Adenine Nucleotide Translocator 1
Mitochondrial ADP, ATP Translocases
Adenine Nucleotide Translocator 2
Nucleotides
Adenosine Diphosphate
Atractyloside
Adenosine Triphosphate
Adenosine Monophosphate
Adenine Nucleotide Translocator 3
Bongkrekic Acid
Molecular Sequence Data
Purine Nucleotides
Mitochondria, Liver
Adenosine
Hypoxanthines
Oxidative Phosphorylation
Inosine
Amino Acid Sequence
Polymorphism, Single Nucleotide
Hypoxanthine
Inosine Monophosphate
NAD
Mitochondria
Base Sequence
5'-Nucleotidase
Cloning, Molecular
Magnesium
Binding Sites
Oxygen Consumption
Escherichia coli
Adenylate Kinase
Proton-Translocating ATPases
Purines
Nucleotide Transport Proteins
Oligomycins
DNA
Cyclophilins
Adenylyl Imidodiphosphate
Coformycin
Voltage-Dependent Anion Channels
Mitochondrial Swelling
Intracellular Membranes
Mutation
Nucleotidases
Nucleic Acid Conformation
Guanosine Triphosphate
Adenosine Triphosphatases
Calcium
Apyrase
Pyrimidine Nucleotides
Glycolysis
NADP
Mitochondrial Membrane Transport Proteins
Hydrogen-Ion Concentration
Energy Metabolism
Guanine Nucleotide Exchange Factors
Sequence Homology, Nucleic Acid
Liver
Cattle
Sequence Analysis, DNA
Protein Binding
Rats, Inbred Strains
Receptors, Purinergic
Myocardium
Affinity Labels
Genes
Plasmids
Uncoupling Agents
RNA, Messenger
Xanthine
Transcription, Genetic
Sequence Homology, Amino Acid
Guanosine Diphosphate
Phosphotransferases
Substrate Specificity
Hexokinase
Models, Molecular
Receptors, Purinergic P2
Permeability
Mitochondria, Muscle
Saccharomyces cerevisiae
Sequence Alignment
Site-Specific DNA-Methyltransferase (Adenine-Specific)
Biological Transport
Ribonucleotides
Aurovertins
Glycosides
Ribonucleosides
Cell Respiration
Deoxyadenosines
Phosphocreatine
Adenosine Kinase
Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone
Nucleosides
Oxidation-Reduction
Adenosine Deaminase
Polymerase Chain Reaction
Glucose
Cyclic AMP
4-Aminobenzoic Acid
Rats, Wistar
Receptors, Purinergic P2Y1
Protein Conformation
DNA Restriction Enzymes
Ophthalmoplegia, Chronic Progressive External
Phosphofructokinase-1, Muscle Type
Tubercidin
Uridine Triphosphate
Cells, Cultured
Restriction Mapping
Codon
Structure-Activity Relationship
Antimycin A
Species Specificity
Blood Platelets
Mitochondrial Proteins
Creatine Kinase
Genotype
Chromatography, High Pressure Liquid
Rabbits
Ion Channels
Suramin
Theophylline
Promoter Regions, Genetic
Cell Membrane Permeability
Submitochondrial Particles
Models, Biological
Membrane Potentials
Open Reading Frames
Biological Transport, Active
Dose-Response Relationship, Drug
Flavin-Adenine Dinucleotide
Temperature
DNA, Mitochondrial
Succinates
Protein Biosynthesis
Mitochondrial Membranes
Voltage-Dependent Anion Channel 2
DNA Primers
Thymine Nucleotides
Ammonia
Isocitrate Dehydrogenase
Pentosyltransferases
Immunophilins
Cytosol
Pyrophosphatases
Pentostatin
Tyrothricin
Catalysis
Azaserine
Electrophoresis, Polyacrylamide Gel
Membrane Potential, Mitochondrial
DNA Repair
Extracellular Space
Dinucleoside Phosphates
Phosphofructokinase-1
Cross-linking of two beta subunits in the closed conformation in F1-ATPase. (1/2294)
In the crystal structure of mitochondrial F1-ATPase, two beta subunits with a bound Mg-nucleotide are in "closed" conformations, whereas the third beta subunit without bound nucleotide is in an "open" conformation. In this "CCO" (beta-closed beta-closed beta-open) conformational state, Ile-390s of the two closed beta subunits, even though they are separated by an intervening alpha subunit, have a direct contact. We replaced the equivalent Ile of the alpha3beta3gamma subcomplex of thermophilic F1-ATPase with Cys and observed the formation of the beta-beta cross-link through a disulfide bond. The analysis of conditions required for the cross-link formation indicates that: (i) F1-ATPase takes the CCO conformation when two catalytic sites are filled with Mg-nucleotide, (ii) intermediate(s) with the CCO conformation are generated during catalytic cycle, (iii) the Mg-ADP inhibited form is in the CCO conformation, and (iv) F1-ATPase dwells in conformational state(s) other than CCO when only one (or none) of catalytic sites is filled by Mg-nucleotide or when catalytic sites are filled by Mg2+-free nucleotide. The alpha3beta3gamma subcomplex containing the beta-beta cross-link retained the activity of uni-site catalysis but lost that of multiple catalytic turnover, suggesting that open-closed transition of beta subunits is required for the rotation of gamma subunit but not for hydrolysis of a single ATP. (+info)Physiological characterization of viable-but-nonculturable Campylobacter jejuni cells. (2/2294)
Campylobacter jejuni is a pathogenic, microaerophilic, gram-negative, mesophilic bacterium. Three strains isolated from humans with enteric campylobacteriosis were able to survive at high population levels (10(7) cells ml-1) as viable-but-nonculturable (VBNC) forms in microcosm water. The VBNC forms of the three C. jejuni strains were enumerated and characterized by using 5-cyano-2,3-ditolyl tetrazolium chloride-4',6-diamino-2-phenylindole staining. Cellular volume, adenylate energy charge, internal pH, intracellular potassium concentration, and membrane potential values were determined in stationary-phase cell suspensions after 48 h of culture on Columbia agar and after 1 to 30 days of incubation in microcosm water and compared. A notable increase in cell volume was observed with the VBNC state; the average cell volumes were 1.73 microliter mg of protein-1 for the culturable form and 10.96 microliter mg of protein-1 after 30 days of incubation in microcosm water. Both the internal potassium content and the membrane potential were significantly lower in the VBNC state than in the culturable state. Culturable cells were able to maintain a difference of 0.6 to 0.9 pH unit between the internal and external pH values; with VBNC cells this difference decreased progressively with time of incubation in microcosm water. Measurements of the cellular adenylate nucleotide concentrations revealed that the cells had a low adenylate energy charge (0.66 to 0.26) after 1 day of incubation in microcosm water, and AMP was the only nucleotide detected in the three strains after 30 days of incubation in microcosm water. (+info)Regulation of a volume-sensitive anion channel in rat pancreatic beta-cells by intracellular adenine nucleotides. (3/2294)
1. The patch-clamp technique in the whole-cell configuration was used to measure the effects of intracellular adenine nucleotides on activity of the volume-sensitive anion channel in single, isolated rat pancreatic beta-cells. 2. In the absence of intracellular nucleotides, swelling of cells with a hypertonic pipette solution failed to activate the conductance. Addition of ATP over the range 2-10 mM maintaining the same degree of hypertonicity caused a progressive activation of the conductance. An increase in ATP produced a similar activation of the conductance in non-swollen cells, albeit with reduced current amplitudes. 3. Activation of the conductance was also observed in the presence of ATPgammaS, adenylyl imidophosphate (AMP-PNP), ADP, diadenosine tetraphosphate and GTPgammaS. Neither ADP nor GDPbetaS inhibited activation of the conductance by ATP. 4. It is concluded that activity of the beta-cell volume-sensitive anion channel can be modulated by changes in intracellular concentrations of ATP within the physiological concentration range by a mechanism that does not require nucleotide hydrolysis. Activity of the channel does not appear to be modulated by a G protein-coupled mechanism. (+info)Comparison of the mechanism of cytotoxicity of 2-chloro-9-(2-deoxy-2- fluoro-beta-D-arabinofuranosyl)adenine, 2-chloro-9-(2-deoxy-2-fluoro- beta-D-ribofuranosyl)adenine, and 2-chloro-9-(2-deoxy-2,2-difluoro- beta-D-ribofuranosyl)adenine in CEM cells. (4/2294)
In an effort to understand biochemical features that are important to the selective antitumor activity of 2-chloro-9-(2-deoxy-2-fluoro-beta-D-arabinofuranosyl)adenine [Cl-F( upward arrow)-dAdo], we evaluated the biochemical pharmacology of three structurally similar compounds that have quite different antitumor activities. Cl-F( upward arrow)-dAdo was 50-fold more potent as an inhibitor of CEM cell growth than were either 2-chloro-9-(2-deoxy-2-fluoro-beta-D-ribofuranosyl)adenine [Cl-F( downward arrow)-dAdo] or 2-chloro-9-(2-deoxy-2, 2-difluoro-beta-D-ribofuranosyl)adenine [Cl-diF( upward arrow downward arrow)-dAdo]. The compounds were similar as substrates of deoxycytidine kinase. Similar amounts of their respective triphosphates accumulated in CEM cells, and the rate of disappearance of these metabolites was also similar. Cl-F( upward arrow)-dAdo was 10- to 30-fold more potent in its ability to inhibit the incorporation of cytidine into deoxycytidine nucleotides than either Cl-F( downward arrow)-dAdo or Cl-diF( upward arrow downward arrow)-dAdo, respectively, which indicated that ribonucleotide reductase was differentially inhibited by these three compounds. Thus, the differences in the cytotoxicity of these agents toward CEM cells were not related to quantitative differences in the phosphorylation of these agents to active forms but can mostly be accounted for by differences in the inhibition of ribonucleotide reductase activity. Furthermore, the inhibition of RNA and protein synthesis by Cl-F( downward arrow)-dAdo and Cl-diF( upward arrow downward arrow)-dAdo at concentrations similar to those required for the inhibition of DNA synthesis can help explain the poor antitumor selectivity of these two agents because all cells require RNA and protein synthesis. (+info)Hypotension induced by exercise is associated with enhanced release of adenyl purines from aged rat artery. (5/2294)
To determine whether the antihypertensive effects of exercise are associated with release of ATP and its metabolites from arteries, we assayed blood pressure and the release of adenine nucleotides and nucleosides from the caudal arteries of exercised and sedentary aged hypercholesterolemic rats. Exercise on a treadmill for 12 wk significantly decreased the rise in systolic and diastolic blood pressure by 7.5 and 15.9%, respectively, with advanced age. The concentrations of oleic, linoleic, and linolenic acids in the caudal artery decreased significantly with exercise, demonstrating an association between exercise and the unsaturation index of caudal arterial fatty acids. The amounts of total adenyl purines released by the arterial segments from exercised rats, both spontaneously and in response to norepinephrine, were significantly greater by 80.0 and 60.7%, respectively, than those released by tissues from sedentary rats. These results suggest that exercise alters the membrane fatty acid composition in aged rats as well as the release of ATP from vascular endothelial cells and that these factors are associated with the regression of the rise in blood pressure normally observed with advanced age. (+info)Effect of zinc on adenine nucleotide pools in relation to aflatoxin biosynthesis in Aspergillus parasiticus. (6/2294)
The adenylic acid systems of Aspergillus parasiticus were studied in zinc-replete and zinc-deficient media. The adenosine 5'-triphosphate levels of the fungus were high during exponential phase and low during stationary phase in zinc-replete cultures. On the other hand, the levels of adenosine 5'-diphosphate and adenosine 5'-monophosphate were low during exponential phase of growth and high during stationary phase. The adenosine 5'-triphosphate levels during exponential phase may indicate higher primary metabolic activity of the fungus. On the other hand, high adenosine 5'-monophosphate levels during stationary phase may inhibit lipid formation and may enhance aflatoxin levels. The inorganic phosphorus content was low in a zinc-replete medium throughout the growth period, thereby favoring aflatoxin biosynthesis. The energy charge during the exponential phase was high but low during the stationary phase. In general the energy charge values were lower because of high adenosine 5'-monophosphate content. (+info)Metabolism and the triggering of germination of Bacillus megaterium. Concentrations of amino acids, organic acids, adenine nucleotides and nicotinamide nucleotides during germination. (7/2294)
A considerable amount of evidence suggests that metabolism of germinants or metabolism stimulated by them is involved in triggering bacterial-spore germination. On the assumption that such a metabolic trigger might lead to relatively small biochemical changes in the first few minutes of germination, sensitive analytical techniques were used to detect any changes in spore components during the L-alanine-triggered germination of Bacillus megaterium KM spores. These experiments showed that no changes in spore free amino acids or ATP occurred until 2-3 min after L-alanine addition. Spores contained almost no oxo acids (pyruvate, alpha-oxoglutarate, oxaloacetate), malate or reduced NAD. These compounds were again not detectable until 2-3 min after addition of germinants. It is suggested, therefore, that metabolism associated with these intermediates is not involved in the triggering of germination of this organism. (+info)Cyanobacterial PPP family protein phosphatases possess multifunctional capabilities and are resistant to microcystin-LR. (8/2294)
The structural gene for a putative PPP family protein-serine/threonine phosphatase from the microcystin-producing cyanobacterium Microcystis aeruginosa PCC 7820, pp1-cyano1, was cloned. The sequence of the predicted gene product, PP1-cyano1, was 98% identical to that of the predicted product of an open reading frame, pp1-cyano2, from a cyanobacterium that does not produce microcystins, M. aeruginosa UTEX 2063. By contrast, PP1-cyano1 displayed less than 20% identity with other PPP family protein phosphatases from eukaryotic, archaeal, or other bacterial organisms. PP1-cyano1 and PP1-cyano2 were expressed in Escherichia coli and purified to homogeneity. Both enzymes exhibited divalent metal dependent phosphohydrolase activity in vitro toward phosphoserine- and phosphotyrosine-containing proteins and 3-phosphohistidine- and phospholysine-containing amino acid homopolymers. This multifunctional potential also was apparent in samples of PP1-cyano1 and PP1-cyano2 isolated from M. aeruginosa. Catalytic activity was insensitive to okadaic acid or the cyanobacterially produced cyclic heptapeptide, microcystin-LR, both potent inhibitors of mammalian PP1 and PP2A. PP1-cyano1 and PP1-cyano2 displayed diadenosine tetraphosphatase activity in vitro. Diadenosine tetraphosphatases share conserved sequence features with PPP family protein phosphatases. The diadenosine tetraphosphatase activity of PP1-cyano1 and PP1-cyano2 confirms that these enzymes share a common catalytic mechanism. (+info)The symptoms of CPEO usually begin in adulthood and can progress slowly over time. They may include:
* Difficulty looking down and outward
* Double vision or diplopia
* Eye fatigue or strain
* Difficulty reading or performing other close-up tasks
* Weakness or paralysis of the eyelids
CPEO is caused by damage to the oculomotor nerve, which controls the lateral rectus muscles. This damage can result from a variety of factors, including:
* Trauma to the head or eye
* Inflammatory conditions such as myasthenia gravis or orbital pseudotumor
* Tumors or cysts in the orbit
* Infections such as neuroretinitis or optic neuropathy
* Genetic disorders such as oculopharyngeal muscular dystrophy
There is no cure for CPEO, but various treatments can help manage the symptoms. These may include:
* Eye exercises to strengthen the remaining muscles and improve eye movement
* Prism lenses to correct double vision
* Strabismus surgery to align the eyes properly
* Botulinum toxin injections to weaken the affected muscles and reduce spasms
* Physical therapy to improve eye movement and strength
It is important for individuals with CPEO to work closely with their healthcare provider to develop a personalized treatment plan that addresses their specific needs and symptoms. With appropriate management, many people with CPEO can maintain good vision and quality of life.
The signs and symptoms of CE can vary depending on the location of the tumor, but they may include:
* Lumps or swelling in the neck, underarm, or groin area
* Fever
* Fatigue
* Weight loss
* Night sweats
* Swollen lymph nodes
* Pain in the affected area
CE is caused by a genetic mutation that leads to uncontrolled cell growth and division. The exact cause of the mutation is not fully understood, but it is believed to be linked to exposure to certain viruses or chemicals.
Diagnosis of CE typically involves a combination of physical examination, imaging tests such as CT scans or PET scans, and biopsy to confirm the presence of cancer cells. Treatment options for CE depend on the stage and location of the tumor, but may include:
* Chemotherapy to kill cancer cells
* Radiation therapy to shrink the tumor
* Surgery to remove the tumor
* Immunotherapy to boost the immune system's ability to fight the cancer
Overall, CE is a rare and aggressive form of cancer that requires prompt diagnosis and treatment to improve outcomes.
Explanation: Genetic predisposition to disease is influenced by multiple factors, including the presence of inherited genetic mutations or variations, environmental factors, and lifestyle choices. The likelihood of developing a particular disease can be increased by inherited genetic mutations that affect the functioning of specific genes or biological pathways. For example, inherited mutations in the BRCA1 and BRCA2 genes increase the risk of developing breast and ovarian cancer.
The expression of genetic predisposition to disease can vary widely, and not all individuals with a genetic predisposition will develop the disease. Additionally, many factors can influence the likelihood of developing a particular disease, such as environmental exposures, lifestyle choices, and other health conditions.
Inheritance patterns: Genetic predisposition to disease can be inherited in an autosomal dominant, autosomal recessive, or multifactorial pattern, depending on the specific disease and the genetic mutations involved. Autosomal dominant inheritance means that a single copy of the mutated gene is enough to cause the disease, while autosomal recessive inheritance requires two copies of the mutated gene. Multifactorial inheritance involves multiple genes and environmental factors contributing to the development of the disease.
Examples of diseases with a known genetic predisposition:
1. Huntington's disease: An autosomal dominant disorder caused by an expansion of a CAG repeat in the Huntingtin gene, leading to progressive neurodegeneration and cognitive decline.
2. Cystic fibrosis: An autosomal recessive disorder caused by mutations in the CFTR gene, leading to respiratory and digestive problems.
3. BRCA1/2-related breast and ovarian cancer: An inherited increased risk of developing breast and ovarian cancer due to mutations in the BRCA1 or BRCA2 genes.
4. Sickle cell anemia: An autosomal recessive disorder caused by a point mutation in the HBB gene, leading to defective hemoglobin production and red blood cell sickling.
5. Type 1 diabetes: An autoimmune disease caused by a combination of genetic and environmental factors, including multiple genes in the HLA complex.
Understanding the genetic basis of disease can help with early detection, prevention, and treatment. For example, genetic testing can identify individuals who are at risk for certain diseases, allowing for earlier intervention and preventive measures. Additionally, understanding the genetic basis of a disease can inform the development of targeted therapies and personalized medicine."
Adenine nucleotide translocator
Thromboxane receptor
CLCN5
Tetrafluoroberyllate
Malate oxidase
Quantum biology
Nucleic acid metabolism
Dehydrogenase
PPAN
Adenosine thiamine triphosphate
P2RY11
Polynucleotide adenylyltransferase
Plasma gelsolin
Adenosine-phosphate deaminase
Glutaminase
Cruciform DNA
Herbert Zimmermann (neuroscientist)
Miodrag Radulovacki
John Thompson Shepherd
XDNA
Nicotinamide adenine dinucleotide
BCL2L13
Dense granule
Bongkrek acid
ARL2
Walter Jennings Jones
Foldamer
Heat stabilization
Adenosine thiamine diphosphate
PFKM
Metabolism
HSPA1B
Echinoderm and flatworm mitochondrial code
LECT2
NAD+ kinase
Cyclophilin
Glucose-6-phosphate dehydrogenase
Enzyme inhibitor
Index of biochemistry articles
DNA damage theory of aging
CAAT box
Hypochlorous acid
Substrate-level phosphorylation
Epigenomics
Chimeric RNA
Phage-assisted continuous evolution
Riboswitch
FMN adenylyltransferase
Robert MacLaren
Glycolysis
MicroRNA
RNA world
Adenosine monophosphate
Ribonucleotide
Chargaff's rules
Maximum parsimony (phylogenetics)
DNA repair
Pages that link to "Adenine nucleotides" - Bioblast
SERCA1 ATPase Antibody (4B8) (H00000487-M05): Novus Biologicals
Programming DNA to deliver cancer drugs
SLC25A4 gene: MedlinePlus Genetics
JCI -
Comments
AMD1 is required for the maintenance of leukemic stem cells and promotes chronic myeloid leukemic growth | Oncogene
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DeCS
ISOGG 2015 Y-DNA Glossary
SMART: Secondary literature for CSP domain
MH DELETED MN ADDED MN
Adenosine Monophosphate (definition)
Guanine7
- Identify the four types of nucleotides: adenine (A), thymine (T), guanine (G) and cytosine (C). (al.us)
- DNA contains only four nucleotides - adenine (A), thymine (T), cytosine (C), and guanine (G) - but this simple genetic alphabet is the starting point for making all of the proteins in the human body, estimated to be as many as one million. (nih.gov)
- Its chemical composition was known, and Erwin Chargaff had noted that the amounts of adenine and cytosine bases always matched, respectively, the amounts of thymine and guanine bases in any given DNA sample. (nih.gov)
- If the nucleotides--a nitrogenous base (adenine, cytosine, guanine, thymine, or uracil) attached to a sugar (ribose or deoxyribose) and a phosphate group--were the basic building blocks, Kornberg needed to know how to make them. (nih.gov)
- Several other researchers were working on the synthesis of adenine and guanine nucleotides, so Kornberg began with those of cytosine, thymine, and uracil. (nih.gov)
- From there, Kornberg and his colleagues quickly found additional enzymes that could make three other nucleotides (those of cytosine, adenine, and guanine) using uridine or PRPP as starting points. (nih.gov)
- In a sense, all life as we have known it boils down to four letters: G, C, A and T. Organized in unique patterns and repetition, these nucleotides (guanine, cytosine, adenine and thymine) form all DNA. (discovermagazine.com)
Thymine1
- Now able to synthesize all five nucleotides (a colleague at Washington University had found an enzyme that made the thymine nucleotide), Kornberg felt ready to look for the enzymes that assemble nucleotides into RNA or DNA. (nih.gov)
Translocase1
- The SLC25A4 gene provides the instructions for making a protein called adenine nucleotide translocase type 1 (ANT1). (medlineplus.gov)
Mitochondrial4
- The mitochondrial adenine nucleotide transporters in myogenesis. (bvsalud.org)
- Adenine Nucleotide Translocator isoforms ( ANTs ) exchange ADP / ATP across the inner mitochondrial membrane , are also voltage-activated proton channels and regulate mitophagy and apoptosis . (bvsalud.org)
- Effects of antimony on mitochondrial function and protein thiol and adenine nucleotide status in cultured cardiac myocytes. (cdc.gov)
- Some of the genetic changes alter single DNA building blocks (nucleotides), whereas others rearrange larger segments of mitochondrial DNA. (nih.gov)
Extracellular2
Appropriate nucleotides1
- To find the crucial enzyme in broken cell extracts from E. coli bacteria, he added ATP, plus the appropriate nucleotides, tagged with radioactive isotopes to trace their incorporation into the nucleic acid chain, and then added DNA as a primer for the chain. (nih.gov)
Complementary nucleotides2
- Students are able to manipulate models to explore transcription to demonstrate how complementary nucleotides bind to ensure a correct copy. (al.us)
- The twisted-ladder shape that two linear strands of DNA assume when complementary nucleotides on opposing strands bond together. (theodora.com)
Phosphate1
- Mediates the reversible, electroneutral exchange of Mg-ATP or Mg-ADP against phosphate ions, catalyzing the net uptake or efflux of adenine nucleotides a. (xenbase.org)
Strands1
- The authors of this study believe G4s temporarily hold the DNA strands apart so that proteins can read the nucleotide code and produce proteins. (iflscience.com)
Synthesis2
- The catecholamine-induced increase in cAMP was associated with an enhancement of adenine nucleotide catabolism resulting in an increase in release of inosine and hypoxanthine which can not be reutilized for adenine nucleotide synthesis. (jci.org)
- Working with a team that included Robert Lehman, Maurice Bessman, and others, Kornberg began his investigation into nucleotide synthesis by looking at orotic acid, a likely precursor of uracil, because it is uracil with a carbon dioxide molecule added. (nih.gov)
Enzymes1
- Enzymes called kinases move the missing pieces to these larger fragments to complete the nucleotide. (nih.gov)
Cellular2
- Therefore, one-third of total cellular adenine nucleotides were irreversibly lost in the presence of 1 mumol/liter isoproterenol. (jci.org)
- MBDB caused not only concentration (0-4.0 mM)- and time (0-2 h)-dependent cell death accompanied by the formation of cell blebs, and the loss of cellular ATP and adenine nucleotide pools, and reduced glutathione levels, but also the accumulation of oxidized glutathione. (erowid.org)
Molecule2
- Nanopore DNA sequencing is a laboratory technique for determining the exact sequence of nucleotides, or bases, in a DNA molecule. (genome.gov)
- DNA is a double-stranded molecule held together by weak bonds between base pairs of nucleotides. (theodora.com)
Proteins1
- Within each strand, chemicals called nucleotides are used as a code for making proteins. (nih.gov)
Mitochondria1
- Thus, the current study was undertaken in a rat model of CA to test the hypothesis that prolonged VF will lead to significantly impaired functional capacity of cerebral mitochondria and complete depletion of high-energy nucleotides. (hindawi.com)
Breakdown2
Bind1
- Trinitrophenyl derivatives bind differently from parent adenine nucleotides to Ca2+-ATPase in the absence of Ca2+. (expasy.org)
Intense1
- The decay mechanism of adenine in particular has been the focus of intense investigation, as has how these correlate to those of its more biologically relevant nucleotide and oligonucleotides in aqueous solution. (warwick.ac.uk)
Made1
- Based on his experience with coenzymes, Kornberg guessed that DNA or RNA would be made in cells by an enzyme that would string together whole nucleotides rather than assemble smaller chemical pieces. (nih.gov)
Code1
- Describe how it takes three nucleotides (called a triplet) to code for each amino acid of a protein. (al.us)
Complete1
- A third enzyme then splits the CO2 off the orotic ribose P, leaving uracil ribose P, also known as uridine monophosphate, which is a complete nucleotide. (nih.gov)
Levels1
- Nucleotide transport is inactive when cytosolic calcium levels are low, and is activated by an increase in cytosolic calcium levels. (xenbase.org)
Specific1
- B) Graphical representation of the 940 single-nucleotide polymorphisms specific to the 8 genotypes, showing interdifferences and intradifferences of all genomes. (cdc.gov)