N-terminal reactivity

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Metabolite Name

Cucurbitacin B 2-Sulfate (1)
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Quilseconazole (1)
Pseudouridine 5'-Phosphate (1)
2'',6''-Di-O-Acetylononin (1)
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Ceftezole (1)
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Cis-P-Coumaric Acid 4-[Apiosyl-(1->2)-Glucoside] (1)
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2,6-Diamino-4-Hydroxy-5-Formamidopyrimidine (1)

First Public Date

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2014 (1)
2013 (1)

Classification

bacteria (1)

Study type

Transcription profiling by array (512)
RNA-seq of coding RNA (45)
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DNA-seq (1)
RNA-seq of coding RNA from single cells (1)
Methylation profiling by high throughput sequencing (1)

Release Date

2010 (135)
2008 (86)
2013 (83)
2015 (81)
2014 (70)
2011 (64)
2012 (63)
2016 (51)
2023 (46)
2009 (45)
2022 (43)
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2007 (37)
2020 (33)
2024 (26)
2005 (24)
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2019 (23)
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2004 (8)
2000 (7)
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2002 (4)
2003 (3)
2001 (3)
1999 (3)
1998 (2)
1997 (1)

Lab affiliation

University of Vienna, Faculty of Chemistry, Department of Analytical Chemistry (5)
Beijing National Laboratory for Molecular Sciences, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, China. (2)
Department of Chemical and Structural Biology, Weizmann Institute of Science, Rehovot, Israel (2)
Division of Medical Inflammation Research, Dept. Medical Biochemistry and Biophysics, Karolinska Institute, Sweden (2)
Lab Head (2)
Assistant Professor of Neurosurgery Department of Neurosurgery Houston Methodist Research Institute Weill Cornell Medical College (1)
Bioanalytical Mass Spectrometry group, Max-Planck-Institute for Biophysical Chemistry, Goettingen, Germany (1)
Biology department, Washington University in St Louis, MO, USA (1)
CBMN UMR5248 CNRS-Univ. Bordeaux (1)
CRG, UPF (1)
Center for Functional Protein Assemblies, Technical University of Germany, Germany (1)
Core Facility for Omics Sciences, IRCCS Istituto Giannina Gaslini, Genoa, Italy (1)
Dalian Institute of Chemical Physics, Chinese Academy of Sciences (1)
Department for Molecular and Applied Microbiology, Leibniz Institute for Natural Product Research and Infection Biology - Hans Knöll Institute Jena - Leibniz-HKI, Jena Germany (1)
Department of Analytical Chemistry, University of Vienna, Austria (1)
Department of Biotechnology, Technical University Delft, Julianalaan 67. 2682 BC Delft, The Netherlands (1)
Department of Chemistry The Scripps Research Institute Jupiter FL, USA (1)
Department of Chemistry, Ulsan National Institute of Science and Technology (1)
Department of Pharmaceutical Chemistry and Bioanalytics, Institute of Pharmacy, Martin Luther University Halle-Wittenberg, Kurt-Mothes-Str. 3, Halle/Saale D-01620, Germany Center for Structural Mass Spectrometry, Martin Luther University Halle-Wittenberg, Kurt-Mothes-Str. 3, Halle/Saale D-01620, Germany (1)
Department of Structural and Computational Biology, Max Perutz Labs, Campus Vienna Biocenter 5, 1030 Vienna, Austria (1)
Dept. Oncology Pathology, Karolinska Institutet and Scilifelab, Stockholm, Sweden (1)
Emory University (1)
Emory University, Department of Chemistry (1)
Faculty of Medicine, Health and Human Sciences, MacquarieUniversity. (1)
Head of Proteomics, Beatson Institute for Cancer Research (1)
IMBA - Institute of Molecular Biotechnology Dr. Bohrgasse 3 1030 Vienna Austria (1)
Istituto Zooprofilattico Sperimentale dell'Abruzzo e del Molise "G. Caporale" - Immunology and Serology Unit (1)
Jacqui Wood Cancer Centre, Medical Research Institute, Ninewells Hospital and Medical School, University of Dundee, James Arrott Drive, Dundee DD1 9SY, Scotland (1)
Khon Kaen University National Phenome Institute, Regional Science Park Northeast 1, Khon Kaen University, Khon Kaen, 40002, Thailand (1)
Laboratório de Biotecnologia, Centro de Biociências e Biotecnologia (CBB), Universidade Estadual do Norte Fluminense Darcy Ribeiro (UENF), Av. Alberto Lamego, Campos dos Goytacazes, RJ, Brazil. Unidade de Biologia Integrativa, Setor de Genômica e Proteômica, UENF, Campos dos Goytacazes, RJ, Brazil. (1)

Tags

xref:PubMed:22436172 (1)
pathogen (1)
pathogen:bacterium (1)

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NHS Carbamate Cross-Linkers Provide Complementary XL-MS Restraints via Preferential N-Terminal Targeting

Cross-linking mass spectrometry (XL-MS) has become a valuable tool for investigating the structural morphology and plasticity of proteins. Traditional cross-linkers contain two N-hydroxy succinimide (NHS) esters that mainly react with lysine residues. In this work, we optimized the in-solution react...

ORGANISM(S): Bos taurus (Bovine) Homo sapiens (Human)

2026-03-30 | PXD069252 | Pride

Identification of drought stress related genes in NatA depleted mutants

N-terminal protein acetylation is one of the most common protein modifications in eucaryotes and is catalyzed co-translationally by N-terminal aceytltransferases (Nats). Regarding the number of predictaed substrates, NatA is the main Nat complex in human and yeast and is composed of the catalytic su...

ORGANISM(S): Arabidopsis thaliana

2015-07-23 | E-GEOD-65414 | biostudies-arrayexpress

Reactivity of commercial antibodies targeting human histone H2B N-terminal tail on the Intel array platform

The aim of the study was to test the Intel array platform and map the H2B epitopes bound by commercial antibody reagents. We also tested the ability of SET7 PKMT to methylate Intel array peptides. We diluted antibody reagents 1:1000 and incubated dilutions on the silicon-based Intel array platorm. ...

ORGANISM(S): Oryctolagus cuniculus

2011-12-02 | E-GEOD-34034 | biostudies-arrayexpress

Effect of Pyridinecarboxaldehyde Functionalization on Reactivity and N-Terminal Protein Modification.

Not available

S-EPMC12042018 | biostudies-literature

Reactivity of the N-terminal region of fibronectin protein to transglutaminase 2 and factor XIIIA.

Not available

S-EPMC3173148 | biostudies-literature

Involvement of N- and C-terminal region of recombinant cervid prion protein in its reactivity to CWD and atypical BSE prions in real-time quaking-induced conversion reaction in the presence of high concentrations of tissue homogenates.

Not available

S-EPMC7757825 | biostudies-literature

Oryctolagus cuniculus