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aspartic

aspartic Sentence Examples

  • CH(NH 2) � Cooh, isoleucin, probably 0-aminocaproic acid, serin or a-amino-(-hydroxy propionic acid, aspartic acid or aminosuccinic acid, HOOC�CH 2 �CH(NH 2)�Cooh, glutaminic acid or a-amino-n-glutaric acid,HOOC� (CH 2) � CH(NH 2) � Cooh, diaminoacetic acid, a-O-diaminopropionic acid, lysin.

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  • Diazosuccinic ester, N2 C(C02C2H5)2, is similarly prepared by the action of nitrous acid on the hydrochloride of aspartic ester.

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  • Ital., 1887, 17, p. 126; 1888, 18, p. 457) synthesized the asparagines from the monomethyl ester of inactive aspartic acid by heating it with alcoholic ammonia.

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  • Hydrolysis by means of acids or alkalis converts the asparagines into aspartic acid; whilst on heating with water in a sealed tube they are converted into ammonium aspartate.

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  • metabolized in the body to its components: aspartic acid, phenylalanine, and methanol.

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  • This could be an activated water molecule as seen in aspartic proteinases or an amino acid side chain.

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  • In aspartic peptidases, the water molecule is directly bound by the side chains of aspartic residues.

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  • The predicted catalytic serine, histidine and aspartic acid residues are shown in ball-and-stick representation.

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  • CH(NH 2) � Cooh, isoleucin, probably 0-aminocaproic acid, serin or a-amino-(-hydroxy propionic acid, aspartic acid or aminosuccinic acid, HOOC�CH 2 �CH(NH 2)�Cooh, glutaminic acid or a-amino-n-glutaric acid,HOOC� (CH 2) � CH(NH 2) � Cooh, diaminoacetic acid, a-O-diaminopropionic acid, lysin.

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  • It may be prepared by heating racemic acid (see TARTARIC Acid) with fuming hydriodic acid; by heating fumaric acid (q.v.) with water at 150-200° C.; by the action of nitrous acid on inactive aspartic acid; and by the action of moist silver oxide on monobromsuccinic acid.

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  • Diazosuccinic ester, N2 C(C02C2H5)2, is similarly prepared by the action of nitrous acid on the hydrochloride of aspartic ester.

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  • Ital., 1887, 17, p. 126; 1888, 18, p. 457) synthesized the asparagines from the monomethyl ester of inactive aspartic acid by heating it with alcoholic ammonia.

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  • Hydrolysis by means of acids or alkalis converts the asparagines into aspartic acid; whilst on heating with water in a sealed tube they are converted into ammonium aspartate.

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  • In aspartic peptidases, the water molecule is directly bound by the side chains of aspartic residues.

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  • The predicted catalytic serine, histidine and aspartic acid residues are shown in ball-and-stick representation.

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