of Coronary Heart Disease: A Critical Review
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Probing intermolecular interactions and binding stability of kaempferol, quercetin and resveratrol derivatives with PPAR-γ: docking, molecular dynamics and MM/GBSA approach to reveal potent PPAR- γ agonist against cancer
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Computational analysis of single nucleotide polymorphisms (SNPs) in PPAR gamma associated with obesity, diabetes and cancer
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Cutoff Errors in the Ewald Summation Formulae for Point Charge Systems
inferredcites →https://doi.org/10.1093/ajcn/75.1.119openalex-extracted
Unsaturated fatty acids selectively induce an inflammatory environment in human endothelial cells
inferredcites →https://doi.org/10.1093/carcin/bgg131openalex-extracted
Activation of PPAR in colon tumor cell lines by oxidized metabolites of linoleic acid, endogenous ligands for PPAR
inferredcites →https://doi.org/10.1124/mol.111.076216openalex-extracted
Mode of Peroxisome Proliferator-Activated Receptor γ Activation by Luteolin
inferredcites →https://doi.org/10.1146/annurev.med.53.082901.104018openalex-extracted
The Mechanisms of Action of PPARs
inferredcites →https://doi.org/10.1155/2010/861238openalex-extracted
Virtual Screening as a Technique for PPAR Modulator Discovery
inferredcites →https://doi.org/10.1186/s40001-023-01477-wopenalex-extracted
PPARG is a potential target of Tanshinone IIA in prostate cancer treatment: a combination study of molecular docking and dynamic simulation based on transcriptomic bioinformatics
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Generation and Dietary Modulation of Anti-Inflammatory Electrophilic Omega-3 Fatty Acid Derivatives
inferredcites →https://doi.org/10.1538/expanim.60.7openalex-extracted
Lipid Mediators in Life Science
inferredcites →https://doi.org/10.2147/dmso.s265399openalex-extracted
Anti-Diabetic Effect of Telmisartan Through its Partial PPARγ-Agonistic Activity
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STABILITY OF OMEGA-3 COMPOUNDS COMPLEX WITH PPAR-γ RECEPTOR AS AN ANTI-OBESITY USING MOLECULAR DYNAMIC SIMULATION
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Molecular Modeling Study for the Design of Novel Peroxisome Proliferator-Activated Receptor Gamma Agonists Using 3D-QSAR and Molecular Docking
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The Plasma Oxylipin Signature Provides a Deep Phenotyping of Metabolic Syndrome Complementary to the Clinical Criteria
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Osteoarthritis: Role of Peroxisome Proliferator-Activated Receptors
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