(a)
Interpretation:
The percentage of α-amino group of lysine will be protonated at its
Concept introduction:
The isoelectric point (
The value of
If the amino acid has no ionizable side chain, then the
If the amino acid has ionizable side chain, then the
The
(b)
Interpretation:
The percentage of β-amino group of lysine will be protonated at its
Concept introduction:
The isoelectric point (
The value of
If the amino acid has no ionizable side chain, then the
If the amino acid has ionizable side chain, then the
The
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ORGANIC CHEMISTRY
- Give typed solution only Which of the amino acids shown represents the structure of Ile at pH 10?arrow_forwardPlease help me with the following 1) sketch a phosphodiester bond 2) Make the two amino from the image below. And contrast the polarity of the side chainsarrow_forwardWhat is the name of this amino acid side chain and it's 3 letter abberivation? How do you find out what amino acid this is?arrow_forward
- Glutamic acid is a naturally occurring α-amino acid that contains acarboxy group in its R group side chain. (Glutamic acid isdrawn in its neutral form with no charged atoms, a form that does not actually exist at any pH.) a.) What form of glutamic acid exists at pH = 1?b.) If the pH is gradually increased, what form of glutamic acid exists afterone equivalent of base is added? After two equivalents? After threeequivalents?c.) Propose a structure of monosodium glutamate, the common flavorenhancer known as MSG.arrow_forwardUsing resonance structures, show why the amino group is activating. Consider an attack by the electrophile E+ at the para position.arrow_forwardFor each amino acid [RCH(NH2)COOH], draw its neutral, positively changed, and negatively charged forms. Which form predominates at pH = 1, 6, and 11? What is the structure of each amino acid at its isoelectric point?a. methionine (R = CH2CH2SCH3)b. serine (R = CH2OH)arrow_forward
- is NH2 stays pronated at pH 1 for Proline in this amino acids chain??? what would be the NH2's charge of proline??? since my professor said that proline does not have a ionizable side chain, so would it be NH2 or NH2+ for a given amino acid At pH1, is it NH2-Pro-Leu-COOH??? or NH3-Pro-Leu-COOH?????arrow_forwardWhat is the correct structure for the peptide SGHKRY at pH 5.0?arrow_forwardLysine and tryptophan are two amino acids that contain an additional Natom in the R group bonded to the a carbon. While lysine is classified asa basic amino acid because it contains an additional basic N atom,tryptophan is classified as a neutral amino acid. Explain why thisdifference in classification occurs.arrow_forward
- Calculate an approximate pI for Peptide E-G-E-Aarrow_forwardHow many of the -amino acids shown in Table 26-1 contain aromatic rings? How many contain sulfur? How many contain alcohols? How many contain hydrocarbon side chains?arrow_forwardThe peptide structure attached below is most likely a? P.S. Both images are the same.arrow_forward
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