Identification of protein targets of 4-hydroxynonenal using click chemistry for ex vivo biotinylation of azido and alkynyl derivatives. - Wikidata - wikimedia - TriplyDB

Identification of protein targets of 4-hydroxynonenal using click chemistry for ex vivo biotinylation of azido and alkynyl derivatives.

Identification of protein targets of 4-hydroxynonenal using click chemistry for ex vivo biotinylation of azido and alkynyl derivatives.

http://www.wikidata.org/entity/Q37382938

about

4-Hydroxy-nonenal-A Bioactive Lipid Peroxidation Product Endogenous Generation and Signaling Actions of Omega-3 Fatty Acid Electrophilic Derivatives Protein lipoxidation: Detection strategies and challenges Redox modification of proteins as essential mediators of CNS autophagy and mitophagy.Chemical proteomics approaches for identifying the cellular targets of natural products The electrophile responsive proteome: integrating proteomics and lipidomics with cellular function Generation and biological activities of oxidized phospholipids Protein adducts of aldehydic lipid peroxidation products identification and characterization of protein adducts using an aldehyde/keto-reactive probe in combination with mass spectrometry Transduction of redox signaling by electrophile-protein reactions Redox proteomics in selected neurodegenerative disorders: from its infancy to future applications.Identification of selective inhibitors of uncharacterized enzymes by high-throughput screening with fluorescent activity-based probes.Chemoproteomic profiling of targets of lipid-derived electrophiles by bioorthogonal aminooxy probe.Selective gamma-ketoaldehyde scavengers protect Nav1.5 from oxidant-induced inactivation.Site-specific protein adducts of 4-hydroxy-2(E)-nonenal in human THP-1 monocytic cells: protein carbonylation is diminished by ascorbic acid.Comparative methods for analysis of protein covalent modification by electrophilic quinoids formed from xenobiotics.Redox regulation of antioxidants, autophagy, and the response to stress: implications for electrophile therapeutics.Oxysterols from free radical chain oxidation of 7-dehydrocholesterol: product and mechanistic studies.Systems analysis of protein modification and cellular responses induced by electrophile stress.A Click Chemistry Approach to Identify Protein Targets of Cancer Chemopreventive Phenethyl Isothiocyanate.Proteins modified by the lipid peroxidation aldehyde 9,12-dioxo-10(E)-dodecenoic acid in MCF7 breast cancer cells.ω-Alkynyl lipid surrogates for polyunsaturated fatty acids: free radical and enzymatic oxidations.Differential metabolism of 4-hydroxynonenal in liver, lung and brain of mice and rats.Small molecule activators of the heat shock response: chemical properties, molecular targets, and therapeutic promise.Assay of protein and peptide adducts of cholesterol ozonolysis products by hydrophobic and click enrichment methods Chemical biology applied to the study of bacterial pathogens.Structure-activity analysis of diffusible lipid electrophiles associated with phospholipid peroxidation: 4-hydroxynonenal and 4-oxononenal analogues.Probing lipid-protein adduction with alkynyl surrogates: application to Smith-Lemli-Opitz syndrome.The lipid peroxidation product 4-hydroxy-2-nonenal: Advances in chemistry and analysis Selective enrichment and identification of azide-tagged cross-linked peptides using chemical ligation and mass spectrometry.Detection and quantification of protein adduction by electrophilic fatty acids: mitochondrial generation of fatty acid nitroalkene derivatives.Protein-selective capture to analyze electrophile adduction of hsp90 by 4-hydroxynonenal.Relationship of electrophilic stress to aging Exploring the biology of lipid peroxidation-derived protein carbonylation.Site-specific proteomic analysis of lipoxidation adducts in cardiac mitochondria reveals chemical diversity of 2-alkenal adduction Site-specific, intramolecular cross-linking of Pin1 active site residues by the lipid electrophile 4-oxo-2-nonenal.Cell signalling by reactive lipid species: new concepts and molecular mechanisms.Formation and signaling actions of electrophilic lipids Inflammation and cancer: chemical approaches to mechanisms, imaging, and treatment.Protein modification by oxidized phospholipids and hydrolytically released lipid electrophiles: Investigating cellular responses.Metabolic impact of 4-hydroxynonenal on macrophage-like RAW 264.7 function and activation.

P2860

Q26782039-F704F47A-A9FC-4A90-B10A-AA6D8D3A476D Q26784513-D3C4498F-384C-4314-8B3C-E43E716E2F2A Q26824737-0295069D-E224-412A-A463-FE8D17EB57B2 Q27687119-693CCB73-1AF3-48F5-8927-4CE6C836A774 Q28072634-2875A957-020B-43D8-8331-9BBCCEBF61E5 Q28388959-6C301178-47E9-4DBD-8919-D4B1567A2148 Q28389691-F823F746-B3D2-41B1-874E-83093CD6988C Q28654792-B8052CD6-34A9-4DDA-B5BA-DDBAC0B46B9A Q30381222-BD90F602-CC40-4CAA-A467-D069767E408B Q30446460-7ADC400E-9A49-4415-95F9-C55AFB929509 Q30860145-20AA2A7E-E57B-4D02-A3A2-F16B4738815C Q33561568-6A074525-9DED-48DE-AE3C-69B0B30D2CBC Q33638480-C81B498C-73B5-4B74-A0BF-175D3ED3E0EA Q33674371-BB1C0F16-D9EC-47F3-AB4F-762A65684682 Q33682246-88C6BCFC-B143-4EC8-9D1B-A3A0AD7CD9A2 Q33702016-8BCF51A3-A28F-4BE0-B879-9DE2905B3F0E Q33730805-68CF3969-15CC-42D8-9A54-4532FE681114 Q33865889-5328DE76-37BA-4892-A90C-44F9B5990945 Q33907551-4C0E3206-694A-4B49-956F-1C9994AF4D5C Q34013171-9D236742-92F2-4927-A62B-8CA0D7736C42 Q34074547-61EB8332-5269-4A94-BA9D-0460D873B164 Q34202618-9DBB6546-CFEE-42AB-B098-C0C0542CC682 Q34338604-1C967BDA-EA40-488D-8B6A-BBAE4DCA0ED6 Q34372452-66C69027-40FB-43E9-ACF3-AEB7D10A803D Q34448285-E6D125B6-8DE6-4935-BCC5-76E76C73BCCD Q34711173-8AB5EEB6-5577-4A73-ADFB-BD0EDEC2B73E Q34799626-A220E830-68CC-4A59-9EDD-ED1D31401772 Q34984799-AD5F986E-BAD1-4462-810A-ACA202D20595 Q35057799-1C193B4E-AC46-45E8-BBAE-9CA5B99C0DC3 Q35129775-EFE91CC9-59A7-4134-A60F-FF8174BDA2BE Q35164081-4FDE861C-823F-4B3A-9342-D0F0CA30EF34 Q35165294-400A689F-833B-416A-B769-E2BB0442CCFB Q35226317-E5FBFFB0-7BAF-4D6A-B386-DF0E03FD5C6A Q35420953-F57FA2DE-4FF1-46B9-9236-B05F5861A826 Q35571550-51351702-99C5-4DDA-BB5B-B8FC9C37BDBA Q35778758-84DE3ABD-82A4-4F26-A2AB-041B652A4B35 Q35804051-BD1F24A9-3DDE-4F46-A540-2C708B5AE918 Q36033937-B79CF4EF-AD1E-49FD-B183-541AC2112076 Q36100380-4411890E-E3EC-412D-A83E-6595D86A587C Q36239558-5AAC717D-3712-41F0-9451-40F5D7456811

P2860

Identification of protein targets of 4-hydroxynonenal using click chemistry for ex vivo biotinylation of azido and alkynyl derivatives.

http://www.wikidata.org/entity/Q37382938

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 31 January 2008

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Identification of protein targ ...... azido and alkynyl derivatives.

@en

Identification of protein targ ...... azido and alkynyl derivatives.

@nl

type

label

Identification of protein targ ...... azido and alkynyl derivatives.

@en

Identification of protein targ ...... azido and alkynyl derivatives.

@nl

prefLabel

Identification of protein targ ...... azido and alkynyl derivatives.

@en

Identification of protein targ ...... azido and alkynyl derivatives.

@nl

P1433

Q37382938-6008B84C-A8C5-4BDE-83F2-A283FA4956FE

P1476

Q37382938-E2E41FE8-3008-40B3-9654-10E9E358E49E

P2093

Q37382938-2A8CCD58-F1D5-4BAC-903A-79ED239A7EEC

Q37382938-329E406D-0E4E-4127-8E5F-A19B9EAB4BA0

Q37382938-33430F2E-8668-44D2-ADC3-1BC517192EFA

Q37382938-5E016F4F-B5EC-450C-A606-8C0A6BECEC42

Q37382938-E00C8454-2749-4835-BE80-42B953AA300C

P2860

Q37382938-062B6EF8-BE27-4595-851C-BAB9899F8697

Q37382938-0ABA482A-4B44-4907-8005-BBF1110B08CF

Q37382938-0B93CAFC-105E-4386-9B20-C66AA80BAF8F

Q37382938-1625A1D7-7CC0-4244-9A3A-850BB9922D2A

Q37382938-162EC524-C667-4952-A86E-575759B4FB32

Q37382938-19631576-2A0A-4829-A8AD-0C86778B3CDE

Q37382938-20AFDA28-DC05-4224-A458-ECDC3C4237CA

Q37382938-21CB7868-88D4-42FD-9482-15743BF85529

Q37382938-2888493A-4456-4EC2-A91E-D42E775D38A8

Q37382938-2B766C48-5F12-4B1E-B56F-7040E7CC1A19

P304

Q37382938-93695FE0-2BCD-40E5-BAA3-05CE07AAFCE9

P31

Q37382938-74B9E96A-F0B0-44A5-8F7B-B204BC8F412A

P356

Q37382938-EBCDAC83-1F08-47CD-9886-1DA8ECD7D299

P433

Q37382938-A7049FA4-FC6A-4244-BE3B-00B0BB617D9D

P478

Q37382938-359BC665-6ECA-4B61-B5C3-D38DDA10C286

P50

Q37382938-F7971FE9-0DD6-4ED5-9DBC-6708BF684870

P577

Q37382938-B9AD60C4-0251-4971-96E5-FFE762784C7B

P5875

Q37382938-650287A1-C808-45F3-A35D-E5B0329D2880

P698

Q37382938-C4819CC4-0580-41B1-BA40-0D46FEF9588B

P932

Q37382938-0D61A47F-51AD-4B8D-AF78-D2871EE54A24

P356

P1433

Chemical Research in Toxicology

P1476

Identification of protein targ ...... azido and alkynyl derivatives

@en

P2093

Aaron T Jacobs

http://www.w3.org/2001/XMLSchema#string

Andrew Vila

http://www.w3.org/2001/XMLSchema#string

Keri A Tallman

http://www.w3.org/2001/XMLSchema#string

Lawrence J Marnett

http://www.w3.org/2001/XMLSchema#string

Ned A Porter

http://www.w3.org/2001/XMLSchema#string

P2860

Cell surface engineering by a modified Staudinger reaction

Click Chemistry: Diverse Chemical Function from a Few Good Reactions

Direct evidence that sulfhydryl groups of Keap1 are the sensors regulating induction of phase 2 enzymes that protect against carcinogens and oxidants

Mitochondrial HSP60 (P1 protein) and a HSP70-like protein (mortalin) are major targets for modification during S-(1,1,2,2-tetrafluoroethyl)-L-cysteine-induced nephrotoxicity

Identification of seven proteins in the endoplasmic reticulum as targets for reactive metabolites of bromobenzene

"Click labeling" with 2-[18f]fluoroethylazide for positron emission tomography.

Identification of protein targets for mycophenolic acid acyl glucuronide in rat liver and colon tissue.

Identification of the hepatic protein targets of reactive metabolites of acetaminophen in vivo in mice using two-dimensional gel electrophoresis and mass spectrometry.

Covalent modification of epithelial fatty acid-binding protein by 4-hydroxynonenal in vitro and in vivo. Evidence for a role in antioxidant biology.

Modification of Cytochrome c by 4-hydroxy- 2-nonenal: evidence for histidine, lysine, and arginine-aldehyde adducts.

P304

432-444

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1021/TX700347W

http://www.w3.org/2001/XMLSchema#string

P433

2

http://www.w3.org/2001/XMLSchema#string

P478

21

http://www.w3.org/2001/XMLSchema#string

P50

Daniel C. Liebler

P577

2008-01-31T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

5618608

http://www.w3.org/2001/XMLSchema#string

P698

18232660

http://www.w3.org/2001/XMLSchema#string

P932

2760080

http://www.w3.org/2001/XMLSchema#string