Adenosine triphosphate
Description
Description of Adenosine triphosphate with associated disease summary
Extracellular
adenosine triphosphate
(ATP) and its metabolites in
airway surface liquid are important agonists for purinergic signaling pathways.
They regulate airway defense mechanisms, including mucociliary clearance, airway inflammation and smooth muscle reactivity.
ATP in exhaled breath condensate has been studied among middle-aged COPD patients, adult asthma patients and children with cystic fibrosis to aid diagnosis and disease
follow-ups.
EBC
ATP levels were reported to be increased in CF patients relative to healthy
controls, and they decreased after treatment. The improvement of lung function
after antibiotic treatment was associated with a three-fold fall in EBC ATP
levels. (Eur Respir (2008))
But
no significant differences in EBC ATP levels were found either between COPD
patients with severe exacerbation and healthy controls (Inflamm. Res. (2008)). Nor
were there significant differences found between non-exacerbating asthma patients
and their healthy counterparts (Lazar et al., Chest 2010).
In these studies, EBC ATP were detected through luminometry (luciferin-luciferase
assay).
In
a pilot study by Esther Jr. et al., analyses using etheno-derivatisation and
HPLC revealed that EBC purine concentrations were below the detection threshold
in most individuals. When optimal separation and detection of adenosine and AMP
were achieved, ATP-specific signal was not detected in 20-fold concentrated EBC
samples. In another study by Lazar et al., using HPLC was not able to detect
ATP in EBC, even in 10-fold concentrated samples from COPD patients and
controls.
EBC
may be a better source of sampling for ATP measurement in comparison to broncho-alveolar
or nasal lavage fluids. It exerts negligible mechanical stress that stimulates
airway ATP release; the low protein content implies low ATPase activity, while
the low cellular components prevents cellular leakage. Nonetheless, salivary
contamination may be confounding, since ATP level in human saliva is 105-6
Description of disease(s) related to Adenosine
triphosphate (ATP):
Disease summary
Cystic Fibrosis (CF)
EBC ATP levels were reported to be increased in CF patients relative to healthy controls, and they decreased after treatment. The improvement of lung function after antibiotic treatment was associated with a three-fold fall in EBC ATP levels (Eur Respir (2008)).Summary of extracted biomedical information
Adenosine triphosphate is associated with abnormalities such as Ischemia, Spastic syndrome, Septicemia and Sphincter. The involved biomedical functions are known as Signal Transduction, Phosphorylation, ATP binding, inhibitors and Oxidative Phosphorylation. The associated genes/proteins with Adenosine triphosphate are PDPK1 gene, CD28 gene, IL2 gene, Mutant Proteins and PANX1 gene. Adenosine triphosphate is associated with Succinates, Purines, Neurotransmitters, Protons and cofactor.Associated references with human 52
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Reference title
with link to reference page |
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Intersample fluctuations in phosphocreatine concentration determined by 31P-magnetic resonance spectroscopy and parameter estimation of metabolic responses to exercise in humans. | J. Physiol. (Lond.) | 2000 |
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Associated curated diseases 1
Download diseasesAssociated disease mapping
Mapping of all associated diseases to Adenosine triphosphate is displayed in red.
Disease Name
with link to disease page |
Description of MeSH term
with link to MeSH Database |
Number of references |
---|---|---|
Cystic Fibrosis |
MeSH:
Cystic Fibrosis
An autosomal recessive genetic disease of the EXOCRINE GLANDS. It is caused by mutations in the gene encoding the CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE
REGULATOR expressed in several organs including the LUNG, the PANCREAS, the
BILIARY SYSTEM, and the SWEAT GLANDS. Cystic fibrosis is characterized by
epithelial secretory dysfunction associated with ductal obstruction resulting in
AIRWAY OBSTRUCTION; chronic RESPIRATORY INFECTIONS; PANCREATIC INSUFFICIENCY;
maldigestion; salt depletion; and HEAT PROSTRATION.
Year introduced: 1967
Link to MeSH Database: D003550
|
20 |
Associated abnormalities 3
Concept Name | External ID | Weighted Score | Hits | References | |
Ischemia | 1000.0 | 1 |
|
||
Spastic syndrome | 605.25 | 1 |
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Septicemia | ICD9-CM:038 | 744.0 | 1 |
|
Associated chemicals 19
Concept Name | External ID | Definition | Weighted Score | Hits | References | |
Purines | 929.54 | 2 |
|
|||
carboxyatractyloside | 1000.0 | 1 |
|
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second messenger | 1000.0 | 1 |
|
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Heavy Ions | 817.0 | 1 |
|
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latrunculin B | 1000.0 | 1 |
|
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carbonyl 3-chlorophenylhydrazone | 1000.0 | 1 |
|
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Polyphosphates | 900.29 | 1 |
|
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Liquid nitrogen | 1000.0 | 1 |
|
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Bicarbonates | 610.67 | 1 |
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Anions | 847.17 | 1 |
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Pyrimidines | CHEBI:16898 | 1000.0 | 1 |
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Neurotransmitters | CHEBI:25512 | 939.84 | 1 |
|
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Protons | CHEBI:24636 | 899.86 | 1 |
|
||
triphosphate | 913.5 | 1 |
|
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Sulfuric Acid Esters | 619.0 | 1 |
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cofactor | 996.5 | 1 |
|
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Hydroxide Ion | 694.73 | 1 |
|
|||
Signaling Molecule | CHEBI:62488 | 1000.0 | 1 |
|
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Ligands | CHEBI:52214 | 930.5 | 1 |
|
Associated functions 52
Concept Name | External ID | Definition | Weighted Score | Hits | References | |
Signal Transduction | GO:0007165 | 671.92 | 8 |
|
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Phosphorylation | 952.0 | 7 |
|
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Oxidative Phosphorylation | 988.06 | 5 |
|
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ATP binding | 968.88 | 5 |
|
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Synthesis | 911.88 | 4 |
|
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Glycolysis | GO:0006096 | 987.75 | 3 |
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T-Cell Activation | 998.17 | 3 |
|
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Cell physiology | 1000.0 | 3 |
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Feedback | 923.17 | 3 |
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Respiration | 963.64 | 3 |
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Hypoxia | 981.33 | 3 |
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Stimulus | 893.67 | 3 |
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Macromolecular alteration | 931.5 | 3 |
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inhibitors | 950.2 | 3 |
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adenosinetriphosphatase activity | GO:0016887 | 741.96 | 2 |
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Bioluminescence | 884.33 | 2 |
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Citric Acid Cycle | 735.38 | 2 |
|
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purinergic nucleotide receptor activity | 658.17 | 2 |
|
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Chromosome Pairing | 644.47 | 2 |
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Exocytosis | GO:0006887 | 1000.0 | 2 |
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Neuronal Transmission | 951.92 | 2 |
|
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Force | 965.25 | 2 |
|
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Regulation | 1000.0 | 2 |
|
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Adjudication | 1000.0 | 2 |
|
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Binding (Molecular Function) | 520.84 | 2 |
|
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Cell Survival | 1000.0 | 1 |
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Anoxia | 926.5 | 1 |
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ATP Hydrolysis | 959.8 | 1 |
|
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T-Cell Proliferation | GO:0042098 | 1000.0 | 1 |
|
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Mitochondrion in division | 812.5 | 1 |
|
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Anabolism | 1000.0 | 1 |
|
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depolarization | 944.0 | 1 |
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Polymerization | 944.0 | 1 |
|
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Electron Transport | 911.33 | 1 |
|
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synaptogenesis | 1000.0 | 1 |
|
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Autocrine Communication | 1000.0 | 1 |
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Transcription, Genetic | 745.95 | 1 |
|
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Membrane Potentials | 924.18 | 1 |
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uptake | 891.25 | 1 |
|
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Inflammation | 944.0 | 1 |
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Physiological action | 1000.0 | 1 |
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respiratory reflex | 1000.0 | 1 |
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Excitatory Postsynaptic Potentials | 495.53 | 1 |
|
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Inspiration function | 644.0 | 1 |
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sensory transduction | 1000.0 | 1 |
|
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Synaptic Potentials | 888.0 | 1 |
|
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paracrine | 847.0 | 1 |
|
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Summation | 1000.0 | 1 |
|
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Physiologic pulse | 676.47 | 1 |
|
|||
Transferring | 1000.0 | 1 |
|
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Entropy | 1000.0 | 1 |
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Mutation | 996.0 | 1 |
|
Associated genes 5
Concept Name | External ID | Definition | Weighted Score | Hits | References | |
CD28 gene | EntrezGene:940 | 647.09 | 3 |
|
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IL2 gene | EntrezGene:3558 | 700.5 | 2 |
|
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PDPK1 gene | EntrezGene:5170 | 606.76 | 2 |
|
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PANX1 gene | EntrezGene:24145 | 881.0 | 1 |
|
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Heavy Meromyosin | 1000.0 | 1 |
|
NCBI Entrez Crosslinks
Chemical Information
Formula | C10H16N5O13P3 |
Mass | 507.181 |
Synonyms | Adenosine triphosphate Adenosine 5'-triphosphate Atriphos Striadyne Triphosphaden Myotriphos Triadenyl Glucobasin 56-65-5 Adephos Adetol Adynol Atipi ATP Triphosaden 5'-Atp adenosine-5'-triphosphate Adenylpyrophosphoric acid Adenosine 5'-(tetrahydrogen triphosphate) Triphosphoric acid adenosine ester |
PubChem CID | 5957 |