ANS A. Isoelectric points of Serine,Aspartic Acid and Histidine are 5.68,2.98 and 7.60 respectively. Isoelectric point indicate that at pH equal to pI the molecule will not move under electric field because it will stay neutral. At pH above pI, the molecule will get deprtonated and acquire a -ve charge and so will move towards +ve electrode. When pH will be below pI the molecule will get protonated at N site and acquire a +ve charge and so will move towards -ve electrode.
So the ideal pH to separate all three amino acid will be 5.68 . At this pH , serine will not move, histidine will get protonated and move towards -ve electrode, and aspartic acid will get deprotonated and move towards +ve electrode.
ANS B. At pH = 5.68,
Serine HO-CH2-CH(NH2)-COOH Neutral
Aspartic Acid COO--CH2-CH(NH2)-COO-
Histidine
ANS C . I have already answer this at the beginning.You can draw the same and show it properly in your text.
) You have a mixture of serine, aspartic acid, and histidine. A) Find a pH value...
Write equations to show the ionic dissociations of the following amino acids: aspartic acid, histidine, serine, and lysine.
19) The form of dipeptide aspatylserine (Asp-Ser) obtained from two amino acids, aspartic acid and serine, whose structures are shown here, is HiN-CH-C-0HIN-CH-C-0 CH2 CH OH aspartic acid serine A HN-CH-C-o-N-CH-C-o CH OH CH2 coo -(H-C-o-H-c-o CH OH CH2 HIN CH-C-N-CH-C-O CH OH CH H-CH-CH CH CH OH coo- 20) Where is the peptide bond located in this dipeptide? serine valine a) the CO-NH joining serine and the valine b) the doubly bonded oxygen just left of center between the...
c) You place your pentapeptide into a buffer with a pH=4. What direction will your pentapeptide move: Circle the correct answer. (2 marks) It will not move. Towards the positive electrode Towards the negative electrode Briefly Explain why: (2 marks) d) You are trying to separate 2 other peptides from your pentapeptide. Peptide 1 is made up of the amino acids: ARKS Peptide 2 is made up of the amino acids: ADES At what pH would you be able to...
please explain thoroughly and show all work If you applied an amino acid mixture containing Histidine and Lysine onto ion exchange chromatography, at what pH should the chromatography be performed? Explain your reasoning. Lysine: pKa1-2.2, pKa2-9.1 and pKaR- 10.5 Histidine: pKa1=1.8, pKa2-9.3 and pKaR-6.0 If you applied an amino acid mixture containing Histidine and Lysine onto ion exchange chromatography, at what pH should the chromatography be performed? Explain your reasoning. Lysine: pKa1-2.2, pKa2-9.1 and pKaR- 10.5 Histidine: pKa1=1.8, pKa2-9.3 and...
1. Explain why polyaspartatic acid (a peptide containing only aspartic acid residues) does NOT form an alpha helix at pH 7.0 but can at pH 2. 6. 2. What kind of non-covalent interaction would the following pairs of amino acids have in the three dimensional structure of a protein at pH 7.0? a) His-Asp b) Tyr-Asp c) Val-Leu d) Trp-Gln 3. Explain how the difference in structure of hemoglobin and myoglobin contribute to their different functions.
6. At neutral pH, which of the following amino acids has a net positive charge, which has a net negative charge, and which is neutral? (Hint: Draw the various charged forms of each amino acid before deciding.) a) Aspartic acid b) Histidine c) Valine 7. Which of the following forms of aspartic acid would you expect to predominate at low pH, neutral pH, and high pH? a) 10_char Line HOC-CH-CH-CO- +NH, b) ._ança do OC-CH-CH-CO- NH2 HOC-CH.CH +NH
what is the net charge of the following amino acid? Draw the corresponding structure. 1. Serine at 5.8 2.Isoleucine at pH 1.0 and can you explain if there is math to do or how would I get the structure for different pH
1. draw the structure of amino acid lysine at pH=1.00 and pH=12.00. 2. find the overall charge of the amino acid at each pH. 3. what will be the overall charge on the peptide alanine-glycine-lysine-serine-aspartate at pH=1.00 and pH=12.00?
TABLE 5.1 PK values for amino acids 2.36 Amino acid Alanine Arginine Asparagine Aspartic acid Cysteine Glutamic acid Glutamine Glycine Histidine Isoleucine Leucine Lysine Methionine Phenylalanine Proline Serine Threonine Tryptophan Tyrosine Valine PK, PK₂ 2.34 9.69 2.17 9.04 2.02 8.80 1.88 9.60 1.96 10.28 2.19 9.67 2.17 9.13 2.34 9.60 1.82 9.17 9.60 9.60 2.18 8.95 2.28 1.83 9.13 1.99 10.60 2.219.15 2.09 9.10 2.83 9.39 2.20 9.11 2.32 9.62 2.36 9.21 5.56. Of the amino acids listed in Table...
i have no clue what amino acid this unknown is . maybe serine ?? pleade help! i also need to locate the eq points it can be from 1-3 points but atleasy 2 , the pka2 location , and the expermental molecular weight value. if you can label it on one of the graphs ( they are the same) the chocies are below ( it most likely will not be glycine ) . other data: unknown weight obtained was =...