Fp-biotin - OmicsDI

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Schizophyllum commune H4-8 (28)
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Metabolite Name

Riboflavin (6)
FP-biotin (5)
Succinyladenosine (5)
L-Histidine (5)
Taurine (5)
L-Glutamine (5)
Deoxyinosine (5)
Deoxyribose (5)
Guanosine (5)
Thymidine (5)
Uridine (5)
N-[(3s)-2-Oxotetrahydrofuran-3-Yl]butanamide (4)
Glycylprolylarginine (4)
Glucosyl 6-hydroxy-2,6-dimethyl-2E,7-octadienoate (4)
(3S,5R,6R,7E)-3,5,6-Trihydroxy-7-megastigmen-9-one (4)
Phosphate (4)
Deoxypyridinoline (4)
Fasoracetam (4)
Jasmolone (4)
(+/-)-Pelletierine (4)
Hymenoxon (4)
28-Norbrassinolide (4)
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Tazobactam (4)
2'-Deoxyuridine (4)
Trinexapac-ethyl (4)
(S)-Reticuline (4)
Vanillin (4)
Hydroquinone (4)

First Public Date

2014 (1)

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Transcription profiling by array (23)
RNA-seq of coding RNA (3)
Transcription profiling by SAGE (1)
ChIP-chip by tiling array (1)
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2011 (8)
2013 (5)
2012 (5)
2014 (4)
2010 (4)
2015 (3)
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2007 (2)
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2008 (1)

Lab affiliation

Boston College (3)
Analytics Core Facility Essen (ACE), Chemische Biologie, Universität Duisburg-Essen, ZMB, Germany (3)
Department of Biology, IISER Pune (2)
Host-Microbe interactions group, the department of medical biology, UiT - The Arctic University of Norway, Tromsø, Norway. (1)
Department of Molecular Physiology, Leiden Institute of Chemistry, Leiden University, Einsteinweg 55, 2333 CC, Leiden, The Netherlands (1)
Department of Molecular Physiology, Leiden Institute of Chemistry, Leiden University, Einsteinweg 55, 2333 CC, Leiden, Netherlands. (1)
Associate Professor, Department of Biology, IISER Pune (1)
Clayton Foundation Laboratories for Peptide Biology The Salk Institute for Biological Studies 10010 North Torrey Pines Road La Jolla, CA, USA (1)
Department of Pathology, Stanford University School of Medicine; Stanford, CA, USA (1)
USACEHR (1)
Department of Obstetrics and Gynecology, Medical University of Graz, Austria (1)
Department of Chemistry, The Scripps Research Institute (1)
The Francis Crick Institute, London, NW1 1AT, United Kingdom (1)
Division of Endocrinology, Diabetes, and Metabolism, Beth Israel Deaconess Medical Center Harvard Medical School Broad Institute of Harvard and MIT (1)
Department of Pathology and Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305 (1)
TUM School of Natural Sciences, Department Biosciences, Chair of Organic Chemistry II, Center for Functional Protein Assemblies (CPA), Technical University Munich (TUM), Ernst-Otto-Fischer Str. 8, Garching, 85748, Germany (1)
Department of Biology, Institute of Molecular Systems Biology, ETH Zurich, Zurich, Switzerland Faculty of Science, University of Zurich, Zurich, Switzerland (1)
Department of Molecular Physiology, Leiden University & Oncode Institute, Leiden 2333 CC, Netherlands (1)
Alzheimer’s Research UK UCL Drug Discovery Institute, University College London, Cruciform Building, Gower Street, London, WC1E 6BT, U.K. (1)
Molecular Physiology, Leiden Institute for Chemistry, Leiden University, The Netherlands (1)
School of Health and Life Sciences, Teesside University, UK (1)
Lundbeck La Jolla Research, San Diego, USA (1)
Department of Molecular Physiology, Leiden Institute of Chemistry, Leiden University (1)

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xref:PubMed:25118238 (1)

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FP-biotin enrichment of serine hydrolases in Enterococcus faecium

In our study, we employed activity-based protein profiling (ABPP), a technique that uses specialized inhibitors to identify active serine hydrolases in different strains of E. faecium (clade A1 and A2) and E. lactis under various growth conditions. Serine hydrolases, a large and diverse family of en...

ORGANISM(S): Enterococcus faecium Bacteria

2024-06-22 | PXD048798 | Pride

Detection of Dichlorvos Aducts in Hepatocyte Cell Line LC-MS/MS

Toxicity of dichlorvos (DDVP), an organophosphate (OP) pesticide, classically results from modification of the serine in the active sites of cholinesterases. However, DDVP also forms adducts on unrelated targets such as transferrin and albumin, suggesting that DDVP causes cellular perturbation by mo...

ORGANISM(S): Homo sapiens (Human)

2014-07-31 | PXD001107 | Pride

Hepatocyte cell line Dichorvos Lc-ms/ms

Five tyrosines and two serines in human albumin are labeled by the organophosphorus agent FP-biotin.

Not available

S-EPMC2646670 | biostudies-literature

An improved synthesis of a fluorophosphonate-polyethylene glycol-biotin probe and its use against competitive substrates.

Not available

S-EPMC3566859 | biostudies-literature

Pretargeted radioimmunotherapy using genetically engineered antibody-streptavidin fusion proteins for treatment of non-hodgkin lymphoma.

Not available

S-EPMC3229652 | biostudies-literature

Comparative Analysis of Bispecific Antibody and Streptavidin-Targeted Radioimmunotherapy for B-cell Cancers.

Not available

S-EPMC5290195 | biostudies-literature

Chemoproteomic profiling of host and pathogen enzymes active in cholera

Activity-based protein profiling (ABPP) is a chemoproteomic tool for detecting active enzymes in complex biological systems. We used ABPP to identify secreted bacterial and host serine hydrolases that are active in animals infected with the cholera pathogen Vibrio cholerae. Four V. cholerae protease...

ORGANISM(S): Vibrio cholerae O1 str. VC91

2016-02-22 | PXD003000 | Pride

Vibrio cholerae rabbit

Synergism of Fusobacterium periodonticum and N-nitrosamines promote the formation of EMT subtypes in ESCC by modulating Wnt3a palmitoylation.

Not available

S-EPMC11364064 | biostudies-literature

Quantitative, High-Throughput Assays for Proteolytic Degradation of Amylin.

Not available

S-EPMC7711817 | biostudies-literature

Identification of a S. aureus virulence factor by activity-based protein profiling (ABPP)

Serine hydrolases play diverse roles in regulating host-pathogen interactions in a number of organisms, yet few have been characterized in the human pathogen Staphylococcus aureus. Here, we describe a chemical proteomic screen that identified 10 previously uncharacterized S. aureus serine hydrolases...

ORGANISM(S): Staphylococcus aureus

2018-05-17 | PXD009210 | Pride

Abpp S. aureus Serine hydrolase

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