Alkylation of cytochrome c by (glutathion-S-yl)-1,4-benzoquinone and iodoacetamide demonstrates compound-dependent site specificity.
about
Reactive intermediates: molecular and MS-based approaches to assess the functional significance of chemical-protein adducts.Protein damage by reactive electrophiles: targets and consequencesMonocyclic aromatic amines as potential human carcinogens: old is new againUtilization of MALDI-TOF to determine chemical-protein adduct formation in vitro.Effect of Low-Power Laser (LPL) and Light-Emitting Diode (LED) on Inflammatory Response in Burn Wound Healing.Bioactivation of the cancer chemopreventive agent tamoxifen to quinone methides by cytochrome P4502B6 and identification of the modified residue on the apoproteinNovel pathways associated with quinone-induced stress in breast cancer cells.Covalent adducts arising from the decomposition products of lipid hydroperoxides in the presence of cytochrome c.Protein electrophile-binding motifs: lysine-rich proteins are preferential targets of quinones.Covalent modification of cytochrome c by reactive metabolites of furan.Regulation of quinone detoxification by the thiol stress sensing DUF24/MarR-like repressor, YodB in Bacillus subtilis.Identification of protein adduction using mass spectrometry: Protein adducts as biomarkers and predictors of toxicity mechanisms.The frequency of 1,4-benzoquinone-lysine adducts in cytochrome c correlate with defects in apoptosome activation.Utilization of LC-MS/MS analyses to identify site-specific chemical protein adducts in vitro.
P2860
Q30424520-EFB060EC-673C-466D-9484-296E8524F203Q33308185-77512294-077E-419F-BBEF-23D3C81097BBQ33575727-58100C90-D0B0-4F27-8BB6-8E3D4D957B67Q33726934-716D585F-A4DD-4CF1-8C2B-D65D0ACB4FC8Q36024555-DB2FBD72-0E59-4840-8CE9-4AA47002B124Q36406301-A04B5EA3-4B12-4B4F-B0AD-275F5C839003Q36673564-4B1187CC-D008-48DF-BE38-A17832804FDEQ36853893-9A60498D-E82E-4F78-A79D-D63EAF07E5C8Q37196117-862A39EB-5A2B-498A-8E8F-89A439C184B5Q37537251-431B80B8-78E1-4CEF-AA39-EA4162E89BCCQ38294363-526AAC1D-A3F2-422C-8C86-A06ABC108DABQ38722096-98FDE174-F946-4B4A-9852-210C389E5E76Q38851577-B8C03DFE-D904-4E83-913E-379F8BDCA619Q42766980-D0F716FA-74A0-4FCF-A814-BCF5DA05CCB8
P2860
Alkylation of cytochrome c by (glutathion-S-yl)-1,4-benzoquinone and iodoacetamide demonstrates compound-dependent site specificity.
description
2005 nî lūn-bûn
@nan
2005 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年学术文章
@wuu
2005年学术文章
@zh-cn
2005年学术文章
@zh-hans
2005年学术文章
@zh-my
2005年学术文章
@zh-sg
2005年學術文章
@yue
name
Alkylation of cytochrome c by ...... nd-dependent site specificity.
@ast
Alkylation of cytochrome c by ...... nd-dependent site specificity.
@en
type
label
Alkylation of cytochrome c by ...... nd-dependent site specificity.
@ast
Alkylation of cytochrome c by ...... nd-dependent site specificity.
@en
prefLabel
Alkylation of cytochrome c by ...... nd-dependent site specificity.
@ast
Alkylation of cytochrome c by ...... nd-dependent site specificity.
@en
P2093
P356
P1476
Alkylation of cytochrome c by ...... und-dependent site specificity
@en
P2093
Daniel E Mason
Maria D Person
Serrine S Lau
Terrence J Monks
P356
10.1021/TX049873N
P577
2005-01-01T00:00:00Z