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Unknown
(214)
Proteomics
(60)
Transcriptomics
(44)
Genomics
(7)
Metabolomics
(3)
Organisms
Andropogon gerardi
(53)
Bacteria
(53)
Canis lupus familiaris
(53)
Cnidaria
(53)
Cricetulus griseus
(53)
Eukaryota
(53)
Fasciola
(53)
Hepatitis B virus
(53)
Human betaherpesvirus 5
(53)
Madurella mycetomatis
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Mesocricetus auratus
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Miscanthus x giganteus
(53)
Homo sapiens
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Candida dubliniensis
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Organisms
Mus musculus
(3)
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Repository
pride
(53)
biostudies-arrayexpress
(47)
ENA
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geo
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MetaboLights
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MetabolomicsWorkbench
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Cell culture
(17)
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(2)
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(1)
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(1)
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(1)
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(1)
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(1)
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(1)
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(1)
Technology Type
Mass Spectrometry
(54)
Shotgun proteomics
(26)
Bottom-up proteomics
(20)
Chemical cross-linking coupled with mass spectrometry proteomics
(5)
Affinity purification coupled with mass spectrometry proteomics
(4)
Data-dependent acquisition
(4)
Mass spectrometry assay
(1)
Mass spectrometry
(1)
ESI
(1)
Gel-based experiment
(1)
Instrument Platform
Liquid Chromatography MS - positive - reverse-phase
(2)
Genetix aQuire
(1)
GenePix 4000B scanner
(1)
Axon- GenePix4000B
(1)
Illumina MiSeq
(1)
NextSeq 500
(1)
LTQ Orbitrap Velos
(1)
Q Exactive
(1)
Liquid Chromatography MS - negative - reverse-phase
(1)
Publication Date
2025
(21)
2010
(18)
2018
(7)
2013
(7)
2023
(6)
2021
(6)
2015
(6)
2012
(5)
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(5)
2020
(5)
2014
(4)
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(4)
2009
(3)
2016
(3)
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(3)
2026
(1)
2024
(1)
2022
(1)
2019
(1)
Metabolite Name
3-[(2,2-Dichlorovinyl)thio]-L-alanine
(1)
O,O,S-Trimethyl phosphorothioate
(1)
5alpha-Androstenone
(1)
Indalpine
(1)
(R)-5-Hydroxy-2-(4-hydroxyphenyl)-7-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)chroman-4-one
(1)
N-Hydroxysuccinimide
(1)
1,2,4,5,7,8-Hexathionane
(1)
(8R,9R,10R,13S,14S)-10,13-Dimethyl-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthrene-3,17-diol
(1)
1-Chlorodibenzo-p-dioxin
(1)
1-Methyl-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-5-ol
(1)
(2R,3R,4R,5S,6S)-3,4,5,6-Tetrahydroxyoxane-2-carboxylic acid
(1)
2,3-dihydroxyisovaleric acid
(1)
Syringol sulfate
(1)
(E)-8-(3,4-Dimethoxystyryl)-7-methyl-1,3-dipropylxanthine
(1)
Octoxynol-1
(1)
Nonoxinol
(1)
6-(3,4-Methylenedioxyphenyl)-3,5-hexadien-2-one
(1)
2,3,4-Trichlorophenol
(1)
(1S,4S,9R,10S,13R,14R)-5,5,9,14-Tetramethyltetracyclo[11.2.1.01,10.04,9]hexadec-6-ene
(1)
Phenyl phosphonothioate
(1)
Isocaproylglycine
(1)
2-Butenoylglycine
(1)
Phygrine
(1)
N-Phenylpropionamide
(1)
N,N'-Dibenzylethylenediamine
(1)
N-(6-Chloro-9h-pyrido[3,4-b]indol-8-yl)-3-pyridinecarboxamide
(1)
(Z)-1-[4-(4-Diethylaminobutoxy)phenyl]-1,2-diphenyl-2-chloro-ethylene
(1)
Tri-P-cresyl phosphate
(1)
1-Chlorobutane
(1)
Piperidine, 1-(4-(1-methyl-1-(4-methylcyclohexyl)ethoxy)phenyl)-, cis-
(1)
First Public Date
2014
(3)
2023
(1)
2017
(1)
Modification
15.994915
(5)
42.010565
(5)
-17.026549
(4)
58.005479
(4)
45.029395
(3)
10.008269
(2)
3x(2)H labeled N6-acetyl-L-lysine
(2)
4x(15)N labeled L-arginine
(2)
+3amu)
(1)
32.056407
(1)
4-tetrahydrothiazine-3-carboxylic acid
(1)
47.036105
(1)
56.026215
(1)
59.036279
(1)
Study type
Transcription profiling by array
(37)
Unknown experiment type
(3)
Proteomic profiling by array
(3)
ChIP-seq
(2)
RNA-seq of coding RNA
(2)
Release Date
2025
(29)
2022
(27)
2021
(26)
2010
(23)
2024
(18)
2019
(18)
2018
(15)
2012
(13)
2020
(13)
2017
(13)
2016
(11)
2013
(10)
2023
(9)
2014
(7)
2011
(7)
2015
(6)
2008
(6)
2009
(5)
2026
(2)
2006
(2)
2004
(1)
Lab affiliation
NCI/NIH CSB
(10)
VIB, department of Medical Protein Research Ugent, department of Biochemistry
(2)
1 Department of Genetics, Harvard Medical School, Boston, MA 02115
(1)
1 The Rosalind Franklin Institute, Oxfordshire, United Kingdom 2 Department of Pharmacology, University of Oxford
(1)
1. University of Victoria Genome BC Proteomics Centre, University of Victoria, Victoria, British Columbia, Canada 2. Segal Cancer Proteomics Centre, Lady Davis Institute, Jewish General Hospital, McGill University, Montreal, Quebec, Canada 3. Department of Biochemistry and Microbiology, University of Victoria, Victoria, British Columbia, Canada 4. Gerald Bronfman Department of Oncology, Jewish General Hospital, Montreal, Quebec, Canada
(1)
1VIB Center for Medical Biotechnology, VIB, Ghent, 9052, Belgium 2Department of Biomolecular Medicine, Ghent University, Ghent, 9052, Belgium
(1)
Center for Theragnosis, Korea Institute of Science and Technology, Seoul 02792, Korea
(1)
DKFZ Heidelberg
(1)
Department of Biochemistry, Ghent University, Belgium
(1)
Department of Biochemistry, University of California, Riverside Riverside, CA, USA
(1)
Department of Chemistry, Umeå University, Umeå, Sweden
(1)
Department of Chemistry, University of Illinois Chicago, Chicago, USA
(1)
Department of Molecular Biology, University of Bergen, N-5020 Bergen
(1)
Department of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, NY 10461, USA
(1)
Department of Parasitology, Faculty of Science, Charles University, BIOCEV, Prague, Czech Republic ORCID logohttp://orcid.org/0000-0001-6976-8446
(1)
Department of biochemistry, molecular and structural biology Jozef Stefan Institute Ljubljana Slovenia
(1)
Ghent University Department of Biochemistry B-9000 Ghent Belgium
(1)
Ghent University, VIB
(1)
Harvard Medical School, Department of Cell Biology Howard Hughes Medical Institute
(1)
Head of Medical Microbiology and Immunology, Department of Health Science and Technology, Medical Faculty, Aalborg Universtity, Denmark
(1)
Istituto di Cristallografia, Consiglio Nazionale delle Ricerche, Sede Secondaria di Catania, Via Paolo Gaifami 18, 95126 Catania, Italy
(1)
Jožef Stefan Institute, Department of Biochemistry and Molecular and Structural Biology, Jamova cesta 39, 1000 Ljubljana, Slovenia Centre of Excellence for Integrated Approaches in Chemistry and Biology of Proteins (CIPKeBiP), Jamova cesta 39, 1000 Ljubljana, Slovenia
(1)
Leibniz-Institut für Analytische Wissenschaften – ISAS – e.V. Head of the department of Systems Analysis
(1)
Leibniz-Institut für Analytische Wissenschaften – ISAS – e.V. Otto-Hahn-Straße 6b 44227 Dortmund, Germany P: +49 (0)2 31.13 92-100 F: +49 (0)2 31.13 92-200 www.isas.de
(1)
MRC Laboratory of Molecular Biology Francis Crick Avenue Cambridge CB2 0QH United Kingdom
(1)
Medical Biotechnology Center, VIB, 9000 Ghent, Belgium and Department of Biochemistry, Ghent University, 9000 Ghent, Belgium
(1)
Medical Biotechnology Center, VIB, B-9000 Ghent, Belgium, Department of Biochemistry, Ghent University, B-9000 Ghent, Belgium.
(1)
NIH/NCI CSB
(1)
Nuffield Department of Medicine
(1)
Nutrigenomics and Fish Growth Endocrinology Group, Institute of Aquaculture Torre de la Sal (IATS-CSIC), 12595 Ribera de Cabanes, Castellón, Spain
(1)
Tags
xref:PubMed:29163519
(1)
xref:PubMed:17785846
(1)
xref:PubMed:18483551
(1)
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Gas phase reactivity of carboxylates with N-hydroxysuccinimide esters.
Not available
S-EPMC4654944
|
biostudies-literature
Cite
Covalent modification of gaseous peptide ions with N-hydroxysuccinimide ester reagent ions.
Not available
S-EPMC3010255
|
biostudies-literature
Cite
N-Hydroxysuccinimide-Modified Ethynylphosphonamidates Enable the Synthesis of Configurationally Defined Protein Conjugates.
Not available
S-EPMC7003776
|
biostudies-literature
Cite
Antibody conjugation to carboxyl-modified microspheres through N-hydroxysuccinimide chemistry for automated immunoassay applications: A general procedure.
Not available
S-EPMC6594677
|
biostudies-literature
Cite
Site-Specific Protein Labeling with N-Hydroxysuccinimide-Esters and the Analysis of Ubiquitin Ligase Mechanisms.
Not available
S-EPMC6093203
|
biostudies-literature
Cite
Gas-phase conjugation to arginine residues in polypeptide ions via N-hydroxysuccinimide ester-based reagent ions.
Not available
S-EPMC3404623
|
biostudies-literature
Cite
Facile spectrophotometric assay of molar equivalents of N-hydroxysuccinimide esters of monomethoxyl poly-(ethylene glycol) derivatives.
Not available
S-EPMC3542108
|
biostudies-literature
Cite
Differential binding of tropomyosin isoforms to actin modified with m-maleimidobenzoyl-N-hydroxysuccinimide ester and fluorescein-5-isothiocyanate.
Not available
S-EPMC2739935
|
biostudies-literature
Cite
Direct Cα-heteroarylation of structurally diverse ethers
via
a mild
N
-hydroxysuccinimide mediated cross-dehydrogenative coupling reaction.
Not available
S-EPMC6094177
|
biostudies-literature
Cite
An accurate TMT-based approach to quantify and model lysine susceptibility to conjugation via N-hydroxysuccinimide esters in a monoclonal antibody.
Not available
S-EPMC6281681
|
biostudies-literature
Cite
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