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Adenylation

The first technique is very intuitive. Out of the few proteins that could be crystallized in a number of different conformations, adenylate kinase is probably the best-studied example. By combining nine observed crystal structures and interpolating between them, a movie was constructed that visualized a hypothetical path of its hinge-bending transition (jVonrhein et al. 1995]). [Pg.67]

To facilitate conformational transitions in the before-mentioned adenylate kinase, Elamrani and co-workers scaled all atomic masses by a large factor thus allowing the use of a high effective simulation temperature of 2000K ([Elamrani et al. 1996]). To prevent protein unfolding, elements of secondary structure had to be constrained. [Pg.73]

Elamrani et al. 1996] Elamrani, S., Berry, M.B., Phillips Jr., G.N., McCammon, J.A. Study of Global Motions in Proteins by Weighted Masses Molecular Dynamics Adenylate Kinase as a Test Case. Proteins 25 (1996) 79-88 [Elcock et al. 1997] Elcock, A.H., Potter, M.J., McCammon, J.A. Application of Poisson-Boltzmann Solvation Forces to Macromolecular Simulations. In Computer Simulation of Biomoleeular Systems, Vol. 3, A.J. Wilkinson et al. eds., ESCOM Science Publishers B.V., Leiden... [Pg.76]

Adenoviridae Adenovirus, type 2 Adenylate cyclase Adenyl cyclase O-Adenylylation Adenylyl cyclase... [Pg.16]

Brain adenylate cyclase Brain imaging Brains Brake bands Brake blocks Brake facings Brake fluids... [Pg.126]

Luciferin (41) (R = H) reacts with adenosiae triphosphate (ATP) and the en2yme to give a complex (42) of the adenylate ester (41) R =... [Pg.272]

Vanadium. Vanadium is essential in rats and chicks (85,156). Estimated human intake is less than 4 mg/d. In animals, deficiency results in impaired growth, reproduction, and Hpid metaboHsm (157), and altered thyroid peroxidase activities (112). The levels of coen2yme A and coen2yme Q q in rats are reduced and monoamine oxidase activity is increased when rats are given excess vanadium (157). Vanadium may play a role in the regulation of (NaK)—ATPase, phosphoryl transferases, adenylate cyclase, and protein kinases (112). [Pg.388]

Two AT-II receptors, AT and AT2 are known and show wide distribution (27). The AT receptor has been cloned and predominates ia regions iavolved ia the regulation of blood pressure and water and sodium retention, eg, the aorta, Hver, adrenal cortex, and ia the CNS ia the paraventricular nucleus, area postrema, and nucleus of the soHtary tract. AT2 receptors are found primarily ia the adrenal medulla, utems, and ia the brain ia the locus coeruleus and the medial geniculate nucleus. AT receptors are GCPRs inhibiting adenylate cyclase activity and stimulating phosphoHpases C, A2, and D. AT2 receptors use phosphotyrosiae phosphatase as a transduction system. [Pg.527]

Opiates iateract with three principal classes of opioid GPCRs )J.-selective for the endorphiQS,5-selective for enkephalins, and K-selective for dynorphias (51). AU. three receptors have been cloned. Each inhibits adenylate cyclase, can activate potassium channels, and inhibit A/-type calcium channels. The classical opiates, morphine and its antagonists naloxone (144) and naltrexone (145), have moderate selectivity for the. -receptor. Pharmacological evidence suggests that there are two subtypes of the. -receptor and three subtypes each of the 5- and K-receptor. An s-opiate receptor may also exist. [Pg.545]

Vasoactive Intestinal Peptide and Pituitary Adenylate Cyclase Activating Peptide. Vasoactive intestinal peptide (VIP)... [Pg.578]

J (339), a 28-amino acid peptide, is a member of a family of stmctuially related peptides that includes secretin [1393-25-5] (340), growth hormone releasing factor (GRF), and pituitary adenylate cyclase-activating peptide (PACAP) [137061(341) (83). [Pg.578]

Lithium. In the lithium carbonate treatment of certain psychotic states, a low incidence (3.6%) of hypothyroidism and goiter production have been observed as side effects (6,36) (see Psychopharmacologicalagents). It has been proposed that the mechanism of this action is the inhibition of adenyl cyclase. Lithium salts have not found general acceptance in the treatment of hyperthyroidism (see Lithiumand lithium compounds). [Pg.53]

Resistance to Lincomycin. Resistance to lincomycin is developed slowly, and is usually caused by modification of 23S ribosomal RNA, which leads to co-resistance to macroHde, lincosaminide, and streptogramin B antibiotics (25). Inactivation of lincomycin by clinical isolates of strains of Staphjlococcus aureus and Staphjlococcus haemoljticus, though retention of sensitivity to macroHdes (see Antibiotics, macrolides) and streptogramins (see Antibiotics, peptides), has been found to be the consequence of the conversion of the antibiotic into its 3-(5 -adenylate) (26). [Pg.87]

Cross-resistance between lincomycin and clindamycin is complete (64), and co-resistances of lincomycin also apply to clindamycin. However, the inactivation of clindamycin by clinical isolates of Staphylococcus haemolyticus and Staphylococcus aureus is caused by adenylylation at the 4-position to form clindamycin 4-(5 -adenylate) [29752-38-3] (7) in contrast to the lincomycin 3-(5 -adenylate) [117785-83-8] (8) that forms (26). [Pg.89]

Clindamycin 3-phosphate [28708-34-17, antibacterially inactive in vitro, and the ribonucleotides clindamycin 3-(5 -cytidylate) [31186-90-0], clindamycin 3-(5 -adenylate) [31186-91-1], clindamycin 3-(5 -uridylate) [36010-69-2], and clindamycin 3-(5 -guanylate) [36010-70-5], all inactive in vitro, can be generated... [Pg.90]

Forskolin (5-[acetyloxy]-3-ethenyldodecahydro-6,10,10b-trihydroxy-3,4a,7,7,10a-penta-methyl-[3R- 3a-4aP, SP, 6P, 6aa,10a, lOaP, 10ba -lFf-naphtho[2,l-b]pyran-l-one) [66575-29-9] M 410.5, m 229-232°, 228-233°. Recrystd from CfiH6-pet ether. It is antihypertensive, positive ionotropic, platelet aggregation inhibitory and adenylate cyclase activating properties [Chem AbstrS9 1978 244150, de Souza et al. Med Res Rev 3 201 1983]. [Pg.246]

Adenosine-3 -monophosphoric acid hydrate [3 -adenylic acid, 3 -AMP] [84-21-9] M 347.3, m 197°(dec, as 2H2O), 210°(dec), m 210°(dec), [a]s46 -50° (c 0.5, 0.5M Na2HP04), pK 3.65, pKz 6.05. It crystallises from large volumes of H2O in needles as the monohydrate, but is not very soluble in boiling H2O. Under acidic conditions it forms an equilibrium mixture of 2 and 3 adenylic acids via the 2, 3 -cyclic phosphate. When heated with 20% HCl it gives a quantitative yield of furfural after 3hours, unlike 5 -adenylic acid which only gives traces of furfural. The yellow monoacridine salt has m 175°(dec) and... [Pg.508]

Figure 4.14 Examples of different types of open twisted a/p structures. Both schematic and topological diagrams are given. In the topological diagrams, arrows denote strands of p sheet and rectangles denote a helices, (a) The FMN-binding redox protein flavodoxln. (b) The enzyme adenylate kinase, which catalyzes the reaction AMP +... Figure 4.14 Examples of different types of open twisted a/p structures. Both schematic and topological diagrams are given. In the topological diagrams, arrows denote strands of p sheet and rectangles denote a helices, (a) The FMN-binding redox protein flavodoxln. (b) The enzyme adenylate kinase, which catalyzes the reaction AMP +...

See other pages where Adenylation is mentioned: [Pg.15]    [Pg.15]    [Pg.217]    [Pg.1162]    [Pg.227]    [Pg.227]    [Pg.191]    [Pg.275]    [Pg.95]    [Pg.381]    [Pg.516]    [Pg.518]    [Pg.532]    [Pg.547]    [Pg.553]    [Pg.566]    [Pg.575]    [Pg.279]    [Pg.280]    [Pg.438]    [Pg.438]    [Pg.443]    [Pg.156]    [Pg.205]    [Pg.206]    [Pg.492]    [Pg.152]    [Pg.129]    [Pg.359]    [Pg.509]    [Pg.532]    [Pg.355]    [Pg.355]   
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See also in sourсe #XX -- [ Pg.83 ]

See also in sourсe #XX -- [ Pg.127 ]

See also in sourсe #XX -- [ Pg.247 , Pg.248 ]




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3 ,5 -Cyclic adenyl phosphate

3 ,5 -Cyclic adenyl phosphate 3 ,5 -CAMP)

3 ,5 -Cyclic adenylate

3 ,5 -Cyclic adenylic acid

5 -Adenylic acid aminohydrolase

5 -Adenylic acid aminohydrolase chemical and physical properties

5 -Adenylic acid aminohydrolase kinetics

5 -Adenylic acid aminohydrolase specificity

5 -Adenylic deaminase, application

ACTH adenylate cyclase in action

ADP in adenylate system

AMP in adenylate system

ATP in adenylate system

Acetyl adenylate

Acetyl adenylate and

Acetyl adenylate preparation

Acetyl adenylate, hydrolysis

Activation of adenylate cyclase

Activation of adenylate cyclase activity

Acyl adenylate

Acyl adenylate, from carboxylic acids

Acyl adenylate, from carboxylic acids mechanism of formation

Acyl adenylates

Acyl adenylates and

Adenosine monophosphate Fatty acid adenylates

Adenosine monophosphate under Adenylic acid

Adenyl cyclase

Adenyl cyclase activity

Adenyl cyclase glucagon

Adenyl cyclase hormonal activation

Adenyl cyclase hormone receptor model

Adenyl cyclase protein inhibitor

Adenyl cyclase system

Adenyl cyclase system subunits

Adenyl cyclase, stimulation

Adenyl cyclase/phosphokinase

Adenyl formation

Adenyl nucleotides

Adenyl radical

Adenyl-amino acids

Adenyl-peptide conjugates

Adenylate

Adenylate

Adenylate Bordetella pertussis

Adenylate Cyclase-Dependent Signaling

Adenylate anhydride

Adenylate anticytokinins

Adenylate binding pockets

Adenylate catabolism

Adenylate charge

Adenylate cyclase

Adenylate cyclase activation

Adenylate cyclase activator

Adenylate cyclase activity

Adenylate cyclase activity stimulation

Adenylate cyclase activity stimulatory effects

Adenylate cyclase activity, inhibition

Adenylate cyclase adrenergic receptors

Adenylate cyclase assay

Adenylate cyclase blood levels

Adenylate cyclase catalytic subunit

Adenylate cyclase cell culture

Adenylate cyclase characterization

Adenylate cyclase coupling

Adenylate cyclase coupling with dopamine receptors

Adenylate cyclase dopamine receptor

Adenylate cyclase dopaminergic receptors

Adenylate cyclase enzyme, effect

Adenylate cyclase factor

Adenylate cyclase hormones affecting

Adenylate cyclase inhibition

Adenylate cyclase lead inhibition

Adenylate cyclase magnesium ions

Adenylate cyclase mechanism

Adenylate cyclase mechanism transfer

Adenylate cyclase metabolism

Adenylate cyclase negative coupling

Adenylate cyclase opioid receptors

Adenylate cyclase pathway, triggering

Adenylate cyclase platelets

Adenylate cyclase postsynaptic

Adenylate cyclase postsynaptic nerve

Adenylate cyclase reaction catalyzed

Adenylate cyclase receptor linked

Adenylate cyclase receptor system

Adenylate cyclase signal transduction

Adenylate cyclase stimulants

Adenylate cyclase stimulation

Adenylate cyclase substituted-phenyl

Adenylate cyclase system

Adenylate cyclase toxic

Adenylate cyclase vanadium

Adenylate cyclase vasopressin-stimulated

Adenylate cyclase, G-proteins

Adenylate cyclase, adenylyl

Adenylate cyclase, in brain

Adenylate cyclase, stereochemical

Adenylate cyclase, thyroid hormones

Adenylate cyclase-cyclic adenosine

Adenylate cyclase-cyclic adenosine monophosphate system

Adenylate cyclases

Adenylate cydase

Adenylate deaminase

Adenylate deaminase and

Adenylate deaminase deficiency

Adenylate definition

Adenylate dephosphorylation

Adenylate energy charge

Adenylate energy charge ratio

Adenylate energy charge, metabolic

Adenylate energy charge, phosphorylation

Adenylate formation from adenosine

Adenylate formation from inosinate

Adenylate groups

Adenylate isopentenyltransferases

Adenylate kinase

Adenylate kinase and

Adenylate kinase assay

Adenylate kinase catalytic activity

Adenylate kinase deficiency

Adenylate kinase effects

Adenylate kinase functions

Adenylate kinase in intermembrane space

Adenylate kinase location

Adenylate kinase mitochondrial enzyme

Adenylate kinase nucleotide binding site

Adenylate kinase reaction

Adenylate kinase reaction mechanism

Adenylate kinase reaction, adenosine triphosphate

Adenylate kinase structure

Adenylate kinase substrate specificity

Adenylate kinase thermodynamics

Adenylate kinase, catalysis

Adenylate kinase, induction

Adenylate oligomers

Adenylate sequence interactions

Adenylate system

Adenylate system storage of energy

Adenylate through

Adenylate translocator

Adenylate, synthesis

Adenylate-binding protein

Adenylates

Adenylates monophosphate adenosine

Adenylates, aminoacyl

Adenylates, chemistry

Adenylation substrates

Adenylation, enzyme regulation

Adenylic 1-methyl

Adenylic 2-deoxy

Adenylic acid

Adenylic acid 5-nucleotidase

Adenylic acid analogues

Adenylic acid deaminase

Adenylic acid isomers

Adenylic acid kinase

Adenylic acid monophosphates

Adenylic acid muscle

Adenylic acid phosphorylation

Adenylic acid ribosidase

Adenylic acid ribosidase and

Adenylic acid yeast

Adenylic acid, AMP

Adenylic acid, deamination

Adenylic acid, deamination formation

Adenylic acid, deamination hydrolysis

Adenylic acid, structure

Adenylic acid-2 -phosphate

Adenylic add

Adenylic deaminase

Adenylic deaminase and

Adenylic kinase

Alanyl adenylate

Amino acid adenylate-sRNA incorporation pathway

Amino acid adenylate-sRNA pathway

Amino acid adenylates

Amino acid synthesis adenylation

Amino acyl adenylates

Aminoacyl adenylates and

Aminoacyl-adenylate

Aziridine adenylates

Bacteria adenylates

Bordetella Adenylate cyclase

Butyryl adenylate

Carboxylic acids, 5 -adenylic acid

Classification adenylate cyclase

Coupling agents adenylate system

Coupling with adenylate cyclase

Cyclic AMP and adenyl cyclase

Cyclic Adenyl cyclase

Cyclic adenylic acid, cAMP

De-adenylation

Delta receptors adenylate cyclase

Dopamine-sensitive adenylate cyclase

Enzymes Adenylate cyclase

Enzymes Adenylate kinase

Enzymes, adenylate-forming

Escherichia coli adenylate kinase

Escherichia coli adenylation

Fatty acid adenylates

Fatty acyl adenylates

Firefly luciferyl adenylate

Flupenthixol effects, adenylate cyclase

Forskolin, which is isolated from Coleus forskohlii, stimulates adenylate cyclase

G-protein-coupled adenylate cyclase-cAMP system

Glucagon adenylate cyclase in action

Glutamine synthetase adenylation

Inhibition of adenylate cyclase

Insulin Adenylate cyclase

Intermediate lobe adenylate cyclase

Kinases adenylate kinase

Luciferase adenylate binding

Luciferyl adenylate

Magnesium ion in adenylate system

Membrane-bound enzymes adenylate cyclase

Modulation of Insulin Secretion via Adenylate Cyclase and Phospholipase C (PLC)

Muscle adenylate kinase

Muscle-adenylic acid deaminase

NMR spectroscopy of adenylate system

Neuroleptics, adenylate cyclase inhibition

Oligo-2 -5 -adenylates

Oxyluciferyl-adenylate

Phosphate, inorganic in adenylate system

Phosphoryl transfer adenylate kinase

Phosphorylation adenyl cyclase regulation

Phosphorylation state ratio adenylate system

Pituitary adenylate cyclase

Pituitary adenylate cyclase-activating

Pituitary adenylate cyclase-activating peptide

Pituitary adenylate cyclase-activating peptide PACAP)

Pituitary adenylate cyclase-activating polypeptide

Pituitary adenylate cyclase-activating polypeptide-38 (PACAP

Platelet activation adenyl cyclase

Platelet adenylate cyclase activation

Prostacyclin adenylate cyclase

Prostaglandin adenylate cyclase activation

Protein adenylate cyclase

Purines adenylate cyclase

Purines adenylate kinase

Pyrophosphate in adenylate system

Second messengers adenylate cyclase control

Striatal adenylate cyclase activity

Striatal adenylate cyclase activity stimulation

Striatal adenylate cyclase, agonists

The Adenylate System

The Membrane Receptor-Non-Adenylate-Cyclase System

The adenylate cyclase-cAMP system

Three-dimensional structures adenylate kinase

Translation adenylation

Tryptophan adenylate

Tyrosine adenylation

Tyrosyl adenylate

Yeast adenylate kinase

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