What is the amino acid sequence of bradykinin? (5 pts) 2. Given four D-aldopentoses A, B,...
Compound A is a D-aldopentose that can be oxidized to an optically active aldaric acid B. On Kiliani-Fischer chain extension, A is converted into C and D; C can be oxidized to an optically inactive aldaric acid E, but D is oxidized to an optically active aldaric acid F. What is the structure of compound C? PLEASE SPECIFY WHAT IS COMPOUND C Also please take into account the instructions for the answer shown Compound A is a D-aldopentose that can...
Can you please explain this? Thank you. 14) An L-aldohexose, X, is treated with nitric acid to yield optically inactive aldaric acid (a diacid). The same L-aldohexose is subjected to Ruff degradation and the degradation product is oxidized with nitric acid to produce another optically inactive aldaric acid. What is a possible structure of L-aldohexose X? он он он он НОЕНН-Нон нон нон н -он н -он нон но -н НЕОН нон но -н но-н но -н но -н но-н...
Please answer in full An unknown pentose (C_5H_10O_5) A is treated with conc. HNO_3 giving optically inactive diacid B. Kiliani-Fischer chain elongation of A results in the formation of two epimeric hexose sugars, C and D, whose diacids (from HNO_3 oxidation) are both optically active (E and F, respectively). When subjected to the Fisher sequence (C1 - C6 interchange), hexose D affords L-glucose. Treatment of pentose A with aqueous bromine gives G, which undergoes decarboxylation in the presence of iron...
11.a) Draw the open chain (Fischer) structure of D-altrose. (1pt) (b) How many chiral centers are in D-altrose? ______ (1pt) (c) What is the maximum number of possible stereoisomers whch can exist for D-altrose? _____ (1pt) (d) Draw L-altrose in open chain form (use Fischer projection) – you may use the space above. (1pt) (e) Use the information above to draw a Haworth projection for alpha-D-altropyranose. (2pt) Ruff degradation on a monosaccharide causes C1 to be lost as carbon dioxide,...
5. D-sorbital is found in 'sugar-free' chewing gum. It is formed by reducing D-glucose with NaBH Draw the structure of D-sorbital. s. (4 pts) Classify the following amino acid as polar, non- polar, acidic, or basic: 6 (4 pts) The amino acid threonine (thr) has two chiral carbons. Draw a Fischer projection of the 2S,3S configuration of threonine. キ 7.(11 pts) Draw the tripeptide lys-asp-ser at physiological pH 8. (8 pts) The pK, values for aspartic acid are 2.10, 9.82...
Question 5 2 pts Given the following mRNA codon sequence, what will be the resulting amino acid sequence after translation? 5'| AUG - GCG-GGU - GCC - UUA - UGA13' sequenci [Select] [Select] Thr Ala [Select] Met lle Tyr Leu [Select] codon table.png
can you please explain this answer 7. (2 pts) is the given amino acid (histidine) below L or D configured and is it the natural/common or the unnatural/uncommon form? AUDroble NH2 A) D, natural C) L, natural B) D, unnatural D) L, unnatural histidine OH
2. (7 pts) What is the sequence of the following HEXAPEPTIDE? *PROVIDE WORK/ANSWER for B-F! (Use deductive reasoning) Observations from Sequencing Experiments: A. The Sequence contains the following amino acids: Y, R, M, K, G,D B. Reaction with 1-fluoro-2,4-dinitrobenzene yielded DNP-G. C. Treatment with chymotrypsin yielded two tripeptides. D. Treatment with trypsin yielded three dipeptides. E. Treatment with carboxypeptidase yielded methionine. F. N-terminal sequencing of one of the chymotrypsin-produced tripeptides yielded DNP-K Explanation and summary of protein sequencing techniques •...