1. Draw the structure for Deoxythymidine
2. Draw the structure for the polypeptide M-P-F-W
3. Draw the structure for the polypeptide H-D
1. Draw the structure for Deoxythymidine 2. Draw the structure for the polypeptide M-P-F-W 3. Draw...
Draw the structure of the following amino acids, at pH 9 i) F ii) P iii) H iv) E v) C vi) G vii) W viii) L
Draw the shear and moment diagrams for the structure. 20 KN w=25kN/m 2 m to A В с 4 m 2 m 4 m 4 m
Draw a model of a very small section of a polypeptide, just 3-4 amino acids in length. Relate this structure to the three main types of Secondary structure formed; α-helix, β-strand and turns. Be sure to show where each of the following is found on the polypeptide: amine groups, carboxyl Groups , R-Groups , peptide bond, φ angles, ψ angles.
1. f(m, n) w = w+1; n = 3; m = n * 10; main W = 0; int z[] = {10, 20, 30}; f(z[w], z[0]); print (z[w], z[0]); Given the code above, what is the output of the program if the values are passed by: a) Value. b) Value-result and address of z[w] is computed at the time of the call. c) Reference. d) Name. (Note: The order of evaluating the parameters of a subprogram are from left to...
4. Write out the 10 structure for the following polypeptide: он он HyN-CH-C-N-CH-C-N-CH-COO CH2 CH-OH CH C-NH2 CH3 COO 5. Illustrate the possible 2° structure interactions in the following polypeptide: R. 6. Identify the type of 3° structure interaction that will occur between the following pairs of amino acids: a) Aspartic acid and lysine b) Serine and tyrosine c) Leucine and valine d) Cysteine and cysteine 7. Draw out the products of the hydrolysis of the following polypeptide: HsN CH-C-N-C-C-N-C-C-N-CH-C-N-CH-COo...
Homework H26.B Given: A sign/pole structure is acted up by three forces F, P and W, in the –y, -z and –y directions, respectively. Find: Determine internal resultants acting on section OB of the pole at location B. For this problem, use the following parameters: W = 800 lb, F = 600 lb and P = 1200 lb. The answer will be in terms of h and L.
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.
Deduce the primary structure of the polypeptide described: 1) N-terminal residue analysis Result: Isoleucine 2) Protease digestion followed by Edman degradation sequencing (refer to textbook for specificity information). A) Trypsin Results: T-1 T-2 T-3 TGVDIQCCSTDNCNPFPTR VDLGCAATCPTVK DCPNGHVCYTK CEITPDITSK TWCDAFCSIR T-4 T-5 T-7 T-8 T-9 T-10 T-11 IR K P R R B) Chymotrypsin Results: C-1 C-2 C-3 CSIRGKRVDLGCAATCPTVKTGVDIQCCSTDNCNPE ITPDITSKDCPNGHVCY PTRKRP CDAF TKTW IRCE C-5 C-6 To answer the question, place the polypeptide fragments resulting from chymotrypsin digestion in the appropriate...
please answer 4. Secondary structure (a-helix): The image below is of a polypeptide in secondary (2) structure level of protein folding. Specifically it is of an a-helix. Use the image on the left to answer the questions a-e below. The image on the right is to help with question "f' only. a. Name the specific bond/interaction indicated by the dotted lines. b. Is this bond/interaction covalent or non-covalent? c. Is this bond/interaction permanent or transient? d. What parts of the...
1. Draw the structure of 4-chloro-2-methylcyclohexanol. 2. Draw the structure of 3-chloro-2-iodo-N,N-dimethylaniline. 3. Draw the structure of the products of the basic hydrolysis of 2-propyl pentanoate using sodium hydroxide.