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Alanine function

Supramolecular electrostatically driven assembly of the L-alanine-functionalized calix[4]arene... [Pg.167]

In addition to illustrating the mechanics of translation Figure 28 12 is important m that It shows the mechanism of peptide bond formation as a straightforward nude ophilic acyl substitution Both methionine and alanine are attached to their respective tRNAs as esters The ammo group of alanine attacks the methionine carbonyl displac mg methionine from its tRNA and converting the carbonyl group of methionine from an ester to an amide function... [Pg.1178]

From a map at low resolution (5 A or higher) one can obtain the shape of the molecule and sometimes identify a-helical regions as rods of electron density. At medium resolution (around 3 A) it is usually possible to trace the path of the polypeptide chain and to fit a known amino acid sequence into the map. At this resolution it should be possible to distinguish the density of an alanine side chain from that of a leucine, whereas at 4 A resolution there is little side chain detail. Gross features of functionally important aspects of a structure usually can be deduced at 3 A resolution, including the identification of active-site residues. At 2 A resolution details are sufficiently well resolved in the map to decide between a leucine and an isoleucine side chain, and at 1 A resolution one sees atoms as discrete balls of density. However, the structures of only a few small proteins have been determined to such high resolution. [Pg.382]

Certain amino acids and their derivatives, although not found in proteins, nonetheless are biochemically important. A few of the more notable examples are shown in Figure 4.5. y-Aminobutyric acid, or GABA, is produced by the decarboxylation of glutamic acid and is a potent neurotransmitter. Histamine, which is synthesized by decarboxylation of histidine, and serotonin, which is derived from tryptophan, similarly function as neurotransmitters and regulators. /3-Alanine is found in nature in the peptides carnosine and anserine and is a component of pantothenic acid (a vitamin), which is a part of coenzyme A. Epinephrine (also known as adrenaline), derived from tyrosine, is an important hormone. Penicillamine is a constituent of the penicillin antibiotics. Ornithine, betaine, homocysteine, and homoserine are important metabolic intermediates. Citrulline is the immediate precursor of arginine. [Pg.87]

A set of low-energy conformers has been provided for alanine (R=CH3) tetramer (terminated at both ends by amide functionality). For each conformer, identify each of the a carbons and measure the (j) and v(/ dihedral angles (see table below). [Pg.226]

Therapeutic Function Cancer chemotherapy Chemical Name 4-[bis(2-chloroethyl)amino]-L-phenylalanine Common Name Alanine nitrogen mustard L-sarcolysine Structural Formula... [Pg.924]

The solution to the specificity problem is to protect those functional groups vve want to render unreactive while leaving exposed only those functional groups we want to react. For example, if we wanted to couple alanine with leucine to synthesize Ala-Leu, we could protect the -NH2 group of alanine and... [Pg.1033]

The classical cadherins are translated as precursor because they are N-terminally cleaved to reveal the mature proteins. This processing is required to activate the cell adhesion function of cadherins. Cadherins interact in trans (i.e., from opposite cells) via the most N-terminal cadherin rqDeats. A short amino acid sequence within this repeat, histidine-alanine-valine (HAV), has been implicated in mediating cell-cell contacts as HAV peptides can disrupt cadherin-dependent cell adhesion. Besides the trans-interactions of cadherins, the extracellular domains are also capable of forming cis-dimers through lateral amino acid contacts between cadherin molecules on one cell. This dimerization again mainly involves the first cadherin repeat. A zipper model based on the pattern of alternating cis- and trans-dimers [1] for the adhesive interactions has been proposed. [Pg.307]

The nurse immediately reportsany elevated alanine aminotransferase (ALT) level to the primary health care provider. The primary health care provider may want to continue monitoring the ALT level or discontinue use of the drug because of the danger of hepatotoxidty. However, abrupt discontinuation may cause a decline in cognitive functioning. [Pg.308]

FIGURE 19.5 The fractional composition of a solution of alanine, a typical amino acid, as a function of pH. Notice that the concentration of the molecular form is extremely low at all pH values its concentration had to be multiplied by a factor of 10 l for it to be visible on the graph. Amino acids are present almost entirely in ionic form in aqueous solution. [Pg.879]

Fmoc-y9-alanine was pre-activated by introducing the pentafluorophenyi function as an ester group [88]. Dmab-y0-alanine and the pentafluorophenyi ester of Fmoc-/ -alanine reacted and the synthesis of the corresponding y0-dipeptide was realized. [Pg.435]

N-f-Boc-L-lysine is a more complex peptide owing to the additional amino function [5] Dmab-y0-alanine and N-f-Boc-i-lysine were reacted to give the dipeptide. [Pg.436]

OS 24] [R 5] [P 16/Dmab-y0-alanineand Emoc-yS-alanine were reacted to give a dipeptide [5], After cleavage of the Emoc function, Emoc-yS-alanine was added to such a dipeptide resulting in tripeptide formation with 30% yield [5]. [Pg.441]


See other pages where Alanine function is mentioned: [Pg.1801]    [Pg.229]    [Pg.89]    [Pg.149]    [Pg.1801]    [Pg.229]    [Pg.89]    [Pg.149]    [Pg.475]    [Pg.562]    [Pg.600]    [Pg.330]    [Pg.63]    [Pg.180]    [Pg.296]    [Pg.23]    [Pg.246]    [Pg.222]    [Pg.142]    [Pg.76]    [Pg.161]    [Pg.215]    [Pg.235]    [Pg.323]    [Pg.554]    [Pg.789]    [Pg.340]    [Pg.879]    [Pg.70]    [Pg.66]    [Pg.7]    [Pg.12]    [Pg.18]    [Pg.306]    [Pg.7]    [Pg.194]    [Pg.195]    [Pg.231]    [Pg.247]    [Pg.196]   
See also in sourсe #XX -- [ Pg.291 ]




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