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Valin

A likely exit path for the xenon was identified as follows. Different members of our research group placed the exit path in the same location and were able to control extraction of the xenon atom with the tug feature of the steered dynamics system without causing exaggerated perturbations of the structure. The exit path is located between the side chains of leucines 84 and 118 and of valine 87 the flexible side chain of lysine 83 lies just outside the exit and part of the time is an obstacle to a linear extraction (Fig. 1). [Pg.142]

Water-soluble globular proteins usually have an interior composed almost entirely of non polar, hydrophobic amino acids such as phenylalanine, tryptophan, valine and leucine witl polar and charged amino acids such as lysine and arginine located on the surface of thi molecule. This packing of hydrophobic residues is a consequence of the hydrophobic effeci which is the most important factor that contributes to protein stability. The molecula basis for the hydrophobic effect continues to be the subject of some debate but is general considered to be entropic in origin. Moreover, it is the entropy change of the solvent that i... [Pg.531]

The influence of a large number of oc-amino acids on the values of and k at have been determined. These a-amino acids included glycine, L-valine, L-leucine, L-phenylalanine, L-tyrosine, L-tryptophan, NOrmethyl-L-tryptophan (L-abrine), N-methyl-L-tyrosine, N,N-dimethyl-L-tyrosine and p -me thoxy-N-me thyl -L -phenyl al anine. [Pg.175]

Under the right conditions, hydrolysis of the eyanide A oceurs during the reaction to give the amino acid B. How could you make the amino acid Valine (TM 138) ... [Pg.44]

Outline the steps in a synthesis of valine from 3 methylbutanoic... [Pg.1121]

Outline the steps in the synthesis of valine from diethyl... [Pg.1122]

Digestion of the tetrapeptide of Problem 27 13 with chy motrypsin gave a dipeptide that on ammo acid analysis gave phenylalanine and valine in equimolar amounts What ammo acid sequences are possible for the tetrapeptide ... [Pg.1131]

ANTIBIOTICS - BETA-LACTAMS - PENICILLINS AND OTHEPE] (Vol 3) d-(L-a-Aminoadipyl)-L-cysteinyl-D-valine (LLD-ACV) [32467-88-2]... [Pg.41]


See other pages where Valin is mentioned: [Pg.28]    [Pg.416]    [Pg.546]    [Pg.453]    [Pg.562]    [Pg.553]    [Pg.437]    [Pg.439]    [Pg.439]    [Pg.86]    [Pg.87]    [Pg.102]    [Pg.232]    [Pg.183]    [Pg.1111]    [Pg.1113]    [Pg.1114]    [Pg.1119]    [Pg.1122]    [Pg.1122]    [Pg.1130]    [Pg.1150]    [Pg.1150]    [Pg.1153]    [Pg.1253]    [Pg.581]    [Pg.612]    [Pg.899]    [Pg.899]    [Pg.899]    [Pg.899]    [Pg.906]    [Pg.1179]    [Pg.363]    [Pg.739]    [Pg.290]    [Pg.20]    [Pg.41]    [Pg.160]    [Pg.1045]    [Pg.1045]    [Pg.1045]    [Pg.1045]   
See also in sourсe #XX -- [ Pg.505 , Pg.563 ]

See also in sourсe #XX -- [ Pg.402 ]

See also in sourсe #XX -- [ Pg.402 ]




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2-Oxoisovalerate as precursor to valine

A valine

A-Aminoadipyl-cysteinyl-valine

A-methyl valine

Acetolactate synthase valine synthesis

Alanine-valine structural

Alanine-valine structural change

Amino acid degradation valine

Amino acid valine

Amino acids valine replaced

Amino valine

Amino-acid residues valine

Biosynthesis valine

Cysteinyl-valine

D-Valine

DL-Valine

Dehydro valine

Dehydrogenase valine

Di-Valine

Esters formed from valine

Geometry valine

Glucose with valine

Glutamine valine

Glycyl-L-valine

Hydroxyl radical valine

Isoleucine-valine enzyme, biosynthetic

J Valine

L Valine

L-valine hydrochloride

Leucine following alanine-valine

Leucine, and Valine

Leucine-isoleucine-valine binding protein

Loading tests, metabolic valine

Maple Valine

Metabolism of valine, leucine, isoleucine, and lysine

Methyl group of valine

Muscle valine

N- valine

N-Benzyl-L-valine

N-Lauroyl-L-valine

N-Methyl-L-valine

Nor valine

Of valine

Plasma valine

Poly-L-valine

Protein hydroperoxides valine

Rearrangements in the biosynthesis of valine and isoleucine

S- valine

Secondary Products Originating from L-Valine

Sorption of Valine on Montmorillonite

Spectra valine

Succinate from valine

T.-Valine

Urine valine

Valin Hydrochlorid

Valine

Valine (Val

Valine (Val biosynthesis

Valine (Val branched fatty acids from

Valine (Val catabolism of, scheme

Valine (Val scheme

Valine (revised)

Valine 692 / INDEX

Valine Biosynthesis Share Four Enzymes

Valine V-acyl-2-oxazolidone from

Valine Valinol

Valine acid intermediates

Valine activating enzyme

Valine alkylation

Valine analogs

Valine anhydride

Valine asymmetric reduction

Valine biochemical structure

Valine bislactim ethers from

Valine borane modifier

Valine carbon catabolism

Valine catabolic pathway

Valine catabolism

Valine characterisation

Valine chemical structure

Valine chiral auxiliary from

Valine codons

Valine cytochrome

Valine deamination

Valine deficiency symptoms

Valine degradation

Valine derivatives

Valine dipeptide

Valine discovery

Valine enantioselective aldol cyclizations

Valine essential amino acid

Valine ethyl ester

Valine excretion

Valine f-butyl ester

Valine following alanine

Valine formula

Valine hydroperoxide formation

Valine hydroperoxides, structure

Valine imine anion alkylation

Valine ionic properties

Valine isoelectric point

Valine isolation

Valine load test

Valine manufacture

Valine metabolism

Valine methyl ester

Valine methyl ester, -, hydrochloride

Valine methyl group

Valine mixtures

Valine molecular weight

Valine nucleus

Valine occurrence

Valine operon

Valine pathway

Valine plasma concentration

Valine polymer

Valine polypeptide, 0-form

Valine purification

Valine r-butyl ester

Valine racemization

Valine reactions

Valine relative hydrophobicity

Valine requirements

Valine residues

Valine residues cytochrome

Valine residues dehydrogenases

Valine resolution

Valine rotation

Valine scheme

Valine solubility

Valine synthesis

Valine transamination

Valine transition

Valine, 3-hydroxy

Valine, 827 table

Valine, acidity

Valine, characteristics

Valine, chiral

Valine, hydrogenation modifier

Valine, infrared spectrum

Valine, load

Valine, load metabolism

Valine, oxidation

Valine, protonated

Valine, structure

Valine-3-methyl-2-oxovalerate

Valine-derived catalysts

Valine-derived formamide

Valine-gramicidin

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