In the box below, draw the structure of the tripeptide Gly-His-Cys as it would appear at pH 7.0.
In the box below, draw the structure of the tripeptide Gly-His-Cys as it would appear at...
7a. Glutathione (GSH) is a cys-containing tripeptide with the sequence Y-glu-cys-gly. The y- glu-cys means that the first peptide bond is between the y-carboxylate group and not the a-carboxylate group that is more typical. Draw the structure of glutathione. 75. GSH helps cells cope with oxidative stress (e.g. peroxides) by becoming oxidized in place of other biomolecules: 2 GSH +R-O-O-H (a peroxide) -> GSSG + ROH (an alcohol) + H2O Draw the structure of oxidised glutathione.
Part A Provide the structure of the tripeptide val-gly-ser at pH 2 Draw the molecule on the canvas by cho sing buttons from the T The single bond is active by default. 12D L3
Draw the structure for Asp-Cys-Gly-Tyr. Draw the molecule on the canvas by choosing buttons from the Tools (for bonds an Templates toolbars, including charges where needed. (Express vour answer Enter the one-letter abbreviation for Asp-Cys-Gly-Tyr. Spell out the one-letter abbreviation for the peptide. Draw the structure for Asn-Tyr-Asp-Glu-Tyr. Draw the molecule on the canvas by choosing buttons from the 1 Templates toolbars, including charges where needed. (Express y Trna Aqu. t2D A Part D Enter the one-letter abbreviation for Asn-Tyr-Asp-Glu-Tyr....
Draw the tripeptide gly-lys-glu as it exists under physiological pH. Write the reaction for the hydrolysis of this tripeptide into the individual amino acids. Be sure to show the reaction conditions and the final products that result under these conditions.
1. Draw the structure of the following tripeptide as it would exist at physiological pH. Be sure to indicate any positive or negatively charged groups in the tripeptide. lle-Lys-Tyr
1. A.) Draw the tripeptide corresponding to Cys-Met-Arg with the correct stereochemistry for L-amino acids found in most proteins. B.) Draw the principle structural form the amino acid with the one-letter code of E. Assume that the pH of the solution is 7.4.
5. Draw the structure of a polypeptide with the sequence N–Thr-Val-Pro-C at pH 7.0. This tripeptide is found in the chemotherapeutic agent dactinomycin.
please explain each question thoroughly. thanks Question 3: Arg-Cys-Met-Ala-Cys-Gly-Arg-Pro-Asn-Tyr-Leu-Trp-Ala-Ile-His-Phe-Ser-Cys-Lys a. What would happen if this peptide were to be incubated with dinitrofluorobenzene (FDNB) followed by 6M HCl hydrolysis at 1100C for 24 hrs. What labeled product(s) would be detected? Consider the following pepide: What would happen if the peptide were treated with CNBr? What would the products be? Why? b. What would happen if the peptide were treated with chymotrypsin? What would the c. products be? Why? Arg-Cys-Met-Ala-Cys-Gly-Arg-Pro-Asn-Tyr, Leu-Trp, Ala-Ile-His-Phe,...
Draw the chemical structure of the following tripeptide: Asn - His - Glu. Point out all locations in this peptide that carry a charge.
Calculate the pI for this peptide. Gly Asp Lys Cys Glu His Met Table 1. Group pka c-teminus 3.5 his 6.0 n-terminus 9.0 lys 10.5 asp/glu 4.0 cys 8.4 tyr 10.5 arg 12.5