Given a Glucuromic acid omd glutathione for A) are impartantto PhaseI xemabistic melabolism B) sronder molecules mare lwater doluble desivatives 2are glucadde code amino acid desivatives E) Both A amd B
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Give a clear handwritten answer asap...Explain
![Griven a
Gilucuronic acid amd
glutathione e tor
r
: लपर
A] are impartantto
Phasett xenabiatic melabolism
B) sronder molecules more water deluble
desivatives
2 are glucode
2 0re amímo acid desivatives
E) Both A amd B
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- Second letter A UUU UCU) UC UCA UCG UAU UUC Phe UUA Tyr UGU UGCJ Ser UAA Stop UGA Stop A UAG Stop UGG Trp UUG Leu CAUHIS CUU CUC CUA CUG CCU* C ССА CCG CGU His САС Leu CGC Arg CGA Pro CAA Gin CGGJ Gln Which amino acid is carried by the TRNA with the anticodon 5'-UCA-3? ACU ACC ACA AAU AAC. AGU AGC AGA AUU Ser Asn AUC Ile A AUA Thr AAA Lys AAG Lys AGG Arg AUG Met ACG GAU GGU] GUU GUC GUA GUGJ GCU GCC GCA GCG GAC Asp Ala GAA GGC Gly GGA Val GAG Glu GGGJ Isoleucine. None-this is a stop codon. Aspartic acid. Histidine. IV. Leucine O V. Third letter UCAG UCAG UCAG First lettertide c lirectir as ques ar to t synthr direct s, the secon aft 43. Peptide bond formation has a positive AG. What is ATP's role in making protein synthesis favorable?Nucleic Acids Convey polypeptide c' minal directi This ques similar to t' carboxy-ter- hesis ing synth to direct sis, the Secon yase aft e genetic groups of 44. Why is ATP important to protein function, and how is it used to accomplish this? which st is. The m fatthaei, synthetic able of r ataining r thus mus ucleotid h of mor Cwas the chemis re critir a 1966 ponded han our PROT mine the s tetail sizer
- Wild type SSL2 reference sequence from amino acid 621 through 680 621 Lys Met Gly Lys Pro Phe Ile Tyr Gly Ser Thr Pro Gln Gln Glu Arg Met Asn Ile Leu 640 1861 AAA ATG GGA AAA CCA TTT ATT TAT GGT TCC ACA CCA CAA CAA GAG CGT ATG AAC ATT CTG 1920 641 Gln Asn Phe Gln Tyr Asn Asp Gln Ile Asn Thr Ile Phe Leu Ser Lys Val Gly Asp Thr 660 1921 CAA AAT TTC CAG TAC AAT GAC CAA ATC AAT ACC ATA TTT CTA TCA AAA GTT GGT GAT ACT 1980 661 Ser Ile Asp Leu Pro Glu Ala Thr Cys Leu Ile Gln Ile Ser Ser His Tyr Gly Ser Arg 680 1981 TCC ATC GAT TTA CCA GAA GCT ACC TGT TTA ATT CAA ATA TCT TCG CAC TAT GGG TCT CGT 2040 Candidate mutant SSL2 sequence from amino acid 621 through 680 621 Lys Met Gly Lys Pro Phe Ile Tyr Gly Ser Thr Pro Gln Gln Glu Arg Met Asn Ile Leu 1861 AAA ATG GGA AAA CCA TTT ATT TAT GGT TCC ACA CCA CAA CAA GAG CGT ATG AAC ATT CTG 641 Arg Asn Phe Gln Tyr Asn Asp Gln Ile Asn Thr Ile Phe Leu Ser Lys Val Gly Asp Thr 1921 CGA AAT TTC CAG TAC AAT GAC CAA ATC AAT ACC ATA TTT CTA TCA AAA GTT GGT GAT ACT…Is phosphate H2PO4 non polar or polarSubjecting this peptide to trypsin would result in L-M-F-V-W-E-Q-A-P-S-P O A. Lys and Met-Phe-Val-Trp-Glu-Gln-Arg and Pro-Ser-Pro OB, Leu-Met-Phe-Val-Trp-Glu-Gin-Ala-Pro-Ser-Pro Leu and Met-Phe-Val-Trp-Glu-Gln-Arg-Pro-Ser-Pro OC. Op. Lys and Met-Phe-Val-Trp-Glu-Gln-Ala-Pro-Ser-Pro Leu and Met-Phe-Val-Trp-Glu-Gin-Arg-Pro-Ser-Pro OE.
- The peptlde bradykinln is a nonapeptlde. Give the name of the peptide (shown below) by namlng the amlno aclds from the N-terminal to the C- terminal. Use the long name, the 3-letter abbreviation and the 1-letter abbreviation. What is the pl of this peptide? Name Compositon Fxnction LOcalizatio Bradykinl Inflammatio Different n and H N vasodilation Cells HNH n Animal H. HNH H NH он HN N HO. The following diagram shows the biosynthesis of B12 coenzymes, starting with the vitamin. DMB is dimethylbenzimidazole. (a) What one additional substrate or cofactor is required by enzyme B? (b) Genetic deficiency in animals of enzyme C would result in exces- sive urinary excretion of what compound?1. The amino acid sequence for the protein lysozyme is given below. Estimate the isoelectric point for lysozyme protein. The pK, values are provided in Table 3.1. KVFGRCELAAAMKRHGLDNYRGYSLGNWVCAAKFESNFNTQATNRNT DGSTDYGILQINSRWWCNDGRTPGSRNLCNIPCSALLSSDITASVNCAKK IVSDGNGMNAWVAWRNRCKGTDVQAWIRGCRL Here's the sequence in this form: LYS VAL PHE GLY ARG CYS GLU LEU ALA ALA ALA MET LYS ARG HIS GLY Table 3.1 Typical pk, values of ionizable groups in proteins Group Acid Typical pK, Base Terminal a-carboxyl 3.1 group Aspartic acid Glutamic acid 4.1 N. Histidine 6.0 -N + H Terminal a-amino group 8.0 Cysteine 8.3 Тутosine 10.9 + H Lysine 10.8 H H. + N-H Arginine 12.5 N-H N-H Note: Values of pk, depend on temperature, ionic strength, and the microenvironment of the ionizable group. in
- L-Ala -NAM-NAG-NAM-NAG L-Ala D-Glu D-Ala DA Transpeptidase D-Ala DAP I D-Ala D-Glu I L-Ala NAG-NAM-NAG-NAM 21. Modification of the enzyme pictured (above) might result in resistance to A. quinolone B. streptomycin C. chloramphenicol D. penicillin E. trimethoprimDraw the peptide at a pH @1 of Cys-His-Glu-Met-Ile-Ser-Thr-Arg-TyrN- HO sta on e yor current pH the peptide? Explain your yor a) Based the charge state shown, what is a possible vahe amswer wsi'ng 2-3 sentences. Show the qull pH ramge yor this protonation otate 6) Hypo thesize a oingle amino acid substitution Cmutation) that wonld make Your amswer must include the which residue this lic You. peptide more hydrophi you would mutate and what new re sidue would take its place Include a 1 sentence explanation g your reasoning your
