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The P-type adenosinetriphosphatases (P-type ATPases) are a family of proteins which use the free energy of ATP hydrolysis to drive uphill transport of ions across membranes. Additionally we are shipping ATPase, Class I, Type 8A, Member 1 Proteins (6) and and many more products for this protein.
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Single-nucleotide polymorphism, rs17448506, located in ATP8A1 intron, reached the significance threshold for interaction with tobacco smoke expose and bronchial hyperresponsiveness (p=10-5).
Over-expression of ATP8A1 alleviated ethanol-induced hepatocyte injury. Moreover, the PI3K/Akt signaling pathway appears to participate in inhibition of ethanol-induced hepatocyte apoptosis.
A pronounced induction of the flippase Atp8a1 was observed in post-mortem tissue homogenates from the hippocampus and temporal lobe of juvenile autistic subjects compared to age-matched controls.
Knockdown of ATP8A1 (a recycling endosome phosphatidlyserine-flippase) suppresses nuclear localization of YAP and YAP-dependent transcription. ATP8A1 knockdown increases the phosphorylated (activated) form of Lats1 that phosphorylates and inactivates YAP.
The increased level of intracellular ATP8A1 protein attenuated the inhibitor role of miR-140-3p in the growth and mobility of NSCLC cell.
Depletion of ATP8A1 impaired the asymmetric transbilayer distribution of phosphatidylserine in recycling endosomes, dissociated EHD1 from recycling endosomes, and generated aberrant endosomal tubules that appear resistant to fission.
the phospholipid flippase complex of ATP8A1 and CDC50A proteins has a role in cell migration
APLT has a role in macrophage-induced nitrosylation/oxidation plays an important role in cell clearance
In a sociability test, the Atp8a1+ mice displayed no preference for an encaged stranger mouse over a novel object, which is a characteristic autistic-like behavior. In sharp contrast, Atp8a1 (-/-) mice displayed a preference for a stranger mouse over the novel object, which is characteristic of neurotypical mouse behavior.
The data of this study strongly indicated that Atp8a1 plays a central role in the PM-APLT activity of some mammalian cells.
role in normal phospholipid distribution in the bilayer, and for normal binding, penetration, and signaling by the zona pellucida
ATPase activity of the secretory granule Atp8a1 is activated by phospholipids binding to a specific site
Such observations suggest tissue-specific differences in transcription initiation complex assembly and regulation of ATPase II gene expression.
Asparagine 905 of the mammalian phospholipid flippase ATP8A2 is essential for lipid substrate-induced activation of ATP8A2 dephosphorylation.
The P-type adenosinetriphosphatases (P-type ATPases) are a family of proteins which use the free energy of ATP hydrolysis to drive uphill transport of ions across membranes. Several subfamilies of P-type ATPases have been identified. One subfamily catalyzes transport of heavy metal ions. Another subfamily transports non-heavy metal ions (NMHI). The protein encoded by this gene is a member of the third subfamily of P-type ATPases and acts to transport amphipaths, such as phosphatidylserine. Two transcript variants encoding different isoforms have been found for this gene.
probable phospholipid-transporting ATPase IA
, ATPase II
, ATPase class I type 8A member 1
, aminophospholipid translocase
, chromaffin granule ATPase II
, ATPase 8A1, aminophospholipid transporter (APLT), class I
, ATPase 8A1, p type