Q1 - all the fragments can be found in the given sequence in option no 2. Further, option 3 and 4 can be eliminated coz it's given in question that, the sequence should contain, 2Arg molecules, and option 3 and 4 doesn't have that. So we are left with option 1 and 2. Out of these, the fragments, after partial hydrolysis, can be found in option no. 2 sequence. The order is also same. Hence 2ND OPTION is the CORRECT one.
Q2. Number of NMR signals are 5. The question can be solved by just counting the no. Of signals in all the molecules. Option 1 has 5 signals. Option 2 has 6 signals. Option 3 has 4 signals. And option 4 has 3 signals only. Hence the CORRECT option is OPTION NO 1.
A decapeptide that is part of an insulin-like peptide has the molecular formula: Asn, Arg(2), Ser(3),...
Arrange the following compounds by how fast they undergo hydrolysis in H20, fastest first: hom CI OCH2CH3 NH2 11 III | > || > III III > | > || OT> ||| > || Oil > I > III A decapeptide that is part of an insulin-like peptide has the molecular formula: Asn, Arg(2), Ser(3), Phe, Cys, Leu, Thr. After partial hydrolysis, the fragments are: Cys-Ser-Phe-Ser- Arg-Asn-Ser-Cys Thr-Leu-Arg Ser-Thr What is the sequence? Ser-Phe-Ser-Thr-Leu-Arg-Arg-Asn-Ser-Cys Arg-Asn-Ser-Cys-Ser-Phe-Ser-Thr-Leu-Arg Ser-Thr-Arg-Asn-Ser-Cys-Ser-Phe-Ser. Asn Thr-Leu-Arg-Asn-Ser-Cys-Ser-Phe-Ser-Phe A compound...
plz help Which aldehyde or ketone AND amine reactants are needed to complete the following reaction? CEO NaBH,CN Amine dil. H30+ N(CH3)3 NH(CH3 N(CH3)3 Predict the product(s) for the following reaction series: ОН -Br 1) NaH 2) ОН + -ONa A decapeptide that is part of an insulin-like peptide has the molecular formula: Asn, Arg(2), Ser(3), Phe, Cys, Leu, Thr. After partial hydrolysis, the fragments are: Cys-Ser-Phe-Ser- Arg-Asn-Ser-Cys Thr-Leu-Arg Ser-Thr What is the sequence? Ser-Phe-Ser-Thr-Leu-Arg-Arg-Asn-Ser-Cys Ser-Thr-Arg-Asn-Ser-Cys-Ser-Phe-Ser- Asn Arg-Asn-Ser-Cys-Ser-Phe-Ser-Thr-Leu-Arg Thr-Leu-Arg-Asn-Ser-Cys-Ser-Phe-Ser-Phe
5. Consider the following peptide: His-Ser-Gln-Gly-Thr-Phe-Thr-Ser-Asp-Tyr-Ser-Lys-Tyr-Leu-Asp-Ser-Arg-Arg-Ala-Gin- Asp-Phe-Val-Gln-Trp-Leu-Met-Asn-Thr a. What are the fragments, if it is cleaved by trypsin? b. What are the fragments, if it is cleaved by chymotrypsin? c. What are the fragments, if it is cleaved by pepsin?
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,...
10. The peptide shown has the amino acid sequence: A. Val-Ser-Ile-Glu-Lys B. Lys-Glu-Ile-Ser-Val C. Thr-Asp-Leu-Gln-Arg D. Val-Asp-Ile-Glu-Arg 11. Which of the following describes the entire three- dimensional structure of a single polypeptide? A. Secondary structure B. Quaternary structure C. Tertiary structure D. Primary structure 12. What is the primary driving force in the formation of protein tertiary structure? A. Energy released when additional ion pairs are formed. B. The exclusion of non-polar substances from aqueous solution. C. The formation of...
C,D, and E i need help with. 17. The following peptide forms part of Human Hemoglobin subunit gammaa Asp-Leu-Lys-Gly-Thr-Phe-Ala A) Which amino acids are likely to be on the side of peptid acids are likely to be on the side of peptide that faces the interior of the protein? Insert your answer leu, Gto.Pne, Ala B) Which are likely to be facing the aqueous environment? Insert your answer Asp, lys, Thr Draw the structure of the sequence at pH7.4. Using...