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Azalysine Analogues as Probes for Protein Lysine Deacetylation and Demethylation
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/anie.200501705openalex-snapshot
An Aldimine Cross‐Coupling for the Diastereoselective Synthesis of Unsymmetrical 1,2‐Diamines
inferredcites →https://doi.org/10.1002/anie.201103754openalex-snapshot
A Direct Method for Site‐Specific Protein Acetylation
inferredcites →https://doi.org/10.1002/jbt.2570010106openalex-snapshot
Oxidative metabolism of some hydrazine derivatives by rat liver and lung tissue fractions
inferredcites →https://doi.org/10.1007/978-1-4419-6382-6openalex-snapshot
Post-Translational Modifications in Health and Disease
inferredcites →https://doi.org/10.1007/s13148-010-0012-4openalex-snapshot
Histone deacetylase (HDAC) inhibitors in recent clinical trials for cancer therapy
inferredcites →https://doi.org/10.1016/j.bbapap.2010.01.021openalex-snapshot
Sirtuin chemical mechanisms
inferredcites →https://doi.org/10.1016/j.bioorg.2009.10.001openalex-snapshot
Substrate specificity of SIRT1-catalyzed lysine Nε-deacetylation reaction probed with the side chain modified Nε-acetyl-lysine analogs
inferredcites →https://doi.org/10.1016/j.bmc.2010.06.035openalex-snapshot
N-Modified lysine containing inhibitors for SIRT1 and SIRT2
inferredcites →https://doi.org/10.1016/j.bmcl.2006.04.075openalex-snapshot
Nε-Thioacetyl-lysine: A multi-facet functional probe for enzymatic protein lysine Nε-deacetylation
inferredcites →https://doi.org/10.1016/j.bmcl.2009.04.028openalex-snapshot
Synthesis and reactivity of novel γ-phosphate modified ATP analogues
inferredcites →https://doi.org/10.1016/j.cbpa.2007.07.014openalex-snapshot
LSD1 and the chemistry of histone demethylation
inferredcites →https://doi.org/10.1016/j.cell.2007.02.005openalex-snapshot
Chromatin Modifications and Their Function
inferredcites →https://doi.org/10.1016/j.cell.2008.05.020openalex-snapshot
SnapShot: p53 Posttranslational Modifications
inferredcites →https://doi.org/10.1016/j.chembiol.2006.05.004openalex-snapshot
Histone H3 Lysine 4 Demethylation Is a Target of Nonselective Antidepressive Medications
inferredcites →https://doi.org/10.1016/j.chembiol.2008.09.009openalex-snapshot
Mechanisms and Molecular Probes of Sirtuins
inferredcites →https://doi.org/10.1016/j.dnarep.2005.06.013openalex-snapshot
Sirtuins (histone deacetylases III) in the cellular response to DNA damage—Facts and hypotheses
inferredcites →https://doi.org/10.1016/j.drudis.2009.06.008openalex-snapshot
Histone acetyl transferases as emerging drug targets
inferredcites →https://doi.org/10.1016/j.gde.2008.01.012openalex-snapshot
The emerging field of dynamic lysine methylation of non-histone proteins
inferredcites →https://doi.org/10.1016/j.gene.2005.09.010openalex-snapshot
Acetylation and deacetylation of non-histone proteins
inferredcites →https://doi.org/10.1016/j.molcel.2007.07.012openalex-snapshot
Modulation of p53 Function by SET8-Mediated Methylation at Lysine 382
inferredcites →https://doi.org/10.1016/j.str.2008.05.015openalex-snapshot
Structural Insights into Intermediate Steps in the Sir2 Deacetylation Reaction
inferredcites →https://doi.org/10.1016/j.tibs.2008.01.003openalex-snapshot
LSD1: oxidative chemistry for multifaceted functions in chromatin regulation
inferredcites →https://doi.org/10.1016/s0021-9258(18)50153-8openalex-snapshot
Esters of Methanesulfonic Acid as Irreversible Inhibitors of Acetylcholinesterase
inferredcites →https://doi.org/10.1016/s0076-6879(02)53056-1openalex-snapshot
SIR2 Family of NAD+-Dependent Protein Deacetylases
inferredcites →https://doi.org/10.1021/bi034959lopenalex-snapshot
Sir2 Regulation by Nicotinamide Results from Switching between Base Exchange and Deacetylation Chemistry
inferredcites →https://doi.org/10.1021/bi0618621openalex-snapshot
trans-2-Phenylcyclopropylamine Is a Mechanism-Based Inactivator of the Histone Demethylase LSD1
inferredcites →https://doi.org/10.1021/bi100299ropenalex-snapshot
Structurally Designed trans-2-Phenylcyclopropylamine Derivatives Potently Inhibit Histone Demethylase LSD1/KDM1,,
inferredcites →https://doi.org/10.1021/bi700414bopenalex-snapshot
Mechanistic Analysis of a Suicide Inactivator of Histone Demethylase LSD1
inferredcites →https://doi.org/10.1021/bi700664yopenalex-snapshot
Structural Basis for the Inhibition of the LSD1 Histone Demethylase by the Antidepressant trans-2-Phenylcyclopropylamine,
inferredcites →https://doi.org/10.1021/bi7013294openalex-snapshot
Mechanism-Based Inhibition of Sir2 Deacetylases by Thioacetyl-Lysine Peptide
inferredcites →https://doi.org/10.1021/bi800767topenalex-snapshot
Plasmodium falciparum Sir2 is an NAD+-Dependent Deacetylase and an Acetyllysine-Dependent and Acetyllysine-Independent NAD+ Glycohydrolase
inferredcites →https://doi.org/10.1021/cb200171dopenalex-snapshot
Kinase Consensus Sequences: A Breeding Ground for Crosstalk
inferredcites →https://doi.org/10.1021/cb6002306openalex-snapshot
Histone Citrullination by Protein Arginine Deiminase: Is Arginine Methylation a Green Light or a Roadblock?
inferredcites →https://doi.org/10.1021/ja0602748openalex-snapshot
A Mechanism-Based Inactivator for Histone Demethylase LSD1
inferredcites →https://doi.org/10.1021/ja070162wopenalex-snapshot
Sir2 Deacetylases Exhibit Nucleophilic Participation of Acetyl-Lysine in NAD+ Cleavage
inferredcites →https://doi.org/10.1021/ja101557kopenalex-snapshot
Biochemical, Structural, and Biological Evaluation of Tranylcypromine Derivatives as Inhibitors of Histone Demethylases LSD1 and LSD2
inferredcites →https://doi.org/10.1021/ja103954uopenalex-snapshot
Site-Specific Introduction of an Acetyl-Lysine Mimic into Peptides and Proteins by Cysteine Alkylation
inferredcites →https://doi.org/10.1021/ja807269jopenalex-snapshot
Highly Dissociative and Concerted Mechanism for the Nicotinamide Cleavage Reaction in Sir2Tm Enzyme Suggested by Ab Initio QM/MM Molecular Dynamics Simulations
inferredcites →https://doi.org/10.1021/ja909996popenalex-snapshot
Comparative Analysis of Small Molecules and Histone Substrate Analogues as LSD1 Lysine Demethylase Inhibitors
inferredcites →https://doi.org/10.1021/ja910342dopenalex-snapshot
Transition State of ADP-Ribosylation of Acetyllysine Catalyzed by Archaeoglobus fulgidus Sir2 Determined by Kinetic Isotope Effects and Computational Approaches
inferredcites →https://doi.org/10.1021/jo01333a048openalex-snapshot
Removal of benzyl-type protecting groups from peptides by catalytic transfer hydrogenation with formic acid
inferredcites →https://doi.org/10.1038/227680a0openalex-snapshot
Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4
inferredcites →https://doi.org/10.1038/cr.2011.22openalex-snapshot
Regulation of chromatin by histone modifications
inferredcites →https://doi.org/10.1038/nature06092openalex-snapshot
p53 is regulated by the lysine demethylase LSD1
inferredcites →https://doi.org/10.1038/nchembio.111openalex-snapshot
Chemical probes for histone-modifying enzymes
inferredcites →https://doi.org/10.1038/nrd2133openalex-snapshot
Anticancer activities of histone deacetylase inhibitors
inferredcites →https://doi.org/10.1038/nrg2485openalex-snapshot
The many roles of histone deacetylases in development and physiology: implications for disease and therapy
inferredcites →https://doi.org/10.1038/onc.2008.436openalex-snapshot
Salermide, a Sirtuin inhibitor with a strong cancer-specific proapoptotic effect
inferredcites →https://doi.org/10.1039/b617185kopenalex-snapshot
N ε -Methanesulfonyl-lysine as a non-hydrolyzable functional surrogate for N ε -acetyl-lysine
inferredcites →https://doi.org/10.1039/c0mb00033gopenalex-snapshot
Sirtuin mechanism and inhibition: explored with Nε-acetyl-lysine analogs
inferredcites →https://doi.org/10.1039/c1cc13515eopenalex-snapshot
Accessing the disallowed conformations of peptides employing amide-to-imidate modification
inferredcites →https://doi.org/10.1042/bj20021321openalex-snapshot
Histone deacetylases (HDACs): characterization of the classical HDAC family
inferredcites →https://doi.org/10.1055/s-1991-26511openalex-snapshot
Sodium Cyanoborohydride Reduction of (Benzyloxycarbonyl)- and (tert-Butoxycarbonyl)hydrazones
inferredcites →https://doi.org/10.1073/pnas.0610993104openalex-snapshot
Long-distance combinatorial linkage between methylation and acetylation on histone H3 N termini
inferredcites →https://doi.org/10.1074/jbc.c200578200openalex-snapshot
Acetylation of p53 Inhibits Its Ubiquitination by Mdm2
inferredcites →https://doi.org/10.1074/jbc.m109.024521openalex-snapshot
Structure-based Mechanism of ADP-ribosylation by Sirtuins
inferredcites →https://doi.org/10.1074/jbc.m707613200openalex-snapshot
Acetylation-dependent ADP-ribosylation by Trypanosoma brucei Sir2
inferredcites →https://doi.org/10.1097/jcp.0b013e31820469eaopenalex-snapshot
Advances Pertaining to the Pharmacology and Interactions of Irreversible Nonselective Monoamine Oxidase Inhibitors
inferredcites →https://doi.org/10.1101/gad.1467506openalex-snapshot
Mammalian sirtuins—emerging roles in physiology, aging, and calorie restriction
inferredcites →https://doi.org/10.1111/j.1742-4658.2009.07142.xopenalex-snapshot
New roles of flavoproteins in molecular cell biology: Histone demethylase LSD1 and chromatin
inferredcites →https://doi.org/10.1111/j.1742-4658.2009.07427.xopenalex-snapshot
Side chain specificity of ADP‐ribosylation by a sirtuin
inferredcites →https://doi.org/10.1126/science.1175371openalex-snapshot
Lysine Acetylation Targets Protein Complexes and Co-Regulates Major Cellular Functions
inferredcites →https://doi.org/10.1128/mcb.20.22.8458-8467.2000openalex-snapshot
Multiple C-Terminal Lysine Residues Target p53 for Ubiquitin-Proteasome-Mediated Degradation
inferredcites →https://doi.org/10.1139/jpn.0730openalex-snapshot
Amine oxidases and their inhibitors: what can they tell us about neuroprotection and the development of drugs for neuropsychiatric disorders?
inferredcites →https://doi.org/10.1146/annurev.biochem.74.082803.133500openalex-snapshot
The Biochemistry of Sirtuins
inferredcites →https://doi.org/10.1158/1078-0432.ccr-09-1293openalex-snapshot
Novel Oligoamine Analogues Inhibit Lysine-Specific Demethylase 1 and Induce Reexpression of Epigenetically Silenced Genes
inferredcites →https://doi.org/10.1158/1541-7786.mcr-07-0324openalex-snapshot
Histone Deacetylase Inhibitors: Overview and Perspectives
inferredcites →https://doi.org/10.1159/000350087openalex-snapshot
Short-Term Effects of Nose-Only Cigarette Smoke Exposure on Glutathione Redox Homeostasis, Cytochrome P450 1A1/2 and Respiratory Enzyme Activities in Mice Tissues
inferredcites →https://doi.org/10.2174/0929867043455675openalex-snapshot
SIR2: The Biochemical Mechanism of NAD+-Dependent Protein Deacetylation and ADP-Ribosyl Enzyme Intermediates
inferredcites →https://doi.org/10.3892/ijo_00000049openalex-snapshot
Histone deacetylase inhibitors: Apoptotic effects and clinical implications (Review)
inferredcites →https://doi.org/10.7150/ijbs.7.575openalex-snapshot
Mammalian Sirtuins and Energy Metabolism
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Mariannamides C and D, Two New Lipohexapeptides, Isolated from Mariannaea Elegans NBRC102301
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Isoxazole‐Derived Amino Acids are Bromodomain‐Binding Acetyl‐Lysine Mimics: Incorporation into Histone H4 Peptides and Histone H3
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Mechanism‐Based Inhibitors of the Human Sirtuin 5 Deacylase: Structure–Activity Relationship, Biostructural, and Kinetic Insight
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Chemische Epigenetik: der Einfluss chemischer und chemo‐biologischer Techniken auf die Zielstruktur‐Validierung von Bromodomänen
inferred← citeshttps://doi.org/10.1002/ange.202200303openalex-snapshot
Chemical Biology Tools for Protein Lysine Acylation
inferred← citeshttps://doi.org/10.1002/anie.201602908openalex-snapshot
Isoxazole‐Derived Amino Acids are Bromodomain‐Binding Acetyl‐Lysine Mimics: Incorporation into Histone H4 Peptides and Histone H3
inferred← citeshttps://doi.org/10.1002/anie.201709050openalex-snapshot
Mechanism‐Based Inhibitors of the Human Sirtuin 5 Deacylase: Structure–Activity Relationship, Biostructural, and Kinetic Insight
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Chemical Epigenetics: The Impact of Chemical and Chemical Biology Techniques on Bromodomain Target Validation
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Chemical Biology Tools for Protein Lysine Acylation
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A Fluorescent Probe for Imaging Sirtuin Activity in Living Cells, Based on One‐Step Cleavage of the Dabcyl Quencher
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Photo Cross‐Linking Probes Containing ϵ‐ N ‐Thioacyllysine and ϵ‐ N ‐Acyl‐(δ‐aza)lysine Residues
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Practical synthesis of novel phosphonopeptides containing AibP
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Novel Therapeutics Targeting Epigenetics
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Bicyclic 5-6 Systems: Four Heteroatoms 1:3
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Targeting Sirtuins: Substrate Specificity and Inhibitor Design
inferred← citeshttps://doi.org/10.1016/j.apsb.2019.05.007openalex-snapshot
A one-step specific assay for continuous detection of sirtuin 2 activity
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Design of small molecule epigenetic modulators
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The mimics of Nε-acyl-lysine derived from cysteine as sirtuin inhibitors
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Acetyl-CoA and the regulation of metabolism: mechanisms and consequences
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Chemical Methods for Encoding and Decoding of Posttranslational Modifications
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Identification of a sirtuin 3 inhibitor that displays selectivity over sirtuin 1 and 2
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Cysteine derivatives as acetyl lysine mimics to inhibit zinc-dependent histone deacetylases for treating cancer
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The growing structural and functional complexity of the LSD1/KDM1A histone demethylase
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Synthesis of lactam-bridged cyclic peptides using sequential olefin metathesis and diimide reduction reactions
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Small molecule epigenetic inhibitors targeted to histone lysine methyltransferases and demethylases
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Small Changes Make the Difference for SIRT2: Two Different Binding Modes for 3-Arylmercapto-Acylated Lysine Derivatives
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Structure-Based Identification of Potent Lysine-Specific Demethylase 1 Inhibitor Peptides and Temporary Cyclization to Enhance Proteolytic Stability and Cell Growth-Inhibitory Activity
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Covalent Peptide LSD1 Inhibitor Specifically Recognizes Cys360 in the Enzyme-Active Region
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Uncovering Robust Delactoylase and Depyruvoylase Activities of HDAC Isoforms
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Lysine-Specific Demethylase 1 (LSD1) Inhibitors: Peptides as an Emerging Class of Therapeutics
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Hyperbranched Polyester-Based Fluorescent Probe for Histone Deacetylase via Aggregation-Induced Emission
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A Selective Phenelzine Analogue Inhibitor of Histone Demethylase LSD1
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Development of a Fluorogenic Probe with a Transesterification Switch for Detection of Histone Deacetylase Activity
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Hydrazide Mimics for Protein Lysine Acylation To Assess Nucleosome Dynamics and Deubiquitinase Action
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The nucleophilic amino group of lysine is central for histone lysine methyltransferase catalysis
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Methylation of geometrically constrained lysine analogues by histone lysine methyltransferases
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Mechanism-based inhibitors of SIRT2: structure–activity relationship, X-ray structures, target engagement, regulation of α-tubulin acetylation and inhibition of breast cancer cell migration
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Mitochondria-targeted inhibitors of the human SIRT3 lysine deacetylase
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Probing lysine posttranslational modifications by unnatural amino acids
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Installation of electrophiles onto the C-terminus of recombinant ubiquitin and ubiquitin-like proteins
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Histone probes for reader and eraser investigations
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Sirtuin Catalysis and Regulation
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N ɛ -acetyl lysine derivatives with zinc binding groups as novel HDAC inhibitors
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Selective inhibitors of SIRT2 regulate perinuclear α-tubulin acetylation, migration, and invasion of breast cancer cells
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Epigenetic pathway targets for the treatment of disease: accelerating progress in the development of pharmacological tools: IUPHAR Review 11
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A Structure–Activity Relationship Study of SNAIL1 Peptides as Inhibitors of Lysine-Specific Demethylase 1
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Insight into the binding mode of a novel LSD1 inhibitor by molecular docking and molecular dynamics simulations
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Stereochemistries of Mariannamides C and D, Two Lipohexapeptides, Isolated from Mariannaea elegans NBRC102301
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Development of Sirtuin Fluorescence Probes and Medicinal Chemistry Research Targeting SIRT Family
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Investigations of sirtuin metabolism
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