Academic cross-fertilization by public screening yields a remarkable class of protein phosphatase methylesterase-1 inhibitors.
about
The biogenesis of active protein phosphatase 2A holoenzymes: a tightly regulated process creating phosphatase specificityAdvancing Biological Understanding and Therapeutics Discovery with Small-Molecule ProbesThe pharmacological landscape and therapeutic potential of serine hydrolasesChanges in Carboxy Methylation and Tyrosine Phosphorylation of Protein Phosphatase PP2A Are Associated with Epididymal Sperm Maturation and MotilityDesign of activated serine–containing catalytic triads with atomic-level accuracyProtein Phosphatase Methyl-Esterase PME-1 Protects Protein Phosphatase 2A from Ubiquitin/Proteasome DegradationActivity-Based Protein Profiling of Oncogene-Driven Changes in Metabolism Reveals Broad Dysregulation of PAFAH1B2 and 1B3 in Cancer.Activity-based proteomic and metabolomic approaches for understanding metabolismIdentification of influenza endonuclease inhibitors using a novel fluorescence polarization assay.Metabolic profiling reveals PAFAH1B3 as a critical driver of breast cancer pathogenicity.A road map to evaluate the proteome-wide selectivity of covalent kinase inhibitors.How chemoproteomics can enable drug discovery and developmentExploring metabolic pathways and regulation through functional chemoproteomic and metabolomic platformsTarget deconvolution techniques in modern phenotypic profiling.Translational synthetic chemistry.Discovery and optimization of sulfonyl acrylonitriles as selective, covalent inhibitors of protein phosphatase methylesterase-1.A substrate-free activity-based protein profiling screen for the discovery of selective PREPL inhibitors.A high-throughput, multiplexed assay for superfamily-wide profiling of enzyme activity.The metabolic serine hydrolases and their functions in mammalian physiology and disease.Selective inhibitor of platelet-activating factor acetylhydrolases 1b2 and 1b3 that impairs cancer cell survival.Single-pot enzymatic synthesis of Dicer-substrate siRNAsMapping proteome-wide interactions of reactive chemicals using chemoproteomic platforms.Competitive activity-based protein profiling identifies aza-β-lactams as a versatile chemotype for serine hydrolase inhibition.Identification of selective covalent inhibitors of platelet activating factor acetylhydrolase 1B2 from the screening of an oxadiazolone-capped peptoid-azapeptoid hybrid library.Discovery of Small Molecule Kappa Opioid Receptor Agonist and Antagonist Chemotypes through a HTS and Hit Refinement Strategy.A LCMT1-PME-1 methylation equilibrium controls mitotic spindle sizeDAGLβ inhibition perturbs a lipid network involved in macrophage inflammatory responses.Selective inhibitors and tailored activity probes for lipoprotein-associated phospholipase A(2)Chemical approaches to study metabolic networksPP2A ligand ITH12246 protects against memory impairment and focal cerebral ischemia in mice.Proteome-wide reactivity profiling identifies diverse carbamate chemotypes tuned for serine hydrolase inhibition.A chemoproteomic platform to quantitatively map targets of lipid-derived electrophiles.Genetic amplification of PPME1 in gastric and lung cancer and its potential as a novel therapeutic target.Remodeling natural products: chemistry and serine hydrolase activity of a rocaglate-derived β-lactone.Development and optimization of piperidyl-1,2,3-triazole ureas as selective chemical probes of endocannabinoid biosynthesis.Discovery and optimization of piperidyl-1,2,3-triazole ureas as potent, selective, and in vivo-active inhibitors of α/β-hydrolase domain containing 6 (ABHD6)Determining target engagement in living systemsActivity-based probes for the study of proteases: recent advances and developments.Activity-based protein profiling: recent advances in probe development and applications.All roads lead to PP2A: exploiting the therapeutic potential of this phosphatase.
P2860
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P2860
Academic cross-fertilization by public screening yields a remarkable class of protein phosphatase methylesterase-1 inhibitors.
description
2011 nî lūn-bûn
@nan
2011 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի մարտին հրատարակված գիտական հոդված
@hy
2011年の論文
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2011年学术文章
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2011年学术文章
@zh-cn
2011年学术文章
@zh-hans
2011年学术文章
@zh-my
2011年学术文章
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2011年學術文章
@yue
name
Academic cross-fertilization b ...... e methylesterase-1 inhibitors.
@ast
Academic cross-fertilization b ...... e methylesterase-1 inhibitors.
@en
type
label
Academic cross-fertilization b ...... e methylesterase-1 inhibitors.
@ast
Academic cross-fertilization b ...... e methylesterase-1 inhibitors.
@en
prefLabel
Academic cross-fertilization b ...... e methylesterase-1 inhibitors.
@ast
Academic cross-fertilization b ...... e methylesterase-1 inhibitors.
@en
P2093
P2860
P356
P1476
Academic cross-fertilization b ...... e methylesterase-1 inhibitors.
@en
P2093
Anna E Speers
Daniel A Bachovchin
Daniel K Nomura
Gregory C Fu
Hugh Rosen
Jacob M Berlin
Justin T Mohr
Peter Chase
Peter S Hodder
Stephan C Schürer
P2860
P304
P356
10.1073/PNAS.1015248108
P407
P577
2011-03-11T00:00:00Z