Water permeation was not affected by mercurial sulfhydryl agents and glucose transport inhibitors.
2
Perturbation of sulfhydryl homeostasis is a hallmark of many diseases, including neurodegenerative disorders.
3
Agonists alter the sulfhydryl redox status of the beta-adrenergic receptors in the presence of Gs.
4
The mammalian enzyme but not the bacterial one was inhibited by a sulfhydryl alkylating agent.
5
A domain in the C-terminal non-collagenous portion of the molecules which forms sulfhydryl-dependent oligomers was identified.
6
Only the free sulfhydryl groups of plasma fibronectin were modified by the label under the experimental conditions.
7
Eleven of these mutants reacted with charged sulfhydryl-specific reagents, and bound antagonist protected nine of these from reaction.
8
This sulfhydryl amino acid specifically modified the effect of ethanol on locomotion because cocaine- or caffeine-induced locomotion was unaffected.
9
Enzymatic activity was exhibited only in the presence of sulfhydryl compounds and further enhanced by addition of 5 mM EDTA.
10
High molecular weight aggregates of APP-34 and APP-62 were the result of sulfhydryl-dependent and non-sulfhydryl-dependent cross-linking.
11
This work aims at assessing if T cells can sense redox stress through protein sulfhydryl oxidation and respond with tyrosine phosphorylation changes.
12
The three fragments as well as their corresponding free sulfhydryl forms were well separated by chromatography and identified online by mass spectrometry.
13
Background: The vasodilator effects of nitroglycerin are mediated by sulfhydryl-dependent bioconversion and influenced by local and systemic neural and hormonal counter-regulatory factors.
14
The high sensitivity of 4-methylmuconolactone methylisomerase to heavy metals and thiol-modifying reagents implicates the involvement of sulfhydryl groups in the catalytic reaction.
15
Dithiothreitol protected the sulfhydryl groups in the membrane and caused a concentration- and time-dependent increase of phospholipid N-methylation at three different catalytic sites.
16
Molecular docking assay suggested that ASB made contacts with the important sulfhydryl group Cys-592 residue and restricted the mobility of the active-site flap.