Target type: molecularfunction
Catalysis of the reaction: ATP + H2O = AMP + H+ + diphosphate. [RHEA:14245]
ATP diphosphatase activity is a critical enzymatic process that hydrolyzes adenosine triphosphate (ATP) into adenosine diphosphate (ADP) and inorganic phosphate (Pi). This reaction is essential for various cellular functions, including energy production, signal transduction, and cellular transport.
ATP diphosphatases, also known as ATPases, act as molecular motors that utilize the energy released from ATP hydrolysis to drive cellular processes. They function by binding ATP and then catalyzing its breakdown, releasing energy that can be used to power other reactions or mechanical work.
Specifically, ATP diphosphatases play a key role in the following processes:
- **Energy production:** The hydrolysis of ATP by ATP diphosphatases provides the energy required for cellular processes such as muscle contraction, protein synthesis, and active transport.
- **Signal transduction:** ATP diphosphatases are involved in signal transduction pathways by hydrolyzing ATP to generate ADP, which can act as a signaling molecule.
- **Cellular transport:** ATP diphosphatases power active transport systems that move molecules across cell membranes against their concentration gradient, ensuring the proper distribution of nutrients, ions, and waste products.
ATP diphosphatases are diverse in their structure and function, with different isoforms exhibiting specific roles in various cellular compartments. Their activity is regulated by factors such as substrate concentration, pH, and the presence of specific ions or cofactors.
Overall, ATP diphosphatase activity is a fundamental enzymatic process that underpins a wide range of cellular functions, making it crucial for maintaining cell viability and organismal survival.'
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Protein | Definition | Taxonomy |
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7,8-dihydro-8-oxoguanine triphosphatase | An oxidized purine nucleoside triphosphate hydrolase that is encoded in the genome of human. [PRO:DNx, UniProtKB:P36639] | Homo sapiens (human) |
Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 | An ectonucleotide pyrophosphatase/phosphodiesterase family member 1 that is encoded in the genome of human. [PRO:DNx, UniProtKB:P22413] | Homo sapiens (human) |
Compound | Definition | Classes | Roles |
---|---|---|---|
kinetin | cytokinin : A phytohormone that promote cell division, or cytokinesis, in plant roots and shoots. kinetin : A member of the class of 6-aminopurines that is adenine carrying a (furan-2-ylmethyl) substituent at the exocyclic amino group. Kinetin: A furanyl adenine found in PLANTS and FUNGI. It has plant growth regulation effects. | 6-aminopurines; furans | cytokinin; geroprotector |
7-azaindole | pyrrolopyridine | ||
2-aminobenzimidazole | 2-aminobenzimidazole : A member of the class of benzimidazoles that is benzimidazole in which the hydrogen at position 2 is replaced by an amino group. 2-aminobenzimidazole: metabolite of benomyl; RN given refers to parent cpd | benzimidazoles | marine xenobiotic metabolite |
imiquimod | imiquimod : An imidazoquinoline fused [4,5-c] carrying isobutyl and amino substituents at N-1 and C-4 respectively. A prescription medication, it acts as an immune response modifier and is used to treat genital warts, superficial basal cell carcinoma, and actinic keratosis. Imiquimod: A topically-applied aminoquinoline immune modulator that induces interferon production. It is used in the treatment of external genital and perianal warts, superficial CARCINOMA, BASAL CELL; and ACTINIC KERATOSIS. | imidazoquinoline | antineoplastic agent; interferon inducer |
1h-imidazo(4,5-b)pyridine | 1H-imidazo(4,5-b)pyridine: structure given in first source 4-azabenzimidazole : The [4,5-b]-fused isomer of imidazopyridine. | imidazopyridine | |
alpha,beta-methyleneadenosine 5'-triphosphate | alpha,beta-methyleneadenosine 5'-triphosphate: do not confuse with beta,gamma-methylene ATP; RN given refers to parent cpd | nucleoside triphosphate analogue | |
adenosine 5'-methylenediphosphate | nucleoside diphosphate analogue | ||
3'-o-(4-benzoyl)benzoyladenosine 5'-triphosphate | 3'-O-(4-benzoyl)benzoyladenosine 5'-triphosphate: purinergic receptors agonist; structure given in first source | purine ribonucleoside triphosphate | |
methylthio-adp | |||
resiquimod | S 28463: structure given in first source | imidazoquinoline | |
4-methyl-2-quinazolinamine | 4-methyl-2-quinazolinamine: from Streptomyces of TCM plant; structure in first source | ||
8-deoxygartanin | 8-deoxygartanin: a butyrylcholinesterase inhibitor; isolated from Garcinia mangostana; structure in first source | xanthones | |
zeatin | Zeatin: An aminopurine factor in plant extracts that induces cell division. (Grant & Hackh's Chemical Dict, 5th ed) | zeatin | plant metabolite |
Reactive blue 2 | anthraquinone | ||
mangostin | alpha-mangostin : A member of the class of xanthones that is 9H-xanthene substituted by hydroxy group at positions 1, 3 and 6, a methoxy group at position 7, an oxo group at position 9 and prenyl groups at positions 2 and 8. Isolated from the stems of Cratoxylum cochinchinense, it exhibits antioxidant, antimicrobial and antitumour activities. mangostin: xanthone from rind of Garcinia mangostana Linn. fruit | aromatic ether; phenols; xanthones | antimicrobial agent; antineoplastic agent; antioxidant; plant metabolite |
norathyriol | norathyriol : A member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy groups at positions 1, 3, 6 and 7. Isolated from Garcinia mangostana and Maclura pomifera, it exhibits inhibitory activity against protein kinase C. norathyriol: from Gentinanaceae; has vasorelaxing action on rat thoracic aorta; structure given in first source | polyphenol; xanthones | antineoplastic agent; EC 2.7.11.13 (protein kinase C) inhibitor; plant metabolite |
2-methylthio-atp | 2-methylthio-ATP: purinergic receptors agonist; relaxes mammalian gut preparations; structure given in first source | ||
gamma-mangostin | gamma-mangostin : A member of the class of xanthones that is 9H-xanthene substituted by hydroxy group at positions 1, 3, 6 and 7, an oxo group at position 9 and prenyl groups at positions 2 and 8. Isolated from the stems of Cratoxylum cochinchinense, it exhibits antitumour activity. | phenols; xanthones | antineoplastic agent; plant metabolite; protein kinase inhibitor |
adenosine 5'-diphosphate 2',3'-dialdehyde | |||
1,3,7-trihydroxy-2-(3-methylbut-2-enyl)-xanthone | 1,3,7-trihydroxy-2-(3-methylbut-2-enyl)-xanthone: from stems of Kielmeyera coriacea; structure in first source | ||
sch 51344 | SCH 51344: inhibits ras transformation; structure given in first source SCH51344 : A pyrazoloquinoline that is 6-methoxy-3-methyl-1H-pyrazolo[3,4-b]quinoline bearing an additional 2-[(2-hydroxyethoxy)ethyl]amino substituent at position 4 | aromatic amine; aromatic ether; primary alcohol; pyrazoloquinoline; secondary amino compound | antineoplastic agent |
3,4,5,6-tetrahydroxyxanthone | |||
sm360320 | SM360320: Proc Natl Acad Sci U S A 2006 Feb 7;103(6):1828-33 | ||
arl-67156 | 6-N,N-diethyl-beta,gamma-dibromomethylene-D-ATP: an inhibitor of ecto-ATPase | ||
3-isomangostin | 3-isomangostin: structure in first source | xanthones | |
garcinone c | garcinone C: an acetylcholinesterase inhibitor; isolated from Garcinia mangostana; structure in first source | xanthones | |
ent-crizotinib | ent-crizotinib : A 3-[1-(2,6-dichloro-3-fluorophenyl)ethoxy]-5-[1-(piperidin-4-yl)pyrazol-4-yl]pyridin-2-amine that is the (S)-enantiomer of crizotinib. | 3-[1-(2,6-dichloro-3-fluorophenyl)ethoxy]-5-[1-(piperidin-4-yl)pyrazol-4-yl]pyridin-2-amine |