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Phosphates terminal

Phosphate terminal nucleotide" 5 -OH terminal nucleotide6 5 -OH penultimate nucleotide6... [Pg.284]

Conduct the assays for Series A, B, and C, initiating each reaction with 100 /id 0.036 M carbamyl phosphate, terminating after 30 min of reaction with 1 ml of 2% perchloric acid, and developing the color by adding 3.0 ml of freshly prepared color reagent as described above. Include a series of carbamyl aspartate standards also as described above. [Pg.154]

Recently, Brzozowska et al. used NR and ex situ electrochemical techniques to characterize an innovative type of monolayer system intended to serve as a support for a bUayer lipid membrane on a gold electrode surface [51]. Zr ions were used to noncovalendy couple a phosphate-terminated self-assembled monolayer (SAM) formed on a gold surface to the carboxylate groups of negatively charged phos-phatidylserrne (PS). This tethered surface was then used for the formation of a PS hpid bilayer structure formed by vesicle fusion and spreading. NR studies revealed the presence of an aqueous environment associated with the tether layer which arises from nonstoichiometric water associated with the zirconium phosphate moieties [52]. [Pg.170]

Theory has been used predominantly to probe the nature of the sites on vanadium clusters and model vanadium oxide surfaces. Cluster and p>eriodic DFT calculations [68,69] have been carried out in order to imderstand the electronic and structural properties of the exposed (100) surface of (VO)2P207. Both cluster and slab calculations reveal that surface vanadium sites can act as both local acid and base sites, thus enhancing the selective activation of n-butane as well as the adsorption of 1-butene. Vanadium accepts electron density from methylene carbon atoms and, thus aids in the subsequent activation of other C-H bonds. Calculations reveal that that the terminal P=0 bonds lie close to the Fermi level and thus present the most nucleophihc oxygen species present at the surface for both the stoichiometric as well as phosphate-terminated surfaces. These sites may be involved in the nucleophilic activation of subsequent CCH bonds necessary in the selective oxidative conversion of butane into maleic anhydride. Full relaxation of the surface, however, tends to lead to a contraction of the terminal P=0 bonds and a lengthening of the P V bonds. This pushes the P V states, initially centered on the oxygen atoms, higher in energy and thus increases their tendency to be involved in nucleophilic attack . [Pg.248]

Following conversion into its kinetic enol phosphate (terminal olefinic bond), treatment of a methyl ketone with LDA or lithium 2,2,6,6-tetramethylpiperidide effects highly regioselective /3-elimination to give a terminal acetylene e.g. Scheme 107).This is the first method for this transformation that works consistently, even for methyl ketones with a-methylene or a-methine hydrogen atoms, without significant quantities of allenes being formed concurrently. [Pg.49]

Each nucleic acid has its own unique sequence of bases, which is known as its primary structure. It is this sequence of bases that carries the genetic information from one cell to the next. In any nucleic acid, the sugar at the one end has an unreacted or free 5 -phosphate terminal end, and the sugar at the other end has a free 3 -hydroxyl group. [Pg.595]

Cationic, anionic, and amphoteric surfactants derive thek water solubiUty from thek ionic charge, whereas the nonionic hydrophile derives its water solubihty from highly polar terminal hydroxyl groups. Cationic surfactants perform well in polar substrates like styrenics and polyurethane. Examples of cationic surfactants ate quaternary ammonium chlorides, quaternary ammonium methosulfates, and quaternary ammonium nitrates (see QuARTERNARY AMMONIUM compounds). Anionic surfactants work well in PVC and styrenics. Examples of anionic surfactants ate fatty phosphate esters and alkyl sulfonates. [Pg.297]

Basically, AZT is anabohcaHy phosphorylated to AZT mono-, di-, and tri-phosphates by various enzymes (kinases) of a target ceU (159). AZT-triphosphate competes with other phosphorylated pyrimidine nucleosides for incorporation into HIV DNA by the viral reverse transcriptase. Incorporation of the AZT-triphosphate into reverse transcriptase results in viral DNA chain termination. Reverse transcriptase is essential in the repHcative cycle of HIV. [Pg.314]

Bis-Pyndoxal Tetraphosphate. A second class of bifunctional reagents, described in 1988, involves two pyridoxal groups linked by phosphates of different lengths (89). As shown in Table 4, the yield of intramolecularly cross-linked hemoglobin increases dramatically with increasing length of the phosphate backbone. It is beheved that the site of reaction of (bis-PL) is between the amino-terminal amino group of one P-chain and the... [Pg.165]

Figure 4.6 The bifunctional enzyme PRA-isomerase (PRAI) IGP-synthase (IGPS) catalyzes two sequential reactions in the biosynthesis of tryptophan. In the first reaction (top half), which is catalyzed by the C-terminal PRAI domain of the enzyme, the substrate N-(5 -phosphoribosyl) anthranilate (PRA) is converted to l-(o-carboxyphenylamino)-l-deoxyribulose 5-phosphate (CdRP) by a rearrangement reaction. The succeeding step (bottom half), a ring closure reaction from CdRP to indole-3-glycerol phosphate (IGP), is catalyzed by the N-terminal IGPS domain. Figure 4.6 The bifunctional enzyme PRA-isomerase (PRAI) IGP-synthase (IGPS) catalyzes two sequential reactions in the biosynthesis of tryptophan. In the first reaction (top half), which is catalyzed by the C-terminal PRAI domain of the enzyme, the substrate N-(5 -phosphoribosyl) anthranilate (PRA) is converted to l-(o-carboxyphenylamino)-l-deoxyribulose 5-phosphate (CdRP) by a rearrangement reaction. The succeeding step (bottom half), a ring closure reaction from CdRP to indole-3-glycerol phosphate (IGP), is catalyzed by the N-terminal IGPS domain.
TFIIB is arranged in two domains, both of which have the cyclin fold described in Chapter 6. Both domains bind to the TBP-TATA box complex at the C-terminal stirrup and helix of TBP. The phosphate and sugar moities of DNA form extensive non-sequence-specific contacts with TFIIB both upstream and downstream of the middle of the TATA box. [Pg.159]

Long-chain polyisoprenoid. molecules with a terminal alcohol moiety are called, polyprenols. The dolichols, one class of polyprenols (Figure 8.18), consist of 16 to 22 isoprene units and, in the form of dolichyl phosphates, function to carry carbohydrate units in the biosynthesis of glycoproteins in animals. Polyprenyl groups serve to anchor certain proteins to biological membranes (discussed in Chapter 9). [Pg.252]


See other pages where Phosphates terminal is mentioned: [Pg.303]    [Pg.171]    [Pg.337]    [Pg.3427]    [Pg.3629]    [Pg.13]    [Pg.157]    [Pg.290]    [Pg.457]    [Pg.3426]    [Pg.3628]    [Pg.342]    [Pg.1202]    [Pg.193]    [Pg.246]    [Pg.135]    [Pg.126]    [Pg.156]    [Pg.303]    [Pg.171]    [Pg.337]    [Pg.3427]    [Pg.3629]    [Pg.13]    [Pg.157]    [Pg.290]    [Pg.457]    [Pg.3426]    [Pg.3628]    [Pg.342]    [Pg.1202]    [Pg.193]    [Pg.246]    [Pg.135]    [Pg.126]    [Pg.156]    [Pg.217]    [Pg.450]    [Pg.296]    [Pg.550]    [Pg.66]    [Pg.391]    [Pg.121]    [Pg.164]    [Pg.164]    [Pg.2133]    [Pg.224]    [Pg.116]    [Pg.178]    [Pg.198]    [Pg.260]    [Pg.264]    [Pg.184]    [Pg.1115]    [Pg.68]   
See also in sourсe #XX -- [ Pg.148 ]




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Nucleotides terminal phosphate, reactions

Self phosphate-terminated

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