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2 ,3 -cAMP

Grossmann, I. E., Mixed Integer Programming Approach for the Synthesis of Integrated Process Flowsheets, Camp. Chem. Eng., 9 463, 1985. [Pg.14]

C with partial decomposition. Synthesized from methanal and ammonia. Hexamine is used as starter fuel for camping stoves, as an... [Pg.203]

Bettelheim draws on his experience in concentration camps to illuminate the dangers inherent in all mass societies in this profound and moving masterpiece. [Pg.447]

If drilling and service personnel require accommodation at the well site a camp will need to be constructed. For safety reasons the camp will be located at a distance from the drilling rig and consist of various types of portacabins. For the camp, waste pits will be required, access roads, parking space and drinking water supplies. [Pg.43]

Camp P J and Patey G N 1999 Ion association and condensation in primitive models of electrolytes J. Chem. Phys. [Pg.553]

Camp P J, Mason C P, Allen M P, Khare A A and Kofke D A 1996 The isotropic-nematic transition in uniaxial hard ellipsoid fluids coexistence data and the approach to the Onsager limit J. Chem. Phys. 105 2837-49... [Pg.2284]

We have previously calculated conformational free energy differences for a well-suited model system, the catalytic subunit of cAMP-dependent protein kinase (cAPK), which is the best characterized member of the protein kinase family. It has been crystallized in three different conformations and our main focus was on how ligand binding shifts the equilibrium among these ([Helms and McCammon 1997]). As an example using state-of-the-art computational techniques, we summarize the main conclusions of this study and discuss a variety of methods that may be used to extend this study into the dynamic regime of protein domain motion. [Pg.68]

Fig. 1. Superposition of three crystal structures of cAMP-dependent protein kinase that show the protein in a closed conformation (straight line), in an intermediate conformation (dashed line), and in an open conformation (broken line). The structures were superimposed on the large lobe. In three locations, arrows identify corresponding amino acid positions in the small lobe. Fig. 1. Superposition of three crystal structures of cAMP-dependent protein kinase that show the protein in a closed conformation (straight line), in an intermediate conformation (dashed line), and in an open conformation (broken line). The structures were superimposed on the large lobe. In three locations, arrows identify corresponding amino acid positions in the small lobe.
Fig. 2. Conformational free energy of closed, intermediate and open protein kinase conformations. cAPK indicates the unbound form of cAMP-dependent protein kinase, cAPKiATP the binary complex of cAPK with ATP, cAPKiPKP the binary complex of cAPK with the peptide inhibitor PKI(5-24), and cAPK PKI ATP the ternary complex of cAPK with ATP and PKI(5-24). Shown are averaged values for the three crystal structures lATP.pdb, ICDKA.pdb, and ICDKB.pdb. All values have been normalized with respect to the free energy of the closed conformations. Fig. 2. Conformational free energy of closed, intermediate and open protein kinase conformations. cAPK indicates the unbound form of cAMP-dependent protein kinase, cAPKiATP the binary complex of cAPK with ATP, cAPKiPKP the binary complex of cAPK with the peptide inhibitor PKI(5-24), and cAPK PKI ATP the ternary complex of cAPK with ATP and PKI(5-24). Shown are averaged values for the three crystal structures lATP.pdb, ICDKA.pdb, and ICDKB.pdb. All values have been normalized with respect to the free energy of the closed conformations.
The procedure is computationally efficient. For example, for the catalytic subunit of the mammalian cAMP-dependent protein kinase and its inhibitor, with 370 residues and 131 titratable groups, an entire calculation requires 10 hours on an SGI 02 workstation with a 175 MHz MIPS RIOOOO processor. The bulk of the computer time is spent on the FDPB calculations. The speed of the procedure is important, because it makes it possible to collect results on many systems and with many different sets of parameters in a reasonable amount of time. Thus, improvements to the method can be made based on a broad sampling of systems. [Pg.188]

Left side of Fig. 4 shows a ribbon model of the catalytic (C-) subunit of the mammalian cAMP-dependent protein kinase. This was the first protein kinase whose structure was determined [35]. Figure 4 includes also a ribbon model of the peptide substrate, and ATP (stick representation) with two manganese ions (CPK representation). All kinetic evidence is consistent with a preferred ordered mechanism of catalysis with ATP binding proceeding substrate binding. [Pg.190]

Karlsson, R., Zheng, J., Zheng, N.-H., Taylor, S. S., Sowadski, J. M. Structure of the mamalian catalytic subunit of cAMP-dependent protein kinase and an inhibitor peptide displays an open conformation. Acta Cryst. D 49 (1993) 381-388. [Pg.196]

Earl Sutherland of Vanderbilt University won the 1971 Nobel Prize in physiology or medicine for uncovering the role of cAMP as a second messenger in connection with his studies of the fight or flight hormone epineph rine (Section 27 6)... [Pg.1161]

H2 The H2 receptor mediates effects, through an increase in cycHc adenosine monophosphate (cAMP), such as gastric acid... [Pg.139]

Biosynthesis. CRE is derived from a precursor of 196 amino acids (84,85). This gene contains one copy of CRE, which is flanked by double basic amino acids. The amino acid sequence of the CRE precursor suggests that it may arise from proteins related to POMC and neurophysins (31). The CRE precursor contains a cAMP responsive element which aHows stimulation of mRNA synthesis when intraceHular levels of cAMP are increased (86). [Pg.203]

Factors controlling calcium homeostasis are calcitonin, parathyroid hormone(PTH), and a vitamin D metabolite. Calcitonin, a polypeptide of 32 amino acid residues, mol wt - SGOO, is synthesized by the thyroid gland. Release is stimulated by small increases in blood Ca " concentration. The sites of action of calcitonin are the bones and kidneys. Calcitonin increases bone calcification, thereby inhibiting resorption. In the kidney, it inhibits Ca " reabsorption and increases Ca " excretion in urine. Calcitonin operates via a cyclic adenosine monophosphate (cAMP) mechanism. [Pg.376]

Parathyroid hormone, a polypeptide of 83 amino acid residues, mol wt 9500, is produced by the parathyroid glands. Release of PTH is activated by a decrease of blood Ca " to below normal levels. PTH increases blood Ca " concentration by increasing resorption of bone, renal reabsorption of calcium, and absorption of calcium from the intestine. A cAMP mechanism is also involved in the action of PTH. Parathyroid hormone induces formation of 1-hydroxylase in the kidney, requited in formation of the active metabolite of vitamin D (see Vitamins, vitamin d). [Pg.376]

CycHc adenosine monophosphate (cAMP), produced from ATP, is involved in a large number of ceUular reactions including glycogenolysis, Hpolysis, active transport of amino acids, and synthesis of protein (40). Inorganic phosphate ions are involved in controlling the pH of blood (41). The principal anion of interceUular fluid is HP (Pig. 3) (41). [Pg.377]

A subset of ion channels not gated by traditional neurotransmitters represents another receptor class. These iaclude potassium, calcium, sodium, and cychc adenosiae monophosphate (cAMP)-gated channels (14—16) for which a large number of synthetic molecules exist that alter ceUular function. [Pg.518]

Researchers at the MoneU Center (Philadelphia, Pennsylvania) are using a variety of electrophysical and biochemical techniques to characterize the ionic currents produced in taste and olfactory receptor cells by chemical stimuli. These studies are concerned with the identification and pharmacology of the active ion channels and mode of production. One of the techniques employed by the MoneU researchers is that of "patch clamp." This method aUows for the study of the electrical properties of smaU patches of the ceU membrane. The program at MoneU has determined that odors stimulate intraceUular enzymes to produce cycUc adenosine 3, 5 -monophosphate (cAMP). This production of cAMP promotes opening of the ion channel, aUowing cations to enter and excite the ceU. MoneU s future studies wiU focus on the connection of cAMP, and the production of the electrical response to the brain. The patch clamp technique also may be a method to study the specificity of receptor ceUs to different odors, as weU as the adaptation to prolonged stimulation (3). [Pg.292]

Pig. 3. Representation of promoter sites on the pro-enkephalin gene. The numbers represent the distance in nucleotides from the pro-enkephalin initiation codon the arrow indicates the direction of transcription. The TATA promoter box occurs immediately before the pro-enkephalin initiation site the AP-2 site, which binds immediate-early gene products, is 70 nucleotides upstream, and the CRE site, which binds a regulatory protein involved in cAMP induction of mRNA synthesis, is 107 nucleotides upstream from the initiation codon. The expanded section shows that the CRE site actually consists of two elements, ENKCRE-1 and ENKCRE-2, which separately confer cAMP sensitivity to pro-enkephalin mRNA synthesis. [Pg.446]


See other pages where 2 ,3 -cAMP is mentioned: [Pg.71]    [Pg.553]    [Pg.2265]    [Pg.3066]    [Pg.66]    [Pg.196]    [Pg.45]    [Pg.158]    [Pg.510]    [Pg.1161]    [Pg.1161]    [Pg.1162]    [Pg.157]    [Pg.157]    [Pg.234]    [Pg.468]    [Pg.26]    [Pg.372]    [Pg.200]    [Pg.132]    [Pg.80]    [Pg.548]    [Pg.579]    [Pg.29]    [Pg.446]    [Pg.446]    [Pg.449]    [Pg.264]    [Pg.278]   
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3 ,5 -Cyclic adenyl phosphate 3 ,5 -CAMP)

3-Adrenergic receptors cAMP accumulation

8- Bromo-cAMP

8-azido-cAMP

AMP, cAMP

Adenylyl Cyclase and cAMP as Second Messenger

Adenylyl cyclase cAMP derived from

Adenylyl cyclase/cAMP system

Adrenaline cAMP formation

Allosteric model for cAMP oscillations

Aperiodic oscillations of cAMP chaos

Au-rich volcanogenic massive sulfide deposits Examples from the world-class Doyon-Bousquet-LaRonde mining camp, Abitibi Greenstone Belt, Canada

Biological rhythms cAMP oscillations

Boot camp

Brain camp

CAMP (cyclic adenosine

CAMP (cyclic adenosine monophosphate action

CAMP Analogs

CAMP accumulation

CAMP accumulation activation

CAMP accumulation agonists

CAMP accumulation inhibition

CAMP accumulation release

CAMP accumulation, forskolin-stimulated

CAMP and DIPAMP

CAMP assays

CAMP caffeine

CAMP cascade

CAMP formation

CAMP formation dopamine

CAMP formation receptor

CAMP generators

CAMP gradient

CAMP ligand

CAMP phosphodiesterase

CAMP phosphodiesterase inhibition

CAMP phosphodiesterase inhibitors

CAMP production

CAMP production materials

CAMP production methods

CAMP receptor

CAMP receptor protein

CAMP resistance

CAMP response element

CAMP response element binding

CAMP response element binding protein

CAMP response element binding protein CREB)

CAMP response element binding receptors

CAMP response element modulator

CAMP response element modulator CREM)

CAMP response protein

CAMP responsive element -mediated

CAMP responsive element -mediated signaling

CAMP responsive element binding protein

CAMP responsive element binding protein CREB)

CAMP responsive elements

CAMP signal transduction

CAMP signaling

CAMP signaling pathway

CAMP stimulation

CAMP system

CAMP waves

CAMP, fluorescent assays

CAMP, intracellular concentration

CAMP, protein kinase interactions

CAMP-CRP

CAMP-GEFs

CAMP-activating compounds

CAMP-dependent Protein Kinase A

CAMP-dependent channels

CAMP-dependent phosphorylation

CAMP-dependent protein kinase

CAMP-dependent protein kinase (PKA

CAMP-dependent protein kinase activation

CAMP-dependent protein kinase pathway

CAMP-dependent protein phosphorylation

CAMP-dependent triacylglycerol

CAMP-dependent triacylglycerol lipase

CAMP-gated Na+channels

CAMP-gated ion channels

CAMP-increasing agents

CAMP-induced influx

CAMP-mediated cascade

CAMP-protein kinase

CAMP-regulated phosphoprotein

CAMP-response element binding CREB)

CAMP-response element binding monophosphate

CAMP-sensitive ion channels

CAMP/PKA signaling pathway

CAMP—See Cyclic adenosine

CAMP—See Cyclic adenosine monophosphate

CAP-cAMP

CREB (cAMP

Caged cAMP

Calcium cAMP pathway interaction

Calcium/cAMP response element binding

Calcium/cAMP response element binding protein

Calcium/cyclic adenosine monophosphate cAMP)

Camp American University

Camp Beale

Camp Bowie

Camp Detrick

Camp Detrick activation

Camp Detrick biological warfare research

Camp Detrick construction

Camp Detrick, Maryland

Camp Dresser McKee

Camp Edwards

Camp Fortune

Camp Gordon

Camp Leach

Camp Lee

Camp McCoy

Camp Roberts

Camp Sibert

Camp Sibert training facilities

Camp layouts

Camp number

Campe sterol

Camping gas

Camping gear

Camping issues

Camps quinoline synthesis

Camps quinolinol synthesis

Camps, Francis

Catabolite repression cAMP-mediated

Complex oscillations in a seven-variable model for cAMP signalling

Complex oscillatory phenomena in a three-variable model for cAMP signalling

Concentration camp inmates

Concentration camps

Concentration/extermination camps

Concentration/extermination camps inmates

Contemporary hunting camp next to the abandoned village of Nuniamo

Cougar Summer Science Camp

Cyclic AMP, cAMP

Cyclic adenine monophosphate CAMP)

Cyclic adenosine monophosphate cAMP response element binding protein

Cyclic adenosine monophosphate cAMP)

Cyclic adenosine monophosphate cAMP)-stimulated acid secretion

Cyclic adenylic acid, cAMP

Dadaab refugee camp

De-camping

Developmental path in parameter space a molecular basis for the ontogenesis of cAMP oscillations

Dibutyryl-cAMP

Dictyostelium cells cAMP oscillations

Dictyostelium discoideum cAMP as messenger

Dictyostelium discoideum cAMP stimulation

Dopamine- and cAMP-regulated

Dopaminergic agonists, cAMP

Exogenous cAMP

Extermination camps

Forskolin-activated cAMP cascade

From cAMP signalling in Dictyostelium to pulsatile hormone secretion

Function of cAMP oscillations in Dictyostelium

G-CaMP

G-protein-coupled adenylate cyclase-cAMP system

Gas Chamber in the Auschwitz I Main Camp

Germany, Nazi concentration camps

Glucagon and cAMP

Glucagon-cAMP-kinase pathway

Hydrolysis 2 ,3 -cAMP

In camps

Inhibition cAMP)

Inhibition of cAMP phosphodiesterase

Intercellular cAMP

Intracellular signaling cAMP levels

Johnson Camp, Arizona

Kinase cAMP-dependent

Kinases cAMP-dependent protein kinase

Labour camps

Link between relay and oscillations of cAMP

Model based on desensitization of the cAMP receptor

Monophosphine CAMP

Necessity of amending the allosteric model for cAMP signalling

Phosphodiesterases cAMP hydrolyzed

Phosphorylation by cAMP-dependent protein kinase

Phosphorylation cAMP dependent, biochemical

Protein cAMP-dependent

Protein kinase Activation by cAMP

Protein kinase, cAMP-dependent active sit

Purines cAMP phosphodiesterase

Pyramid, Camp

R-camp

Rare earth element variations in volcanogenic massive sulfides, Bathurst Mining Camp, New Brunswick evidence from laser-ablation ICPMS analyses of phosphate accessory phases

Refugee camps

Regulation of Platelet Activation By cAMP and cGMP

Relaxation cAMP contributing

Replacement Training Center, Camp Sibert

Rp-cAMPS

Second messenger, cAMP

Signal transduction cAMP-dependent protein kinase activation

Sprague de Camp

Summer Science Camp

The adenylate cyclase-cAMP system

Union Camp

Unit Training at Camp Sibert

Urinary cAMP Excretion in Gouty Patients with and without Nephrolithiasis

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