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Structures inosine

The 5 nucleotide of inosine inosimc acid (CioHi3N40gP) is added to foods as a flavor enhancer What is the structure of mosinic acid" (The structure of inosine is given in Problem 28 21)... [Pg.1190]

RNA-editing is a posttranscriptional mechanism mediated by RNA editases, which results in a site-selective deamination of adenosine to inosine. This alters codons and splicing in nuclear transcripts and thereby alters the structure and function of proteins. [Pg.1090]

Inosine 5 -Monophosphate Dehydrogenase. A series of 21 known inosine 5 -monophosphate dehydrogenase (IMPDH) inhibitors was used to validate a virtual screening protocol. By application of a molecular weight filter (80 < MW < 400), 3425 compounds were extracted from an in-house reagent inventory system. Docking of these compounds into a substrate-IMPDH complex 3D structure was performed with the program FlexX three... [Pg.401]

Figure 7.9 Chemical structures of ligands of the enzyme PNP. (A) The substrate inosine, (B) the inosine and phosphate transition state, and (C) the transition state mimic inhibitor Imucillin H. Figure 7.9 Chemical structures of ligands of the enzyme PNP. (A) The substrate inosine, (B) the inosine and phosphate transition state, and (C) the transition state mimic inhibitor Imucillin H.
Tipson devoted most of his years in Levene s laboratory accomplishing seminal work on the components of nucleic acids. To determine the ring forms of the ribose component of the ribonucleosides he applied Haworth s methylation technique and established the furanoid structure for the sugar in adenosine, guanosine, uridine, and thymidine. He showed that formation of a monotrityl ether is not a reliable proof for the presence of a primary alcohol group in a nucleoside, whereas a tosyl ester that is readily displaced by iodide affords clear evidence that the ester is at the 5-position of the pentofuranose. Acetonation of ribonucleosides was shown to give the 2, 3 -C -isopropyl-idene derivatives, which were to become extensively used in nucleoside and nucleotide chemistry, and were utilized by Tipson in the first chemical preparation of a ribonucleotide, inosinic acid. [Pg.422]

All muscarinic receptors are members of the seven transmembrane domain, G protein-coupled receptors, and they are structurally and functionally unrelated to nicotinic ACh receptors. Activation of muscarinic receptors by an agonist triggers the release of an intracellular G-protein complex that can specifically activate one or more signal transduction pathways. Fortunately, the cellular responses elicited by odd- versus even-numbered receptor subtypes can be conveniently distinguished. Activation of Ml, M3, and M5 receptors produces an inosine triphosphate (IP3) mediated release of intracellular calcium, the release of diacylglyc-erol (which can activate protein kinase C), and stimulation of adenylyl cyclase. These receptors are primarily responsible for activating calcium-dependent responses, such as secretion by glands and the contraction of smooth muscle. [Pg.122]

The structure of the urease active center is similar to that of adenosine deaminase, an enzyme containing one zinc(II) per active site (though see 48). This enzyme catalyzes the deamination of adenosine to inosine and NH3 (see Scheme 9), a reaction mechanistically related... [Pg.251]

The first surprise was that these molecules are much longer than seems necessary for the formation of adapters. In addition, 10-20% of their bases are modified greatly from their original form.171 Another surprise was that the anticodons are not all made up of "standard" bases. Thus, hypoxanthine (whose nucleoside is inosine) occurs in some anticodons. Conventional "cloverleaf" representations of tRNA, which display their secondary structures, are shown in Figs. 5-30 and 29-7. However, the molecules usually have an L shape rather than a cloverleaf form (Figs. 5-31 and 29-6),172 and the L form is essential for functioning in protein synthesis as indicated by X-ray and other data.173 Three-dimensional structures, now determined for several different tRNAs,174 175 are all very similar. Structures in solution are also thought to be... [Pg.1687]

A number of zinc and cadmium complexes of adenine (82),554,555 adenine N-oxide,556 guanine,557 inosine,558 cytidine559 and other nucleosides560 have been studied. The structure of (9-methyladenine)ZnCl2 is polymeric each zinc ion is tetrahedrally coordinated to two chlorine atoms (Zn—Cl = 2.22 A), and to N-l and N-7 of neighbouring adenine moieties (Zn— N = 2.05A).561 A structural study of the related cadmium complex, CdCl2(DMSO)L (L = 9-methyladenine), has shown the complex to form a one-dimensional polymer. 2... [Pg.957]

The purine bases, adenine and guanine, participate in nature by providing structural elements of nucleic acids and numerous cofactors. The deaminated products of adenine and guanine do not participate in these coenzymic functions except in a relatively few instances. For example, the relative ineffectiveness of inosine monophosphate (IMP) vs. [Pg.47]


See other pages where Structures inosine is mentioned: [Pg.331]    [Pg.387]    [Pg.36]    [Pg.108]    [Pg.284]    [Pg.200]    [Pg.200]    [Pg.126]    [Pg.87]    [Pg.420]    [Pg.158]    [Pg.335]    [Pg.544]    [Pg.97]    [Pg.338]    [Pg.234]    [Pg.565]    [Pg.396]    [Pg.194]    [Pg.1049]    [Pg.1454]    [Pg.1648]    [Pg.1117]    [Pg.836]    [Pg.34]    [Pg.426]    [Pg.711]    [Pg.235]    [Pg.18]    [Pg.81]    [Pg.306]   
See also in sourсe #XX -- [ Pg.181 ]




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Inosin

Inosinate

Inosine, crystal structure

Inosine-5 -monophosphate, structure

Inosinic acid, structure

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