The adenosine A ₂ ₐ receptor is the main adenosine receptor expressed on immune cell subsets including T - cells, NK cells and dendritic cells and
binding of adenosine to the A ₂ ₐ receptor on immune cells blocks the activation and effector functions of anti-tumor immune cells and promotes a regulatory, immune - suppressive phenotype.
Binding of adenosine to the A2A receptor on immune cells blocks the activation and effector functions of anti-tumor immune cells and promotes a regulatory, immune - suppressive phenotype.
Not exact matches
Bound to the cell membrane, Na ± K+ATP ase uses the energy
of adenosine triphosphate (ATP) molecules to pump sodium out
of the cell and potassium into the cell, maintaining a charge gradient that allows ions to flow through open channels.
In this pathway, dopamine - and an
adenosine 3 ′, 5 ′ - monophosphate (cAMP)-- regulated phospho - protein
of 32 kilodaltons (DARPP - 32) is phosphorylated or dephosphorylated at three sites, in a pattern predicted to cause a synergistic inhibition
of protein phosphatase — 1 and concomitant regulation
of its downstream effector proteins glycogen synthesis kinase — 3 (GSK - 3), cAMP response element —
binding protein (CREB), and c - Fos.
In a new report published in the January 2015 issue
of the FASEB Journal, scientists use mice to show that a human membrane -
bound enzyme called CD39, which can clear the dangerous buildup
of adenosine triphosphate (ATP) from the bloodstream, significantly improves survival
of mice in sepsis.
MinE activates the enzymatic activity
of membrane -
bound MinD, thus triggering the conversion
of its
bound nucleotide
adenosine triphosphate (ATP) to
adenosine diphosphate (ADP), which causes the release
of MinD - ADP into the cell cytoplasm.
When a substance is
bound to zebrafish Abcb4, this triggers cleavage
of the energy transfer substance
adenosine triphosphate (ATP).
The Escherichia coli methyl - directed reaction has been reconstituted in a purified system consisting
of MutH, MutL, and MutS proteins, DNA helicase II, single - strand DNA
binding protein, DNA polymerase III holoenzyme, exonuclease I, DNA ligase, along with ATP (
adenosine triphosphate), and the four deoxynucleoside triphosphates.
Two specific long - range interactions clamp the two halves
of the domain together: a two - Mg2 + - coordinated
adenosine - rich corkscrew plugs into the minor groove
of a helix, and a GAAA hairpin loop
binds to a conserved 11 - nucleotide internal loop.
The Mfd protein was shown to (i) displace RNAP stalled at a lesion in an
adenosine triphosphate - dependent reaction, (ii)
bind to the damage recognition subunit (UvrA)
of the excision nuclease, and (iii) stimulate the repair
of the transcribed strand only when transcription is taking place.
[1,5,7] The direct inhibition
of cdks 1, 2, and 4 via competitive inhibition
of adenosine triphosphate
binding by flavopiridol has been demonstrated.
«They always include an
adenosine triphosphate
binding site and a set
of conserved amino acid residues.
It
binds to the receptors, substituting
adenosine, which in turn prevents the increase
of pain levels.
This happens because
of caffeine's affinity to
bind with
adenosine receptors in the muscles.
Now
adenosine is a neurotransmitter and it's an inhibitory neurotransmitter and what that means is that it suppresses the level
of the activity
of the neurons that it interacts with so if we take the caffeine molecule and we block the ability
of the
adenosine molecule to
bind to the receptor, to the
adenosine receptor, we keep ourselves more alert, we keep
adenosine from
binding.
It is found in all human cells where it is required to
bind to and activate
adenosine triphosphate (ATP), the chief energy molecule
of cells.
For a chemical perspective
adenosine triphosphate is an adenine nucleotide, which
binds itself to 3 different groups
of phosphatee types.