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This protein encoded by MPST catalyzes the transfer of a sulfur ion from 3-mercaptopyruvate to cyanide or other thiol compounds. Zusätzlich bieten wir Ihnen MPST Antikörper (33) und MPST Proteine (14) und viele weitere Produktgruppen zu diesem Protein an.
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3-Mercaptopyruvate sulphurtransferase and not cystathionine gamma-lyase is the primary regulator of coronary artery hydrogen sulfide production and function.
In this review, we discuss the roles of non-canonical Hippo/Mst (zeige MAP3K10 ELISA Kits) signaling pathways in lymphocyte development and functions. [review]
The crystal structure analysis allows us to propose a detailed mechanism for MST (zeige MAP3K10 ELISA Kits) in which an Asp (zeige ASIP ELISA Kits)-His-Ser (zeige SIGLEC1 ELISA Kits) catalytic triad is positioned to activate the nucleophilic cysteine residue and participate in general acid-base chemistry
In all the investigated cell lines, the activity of MPST was higher than that of CST (zeige GAL3ST1 ELISA Kits), which suggests that in these cells, the main pathway of sulfane sulfur formation is the MPST-catalyzed reaction.
Data suggest that impaired rhodanese expression is associated with increased whole cell reactive oxygen species as well as higher mitochondrial superoxide production and predicts mortality in hemodialysis patients.
This work is the first report of a functional genetic polymorphism affecting MPST and should help in investigation of disorders such as mercaptolactate-cysteine disulfiduria.
the findings of this study indicate that a deficiency in 3MST does not significantly affect endotoxemia, while a deficiency in CBS (zeige CBS ELISA Kits) or CSE (zeige CTH ELISA Kits) slightly ameliorates the outcome of LPS (zeige TLR4 ELISA Kits)-induced endotoxemia in vivo.
Up-regulation of 3-MST was located in living neurons and followed neuronal autophagy after traumatic brain injury.
H2S3 and H2S are produced in the brain by 3-mercaptopyruvate sulfurtransferase.
behavioral abnormality in MST-KO mice is caused by MST function defects such as an antioxidant insufficiency or a new transducer, H2S (or HS(-)) and/or SOx (zeige QSOX1 ELISA Kits) deficiency.
SiRNA silencing of 3-MPST reduced basal bioenergetic parameters and prevented the stimulating effect of 3-MP on mitochondrial bioenergetics.
This protein encoded by this gene catalyzes the transfer of a sulfur ion from 3-mercaptopyruvate to cyanide or other thiol compounds. It may be involved in cysteine degradation and cyanide detoxification. There is confusion in literature between this protein (mercaptopyruvate sulfurtransferase, MPST), which appears to be cytoplasmic, and thiosulfate sulfurtransferase (rhodanese, TST, GeneID:7263), which is a mitochondrial protein. Deficiency in MPST activity has been implicated in a rare inheritable disorder known as mercaptolactate-cysteine disulfiduria (MCDU). Alternatively spliced transcript variants encoding same or different isoforms have been identified for this gene.
, human liver rhodanese
, thiosulfate sulfurtransferase (rhodanese)
, mercaptopyruvate sulfurtransferase
, thiosulfate sulfurtransferase
, mercaptopyruvate sulfurtransferase S homeolog